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WO2003087248A1 - Water-dispersed powder coating, process for the production thereof, and color matching method - Google Patents

Water-dispersed powder coating, process for the production thereof, and color matching method Download PDF

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Publication number
WO2003087248A1
WO2003087248A1 PCT/JP2003/004677 JP0304677W WO03087248A1 WO 2003087248 A1 WO2003087248 A1 WO 2003087248A1 JP 0304677 W JP0304677 W JP 0304677W WO 03087248 A1 WO03087248 A1 WO 03087248A1
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WO
WIPO (PCT)
Prior art keywords
coating
water
paint
powder
dispersed
Prior art date
Application number
PCT/JP2003/004677
Other languages
French (fr)
Japanese (ja)
Inventor
Masakazu Teramoto
Tatuya Kawamura
Original Assignee
Kuboko Paint Co., Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2003011333A external-priority patent/JP2004224833A/en
Application filed by Kuboko Paint Co., Ltd. filed Critical Kuboko Paint Co., Ltd.
Priority to AU2003236237A priority Critical patent/AU2003236237A1/en
Publication of WO2003087248A1 publication Critical patent/WO2003087248A1/en

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02Emulsion paints including aerosols

Definitions

  • the present invention relates to a water-dispersible powder coating, a method for producing the same, and a toning method using the water-dispersible powder paint, and particularly to a coating having excellent coating workability and storage stability and having a smooth and excellent appearance.
  • the present invention relates to a toning method capable of finely adjusting the brightness and color to a desired brightness and color by a simple operation without causing color unevenness or the like.
  • a water-dispersed powder paint in which a powder paint component is dispersed in water is considered.
  • Japanese Patent Publication No. 11-34-34-32 and Japanese Patent Publication No. 11-150-34878 have been proposed.
  • Many of these water-dispersible powder coatings are prepared by melt-mixing a thermosetting resin or its pigment component at a temperature equal to or higher than the melting temperature but lower than the curing temperature, then coarsely pulverizing, and then finely pulverizing in a dry system. And a method of dispersing in water using a dispersing agent or the like, or a method of dispersing coarsely ground material in water together with a dispersing agent and then finely pulverizing by wet method.
  • the water-dispersible powder coatings disclosed in the prior art contain resin components constituting the water-dispersible powder coating in consideration of storage stability and uniformity of the coating film. It is said that the particle size of the particles is preferably small, and specifically, those having an average particle size (cumulative 50% particle size: D50) of 10 m or less are recommended.
  • the water-dispersed powder coating has poor storage stability because the resin powder, which is originally insoluble in water, is dispersed in water, and the powder components are liable to settle and separate during storage. In addition, cracking is likely to occur during heating and drying, and it is difficult to obtain a smooth coating film. For this reason, much research has been conducted on dispersants and surfactants for improving storage stability and coating film performance.
  • Japanese Unexamined Patent Publication (Kokai) No. 58-191 677 discloses a metal salt of a polycarboxylic acid, a diamine salt, an alkyl ether or an alkylphenyl ether of polyoxyethylene, a sorbitan fatty acid ester, or the like as a dispersant. Techniques for improving storage stability and coating film performance by adding an appropriate amount have been disclosed.
  • Japanese Patent Application Laid-Open No. 58-17757 discloses a nonionic surfactant having an HLB of 10 or less. A technique has been disclosed in which an agent is contained in an appropriate amount as a fluidity aid to suppress cracking and cracking.
  • H11-15034878 specifies the type of resin constituting the coating powder, a crosslinking agent, etc., as well as a nonionic thickener, a defoaming agent,
  • aqueous components including dispersants and water retention agents
  • Water-dispersible lacquers have been disclosed that provide transparent coatings of excellent performance for car bodies.
  • the solid content concentration of the paint is lowered to ensure fluidity, sagging and see-through of the substrate tend to occur, and the water-dispersed paint described in Japanese Patent Application Laid-Open No. 58-17557
  • the water resistance of the coating film is secured by using the selected surfactant, but the fluidity of the paint deteriorates as the powder particles become finer, and the surfactant is selected. Doing so alone does not ensure satisfactory liquidity.
  • the amount of the surfactant is increased to increase the fluidity, or the solid content concentration of the coating material is reduced, the puffiness is likely to occur as described above. Further, the addition of a large amount of a low HLB nonionic surfactant causes a serious defect that powder particles adhere to each other.
  • the transparent lacquer aqueous dispersion disclosed in Japanese Patent Application Laid-Open No. H11-5303478 can be used to convert a specific paint powder into a nonionic thickener, a surfactant and a dispersant. It is produced by wet dispersing in the coexistence of water, but it is pointed out that the finely divided coating powder tends to agglomerate, resulting in poor storage stability and poor water resistance of the coating film.
  • water-dispersed powder coatings are highly versatile and can be produced in a variety of small quantities, but when the color and lightness of the finished coating film is slightly different from the intended If the particle size and particle size distribution of the body paint are not precisely controlled, simply mixing the water-dispersed powder paint will cause color mixing and color unevenness, making it impossible to adjust the color. Therefore, in such a case, in order to readjust the color and brightness of the finished coating film, the water-dispersed powder coating is filtered or centrifuged to separate and dry the solid components. After blending the toning pigments and dyes, they must be heated and melted and then coarsely ground and finely ground again, which ultimately requires the same steps as preparing a new water-dispersed powder coating. become.
  • the present invention has been made by focusing on the problems of the prior art as described above. Eliminates the above-mentioned drawbacks of water-dispersed powder coatings, improves storage stability and coating workability as coatings, and is excellent in smoothness and gloss, and has no dullness
  • An object of the present invention is to provide a water-dispersed powder coating material that gives a beautiful coating film appearance and a useful production method thereof.
  • Another object of the present invention is to provide a toning method capable of easily performing toning using a water-dispersed powder coating even at a painting site or the like.
  • the water-dispersible powder coating material of the present invention which can solve the above-mentioned problems includes a coating resin, and has an average particle size (D50) of l to 30 ⁇ m, more preferably 5 to It is characterized in that the powder of 152 m is dispersed in water.
  • D50 average particle size
  • the particle size distribution of the powder in the water-dispersed powder coating material of the present invention is 50 m or more, more preferably 20% or more of the particles occupying 10 mass% or less, and 0.5 m or less, More preferably, the ratio of particles of 3 xm or less is 10% by mass or less.
  • the powder containing the coating resin having the above-mentioned particle size composition is prepared by adding water to an alkylene oxide adduct of a styrene / maleic acid copolymer and a surfactant.
  • the styrene / maleic acid copolymer is dispersed in an alkylene oxide.
  • Particularly preferred as an additive is a co-adduct of ethylene oxide and propylene oxide.
  • Non-ionic surfactants are particularly preferred as the surfactant, and among them, surfactants having an HLB in the range of 4 to 13 are preferred.
  • alkylene oxide adducts of alkyne diols having a weight-average molecular weight in the range of 300 to 300, and alkylene oxide addition of the alkyne diol.
  • Particularly preferred as the product is an ethylene oxide adduct of tetramethyldecinediol.
  • the content of the alkylene oxide adduct of the styrene / maleic acid copolymer is preferably from 0.1 to 1% by mass in terms of solid content with respect to the resin powder for coating, and the content of the surfactant is preferable. Is preferably in the range of 0.1 to 1% by mass in terms of solid content with respect to the resin powder for coating.
  • the preferred solid content concentration of the water-dispersed powder coating according to the present invention is 30 to 60% by mass, and the viscosity of the dispersion is 100 to 500 mPa ⁇ at 23 ° C. s,
  • the glass transition temperature of the paint resin powder is preferably in the range of 30 to 80 ° C.
  • the type of the resin for the coating material is not particularly limited, but is particularly preferably at least one selected from the group consisting of an epoxy resin, a polyester resin, and an acrylic resin.
  • a colored paint containing a pigment together with a paint resin may be used.
  • the production method of the present invention is positioned as a useful production method of a water-dispersed powder coating material having the above-mentioned properties.
  • the composition is constituted by melting and mixing raw material components for a coating material including a resin for a coating material and cooling the mixture. After the coarse pulverization, the coarsely pulverized material is dispersed in water in an amount of 0.3 to 2.3 times and treated with a circulation type bead mill to obtain a solid component having an average particle diameter (D50). Is 5 to 15 zm, the ratio of particles occupying 20 / m or more is 10% by mass or less, and the ratio of particles occupying 3m or less is 10% by mass or less. have.
  • the molten mixture is formed into a sheet, which is roughly pulverized or processed by the circulation type bead mill.
  • the pigment is melt-mixed and used, a water-dispersed colored powder coating can be obtained.
  • the powder containing the paint resin and the pigment as one body is made of water.
  • the average particle size (D50) of the powder is 5 to 15 m and the proportion of particles having a particle size of 20 m or more is 10 mass% or less.
  • One kind of toning paint is prepared, and at least one kind of the toning paint is mixed with the base paint in an appropriate amount in accordance with the brightness and Z or color of the base paint.
  • the feature is that the brightness and / or color of the base paint is finely adjusted.
  • the ratio (A / B) to (B) is preferably 1 or more and 5 or less, and the mixing amount of the toning paint with respect to the base paint is 0.1 mass based on the solid content. % Or more and 20% by mass or less.
  • FIG. 1 is a graph showing the relationship between the particle size of the resin powder for coating and the circulation time when a circulation type bead mill is used
  • FIG. 2 is a graph showing the number of passes when a multi-pass operation type bead mill is used.
  • 4 is a graph showing the relationship with the particle size of a coating resin powder.
  • the water-dispersed powder coating composition of the present invention contains a coating resin, and has an average particle size (D 50) of 1 to 30 m, more preferably 5 to 30 m. It is more preferable that the powder having a particle size of ⁇ 15 ⁇ is dispersed in water, and the particle size of the powder is 50 zm or more, more preferably 20 m or more. Is less than 10% by mass (more preferably 5% by mass or less, more preferably substantially 0%) and 0.5 // m or less, more preferably 3% or less. The proportion occupied by the fine particles is 10% by mass or less (more preferably 5% by mass or less, further preferably substantially 0%).
  • the styrene / maleic acid copolymer with an alkylene oxide adduct in combination with a surfactant to increase the fluidity as an aqueous dispersion.
  • a surfactant to increase the fluidity as an aqueous dispersion.
  • the average particle size (D 50) of the powder is too small, the above surfactant or the like must be added more than necessary, which may adversely affect the coating properties such as water resistance. .
  • the average particle diameter (D50) exceeds 30 and becomes excessively coarse, the powder components in the paint tend to settle during storage and the like, and not only does the handling of the paint deteriorate, but also the The texture of the film becomes coarse, making it difficult to obtain a smooth coating film appearance.
  • the particle size distribution of the powder affects the smoothness of the coating film, the filterability when preparing a water-dispersed paint, and the workability of coating, and occupies 50% of the solid component (powder).
  • the ratio of particles having a particle size of at least m is 10% by mass or less, and the ratio of particles having a particle size of 0.5 ⁇ m or less (more preferably 3m or less) is 10% by mass or less.
  • the ratio of particles falling within the preferred particle size range of 0.5 ⁇ 1! 1 or more and 50 ⁇ 111 or less, more preferably 3 m or more and 2 m or less, is preferably 8%. It is desirably 0% by mass or more.
  • the unevenness interval is short and the coated film has a large unevenness height difference, and it is difficult to obtain a uniform finished coated film.
  • the amount of coarse particles of 50 zm or more exceeds 10% by mass, the filter is likely to be clogged in the filtration step at the time of paint production, and 0.5% If the amount of fine particles of less than 10% by mass (more preferably 3 m or less) exceeds 10% by mass, the fluidity of the paint tends to decrease and the coating workability tends to deteriorate.
  • the proportion of particles having an average particle diameter (D50) of 1 m or more and 30 m or less and 50 / im or more (more preferably 20 m or more) is 10 mass% or less, and 0.5 im
  • D50 average particle diameter
  • the proportion of particles of less than 3 / xm (more preferably 3 / xm or less) is 10% by mass or less
  • problems such as deterioration of coating workability and handleability due to excessively high paint viscosity may occur.
  • No coating occurs, and the formed coating film has a more uniform and smoother appearance.
  • only impurities can be easily removed without causing clogging of the filter in the filtration step in the production of paint.
  • the solid content concentration of the water-dispersed powder coating used in the present invention is also a factor that affects coating workability and coating film characteristics, and is preferably 30 to 60. It is desirable to adjust to the range of mass%. By the way, the solid content concentration
  • the solid content concentration of the water-dispersed powder coating is preferably adjusted to 30% by mass or more and 60% by mass or less.
  • the water-dispersible powder coating of the present invention is obtained by dispersing a powder containing the coating resin in water in the presence of an alkylene oxide adduct of a styrene / maleic acid copolymer and a surfactant. It is preferred that
  • the alkylene oxide adduct of the styrene / maleic acid copolymer is a compound in which an alkylene oxide is added to a copolymer obtained by copolymerizing styrene and (anhydrous) maleic acid. Is a copolymer obtained by the method represented by the formula
  • r is an integer of 1 to 5
  • s is an integer of 5 to 20
  • t is an integer of 1 to 50
  • R is hydrogen, an alkyl alcohol residue having 1 to 20 carbon atoms, and a carbon number of the alkyl group.
  • Is 1 to 20 alkylphenol residues Group fatty acid residue with 8 to 40 carbon atoms, fatty acid amide residue with 8 to 40 carbon atoms, fatty acid amide residue with 8 to 40 carbon atoms, ester residue of glycerin or dalyserin and fatty acid Sorbitol or sorbitol or an ester residue of a fatty acid with sorbitol, a fatty acid alkanol amide residue having 8 to 40 carbon atoms, and the like.
  • This adduct is preferably a styrene / maleic acid skeleton constituting the main chain, an alkylene oxide chain added to an unneutralized carboxyl group and one of the carboxylic acid groups in the maleic acid unit contained in the skeleton, and particularly preferably.
  • a water-dispersed powder coating it provides high-quality coatings that have excellent storage stability and coating workability, are free from sagging, and have excellent performance in water resistance and coating smoothness.
  • the weight average molecular weight of the above-mentioned adduct should be in the range of 2,000 to 100,000, more preferably 100,000 to 50,000.
  • the molar ratio of styrene units to maleic acid units ranges from 0.2 to 1 for the former, and the co-addition molar ratio of propylene oxide ranges from 0.1 to 0.5 for ethylene oxide. It is better to use one.
  • the weight average molecular weight is too small, the adsorption ratio (carboxyl group ratio) to the powder particles and the alkylene oxide chain are small, so that the finely divided powder particles tend to aggregate and storage stability tends to deteriorate. If the weight-average molecular weight is too large, the alkylene oxide chain becomes too large to improve the storage stability, but the water resistance tends to deteriorate.
  • the proportion of ethylene oxide contained in the alkylene oxide chain becomes too large, the water resistance tends to decrease due to the increase in hydrophilicity.
  • the proportion of propylene oxide is too large, the hydrophobicity becomes too strong, the solubility in water is reduced, and the function as a dispersant is hardly exhibited effectively.
  • the ratio of styrene constituting the main chain increases, the fluidity of the coating material improves and the coating workability improves, but the adsorption ratio (the ratio of lipoxyl groups) to the powder particles and the alkylene oxide chain increase. As the particle size becomes smaller, the coating powder particles tend to agglomerate and storage stability decreases.
  • the ratio of maleic acid is too large, the number of alkylene oxide chains increases and the storage stability is improved, but the water resistance tends to be insufficient.
  • Alkylene oxide adducts of styrene / maleic acid copolymers satisfying these preferred requirements are, for example, trade names of Pick Chemical Co., Ltd.
  • the type of surfactant used in combination with the alkylene oxide adduct is not particularly limited, and various surfactants usable for general water-based paints, for example, anionic, cationic, amphoteric, and nonionic surfactants can be used. Various surfactants can be used.
  • anionic surfactants include fatty acid trienol amine amine salt, (linear) alkyl benzene sulfonate, ⁇ -sulfo fatty acid (methyl) ester alkali salt, and «-olefin sulfonate alkyl ether sulfate Alkali salts, monoalkyl phosphates Lauryl sulfate, acyl-methyl taurate, sodium salts of carboxylic acids, sulfate esters of higher alcohols, sulfated fatty acid esters, sulfated olefins, alkylnaphthalene sulfonates, para Examples thereof include a fin sulfonate and a higher alcohol phosphate, and as the above salts, a sodium salt and a potassium salt are preferably used.
  • Examples of the cationic surfactant include ammonium chloride, monoalkyl ammonium chloride, dialkyl ammonium chloride, trialkyl ammonium chloride, and cetyl chloride.
  • Methylammonium, etc., and examples of the amphoteric surfactant include amino acid-type amphoteric surfactants, bayone-type amphoteric surfactants, sulfate ester-type amphoteric surfactants, sulfonate-type amphoteric surfactants, and phosphorus Acid ester salt-type amphoteric surfactants are exemplified.
  • nonionic surfactants include alkyl polydarcosides, fatty acid alkanolamides, polyoxyethylene alkyl ethers, glycerin fatty acid esters, fatty acid esters of sorbitan and sorbitan, and fatty acid esters of sucrose.
  • Propylene glycol fatty acid ester higher alcohol ethylene oxide adduct, alkyl phenol ethylene oxide adduct, fatty acid ethylene oxide adduct, polyhydric alcohol fatty acid ester ethylene oxide adduct, higher alkylamine ethylene oxide Fatty acid amido ethylene oxide adduct, fatty acid ester of glycerol, fatty acid ester of pentaerythritol, alkyl ether of polyhydric alcohol, fatty acid amine of alkanolamines For example.
  • non-ionic surfactants are particularly preferably used in the present invention, and HLB having a HLB in the range of 4 to 13, more preferably 4 to 9 is preferred. Things.
  • nonionic surfactants particularly preferred are alkylene oxide adducts of alkynediols, and more specifically, ethylene oxide adducts of tetramethyldecinediol represented by the following general formula.
  • the average molecular weight is in the range of 300 to 300, more preferably in the range of 300 to 1000.
  • alkylene oxide adduct of alkynediol satisfying these requirements is For example, it can be obtained as a product name “Surfinol” series manufactured by Air Products.
  • the water-dispersed powder coating material of the present invention it is effective to use the above-mentioned alkylene oxide adduct of styrene / maleic anhydride copolymer and the above-mentioned surfactant in combination, and only one of them is used. In this case, it is difficult to obtain comprehensively excellent paint performance intended in the present invention.
  • the alkylene oxide adduct of the styrene / maleic acid copolymer and the surfactant are added to the resin powder for coating in a solid content.
  • each of them is contained in the range of 0.1 to 1% by mass in terms of conversion, and the use ratio of the alkylene oxide adduct of the styrene-maleic acid copolymer and the surfactant is the former 1 by mass ratio.
  • coating resin used in the present invention there are no particular restrictions on the type of coating resin used in the present invention, and known resins used for water-dispersed powder coatings, such as epoxy resins, polyester resins, acrylic resins, polyvinyl chloride resins, Polyethylene resin, polyamide resin, alkyd resin, amino alkyd resin, phenol alkyd resin, polybutadiene resin Silicone resin, isocyanate resin, melamine resin, fluorine resin, etc. can be used. These can be used alone or in combination of two or more as needed. .
  • resins used for water-dispersed powder coatings such as epoxy resins, polyester resins, acrylic resins, polyvinyl chloride resins, Polyethylene resin, polyamide resin, alkyd resin, amino alkyd resin, phenol alkyd resin, polybutadiene resin Silicone resin, isocyanate resin, melamine resin, fluorine resin, etc.
  • resins having a glass transition temperature of 30 ° C or higher, more preferably 40 ° C or higher, and 80 ° C or lower, more preferably 70 ° C or lower. is there.
  • the glass transition temperature of the resin is less than 30 ° C, not only the powder particles in the paint may cause blocking during storage or transportation, but also cause the fusion during mechanical pulverization to cause fine particles.
  • the glass transition temperature is too high, the fluidity at the time of baking is deteriorated, and the smoothness of the finished coating film tends to decrease.
  • the coating resin used in the present invention for example, the above-mentioned epoxy resin, polyester resin, acrylic resin, alkyd resin, polybutadiene resin, silicon resin, polyurethane resin, fluorine resin, etc.
  • a hydroxyl group-containing resin in which a hydroxyl group is introduced into the resin by a known method and a curing agent having a functional group that reacts with the hydroxyl group in the resin are combined, a curable paint by heat, ultraviolet light, or the like can be obtained.
  • suitable hardeners include amino resins (paints incorporating these are sometimes referred to as amino resin-curable paints), blocked polyisocyanate compounds (paints containing these are cured with isocyanates) Paints).
  • amino resin examples include those obtained by condensation or co-condensation of melamine, benzoguanamine, urea dicyandiamide, and the like with formaldehyde, and further modified with alcohols having 1 to 8 carbon atoms. Also, an amino resin containing a carboxylic acid group can be used.
  • Acids such as para-toluenesulfonic acid dodecylbenzenesulfonic acid, dinonylnaphthalenesulfonic acid, and dinoernaphthalenedisulfonic acid, and amine-neutralized products of these acids can be blended as a curing catalyst for the hydroxyl group and the amino resin.
  • the blocked polyisocyanate compound is a polyisocyanate compound obtained by blocking a free isocyanate compound with a blocking agent.
  • polyisocyanate compound having a free isocyanate group examples include aliphatic diisocyanates such as hexamethylene diisocyanate or trimethyl hexamethylene diisocyanate, and xylene diisocyanate.
  • organic diisocyanates such as cycloaliphatic diisocyanates such as isophorone diisocyanate, aromatic diisocyanates such as tolylene diisocyanate or 4,4'-diphenylmethane diisocyanate
  • cycloaliphatic diisocyanates such as isophorone diisocyanate
  • aromatic diisocyanates such as tolylene diisocyanate or 4,4'-diphenylmethane diisocyanate
  • blocking agent examples include oxime, phenol, alcohol, lactam, malonate, and mercapone.
  • a dissociation catalyst for the blocking agent a lead-based catalyst (such as lead 2-ethylethylhexanoate, lead benzoate, and lead oleate), and a tin-based catalyst (tetrabutyltin, tin octoate, tin oleate, tin tartrate) , Dibutyltin di (2-ethylhexylate), dibenzyltin di (2-ethylhexylate), dibutyltin dilaurate, dibutyltin diisooctyl maleate, dibutyltin sulfide, dibutyltin dibutoxide, etc.)
  • a catalyst such as zinc naphthenate
  • an antimony-based catalyst such as antimony trichloride
  • the above-mentioned resins such as polyester resin, acryl resin, alkyd resin, polybutylene resin, silicon resin, polyurethane resin, fluorine resin, etc.
  • a carboxyl group-containing resin into which a carboxylic acid group is introduced by a known method and a curing agent having a functional group that reacts with the carboxylic acid group in the resin are blended, a curable paint by heat or ultraviolet light can be obtained.
  • a polyepoxy compound (a paint containing this compound may be referred to as an epoxy curable paint) may be used.
  • a polyepoxy compound is a compound having at least two epoxy groups in one molecule. Typical examples thereof include ethylene glycol. Diglycidyl ether, neopentyldaricol ⁇ diglycidyl ether, glycerin Polyglycidyl ether of polyhydric alcohols such as diglycidyl ether, glycerintriglycidyl ether, diglycerin 'triglycidyl ether, hydrogenated bisphenol Adiglycidyl ether or bisphenol Adiglycidyl ether Examples include vinyl-based polymers having an epoxy group in the side chain.
  • ethoxy dimethyl silane ethoxy ethoxyl silane, trimethoxy propyl silane, trimethoxy butyl silane, trimethoxy phenyl silane, tetraethoxy silane, r-N- (2-aminoethyl And silane compounds such as aminopropyltrimethoxysilane and aminocaptopropyltrimethoxysilane.
  • the above-mentioned epoxy resin bis (phenol) -type glycidyl ether type, (meth) acrylic (co) polymer having glycidyl (meth) acrylate as an essential component, Etc.
  • a curing agent having a functional group that reacts with the epoxy group paints containing these are sometimes called epoxy-curable paints. It can be used as a paint that can be cured by heat or ultraviolet light.
  • Cationic polymerization catalysts include, for example, aryldiazonium salts, arylodenium salts, arylsulfonium salts, and the like.
  • Curing agents include, for example, polycarboxylic acid resins (acrylic resins) Resins, polyester resins, etc.), phenolic resins (nopolac-type phenolic resins, resole-type phenolic resins, etc.), polycarboxylic compounds (eg, adipic acid, sebacic acid, trimellitic acid, dodecane diacid, phthalic acid) Phosphoric acid) and amides (such as dicyandiamide).
  • a curing agent in addition to the above resin for paint, a curing agent, a curing accelerator, a flow regulator, a foaming inhibitor, an antistatic agent, an ultraviolet absorber, an antioxidant, which may be added to ordinary powder coating materials. It is, of course, possible to further improve the properties of the coating film by blending an agent.
  • acrylic acid-based copolymer copolymer of acrylic acid and acrylic ester
  • cellulose-based methylcellulose, hydroxyshethyl cellulose, propyl Cellulose, carboxymethylcellulose, etc.
  • polyurethane polyether-modified urethane compounds, etc.
  • polyamide polyamide
  • clay bentonite, heptrite, saponite, etc.
  • thickeners mineral oils and minerals
  • a defoaming agent such as a metal-based or silicon-based material, and also a heat-proofing agent that provides a stopping function to the metal to be coated (especially an iron-based alloy).
  • the water-dispersed powder coating of the present invention when a powder substantially consisting only of a coating resin is used, it becomes a coating for forming a so-called clear coating film.
  • a powder containing an appropriate amount of a pigment or a dye is used together with the resin for a coating, a colored coating having a color corresponding to the color tone or the like of the pigment or the dye can be obtained.
  • the pigments used here include coloring pigments and anti-pigmenting pigments.
  • coloring pigments include iron oxide such as red iron oxide, titanium oxide, titanium yellow, zinc white, zinc sulfide, lithium sulfide, antimony oxide, and cobalt.
  • Inorganic pigments such as blue and Rikiichi pump racks, quinacridone red, phthalocyanine blue, phthalocyanine green, permanent red, hanzaeroel, indian sable, brilliant
  • organic pigments such as first scarlet and variogen red. These can be used alone, or two or more can be used in combination as needed.
  • calcium carbonate, barium sulfate, barium carbonate, clay, talc, diatomaceous earth, silica powder, basic magnesium carbonate, alumina white, or the like may be used as an extender and an anti-glare agent.
  • the amount of the above pigments there is no limitation on the amount of the above pigments, and it may be arbitrarily selected according to the type of pigment to be used and the color tone, lightness, saturation, etc. required for the coating film. It is in the range of 1 to 80 parts by mass, more usually in the range of 2 to 70 parts by mass, per 100 parts by mass. It should be noted that when clear paint is used, the blending of the pigment is naturally omitted. If necessary, any dye may be used in addition to or instead of the pigment.
  • the water-dispersed powder coating of the present invention has excellent leveling properties and facilitates the formation of a coating film having higher smoothness, without causing the coating to be dull or transparent during spray coating. Therefore, the viscosity of the water-dispersed powder coating at 23 ° C. is not less than 100 mPas, more preferably not less than 200 mPas and not more than 500 mPas. It is more preferable to adjust the pressure to 400 mPas or less.
  • the paint viscosity is too low, the repelling property at the time of painting is good, but sagging occurs at the time of spray painting and cracking tends to occur at the time of heating and drying, making it difficult to obtain a uniform coating film. If the paint viscosity is too high, the sagging property will be good, but the workability of painting and the leveling property at the time of painting will deteriorate, and it tends to be difficult to obtain a smooth coating film.
  • the water-dispersed powder coating is a coating resin as a raw material or It is preferable to melt and mix the ingredients and dyes, cool and solidify, coarsely pulverize to an appropriate size (usually 1 mm or less), disperse them in an appropriate amount of water, and treat the aqueous dispersion with a circulation type bead mill or the like. Finely pulverize so as to satisfy the average particle size (D50) and the particle size distribution.
  • D50 average particle size
  • the recirculating bead mill circulates the coarsely ground dispersion liquid between a bead mill containing steel balls, ceramic balls, etc. as a crushing medium and a processing liquid tank to reduce the size of the powder in the dispersion liquid.
  • the progress of atomization depends on the material, size, filling amount, rotation speed of agitator / evening shaft, circulation flow rate of dispersion liquid, etc.
  • the degree of miniaturization can be arbitrarily adjusted by adjusting the operation time.
  • the powders in the aqueous dispersion may block (fuse) with each other. It is preferable to use a mold equipped with a cooling mechanism and to carry out the fine pulverization treatment while keeping the temperature of the processing solution low, since fine particles can be smoothly reduced without blocking. At this time, if the paint viscosity is too high, the temperature tends to rise during pulverization, which may cause blocking. Therefore, the paint viscosity is preferably suppressed to about 500 mPa ⁇ s or less at room temperature.
  • Fig. 1 is a graph showing the relationship between the circulating operation time and the particle size of the powder in the aqueous dispersion when performing the fine processing by the circulating bead mill. It is possible to easily obtain an aqueous dispersion having the following particle size configuration. On the other hand, even if a bead mill is used to refine the coarsely divided aqueous dispersion, when the multi-pass operation method is adopted, for example, the particle size changes stepwise with each pass, as shown in Fig. 2. It is difficult to adjust the particle size to a desired range. Therefore, in order to obtain the above-mentioned preferable average particle size (D50) and particle size distribution, it is desirable to use a circulation type bead mill.
  • D50 preferable average particle size
  • the particle size composition of the coarsely ground aqueous dispersion to be subjected to the circulation type bead mill is not particularly limited, and may be blended with the paint resin as necessary as described above.
  • the melt mixture of pigments may be used by appropriately pulverizing it.However, in order to narrow the particle size range after refining by a circulating bead mill as much as possible and to narrow the particle size distribution, the particle size range of the coarsely pulverized product It is also desirable to make the molten mixture as narrow as possible. For this purpose, it is preferable to use a coarsely crushed material obtained by processing the molten mixture into a sheet having an appropriate thickness (preferably around 1 mm) and then crushing it. desirable.
  • the coarsely crushed material when crushed after being formed into a sheet, the coarsely crushed material has a relatively uniform particle size as compared with crushed lump material, and it becomes easier to obtain coarsely crushed material having a narrow particle size distribution. As a result, the particle size composition of the finely pulverized product obtained by treating with a circulation type bead mill becomes more uniform.
  • a circulation type bead mill can be used to adjust the circulation time as appropriate according to the material, size, filling amount, rotation speed of the agitator shaft, circulation flow rate of the paint, etc. It is possible to easily obtain the water-dispersed powder coating material having the above-mentioned preferred particle size range and particle size distribution.
  • the alkylene oxide adduct of the styrene / maleic acid copolymer and the surfactant which are preferably blended when the resin powder for coating is dispersed in water, or other water-based additives, are used for coating. It may be contained in the compounding raw material when producing the resin powder, or added to the aqueous dispersion when coarsely pulverized, or may be added before or during the treatment by the circulating bead mill. Alternatively, it may be added after the bead mill treatment.
  • the thus obtained finely pulverized dispersion liquid is optionally pressurized in the final step.
  • the water-dispersed powder of the present invention is obtained by filtering foreign substances and impurities through a screen equipped with suction or an ultrasonic vibrating mechanism. Paint can be obtained.
  • the type of the object to be coated with the water-dispersed powder coating is not limited at all, and examples thereof include materials and parts used for automobiles, ships, trains, and the like, building materials such as outer panel materials, home electric appliances and office work. It is widely applied to the coating of materials such as components, outer shells, various containers, machine parts and members, pipes, various metal members used for cans and furniture, and plastic members. Can be
  • plastics examples include various known plastics irrespective of whether they are transparent or opaque, and specific examples thereof include polyolefins, polyesters, polyamides, polyurethanes, polyimides, and polycarbonates. These plastics can be appropriately surface-treated as necessary.
  • Metals include the most versatile iron-based metal materials such as steel and alloy steel, as well as non-ferrous metals and alloys such as aluminum, titanium, and brass, as well as zinc-plated steel and tin-plated steel.
  • Nozzle metal material chromate-treated phosphate-treated surface-treated steel material; applicable to aluminum or aluminum alloy materials that have been subjected to anodic oxidation, cathodic oxidation, sealing, etc. .
  • inorganic materials other than metal for example, it is also possible to apply to concrete, mortar, glass, etc., and it is possible to apply an appropriate surface treatment to these objects to be coated as necessary. .
  • the water-dispersed powder coating of the present invention often uses a thermosetting resin as a coating resin in order to enhance water resistance, chemical resistance, weather resistance, and scratch resistance.
  • baking treatment is performed.
  • any drying furnace such as an electric hot air drying oven, a gas hot air drying oven (indirect hot air a hot air blowing), a far infrared drying oven, or a jet heater drying oven is used.
  • Use for example, 120 to 350, more generally 140 to 25 O: 10 seconds to 60 minutes, and more generally, heat drying in about 5 minutes to 40 minutes do it. It is also effective to carry out preliminary drying prior to the above heat drying.
  • the method of applying the water-dispersed powder coating material of the present invention to an object to be coated or printed is not limited at all, and any of the conventionally known methods, electrostatic coating (rotary, air atomizing, airless, air assist, etc.) Type), electrodeposition coating, air spray coating, airless coating, natural roll coater coating, rib-roll coating, roller-coating, roller-coating, roller-coating, die coater coating, immersion coating, brushing Painting, screen Any method such as printing can be adopted.
  • the thickness of the coating film may be appropriately determined according to the performance and appearance required of the coating film, but is usually from 20 to 500 im, particularly preferably from 30 to 100 m. In the case of coating, it is of course effective to adopt a multilayer coating such as two-coating or three-coating.
  • the water-dispersed powder coating material of the present invention is obtained by uniformly and stably finely dispersing the resin powder for coating as described above.
  • the coating components other than the material to be coated are not included. Overspray is performed, but since redispersibility in water is good unless heat treatment is performed, powder paint sprayed with these bars is collected as powder at any time, or washed with water or the like. By collecting as a dispersion, it can be recovered.
  • the water-dispersed powder coating of the present invention can be used as an undercoat, an intermediate coating, or a top coating (including, for example, a coloring coating, a coloring base coating, and a clear top coating).
  • undercoat paint When used as an undercoat paint, besides the above-mentioned resin powder for paint, for example, coloring pigments, anticorrosion pigments, inorganic fillers, plasticizers, surfactants other than the above, defoamers, or other additives Agents (preservatives, solvents, etc.) can be added without any particular limitation.
  • coloring pigments, anticorrosion pigments, inorganic fillers, plasticizers, surfactants other than the above, defoamers, or other additives Agents can be added without any particular limitation.
  • the water-dispersed powder coating of the present invention is used as an intermediate coating, in addition to the above-mentioned resin powder for coating, for example, a coloring pigment, an inorganic filler, a plasticizer, a surfactant other than the above, Foaming agents and other additives (preservatives, solvents, etc.) can be added.
  • a coloring pigment for example, a coloring pigment, an inorganic filler, a plasticizer, a surfactant other than the above, Foaming agents and other additives (preservatives, solvents, etc.)
  • Foaming agents and other additives preservatives, solvents, etc.
  • the water-dispersed powder coating of the present invention is used as a top-coating colored coating, other than the above-mentioned coating resin powder, for example, a coloring pigment Inorganic fillers, plasticizers, surfactants other than the above, antifoaming agents, stabilizers, and other additives (such as anti-glazing agents, glazing agents, preservatives, anti-scratch agents, solvents, etc.) be able to.
  • a polyester resin-based curable paint acrylic resin-based curable paint from the viewpoints of weather resistance, finish properties, and the like.
  • the water-dispersible powder coating of the present invention is used as a clear top coating of a top coating type, other than the above-mentioned resin powder for coating, for example, a coloring pigment (to the extent that the base is not completely hidden), inorganic Fillers, plasticizers, surfactants other than the above, defoamers, stabilizers, and other additives (such as anti-glazing agents, glazing agents, preservatives, anti-scratch agents, solvents, etc.) may be added. it can.
  • a known curable coating, or a water-dispersible powder coating of the present invention is applied as a top coating
  • the top coat is cured at a predetermined baking temperature (when the undercoat and Z or the intermediate coat are not cured, they are cured simultaneously).
  • a known curable paint or the water-dispersible powder paint of the present invention is applied as a top coat
  • a baking treatment is performed at a predetermined temperature to cure the overcoat film (when the undercoat film and Z or the intermediate coat film are uncured, they are simultaneously cured).
  • a known curable paint is directly applied as an undercoat paint on the surface of a material such as metal,
  • a baking process is performed at a predetermined temperature to cure the top coat (or simultaneously cure the undercoat and / or intermediate coat if uncured).
  • curable paints used when carrying out each of the above film forming methods 1 to 3 include, for example, amino-curable resin paints, isocyanate-curable resin paints, acid epoxy-curable resin paints, and hydrolyzable resins.
  • Curable resin paints can be mentioned, and these can be used alone or in combination of two or more as needed if necessary.
  • curable paints may include additives conventionally incorporated into paints as needed, such as coloring pigments, extender pigments, metallic pigments, Color pearl pigments, flow control agents, anti-cissing agents, anti-sagging agents, ultraviolet absorbers, antioxidants, UV stabilizers, delustering agents, glazing agents, preservatives, curing accelerators, curing catalysts, An abrasion inhibitor, an antifoaming agent, a solvent and the like can be contained without particular limitation.
  • curable paints there is no particular limitation on the form of these curable paints, and any form of powder paint, solvent-free paint, water-based paint, organic solvent-based paint (including non-aqueous dispersion paint), etc. may be used. Absent.
  • curable coatings include, for example, electrostatic coating (rotary, air atomizing, airless, air assist, etc.), air spray coating, airless coating, brush coating, 'roll coating, dip coating, etc. It can be painted in any way.
  • top coat when made to be a clear finish, it is also possible to employ a three coat / three bake method, a three coat / two bake method, a three coat / one bake method, or the like.
  • the water-dispersed powder coating of the present invention has excellent storage stability, spray coating properties, and the like, and gives a coating film having a uniform, excellent surface appearance without unevenness or transparency. If the film is different from the intended color or lightness, or if the color or lightness is to be changed aggressively, the toning is performed in substantially the same manner as preparing a new paint as described above. It takes power.
  • a water-dispersed powder coating having the above characteristics is used as a base coating, and the color can be easily adjusted to any desired color and brightness without harming the above characteristics of the base coating. Also provides toning methods You.
  • the toning method defined as another configuration of the present invention is, as described above, a water-dispersed powder coating material in which a powder containing a coating resin and a pigment is dispersed in water, and an average particle size of the powder.
  • the diameter (D50) is 5 to 15 im and the proportion of particles of 20 m or more occupies 10 mass% or less, and the proportion of particles of 3 m or less occupies 10 mass% or less
  • the solid content concentration Is used as a base paint and as a method for finely adjusting the color and Z or lightness of the base paint
  • It is composed of a water-dispersed powder coating material in which a powder containing the same or different coating resin as the above-mentioned coating resin and a pigment is dispersed in water, and the powder has an average particle size (D50). 5 m or less (substantially free of coarse particles having a particle size of more than 10 m) and at least one toning containing white, black, red, blue or yellow pigments A paint is prepared in advance, and at least one of the toning paints is mixed with the base paint in an appropriate amount in accordance with the lightness and Z or color of the base paint. This is a toning method for finely adjusting the color.
  • the toning paint used in this case a water-dispersion type powder coating which is essentially the same as the above-mentioned base coating is used, but the minimum required characteristics required for the toning paint are used. It is preferable to use those having an average particle diameter (D 50) of the solid component contained in the coating material of 5 / m or less. The reason is that if the average particle size (D50) of the solid component contained in the toning paint exceeds 5 m, even if the amount of the toning paint is within an appropriate range, the toning after the toning is not possible. This is because a partial color tone difference (color unevenness) easily occurs on the coating film surface.
  • the average particle diameter (D50) In order to enhance the uniformity of the color and lightness of the paint after toning, it is desirable to use a paint having an average particle diameter (D50) of 5 m or less. However, if the average particle size (D50) is too small, the viscosity of the entire water-dispersed powder coating after toning becomes too high, which adversely affects the coating workability. Therefore, it is desirable to set the average particle diameter (D50) to about 2 m or more.
  • the average particle size (D 50) of the solid component in the toning paint is 5 m. Even if it is below, if more than 10 coarse particles are present in the solid component of the paint, color mixing will occur in the paint film after toning, and the particles of each color will be clearly distinguished and observed. It is difficult to obtain a toned coating film having a uniform color and brightness. Therefore, in order to obtain a uniform toned coating film without color unevenness or color mixture, it is required that the solid component of the coating material contains substantially no coarse particles exceeding 10%.
  • substantially absent does not necessarily mean that there is no “absence”, but a small amount of contamination is permissible as long as it is recognized as uniform by visual observation as a toning coating film. However, it is desirable that the amount of coarse particles exceeding 10 m in the total amount of the solid components is suppressed to about 2% by mass or less, more preferably about 0.5% by mass or less.
  • the pigment to be blended by selecting a pigment to be blended, at least one selected from five types of white, black, red, blue, and yellow, preferably at least five types is selected.
  • white and black toning paints are used to fine tune the lightness and darkness of the base paint
  • red, blue and yellow toning paints are colors. These three primary colors are used for fine adjustment of color.
  • the base paint is gray and you only need to make fine adjustments to light and dark, prepare two types of toning paints, white and black, and use one or two of them. You just have to color it.
  • No special technology is required for the method of producing the above-mentioned toning paint, and if the particle size composition of the solid components is sufficiently understood, a method substantially similar to the above-mentioned method of producing the base paint is required.
  • the dispersant, emulsifier, anti-settling agent and the like disclosed as additives to the base paint can be similarly added to the toning paint.
  • the characteristics of the toning method are utilized more effectively to achieve the toning.
  • the ratio of the average particle diameter (A) of the powder contained in the base paint to the average particle diameter (B) of the powder contained in the toning paint It is desirable to adjust the average particle size of each solid component so that (A / B) is in the range of 1 to 5.
  • the particle size ratio (A / B) is less than 1 means that the particle size of the powder component in the toning coating is equal to or relative to the particle size of the powder component in the base coating. In this case, the coating film after toning is likely to cause color unevenness and color mixture. Conversely, the particle size ratio (A / B) exceeding 5 means that the particle size of the powder component in the toning coating is too small compared to the particle size of the powder component in the base coating. In this case, the handling of paint and the workability of coating tend to be poor.
  • the mixing ratio of the toning paint to the base paint cannot be determined uniformly because it varies depending on the lightness and color of the base paint to be fine-tuned.
  • color mixing occurs due to particles of the base paint, and it is difficult to obtain a uniform coating film.
  • an anti-glazing agent as an additive other than those described above to make the appearance of the coating film opaque.
  • an anti-glazing agent there are no special restrictions on the type of glossy agent.
  • All known matting agents such as calcium carbonate, barium sulfate, barium carbonate, clay, talc, diatomaceous earth, silica powder, basic magnesium carbonate, alumina white, wax, plastic beads, etc. They can be used alone or in combination of two or more as necessary.
  • the glossing agent can be added at any stage before or after the above-mentioned toning paint is blended with the base paint to be toned. Although it varies depending on the type and degree of the required matte state, it is usually about 0.1 to 20% by mass based on the solid content of the paint. In other words, if you want to make the toning film a matte finish, add an appropriate amount of the matting agent to the paint before toning, in the toning process, or after finishing the toning, It is possible to obtain a toned coating film in a correspondingly matt state.
  • a special method is not required for the coating method and baking conditions using the water-dispersed powder paint toned by the above method, and the methods described above, including the type of the object to be coated, are not required. All objects to be coated can be applied.
  • the average particle size (D50), particle size distribution, nonvolatile content, measurement method of paint viscosity, coating workability, and evaluation method of coating film performance used in the following experiments were as follows.
  • Each water-dispersed powder coating is mixed with water until the solid content concentration becomes 5% by mass or less. After dilution, this diluted solution is treated with an ultrasonic homogenizer "Ultrasonic homogenizer 1" manufactured by Nippon Seiki Seisaku-sho, Ltd., and then a particle size distribution analyzer manufactured by Nikkiso Co., Ltd.
  • the particle size distribution is measured using "Microtrack MT330 EL", and the cumulative 50% particle size is determined as the average particle size (D50) from the particle size distribution curve.
  • the glass transition temperature (T g) of the powder particles was measured using a differential scanning calorimeter “DSC 6200” manufactured by Seiko Instruments Inc.
  • Spray coating is performed three times in a row, spray-dried at a setting time of 20 minutes at 20 ° C, and baked and dried. Is evaluated on a 5-point scale based on the following criteria.
  • the spray gun and spray air pressure are the same as those adopted in the above-mentioned evaluation of coating workability.
  • a water-dispersed powder coating is applied in the same manner as in the above-mentioned dullness test, and the test piece is allowed to stand at 20 ° C for 10 minutes. Then, the size of the unevenness on the surface is visually evaluated in five steps.
  • Coating is performed in the same manner as in the sagging evaluation described above, and the paint state of the obtained coating film is evaluated on a 5-point scale according to the following criteria.
  • the spray gun and spray air pressure shall be the same as those adopted in the above-mentioned evaluation of coating workability.
  • Print area is less than 1 Z 4 of total coating area
  • the area where the peeling occurred was 1/4 or more of the total coating area, but less than 12 2: The area where the peeling occurred was 1/2 or more of the total coating area, and less than 3/4. 1: The area where the peeling occurred was 3/4 or more of the total coating area.
  • Benzoin Degassing agent manufactured by MIWON COMMERCIAL
  • Imidazole a curing accelerator manufactured by Shikoku Chemicals
  • AER6002 Epoxy resin manufactured by Asahi Kasei Epoxy Co., Ltd.
  • AER6004 Epoxy resin manufactured by Asahi Kasei Epoxy Co., Ltd.
  • Acronal 4F Flow modifier manufactured by BASF
  • Titanium oxide CR97 Titanium oxide manufactured by Ishihara Sangyo
  • ADEKINOL UH_540 Viscosity adjuster manufactured by Asahi Denka Kogyo Co., Ltd.
  • ADEKANOL UH_752 Viscous adjuster manufactured by Asahi Denka Kogyo Co., Ltd.
  • Sudfinol 420 Air Products Surfactant
  • Dispersant manufactured by BIC CHEMI
  • AD H curing agent manufactured by Otsuka Chemical Co., Ltd.
  • Almatex PD 7310 Acrylic resin manufactured by Mitsui Chemicals, Inc.
  • Decanedicarboxylic acid a curing agent manufactured by Ube Industries
  • a C E MA T T HK 460 silica particles manufactured by DeDasa AG, Inc.
  • the raw materials are used in the ratio shown in Formulation 1 below, uniformly mixed with a high-speed mixer, then hot-melt kneaded and extruded using a melt extruder. Cool and solidify into a sheet of about 1 mm. This sheet is coarsely crushed by passing through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed polyester resin.
  • Polyester resin coarse powder (Note) 50.0 (parts)
  • Example 11 the solid content concentration of the water-dispersed powder coating material, the total amount of the additives [components other than the coarsely pulverized product and the dispersion medium (water)], and the dispersion time by the circulating bead mill were determined.
  • a water-dispersed powder coating material is prepared in the same manner as in Example 11 except that each is changed as shown in Table 1 below.
  • Table 1 shows the average particle size (D50) and the particle size distribution of the paint powder contained in each paint.
  • Example 1 Using the epoxy resin coarse powder obtained above, a water-dispersed powder coating was obtained in the same manner as in Example 11 below. Table 1 shows the properties and characteristics of the obtained water-dispersed powder coating. The T g of the powder particles was 62. Example 1 1 7
  • Example 18 A total of 100.0 The water-dispersed powder coating was obtained in the same manner as in Example 11 above using the coarsely pulverized acrylic resin obtained above. Table 1 shows the properties and characteristics of the obtained water-dispersed powder coating. The T g of the powder particles was 60 ° C. Example 18
  • the raw materials are used in the ratio shown in Formulation 5 below, uniformly mixed with a high-speed mixer, and then hot-melt kneaded using a melt extruder.
  • the mixture is extruded and cooled and solidified into a sheet with a thickness of about 1 mm.
  • This sheet-like material is coarsely ground through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely ground epoxy-polyester resin.
  • a water-dispersed powder coating was obtained in the same manner as in Example 11 below using the epoxy-polyester resin coarse powder obtained above.
  • Table 1 shows the properties of the obtained water-dispersed powder coating.
  • the T g of the powder particles was 65 ° C.
  • each of the obtained water-dispersed powder coatings was applied three times to SPCC steel plates (same as above) using a spray gun “W-100” (nozzle diameter: 1.3 mm) manufactured by Annest Iwata. Spray-painted and then placed in a hot-air dryer.
  • W-100 spray gun
  • the raw materials are used in the ratio shown in Formulation 1 below, mixed uniformly with a high-speed mixer, then hot-melt kneaded and extruded using a melt extruder, and cooled and solidified into a sheet with a thickness of about 1 mm. After the sheet material is coarsely crushed by passing through a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed material.
  • the average particle diameter (D50) of the powder particles is 13 m, and the content of coarse particles having a particle diameter of 50 m or more and fine particles having a particle diameter of 0.5 m or less is determined. Was also 0%.
  • the T g of the powder particles was 65 ° C.
  • Example 2-1 the surfactant shown in Table 3 was used in place of the surfactant "Safinol 420" used in the above Formulation 2, or "Disperbyk-19" in Formula 1 was used.
  • “Huichi Ichiren TG-7500 W” a dispersant manufactured by Kyoei Chemical Co., Ltd.
  • a polyester resin-based water-dispersible powder was used instead of “0”
  • Body paint was manufactured. The average particle size (D50), particle size distribution, and solid content of each water-dispersed powder coating material were adjusted to be the same as those in Example 2-1.
  • the surfactant used here is as follows:
  • An epoxy resin-based coarse powder is obtained in the same manner as in a-1) of Example 2-1 except that the raw materials are used in the ratio shown in the following formulation 3.
  • a water-dispersible powder coating was produced in the same manner as in Example 2-1 b-1), except that the raw material mixture used in the ratio shown in Formula 4 below was used.
  • Table 3 shows the properties and characteristics of the powder coating.
  • the average particle size (D 50) of the powder particles contained in the obtained powder coating material was 13 m, and the coarse particles having a particle size of 50 m or more and the particles having a particle size of 0.5 m or more were 0.5 m or more.
  • the content of fine particles below zm was 0% in all cases.
  • the T g of the powder particles was 62 ° C.
  • the average particle diameter (D50) of the body particles is 13 ⁇ m, and the content of coarse particles having a particle diameter of 50 ⁇ m or more and fine particles having a particle diameter of 0.5 / m or less
  • the powder particles had a T g of 62 ° C.
  • An acryl resin-based water-dispersed powder coating is obtained in the same manner as in Example 2-1 except that the raw material mixture having the ratio shown in the following formulation 6 is used.
  • Table 3 shows the properties and characteristics of the obtained water-dispersed powder coating.
  • the average particle size (D50) of the powder particles is 13 ⁇ m, and the content of coarse particles having a particle size of 50 m or more and fine particles having a particle size of 2.5 or less is determined. Was also 0%.
  • the T g of the powder particles was 60 ° C.
  • Coarse pulverized material (Note) 1 0 0.0 (Parts) Zion exchange water 1 0 0.0 "Adecanol UH—5 4 0" 0.4
  • Table 3 shows the properties and characteristics of the obtained water-dispersed powder coating.
  • the average particle size (D50) of the powder particles is 13 m, and the content of coarse particles having a particle size of 50 m or more and fine particles having a particle size of 0.5 m or less is as follows. All were 0%.
  • the T g of the powder particles was 60.
  • Paint 1 Production example (Polyester-based water-dispersed powder coating; for Examples) a-1) Production of coarsely ground polyester resin
  • the raw materials are used in the ratio shown in Formulation 1 below, uniformly mixed with a high-speed mixer, then hot melt kneaded and extruded using a melt extruder, extruded into a sheet with a thickness of about 1 mm, and cooled and solidified. Let it. This sheet is coarsely pulverized through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a polyester resin coarse powder.
  • the raw material mixture used in the ratio shown in the following formulation 2 was mixed with a 100. O kg by a disperser, and the mixture was wet-circulated bead mill with a built-in cooling mechanism [dispersion media: Nitkato with a diameter of 1.0 mm Zirconiapole "YTZ" manufactured by one company was charged into a circulation tank connected to 80% (4.4 kg) of the vessel volume], and the agitator disk was rotated at a peripheral speed of 1 O mZ s Fine grinding is performed by circulating while rotating. Next, the mixture is filtered through a 502 m filter to obtain a polyester resin-based water-dispersed powder coating material 1. Table 5 shows the properties and characteristics of the obtained water-dispersed powder coating material 1.
  • the average particle size (D50) of the powder particles in the powder coating material 1 was 13 / m, and the coarse particles having a particle size of 50 ⁇ m or more and the particle size of 0.5 m or less were used. In each case, the content of fine particles was 0%.
  • the T g of the powder particles was 65.
  • Formula 2 Coarse pulverized polyester resin (Note) 1 0.0 0 (parts) Ion exchange water 100 0 0
  • a polyester resin-based water-dispersed powder coating material 2 was obtained in the same manner as described above, except that in the production example of the coating material 1, the following formulation 3 was used instead of the formulation 2.
  • Polyester resin coarsely pulverized product (Note) 10.0 (Parts) Ion-exchanged water 1 00.0
  • Polyester resin coarsely pulverized product obtained by the above formulation 1 Paint 3 Production example (Epoxy resin water-dispersed powder coating; for example) a-2) Epoxy resin Manufacture of coarse powder
  • a coarsely pulverized epoxy resin material is obtained in the same manner as in a-1) of the above-mentioned Production Example 1 for the coating material, except that the raw materials are used in the ratio shown in the following formulation 4.
  • An epoxy resin-based water-dispersed powder coating material 3 was produced in the same manner as in the above-mentioned coating material 1 Production Example b-1), except that the raw material mixture used in the ratio shown in the following formulation 5 was used.
  • Table 5 shows the properties and characteristics of the water-dispersed powder coating material 3.
  • the average particle size (D 50) of the powder particles contained in the obtained paint 3 was 13 m, coarse particles having a particle size of 50 m or more and particle sizes of 0.5 m or less. Was 0% in all cases.
  • the T g of the powder particles was 62 ° C.
  • Epoxy resin coarse pulverized product (Note) 10.0 (Parts) Deionized water 10.0
  • Epoxy resin-based coarsely pulverized product obtained by the above-mentioned formulation 4 Paint 4 Production Example (Epoxy resin-based water-dispersed powder paint; for Example) An epoxy resin-based water-dispersed powder coating material 4 was produced in the same manner except that the following formulation 6 was used instead of the formulation 5.
  • Epoxy resin coarse pulverized product (Note) 10.0 (parts) Ion exchange water 1 0 0 0
  • Acrylic resin-based water-dispersed powder coating material 5 is obtained in the same manner as in the above-mentioned coating material 1 production example, except that the raw material mixture having the ratio shown in the following formulation 8 is used.
  • Table 5 shows the properties and characteristics of the obtained water-dispersed powder coating material 5.
  • the average particle diameter (D 50) of the powder particles contained in the coating is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 m or less are used. The contents were all 0%.
  • the T g of the powder particles was 60 ° C.
  • Acrylic resin-based coarse powder (Tg: 60 ° C) obtained by the above Formulation 7 Paint 6 Production example (Acrylic resin-based water-dispersed powder coating; for Examples) “Floren TG—750 W” (Kyoei Chemical Co., Ltd.) was used instead of “Disperbyk—190” used in Formulation 8 in the production of the acrylic resin-based water-dispersible powder coating 5 shown in 3).
  • Acrylic resin-based water-dispersible paint 6 was produced in exactly the same manner as in the above-mentioned Paint 5 Production Example, except that a dispersant manufactured by Co., Ltd. was used.
  • the average particle diameter (D 50) of the powder particles contained in the paint 6 is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 m or less are used. The contents were all 0%.
  • the T g of the powder particles was 60 ° C. Paint 7 Production example (acrylic resin-based water-dispersed powder coating; for example) Admixture shown in Table 5 was adopted, and acryl resin-based water-dispersed powder-based coating was performed in the same manner as in the above-mentioned coating 1 Production Example. 7 was manufactured.
  • the average particle size (D 50) of the powder particles contained in the paint 7 is 13 m, coarse particles having a particle size of 50 ⁇ m or more and fine particles having a particle size of 0.5 ⁇ m or less. The content of all substances was 0%.
  • the T g of the powder particles was 60 ° C.
  • Paint 8 Production Example (acrylic resin-based water-dispersed powder coating; for example) In the above-mentioned Paint 5 Production Example, an acrylic resin-based water-based Dispersion type powder coating 8 was produced.
  • the average particle diameter (D 50) of the powder particles contained in the paint 8 is 13 ⁇ m, the content of coarse particles having a particle size of 50 ⁇ m or more and the content of fine particles having a particle size of 0.511 or less were 0%.
  • the T g of the powder particles was 58 ° C. Paint 9 Production example (Polyester resin-based water-dispersed powder paint; for comparative example)
  • the formulation shown in Table 5 was adopted, and a polyester resin-based water-dispersed powder coating material 9 was manufactured in the same manner as in the above-mentioned coating material 1 manufacturing example.
  • the average particle size (D50) of the powder particles contained in the coating material 9 is 13 m, and the coarse particles having a particle size of 50 m or more and the fine particles having a particle size of 0.5 Xm or less are fine. The contents were all 0%.
  • the T g of the powder particles was 65 ° C., and the composition of the paint 10 was prepared as shown in Table 5 below.
  • An epoxy resin-based water-dispersed powder coating material 10 was produced in the same manner as in the coating material 1 production example.
  • the average particle diameter (D 50) of the powder particles contained in the paint 10 is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 xm or less are fine. The contents were all 0%.
  • the T g of the powder particles was 62. Paint 11 Production Example (acrylic resin-based water-dispersed powder paint; for comparative example) The formulation shown in Table 5 was adopted. An acrylic resin-based water-dispersed powder coating material 11 was produced in the same manner as in the production example.
  • the average particle size (D50) of the powder particles contained in the coating material 11 is 13 ⁇ m, and coarse particles having a particle size of 50 m or more and fine particles having a particle size of 0.5 xm or less are provided. Was 0% in all cases.
  • the T g of the powder particles was 60 ° C.
  • the properties and characteristics of each of the obtained water-dispersed powder coating materials 1 to 11 are shown in Table 5. Table 5
  • Paint i "Rethane PG-80 Metallic” (Kansai Paint Co., Ltd.'s isocyanate-curable acryl resin paint, used as a two-component curable organic solvent-based colored topcoat.
  • Paint ii "Electron G T-10 Gray” (Kansai Paint Co., Ltd. block isocyanate curable epoxy resin cationic electrodeposition paint, used as undercoat.
  • Paint iii Mix 140 parts of neutralized aqueous acrylic resin (1) with 50% solids and 34 parts of Cymel 370 (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) Then, 25 parts of “Aluminum Paste 891 K” (manufactured by Toyo Aluminum Co., Ltd.) was added and dispersed, and the solid content was adjusted to 35% with deionized water to obtain a colored base paint.
  • a number-average molecular weight: about 100,000 acryl resin solution (solid content: 60%) is prepared, di'methylaminoethanol is added to this solution, neutralized, and then solidified with isopropyl alcohol. Diluted to 50% per minute.
  • Paint iv Acrylic resin neutralization solution with 50% solids (same as 1 * above) 140 parts and “Cymel 370” (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) 3 Mix 4 parts and adjust to a solid content of 35% with deionized water. Use as a clear top coating.
  • Paint V Acrylic resin neutralization solution with 50% solids (same as 1 * above) 140 parts and “Symel 370” (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) 3 Four parts are mixed, 55 parts of titanium white and 2 parts of carbon black are added and dispersed, and then adjusted to a solid content of 35% with deionized water, and used as a colored overcoat.
  • Neo-Amirac # 600 White (Kansai Paint Co., Ltd., an organic solvent-based, acrylic melamine-cured paint, colored top coat Used as a paint.
  • Polyester resin (neopentyldaricol; ⁇ 56 parts; trimethylolpropane; 109 parts; hexahydrofuric acid; 370 parts; adipic acid; 292 parts and isofuric acid; Put 398 parts in a reaction vessel and react at 220 ° C for 6 hours, then add trimellitic anhydride; 45 parts, and react at 170 ° C for 30 minutes.
  • the polyester resin obtained has a number average molecular weight of about 800, an acid value of 2 O mg KOH / g. A hydroxyl value of 95 mg KO HZ g) 100 parts (solid equivalent, hereinafter the same).
  • Material A (zinc phosphate-treated steel sheet) was spray-coated with the above-mentioned “Paint 4” as an undercoat paint to a dry film thickness of 40 zm, and then baked at 180 ° C for 20 minutes. After the treatment, the above “paint i” was spray-coated as a colored overcoat paint so as to have a dry film thickness of 80 xm, and was cured by heating at 80 ° C for 30 minutes.
  • the coating film obtained is a two-layer multi-layer coating film consisting of an undercoat film and a colored overcoat film, and the coating method is ⁇ 2 coats and 2 coatings, 2 coating films and 2 baking times ''.
  • Example 3 is an example of the present invention in which an epoxy resin-based water-dispersed powder coating is applied as an undercoat.
  • the bath temperature of the electrodeposition bath is 15 to 35 ° C
  • the load voltage is 100 to 400 V
  • the film thickness is 40 / m was applied between the object to be coated and the electrode to perform cationic electrodeposition coating.
  • excess electrodeposition paint was washed with industrial water to prevent the electrodeposition paint from remaining on the surface of the coating.
  • Tables 6 to 8 collectively show the configurations and coating film performances of the coating films formed in Example 3-1 to 3-24 and Comparative Example 3-1 to 3-6.
  • “2C1B” means 2 coats and 1 bake
  • “3C2B” means 3 coats and 2bake
  • “3C3B” means 3 coats and 3bake
  • “4C2B” Means 4 coats 2 bake
  • 4 C 4 B means 4 coats 4 bake
  • material A is zinc phosphate treated steel sheet
  • material B is molten zinc plated steel sheet
  • material C is material “SP” means spray painting
  • ED means electrodeposition coating, which is used as a painting method to represent “phosphoric aluminum plate”.
  • Baking 180 180 Coating type iv 8 8 Coating method SP SP SP Top-coat clear coating Dry film thickness (im) 80 80 80 80 Drying (° C, 10 minutes)
  • Baking 140 180 180 Number of layers 2 2 2 3 2 3 4 2 2 3 Undercoat a a a a a a a a a a a a a a a a a a
  • Membrane a Use of invention product Colored top coat b b b b a a a a
  • Coloring base b a b Clear b a Baking process 2G2B 2G1 B 2C2B 2G2B 2C2B 3C3B 4G3B 2C1 B 2C2B 3C2B
  • Baking 180 180 180 180 Number of multilayer films 3 2 2 2 2 2 2 3 3 4 3 Undercoating a a a a a b b b b b b b Coating process Intermediate coating a Film a: Use of invention
  • Baking 180 180 140 140 140 140 140 140 140 Number of layers 3 3 3 4 2 2 3 3 4 Undercoat b b b b b b b b b b b b Intercoat b a b b b Coating coating
  • the raw materials are used in the ratio shown in Formulation 1 below, mixed uniformly with a high-speed mixer, melt-kneaded using a melt extruder, and extruded into a sheet with a thickness of about 1 mm to be cooled and solidified.
  • This sheet material is coarsely crushed through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed material.
  • a coarsely pulverized product is obtained in the same manner as above except that the following formulation 3 is used.
  • a coarse powdered material was obtained by the same raw material blend as shown in the above-mentioned blend 1, and this was used in the same blend ratio as in the above-mentioned blend 2, except that the circulation time for the fine grinding treatment was reduced to 30 minutes.
  • a comparative base coating (al) was obtained.
  • the properties and properties of the base paint (al) are shown in Table 11 below.
  • Coarse ground material was obtained with the same raw material composition as shown in Formulation 1, and this was used in the same composition ratio as in Formulation 2 above, and the circulation time for fine pulverization was extended to 120 minutes.
  • a comparative base paint (a2) was obtained in the same manner as in the above example, except for the above. The properties and characteristics of the comparative base paint (a2) are shown in Table 11 below.
  • the raw materials are blended in the ratio shown in the following Formulation 6, uniformly mixed by a high-speed mixer, heated and kneaded using a melt extruder, extruded into a sheet shape, and cooled and solidified to obtain a thickness of about lmm. Sea 1, get a thing. After the sheet material is crushed by a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain a coarsely ground clear material having an average particle size of about 0.5 mm.
  • the reference black paint for color matching (b3) and the reference paint for color matching (b4) shown in Table 13 above were used as the paint base as described above.
  • Powder and color pigment are mixed in a powder state.Mikuguchi is a mixture of resin powder and pigment powder separately dispersed and mixed. The color pigment is melt-mixed with the resin, then finely pulverized, and mixed with the resin. This is different from the toning paint of the present invention in which the pigment is integrated.
  • pigment dispersions for aqueous paints shown in Table 14 below were used as toning paints (b5) and (b6). These pigment dispersions are obtained by dispersing an extremely fine pigment powder in an aqueous medium, and the color pigment is melt-mixed with a base resin and then finely pulverized to form the resin and pigment of the present invention. Is different from the toning paint. Table 14
  • the base paint and toning paint obtained above are used in various mixing ratios and combinations, and the toning is prepared by uniformly mixing with a disperser to prepare a toning paint.
  • the coating performance was examined. The results are shown in Table 15 and Tables 16 and 17.
  • Spray gun “W-100” (nozzle diameter: 1.3 mm) manufactured by Annest Iwata Co., Ltd. was used for spray painting, and the SPCC steel plate (same before) was spray-painted three times and then hot-air dried. The film was loaded into the machine and baked at 190 ° C for 20 minutes, and then the coating film performance was evaluated.
  • A1 B1 B2 B3 B4 B5 Control agent Particle size (m) Particle size () Stability Workability (jum) Blended Smoothness Ra (jum)
  • Table 15 above is an example that satisfies all of the preferable requirements defined in the present invention.
  • the coating workability is good and the coating film properties (color mixing and smoothness) are also extremely excellent.
  • the blending amount of the toning paint was specified to be 10 parts or 20 parts.However, when actually performing the toning, the toning was performed according to the target color tone of the base paint. It is natural that the blending amount of the toning paint is properly adjusted, and it is of course possible to perform delicate color matching using two or more kinds of toning paints.
  • reference numerals 7 and 8 shown in Tables 16 and 17 indicate that the particle size composition of the base paint and the toning paint is both appropriate, but the amount of the toning paint is too large. This is an example, and slight color mixing is observed.
  • Reference numerals 9, 10 are comparative examples in which the particle size composition of the base paint is appropriate but the particle size composition of the toning paint does not satisfy the specified requirements, and clear color mixing is observed.
  • Reference numeral 11 is a comparative example in which the average particle size of the base paint is too coarse
  • reference numeral 12 is a comparative example in which the average particle size of the base paint and the toning paint is too coarse. Are observed and the coating film performance (smoothness sagging) is poor.
  • Reference numerals 13 and 14 are comparative examples in which the average particle size of the base paint is too small, and the paint workability is poor irrespective of the toning paint, making it impossible to paint.
  • Reference numerals 15 and 16 and reference numerals 17 and 18 are examples in which a mixed dispersion of clear resin powder and fine pigment powder was used as a toning coating for a base coating with an appropriate particle size composition. Yes, the workability of coating and the smoothness of the coating film are good due to the appropriate particle size composition of the base paint, but the finished coating film surface is pigmented by the presence of ultrafine pigment powder alone. The color is floated by the powder, and the gloss is reduced. During storage, the pigment component and the base paint undergo phase separation.
  • the separation stability as a coating and coating using a spray gun It is possible to provide a water-dispersed powder coating material that has a fine surface, has little unevenness, and provides an excellent coating appearance without causing problems such as workability and waste liquid treatment.
  • the alkylene oxide adduct of the styrene / maleic acid copolymer preferably used in the present invention is composed of a saturated hydrocarbon bond.
  • the olepoxyl group derived from maleic acid has a high polarity, it has excellent adhesion to almost any object to be coated, including plastics, metals, and inorganic materials.
  • the alkylene oxide adduct is present in the molecule as a hydrophilic side chain away from the main chain of the styrene / maleic acid copolymer, so it has little steric hindrance to the main chain and functions as a hydrophilic group. Is fully demonstrated.
  • the surface of the coating particles is protected by the hydrophilic group, and rapid water evaporation does not occur on the particle surface even in the baking process. Less coating film defects such as pinholes.
  • the alkylene oxide adduct of a styrene / maleic acid copolymer preferably used in the present invention has a good balance between hydrophobicity and hydrophilicity, and thus exhibits excellent coating performance stably.
  • a coating resin or a pigment and a pigment are melt-mixed, preferably processed into a sheet, coarsely pulverized, and then finely pulverized using a circulation type bead mill.
  • a water-dispersed powder coating material satisfying the requirements of the above average particle size (D50) and particle size distribution can be easily produced.
  • the average particle size and the particle size distribution of the resin powder in the water-dispersed powder coating material, and further, the solid component concentration is used for the specified base coating material,
  • a water-dispersed toning powder coating with a specified particle size composition it is possible to adjust the delicate color matching of the base coating and toning with a paint sprayer, which is difficult with a water-dispersed powder coating. Easy to implement.

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Abstract

A water-dispersed powder coating which comprises a coating resin powder having a median diameter (D50) of 1 to 30µm, preferably 5 to 15µm, and still preferably a uniform particle size distribution wherein the content of particles of 50µm or above in diameter and that of particles of 0.5µm or below in diameter are each 10 % by mass or below, and is prepared by dispersing the coating resin powder in water preferably in the presence of an adduct of a styrene-maleic acid copolymer with an alkylene oxide and a surfactant and which is excellent in workability in application and storage stability and can give smooth coating films excellent in surface appearance and properties; a process for producing the water-dispersed powder coating; and a method of color matching with the powder coating.

Description

明 細 書 水分散型粉体塗料とその製法、 並びに調色方法 -  Description Water-dispersible powder coating, its production method and toning method-
技術分野 本発明は水分散型粉体塗料とその製法、 並びに水分散型粉体塗料 を用いた調色方法に関し、 特に、 塗装作業性や貯蔵安定性に優れ且 つ平滑で優れた外観の塗膜を与え、 更には廃水処理性にも優れた水 分散タイプの粉体塗料と該塗料の製法、 並びに、 それらの水分散型 粉体塗料を使用し、 明度や色彩が微妙に異なるベース塗料の該明度 や色彩を、 色ムラなどを生じることなく簡単な操作で希望する明度 や色彩に微調整することのできる調色方法に関するものである。 TECHNICAL FIELD The present invention relates to a water-dispersible powder coating, a method for producing the same, and a toning method using the water-dispersible powder paint, and particularly to a coating having excellent coating workability and storage stability and having a smooth and excellent appearance. A water-dispersed powder coating that gives a membrane and is also excellent in wastewater treatment properties, a method for producing the paint, and a base paint that uses these water-dispersed powder paints to have slightly different brightness and color. The present invention relates to a toning method capable of finely adjusting the brightness and color to a desired brightness and color by a simple operation without causing color unevenness or the like.
背景技術 塗料としては、 従来より有機溶剤を用いた塗料が汎用されてき た。 ところが有機溶剤を使用した塗料は、 環境問題や火災発生の原 因になり得ることから、 有機溶剤を使用しない水性塗料や粉体塗料 が注目されている。 BACKGROUND ART As a paint, a paint using an organic solvent has been widely used. However, paints that use organic solvents can cause environmental problems and fires, so water-based paints and powder paints that do not use organic solvents have attracted attention.
しかし、 水性塗料では満足のいく塗膜性能が得られ難く、 また廃 水処理などの問題を有している。 これに対し粉体塗料は塗膜性能に 優れており、 且つオーバ一スプレーした塗料は回収装置を利用して 循環使用できるため塗料ロスが殆どなく、 経済性にも極めて有用な ものである。 しかし、 粉体塗装のために高価な塗装設備を必要とす ることや、 仕上り塗膜が粉体塗料特有のゆず肌となり、 薄膜塗装が 難しいという問題も指摘される。 更に粉体塗料は、 製造上多品種少 量生産には不向きであり、 また、 異色の粉末や異物が混入するとそ れらの除去が殆ど不可能であり、 汎用化を妨げる大きな原因になつ ている。 こう した粉体塗料の難点を克服する他のタイプの塗料として、 粉 体塗料成分を水に分散させた水分散型の粉体塗料が考えられており 例えば特開平 7 _ 1 9 6 9 5 3号公報、 同 1 1 一 3 4 3 4 3 2号公 報、 特表平 1 1 一 5 0 3 4 7 8号公報などが提案されている。 これ ら水分散型粉体塗料の多くは、 熱硬化性樹脂、 またはこれと顔料成 分を溶融温度以上、 硬化温度未満の温度で溶融混合してから粗粉砕 し、 更に乾式で微粉砕してから分散剤などを用いて水に分散させる 方法、 或いは粗粉碎物を分散剤などと共に水に分散させてから湿式 で微粉砕する方法、 等によって製造される旨記載されている。 However, water-based paints have difficulty obtaining satisfactory coating film performance, and have problems such as wastewater treatment. On the other hand, powder coatings have excellent coating performance, and oversprayed coatings can be recycled using recovery equipment, so there is almost no paint loss and they are extremely useful in terms of economy. However, it is pointed out that powder coating requires expensive coating equipment, and that the finished coating film becomes a pesticide peculiar to powder coating, making thin film coating difficult. Furthermore, powder coatings are unsuitable for high-mix low-volume production in the manufacturing process, and when mixed with powders of different colors or foreign matter, it is almost impossible to remove them, which is a major factor hindering general use. I have. As another type of paint that overcomes the disadvantages of such powder paints, a water-dispersed powder paint in which a powder paint component is dispersed in water is considered. Japanese Patent Publication No. 11-34-34-32 and Japanese Patent Publication No. 11-150-34878 have been proposed. Many of these water-dispersible powder coatings are prepared by melt-mixing a thermosetting resin or its pigment component at a temperature equal to or higher than the melting temperature but lower than the curing temperature, then coarsely pulverizing, and then finely pulverizing in a dry system. And a method of dispersing in water using a dispersing agent or the like, or a method of dispersing coarsely ground material in water together with a dispersing agent and then finely pulverizing by wet method.
前掲の公報を含めて、 先行技術に開示されている水分散型粉体塗 料の殆どは、 貯蔵安定性や塗膜の均一性などを考慮して水分散型粉 体塗料を構成する樹脂成分の粒径は小さいことが好ましいとされて おり、 具体的には、 平均粒径 (積算 5 0 %粒径 : D 5 0 ) で 1 0 m以下のものを推奨している。  Most of the water-dispersible powder coatings disclosed in the prior art, including the above-mentioned gazettes, contain resin components constituting the water-dispersible powder coating in consideration of storage stability and uniformity of the coating film. It is said that the particle size of the particles is preferably small, and specifically, those having an average particle size (cumulative 50% particle size: D50) of 10 m or less are recommended.
また水分散型の粉体塗料は、 本来は水に不溶性の塗料樹脂粉末を 水に分散させたものであるから貯蔵安定性が悪く、 保管時に該粉末 成分が沈降分離し易い。 しかも加熱乾燥時にヮキを起こし易く、 平 滑な塗膜が得られ難い。 そのため、 貯蔵安定性や塗膜性能を高める ための分散剤や界面活性剤などについても多くの研究がなされてい る。  Further, the water-dispersed powder coating has poor storage stability because the resin powder, which is originally insoluble in water, is dispersed in water, and the powder components are liable to settle and separate during storage. In addition, cracking is likely to occur during heating and drying, and it is difficult to obtain a smooth coating film. For this reason, much research has been conducted on dispersants and surfactants for improving storage stability and coating film performance.
例えば特開昭 5 8 — 1 9 1 7 6 7号公報には、 分散剤としてポリ カルボン酸の金属塩ゃァミン塩、 ポリオキシエチレンのアルキルェ 一テルやアルキルフエ二ルェ一テル、 ソルビタン脂肪酸エステル等 を適量含有させることで、 貯蔵安定性や塗膜性能を高める技術が開 示されており、 また特開昭 5 8 — 1 7 5 7号公報には、 H L Bが 1 0以下のノ二オン界面活性剤を流動性助剤として適量含有させるこ とで、 ヮキやひび割れを抑える技術が開示されている。 また前記特 表平 1 1 一 5 0 3 4 7 8号公報には、 塗料粉体を構成する樹脂の種 類や架橋剤などを特定すると共に、 非イオン性増粘剤と、 消泡剤や 分散剤、 保水剤などを含む水性成分を使用することで、 特に自動車 車体用として優れた性能の透明被覆を与える水分散性ラッカーが開 示されている。 For example, Japanese Unexamined Patent Publication (Kokai) No. 58-191 677 discloses a metal salt of a polycarboxylic acid, a diamine salt, an alkyl ether or an alkylphenyl ether of polyoxyethylene, a sorbitan fatty acid ester, or the like as a dispersant. Techniques for improving storage stability and coating film performance by adding an appropriate amount have been disclosed. Japanese Patent Application Laid-Open No. 58-17757 discloses a nonionic surfactant having an HLB of 10 or less. A technique has been disclosed in which an agent is contained in an appropriate amount as a fluidity aid to suppress cracking and cracking. In addition, Japanese Patent Application Laid-Open No. H11-15034878 specifies the type of resin constituting the coating powder, a crosslinking agent, etc., as well as a nonionic thickener, a defoaming agent, The use of aqueous components including dispersants and water retention agents, Water-dispersible lacquers have been disclosed that provide transparent coatings of excellent performance for car bodies.
ところが、 上記特開昭 5 8— 1 9 1 7 6 7号公報に記載された水 分散性塗料の場合、 記載の界面活性剤を使用すると、 粉体粒子を微 細化するにつれて塗料の流動性が悪くなるため塗装作業性が低下し 均一な塗膜が得られ難くなるだけでなく、 分散工程で発熱し易くな り、 粉体粒子同士が融着し易くなる。 そこで、 流動性を高めるため に界面活性剤の量を増大させると、 タレやヮキが生じ易くなると共 に塗膜の耐水性や光沢が低下する。 或いは、 流動性を確保するため に塗料の固形分濃度を下げると、.タレや素地の透けを生じ易くなる, また特開昭 5 8 — 1 7 5 7号公報に記載された水分散型塗料の場 合、 選択された界面活性剤を使用することで塗膜の耐水性は確保さ れるが、 粉体粒子を微細化するにゥれて塗料の流動性が悪くなり、 界面活性剤を選択するだけでは満足のいく流動性を確保することが できない。 また、 流動性を高めるべく界面活性剤の量を増大し、 或 いは塗料の固形分濃度を下げると、 前記と同様にヮキゃタレが生 易くなる。 更に、 低 H L Bのノニオン系界面活性剤を多量添加する と、 粉体粒子同士が凝着するという重大な欠陥を招く。  However, in the case of the water-dispersible paint described in the above-mentioned Japanese Patent Application Laid-Open No. 58-197167, when the surfactant described is used, the fluidity of the paint becomes smaller as the powder particles become finer. In addition, not only does the coating workability deteriorate, making it difficult to obtain a uniform coating film. In addition, heat is easily generated in the dispersing step, and the powder particles are easily fused to each other. Therefore, when the amount of the surfactant is increased in order to enhance the fluidity, sagging and rubbing are likely to occur, and the water resistance and gloss of the coating film decrease. Alternatively, if the solid content concentration of the paint is lowered to ensure fluidity, sagging and see-through of the substrate tend to occur, and the water-dispersed paint described in Japanese Patent Application Laid-Open No. 58-17557 In this case, the water resistance of the coating film is secured by using the selected surfactant, but the fluidity of the paint deteriorates as the powder particles become finer, and the surfactant is selected. Doing so alone does not ensure satisfactory liquidity. Further, if the amount of the surfactant is increased to increase the fluidity, or the solid content concentration of the coating material is reduced, the puffiness is likely to occur as described above. Further, the addition of a large amount of a low HLB nonionic surfactant causes a serious defect that powder particles adhere to each other.
更に、 特表平 1 1 — 5 0 3 4 7 8号公報に開示されている透明ラ ッカー水性分散体は、 特定の塗料粉体を非イオン性増粘剤および界 面活性剤や分散剤などの共存下で湿式分散することにより製造され るが、 微粒化した塗料粉体の凝集が起こり易くて貯蔵安定性が悪く 更には塗膜の耐水性が劣るという欠点も指摘される。  Furthermore, the transparent lacquer aqueous dispersion disclosed in Japanese Patent Application Laid-Open No. H11-5303478 can be used to convert a specific paint powder into a nonionic thickener, a surfactant and a dispersant. It is produced by wet dispersing in the coexistence of water, but it is pointed out that the finely divided coating powder tends to agglomerate, resulting in poor storage stability and poor water resistance of the coating film.
しかも水分散型粉体塗料は、 多品種少量生産が可能で高い汎用性 を有している反面、 仕上り塗膜の色彩や明度が意図する色彩や明度 と微妙に異なった場合、 水分散型粉体塗料の粒子径および粒度分布 が精度よく制御されていないと、 単に水分散型粉体塗料を混ぜ合わ せても色混じりや色ムラを生じ、 色を調整することができない。 従 つてその様な場合、 仕上り塗膜の色彩や明度を再調整するには、 水 分散型粉体塗料を濾過や遠心分離にかけて固形成分を分離 · 乾燥し 調色用の顔料や染料を配合した後、 加熱溶融してから再度粗粉砕お よび微粉砕しなければならず、 結局のところ新規水分散型粉体塗料 を調製するのと同様の手数が必要になる。 In addition, water-dispersed powder coatings are highly versatile and can be produced in a variety of small quantities, but when the color and lightness of the finished coating film is slightly different from the intended If the particle size and particle size distribution of the body paint are not precisely controlled, simply mixing the water-dispersed powder paint will cause color mixing and color unevenness, making it impossible to adjust the color. Therefore, in such a case, in order to readjust the color and brightness of the finished coating film, the water-dispersed powder coating is filtered or centrifuged to separate and dry the solid components. After blending the toning pigments and dyes, they must be heated and melted and then coarsely ground and finely ground again, which ultimately requires the same steps as preparing a new water-dispersed powder coating. become.
また、 既存の水分散型粉体塗料の色彩等を、 塗装作業現場で若干 変更して使用したい要望が生じた場合も同様であり、 水分散型粉体 塗料ではこう した要望に適合させることができず、 求められる色彩 などに適合する新たな水分散型粉体塗料を発注しなければならない, 本発明は上記の様な従来技術の問題点に着目してなされたもので あって、 その目的は、 水分散型粉体塗料にみられる前掲の欠点を解 消し、 塗料としての貯蔵安定性や塗装作業性を改善すると共に、 平 滑性や光沢に優れ、 且つ夕レゃヮキ等のない美麗な塗膜外観を与え る水分散型粉体塗料を提供すると共に、 その有用な製法を提供する ことにある。 また本発明の他の目的は、 水分散型粉体塗料を用いた 調色を、 塗装現場等においても簡単に行う ことのできる調色方法を 提供することにある。  The same applies when a request arises to use the existing water-dispersed powder coating with a slight change in color, etc., at the painting site, and the water-dispersed powder coating can meet such demands. It is not possible to do so and must order a new water-dispersed powder coating that meets the required colors. The present invention has been made by focusing on the problems of the prior art as described above. Eliminates the above-mentioned drawbacks of water-dispersed powder coatings, improves storage stability and coating workability as coatings, and is excellent in smoothness and gloss, and has no dullness An object of the present invention is to provide a water-dispersed powder coating material that gives a beautiful coating film appearance and a useful production method thereof. Another object of the present invention is to provide a toning method capable of easily performing toning using a water-dispersed powder coating even at a painting site or the like.
発明の開示 上記課題を解決することのできた本発明の水分散型粉体塗料とは 塗料用樹脂を含み、 平均粒径 (D 5 0 ) が l 〜 3 0 ^ m、 より好ま しくは 5〜 1 5 2 mである粉体が水に分散されたものであるところ に特徴を有している。 DISCLOSURE OF THE INVENTION The water-dispersible powder coating material of the present invention which can solve the above-mentioned problems includes a coating resin, and has an average particle size (D50) of l to 30 ^ m, more preferably 5 to It is characterized in that the powder of 152 m is dispersed in water.
本発明の水分散型粉体塗料における上記粉体の粒度分布は、 5 0 m以上、 より好ましくは 2 Ο ΙΏ以上の粒子の占める比率が 1 0 質量%以下で、 且つ 0 . 5 m以下、 より好ましくは 3 x m以下の 粒子の占める比率が 1 0質量%以下であるものが好ましい。  The particle size distribution of the powder in the water-dispersed powder coating material of the present invention is 50 m or more, more preferably 20% or more of the particles occupying 10 mass% or less, and 0.5 m or less, More preferably, the ratio of particles of 3 xm or less is 10% by mass or less.
そして本発明の水分散型粉体塗料は、 上記粒度構成の塗料用樹脂 を含む粉体が、 スチレン · マレイン酸共重合体のアルキレンォキサ ィ ド付加物と界面活性剤の共存下に、 水に分散されたものが好まし く、 上記スチレン · マレイン酸共重合体のアルキレンオキサイ ド付 加物として特に好ましいのは、 エチレンオキサイ ドとプロピレンォ キサイ ドとの共付加物である。 また、 界面活性剤として特に好まし いのは非イオン系界面活性剤であり、 中でも H L Bが 4〜 1 3の範 囲の界面活性剤が好ましい。 In the water-dispersed powder coating composition of the present invention, the powder containing the coating resin having the above-mentioned particle size composition is prepared by adding water to an alkylene oxide adduct of a styrene / maleic acid copolymer and a surfactant. Preferably, the styrene / maleic acid copolymer is dispersed in an alkylene oxide. Particularly preferred as an additive is a co-adduct of ethylene oxide and propylene oxide. Non-ionic surfactants are particularly preferred as the surfactant, and among them, surfactants having an HLB in the range of 4 to 13 are preferred.
界面活性剤の中でもとりわけ好ましいのは、 アルキンジオールの アルキレンォキサイ ド付加物からなり、 重量平均分子量が 3 0 0〜 3 0 0 0の範囲のもので、 該アルキンジオールのアルキレンォキサ ィ ド付加物として特に好ましいのは、 テトラメチルデシンジオール のエチレンォキサイ ド付加物である。  Among the surfactants, particularly preferred are alkylene oxide adducts of alkyne diols having a weight-average molecular weight in the range of 300 to 300, and alkylene oxide addition of the alkyne diol. Particularly preferred as the product is an ethylene oxide adduct of tetramethyldecinediol.
上記スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加 物の含有量は、 塗料用樹脂粉体に対し固形分換算で 0 . 1 〜 1質 量%が好ましく、 また上記界面活性剤の含有量は、 塗料用樹脂粉体 に対し固形分換算で 0 . 1 〜 1質量%の範囲が好ましい。  The content of the alkylene oxide adduct of the styrene / maleic acid copolymer is preferably from 0.1 to 1% by mass in terms of solid content with respect to the resin powder for coating, and the content of the surfactant is preferable. Is preferably in the range of 0.1 to 1% by mass in terms of solid content with respect to the resin powder for coating.
本発明にかかる上記水分散型粉体塗料の好ましい固形分濃度は 3 0〜 6 0質量%で、 該分散体の粘度は、 2 3 °Cにおいて 1 0 0〜 5 0 0 0 m P a · s、 前記塗料樹脂粉体のガラス転移温度は 3 0〜 8 0 °Cの範囲が好適である。  The preferred solid content concentration of the water-dispersed powder coating according to the present invention is 30 to 60% by mass, and the viscosity of the dispersion is 100 to 500 mPa · at 23 ° C. s, The glass transition temperature of the paint resin powder is preferably in the range of 30 to 80 ° C.
上記塗料用樹脂の種類は特に制限されないが、 特に好ましいのは エポキシ系樹脂、 ポリエステル系樹脂、 アク リル系樹脂よりなる群 から選択される少なく とも 1種であり、 これらは無色でクリア一塗 膜を形成するものの他、 塗料用樹脂と共に顔料を含む着色塗料であ つてもよい。  The type of the resin for the coating material is not particularly limited, but is particularly preferably at least one selected from the group consisting of an epoxy resin, a polyester resin, and an acrylic resin. In addition to the above, a colored paint containing a pigment together with a paint resin may be used.
本発明の製法は、 上記特性を備えた水分散型粉体塗料の有用な製 法として位置付けられるもので、 その構成は、 塗料用樹脂を含む塗 料用原料成分を溶融混合し、 これを冷却してから粗粉砕した後、 該 粗粉砕物.を 0 . Ί〜 2 . 3倍量の水に分散させた状態で循環型ビー ズミルにより処理し、 固形成分の平均粒径 (D 5 0 ) が 5〜 1 5 z m、 2 0 / m以上の粒子の占める比率が 1 0質量%以下、 3 m以 下の粒子の占める比率が 1 0質量%以下となる様に微粉砕するとこ ろに特徴を有している。 上記において塗料用樹脂の微粉砕物を得る際には、 溶融混合物を シート状に成形し、 これを粗粉砕してか S前記循環型ビーズミルで 処理するのが好まし 、 この際、 塗料用樹脂と共に顔料を溶融混合 して使用すれば、 水分散型の着色粉体塗料を得ることができる。 更に本発明の調色方法とは、 前掲の水分散型粉体塗料からなるベ ース塗料の色彩及び/又は明度を微調整するに当り、 塗料用樹脂と 顔料を一体として含む粉体が水に分散された水分散型粉体塗料から なり、 前記粉体の平均粒径 (D 5 0 ) が 5〜 : 1 5 mで、 且つ 2 0 m以上の粒子の占める比率が 1 0質量%以下、 3 m以下の粒子 の占める比率が 1 0質量%以下で、 固形分濃度が 3 0〜 6 0質量% であるベース塗料の色彩及び/又は明度を微調整する方法であって 前記塗料用樹脂と同一もしくは異種の塗料用樹脂を顔料と一体と して含む粉体が水に分散された水分散型粉体塗料からなり、 該粉体 の平均粒径 (D 5 0 ) が 5 m以下 (但し、 粒径が 1 0 mを超え る粗粒物を実質的に含まない) で、 且つ白、 黒、 赤、 青または黄色 系の顔料を含む少なく とも 1種の調色用塗料を準備しておき、 前記ベース塗料の明度及び Z又は色彩に応じて、 前記調色用塗料 の少なく とも 1種を前記べ一ス塗料に適量配合することによって、 該ベース塗料の明度及び/又は色彩を微調整するところに特徴を有 している。 The production method of the present invention is positioned as a useful production method of a water-dispersed powder coating material having the above-mentioned properties. The composition is constituted by melting and mixing raw material components for a coating material including a resin for a coating material and cooling the mixture. After the coarse pulverization, the coarsely pulverized material is dispersed in water in an amount of 0.3 to 2.3 times and treated with a circulation type bead mill to obtain a solid component having an average particle diameter (D50). Is 5 to 15 zm, the ratio of particles occupying 20 / m or more is 10% by mass or less, and the ratio of particles occupying 3m or less is 10% by mass or less. have. In the case of obtaining a finely pulverized product of the coating resin in the above, it is preferable that the molten mixture is formed into a sheet, which is roughly pulverized or processed by the circulation type bead mill. When the pigment is melt-mixed and used, a water-dispersed colored powder coating can be obtained. Further, in the color-adjusting method of the present invention, when finely adjusting the color and / or lightness of the base paint composed of the water-dispersible powder paint described above, the powder containing the paint resin and the pigment as one body is made of water. Wherein the average particle size (D50) of the powder is 5 to 15 m and the proportion of particles having a particle size of 20 m or more is 10 mass% or less. A method for finely adjusting the color and / or lightness of a base coating material in which the proportion of particles having a particle size of 3 m or less is 10% by mass or less and the solid content concentration is 30 to 60% by mass. A water-dispersed powder coating material in which a powder containing the same or a different coating resin and a pigment together with a pigment is dispersed in water, has an average particle size (D50) of 5 m or less ( However, it does not substantially contain coarse particles having a particle size exceeding 10 m) and at least contains white, black, red, blue or yellow pigments. One kind of toning paint is prepared, and at least one kind of the toning paint is mixed with the base paint in an appropriate amount in accordance with the brightness and Z or color of the base paint. The feature is that the brightness and / or color of the base paint is finely adjusted.
この調色方法を実施するに当っては、 上記ベース塗料に含まれる 粉体の平均粒径 (D 5 0 ) (A)と、 前記調色用塗料に含まれる粉体 の平均粒径 (D 5 0 ) (B)との比(Aノ B)を 1以上、 5以下とするの がよく、 また、 上記ベース塗料に対する調色用塗料の配合量は、 固 形分基準で 0 . 1質量%以上、 2 0質量%以下とするのがよい。  In carrying out this toning method, the average particle size (D 50) (A) of the powder contained in the base paint and the average particle size (D 50) The ratio (A / B) to (B) is preferably 1 or more and 5 or less, and the mixing amount of the toning paint with respect to the base paint is 0.1 mass based on the solid content. % Or more and 20% by mass or less.
また、 上記調色用塗料を配合する際には、 その前または後に、 艷 調整剤を添加して艷の調整を行う ことも有効である。 図面の簡単な説明 図 1は、 循環型ビーズミルを用いた場合の塗料用樹脂粉体の粒度 と循環時間の関係を示すグラフ、 図 2は、 多パス運転型ビーズミル を使用したときのパス回数と塗料用樹脂粉体の粒度との関係を示す グラフである。 When compounding the above-mentioned toning paint, it is also effective to adjust the gloss by adding an gloss adjuster before or after that. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing the relationship between the particle size of the resin powder for coating and the circulation time when a circulation type bead mill is used, and FIG. 2 is a graph showing the number of passes when a multi-pass operation type bead mill is used. 4 is a graph showing the relationship with the particle size of a coating resin powder.
発明を実施するための最良の形態 上記の様に本発明の水分散型粉体塗料は、 塗料用樹脂を含み、 平 均粒径 (D 5 0 ) が l〜 3 0 m、 より好ましくは 5〜 1 5 ΠΙで ある粉体が水に分散されたものであるところに特徴を有するもので より好ましいのは、 該粉体の粒度構成が、 5 0 z m以上、 より好ま しくは 2 0 m以上の粗粒物の占める比率が 1 0質量%以下 (より 好ましくは 5質量%以下、 更に好ましくは実質的にゼロ%) で、 且 つ 0. 5 // m以下、 より好ましくは 3 m以下の微粒子の占める比 率が 1 0質量%以下 (より好ましくは 5質量%以下、 更に好ましく は実質的に 0 %) であるものである。 BEST MODE FOR CARRYING OUT THE INVENTION As described above, the water-dispersed powder coating composition of the present invention contains a coating resin, and has an average particle size (D 50) of 1 to 30 m, more preferably 5 to 30 m. It is more preferable that the powder having a particle size of ΠΙ15〜 is dispersed in water, and the particle size of the powder is 50 zm or more, more preferably 20 m or more. Is less than 10% by mass (more preferably 5% by mass or less, more preferably substantially 0%) and 0.5 // m or less, more preferably 3% or less. The proportion occupied by the fine particles is 10% by mass or less (more preferably 5% by mass or less, further preferably substantially 0%).
ちなみに平均粒径 (D 5 0 ) が 1 m未満では、 粒子が微細に過 ぎるため構造粘性が高くなつて流動性が低下し、 スプレーガン等を 用いた塗装作業性が低下したり、 仕上り外観 (塗膜の平滑性や均一 性) などが低下する傾向が生じるからである。 そこで、 塗料の固形 分濃度を下げることによって流動性を確保しょうとすると、 固形分 濃度の低下に伴って、 所謂 "塗膜のやせ" や "透け" が問題になつ てくる。 また本発明では、 追って詳述する如く、 スチレン · マレイ ン酸共重合体のアルキレンォキサイ ド付加物と界面活性剤の併用に より、 水性分散液としての流動性を高めて使用することが好ましい が、 該粉末の平均粒径 (D 5 0 ) が小さ過ぎると、 上記界面活性剤 などを必要以上に添加しなければならなくなり、 耐水性などの塗膜 特性に悪影響を及ぼす恐れもでてく る。 他方、 平均粒径 (D 5 0 ) が 3 0 を超えて過度に粗大になる と、 保管時などに塗料中の粉体成分が沈降し易く、 塗料の取扱い性 が低下するばかりでなく、 塗膜のきめが粗くなって平滑な塗膜外観 が得られ難くなる。 By the way, when the average particle size (D50) is less than 1 m, the particles are too fine and the structural viscosity is high, so that the fluidity is reduced, and the coating workability using a spray gun or the like is reduced, or the finished appearance is reduced. (Smoothness and uniformity of the coating film) tend to decrease. Therefore, when trying to secure fluidity by lowering the solids concentration of paint, so-called "thinning" or "transparency" of the coating film becomes a problem as the solids concentration decreases. In the present invention, as will be described in detail later, it is preferable to use the styrene / maleic acid copolymer with an alkylene oxide adduct in combination with a surfactant to increase the fluidity as an aqueous dispersion. However, if the average particle size (D 50) of the powder is too small, the above surfactant or the like must be added more than necessary, which may adversely affect the coating properties such as water resistance. . On the other hand, if the average particle diameter (D50) exceeds 30 and becomes excessively coarse, the powder components in the paint tend to settle during storage and the like, and not only does the handling of the paint deteriorate, but also the The texture of the film becomes coarse, making it difficult to obtain a smooth coating film appearance.
また該粉体の粒度分布は、 塗膜の平滑性や、 水分散型塗料を調製 する際の濾過性、 更には塗装作業性などに影響を及ぼし、 固形成分 (粉体) 中に占める 5 0 m以上 (より好ましくは 2 0 ΠΙ以上) の粒子の比率が 1 0質量%以下で、 且つ 0. 5 ^ m以下 (より好ま しくは 3 m以下) の粒子の占める比率が 1 0質量%以下であるこ とが望ましく 、 その結果として、 0. 5 ^ 1!1以上 5 0 ^ 111以下、 よ り好ましくは 3 m以上 2 m以下の好適粒径範囲に納まる粒子 の全体中に占める比率は 8 0質量%以上であることが望ましい。 ちなみに粒度分布が広い水分散型粉体塗料では、 凹凸間隔が短く て凹凸高低差の大きい塗膜となり、 均一な仕上り塗膜が得られ難く なる。 更に 5 0 z m以上 (より好ましく は 2 0 m以上) の粗粒物 が 1 0質量%を超えると、 塗料製造時の濾過工程でフィルタ一が目 詰りを起こし易くなり、 また、 0. 5 ΠΙ以下 (より好ましくは 3 m以下) の微粒物が 1 0質量%を超えると塗料の流動性が低下し 塗装作業性が悪くなる傾向が見られる。  In addition, the particle size distribution of the powder affects the smoothness of the coating film, the filterability when preparing a water-dispersed paint, and the workability of coating, and occupies 50% of the solid component (powder). The ratio of particles having a particle size of at least m (more preferably at least 20%) is 10% by mass or less, and the ratio of particles having a particle size of 0.5 ^ m or less (more preferably 3m or less) is 10% by mass or less. As a result, the ratio of particles falling within the preferred particle size range of 0.5 ^ 1! 1 or more and 50 ^ 111 or less, more preferably 3 m or more and 2 m or less, is preferably 8%. It is desirably 0% by mass or more. By the way, in the case of a water-dispersed powder coating having a wide particle size distribution, the unevenness interval is short and the coated film has a large unevenness height difference, and it is difficult to obtain a uniform finished coated film. Further, when the amount of coarse particles of 50 zm or more (more preferably 20 m or more) exceeds 10% by mass, the filter is likely to be clogged in the filtration step at the time of paint production, and 0.5% If the amount of fine particles of less than 10% by mass (more preferably 3 m or less) exceeds 10% by mass, the fluidity of the paint tends to decrease and the coating workability tends to deteriorate.
しかし、 平均粒径 (D 5 0 ) が 1 m以上 3 0 m以下で且つ 5 0 /i m以上 (より好ましくは 2 0 m以上) の粒子の占める比率が 1 0質量%以下、 0. 5 i m以下 (より好ましくは 3 /xm以下) の 粒子の占める比率が 1 0質量%以下の水分散型粉体塗料では、 塗料 粘度が過度に高くなつて塗装作業性や取扱い性が劣化するといった 問題を生じる ことなく、 しかも形成される塗膜は均一で平滑性の一 段と優れた仕上り外観を有するものとなる。 更に、 塗料製造時の濾 過工程でフィルターの目詰りを起こすことなく夾雑物のみを容易に 除去することができる。  However, the proportion of particles having an average particle diameter (D50) of 1 m or more and 30 m or less and 50 / im or more (more preferably 20 m or more) is 10 mass% or less, and 0.5 im With water-dispersed powder coatings in which the proportion of particles of less than 3 / xm (more preferably 3 / xm or less) is 10% by mass or less, problems such as deterioration of coating workability and handleability due to excessively high paint viscosity may occur. No coating occurs, and the formed coating film has a more uniform and smoother appearance. Furthermore, only impurities can be easily removed without causing clogging of the filter in the filtration step in the production of paint.
本発明で使用する上記水分散型粉体塗料の固形分濃度も、 塗装作 業性や塗膜特性に影響を及ぼす要因であり、 好ましくは 3 0〜 6 0 質量%の範囲に調整することが望ましい。 ちなみに、 固形分濃度がThe solid content concentration of the water-dispersed powder coating used in the present invention is also a factor that affects coating workability and coating film characteristics, and is preferably 30 to 60. It is desirable to adjust to the range of mass%. By the way, the solid content concentration
3 0質量%未満の低濃度物では、 濃度不足のため塗装時に前述した "塗膜のやせ" や "透け" が生じ易くなる。 逆に 6 0質量%を超え て過度に高濃度になると、 塗料粘度が高くなって流動性が低下し、 塗装時のレペリ ング性が悪くなり、 仕上り塗膜の平滑性などに悪影 響が生じてくる。 この様なことから、 水分散型粉体塗料の固形分濃 度は 3 0質量%以上、 6 0質量%以下に調整するのがよい。 With a low concentration of less than 30% by mass, the above-mentioned "thin film" and "transparency" of the coating film easily occur at the time of painting due to insufficient concentration. Conversely, if the concentration exceeds 60% by mass and the concentration becomes excessively high, the viscosity of the paint increases and the fluidity decreases, resulting in poor repelling properties at the time of painting and adversely affecting the smoothness of the finished coating film. Come up. For this reason, the solid content concentration of the water-dispersed powder coating is preferably adjusted to 30% by mass or more and 60% by mass or less.
また本発明の水分散型粉体塗料は、 上記塗料用樹脂を含む粉体を スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加物と界 面活性剤の共存下に水に分散されたものであることが好ましい。  The water-dispersible powder coating of the present invention is obtained by dispersing a powder containing the coating resin in water in the presence of an alkylene oxide adduct of a styrene / maleic acid copolymer and a surfactant. It is preferred that
上記スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加 物とは、 スチレンと (無水) マレイン酸を共重合することによって 得られる共重合体にアルキレンォキサイ ドが付加した化合物であり 例えば下記一般式で示される方法によつて得られる共重合体である  The alkylene oxide adduct of the styrene / maleic acid copolymer is a compound in which an alkylene oxide is added to a copolymer obtained by copolymerizing styrene and (anhydrous) maleic acid. Is a copolymer obtained by the method represented by the formula
Figure imgf000010_0001
Figure imgf000010_0001
CH2-CH2およひ CH3-CH-CH2  CH2-CH2 and CH3-CH-CH2
\ノ 0 ヽノ 0  \ ノ 0 ヽ ノ 0
Figure imgf000010_0002
上記一般式において、 rは 1 〜 5 、 s は 5 〜 2 0 、 tは 1 〜 5 0 の整数を表わし、 Rは水素、 炭素数 1 〜 2 0のアルキルアルコール 残基、 アルキル基の炭素数が 1 〜 2 0であるアルキルフエノール残 基、 炭素数 8〜 4 0 の脂肪酸残基、 炭素数 8〜 4 0 の脂肪酸ァミ ン 残基、 炭素数 8〜 4 0 の脂肪酸アミ ド残基、 グリセリ ンまたはダリ セリンと脂肪酸のエステル残基、 ソルビトールまたはソルビトール と脂肪酸のエステル残基、 炭素数 8〜 4 0の脂肪酸アル力ノールァ ミ ド残基等から選択される少なく とも 1種の置換基を表わし、 一 A 〇—は、 エチレンオキサイ ドとプロ ピレンオキサイ ドの共重合鎖 (ブロック、 ランダムまたは交互共重合物を含む) を表わす。
Figure imgf000010_0002
In the above general formula, r is an integer of 1 to 5, s is an integer of 5 to 20, t is an integer of 1 to 50, R is hydrogen, an alkyl alcohol residue having 1 to 20 carbon atoms, and a carbon number of the alkyl group. Is 1 to 20 alkylphenol residues Group, fatty acid residue with 8 to 40 carbon atoms, fatty acid amide residue with 8 to 40 carbon atoms, fatty acid amide residue with 8 to 40 carbon atoms, ester residue of glycerin or dalyserin and fatty acid Sorbitol or sorbitol or an ester residue of a fatty acid with sorbitol, a fatty acid alkanol amide residue having 8 to 40 carbon atoms, and the like. Represents the copolymer chain (including block, random or alternating copolymer) of amide and propylene oxide.
この付加物は、 主鎖を構成するスチレン · マレイン酸骨格と、 該 骨格中に含まれるマレイン酸単位における未中和のカルボキシル基 および一方の力ルポキシル基に付加したアルキレンォキサイ ド鎖、 特に好ましくはエチレンォキサイ ドとプロピレンォキサイ ドが共付 加した側鎖部の存在により、 後述する界面活性剤との共存とも相俟 つて、 塗料用樹脂粉体に対して卓越した分散性を与え、 水分散型粉 体塗料として卓越した貯蔵安定性と塗装作業性を保障しつつ、 タレ ゃヮキがなく且つ耐水性や塗膜平滑性においても優れた性能を示す 高品質の塗膜を与える。  This adduct is preferably a styrene / maleic acid skeleton constituting the main chain, an alkylene oxide chain added to an unneutralized carboxyl group and one of the carboxylic acid groups in the maleic acid unit contained in the skeleton, and particularly preferably. Provides excellent dispersibility for resin powders for coatings due to the presence of side chains where ethylene oxide and propylene oxide are co-added, together with the coexistence with surfactants described below. As a water-dispersed powder coating, it provides high-quality coatings that have excellent storage stability and coating workability, are free from sagging, and have excellent performance in water resistance and coating smoothness.
これらの諸機能をより有効に発揮させるには、 上記付加物として 重量平均分子量が 2, 000〜 1 00 , 00 0、 よ り好ま し く は 1 0, 00 0〜 50 , 000 の範囲で、 スチレン単位とマレイ ン酸単位のモル比率が前 者 1 に対して後者 0 . 2〜 1、 プロピレンオキサイ ドの共付加モル 比がエチレンオキサイ ドに対して 0 . 1〜 0 . 5の範囲のものを使 用するのがよい。  In order to make these various functions more effective, the weight average molecular weight of the above-mentioned adduct should be in the range of 2,000 to 100,000, more preferably 100,000 to 50,000. The molar ratio of styrene units to maleic acid units ranges from 0.2 to 1 for the former, and the co-addition molar ratio of propylene oxide ranges from 0.1 to 0.5 for ethylene oxide. It is better to use one.
重量平均分子量が小さ過ぎる場合は、 粉体粒子に対する吸着比率 (カルボキシル基比率) やアルキレンオキサイ ド鎖が小さいため、 微細化された粉体粒子が凝集し易くなって貯蔵安定性が悪くなる傾 向があり、 逆に重量平均分子量が大き過ぎると、 アルキレンォキサ ィ ド鎖も大きくなつて貯蔵安定性は向上するが、 耐水性が悪くなる 傾向が生じてくる。  If the weight average molecular weight is too small, the adsorption ratio (carboxyl group ratio) to the powder particles and the alkylene oxide chain are small, so that the finely divided powder particles tend to aggregate and storage stability tends to deteriorate. If the weight-average molecular weight is too large, the alkylene oxide chain becomes too large to improve the storage stability, but the water resistance tends to deteriorate.
また、 アルキレンォキサイ ド鎖に含まれるエチレンォキサイ ドの 比率が多くなり過ぎると、 親水性が高くなつて耐水性が低下傾向を 示し、 またプロピレンオキサイ ドの比率が多くなり過ぎると、 疎水 性が強くなり過ぎて水への溶解性が低下し、 分散剤としての機能が 有効に発揮され難くなる。 また、 主鎖部分を構成するスチレンの比 率が多くなると、 塗料の流動性は良くなって塗装作業性は向上する が、 粉体粒子に対する吸着比率 (力ルポキシル基比率) やアルキレ ンォキサイ ド鎖が小さくなり、 塗料粉体粒子が凝集し易くなって貯 蔵安定性が低下してくる。 またマレイン酸の比率が多くなり過ぎる と、 アルキレンオキサイ ド鎖も多くなつて貯蔵安定性は向上するも のの、 耐水性不足になる傾向が生じてくる。 On the other hand, if the proportion of ethylene oxide contained in the alkylene oxide chain becomes too large, the water resistance tends to decrease due to the increase in hydrophilicity. In addition, when the proportion of propylene oxide is too large, the hydrophobicity becomes too strong, the solubility in water is reduced, and the function as a dispersant is hardly exhibited effectively. In addition, when the ratio of styrene constituting the main chain increases, the fluidity of the coating material improves and the coating workability improves, but the adsorption ratio (the ratio of lipoxyl groups) to the powder particles and the alkylene oxide chain increase. As the particle size becomes smaller, the coating powder particles tend to agglomerate and storage stability decreases. On the other hand, if the ratio of maleic acid is too large, the number of alkylene oxide chains increases and the storage stability is improved, but the water resistance tends to be insufficient.
これら好ましい要件を満たすスチレン · マレイン酸共重合体のァ ルキレンオキサイ ド付加物は、 例えばピックケミ一社製の商品名 Alkylene oxide adducts of styrene / maleic acid copolymers satisfying these preferred requirements are, for example, trade names of Pick Chemical Co., Ltd.
「D i sp e r byk _ 1 9 0」 、 或いは共栄社化学社製の商品名 「フロー レン T G— 7 5 0 W」 などとして入手できる。 It can be obtained as "Disper byk_190", or as the product name "Floren TG-7500W" manufactured by Kyoeisha Chemical Co., Ltd.
また上記アルキレンォキサイ ド付加物と併用される界面活性剤の 種類は特に制限されず、 一般の水性塗料用として使用可能な様々の 界面活性剤、 例えばァニオン系、 カチオン系、 両性、 ノニオン系の 各種界面活性剤を使用できる。  The type of surfactant used in combination with the alkylene oxide adduct is not particularly limited, and various surfactants usable for general water-based paints, for example, anionic, cationic, amphoteric, and nonionic surfactants can be used. Various surfactants can be used.
ァニオン系界面活性剤の具体例としては、 脂肪酸トリエ夕ノール アミン塩、 (直鎖) アルキルベンゼンスルホン酸塩、 α —スルホ脂 肪酸 (メチル) エステルアルカリ塩、 《—ォレフイ ンスルホン酸塩 アルキルエーテル硫酸エステルアルカリ塩、 モノアルキルリ ン酸塩 ラウリル硫酸塩、 ァシルー Ν —メチルタウレート、 カルボン酸のナ トリウム塩、 高級アルコールの硫酸エステル塩、 硫酸化脂肪酸エス テル、 硫酸化ォレフイ ン、 アルキルナフタレンスルホン酸塩、 パラ フイ ンスルホン酸塩、 高級アルコールリ ン酸エステル塩などが例示 され、 上記塩類としてはナト リゥム塩や力リゥム塩が好ましく使用 される。  Specific examples of anionic surfactants include fatty acid trienol amine amine salt, (linear) alkyl benzene sulfonate, α-sulfo fatty acid (methyl) ester alkali salt, and «-olefin sulfonate alkyl ether sulfate Alkali salts, monoalkyl phosphates Lauryl sulfate, acyl-methyl taurate, sodium salts of carboxylic acids, sulfate esters of higher alcohols, sulfated fatty acid esters, sulfated olefins, alkylnaphthalene sulfonates, para Examples thereof include a fin sulfonate and a higher alcohol phosphate, and as the above salts, a sodium salt and a potassium salt are preferably used.
カチオン系界面活性剤としては、 例えばアンモニゥムクロライ ド モノアルキルアンモニゥムクロライ ド、 ジアルキルアンモニゥムク 口ライ ド、 ト リアルキルアンモニゥムクロライ ド、 塩化セチルト リ メチルアンモニゥム等が、 また両性界面活性剤としては、 アミノ酸 型両性界面活性剤、 ベ夕イン型両性界面活性剤、 硫酸エステル塩型 両性界面活性剤、 スルホン酸塩型両性界面活性剤、 リン酸エステル 塩型両性界面活性剤などが例示される。 Examples of the cationic surfactant include ammonium chloride, monoalkyl ammonium chloride, dialkyl ammonium chloride, trialkyl ammonium chloride, and cetyl chloride. Methylammonium, etc., and examples of the amphoteric surfactant include amino acid-type amphoteric surfactants, bayone-type amphoteric surfactants, sulfate ester-type amphoteric surfactants, sulfonate-type amphoteric surfactants, and phosphorus Acid ester salt-type amphoteric surfactants are exemplified.
非イオン系界面活性剤の具体例としては、 アルキルポリダルコシ ド、 脂肪酸アルカノ一ルアミ ド、 ポリオキシエチレンアルキルエー テル、 グリセリ ン脂肪酸エステル、 ソルピト一ルおよびソルビタン の脂肪酸エステル、 ショ糖の脂肪酸エステル、 プロピレングリコー ル脂肪酸エステル、 高級アルコールエチレンオキサイ ド付加物、 ァ ルキルフエノールエチレンォキサイ ド付加物、 脂肪酸エチレンォキ サイ ド付加物、 多価アルコール脂肪酸エステルエチレンォキサイ ド 付加物、 高級アルキルアミンエチレンオキサイ ド付加物、 脂肪酸ァ ミ ドエチレンォキサイ ド付加物、 グリセロールの脂肪酸エステル、 ペン夕エリスリ トールの脂肪酸エステル、 多価アルコールのアルキ ルェ一テル、 アルカノールァミン類の脂肪酸アミ ドなどが例示され る。  Specific examples of nonionic surfactants include alkyl polydarcosides, fatty acid alkanolamides, polyoxyethylene alkyl ethers, glycerin fatty acid esters, fatty acid esters of sorbitan and sorbitan, and fatty acid esters of sucrose. Propylene glycol fatty acid ester, higher alcohol ethylene oxide adduct, alkyl phenol ethylene oxide adduct, fatty acid ethylene oxide adduct, polyhydric alcohol fatty acid ester ethylene oxide adduct, higher alkylamine ethylene oxide Fatty acid amido ethylene oxide adduct, fatty acid ester of glycerol, fatty acid ester of pentaerythritol, alkyl ether of polyhydric alcohol, fatty acid amine of alkanolamines For example.
上記の界面活性剤は、 各々単独で使用し得る他、 必要により任意 の 2種以上を適宜選択して併用することも可能である。 しかし、 多 くの界面活性剤の中でも本発明で特に好ましく使用されるのは非ィ オン系の界面活性剤であり、 中でも H L Bが 4〜 1 3、 より好まし くは 4〜 9の範囲のものである。 尚、 非イオン系界面活性剤の H L Bは、 「H L B = E / 5 ( Eはポリエチレンオキサイ ド部分の質 量%を表わす) 」 として求める。  The above-mentioned surfactants can be used alone, respectively, and if necessary, any two or more kinds can be appropriately selected and used in combination. However, among many surfactants, non-ionic surfactants are particularly preferably used in the present invention, and HLB having a HLB in the range of 4 to 13, more preferably 4 to 9 is preferred. Things. The HLB of the nonionic surfactant is determined as "HLB = E / 5 (E represents the mass% of the polyethylene oxide portion)".
非イオン系界面活性剤の中でも特に好ましいのは、 アルキンジォ ールのアルキレンオキサイ ド付加物、 より具体的には、 下記一般式 で示されるテトラメチルデシンジオールのエチレンオキサイ ド付加 物で、 重量平均分子量が 3 0 0〜 3 0 0 0、 より好ましくは 3 0 0 〜 1 0 0 0の範囲のものである。 CH3 CH3 CH3 CHs Among the nonionic surfactants, particularly preferred are alkylene oxide adducts of alkynediols, and more specifically, ethylene oxide adducts of tetramethyldecinediol represented by the following general formula. The average molecular weight is in the range of 300 to 300, more preferably in the range of 300 to 1000. CH3 CH3 CH3 CHs
CH3— GH— CH2— C— C≡C— C— CH2— CH— CH3  CH3— GH— CH2— C— C≡C— C— CH2— CH— CH3
0 O  0 O
CH2 CH2  CH2 CH2
CH2 CH2  CH2 CH2
OH OH  OH OH
(式中、 m , nは 0 6の整数で、 少なく とも 1方は 1以上で あり、 m + nは 1 1 2 を表わす) これらの要件を満たすアルキンジオールのアルキレンオキサイ ド 付加物は、 例えばエア一プロダクツ社製の商品名 「サーフィ ノー ル」 シリーズ等として入手できる。 (In the formula, m and n are integers of 06, at least one of which is 1 or more, and m + n represents 112.) The alkylene oxide adduct of alkynediol satisfying these requirements is For example, it can be obtained as a product name “Surfinol” series manufactured by Air Products.
本発明の水分散型粉体塗料では、 前述したスチレン · 無水マレィ ン酸共重合体のアルキレンォキサイ ド付加物と上記界面活性剤を併 用することが有効であり、 それら一方のみを使用したのでは、 本発 明で意図する総合的に優れた塗料性能が得られ難くなる。 そして、 両者の併用による優れた作用効果をより効果的に発揮させるには、 前記スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加物 と界面活性剤を、 塗料用樹脂粉体に対し固形分換算で各々 0 . 1〜 1質量%の範囲で含有させることが望ましく、 また上記スチレン - マレイン酸共重合体のアルキレンォキサイ ド付加物と界面活性剤の 使用比率は、 質量比で前者 1 に対し 0 . 1〜 5、 より好ましくは 0 5〜 2の範囲とすることが望ましい。  In the water-dispersed powder coating material of the present invention, it is effective to use the above-mentioned alkylene oxide adduct of styrene / maleic anhydride copolymer and the above-mentioned surfactant in combination, and only one of them is used. In this case, it is difficult to obtain comprehensively excellent paint performance intended in the present invention. In order to more effectively exert the excellent action and effect of the combined use of both, the alkylene oxide adduct of the styrene / maleic acid copolymer and the surfactant are added to the resin powder for coating in a solid content. It is preferable that each of them is contained in the range of 0.1 to 1% by mass in terms of conversion, and the use ratio of the alkylene oxide adduct of the styrene-maleic acid copolymer and the surfactant is the former 1 by mass ratio. On the other hand, it is desirable to set it in the range of 0.1 to 5, more preferably 0.5 to 2.
本発明で使用する塗料用樹脂の種類には特に制限がなく、 水分散 型粉体塗料用として用いられる公知の榭脂、 例えばエポキシ系樹脂 ポリエステル系樹脂、 アクリル系樹脂、 ポリ塩化ビニル系樹脂、 ポ リエチレン系樹脂、 ポリアミ ド系樹脂、 アルキド系樹脂、 アミノ · アルキド樹脂、 フエノール · アルキド樹脂、 ポリブタジエン系樹脂 シリコン系樹脂、 イソシァネ一ト系樹脂、 メラミン系樹脂、 フッ素 系樹脂などを使用することができ、 これらは各々単独で使用し得る 他、 必要により 2種以上を適宜複合して使用することができる。 There are no particular restrictions on the type of coating resin used in the present invention, and known resins used for water-dispersed powder coatings, such as epoxy resins, polyester resins, acrylic resins, polyvinyl chloride resins, Polyethylene resin, polyamide resin, alkyd resin, amino alkyd resin, phenol alkyd resin, polybutadiene resin Silicone resin, isocyanate resin, melamine resin, fluorine resin, etc. can be used.These can be used alone or in combination of two or more as needed. .
上記塗料用樹脂の中でも特に好ましいのは、 ガラス転移温度が 3 0 °C以上、 より好ましくは 4 0 °C以上で、 8 0 °C以下、 より好まし くは 7 0 °C以下の樹脂である。 ちなみに、 樹脂のガラス転移温度が 3 0 °C未満の場合は、 貯蔵時や輸送時に塗料中の粉体粒子がブロッ キングを起こす恐れが生じるだけでなく、 機械粉砕時に融着を起こ して微粒化し難くなることがあり、 逆にガラス転移温度が高過ぎる 場合は、 焼付時の流動性が悪化して仕上り塗膜の平滑性が低下傾向 を示す様になる。 · 本発明で使用する塗料用樹脂において、 例えば、 上記したェポキ シ系樹脂、 ポリエステル系樹脂、 アクリル系樹脂、 アルキド系樹脂 ポリブタジエン系樹脂、 シリコン系樹脂、 ポリウレタン系樹脂、 フ ッ素系樹脂などの樹脂に水酸基を公知の方法により導入した水酸基 含有樹脂と該樹脂中の水酸基と反応する官能基を有する硬化剤を配 合すれば、 熱や紫外線などによる硬化型の塗料とすることができる このような硬化剤としては、 例えば、 アミノ榭脂 (このものを配 合した塗料をァミノ樹脂硬化型塗料と呼ぶことがある) 、 ブロック 化ポリイソシァネート化合物 (このものを配合した塗料をイソシァ ネート硬化型塗料と呼ぶことがある) などが挙げられる。  Among the above coating resins, particularly preferred are resins having a glass transition temperature of 30 ° C or higher, more preferably 40 ° C or higher, and 80 ° C or lower, more preferably 70 ° C or lower. is there. By the way, if the glass transition temperature of the resin is less than 30 ° C, not only the powder particles in the paint may cause blocking during storage or transportation, but also cause the fusion during mechanical pulverization to cause fine particles. On the other hand, if the glass transition temperature is too high, the fluidity at the time of baking is deteriorated, and the smoothness of the finished coating film tends to decrease. In the coating resin used in the present invention, for example, the above-mentioned epoxy resin, polyester resin, acrylic resin, alkyd resin, polybutadiene resin, silicon resin, polyurethane resin, fluorine resin, etc. If a hydroxyl group-containing resin in which a hydroxyl group is introduced into the resin by a known method and a curing agent having a functional group that reacts with the hydroxyl group in the resin are combined, a curable paint by heat, ultraviolet light, or the like can be obtained. Examples of suitable hardeners include amino resins (paints incorporating these are sometimes referred to as amino resin-curable paints), blocked polyisocyanate compounds (paints containing these are cured with isocyanates) Paints).
ァミノ樹脂として、 例えば、 メラミン、 ベンゾグアナミン、 尿素 ジシアンジアミ ドなどとホルムアルデヒ ドとの縮合又は共縮合によ つて得られるものがあげられ、 更に、 このものを炭素数 1 〜 8のァ ルコール類で変性したものや力ルポキシル基含有アミノ樹脂等も使 用することができる。  Examples of the amino resin include those obtained by condensation or co-condensation of melamine, benzoguanamine, urea dicyandiamide, and the like with formaldehyde, and further modified with alcohols having 1 to 8 carbon atoms. Also, an amino resin containing a carboxylic acid group can be used.
水酸基とァミノ樹脂の硬化触媒として、 パラ トルエンスルホン酸 ドデシルベンゼンスルホン酸、 ジノニルナフタレンスルホン酸、 ジ ノエルナフタレンジスルホン酸などの酸、 これらの酸のアミン中和 物を配合することができる。 ブロック化ポリイソシァネート化合物としては、 フリーのイソシ ァネート化合物をブロック化剤でブロック化したポリイソシァネー ト化合物である。 Acids such as para-toluenesulfonic acid dodecylbenzenesulfonic acid, dinonylnaphthalenesulfonic acid, and dinoernaphthalenedisulfonic acid, and amine-neutralized products of these acids can be blended as a curing catalyst for the hydroxyl group and the amino resin. The blocked polyisocyanate compound is a polyisocyanate compound obtained by blocking a free isocyanate compound with a blocking agent.
フリーのイソシァネ一ト基を有するポリイソシァネート化合物と しては、 へキサメチレンジイソシァネ一 ト、 もしくはトリメチルへ キサメチレンジイソシァネート等の脂肪族ジィソシァネート類、 キ シレンジイソシァネ一ト、 もしくはイソホロンジイソシァネート等 の環状脂肪族ジィソシァネート類、 トリ レンジイソシァネートもし くは 4, 4 ' —ジフエニルメタンジイソシァネート等の芳香族ジィ ソシァ.ネート類等の有機ジイソシァネートそれ自体、 又はこれらの 各有機ジイソシァネートの過剰量と多価アルコール、 低分子量ポリ エステル樹脂もしくは水等との付加物、 あるいは前述した各有機ジ イソシァネート同士の (共) 重合体、 更にはイソシァネート · ピウ レツ ト体等が挙げられる。  Examples of the polyisocyanate compound having a free isocyanate group include aliphatic diisocyanates such as hexamethylene diisocyanate or trimethyl hexamethylene diisocyanate, and xylene diisocyanate. Or organic diisocyanates such as cycloaliphatic diisocyanates such as isophorone diisocyanate, aromatic diisocyanates such as tolylene diisocyanate or 4,4'-diphenylmethane diisocyanate An adduct of an excess amount of each of these organic diisocyanates with a polyhydric alcohol, a low molecular weight polyester resin or water, or a (co) polymer of each of the above-mentioned organic diisocyanates; Lett bodies and the like can be mentioned.
ブロック化剤としては、 才キシム、 フエノール、 アルコール、 ラ クタム、 マロン酸エステル、 メルカプ夕ン等が挙げられる。  Examples of the blocking agent include oxime, phenol, alcohol, lactam, malonate, and mercapone.
また、 ブロック化剤の解離触媒として、 鉛系触媒 ( 2 —ェチルへ キサン酸鉛、 安息香酸鉛、 ォレイン酸鉛など) 、 錫系触媒 (テトラ ブチル錫、 ォクチル酸錫、 ォレイン酸錫、 酒石酸錫、 ジブチル錫ジ ( 2 —ェチルへキシレート) 、 ジベンジル錫ジ ( 2 —ェチルへキシ レー ト) 、 ジブチル錫ジラウレ一卜、 ジブチル錫ジイソォクチルマ レエ一卜、 ジブチル錫スルフィ ド、 ジブチル錫ジブトキシドなど) 亜鉛系触媒 (ナフテン酸亜鉛など) 、 アンチモン系触媒 (三塩化ァ ンチモンなど) などを配合することができる。  In addition, as a dissociation catalyst for the blocking agent, a lead-based catalyst (such as lead 2-ethylethylhexanoate, lead benzoate, and lead oleate), and a tin-based catalyst (tetrabutyltin, tin octoate, tin oleate, tin tartrate) , Dibutyltin di (2-ethylhexylate), dibenzyltin di (2-ethylhexylate), dibutyltin dilaurate, dibutyltin diisooctyl maleate, dibutyltin sulfide, dibutyltin dibutoxide, etc.) A catalyst (such as zinc naphthenate) and an antimony-based catalyst (such as antimony trichloride) can be blended.
また、 本発明で使用する塗料用樹脂において、 例えば、 上記した ボリエステル系樹脂、 アク リル系樹脂、 アルキド系樹脂、 ポリブ夕 ジェン系樹脂、 シリコン系樹脂、 ポリウレタン系樹脂、 フッ素系樹 脂などの樹脂に、 力ルポキシル基を公知の方法で導入したカルポキ シル基含有樹脂と該樹脂中の力ルポキシル基と反応する官能基を有 する硬化剤を配合すれば、 熱や紫外線などによる硬化型の塗料とす ることができる。 In the resin for paint used in the present invention, for example, the above-mentioned resins such as polyester resin, acryl resin, alkyd resin, polybutylene resin, silicon resin, polyurethane resin, fluorine resin, etc. In addition, if a carboxyl group-containing resin into which a carboxylic acid group is introduced by a known method and a curing agent having a functional group that reacts with the carboxylic acid group in the resin are blended, a curable paint by heat or ultraviolet light can be obtained. You Can be
このような硬化剤としては、 例えば、 ポリエポキシ化合物 (この ものを配合した塗料をエポキシ硬化型塗料と呼ぶことがある) など が挙げられる。  As such a curing agent, for example, a polyepoxy compound (a paint containing this compound may be referred to as an epoxy curable paint) may be used.
ポリエポキシ化合物とは、 1分子中に少なく とも 2個のエポキシ 基を有する化合物であり、 その代表的な例としては、 エチレングリ コール . ジグリ シジルエーテル、 ネオペンチルダリコール ■ ジグリ シジルエーテル、 グリセリ ン · ジグリシジルエーテル、 グリセリ ン · トリグリシジルエーテル、 ジグリセリ ン ' トリグリシジルェ一 テル、 水添ビスフエノール A · ジグリシジルェ一テルまたはビスフ ヱノール A · ジグリシジルェ一テルなどの多価アルコールのポリグ リシジルエーテル、 あるいは側鎖にエポキシ基を有するビニル系重 合体などが挙げられる。  A polyepoxy compound is a compound having at least two epoxy groups in one molecule. Typical examples thereof include ethylene glycol. Diglycidyl ether, neopentyldaricol ■ diglycidyl ether, glycerin Polyglycidyl ether of polyhydric alcohols such as diglycidyl ether, glycerintriglycidyl ether, diglycerin 'triglycidyl ether, hydrogenated bisphenol Adiglycidyl ether or bisphenol Adiglycidyl ether Examples include vinyl-based polymers having an epoxy group in the side chain.
カルボキシル基とエポキシ基との硬化触媒としては、 ジェトキシ ジメチルシラン、 ジェトキシジェチルシラン、 トリメ トキシプロピ ルシラン、 トリメ トキシブチルシラン、 トリメ トキシフエ二ルシラ ン、 テトラエ卜キシシラン、 r - N - ( 2 —アミノエチル) ァミノ プロピルトリメ 卜キシシラン、 ァ一メルカプトプロピルトリメ トキ シシランなどのシラン化合物が挙げられる。  As a curing catalyst for a carboxyl group and an epoxy group, ethoxy dimethyl silane, ethoxy ethoxyl silane, trimethoxy propyl silane, trimethoxy butyl silane, trimethoxy phenyl silane, tetraethoxy silane, r-N- (2-aminoethyl And silane compounds such as aminopropyltrimethoxysilane and aminocaptopropyltrimethoxysilane.
また、 本発明で使用する塗料用樹脂において、 例えば、 上述した エポキシ系樹脂 [ビスフエノ一ル型グリシジルエーテルタイプ、 グ リシジル (メタ) ァクリ レートを必須成分とする (メタ) アクリル 系 (共) 重合体など] のエポキシ基をカチオン重合させるカチオン 重合触媒や、 エポキシ基と反応する官能基を有する硬化剤 (このも のを配合した塗料をエポキシ硬化型塗料と呼ぶことがある) を配合 することにより、 熱や紫外線による硬化型の塗料とすることができ る。  In the coating resin used in the present invention, for example, the above-mentioned epoxy resin [bis (phenol) -type glycidyl ether type, (meth) acrylic (co) polymer having glycidyl (meth) acrylate as an essential component, Etc.), and a curing agent having a functional group that reacts with the epoxy group (paints containing these are sometimes called epoxy-curable paints). It can be used as a paint that can be cured by heat or ultraviolet light.
カチオン重合触媒としては、 例えば、 ァリールジァゾニゥム塩、 ァリ一ルョードニゥム塩、 ァリ一ルスルホニゥム塩等が挙げられる また、 硬化剤としては、 例えば、 ポリカルボン酸樹脂 (アクリル 系樹脂、 ポリエステル系樹脂等) 、 フエノール樹脂 (ノポラック型 フエノール樹脂、 レゾール型フエノール樹脂など) 、 ポリカルボン 酸化合物 (例えば、 アジピン酸、 セバシン酸、 トリメ リ ッ ト酸、 ド デカン 2酸、 フタ一ル酸等) 、 アミ ド (ジシアンジアミ ド等) が挙 げられる。 Cationic polymerization catalysts include, for example, aryldiazonium salts, arylodenium salts, arylsulfonium salts, and the like. Curing agents include, for example, polycarboxylic acid resins (acrylic resins) Resins, polyester resins, etc.), phenolic resins (nopolac-type phenolic resins, resole-type phenolic resins, etc.), polycarboxylic compounds (eg, adipic acid, sebacic acid, trimellitic acid, dodecane diacid, phthalic acid) Phosphoric acid) and amides (such as dicyandiamide).
なお必要によっては、 上記塗料用樹脂に加えて、 通常の粉体塗料 に配合されることのある硬化剤、 硬化促進剤、 流動調整剤、 発泡防 止剤、 帯電防止剤、 紫外線吸収剤、 防鲭剤などを配合し、 塗膜特性 を更に改善することも勿論可能である。  If necessary, in addition to the above resin for paint, a curing agent, a curing accelerator, a flow regulator, a foaming inhibitor, an antistatic agent, an ultraviolet absorber, an antioxidant, which may be added to ordinary powder coating materials. It is, of course, possible to further improve the properties of the coating film by blending an agent.
尚、 本発明の水分散型粉体塗料においては、 上記成分に加えて、 例えばアクリル酸系共重合体 (アク リル酸とアク リルエステルの共 重合体) 、 セルロース系 (メチルセルロース、 ヒ ドロキシェチルセ ルロース、 プロピルセルロース、 カルポキシメチルセルロースな ど) 、 ポリウレタン系 (ポリエーテル変性ウレタン化合物など) 、 ポリアマイ ド系、 クレー系 (ベントナイ ト、 ヘク トライ ト、 サポナ イ トなど) の増粘剤や、 ミネラルオイル系や鉱物系、 シリコン系な どの消泡剤、 更には被塗装物である金属 (特に鉄系合金など) に対 して鲭止め機能を与えるための防鲭剤などを添加することも可能で あ 0  In addition, in the water-dispersed powder coating of the present invention, in addition to the above components, for example, acrylic acid-based copolymer (copolymer of acrylic acid and acrylic ester), cellulose-based (methylcellulose, hydroxyshethyl cellulose, propyl Cellulose, carboxymethylcellulose, etc.), polyurethane (polyether-modified urethane compounds, etc.), polyamide, clay (bentonite, heptrite, saponite, etc.) thickeners, mineral oils and minerals It is also possible to add a defoaming agent such as a metal-based or silicon-based material, and also a heat-proofing agent that provides a stopping function to the metal to be coated (especially an iron-based alloy).
本発明の水分散型粉体塗料では、 実質的に塗料用樹脂のみからな る粉体を用いた場合は、 所謂クリア一塗膜形成用の塗料となる。 ま た塗料用樹脂と共に適量の顔料や染料を配合した粉末を使用すれば 当該顔料や染料の有する色調等に応じた色彩の着色塗料として得る ことができる。  In the water-dispersed powder coating of the present invention, when a powder substantially consisting only of a coating resin is used, it becomes a coating for forming a so-called clear coating film. When a powder containing an appropriate amount of a pigment or a dye is used together with the resin for a coating, a colored coating having a color corresponding to the color tone or the like of the pigment or the dye can be obtained.
こ こで用いる顔料としては、 着色顔料ゃ防鲭顔料などが包含され 着色顔料としては例えば、 ベンガラなどの酸化鉄、 酸化チタン、 チ タン黄、 亜鉛華、 硫化亜鉛、 リ トボン、 酸化アンチモン、 コバルト ブルー、 力一ポンプラックなどの無機系顔料や、 キナクリ ドンレツ ド、 フタロシアニンブルー、 フタロシアニングリーン、 パーマネン トレッ ド、 ハンザイエロ一、 イ ンダンスレンブル一、 ブリ リアント ファース トスカーレツ ト、 バリオゲンレツ ドなどの有機顔料が例示 され、 これらも単独で使用し得る他、 必要により 2種以上を組合せ て使用できる。 The pigments used here include coloring pigments and anti-pigmenting pigments. Examples of coloring pigments include iron oxide such as red iron oxide, titanium oxide, titanium yellow, zinc white, zinc sulfide, lithium sulfide, antimony oxide, and cobalt. Inorganic pigments such as blue and Rikiichi pump racks, quinacridone red, phthalocyanine blue, phthalocyanine green, permanent red, hanzaeroel, indian sable, brilliant Examples thereof include organic pigments such as first scarlet and variogen red. These can be used alone, or two or more can be used in combination as needed.
更に、 体質顔料ゃ艷消し剤として、 炭酸カルシウム、 硫酸バリゥ ム、 炭酸バリウム、 クレー、 タルク、 ケイソゥ土、 シリカ粉、 塩基 性炭酸マグネシウム、 アルミナホワイ ト等を使用したり、 塗膜の光 輝性向上を目的として配合される光輝性顔料として、 パール顔料、 アルミニウム粉やステンレス鋼粉などの金属粉や金属フレーク、 ガ ラスビーズやガラスフレーク、 雲母、 リン片状酸化鉄 (M I O) 等 を併用することも有効である。  In addition, calcium carbonate, barium sulfate, barium carbonate, clay, talc, diatomaceous earth, silica powder, basic magnesium carbonate, alumina white, or the like may be used as an extender and an anti-glare agent. Use of pearl pigments, metal powders such as aluminum powder and stainless steel powder, metal flakes, glass beads and glass flakes, mica, flake iron oxide (MIO), etc. as glitter pigments for the purpose of improvement Is also effective.
上記顔料の配合量には一切制限がなく、 用いる顔料の種類や塗膜 に求められる色調、 明度、 彩度などに応じて任意に選定すればよい が、 標準的な配合量は、 塗料用樹脂 1 0 0質量部に対し 1〜 8 0質 量部の範囲、 より一般的には 2〜 7 0質量部の範囲である。 なお、 ク リア一塗料とする場合に顔料の配合が省略されることは当然であ る。 また必要によっては、 顔料に加えて或いは顔料に代えて任意の 染料を使用することも可能である。  There is no limitation on the amount of the above pigments, and it may be arbitrarily selected according to the type of pigment to be used and the color tone, lightness, saturation, etc. required for the coating film. It is in the range of 1 to 80 parts by mass, more usually in the range of 2 to 70 parts by mass, per 100 parts by mass. It should be noted that when clear paint is used, the blending of the pigment is naturally omitted. If necessary, any dye may be used in addition to or instead of the pigment.
本発明の水分散型粉体塗料は、 スプレー塗装時に塗料の夕レゃヮ キ、 透け等を生じることなく、 レべリ ング性に優れ、 より平滑性の 高い塗膜の形成を容易にするため、 該水分散型粉体塗料の 2 3 °Cで の粘度を l O O m P a ' s以上、 より好ましくは 2 0 0 mP a * s 以上で、 5 0 0 0 m P a ' s 以下、 より好ましく は 4 0 0 0 m P a · s以下に調整することが望ましい。  The water-dispersed powder coating of the present invention has excellent leveling properties and facilitates the formation of a coating film having higher smoothness, without causing the coating to be dull or transparent during spray coating. Therefore, the viscosity of the water-dispersed powder coating at 23 ° C. is not less than 100 mPas, more preferably not less than 200 mPas and not more than 500 mPas. It is more preferable to adjust the pressure to 400 mPas or less.
ちなみに塗料粘度が低過ぎる場合は、 塗装時のレペリング性は良 好であるが、 スプレー塗装時にタレを起したり加熱乾燥時にヮキを 生じ易くなって均質な塗膜が得られ難くなり、 逆に塗料粘度が高過 ぎると、 タレ性は良好になるが、 塗装作業性や塗装時のレべリ ング 性が悪化し平滑な塗膜が得られ難くなる傾向が生じてくる。  By the way, if the paint viscosity is too low, the repelling property at the time of painting is good, but sagging occurs at the time of spray painting and cracking tends to occur at the time of heating and drying, making it difficult to obtain a uniform coating film. If the paint viscosity is too high, the sagging property will be good, but the workability of painting and the leveling property at the time of painting will deteriorate, and it tends to be difficult to obtain a smooth coating film.
次に、 本発明に係る水分散型粉体塗料の製法について説明する。 上記水分散型粉体塗料は、 原料となる塗料用樹脂またはこれと顔 料や染料を溶融混合して冷却固化させ、 適当なサイズ (通常は l m m以下) に粗粉砕してから適量の水に分散させ、 該水分散体を循環 型ビーズミル等で処理することによって、 好ましい平均粒径 (D 5 0 ) と粒度分布を満たす様に微粉砕する。 Next, a method for producing the water-dispersed powder coating material according to the present invention will be described. The water-dispersed powder coating is a coating resin as a raw material or It is preferable to melt and mix the ingredients and dyes, cool and solidify, coarsely pulverize to an appropriate size (usually 1 mm or less), disperse them in an appropriate amount of water, and treat the aqueous dispersion with a circulation type bead mill or the like. Finely pulverize so as to satisfy the average particle size (D50) and the particle size distribution.
循環型ビーズミルとは、 破碎用メディアとして鋼球やセラミック ス球などが装入されたビーズミルと処理液タンクとの間で粗粉碎分 散液を循環させ、 分散液中の粉体の微細化を進める装置であり、 微 細化の進行状態は粉砕用メディアの材質、 サイズ、 充填量、 アジテ —夕一シャフ トの回転数、 分散液の循環流量などによって変わって くるが、 何れにしても循環運転時間を調整することで微細化の程度 を任意に調整できる。  The recirculating bead mill circulates the coarsely ground dispersion liquid between a bead mill containing steel balls, ceramic balls, etc. as a crushing medium and a processing liquid tank to reduce the size of the powder in the dispersion liquid. The progress of atomization depends on the material, size, filling amount, rotation speed of agitator / evening shaft, circulation flow rate of dispersion liquid, etc. The degree of miniaturization can be arbitrarily adjusted by adjusting the operation time.
尚、 ビーズミルを用いて微粉砕を行う際に、 処理液温度が高温に なると水分散液中の粉体同士がブロッキング (融着) を起こす恐れ があるが、 循環型ビーズミルとして外付け型もしくは内臓型の冷却 機構を備えたものを使用し、 処理液温度を低めに抑えて微粉砕処理 を行えば、 微粒子同士がプロッキングを起こすことなく円滑に微細 化できるので好ましい。 この際、 塗料粘度が高すぎると微粉碎時に 昇温し易くなつてブロッキングを起こす原因になるので、 塗料粘度 は常温で約 5 0 0 0 m P a · s程度以下に抑えるのがよい。  When finely pulverizing using a bead mill, if the temperature of the treatment liquid is high, the powders in the aqueous dispersion may block (fuse) with each other. It is preferable to use a mold equipped with a cooling mechanism and to carry out the fine pulverization treatment while keeping the temperature of the processing solution low, since fine particles can be smoothly reduced without blocking. At this time, if the paint viscosity is too high, the temperature tends to rise during pulverization, which may cause blocking. Therefore, the paint viscosity is preferably suppressed to about 500 mPa · s or less at room temperature.
図 1は、 循環型ビーズミルで微細化処理を行う際の循環運転時間 と水分散液中の粉体の粒径との関係を示したグラフであり、 循環運 転時間を適宜調整することで目標とする粒度構成の水分散液を容易 に得ることができる。 これに対し、 粗粉碎水分散液の微細化にビー ズミルを使用したとしても、 多パス運転法を採用した場合は、 例え ば図 2に示す如く粒径がパス回数毎に段階的に変化するだけであり 所望する粒径範囲に調整することが難しい。 よって、 前述した好ま しい平均粒径 (D 5 0 ) と粒度分布を得るには、 循環型ビーズミル を使用することが望ましい。  Fig. 1 is a graph showing the relationship between the circulating operation time and the particle size of the powder in the aqueous dispersion when performing the fine processing by the circulating bead mill. It is possible to easily obtain an aqueous dispersion having the following particle size configuration. On the other hand, even if a bead mill is used to refine the coarsely divided aqueous dispersion, when the multi-pass operation method is adopted, for example, the particle size changes stepwise with each pass, as shown in Fig. 2. It is difficult to adjust the particle size to a desired range. Therefore, in order to obtain the above-mentioned preferable average particle size (D50) and particle size distribution, it is desirable to use a circulation type bead mill.
なお、 循環型ビーズミルにかける粗粉碎水分散液の粒度構成は特 に制限的でなく、 前述した如く塗料用樹脂と必要により配合される 顔料の溶融混合物を適当に粗粉碎したものを使用すればよいが、 循 環型ビーズミルによる微細化処理後の粒径範囲を極力狭く して粒度 分布を狭めるには、 粗粉砕物の粒径範囲もできるだけ狭く しておく ことが望ましく、 そのためには、 前記溶融混合物を適当な厚さ. (好 ましくは 1 m m前後) のシート状に加工してから破砕した粗粉碎物 を使用することが望ましい。 しかして、 シート状にしてから破砕す ると、 塊状物を破砕したものに較べて粗粉砕物の粒径が相対的に均 一となつて粒度分布の狭い粗粉碎物が得られ易くなり、 ひいては、 循環型ビーズミルで処理することによつて得られる微粉砕物の粒度 構成もより均一になるからである。 The particle size composition of the coarsely ground aqueous dispersion to be subjected to the circulation type bead mill is not particularly limited, and may be blended with the paint resin as necessary as described above. The melt mixture of pigments may be used by appropriately pulverizing it.However, in order to narrow the particle size range after refining by a circulating bead mill as much as possible and to narrow the particle size distribution, the particle size range of the coarsely pulverized product It is also desirable to make the molten mixture as narrow as possible. For this purpose, it is preferable to use a coarsely crushed material obtained by processing the molten mixture into a sheet having an appropriate thickness (preferably around 1 mm) and then crushing it. desirable. However, when crushed after being formed into a sheet, the coarsely crushed material has a relatively uniform particle size as compared with crushed lump material, and it becomes easier to obtain coarsely crushed material having a narrow particle size distribution. As a result, the particle size composition of the finely pulverized product obtained by treating with a circulation type bead mill becomes more uniform.
そして、 この様な粗粉砕の後、 循環型ビーズミルを使用し、 粉碎 用メディアの材質、 サイズ、 充填量、 アジテーターシャフ トの回転 数、 塗料の循環流量などに応じて循環時間を適宜調整すれば、 前掲 の好適粒度範囲と粒度分布を有する水分散型粉体塗料を容易に得る ことができる。  After such coarse pulverization, a circulation type bead mill can be used to adjust the circulation time as appropriate according to the material, size, filling amount, rotation speed of the agitator shaft, circulation flow rate of the paint, etc. It is possible to easily obtain the water-dispersed powder coating material having the above-mentioned preferred particle size range and particle size distribution.
なお、 該塗料用樹脂粉体を水に分散させる際に好ましく配合され る前記スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加 物や界面活性剤、 或いは更に他の水系添加剤は、 塗料用樹脂粉末を 製造する際に、 その配合原料中に含有させたり、 粗粉砕する際に水 分散液中に添加してもよく、 或いは循環型ビーズミルによる処理の 前または処理途中で添加してもよく、 更にはビーズミル処理後に添 加しても構わない。  The alkylene oxide adduct of the styrene / maleic acid copolymer and the surfactant, which are preferably blended when the resin powder for coating is dispersed in water, or other water-based additives, are used for coating. It may be contained in the compounding raw material when producing the resin powder, or added to the aqueous dispersion when coarsely pulverized, or may be added before or during the treatment by the circulating bead mill. Alternatively, it may be added after the bead mill treatment.
かく して得られる微粉砕分散液を、 最終工程で、 必要により加圧. 吸引あるいは超音波加振機構付のスクリーンに通して異物や夾雑物 を濾別すると、 本発明の水分散型粉体塗料を得ることができる。  The thus obtained finely pulverized dispersion liquid is optionally pressurized in the final step. The water-dispersed powder of the present invention is obtained by filtering foreign substances and impurities through a screen equipped with suction or an ultrasonic vibrating mechanism. Paint can be obtained.
本発明において、 上記水分散型粉体塗料が塗装される被塗物の種 類は一切制限されず、 例えば自動車、 船舶、 電車などに用いる素材 や部品、 外板材などの建材、 家電製品や事務機器などの構成素材や 外殻体、 各種容器、 機械部品 · 部材、 管材、 缶や家具などとして用 いる各種の金属部材ゃプラスチック部材などの塗装に幅広く適用す ることができる。 In the present invention, the type of the object to be coated with the water-dispersed powder coating is not limited at all, and examples thereof include materials and parts used for automobiles, ships, trains, and the like, building materials such as outer panel materials, home electric appliances and office work. It is widely applied to the coating of materials such as components, outer shells, various containers, machine parts and members, pipes, various metal members used for cans and furniture, and plastic members. Can be
プラスチック類と しては、 透明、不透明の如何を問わず公知の 種々のプラスチックが挙げられ、 具体的には、 ポリオレフイ ン、 ポ リエステル、 ポリアミ ド、 ポリウレタン、 ポリイミ ド、 ポリカーボ ネートなどが挙げられる。 これらプラスチック類の被塗物には、 必 要に応じて適宜の表面処理を施しておく ことも可能である。  Examples of the plastics include various known plastics irrespective of whether they are transparent or opaque, and specific examples thereof include polyolefins, polyesters, polyamides, polyurethanes, polyimides, and polycarbonates. These plastics can be appropriately surface-treated as necessary.
金属類としては、 最も汎用性の高い鋼や合金鋼などの鉄基金属材 を始めとして、 アルミニウムやチタン、 真鍮などの非鉄金属や合金 など、 更には、 亜鉛めつき鋼材や錫めつき鋼材などのめつき金属 材 ; クロメート処理ゃリ ン酸塩処理を施した表面処理鋼材 ; 陽極酸 化処理や陰極酸化処理、 封孔処理などの施されたアルミニウム又は アルミニウム合金材、 などに制限なく適用できる。  Metals include the most versatile iron-based metal materials such as steel and alloy steel, as well as non-ferrous metals and alloys such as aluminum, titanium, and brass, as well as zinc-plated steel and tin-plated steel. Nozzle metal material; chromate-treated phosphate-treated surface-treated steel material; applicable to aluminum or aluminum alloy materials that have been subjected to anodic oxidation, cathodic oxidation, sealing, etc. .
金属以外の無機材類として、 例えば、 コンク リート、 モルタル、 ガラスなどに塗布することも可能であり、 これらの被塗物にも、 必 要に応じて適宜の表面処理を施しておく ことができる。  As inorganic materials other than metal, for example, it is also possible to apply to concrete, mortar, glass, etc., and it is possible to apply an appropriate surface treatment to these objects to be coated as necessary. .
また本発明の水分散型粉体塗料は、 耐水性ゃ耐薬品性、 耐候性、 耐傷付き性などを高めるため、 塗料用樹脂として熱硬化性樹脂を使 用することが多いため、 塗装後は大抵の場合焼付け処理されるが、 該焼付けには、 例えば電気熱風乾燥炉、 ガス熱風乾燥炉 (間接熱風 a接熱風) 、 遠赤外乾燥炉、 ジェッ トヒーター乾燥炉など任意の乾 燥炉を使用し、 例えば 1 2 0〜 3 5 0 、 より一般的には 1 4 0〜 2 5 O :で 1 0秒〜 6 0分、 より一般的には 5分〜 4 0分程度で加 熱乾燥すればよい。 上記加熱乾燥に先立って、 予備乾燥しておく こ とも有効である。  In addition, the water-dispersed powder coating of the present invention often uses a thermosetting resin as a coating resin in order to enhance water resistance, chemical resistance, weather resistance, and scratch resistance. In most cases, baking treatment is performed. For this baking, any drying furnace such as an electric hot air drying oven, a gas hot air drying oven (indirect hot air a hot air blowing), a far infrared drying oven, or a jet heater drying oven is used. Use, for example, 120 to 350, more generally 140 to 25 O: 10 seconds to 60 minutes, and more generally, heat drying in about 5 minutes to 40 minutes do it. It is also effective to carry out preliminary drying prior to the above heat drying.
本発明の水分散型粉体塗料を被塗物に塗装したり印刷する手法に も全く制限がなく、 従来から公知の方法、 静電塗装 (回転式、 エア 霧化式、 エアレス式、 エアアシス ト式など) や、 電着塗装、 エアス プレー塗装、 エアレス塗装、 ナチュラルロールコーター塗装、 リバ 一スロールコーター塗装、 力一テンフローコ一夕一塗装、 ローラ一 力一テン塗装、 ダイコーター塗装、 浸漬塗装、 刷毛塗り、 スクリー ン印刷など、 任意の方法を採用できる。 The method of applying the water-dispersed powder coating material of the present invention to an object to be coated or printed is not limited at all, and any of the conventionally known methods, electrostatic coating (rotary, air atomizing, airless, air assist, etc.) Type), electrodeposition coating, air spray coating, airless coating, natural roll coater coating, rib-roll coating, roller-coating, roller-coating, roller-coating, die coater coating, immersion coating, brushing Painting, screen Any method such as printing can be adopted.
塗膜厚さは、 塗膜に要求される性能や外観などに応じて適宜決め ればよいが、 通常は 2 0〜 5 0 0 i m、 特に 3 0〜 1 0 0 mが好 ましく、 厚塗りを行う場合は 2回塗りや 3回塗りなどの多層塗りを 採用することも勿論有効である。  The thickness of the coating film may be appropriately determined according to the performance and appearance required of the coating film, but is usually from 20 to 500 im, particularly preferably from 30 to 100 m. In the case of coating, it is of course effective to adopt a multilayer coating such as two-coating or three-coating.
また本発明の水分散型粉体塗料は、 前述した如く塗料用樹脂粉体 を均一且つ安定に微分散させたもので、 特にスプレー塗装法を採用 した場合は、 被塗物以外に塗料成分がオーバ一スプレーするが、 こ れらは加熱処理しない限り水への再分散性は良好であるので、 これ らォ一バースプレーした粉体塗料は随時粉体として捕集し、 或いは 水洗等により水分散体として捕集することで、 回収することも可能 である。  The water-dispersed powder coating material of the present invention is obtained by uniformly and stably finely dispersing the resin powder for coating as described above. In particular, when the spray coating method is employed, the coating components other than the material to be coated are not included. Overspray is performed, but since redispersibility in water is good unless heat treatment is performed, powder paint sprayed with these bars is collected as powder at any time, or washed with water or the like. By collecting as a dispersion, it can be recovered.
なお本発明の水分散型粉体塗料は、 下塗り塗料、 中塗り塗料ある いは上塗り塗料 (例えば、 着色塗料、 着色べ一ス塗料 クリア一上 塗り塗料などを包含する) として使用できる。  The water-dispersed powder coating of the present invention can be used as an undercoat, an intermediate coating, or a top coating (including, for example, a coloring coating, a coloring base coating, and a clear top coating).
下塗り塗料として使用する際には、 上述した塗料用樹脂粉体以外 に、 例えば、 着色顔料、 防食顔料、 無機充填剤、 可塑剤、 上記以外 の界面活性剤、 消泡剤、 或いは更に他の添加剤 (防腐剤、 溶媒な ど) 等を特に制限なく配合することができる。 下塗り塗料として使 用する場合は、 金属に対する付着性や防食性などの観点からェポキ シ樹脂系硬化型塗料やポリエステル樹脂系硬化型塗料を使用するこ とが好ましい。  When used as an undercoat paint, besides the above-mentioned resin powder for paint, for example, coloring pigments, anticorrosion pigments, inorganic fillers, plasticizers, surfactants other than the above, defoamers, or other additives Agents (preservatives, solvents, etc.) can be added without any particular limitation. When used as an undercoat, it is preferable to use epoxy resin-based curable paints or polyester resin-based curable paints from the viewpoints of adhesion to metals and corrosion resistance.
本発明の水分散型粉体塗料を中塗り塗料として使用する際には、 上述した塗料用樹脂粉体以外に、 例えば、 着色顔料、 無機充填剤、 可塑剤、 上記以外の界面活性剤、 消泡剤、 その他添加剤 (防腐剤、 溶媒等) などを配合することができる。 中塗り塗料としては、 上塗 り塗膜又は下塗り塗膜に対する付着性、 耐候性、 仕上り性などの観 点からポリエステル樹脂系硬化型塗料を使用することが好ましい。  When the water-dispersed powder coating of the present invention is used as an intermediate coating, in addition to the above-mentioned resin powder for coating, for example, a coloring pigment, an inorganic filler, a plasticizer, a surfactant other than the above, Foaming agents and other additives (preservatives, solvents, etc.) can be added. As the intermediate coating, it is preferable to use a polyester resin-based curable coating from the viewpoints of adhesion to an overcoat or undercoat, weather resistance and finish.
本発明の水分散型粉体塗料を上塗りタイプの着色塗料として使用 する場合には、 上述した塗料用樹脂粉体以外に、 例えば、 着色顔料 無機充填剤、 可塑剤、 上記以外の界面活性剤、 消泡剤、 安定剤、 そ の他の添加剤 (艷消し剤、 艷出し剤、 防腐剤、 擦り傷防止剤、 溶媒 等) などを配合することができる。 上塗り塗料としては、 耐候性、 仕上り性などの観点からポリエステル樹脂系硬化型塗料ゃァク リル 樹脂系硬化型塗料を使用することが好ましい。 When the water-dispersed powder coating of the present invention is used as a top-coating colored coating, other than the above-mentioned coating resin powder, for example, a coloring pigment Inorganic fillers, plasticizers, surfactants other than the above, antifoaming agents, stabilizers, and other additives (such as anti-glazing agents, glazing agents, preservatives, anti-scratch agents, solvents, etc.) be able to. As the top coat, it is preferable to use a polyester resin-based curable paint acrylic resin-based curable paint from the viewpoints of weather resistance, finish properties, and the like.
本発明の水分散型粉体塗料を上塗りタイプのク リア一塗料として 使用する際には、 上述した塗料用樹脂粉体以外に、 例えば、 着色顔 料 (下地が完全に隠蔽しない程度) 、 無機充填剤、 可塑剤、 上記以 外の界面活性剤、 消泡剤、 安定剤、 その他の添加剤 (艷消し剤、 艷 出し剤、 防腐剤、 擦り傷防止剤、 溶媒等) などを配合することがで きる。  When the water-dispersible powder coating of the present invention is used as a clear top coating of a top coating type, other than the above-mentioned resin powder for coating, for example, a coloring pigment (to the extent that the base is not completely hidden), inorganic Fillers, plasticizers, surfactants other than the above, defoamers, stabilizers, and other additives (such as anti-glazing agents, glazing agents, preservatives, anti-scratch agents, solvents, etc.) may be added. it can.
次に、 上述した下塗り塗料、 中塗り塗料、 あるいは上塗り塗料と して使用する場合の具体的な塗膜形成法について、 その具体例を以 下に示す。  Next, specific examples of the method of forming a coating film when used as the above-mentioned undercoat, intermediate coat, or topcoat are shown below.
①本発明の水分散型粉体塗料を下塗り塗料として用いる塗装例。 この塗装例は、  (1) A coating example in which the water-dispersed powder coating of the present invention is used as an undercoat. This painting example
1 )金属などの素材表面に直接、 前記水分散型粉体塗料を下塗り塗料 として塗装し、  1) Apply the water-dispersed powder coating directly as a primer on the surface of a material such as metal,
2)必要により焼付処理を行った後、  2) After baking as required,
3)必要に応じて公知の硬化型塗料、 もしくは前述した本発明の水分 散型粉体塗料を中塗り塗料として塗装し、  3) If necessary, a known curable paint, or a water-dispersible powder paint of the present invention described above is applied as an intermediate paint,
4)必要により焼付処理した後、  4) After baking if necessary,
5)公知の硬化型塗料、 もしくは本発明の水分散型粉体塗料を上塗り 塗料として塗装し、  5) A known curable coating, or a water-dispersible powder coating of the present invention is applied as a top coating,
6)最後に所定の焼付温度で上塗り塗膜を硬化させる (下塗り塗膜及 び Z又は中塗り塗膜が未硬化の場合には同時に硬化させる) 方法 である。  6) Finally, the top coat is cured at a predetermined baking temperature (when the undercoat and Z or the intermediate coat are not cured, they are cured simultaneously).
②本発明の水分散型粉体塗料を中塗り塗料として用いる塗装例。 この塗装例は、  (2) A coating example using the water-dispersed powder coating of the present invention as an intermediate coating. This painting example
1 )金属製などの素材表面に公知の硬化型塗料下塗り塗料として直接 塗装し、 1) Directly as a well-known curable undercoat paint on the surface of materials such as metal Painted,
2)必要に応じて焼付けた後、  2) After baking if necessary,
3)本発明の水分散型粉体塗料を中塗り塗料として塗装し、  3) The water-dispersed powder coating of the present invention is applied as an intermediate coating,
4)必要に応じて焼付処理した後、  4) After baking if necessary,
5)公知の硬化型塗料、 もしくは前記本発明の水分散型粉体塗料を上 塗り塗料として塗装し、  5) A known curable paint or the water-dispersible powder paint of the present invention is applied as a top coat,
6)最後に所定温度で焼付処理を行って上塗り塗膜を硬化 (下塗り塗 膜及び Z又は中塗り塗膜が未硬化の場合は同時に硬化) させる方法 である。  6) Finally, a baking treatment is performed at a predetermined temperature to cure the overcoat film (when the undercoat film and Z or the intermediate coat film are uncured, they are simultaneously cured).
③本発明の水分散型粉体塗料を上塗り塗料として用いる塗装例。 この塗膜形成法は  (3) A coating example in which the water-dispersed powder coating of the present invention is used as a top coating. This coating method is
1 )金属などの素材表面に、 公知の硬化型塗料を下塗り塗料として直 接塗装し、  1) A known curable paint is directly applied as an undercoat paint on the surface of a material such as metal,
2)必要により焼付処理した後、  2) After baking if necessary,
3)公知の硬化型塗料を中塗り塗料として塗装し、  3) Apply a known curable coating as an intermediate coating,
4)必要に応じて焼付処理した後、  4) After baking if necessary,
5)本発明の水分散型粉体塗料を上塗り塗料として塗装し、  5) The water-dispersed powder coating of the present invention is applied as a top coating,
6)最後に所定の温度で焼付処理を行って上塗り塗膜を硬化 (下塗り 塗膜及び/又は中塗り塗膜が未硬化の場合,には同時に硬化) させる 方法である。  6) Finally, a baking process is performed at a predetermined temperature to cure the top coat (or simultaneously cure the undercoat and / or intermediate coat if uncured).
上記①〜③の各塗膜形成法を実施する際に使用する公知の硬化型 塗料としては、 例えば、 ァミノ硬化型樹脂塗料、 イソシァネート硬 化型樹脂塗料、 酸エポキシ硬化型樹脂塗料、 加水分解性シラン硬化 型樹脂塗料、 水酸基エポキシ基硬化型榭脂塗料、 ヒ ドラジン硬化型 樹脂塗料、 酸化重合硬化型樹脂塗料、 光 (熱) ラジカル重合型樹脂 塗料、 光 (熱) カチオン重合型樹脂塗料などの硬化型樹脂塗料が挙 げられ、 これらは各々単独で使用し得る他、 必要により任意の組合 せで 2種以上を併用することができる。  Known curable paints used when carrying out each of the above film forming methods ① to ③ include, for example, amino-curable resin paints, isocyanate-curable resin paints, acid epoxy-curable resin paints, and hydrolyzable resins. Silane-curable resin paint, hydroxyl-epoxy group-curable resin paint, hydrazine-curable resin paint, oxidative polymerization-curable resin paint, light (heat) radical polymerizable resin paint, light (heat) cationic polymerizable resin paint, etc. Curable resin paints can be mentioned, and these can be used alone or in combination of two or more as needed if necessary.
これら公知の硬化型塗料には、 必要に応じて従来から塗料に配合 される添加剤、 例えば、 着色顔料、 体質顔料、 メタリ ック顔料、 着 色パール顔料、 流動性調整剤、 ハジキ防止剤、 垂れ止め防止剤、 紫 外線吸収剤、 酸化防止剤、 紫外線安定剤、 艷消し剤、 艷出し剤、 防 腐剤、 硬化促進剤、 硬化触媒、 擦り傷防止剤、 消泡剤、 溶媒などを 特に制限なしに含有させることができる。 These known curable paints may include additives conventionally incorporated into paints as needed, such as coloring pigments, extender pigments, metallic pigments, Color pearl pigments, flow control agents, anti-cissing agents, anti-sagging agents, ultraviolet absorbers, antioxidants, UV stabilizers, delustering agents, glazing agents, preservatives, curing accelerators, curing catalysts, An abrasion inhibitor, an antifoaming agent, a solvent and the like can be contained without particular limitation.
これら硬化性塗料の形態にも格別の制限はなく、 粉体塗料、 無溶 剤型塗料、 水性塗料、 有機溶剤型塗料 (非水分散型塗料も含む) 等 のいずれの形態であっても構わない。  There is no particular limitation on the form of these curable paints, and any form of powder paint, solvent-free paint, water-based paint, organic solvent-based paint (including non-aqueous dispersion paint), etc. may be used. Absent.
これら公知の硬化型塗料は、 例えば静電塗装 (回転式、 エア霧化 式、 エアレス式、 エアアシス ト式など) や、 エアスプレー塗装、 ェ アレス塗装、 刷毛塗り、' ロール塗り、 浸漬塗装など、 任意の方法で 塗装することができる。  These known curable coatings include, for example, electrostatic coating (rotary, air atomizing, airless, air assist, etc.), air spray coating, airless coating, brush coating, 'roll coating, dip coating, etc. It can be painted in any way.
また、 被塗物に水分散型粉体塗料を塗装して焼付乾燥する際には Also, when applying a water-dispersed powder coating to the object to be coated and baking and drying,
1 コート . 1ベーク法を始めとして、 被塗物に下塗り塗料を塗装し 焼付乾燥した後に水分散型塗料を塗り重ねてから焼付乾燥させる 2 コート · 2ベ一ク法や、 下塗り塗料を塗装し、 加熱または焼付乾燥 を行わずにゥエツ ト · オン · ゥエツ トで水分散型粉体塗料を塗り重 ねてから焼付乾燥する 2コート ' 1ベ一ク法などを採用することが できる。 1 coat. 1 Bake method, etc., apply undercoat paint on the object to be coated, bake dry, apply water-dispersion paint, then bake dry. 2 coat2 bake method, apply undercoat paint. However, it is possible to adopt a two-coat / one-bake method in which the water-dispersed powder coating is applied in a wet-on-a-wet manner without heating or baking and drying, and then baking drying is performed.
更に、 トップコートをクリア一仕上げ等にする場合は、 同様に 3 コート · 3ベ一ク法ゃ 3コート ' 2ベーク法、 3コート ' 1ベーク 法等を採用することもできる。  Further, when the top coat is made to be a clear finish, it is also possible to employ a three coat / three bake method, a three coat / two bake method, a three coat / one bake method, or the like.
上記の様に本発明の水分散型粉体塗料は、 優れた貯蔵安定性、 ス プレー塗装性などを有すると共に均質で凹凸や透けのない優れた表 面外観の塗膜を与えるが、 該塗膜が、 意図する色彩や明度と異なる 場合、 或いは該色彩や明度を積極的に変更したい場合に、 その調色 を行うには、 前掲の如く新たに塗料を調製するのと実質的に同じ労 力を要する。  As described above, the water-dispersed powder coating of the present invention has excellent storage stability, spray coating properties, and the like, and gives a coating film having a uniform, excellent surface appearance without unevenness or transparency. If the film is different from the intended color or lightness, or if the color or lightness is to be changed aggressively, the toning is performed in substantially the same manner as preparing a new paint as described above. It takes power.
そこで本発明では、 上記特性を備えた水分散型粉体塗料をベース 塗料として使用し、 該ベース塗料の前記特性を害することなく、 所 望に応じた任意の色彩と明度に簡便に調色できる調色方法も提供す る。 Thus, in the present invention, a water-dispersed powder coating having the above characteristics is used as a base coating, and the color can be easily adjusted to any desired color and brightness without harming the above characteristics of the base coating. Also provides toning methods You.
即ち本発明の他の構成として定める調色方法とは、 前述した如く 塗料用樹脂と顔料を一体として含む粉体が水に分散された水分散型 粉体塗料からなり、 前記粉体の平均粒径 (D 5 0 ) が 5〜 1 5 i m で、 且つ 2 0 m以上の粒子の占める比率が 1 0質量%以下、 3 m以下の粒子の占める比率が 1 0質量%以下で、 固形分濃度が 3 0 〜 6 0質量%である水分散型粉体塗料をべ一ス塗料として使用し、 該ベース塗料の色彩及び Z又は明度を微調整する方法として、  That is, the toning method defined as another configuration of the present invention is, as described above, a water-dispersed powder coating material in which a powder containing a coating resin and a pigment is dispersed in water, and an average particle size of the powder. When the diameter (D50) is 5 to 15 im and the proportion of particles of 20 m or more occupies 10 mass% or less, and the proportion of particles of 3 m or less occupies 10 mass% or less, the solid content concentration Is used as a base paint, and as a method for finely adjusting the color and Z or lightness of the base paint,
前記塗料用樹脂と同一もしくは異種の塗料用樹脂を顔料と一体と して含む粉体が水に分散された水分散型粉体塗料からなり、 該粉体 の平均粒径 ( D 5 0 ) が 5 m以下 (伹し、 粒径が 1 0 mを超え る粗粒物を実質的に含まない) で、 且つ白、 黒、 赤、 青または黄色 系の顔料を含む少なく とも 1種の調色用塗料を準備しておき、 前記ベース塗料の明度及び Z又は色彩に応じて、 前記調色用塗料 の少なく とも 1種を前記ベース塗料に適量配合することによって、 該ベース塗料の明度及び Z又は色彩を微調整する調色法である。  It is composed of a water-dispersed powder coating material in which a powder containing the same or different coating resin as the above-mentioned coating resin and a pigment is dispersed in water, and the powder has an average particle size (D50). 5 m or less (substantially free of coarse particles having a particle size of more than 10 m) and at least one toning containing white, black, red, blue or yellow pigments A paint is prepared in advance, and at least one of the toning paints is mixed with the base paint in an appropriate amount in accordance with the lightness and Z or color of the base paint. This is a toning method for finely adjusting the color.
こ の際に使用する調色用塗料としては、 前述したベース塗料と本 質的には同様の水分散型粉体塗料が使用されるが、 該調色用塗料に 求められる最小限の要求特性として、 該塗料中に含まれる固形成分 の平均粒径 (D 5 0 ) が 5 / m以下のものを使用するのがよい。 そ の理由は、 該調色用塗料に含まれる固形成分の平均粒径 (D 5 0 ) が 5 mを超えると、 調色用塗料の配合量が適正範囲内であっても 調色後の塗膜面に部分的な色調差 (色ムラ) ができ易くなるからで ある。 調色後の塗料の色彩や明度の均一性を高めるうえでも、 平均 粒径 ( D 5 0 ) が 5 m以下のものを使用することが望ましい。 伹 し、 調色用塗料といえども平均粒径 (D 5 0 ) が小さ過ぎると、 調 色後の水分散型粉体塗料全体の粘度が高くなり過ぎて塗装作業性に 悪影響が現れてく るので、 平均粒径 (D 5 0 ) で 2 m程度以上に することが望ましい。  As the toning paint used in this case, a water-dispersion type powder coating which is essentially the same as the above-mentioned base coating is used, but the minimum required characteristics required for the toning paint are used. It is preferable to use those having an average particle diameter (D 50) of the solid component contained in the coating material of 5 / m or less. The reason is that if the average particle size (D50) of the solid component contained in the toning paint exceeds 5 m, even if the amount of the toning paint is within an appropriate range, the toning after the toning is not possible. This is because a partial color tone difference (color unevenness) easily occurs on the coating film surface. In order to enhance the uniformity of the color and lightness of the paint after toning, it is desirable to use a paint having an average particle diameter (D50) of 5 m or less. However, if the average particle size (D50) is too small, the viscosity of the entire water-dispersed powder coating after toning becomes too high, which adversely affects the coating workability. Therefore, it is desirable to set the average particle diameter (D50) to about 2 m or more.
また、 該調色用塗料中の固形成分の平均粒径 (D 5 0 ) が 5 m 以下であったとしても、 当該塗料の固形成分中に 1 0 を超える 粗粒物が存在すると、 調色後の塗膜に色混じりが生じて各色の粒子 がはっきりと区別して観察される様になり、 色彩や明度の均質な調 色塗膜が得られ難くなる。 従って、 均質で色ムラや色混じりのない 調色塗膜を得るには 当該塗料固形成分中に 1 0 を超える粗粒 物が実質的に存在しないことが求められる。 ここで 「実質的に存在 しない」 とは、 必ずしも 「皆無」 でなければならない趣旨ではなく 調色塗膜として肉眼観察で均一と認められる限り微量の混入は許容 される。 しかし、 好ましくは固形成分の全量中に占める比率で、 1 0 mを超える粗粒物の混入量は 2質量%程度以下、 より好ましく は 0 . 5質量%程度以下に抑えることが望ましい。 The average particle size (D 50) of the solid component in the toning paint is 5 m. Even if it is below, if more than 10 coarse particles are present in the solid component of the paint, color mixing will occur in the paint film after toning, and the particles of each color will be clearly distinguished and observed. It is difficult to obtain a toned coating film having a uniform color and brightness. Therefore, in order to obtain a uniform toned coating film without color unevenness or color mixture, it is required that the solid component of the coating material contains substantially no coarse particles exceeding 10%. Here, “substantially absent” does not necessarily mean that there is no “absence”, but a small amount of contamination is permissible as long as it is recognized as uniform by visual observation as a toning coating film. However, it is desirable that the amount of coarse particles exceeding 10 m in the total amount of the solid components is suppressed to about 2% by mass or less, more preferably about 0.5% by mass or less.
そして、 上記調色用塗料の要求特性を満たすことを前提として、 配合する顔料を選択することにより、 白色、 黒色、 赤色、 青色、 黄 色の 5種から選ばれる少なく とも 1種、 好ましくは 5種の調色用塗 料を準備する。 上記 5種の調色用塗料のうち、 白色と黒色の調色用 塗料はベース塗料の明 · 暗を微調整す,るのに使用され、 また赤色、 青色および黄色の調色用塗料は色の 3原色を構成するもので、 色彩 の微調整に用いられる。  Then, assuming that the required characteristics of the toning paint are satisfied, by selecting a pigment to be blended, at least one selected from five types of white, black, red, blue, and yellow, preferably at least five types is selected. Prepare seed toning coatings. Of the above five toning paints, white and black toning paints are used to fine tune the lightness and darkness of the base paint, and red, blue and yellow toning paints are colors. These three primary colors are used for fine adjustment of color.
従って、 これら 5種類の調色用塗料を準備しておき、 ベース塗料 に対するこれら調色用塗料の配合量や配合比率を適宜に調整すれば ベース塗料の色調 (明 ' 暗および色彩) を必要に応じて任意に微調 整することが可能となる。 よって、 これら 5種類の色の調色用塗料 を準備しておけば、 様々の色に合せることができる。 本発明の調色 方法を汎用化するには、 上記 5種類の調色用塗料を準備しておくの が最善であるが、 ベース塗料の色調に'よっては、 上記 5種類のうち 1種〜 4種の調色用塗料を準備しておくだけでも、 便宜的にベース 塗料の調色を行う ことも可能である。  Therefore, if these five types of toning paints are prepared, and the amounts and proportions of these toning paints with respect to the base paint are adjusted as appropriate, the color tone (bright, dark and color) of the base paint becomes necessary. Fine adjustment can be made arbitrarily. Therefore, if these five kinds of toning paints are prepared, they can be adjusted to various colors. In order to generalize the toning method of the present invention, it is best to prepare the above-mentioned five kinds of toning paints, but depending on the color tone of the base paint, one of the above five tones may be used. Even if only four types of toning paints are prepared, it is also possible to conveniently perform the toning of the base paint.
例えばベース塗料が灰色であって、 明 · 暗のみを微調整すればよ い場合は、 白色と黒色の 2種の調色用塗料を準備しておき、 そのう ち 1種または 2種を用いて調色すればよい。 上記調色用塗料の製法には格別特殊な技術が要求されるわけでは なく、 固形成分の粒度構成さえ十分に把握しておけば、 前述したベ —ス塗料の製法と実質的に同様の方法を採用することができ、 また 該調色用塗料中にも前記ベース塗料への添加剤として開示した分散 剤や乳化剤、 沈降防止剤などを同様に添加することができる。 For example, if the base paint is gray and you only need to make fine adjustments to light and dark, prepare two types of toning paints, white and black, and use one or two of them. You just have to color it. No special technology is required for the method of producing the above-mentioned toning paint, and if the particle size composition of the solid components is sufficiently understood, a method substantially similar to the above-mentioned method of producing the base paint is required. The dispersant, emulsifier, anti-settling agent and the like disclosed as additives to the base paint can be similarly added to the toning paint.
ところでこの調色方法では、 上述した通り、 ベース塗料と調色用 塗料に含まれる固形成分の各粒度構成を定める'ことが重要となるが 該調色方法の特徴を一層有効に活かし、 調色後の塗膜の均一性等を 一段と高めるには、 ベース塗料に含まれる粉体の平均粒径(A)と、 調色用塗料に含まれる粉体の平均粒径(B)との比(A/B)が 1 〜 5の範 囲となる様に、 各固形成分の平均粒径を調整することが望ましい。  By the way, in this toning method, as described above, it is important to determine each particle size composition of the solid components contained in the base paint and the toning paint, but the characteristics of the toning method are utilized more effectively to achieve the toning. In order to further improve the uniformity of the subsequent coating film, the ratio of the average particle diameter (A) of the powder contained in the base paint to the average particle diameter (B) of the powder contained in the toning paint ( It is desirable to adjust the average particle size of each solid component so that (A / B) is in the range of 1 to 5.
ちなみに、 粒径比(A/B)が 1未満であると言う ことは、 調色用塗 料中の粉体成分の粒径がベース塗料中の粉体成分の粒径と同等か相 対的に大き過ぎることを意味しており、 この場合は、 調色後の塗膜 が色ムラや色混じりを生じ易くなる。 逆に粒径比(A/B)が 5 を超え ると言う ことは、 調色用塗料中の粉体成分の粒径がベース塗料中の 粉体成分の粒径に比べて小さ過ぎることを意味しており、 この場合 は、 塗料の取扱い性や塗装作業性が悪くなる傾向が生じてくる。  Incidentally, that the particle size ratio (A / B) is less than 1 means that the particle size of the powder component in the toning coating is equal to or relative to the particle size of the powder component in the base coating. In this case, the coating film after toning is likely to cause color unevenness and color mixture. Conversely, the particle size ratio (A / B) exceeding 5 means that the particle size of the powder component in the toning coating is too small compared to the particle size of the powder component in the base coating. In this case, the handling of paint and the workability of coating tend to be poor.
また、 ベース塗料に対する調色用塗料の配合比率は、 微調整され るべきベース塗料の明度や色彩によって変わってくるので一律に決 めることはできないが、 微調整という本発明本来の特徴を活かす上 では、 固形分基準でベース塗料に対する調色用塗料の配合量を 0 . 1 〜 2 0質量%の範囲から選択することが望ましい。 ちなみに、 調 色用塗料の配合量が 0 . 1質量%未満では満足な調色効果 (色合せ 効果) が得られなくなる恐れがあり、 逆に 2 0質量%を超えて多量 の調色用塗料を配合すると、 ベース塗料の粒子による色混じりが生 じて均質な塗膜が得られ難くなる。  In addition, the mixing ratio of the toning paint to the base paint cannot be determined uniformly because it varies depending on the lightness and color of the base paint to be fine-tuned. In the above, it is desirable to select the blending amount of the toning paint with respect to the base paint on the basis of the solid content in the range of 0.1 to 20% by mass. If the amount of the toning paint is less than 0.1% by mass, a satisfactory toning effect (color matching effect) may not be obtained. When the compound is blended, color mixing occurs due to particles of the base paint, and it is difficult to obtain a uniform coating film.
なお本発明の調色法を実用化するに当っては、 前記以外の添加剤 として塗膜外観を艷消し状とするための艷消剤を適量配合すること も可能である。 艷消剤の種類にも格別の制限はなく、 塗料用の艷消 剤として知られた全ての艷消剤、 たとえば炭酸カルシウム、 硫酸バ リウム、 炭酸バリウム、 ク レー、 タルク、 ケイソゥ土、 シリカ粉、 塩基性炭酸マグネシウム、 アルミナホワイ ト、 ワックス、 プラスチ ックビーズ等を、 各々単独で或いは必要により 2種以上を適宜組合 せて使用できる。 When the toning method of the present invention is put to practical use, it is possible to add an appropriate amount of an anti-glazing agent as an additive other than those described above to make the appearance of the coating film opaque. There are no special restrictions on the type of glossy agent. All known matting agents such as calcium carbonate, barium sulfate, barium carbonate, clay, talc, diatomaceous earth, silica powder, basic magnesium carbonate, alumina white, wax, plastic beads, etc. They can be used alone or in combination of two or more as necessary.
該艷消剤は、 調色すべきベース塗料に前掲の調色用塗料を配合す る前または後の任意の段階で添加することができ、 またその好まし い添加量は、 艷消剤の種類や求められる艷消状態の程度によっても 異なるが、 通常は塗料の固形分基準で 0 . 1 〜 2 0質量%程度程度 である。 即ち、 調色塗膜を艷消し状としたい場合、 調色の前、 調色 工程、 あるいは調色を終えた後の段階で、 当該塗料に適量の艷消剤 を添加すると、 その添加量に応じた艷消状態の調色塗膜を得ること ができる。  The glossing agent can be added at any stage before or after the above-mentioned toning paint is blended with the base paint to be toned. Although it varies depending on the type and degree of the required matte state, it is usually about 0.1 to 20% by mass based on the solid content of the paint. In other words, if you want to make the toning film a matte finish, add an appropriate amount of the matting agent to the paint before toning, in the toning process, or after finishing the toning, It is possible to obtain a toned coating film in a correspondingly matt state.
上記方法で調色された水分散型粉体塗料を用いた塗装法や焼付条 件などは格別特殊な手法が求められるわけではなく、 被塗装対象物 の種類などを含めて、 前述した方法や被塗装物が全て適用できる。  A special method is not required for the coating method and baking conditions using the water-dispersed powder paint toned by the above method, and the methods described above, including the type of the object to be coated, are not required. All objects to be coated can be applied.
実施例 以下、 実施例を挙げて本発明をより具体的に説明するが、 本発明 はもとより下記実施例によって制限を受けるものではなく、 前 , 後 記の趣旨に適合し得る範囲で適当に変更を加えて実施することも可 能であり、 それらはいずれも本発明の技術的範囲に含まれる。 尚、 下記において 「%」 または 「部」 とあるのは、 特記しない限り 「質 量%」 または 「質量部」 を意味する。 EXAMPLES Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples, and may be appropriately changed within a range that can be adapted to the spirits described above and below. It is also possible to implement the present invention, and all of them are included in the technical scope of the present invention. In the following, “%” or “parts” means “% by mass” or “parts by mass” unless otherwise specified.
また、 下記実験で採用した平均粒径 (D 5 0 ) および粒度分布、 不揮発分濃度、 塗料粘度の測定法および塗装作業性、 塗膜性能の評 価法などは下記の通り とした。  The average particle size (D50), particle size distribution, nonvolatile content, measurement method of paint viscosity, coating workability, and evaluation method of coating film performance used in the following experiments were as follows.
[平均粒径 (D 5 0 ) および粒度分布]  [Average particle size (D50) and particle size distribution]
各水分散型粉体塗料を固形分濃度が 5質量%以下となるまで水で 希釈し、 この希釈液を日本精機製作所社製の超音波分散機 「超音波 ホモジナイザ一」 で処理した後、 日機装社製の粒度分布測定装置Each water-dispersed powder coating is mixed with water until the solid content concentration becomes 5% by mass or less. After dilution, this diluted solution is treated with an ultrasonic homogenizer "Ultrasonic homogenizer 1" manufactured by Nippon Seiki Seisaku-sho, Ltd., and then a particle size distribution analyzer manufactured by Nikkiso Co., Ltd.
「マイクロ トラック MT 3 3 0 0 E L」 を用いて粒度分布を測定 し、 その粒度分布曲線から累積 5 0 %粒径を平均粒径 (D 5 0 ) と して求める。 The particle size distribution is measured using "Microtrack MT330 EL", and the cumulative 50% particle size is determined as the average particle size (D50) from the particle size distribution curve.
[ T g測定]  [T g measurement]
セイコーインスツルメンッ社製の示差走査熱量分析装置 「D S C 6 2 0 0」 を用いて、 粉体粒子のガラス転移温度 (T g ) を測定。  The glass transition temperature (T g) of the powder particles was measured using a differential scanning calorimeter “DSC 6200” manufactured by Seiko Instruments Inc.
[塗料粘度]  [Paint viscosity]
「 J I S K 5 6 0 0 — 2— 3」 に記載されているコーン ' プ レート粘度計法に従い、 東機産業社製の粘度計 「R E 5 5 0 H」 を 用いて水分散型粉体塗料の粘度を求める。 塗料温度と測定温度は何 れも 2 3 °Cとし、 ずり速度 1 ( s ) で測定した粘度を、 供試塗料 の粘度値とする。  In accordance with the cone-plate viscometer method described in “JISK 550 — 2-3”, water-dispersible powder coatings were prepared using a viscometer “RE550H” manufactured by Toki Sangyo Co., Ltd. Determine the viscosity. Both the paint temperature and the measurement temperature are 23 ° C, and the viscosity measured at a shear rate of 1 (s) is defined as the viscosity value of the test paint.
[塗装作業性]  [Paint workability]
ァネス ト岩田社製の重力式スプレーガン 「W— 1 0 0」 (ノズル 口径 ; 1. 3 mm) を用いて、 各水分散型粉体塗料を塗装したとき の、 ガンノズルからの塗料の噴出状態を観察し、 塗装作業性に支障 がないかどうかを下記の 5段階で評価する。 吹付け空気圧力は 0. Spraying state of paint from gun nozzle when each water-dispersion type powder paint is applied using a gravity spray gun “W-100” (nozzle diameter: 1.3 mm) manufactured by Anest Iwata. And evaluate whether there is any obstacle to painting workability in the following five steps. Spray air pressure is 0.
2 M P a とする。 Let it be 2 MPa.
5 : 塗料の流動性が良好で、 ガンノズルから塗料が均一に噴射する 4 : 塗料の流動性は良好であるが、 噴出ムラを生じることがある 5: Good paint fluidity, spray paint uniformly from gun nozzle 4: Good paint fluidity, but may cause uneven ejection
3 : 塗料の流動性がやや悪く、 常時噴出ムラが観察される 3: The fluidity of the paint is slightly poor, and unevenness of jetting is always observed.
2 : 塗料の流動性が悪くてガンノズルから塗料が噴出し難く、 噴出 が途切れる場合がある  2: The fluidity of the paint is poor, so it is difficult for the paint to be ejected from the gun nozzle, and the ejection may be interrupted.
1 : 塗料の流動性が著しく悪くてガンノズルから塗料が噴出せず、 塗装できない。  1: The fluidity of the paint is remarkably poor, and the paint cannot be sprayed from the gun nozzle and cannot be painted.
[夕レ性]  [Evening]
被塗物を垂直に立て掛け、 各水分散型粉体塗料の温度と塗装環境 温度を 2 0 °Cに設定しから、 「 J I S K 5 6 0 0 - 1 - 1 3 3 . 7吹付け塗り」 に記載されている塗装法に準拠して連続 3回重 ねてスプレー塗装し、 2 0 °Cで 1 0分間のセッティ ングタイムを取 つて焼付乾燥を行い、 タレの状態を下記の基準で 5段階評価する。 尚、 スプレーガンおよび吹付け空気圧力は、 上記塗装作業性評価で 採用したのと同じとする。 Place the object vertically on it, set the temperature of each water-dispersed powder coating and the temperature of the coating environment to 20 ° C, and then set the JISK 560-0-1-13 In accordance with the coating method described in `` 3.7 Spray coating '', spray coating is performed three times in a row, spray-dried at a setting time of 20 minutes at 20 ° C, and baked and dried. Is evaluated on a 5-point scale based on the following criteria. The spray gun and spray air pressure are the same as those adopted in the above-mentioned evaluation of coating workability.
5 : 塗装時のタレが認められず、 焼付後の塗膜にもタレ跡が全く認 められない  5: No sagging was observed at the time of painting, and no sagging marks were observed on the coated film after baking.
4 : 塗装時のタレは認められないが、 焼付後の塗膜にタレ跡が僅か に残る  4: No sagging is observed at the time of painting, but slight sagging marks remain on the coated film after baking
3 : 塗装時にタレが僅かに認められ、 焼付後の塗膜にもタレ跡が僅 かに残る  3: Slight sagging is observed at the time of painting, and slight sagging marks remain on the coated film after baking.
2 : 塗装時のタレが著しく、 焼付後の塗膜にもタレ跡が著しく残る 1 : 塗装時のタレが著しくて焼付後の塗膜が非常に薄くなり、 素地 の透けが著しい。  2: Significant sag at the time of painting, marked sagging remains on the paint film after baking 1: Paint dripping at the time of painting is very thin, and the paint film after baking is extremely thin, and the base material is very transparent.
[レペリ ング性]  [Repelling property]
上記夕レ性試験と同じ方法で水分散型粉体塗料を塗装し、 試験片 を 2 0 °Cで 1 0分間放置してから、 途面の凹凸の大きさを 5段階で 目視評価する。  A water-dispersed powder coating is applied in the same manner as in the above-mentioned dullness test, and the test piece is allowed to stand at 20 ° C for 10 minutes. Then, the size of the unevenness on the surface is visually evaluated in five steps.
5 : 凹凸が全く認められない  5: No unevenness is observed
4 : 凹凸が殆ど認められない  4: Almost no irregularities
3 : 僅かな凹凸が認められるが、 実用上問題なし  3: Slight irregularities are observed, but there is no practical problem
2 : 若干の凹凸が認められる 2: Some irregularities are observed
1 : 凹凸が著しく実用性を欠く。  1: The unevenness is remarkably lacking in practicality.
[ヮキ性]  [Peak property]
上記タレ性評価と同じ方法で塗装を行い、 得られた塗膜のヮキの 状態を下記の基準で 5段階評価する。 尚、 スプレーガンおよび吹付 け空気圧力は、 上記塗装作業性評価で採用したのと同じとする。 Coating is performed in the same manner as in the sagging evaluation described above, and the paint state of the obtained coating film is evaluated on a 5-point scale according to the following criteria. The spray gun and spray air pressure shall be the same as those adopted in the above-mentioned evaluation of coating workability.
5 ヮキが全く認められない 5 No markings are recognized
4 ヮキの部分が全塗膜面積の 1 Z 4未満 4 Printed area is less than 1 Z 4 of total coating area
3 ヮキを生じた部分が全塗膜面積の 1 / 4以上、 1 2未満 2 : ヮキを生じた部分が全塗膜面積の 1 / 2以上、 3 / 4未満 1 : ヮキを生じた部分が全塗膜面積の 3 / 4以上。 3 The area where the peeling occurred was 1/4 or more of the total coating area, but less than 12 2: The area where the peeling occurred was 1/2 or more of the total coating area, and less than 3/4. 1: The area where the peeling occurred was 3/4 or more of the total coating area.
[平滑性]  [Smoothness]
被塗物を垂直に立て掛け、 各水分散型粉体塗料の温度と塗装環境 温度を 2 0 °Cに設定してから、 「 J I S K 5 6 0 0 — 1 二 1 3. 3. 7吹付け塗り」 に記載されている塗装法に準拠して、 乾燥 膜厚が 5 0 mとなる様にスプレー塗装し、 焼付乾燥することによ つて得られる塗膜の平滑性を、 下記の基準で 5段階評価する。  Hold the work vertically, set the temperature of each water-dispersed powder coating and the temperature of the coating environment to 20 ° C, and then spray-coat with “JISK 560-0 — 1 2 1 3.3.7 Spray coating to a dry film thickness of 50 m and baking drying according to the coating method described in `` 5. evaluate.
5 : オレンジピール等が認められず、 塗膜が十分に平滑である 4 : オレンジピールは認められないが、 塗膜に微細な凹凸が認めら れる 5: No orange peel, etc., and the coating film is sufficiently smooth 4: No orange peel, but fine unevenness in the coating film
3 : オレンジピールは認められないが、 塗膜に小さな凹凸が認めら れる  3: No orange peel is observed, but small irregularities are observed in the coating film
2 : 明らかなオレンジピールが観察されるが、 その波長は小さい 1 : 明らかなオレンジピールが観察され、 その波長が大きい。  2: A clear orange peel is observed, but the wavelength is small 1: A clear orange peel is observed, and the wavelength is large.
[塗膜性能]  [Coating performance]
水分散型粉体塗料を S P C C (ブライ ト) 鋼板 ( 1 5 0 X 7 0 X 0. 8 mm) に上記と同じ塗装条件を採用して 3回塗りでスプレー 塗装し、 1 9 0 °Cで 2 0分間の焼付乾燥を行い、得られた塗膜を下 記の a)〜f)によつて評価する。  Spray the water-dispersed powder coating on SPCC (bright) steel plate (150 x 70 x 0.8 mm) using the same coating conditions as above with three coats and spray at 190 ° C. After baking and drying for 20 minutes, the obtained coating film is evaluated according to the following a) to f).
a)膜厚 ; ケッ ト科学研究所社製の電磁式膜厚計 「L Z _ 3 0 0」 を用いて測定する。  a) Film thickness: Measured using an electromagnetic film thickness meter “LZ_300” manufactured by KET Science Institute.
b)耐水性 ; 焼付処理を終えた塗装板を 4 0 °Cの水中に 2 4 0時間 浸漬し、 浸漬後の塗膜外観を下記の基準で 5段階評価する。  b) Water resistance: The coated plate after the baking treatment is immersed in water at 40 ° C for 240 hours, and the appearance of the coated film after immersion is evaluated on a 5-point scale according to the following criteria.
5 塗膜状態に変化が認められない  5 No change in the coating state
4 塗膜に僅かな艷引けが認められるが、 フクレは観察されない 3 塗膜に僅かな艷引けが認められ、 フクレも僅かに観察される 2 塗膜に著しい艷引けとフクレが観察される 4 Slightly glossy, but no swelling is observed in the coating 3 Slightly glossy, swelling is slightly observed in the coating 2
塗膜の著しい剥離が認められる。  Significant peeling of the coating film is observed.
c)表面粗度 ; 小坂研究所製の 「サーフコーダ S E 3 5 0 0」 を使 用し、 J I S B 0 6 0 1 — 1 9 9 4に従って塗膜の平均表面粗さ (R a )を求める(カッ トオフ ; 0. 8 mm、 フィルタ一 ; ガウス、 測定長さ ; 4 m m )。 この値が小さいほど、 平滑性に優れているこ とを表わす。 c) Surface roughness: Use “Surfcoder SE350” manufactured by Kosaka Laboratory. Determine the average surface roughness (R a) of the coating film according to JISB 0601-1994 (cut-off: 0.8 mm, filter: Gauss, measurement length: 4 mm). The smaller this value is, the better the smoothness is.
d)色混じり ; 十分に明るい場所で、 上記方法により得た塗膜から d) Color mixture; in a sufficiently bright place, from the coating film obtained by the above method
2 0 c m離して目視観察し、 下記の基準で評価する。 Visually observe at a distance of 20 cm and evaluate according to the following criteria.
5 : 色が均一で色混じりが認められない 5: Uniform color and no color mixing
4 : 色は均一であるが、 僅かに色のムラが確認できる  4: Color is uniform, but slight unevenness of color can be confirmed
3 : 色のムラが確認できる  3: Color unevenness can be confirmed
2 : 色が不均一で、 僅かに各色の粗粒子が確認できる  2: The color is uneven and coarse particles of each color can be slightly confirmed.
1 : 色が不均一であり、 各色の粗粒子がはっきり と確認できる。  1: The color is uneven and coarse particles of each color can be clearly seen.
0光沢値 ; J I S Κ 5 6 0 0,_ 4— 7 に準拠し、 入射角と受光 角が夫々 6 0度における塗膜の鏡面光沢度を測定する。  0 Gloss value: Measure the specular gloss of the coating film at an incident angle and a light receiving angle of 60 degrees, respectively, in accordance with JIS Κ 560, _4—7.
[塗料の貯蔵安定性]  [Storage stability of paint]
「 J I S K 5 6 0 0 - 2 - 7 加温安定性」 に記載されてい る試験法に従って、 各水分散型粉体塗料を密封可能な容器に入れ、 According to the test method described in `` JISK 560-2-2-7 Heating Stability '', place each water-dispersible powder coating in a sealable container,
3 5 °Cで 9 0 日間静置状態で貯蔵した後に室温に戻し、 貯蔵前と比 ベて 「塗料の状態」 、 「塗装作業性」 および 「塗膜の外観」 の変化 を 5段階で総合評価する。 35 Stored at 90 ° C for 90 days and returned to room temperature.Compared to before storage, changes in “paint state”, “paint workability” and “coating appearance” were evaluated in 5 stages. evaluate.
5 : 貯蔵前と比べて変化が認められず、 非常に安定である  5: No change is observed compared to before storage and it is very stable
4 : 僅かに凝集が認められるが簡単に解れ、 塗装作業性や塗膜外観 に変化は見られない  4: Slight agglomeration is observed but easy to dissolve, no change in coating workability or coating appearance
3 : 著しい凝集が認められるが、 ディスパ一等の撹拌機で撹拌する ことにより貯蔵前の状態に戻る  3: Although remarkable aggregation is observed, it returns to the state before storage by stirring with a stirrer such as Dispa.
2 : 硬い沈殿物が認められ、 撹拌しても貯蔵前の状態に戻らず、 塗 装作業性および塗膜外観が明らかに劣化する  2: A hard precipitate is observed and does not return to the state before storage even after stirring, and the coating workability and the appearance of the coating film are clearly deteriorated.
1 : 硬い沈殿物が認められ、 撹拌しても塗装可能な状態に戻らない また下記実施例に示す配合において、 「〇〇〇」 で示した商品名 (商標名) は、 各々下記製造会社と化学物質名を表す。  1: A hard precipitate is observed and does not return to a paintable state even with stirring. In the formulations shown in the examples below, the trade names (trade names) indicated by “〇〇〇” are the same as those of the following manufacturers, respectively. Indicates a chemical substance name.
「ファイ ンディ ック M— 8 0 2 0」 : 大日本インキ工業社製のポ リエステル系樹脂 “Findick M-820”: A product made by Dainippon Ink Industries, Ltd. Ester resin
「クレラン V P L S 2 2 5 6」 : 住友バイエルウレタン社製 のブロックイソシァネー ト樹脂  “Cleran V P L S 2 2 5 6”: Sumitomo Bayer Urethane Block Isocyanate Resin
ベンゾィ ン : MIWON COMMERCIAL社製の脱ガス剤  Benzoin: Degassing agent manufactured by MIWON COMMERCIAL
ィミダゾール : 四国化成工業社製の硬化促進剤  Imidazole: a curing accelerator manufactured by Shikoku Chemicals
「A E R 6 0 0 2」 : 旭化成エポキシ社製のエポキシ樹脂 「A E R 6 0 1 4」 : 旭化成エポキシ社製のエポキシ樹脂 「ァクロナール 4 F」 : B A S F社製の流動調整剤  "AER6002": Epoxy resin manufactured by Asahi Kasei Epoxy Co., Ltd. "AER6004": Epoxy resin manufactured by Asahi Kasei Epoxy Co., Ltd. "Acronal 4F": Flow modifier manufactured by BASF
「酸化チタン C R 9 7」 : 石原産業社製の酸化チタン  "Titanium oxide CR97": Titanium oxide manufactured by Ishihara Sangyo
「アデ力ノール U H _ 5 4 0」 : 旭電化工業社製の粘度調整剤 「アデカノ一ル UH_ 7 5 2」 : 旭電化工業社製の粘度調整剤 「サーフィ ノール 4 2 0」 : エアープロダクツ社製の界面活性剤 "ADEKINOL UH_540": Viscosity adjuster manufactured by Asahi Denka Kogyo Co., Ltd. "ADEKANOL UH_752": Viscous adjuster manufactured by Asahi Denka Kogyo Co., Ltd. "Surfinol 420": Air Products Surfactant
H L B = 4 H L B = 4
「Disperbyk— 1 9 0」 : ビックケミ一社製の分散剤  "Disperbyk—190": Dispersant manufactured by BIC CHEMI
「ラスミン MK— 9」 ( 1 0 %水溶液) : 共栄社化学社製の防鲭 剤  "Rasmin MK-9" (10% aqueous solution): Kyoeisha Chemical's chemical inhibitor
「AD H」 : 大塚化学社製の硬化剤  "AD H": curing agent manufactured by Otsuka Chemical Co., Ltd.
「アルマテックス P D 7 3 1 0」 : 三井化学社製のアク リル系樹 脂  "Almatex PD 7310": Acrylic resin manufactured by Mitsui Chemicals, Inc.
デカンジカルボン酸 : 宇部興産社製の硬化剤  Decanedicarboxylic acid: a curing agent manufactured by Ube Industries
「ェピコート GV— 2 3 0」 : 日本ュピカ社製のポリエステル系 樹脂  "Epicoat GV-230": Polyester resin manufactured by Nupika Japan
「ェピコート 1 0 0 3 F j : 油化シェルエポキシ社製のエポキシ 樹脂  “Epicoat 103 Fj: Yuka Shell Epoxy resin
「A C E MA T T HK 4 6 0」 : デダサ A G社製のシリカ粒子 実施例 1一 1  “A C E MA T T HK 460”: silica particles manufactured by DeDasa AG, Inc.
[ポリエステル系樹脂粗粉碎物の製造]  [Manufacture of coarsely ground polyester resin]
原料を下記配合 1 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練すると共に押出し、 厚さ 約 1 mmのシート状に冷却固化させる。 このシート状物を破碎機に 通して粗粉砕した後、 篩目が 1. 0 mmのフィルタ一に通してポリ エステル系樹脂粗粉砕物を得る。 The raw materials are used in the ratio shown in Formulation 1 below, uniformly mixed with a high-speed mixer, then hot-melt kneaded and extruded using a melt extruder. Cool and solidify into a sheet of about 1 mm. This sheet is coarsely crushed by passing through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed polyester resin.
配合 1 :  Formula 1:
「ファインディ ック M _ 8 0 2 0」 5 5. 0 (部) “Fine-dick M _ 8 0 2 0” 55.0 (parts)
「クレラン V P L S 2 2 5 6」 8. 2 `` Cleran VPL S 2 2 5 6 '' 8.2
ベンゾィン 0. 4  Benzoin 0.4
「A E R _ 6 0 0 2」 1. 5  `` AER_6002 '' 1.5
「ァクロナール 4 F」 0. 5  「Acronal 4 F」 0.5
「酸化チタン C R 9 7」 3 4. 4  "Titanium oxide CR97" 34.4
合計 1 0 0. 0  Total 1 0 0. 0
[水分散型粉体塗料の製造]  [Manufacture of water-dispersed powder coating]
下記配合 2に示す比率で用いた原料配合物 1 0. 0 k gをデイス パーによって混合し、 この混合物を冷却機構内蔵型の湿式循環型ビ ーズミル [分散メディア ; 直径 1. 0 m mのニツカ ト一社製ジルコ 二アポ一ル 「YT Z」 を、 ベッセル容積に対して 8 0 % ( 4. 4 k g ) 装入したもの] に連結した循環槽に投入し、 アジテーターディ スクを周速 1 0 m/ sで回転させながら、 循環流量 2 リ ッ トルノ分 で 3 0分間循環させることによって微粉砕処理を行う。 次いで、 5 0 mフィルタ一を通して濾過することによって水分散型粉体塗料 を得る。 得られた水分散型粉体塗料の性状 · 特性を表 1 に示す。 尚 粉体粒子の T gは 6 5 °Cであった。  10.0 kg of the raw material mixture used in the ratio shown in the following Formulation 2 was mixed with a disperser, and this mixture was dispersed in a wet circulation type bead mill with a built-in cooling mechanism. With 80% (4.4 kg) of the vessel zirconia porcelain “YT Z” loaded into the circulation tank connected to the vessel, and the agitator disk is rotated at a peripheral speed of 10 m. While rotating at / s, the fine pulverization treatment is performed by circulating for 30 minutes at a circulation flow rate of 2 liters. Next, a water-dispersed powder coating is obtained by filtering through a 50 m filter. Table 1 shows the properties and characteristics of the obtained water-dispersed powder coating. The T g of the powder particles was 65 ° C.
配合 2 :  Formula 2:
ポリエステル系樹脂粗粉碎物(注) 5 0. 0 (部) Polyester resin coarse powder (Note) 50.0 (parts)
「サーフィ ノール 4 4 0」 0. 2 "Surfinol 4 4 0" 0.2
「アデ力ノール UH _ 7 5 2」 0. 5  `` Ade Force Knoll UH _ 7 5 2 '' 0.5
イオン交換水 4 9. 3  Ion exchange water 49.3
合計 1 0 0. 0  Total 1 0 0. 0
(注)上記配合 よって得たポリエステル系樹脂粗粉碎物 ( T ; 6 5 °C) 実施例 1 一 2〜 1 一 5、 比較例 1 一 1〜; L 一 2 (Note) Polyester resin coarse powder obtained by the above blending (T; 65 ° C) Example 1 1-2 1-5, Comparative Example 1 1-1-1; L-1 2
上記実施例 1 一 1 において、 水分散型粉体塗料の固形分濃度、 添 加剤 [粗粉砕物と分散媒 (水) 以外の成分] の総添加量、 循環型ビ —ズミルによる分散時間をそれぞれ下記表 1 に示す様に変更した以 外は、 前記実施例 1 一 1 と同様にして水分散粉体塗料を調製する。 なお、 各塗料中に含まれる塗料粉体の平均粒径 (D 5 0 ) と粒度分 布を表 1 に一括して示す。 実施例 1 一 6  In Example 11 above, the solid content concentration of the water-dispersed powder coating material, the total amount of the additives [components other than the coarsely pulverized product and the dispersion medium (water)], and the dispersion time by the circulating bead mill were determined. A water-dispersed powder coating material is prepared in the same manner as in Example 11 except that each is changed as shown in Table 1 below. Table 1 shows the average particle size (D50) and the particle size distribution of the paint powder contained in each paint. Example 1 1 6
[エポキシ系樹脂粗粉碎物の製造] ' 原料を下記配合 3 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練すると共に押出し、 厚さ 約 1 m mのシート状に冷却固ィ匕させる。 このシート状物を破砕機に 通して粗粉砕した後、 篩目が 1 . 0 mmのフィルタ一に通してェポ キシ系樹脂粗粉砕物を得る。  [Production of epoxy resin coarse powder] 'Use raw materials in the ratio shown in Formulation 3 below, mix uniformly with a high-speed mixer, and then extrude with hot melt kneading using a melt extruder to a thickness of about 1 It is cooled to form a sheet of mm. After the sheet material is coarsely pulverized through a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain a coarsely pulverized epoxy resin material.
配合 3 :  Formula 3:
「A E R— 6 0 1 4」 6 1 . 3 (部) 「 A D H」 2 . 8  “AER—6001 4” 61.3 (parts) “ADH” 2.8
ベンゾィン 0 . 4  Benzoin 0.4
「ァクロナール 4 F」 0 . 5 「酸化チタン C R 9 7」 3 5 . 0  "Acronal 4F" 0.5 "Titanium oxide CR97" 35.0
合計 1 0 0 . 0  Total 1 0 0 .0
上記で得たエポキシ系樹脂粗粉碎物を使用し、 以下は前記実施例 1 一 1 と同様にして水分散型粉体塗料を得た。 得られた水分散型粉 体塗料の性状 · 特性を表 1 に示す。 尚、 粉体粒子の T gは 6 2 で あった。 実施例 1 一 7  Using the epoxy resin coarse powder obtained above, a water-dispersed powder coating was obtained in the same manner as in Example 11 below. Table 1 shows the properties and characteristics of the obtained water-dispersed powder coating. The T g of the powder particles was 62. Example 1 1 7
[ァクリル系樹脂粗粉碎物の製造] 原料を下記配合 4に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練すると共に押出し、 厚さ 約 l mmのシート状に冷却固化させる。 このシート状物を破碎機に 通して粗粉碎した後、 篩目が 1. 0 mmのフィルターに通してァク リル系榭脂粗粉碎物を得る。 [Manufacture of acryl-based resin coarse powder] The raw materials are used in the ratio shown in Formulation 4 below, uniformly mixed with a high-speed mixer, then hot melt kneaded and extruded using a melt extruder, and cooled and solidified into a sheet having a thickness of about 1 mm. After the sheet material is coarsely pulverized through a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain an acrylic resin coarsely pulverized material.
配合 4 :  Formula 4:
「アルマテックス P D 7 3 1 0」 5 3. 0 (部) デカンジカルボン酸 1 1 . 5 ベンゾイン 0. 4  “Almatex PD 7310” 53.0 (parts) Decanedicarboxylic acid 11.5 Benzoin 0.4
「ァクロナ一ル 4 F」 0. 5 "Acronal 4 F" 0.5
「酸化チタン C R 9 7」 3 5. 0 `` Titanium oxide C R 9 7 '' 35.0
合計 1 0 0. 0 上記で得たァク リル系樹脂粗粉砕物を使用し、 以下は前記実施例 1 一 1 と同様にして水分散型粉体塗料を得た。 得られた水分散型粉 体塗料の性状 · 特性を表 1 に示す。 尚、 粉体粒子の T gは 6 0 °Cで あった。 実施例 1 一 8  A total of 100.0 The water-dispersed powder coating was obtained in the same manner as in Example 11 above using the coarsely pulverized acrylic resin obtained above. Table 1 shows the properties and characteristics of the obtained water-dispersed powder coating. The T g of the powder particles was 60 ° C. Example 18
[エポキシ · ポリエステル系樹脂粗粉砕物の製造]  [Manufacture of coarsely crushed epoxy / polyester resin]
原料を下記配合 5 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練す.ると共に押出し、 厚さ 約 1 m mのシート状に冷却固化させる。 このシー ト状物を破砕機に 通して粗粉碎した後、 篩目が 1. 0 mmのフィルターに通してェポ キシ · ポリエステル系樹脂粗粉碎物を得る。  The raw materials are used in the ratio shown in Formulation 5 below, uniformly mixed with a high-speed mixer, and then hot-melt kneaded using a melt extruder. The mixture is extruded and cooled and solidified into a sheet with a thickness of about 1 mm. This sheet-like material is coarsely ground through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely ground epoxy-polyester resin.
配合 5 :  Formula 5:
「ェピコ一卜 GV— 2 3 0」 3 8. 0 (部) “Epico GV—2 3 0” 38.0 (parts)
「ェピコ一卜 1 0 0 3 F」 2 8. 0 “Epicoco 1 0 0 3 F” 28.0
ベンゾィン 0. 4  Benzoin 0.4
「ァクロナール 4 F」 0. 5  「Acronal 4 F」 0.5
イミダゾール 0. 1 「酸化チタン C R 9 7」 3 3. 0 Imidazole 0.1 "Titanium oxide CR97" 33.0
合計 1 0 0. 0  Total 1 0 0. 0
上記で得たエポキシ · ポリエステル系榭脂粗粉碎物を使用し、 以 下は前記実施例 1 一 1 と同様にして水分散型粉体塗料を得た。 得ら れた水分散型粉体塗料の性状 ' 特性を表 1 に示す。 尚、 粉体粒子の T gは 6 5 °Cであった。 A water-dispersed powder coating was obtained in the same manner as in Example 11 below using the epoxy-polyester resin coarse powder obtained above. Table 1 shows the properties of the obtained water-dispersed powder coating. The T g of the powder particles was 65 ° C.
粒度分布(masS%) Particle size distribution (mas S %)
水分散粉体塗料の 分散時間 平均 径  Dispersion time of water-dispersed powder paint Average diameter
m以上 20 m以上 3 II m以下 0.5 μ m以 固形分濃度(mass% :¾1 (mm) D50(jU m) の割合 の割合 の割合 の割合 実施例 1 - 1 50.4 30 27.2 8 66 0 0 実施例 1-2 50.4 40 18.5 0 31 0 0 実施例 1-3 50.4 50 13.0 0 8 0 0 実施例 1 - 4 50.4 100 7.3 0 1 5 0 実施例 1-5 50.4 115 4.4 0 0 13 0 実施例 1-6 50.4 50 13.0 0 8 0 0 実施例 1-7 50.4 50 13.0 0 8 0 0 実施例 1-8 50.4 50 13.0 0 8 0 0 比較例 1-1 50.4 20 35.5 25 72 0 0 比較例 1-2 50.4 10 45.0 32 89 0 0 m or more 20 m or more 3 II m or less 0.5 μm or less Solid content concentration (mass%: ¾1 (mm) D50 (jU m) ratio Ratio of ratio Example 1-1 50.4 30 27.2 8 66 0 0 Implementation Example 1-2 50.4 40 18.5 0 31 0 0 Example 1-3 50.4 50 13.0 0 8 0 0 Example 1-4 50.4 100 7.3 0 15 0 Example 1-5 50.4 115 4.4 0 0 13 0 Example 1 -6 50.4 50 13.0 0 8 0 0 Example 1-7 50.4 50 13.0 0 8 0 0 Example 1-8 50.4 50 13.0 0 8 0 0 Comparative example 1-1 50.4 20 35.5 25 72 0 0 Comparative example 1-2 50.4 10 45.0 32 89 0 0
※ 1;水分散粉体塗料中の固形分濃度(maSS%) * 1: Solid content concentration in water-dispersed powder coating (ma SS %)
得られた各水分散型粉体塗料を使用し、 ァネス ト岩田社製のスプ レーガン 「W— 1 0 0」 (ノズル口径 1. 3 mm) を用いて、 S P C C鋼板 (同前) に 3回塗りでスプレー塗装し、 次いで熱風乾燥機 内に装入して、 ポリエステル系樹脂の場合は 1 9 0 °Cで 2 0分間、 エポキシ系樹脂、 アクリル系樹脂、 エポキシ ' ポリエステル系樹脂 の場合は 1 8 0 °Cで 2 0分間焼付処理してから塗膜性能を評価し、 下記表 2 に示す結果を得た。 Each of the obtained water-dispersed powder coatings was applied three times to SPCC steel plates (same as above) using a spray gun “W-100” (nozzle diameter: 1.3 mm) manufactured by Annest Iwata. Spray-painted and then placed in a hot-air dryer. For polyester resin, at 190 ° C for 20 minutes, 1 for epoxy resin, acrylic resin, epoxy 'polyester resin After baking at 80 ° C for 20 minutes, the coating film performance was evaluated, and the results shown in Table 2 below were obtained.
表 2 Table 2
Figure imgf000042_0001
Figure imgf000042_0001
実施例 2 — 1 Example 2 — 1
a - 1)ポリエステル樹脂系粗粉砕物の製造  a-1) Production of coarsely crushed polyester resin
原料を下記配合 1 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練すると共に押出し、 厚さ 約 1 m mのシート状に冷却固化させる。 このシート状物を破碎機に 通して粗粉砕した後、 篩目が 1. 0 mmのフィルタ一に通して粗粉 砕物を得る。  The raw materials are used in the ratio shown in Formulation 1 below, mixed uniformly with a high-speed mixer, then hot-melt kneaded and extruded using a melt extruder, and cooled and solidified into a sheet with a thickness of about 1 mm. After the sheet material is coarsely crushed by passing through a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed material.
配合 1 :  Formula 1:
「ファインディ ック M— 8 0 2 0」 5 4 · 9 (部) “FINEDIC M—800 200” 5 4 · 9 (parts)
「クレラン V P L S 2 2 5 6」 8. 2 `` Cleran VPL S 2 2 5 6 '' 8.2
「ベンゾイン」 0. 4  “Benzoin” 0.4
「A E R 6 0 0 2」 3. 0  “A E R 6 0 2” 3.0
「ァクロナ一ル 4 F」 0. 5  "Acronal 4 F" 0.5
「酸化チタン C'R 9 7」 3 3. 0  `` Titanium oxide C'R 9 7 '' 33.0
合計 1 0 0. 0  Total 1 0 0. 0
b-1)ポリエステル樹脂系水分散型粉体塗料の製造  b-1) Manufacture of polyester resin-based water-dispersed powder coating
下記配合 2に示す比率で用いた原料配合物 1 0. 0 k gをデイス パーによって混合し、 この混合物を冷却機構内蔵型の湿式循環型ビ —ズミル [分散メディア ; 直径 1. 0 mmのニツカ トー社製ジルコ 二アポ一ル 「Y T Z」 を、 ベッセル容積に対して 8 0 % ( 4. 4 k g ) 装入したもの] に連結した循環槽に投入し、 アジテーターディ スクを周速 l O mZ sで回転させながら循環させることによって微 粉碎処理を行う。 次いで、 5 0 mフィルターを通して濾過するこ とによって水分散型粉体塗料を得る。 得られた水分散型粉体塗料の 性状 · 特性を表 3に示す。 尚、 該粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0. 5 m以下の微粒物の含有量は何れも 0 %であった。 また該粉体粒子 の T gは 6 5 °Cであった。  10.0 kg of the raw material formulation used in the ratio shown in the following formulation 2 was mixed with a disperser, and the mixture was wet-circulated bead mill with a built-in cooling mechanism [dispersion media; Nitka Toe with a diameter of 1.0 mm The Zirco Niapor "YTZ" was charged to a circulation tank connected to 80% (4.4 kg) of the vessel volume], and the agitator disk was rotated at a peripheral speed l O mZ s Fine grinding treatment is performed by circulating while rotating. Then, the mixture is filtered through a 50 m filter to obtain a water-dispersed powder coating. Table 3 shows the properties and characteristics of the obtained water-dispersed powder coating. The average particle diameter (D50) of the powder particles is 13 m, and the content of coarse particles having a particle diameter of 50 m or more and fine particles having a particle diameter of 0.5 m or less is determined. Was also 0%. The T g of the powder particles was 65 ° C.
配合 2 :  Formula 2:
粗粉砕物(注) 1 0 0. 0 (部) イオン交換水 1 0 0. 0 「アデカノ一ル UH— 5 4 0」 0. 4 「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 5 「サ一フィ ノール 4 2 0 J · 0. 4Coarsely pulverized material (Note) 1 0 0.0 (parts) Ion-exchanged water 10.0 0.0 “Adecanol UH—540” 0.4 “Rasmin MK—9” (10% aqueous solution) 0.5 “Safinol 4 20 J · 0.4
「Disperbyk— 1 9 0」 0. 4 合計 2 0 1. 7 “Disperbyk—1 9 0” 0.4 Total 2 0 1.7
(注)上記配合 1 によって得た粗粉砕物 (T g ; 6 5 °C) 実施例 2 - 2〜 2 一 8および比較例 2 — 1〜 2 - 4  (Note) Coarsely pulverized material (Tg; 65 ° C) obtained by the above-mentioned Formulation 1 Example 2-2 to 218 and Comparative Example 2 — 1-2 to 4
実施例 2 — 1 において、 上記配合 2で用いた界面活性剤 「サ一フ ィ ノール 4 2 0」 に代えて表 3 に示す界面活性剤を使用し、 或いは 前記配合 1 の 「Disperbyk— 1 9 0」 に代えて 「フ口一レン T G— 7 5 0 W」 (共栄化学社製の分散剤) を使用した以外は、 前記実施 例 2 — 1 と同様にして、 ポリエステル樹脂系水分散型粉体塗料を製 造した。 各水分散型粉体塗料の平均粒径 (D 5 0 ) や粒度分布およ び固形分濃度は、 何れも実施例 2 — 1 と同じになる様に調整した。  In Example 2-1, the surfactant shown in Table 3 was used in place of the surfactant "Safinol 420" used in the above Formulation 2, or "Disperbyk-19" in Formula 1 was used. In the same manner as in Example 2-1 except that “Huichi Ichiren TG-7500 W” (a dispersant manufactured by Kyoei Chemical Co., Ltd.) was used instead of “0”, a polyester resin-based water-dispersible powder was used. Body paint was manufactured. The average particle size (D50), particle size distribution, and solid content of each water-dispersed powder coating material were adjusted to be the same as those in Example 2-1.
ここで用いた界面活性剤は下記の通り、  The surfactant used here is as follows:
「サ一フィ ノール 4 4 0」 : エア一プロダクツ社製の非イオン界 面活性剤、 H L B = 8、  "Safinol 4440": A non-ionic surfactant manufactured by Air Products, HLB = 8,
「サーフィ ノール 4 6 5」 : エア一プロダクツ社製の非イオン界 面活性剤、 H L B = 1 3、  "Surfinol 4 6 5": A non-ionic surfactant manufactured by Air Products, HLB = 13,
「サ一フィ ノール 4 8 5」 : エア一プロダクツ社製の非イオン界 面活性剤、 H L B = 1 7、  “Surfinol 4 8 5”: A non-ionic surfactant manufactured by Air Products, H L B = 17,
「夕一ジトール TMN— 3」 : ダウケミカル社製の非イオン界面 活性剤、 H L B = 8、  "Yuichi Jitol TMN-3": A nonionic surfactant manufactured by Dow Chemical Company, HLB = 8,
「夕一ジトール TMN— 6」 : ダウケミカル社製の非イオン界面 活性剤、 H L B = 1 2、  "Yuichi Jitol TMN-6": A nonionic surfactant manufactured by Dow Chemical Company, HLB = 12,
「 S Nゥエツ 卜 9 7 0」 : サンノプコ社製のァニオン系界面活性 剤。 実施例 2 — 9 “SN ゥ Jet 970”: An anionic surfactant manufactured by San Nopco. Example 2 — 9
a - 2)エポキシ樹脂系粗粉碎物の製造  a-2) Manufacture of epoxy resin-based coarse powder
原料を下記配合 3 に示す比率で使用した以外は、 前記実施例 2 — 1 の a-1)と同様にして、 エポキシ樹脂系粗粉碎物を得る。  An epoxy resin-based coarse powder is obtained in the same manner as in a-1) of Example 2-1 except that the raw materials are used in the ratio shown in the following formulation 3.
配合 3 :  Formula 3:
「A E R - 6 0 1 4」 6 1 . 3 (部) "A E R -6001 4" 61.3 (parts)
「 A D H」 2. 8 “ADH” 2.8
「ベンゾィン」 0. 4  "Benzin" 0.4
「ァクロナ一ル 4 F」 0. 5  "Acronal 4 F" 0.5
「酸化チタン C R 9 7」 3 5. 0  `` Titanium oxide C R 9 7 '' 35.0
合計 1 0 0. 0  Total 1 0 0. 0
b- 2)エポキシ樹脂系水分散型粉体塗料の製造  b-2) Manufacture of water-dispersible epoxy resin-based powder coatings
下記配合 4に示す比率で用いた原料配合物を使用した以外は、 前 記実施例 2 — 1 の b-1)と同様にして水分散型粉体塗料を製造し、 得られた水分散型粉体塗料の性状 · 特性を表 3 に示した。 尚、 得ら れた粉体塗料中に含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0. 5 z m以 下の微粒物の含有量は何れも 0 %であった。 また該粉体粒子の T g は 6 2 °Cであった。  A water-dispersible powder coating was produced in the same manner as in Example 2-1 b-1), except that the raw material mixture used in the ratio shown in Formula 4 below was used. Table 3 shows the properties and characteristics of the powder coating. The average particle size (D 50) of the powder particles contained in the obtained powder coating material was 13 m, and the coarse particles having a particle size of 50 m or more and the particles having a particle size of 0.5 m or more were 0.5 m or more. The content of fine particles below zm was 0% in all cases. The T g of the powder particles was 62 ° C.
配合 4 :  Formula 4:
粗粉碎物(注) 1 0 0. 0 (部) イオン交換水 1 0 0. 0 Coarse powder (Note) 1 0 0.0 (Parts) Ion exchange water 1 0 0.0
「アデ力ノール UH— 5 4 0」 ' 0. 4“Ade Force Knoll UH—5 4 0” '0.4
「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 5 「サ一フイ ノ一ル 4 2 0」 0. 4 「Disperbyk_ 1 9 0」 0. 4 合計 2 0 1 . 7"Rasmin MK-9" (10% aqueous solution) 0.5 "Sulfur 4-20" 0.4 "Disperbyk_190" 0.4 Total 20.1
(注)上記配合 3 によつて得た粗粉碎物 (T g ; 6 2 °C) 比較例 2 — 5 上記実施例 2 — 9 において、 配合 4で用いた 「Disperbyk— 1 9 0 J に代えて 「ォロタン 7 3 1 D P J (ローム ' アンド ' ハース社 製の分散剤) を使用した以外は、 前記実施例 2 — 9 と同様にして水 分散型粉体塗料を製造し、 得られた水分散型粉体塗料の性状 · 特性 を表 3 に示した。 尚、 得られた粉体塗料中に含まれる粉体粒子の平 均粒径 ( D 5 0 ) は 1 3 ^ mであり、 粒径が 5 0 ^ m以上の粗粒物 および粒径が 0. 5 / m以下の微粒物の含有量は何れも 0 %であつ た。 また該粉体粒子の T gは 6 2 °Cであった。 実施例 2 — 1 0 (Note) Coarse ground material (T g; 62 ° C) obtained by the above-mentioned formulation 3 Comparative Example 2 — 5 In the above Examples 2-9, except that “Orotane 731 DPJ (a dispersant manufactured by Rohm and Haas) was used instead of“ Disperbyk—190 J ”used in Formulation 4, A water-dispersible powder coating was produced in the same manner as in 2-9, and the properties and characteristics of the obtained water-dispersed powder coating are shown in Table 3. The powder contained in the obtained powder coating was also shown. The average particle diameter (D50) of the body particles is 13 ^ m, and the content of coarse particles having a particle diameter of 50 ^ m or more and fine particles having a particle diameter of 0.5 / m or less The powder particles had a T g of 62 ° C. Example 2—10
a - 3)ァク リル樹脂系粗粉砕物の製造  a-3) Manufacture of coarsely ground acrylic resin
原料を下記配合 5 に示す比率で使用した以外は、 前記実施例 2 — 1 の a_l)と同様にして、 ァクリル樹脂系の粗粉碎物を得る。  Except that the raw materials were used in the ratio shown in the following formula 5, a acryl resin-based coarse powder was obtained in the same manner as in a_l) of Example 2-1.
配合 5 :  Formula 5:
「アルマテックス P D 7 3 1 0」 5 3. 0 (部) デカンジカルボン酸 1 1. 5  “Almatex PD 7310” 53.0 (parts) Decanedicarboxylic acid 11.5
「ベンゾイン」 0. 4  “Benzoin” 0.4
「ァクロナール 4 F」 0. 5  「Acronal 4 F」 0.5
「酸化チタン C R 9 7」 3 4. 6  `` Titanium oxide C R 9 7 '' 34.6
合計 1 0 0. 0  Total 1 0 0. 0
b-3)ァクリル樹脂系水分散型粉体塗料の製造  b-3) Manufacture of water-dispersible powder coating of acryl resin
下記配合 6 に示す比率の原料配合物を採用した以外は、 前記実施 例 2 — 1 と同様の方法で、 ァクリル樹脂系の水分散型粉体塗料を得 る。 得られた水分散型粉体塗料の性状 · 特性を表 3 に示す。 尚、 該 粉体粒子の平均粒径 (D 5 0 ) は 1 3 ^ mであり、 粒径が 5 0 m 以上の粗粒物および粒径が 2. 5 以下の微粒物の含有量は何れ も 0 %であった。 また該粉体粒子の T gは 6 0 °Cであった。  An acryl resin-based water-dispersed powder coating is obtained in the same manner as in Example 2-1 except that the raw material mixture having the ratio shown in the following formulation 6 is used. Table 3 shows the properties and characteristics of the obtained water-dispersed powder coating. The average particle size (D50) of the powder particles is 13 ^ m, and the content of coarse particles having a particle size of 50 m or more and fine particles having a particle size of 2.5 or less is determined. Was also 0%. The T g of the powder particles was 60 ° C.
配合 6 :  Formula 6:
粗粉砕物(注) 1 0 0. 0 (部) ィオン交換水 1 0 0. 0 「アデカノ一ル UH— 5 4 0」 0. 4 Coarse pulverized material (Note) 1 0 0.0 (Parts) Zion exchange water 1 0 0.0 "Adecanol UH—5 4 0" 0.4
「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 5  "Rasmin MK-9" (10% aqueous solution) 0.5
「サーフィ ノール 4 2 0」 0. 4  “Surfinol 4 2 0” 0.4
「Disperbyk— 1 9 0」 0. 4 合計 2 0 1. 7  “Disperbyk—1 9 0” 0.4 Total 2 0 1.7
(注)上記配合 5 によって得た粗粉碎物 (T g ; 6 0 °C) 比較例 2 — 6  (Note) Crude powder (T g; 60 ° C) obtained by the above formulation 5 Comparative Example 2 — 6
上記 b - 3)に示したァク リル樹脂系水分散型粉体塗料の製造にお ける配合 6で用いた 「Disperbyk— 1 9 0」 に代えて 「ォロタン 7 3 1 D P」 (同前) を使用した以外は、 上記実施例 2 — 1 0 と全く 同様にして、 ァクリル樹脂系水分散型塗料を製造した。  “Orotane 731 DP” (the same as above) in place of “Disperbyk—190” used in Formulation 6 in the production of the acrylic resin-based water-dispersed powder coating shown in b-3) above An acryl resin-based water-dispersed paint was produced in exactly the same manner as in Example 2-10 except that was used.
得られた水分散型粉体塗料の性状 · 特性を表 3に示す。 尚、 該粉 体粒子の平均粒径 ( D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以 上の粗粒物および粒径が 0. 5 m以下の微粒物の含有量は何れも 0 %であった。 また該粉体粒子の T gは 6 0 であった。 Table 3 shows the properties and characteristics of the obtained water-dispersed powder coating. The average particle size (D50) of the powder particles is 13 m, and the content of coarse particles having a particle size of 50 m or more and fine particles having a particle size of 0.5 m or less is as follows. All were 0%. The T g of the powder particles was 60.
表 3 Table 3
実 施 例 比 較 例  Example Example Comparative Example
り一 1 ゥ一ゥ ゥ _ ゥ一 S 0— R ゥ一 7 ゥ _ Q y ゥ一 1 n _ 0 "t ウー ホ リエス丁ル糸ネ且粉 5?物 H I Π U ΠU i In UnU 1 UU 1 I Π U ΠU I UU 1 I n UnU I UU l UU y u Q Π i 1n un u  Ri 1 1 ゥ 1 ゥ ゥ ゥ S S 0— R ゥ 1 7 _ _ Q y ゥ 1 1 _ 0 "t woo リ 丁 丁 ル ネ n 5 HI HI HI 1 I Π U ΠU I UU 1 In n UnU I UU l UU yu Q Π i 1n un u
ェ 千ン糸ネ fl ¾ί ίι W I UU I UU  D Thousand Threads fl ¾ί ίι W I UU I UU
1 n  1 n
アクリル系祖粉砕物 I UnU 1 I n u  Acrylic crushed material I UnU 1 I n u
1 i Unn  1 i Unn
イオン n  Ion n
父 τΚ 1 UU I UU i UU 1 UU 1 UU 1 UU U i Ίn UU 1 UU i 1n UnU 11 u 11 U I UU inn 1n UnU ■in ァ丁 力ノール UH— ί)4ϋ A U.4 U.4 U.4 Π U.4 /1 n  Father τΚ 1 UU I UU i UU 1 UU 1 UU 1 UU U i Ίn UU 1 UU i 1n UnU 11 u 11 UI UU inn 1n UnU ■ in .4 Π U.4 / 1 n
U.4 U.4 U.4 U.4 n n U.4 Π U.41 n Π 防鑌剤 フス:;ノ ΜΚ一 Ίυ%^ U.0 U.0 U.0 U.0 n u .0 c U.0 U .0 n u .0 ς U , 0 n u .0 ς u .0 π u .0 ς n U .0 u . U.4 U.4 U.4 U.4 nn U.4 Π U.41 n Π Protective agent Hus :; ΜΚ Ίυ% ^ U.0 U.0 U.0 U.0 nu .0 c U.0 U .0 nu .0 ς U, 0 nu .0 ς u .0 π u .0 ς n U .0 u.
Figure imgf000048_0001
sΑp eroyK 1 ιΩ yΠ u - Π U , *f Π Π Π Π n A
Figure imgf000048_0001
s Α p eroyK 1 ιΩ yΠ u-Π U, * f Π Π Π Π n A
分散剤 フローレノ 1 (j— /oUW n Dispersant Floreno 1 (j— / oUW n
'メ lノ / S IUド Π ク u舞 n ク n 'Me / no / S IU
4 V4-一 1 1一 Π Λ 4 V4-1 1 1 1 Π Λ
ノィノ ル Π Λ  ノ ノ ィ
サーフィノール 440 n U .4 * U . ½ U. Π U. l Π U . サ一フィノール 465 0.4  Surfynol 440 n U .4 * U. ½ U. Π U. l Π U.
界面  Interface
サーフィノール 485 0.4  Surfynol 485 0.4
活性剤  Activator
タ一シ'ト一ル TMN— 3 0.4 0.4 0.4 ターシ'トール TMN— 6 0.4  Terminal TMN-30.4 0.4 0.4Terminal TMN-60.4
S ウエット 970 0.4  S wet 970 0.4
塗料粉体の平均粒径 13 13 13 13 13 13 13 13 13 13 13 13 13 13 13 1 13 13 13 13 13 13 13 13 13 13 13 13 13 13 13 1
(D50): m (D50): m
塗料固形分濃度(maSS%) 50 50 50 50 50 50 50 50 50 50 45 45 50 50 50 5 塗料粘度(mPa-s) 2750 2600 2600 2600 2500 2430 2800 2700 2750 2800 3100 3000 3100 2970 2960 31 Paint solids concentration (ma SS %) 50 50 50 50 50 50 50 50 50 50 45 45 50 50 50 50 5 Paint viscosity (mPa-s) 2750 2600 2600 2600 2500 2430 2800 2700 2750 2800 3100 3000 3100 2970 2960 31
得られた各水分散型粉体塗料を使用し、 ァネス ト岩田社製のスプ レーガン 「W— 1 0 0」 (ノズル口径 1 . 3 mm) を用いて、 「 S P C C— S D P B— 3 1 1 8」 鋼板 (同前) に 3回スプレー塗装 し、 次いで熱風乾燥機内に装入して、 ポリエステル系樹脂の場合は 1 9 0 °Cで 2 0分間、 エポキシ系樹脂、 アクリル系樹脂、 ェポキ シ · ポリエステル系樹脂の場合は 1 8 0 °Cで 2 0分間焼付処理して から塗膜性能を評価し、 下記表 4に示す結果を得た。 Using each of the water-dispersible powder coatings obtained, a spray gun “W—100” (nozzle diameter: 1.3 mm) manufactured by Anest Iwata Co., Ltd. was used to “SPCC—SDPB—3118” Spray paint on the steel plate (same as above) three times, then put it in a hot air dryer, and in the case of polyester resin, at 190 ° C for 20 minutes, epoxy resin, acrylic resin, epoxy resin In the case of a polyester resin, the coating film performance was evaluated after baking treatment at 180 ° C. for 20 minutes, and the results shown in Table 4 below were obtained.
表 4 実 施 例 比 較 例 Table 4 Comparative examples
評価項目  Evaluation item
2-1 2-2 2-3 2-4 2-5 2-6 2-7 2-8 2-9 2-10 2-1 2-2 2-3 2-4 2-5 2-6 塗装作業性 5 5 5 5 5 5 5 5 5 5 3 3 3 3 3 3 タレ性 5 5 5 5 5 5 5 5 5 5 3 3 5 5 5 5 ヮキ性 5 5 5 5 5 5 5 5 5 5 4 4 3 3 3 3 平滑性 5 5 5 5 5 5 5 5 5 5 2 2 3 3 3 3 貯蔵安定性 5 5 5 5 5 5 5 5 5 5. 2 2 3 3 3 3 耐水性 5 5 5 4 4 4 3 5 5 5 5 4 3 2 3 3 2-1 2-2 2-3 2-4 2-5 2-6 2-7 2-8 2-9 2-10 2-1 2-2 2-3 2-4 2-5 2-6 Painting work 5 5 5 5 5 5 5 5 5 5 3 3 3 3 3 3 Sagging 5 5 5 5 5 5 5 5 5 5 3 3 5 5 5 5 Grading 5 5 5 5 5 5 5 5 5 5 4 4 3 3 3 3 Smoothness 5 5 5 5 5 5 5 5 5 5 2 2 3 3 3 3 Storage stability 5 5 5 5 5 5 5 5 5 5 5.2 2 3 3 3 3 Water resistance 5 5 5 4 4 4 3 5 5 5 5 4 3 2 3 3
塗料 1製造例 (ポリエステル系水分散型粉体塗料 ; 実施例用) a - 1)ポリェステル樹脂系粗粉砕物の製造 Paint 1 Production example (Polyester-based water-dispersed powder coating; for Examples) a-1) Production of coarsely ground polyester resin
原料を下記配合 1 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて熱溶融混練すると共に押出し、 厚さ 約 1 m mのシ—ト状に押出して冷却固化させる。 このシー ト状物を 破碎機に通して粗粉砕した後、 篩目が 1. 0 mmのフィルターに通 すことによりポリエステル樹脂系粗粉碎物を得る。  The raw materials are used in the ratio shown in Formulation 1 below, uniformly mixed with a high-speed mixer, then hot melt kneaded and extruded using a melt extruder, extruded into a sheet with a thickness of about 1 mm, and cooled and solidified. Let it. This sheet is coarsely pulverized through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a polyester resin coarse powder.
配合 1 :  Formula 1:
「ファイ ンティ ック M - 8 0 2 0」 5 4. 9 (部) 「クレラン V P L S 2 2 5 6」 8. 2  “Finick M-820 0” 54.9 (parts) “Cleran VPL S 2 2 5 6” 8.2
「ベンゾィ ン」 0. 4  `` Benzine '' 0.4
「 A E R 6 0 0 2」 3. 0  “AER6002” 3.0
「ァクロナール 4 F」 0. 5  「Acronal 4 F」 0.5
「酸化チタン C R 9 7」 3 3. 0  "Titanium oxide CR97" 33.0
合計 1 0 0. 0 b-1)ポリエステル樹脂系水分散型粉体塗料 1 の製造  10.0 0.0 b-1) Production of polyester resin water-dispersed powder coating material 1
下記配合 2 に示す比率で用いた原料配合物 1 0. O k gをデイス パーによって混合し、 この混合物を冷却機構内蔵型の湿式循環型ビ —ズミル [分散メディア ; 直径 1. 0 mmのニツカ 卜一社製ジルコ ニァポール 「 Y T Z」 を、 ベッセル容積に対し 8 0 % ( 4. 4 k g ) 装入したもの] に連結した循環槽に投入し、 アジテ一タ一アイ スクを周速 1 O mZ sで回転させながら循環させることによって微 粉砕処理を行う。 次いで、 5 0 2 mフィルターに通して濾過するこ とによりポリエステル樹脂系水分散型粉体塗料 1 を得る。 得られた 水分散型粉体塗料 1の性状 · 特性を表 5 に示す。 尚、 該粉体塗料 1 中の粉体粒子の平均粒径 (D 5 0 ) は 1 3 / mであり、 粒径が 5 0 ^ m以上の粗粒物および粒径が 0. 5 m以下の微粒物の含有量は 何れも 0 %であった。 また該粉体粒子の T gは 6 5 であった。 配合 2 : ポリエステル樹脂系粗粉砕物(注) 1 0.0 0 (部) イオン交換水 1 0 0 0 The raw material mixture used in the ratio shown in the following formulation 2 was mixed with a 100. O kg by a disperser, and the mixture was wet-circulated bead mill with a built-in cooling mechanism [dispersion media: Nitkato with a diameter of 1.0 mm Zirconiapole "YTZ" manufactured by one company was charged into a circulation tank connected to 80% (4.4 kg) of the vessel volume], and the agitator disk was rotated at a peripheral speed of 1 O mZ s Fine grinding is performed by circulating while rotating. Next, the mixture is filtered through a 502 m filter to obtain a polyester resin-based water-dispersed powder coating material 1. Table 5 shows the properties and characteristics of the obtained water-dispersed powder coating material 1. The average particle size (D50) of the powder particles in the powder coating material 1 was 13 / m, and the coarse particles having a particle size of 50 ^ m or more and the particle size of 0.5 m or less were used. In each case, the content of fine particles was 0%. The T g of the powder particles was 65. Formula 2: Coarse pulverized polyester resin (Note) 1 0.0 0 (parts) Ion exchange water 100 0 0
「アデカノ一ル UH— 5 4 0 J 0 4  "Adecanol UH—540 J04
「サーフィ ノール 4 2 0」 0 4  `` Surfinol 4 2 0 '' 0 4
「Disperbyk— 1 9 0」 0 4  “Disperbyk—1 9 0” 0 4
□ 口 2 0 1 2  □ Mouth 2 0 1 2
(注)上記配合 1 によって得たポリエステル榭脂系粗粉砕物 (T g ; 6 5 °C ) 塗料 2製造例 (ポリエステル樹脂系水分散型粉体塗料 ; 実施例 用)  (Note) Coarsely crushed polyester resin-based product (Tg; 65 ° C) obtained by the above Formulation 1 Paint 2 Production example (Polyester resin-based water-dispersed powder coating; for Examples)
前記塗料 1製造例において、 配合 2 に代えて下記配合 3 を採用し た以外は上記と同様にしてポリエステル樹脂系水分散型粉体塗料 2 を得た。  A polyester resin-based water-dispersed powder coating material 2 was obtained in the same manner as described above, except that in the production example of the coating material 1, the following formulation 3 was used instead of the formulation 2.
配合 3 :  Formula 3:
ポリエステル樹脂系粗粉砕物(注) 1 0 0. 0 (部) イオン交換水 1 0 0. 0  Polyester resin coarsely pulverized product (Note) 10.0 (Parts) Ion-exchanged water 1 00.0
「アデ力ノール UH— 5 4 0」 0. 4  “Ade Force Knoll UH—5 4 0” 0.4
「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 5  "Rasmin MK-9" (10% aqueous solution) 0.5
「サ一フィ ノール 4 2 0」 0. 4  「Safinol 4 2 0」 0.4
「Disperbyk— 1 9 0」 0. 4  “Disperbyk—1 9 0” 0.4
合計 2 0 1. 7  Total 2 0 1.7
(注)上記配合 1 によって得たポリエステル樹脂系粗粉砕物 (T g ; 6 5 °C ) 塗料 3製造例 (エポキシ樹脂系水分散型粉体塗料 ; 実施例用) a- 2)エポキシ樹脂系粗粉碎物の製造  (Note) Polyester resin coarsely pulverized product (Tg; 65 ° C) obtained by the above formulation 1 Paint 3 Production example (Epoxy resin water-dispersed powder coating; for example) a-2) Epoxy resin Manufacture of coarse powder
原料を下記配合 4に示す比率で使用した以外は、 前記塗料 1製造 例の a- 1)と同様にして、 エポキシ樹脂系粗粉砕物を得る。  A coarsely pulverized epoxy resin material is obtained in the same manner as in a-1) of the above-mentioned Production Example 1 for the coating material, except that the raw materials are used in the ratio shown in the following formulation 4.
配合 4 : 「A E R— 6 0 1 4」 6 1. 3 (部) 「 A D H」 2. 8 「ベンゾイン」 0. 4 「ァクロナ一ル 4 F」 0. 5 「酸化チタン C R 9 7 J 3 5. 0 Formula 4: “AER— 6 1 4” 6 1.3 (parts) “ADH” 2.8 “Benzoin” 0.4 “Acronal 4 F” 0.5 “Titanium oxide CR 9 7 J 35.0”
合計 1 0 0. 0 b - 2)エポキシ樹脂系水分散型粉体塗料 3の製造  Total 10.0 b-2) Production of epoxy resin-based water-dispersed powder coating material 3
下記配合 5 に示す比率で用いた原料配合物を使用した以外は、 前 記塗料 1製造例の b- 1)と同様にしてエポキシ樹脂系水分散型粉体 塗料 3 を製造し、 得られた水分散型粉体塗料 3の性状 · 特性を表 5 に示した。 尚、 得られた塗料 3 中に含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および 粒径が 0. 5 m以下の微粒物の含有量は何れも 0 %であった。 ま た該粉体粒子の T gは 6 2 °Cであった。  An epoxy resin-based water-dispersed powder coating material 3 was produced in the same manner as in the above-mentioned coating material 1 Production Example b-1), except that the raw material mixture used in the ratio shown in the following formulation 5 was used. Table 5 shows the properties and characteristics of the water-dispersed powder coating material 3. The average particle size (D 50) of the powder particles contained in the obtained paint 3 was 13 m, coarse particles having a particle size of 50 m or more and particle sizes of 0.5 m or less. Was 0% in all cases. The T g of the powder particles was 62 ° C.
配合 5 :  Formula 5:
エポキシ樹脂系粗粉砕物(注) 1 0 0. 0 (部) イオン交換水 1 0 0. 0  Epoxy resin coarse pulverized product (Note) 10.0 (Parts) Deionized water 10.0
「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 5 "Rasmin MK-9" (10% aqueous solution) 0.5
「サ一フィ ノール 4 2 0」 0. 4 「Disperbyk— 1 9 0」 0. 4 合計 2 0 1. 3 “Safinol 4 2 0” 0.4 “Disperbyk— 1 9 0” 0.4 Total 2 0 1.3
(注)前記配合 4によって得たエポキシ樹脂系粗粉砕物 (T g ; 6 2 °C) 塗料 4製造例 (エポキシ樹脂系水分散型粉体塗料 ; 実施例用) 前記塗料 3製造例において、 配合 5 に代えて下記配合 6 を採用し た以外は同様にしてエポキシ樹脂系水分散型粉体塗料 4を製造した 配合 : 6  (Note) Epoxy resin-based coarsely pulverized product (Tg; 62 ° C) obtained by the above-mentioned formulation 4 Paint 4 Production Example (Epoxy resin-based water-dispersed powder paint; for Example) An epoxy resin-based water-dispersed powder coating material 4 was produced in the same manner except that the following formulation 6 was used instead of the formulation 5. Formulation: 6
エポキシ樹脂系粗粉砕物(注) 1 0 0. 0 (部) イオン交換水 1 0 0 0 Epoxy resin coarse pulverized product (Note) 10.0 (parts) Ion exchange water 1 0 0 0
「アデカノ一ル UH— 5 4 0」 0 4  “Adecanol UH—5 4 0” 0 4
「ラスミン MK— 9」 ( 1 0 %水溶液) 0 5  "Rasmin MK-9" (10% aqueous solution) 0 5
「サ一フィ ノール 4 2 0 J 0 4  Safinol 4 2 0 J 0 4
「Disperbyk— 1 9 0」 0 4  “Disperbyk—1 9 0” 0 4
2 0 1 7  2 0 1 7
(注)前記配合 4 よって得たエポキシ樹脂系粗粉碎物 (T g ; 6 2。C) 塗料 5製造例 (ァクリル樹脂系水分散型粉体塗料 ; 実施例用) a- 3)ァクリル樹脂系粗粉砕物の製造  (Note) Epoxy resin coarse powder (Tg; 62.C) paint 5 obtained by the above-mentioned compounding 4 Paint 5 Production example (acrylic resin-based water-dispersible powder paint; for example) a-3) acrylic resin-based Production of coarsely pulverized material
原料を下記配合 7 に示す比率で使用した以外は、 前記塗料 ] 例の a-1)と同様にして、 ァク リル樹脂系粗粉碎物を得る。  Except that the raw materials were used in the proportions shown in the following formulation 7, the same procedure as in a-1) of the above coating example was carried out to obtain an acrylic resin-based coarse powder.
配合 7 :  Formula 7:
「アルマテックス P D 7 3 1 0」 5 3. 0 (郜) デカンジカルボン酸 1 1. 5  “Almatex PD 7310” 53.0 (郜) Decanedicarboxylic acid 11.5
「ベンゾイン」 0. 4  “Benzoin” 0.4
「ァクロナール 4 F」 0. 5  「Acronal 4 F」 0.5
「酸化チタン C R 9 7」 3 4. 6  `` Titanium oxide C R 9 7 '' 34.6
合計 1 0 0. 0 b- 3)ァクリル樹脂系水分散型粉体塗料 5の製造  10.0 0.0 b- 3) Manufacture of acrylyl resin-based water-dispersed powder coating material 5
下記配合 8 に示す比率の原料配合物を採用した以外は、 前記塗料 1製造例と同様の方法で、 アクリル樹脂系水分散型粉体塗料 5 を得 る。 得られた水分散型粉体塗料 5の性状、 特性を表 5に示す。 該塗 料中に含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0. 5 m以下の微粒物 の含有量は何れも 0 %であった。 また該粉体粒子の T gは 6 0 °Cで あった。  Acrylic resin-based water-dispersed powder coating material 5 is obtained in the same manner as in the above-mentioned coating material 1 production example, except that the raw material mixture having the ratio shown in the following formulation 8 is used. Table 5 shows the properties and characteristics of the obtained water-dispersed powder coating material 5. The average particle diameter (D 50) of the powder particles contained in the coating is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 m or less are used. The contents were all 0%. The T g of the powder particles was 60 ° C.
配合 8 : アクリル樹脂系粗粉碎物(注) 1 0 0. 0 (部) ィオン交換水 1 0 0. 0 Formula 8: Acrylic resin coarse powder (Note) 1 0 0.0 (Parts) Zion exchange water 1 0 0.0
「アデカノ一ル UH— 5 4 0」 0. 4  "Adecanol UH—5 4 0" 0.4
「サーフイ ノ一ル 4 2 0」 0. 4  "Surfinol 4 2 0" 0.4
「 Disperbyk - 1 9 0 J 0. 4  "Disperbyk-1 90 J 0.4
合計 2 0 1 . 2  Total 2 0 1.2
(注)前記配合 7 によって得たァク リル樹脂系粗粉碎物 (T g ; 6 0 °C) 塗料 6製造例 (ァク リル樹脂系水分散型粉体塗料 ; 実施例用) 上記 b-3)に示したァク リル樹脂系水分散型粉体塗料 5 の製造に おける配合 8で用いた 「Disperbyk— 1 9 0」 に代えて 「フローレ ン T G— 7 5 0 W」 (共栄化学社製の分散剤) を使用した以外は、 前記塗料 5製造例と全く同様にして、 アクリル樹脂系水分散型塗料 6を製造した。 該塗料 6に含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 ; m以上の粗粒物および粒径が 0. 5 m以下の微粒物の含有量は何れも 0 %であった。 また該粉体粒 子の T gは 6 0 °Cであった。 塗料 7製造例 (ァク リル樹脂系水分散型粉体塗料 ; 実施例用) 表 5に記載した配合を採用し、 前記塗料 1製造例と同様の方法で ァクリル樹脂系水分散型粉体塗料 7 を製造した。 該塗料 7 に含まれ る粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 〃 m以上の粗粒物および粒径が 0. 5 ^ m以下の微粒物の含有量は何 れも 0 %であった。 また該粉体粒子の T gは 6 0 °Cであった。 塗料 8製造例 (ァク リル樹脂系水分散型粉体塗料 ; 実施例用) 前記塗料 5製造例において、 「酸化チタン C R 9 7」 を使用しな かった以外は同様にしてアクリル樹脂系水分散型粉体塗料 8 を製造 した。 該塗料 8 に含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 ^ mであり、 粒径が 5 0 ^ m以上の粗粒物および粒径が 0 . 5 1 1以 下の微粒物の含有量は何れも 0 %であった。 また該粉体粒子の T g は 5 8 °Cであった。 塗料 9製造例 (ポリエステル樹脂系水分散型粉体塗料 ; 比較例 用) (Note) Acrylic resin-based coarse powder (Tg: 60 ° C) obtained by the above Formulation 7 Paint 6 Production example (Acrylic resin-based water-dispersed powder coating; for Examples) “Floren TG—750 W” (Kyoei Chemical Co., Ltd.) was used instead of “Disperbyk—190” used in Formulation 8 in the production of the acrylic resin-based water-dispersible powder coating 5 shown in 3). Acrylic resin-based water-dispersible paint 6 was produced in exactly the same manner as in the above-mentioned Paint 5 Production Example, except that a dispersant manufactured by Co., Ltd. was used. The average particle diameter (D 50) of the powder particles contained in the paint 6 is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 m or less are used. The contents were all 0%. The T g of the powder particles was 60 ° C. Paint 7 Production example (acrylic resin-based water-dispersed powder coating; for example) Admixture shown in Table 5 was adopted, and acryl resin-based water-dispersed powder-based coating was performed in the same manner as in the above-mentioned coating 1 Production Example. 7 was manufactured. The average particle size (D 50) of the powder particles contained in the paint 7 is 13 m, coarse particles having a particle size of 50 μm or more and fine particles having a particle size of 0.5 ^ m or less. The content of all substances was 0%. The T g of the powder particles was 60 ° C. Paint 8 Production Example (acrylic resin-based water-dispersed powder coating; for example) In the above-mentioned Paint 5 Production Example, an acrylic resin-based water-based Dispersion type powder coating 8 was produced. The average particle diameter (D 50) of the powder particles contained in the paint 8 is 13 ^ m, the content of coarse particles having a particle size of 50 ^ m or more and the content of fine particles having a particle size of 0.511 or less were 0%. The T g of the powder particles was 58 ° C. Paint 9 Production example (Polyester resin-based water-dispersed powder paint; for comparative example)
表 5 に記載の配合を採用し、 以下は前記塗料 1製造例と同様にし てポリエステル樹脂系水分散型粉体塗料 9 を製造した。 該塗料 9 に 含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0 . 5 X m以下の微粒物の含有 量は何れも 0 %であった。 また該粉体粒子の T gは 6 5 °Cであった, 塗料 1 0製造例 (エポキシ樹脂系水分散型粉体塗料 ; 比較例用) 表 5 に記載の配合を採用し、 以下は前記塗料 1製造例と同様にし てエポキシ樹脂系水分散型粉体塗料 1 0を製造した。 該塗料 1 0 に 含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0 . 5 x m以下の微粒物の含有 量は何れも 0 %であった。 また該粉体粒子の T gは 6 2 であった, 塗料 1 1製造例 (ァクリル樹脂系水分散型粉体塗料 ; 比較例用) 表 5 に記載の配合を採用し、 以下は前記塗料 1製造例と同様にし てアクリル樹脂系水分散型粉体塗料 1 1 を製造した。 該塗料 1 1 に 含まれる粉体粒子の平均粒径 (D 5 0 ) は 1 3 ^ mであり、 粒径が 5 0 m以上の粗粒物および粒径が 0 . 5 x m以下の微粒物の含有 量は何れも 0 %であった。 また該粉体粒子の T gは 6 0 °Cであった, 得られた各水分散型粉体塗料 1 〜 1 1 の性状、 特性を表 5 に示す, 表 5 The formulation shown in Table 5 was adopted, and a polyester resin-based water-dispersed powder coating material 9 was manufactured in the same manner as in the above-mentioned coating material 1 manufacturing example. The average particle size (D50) of the powder particles contained in the coating material 9 is 13 m, and the coarse particles having a particle size of 50 m or more and the fine particles having a particle size of 0.5 Xm or less are fine. The contents were all 0%. The T g of the powder particles was 65 ° C., and the composition of the paint 10 was prepared as shown in Table 5 below. An epoxy resin-based water-dispersed powder coating material 10 was produced in the same manner as in the coating material 1 production example. The average particle diameter (D 50) of the powder particles contained in the paint 10 is 13 m, and the coarse particles having a particle diameter of 50 m or more and the fine particles having a particle diameter of 0.5 xm or less are fine. The contents were all 0%. The T g of the powder particles was 62. Paint 11 Production Example (acrylic resin-based water-dispersed powder paint; for comparative example) The formulation shown in Table 5 was adopted. An acrylic resin-based water-dispersed powder coating material 11 was produced in the same manner as in the production example. The average particle size (D50) of the powder particles contained in the coating material 11 is 13 ^ m, and coarse particles having a particle size of 50 m or more and fine particles having a particle size of 0.5 xm or less are provided. Was 0% in all cases. The T g of the powder particles was 60 ° C. The properties and characteristics of each of the obtained water-dispersed powder coating materials 1 to 11 are shown in Table 5. Table 5
Figure imgf000057_0001
Figure imgf000057_0001
次に、 上記水分散型粉体塗料 1〜 1 1 と組合せて使用するその他 の塗料について示す。 Next, other paints used in combination with the water-dispersed powder coatings 1 to 11 will be described.
. 塗料 i : 「レタン P G— 8 0メタリ ック」 (関西ペイント社製の ィソシァネー ト硬化型ァクリル樹脂塗料で、 2液硬化型有機溶剤系 の着色上塗り塗料として使用する。  Paint i: "Rethane PG-80 Metallic" (Kansai Paint Co., Ltd.'s isocyanate-curable acryl resin paint, used as a two-component curable organic solvent-based colored topcoat.
塗料 ii : 「エレクロン G T— 1 0 グレー」 (関西ペイント社製の ブロックイソシァネ一ト硬化型エポキシ樹脂カチオン電着塗料で、 下塗り塗料として使用する。  Paint ii: "Electron G T-10 Gray" (Kansai Paint Co., Ltd. block isocyanate curable epoxy resin cationic electrodeposition paint, used as undercoat.
塗料 iii : 固形分 5 0 %のアクリル樹脂中和水溶液 ( 1 ) 1 4 0 部と、 「サイメル 3 7 0」 (三井サイテック社製の 8 8 %水溶性メ ラミン樹脂溶液) 3 4部を混合し、 次いで 「アルミペース ト 8 9 1 K」 (東洋アルミニウム社製) 2 5部を加えて分散し、 脱イオン水 で固形分 3 5 %に調整することにより着色べ一ス塗料としたもの。  Paint iii: Mix 140 parts of neutralized aqueous acrylic resin (1) with 50% solids and 34 parts of Cymel 370 (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) Then, 25 parts of “Aluminum Paste 891 K” (manufactured by Toyo Aluminum Co., Ltd.) was added and dispersed, and the solid content was adjusted to 35% with deionized water to obtain a colored base paint.
( 1 メタク リル酸メチル 3 0部、 アク リル酸ェチル 2 3部、 ァクリル酸ブチル 3 0部、 メタクリル酸ヒ ドロキシェチル 1 2部、 ァクリル酸 5部の共重合体からなり、 酸価 ; 4 0、 水酸基価 ; 5 2 数平均分子量 ; 約 1 0 0 0 0のァクリル樹脂溶液 (固形分 6 0 %) を製造し、 この溶液にジ'メチルアミノエタノールを加えて中和し、 次いでイソプロピルアルコールで固形分 5 0 %に希釈したもの。  (1 A copolymer of 30 parts of methyl methacrylate, 23 parts of ethyl acrylate, 30 parts of butyl acrylate, 12 parts of hydroxyshethyl methacrylate, and 5 parts of acrylic acid, acid value: 40, Hydroxyl value: 52 A number-average molecular weight: about 100,000 acryl resin solution (solid content: 60%) is prepared, di'methylaminoethanol is added to this solution, neutralized, and then solidified with isopropyl alcohol. Diluted to 50% per minute.
塗料 iv : 固形分 5 0 %のアク リル樹脂中和溶液 (上記 1※と同 じ) 1 4 0部と 「サイメル 3 7 0」 (三井サイテック社製の 8 8 % 水溶性メラミン樹脂溶液) 3 4部を混合し、 脱イオン水で固形分 3 5 %に調整したもので、 上塗りクリア一塗料として使用する。  Paint iv: Acrylic resin neutralization solution with 50% solids (same as 1 * above) 140 parts and “Cymel 370” (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) 3 Mix 4 parts and adjust to a solid content of 35% with deionized water. Use as a clear top coating.
塗料 V : 固形分 5 0 %のアク リル樹脂中和溶液 (上記 1 ※と同 じ) 1 4 0部と 「サイメル 3 7 0」 (三井サイテック社製の 8 8 % 水溶性メラミン樹脂溶液) 3 4部を混合し、 これにチタン白 5 5部 とカーボンブラック 2部を加えて分散した後、 脱イオン水で固形分 3 5 %に調整したもので、 着色上塗り塗料として使用する。  Paint V: Acrylic resin neutralization solution with 50% solids (same as 1 * above) 140 parts and “Symel 370” (88% water-soluble melamine resin solution manufactured by Mitsui Cytec) 3 Four parts are mixed, 55 parts of titanium white and 2 parts of carbon black are added and dispersed, and then adjusted to a solid content of 35% with deionized water, and used as a colored overcoat.
塗料 : 「ネオアミラック # 6 0 0 0 ホワイ ト」 (関西ペイン ト社製の有機溶剤系、 アクリルメラミン硬化系の塗料で、 着色上塗 り塗料として使用する。 Paint: Neo-Amirac # 600 White (Kansai Paint Co., Ltd., an organic solvent-based, acrylic melamine-cured paint, colored top coat Used as a paint.
塗料 vii : ポリエステル樹脂 (ネオペンチルダリコール ; Ί 5 6部. トリメチロールプロパン ; 1 0 9部、 へキサヒ ドロフ夕ル酸 ; 3 7 0部、 アジピン酸 ; 2 9 2部およびイソフ夕ル酸 ; 3 9 8部を反応 容器に入れ、 2 2 0 °Cで 6時間反応させた後、 無水ト リ メ リ ッ ト 酸 ; 4 5部添加し、 1 7 0 °Cで 3 0分反応させて得られるポリエス テ樹脂で、 数平均分子量 ; 約 8 0 0 0、 酸価 ; 2 O m g K O H/ g . 水酸基価 ; 9 5 m g K O HZ g ) 1 0 0 0部 (固形換算、 以下同 じ) 、 ジメチルアミノエ夕ノール ; 4 0部、 硬化剤 (へキサメチレ ンジイソシァネー トの 3量体のァダク ト物をメチルェチルケ トォキ シムでブロックしたもの) 4 1 0部、 チタン白顔料 (ティカ社製の 「ティカ J R 8 0 6」 ) 1 4 0 0部及び力一ポンプラック (三菱化 学社製の 「三菱カーボンブラック M— 1 0 0」 ) 2部を、 脱イオン 水 1 8 0 0部と共に混合分散したもので、 中塗り塗料として使用す る。 実施例 3 — 1  Paint vii: Polyester resin (neopentyldaricol; Ί56 parts; trimethylolpropane; 109 parts; hexahydrofuric acid; 370 parts; adipic acid; 292 parts and isofuric acid; Put 398 parts in a reaction vessel and react at 220 ° C for 6 hours, then add trimellitic anhydride; 45 parts, and react at 170 ° C for 30 minutes. The polyester resin obtained has a number average molecular weight of about 800, an acid value of 2 O mg KOH / g. A hydroxyl value of 95 mg KO HZ g) 100 parts (solid equivalent, hereinafter the same). Dimethylaminoethanol; 40 parts, curing agent (hexamethylenediisocyanate trimer adduct blocked with methylethylketoxim) 410 parts, titanium white pigment (Tika's JR 806)) 1400 parts and power pump rack (Mitsubishi Chemical Corporation Mitsubishi Carbon Black M-1000 ") 2 parts mixed and dispersed with 180 parts of deionized water. Used as an intermediate coating. Example 3 — 1
素材 A (燐酸亜鉛処理鋼板) に、 下塗り塗料として前記で得た 「塗料 4」 を乾燥膜厚が 4 0 z mとなる様にスプレー塗装し、 次い で 1 8 0 °Cで 2 0分間焼付処理した後、 前記 「塗料 i」 を着色上塗 り塗料として乾燥膜厚が 8 0 x mとなるようにスプレー塗装し、 8 0 °Cで 3 0分間加熱して硬化させた。  Material A (zinc phosphate-treated steel sheet) was spray-coated with the above-mentioned “Paint 4” as an undercoat paint to a dry film thickness of 40 zm, and then baked at 180 ° C for 20 minutes. After the treatment, the above “paint i” was spray-coated as a colored overcoat paint so as to have a dry film thickness of 80 xm, and was cured by heating at 80 ° C for 30 minutes.
得られる塗膜は、 下塗り塗膜と着色上塗り塗膜との 2層複層塗膜 であ り、 塗装方式は 「 2 コー ト 2ベ一ク、 塗装膜 2、 焼付 2回」 The coating film obtained is a two-layer multi-layer coating film consisting of an undercoat film and a colored overcoat film, and the coating method is `` 2 coats and 2 coatings, 2 coating films and 2 baking times ''.
( 2 C 2 Bと略記する) である。 本例は、 エポキシ樹脂系水分散型 粉体塗料を下塗り として適用した本発明の実施例である。 実施例 3 — 2〜 3 — 2 4、 比較例 3 — 1 〜 3 _ 6 (Abbreviated as 2 C 2 B). This example is an example of the present invention in which an epoxy resin-based water-dispersed powder coating is applied as an undercoat. Example 3 — 2 to 3 — 24, Comparative Example 3 — 1 to 3 _ 6
前記で得た 「塗料 1 〜 1 1」 および 「塗料 i 〜vii」 を使用し、 下 記表 6〜 8に示す塗料、 塗装法、 膜厚、 乾燥、 焼付条件の組合せで 実施例 3 — 2〜 3 — 2 4および比較例 3 _ 1〜 3 — 6 の塗膜を形成 した。 Using “Paints 1 to 11” and “Paints i to vii” obtained above, the combination of paint, coating method, film thickness, drying, and baking conditions shown in Tables 6 to 8 below is used. The coating films of Examples 3-2 to 3-24 and Comparative Examples 3_1 to 3-6 were formed.
なお、 塗装法としてカチオン電着塗装 (E D) を採用する場合は 電着浴の浴温を 1 5〜 3 5 °C, 負荷電圧を 1 0 0〜 4 0 0 Vとし、 膜厚が 4 0 / mになる様に被塗物と電極との間で通電してカチオン 電着塗装を行った。 電着塗装後、 余分に付着した電着塗料を工業用 水で水洗し、 塗装物表面に電着塗料が残らない様にした。  When cation electrodeposition coating (ED) is adopted as the coating method, the bath temperature of the electrodeposition bath is 15 to 35 ° C, the load voltage is 100 to 400 V, and the film thickness is 40 / m was applied between the object to be coated and the electrode to perform cationic electrodeposition coating. After electrodeposition coating, excess electrodeposition paint was washed with industrial water to prevent the electrodeposition paint from remaining on the surface of the coating.
実施例 3 — 1〜 3— 2 4、 および比較例 3 — 1〜 3 — 6で形成さ れた各塗膜の構成と塗膜性能を、 表 6〜 8 にまとめて示す。 尚、 表 6〜 8 において、 「 2 C 1 B」 は 2 コート 1ベーク、 「 3 C 2 B」 は 3 コート 2ベーク、 「 3 C 3 B」 は 3 コート 3ベーク、 「 4 C 2 B」 は 4コート 2ベーク、 「4 C 4 B」 は 4コート 4ベークをそれ ぞれ意味し、 また、 素材 Aは 「燐酸亜鉛処理鋼板」 、 素材 Bは 「溶 融亜鉛メツキ鋼板」 、 素材 Cは 「燐酸処理アルミニウム板」 を表す 塗装方法として示した 「 S P」 はスプレー塗装、 「E D」 は電着塗 装を意味する。 Tables 6 to 8 collectively show the configurations and coating film performances of the coating films formed in Example 3-1 to 3-24 and Comparative Example 3-1 to 3-6. In Tables 6 to 8, “2C1B” means 2 coats and 1 bake, “3C2B” means 3 coats and 2bake, “3C3B” means 3 coats and 3bake, and “4C2B” Means 4 coats 2 bake, 4 C 4 B means 4 coats 4 bake, and material A is zinc phosphate treated steel sheet, material B is molten zinc plated steel sheet, and material C is material “SP” means spray painting, and “ED” means electrodeposition coating, which is used as a painting method to represent “phosphoric aluminum plate”.
表 6 Table 6
実 施 列  Implementation
3-1 3-2 3-3 3-4 3-5 3-6 3-7 3-8 3-9 3-10 3-1 3-2 3-3 3-4 3-5 3-6 3-7 3-8 3-9 3-10
A A A A A A A A A A A A A A A A A A A A A
塗料種 4 4 4 4 3 4 4 4 3 4 塗装方法 SP SP SP SP ED SP SP SP ED SP 乾燥膜厚(ju m) 40 40 40 40 40 40 40 40 40 40 下塗り塗料  Paint type 4 4 4 4 3 4 4 4 3 4 Painting method SP SP SP SP ED SP SP SP ED SP Dry film thickness (jum) 40 40 40 40 40 40 40 40 40 40 Undercoat paint
乾燥 (。C、10分) 20 20 20 20 焼付け条件 180 180 180 180 180 180 (°C、 20分)  Drying (.C, 10 minutes) 20 20 20 20 Baking conditions 180 180 180 180 180 180 (° C, 20 minutes)
塗料種 1 1  Paint type 1 1
塗装方法 SP SP  Painting method SP SP
中塗り塗料 乾燥膜) 1( m) 80 80  Intermediate coating (dry film) 1 (m) 80 80
¾燥 (°C、10分)  ¾ drying (° C, 10 minutes)
焼付け 180 180  Baking 180 180
• 塗料種 i V Vi vi 6 5 5 塗装方法 SP SP SP SP SP SP SP 着色上塗 y塗料 乾燥膜厚 ( / m) 80 80 80 80 40 40 40  • Paint type i V Vi vi 6 5 5 Coating method SP SP SP SP SP SP SP SP Colored top coat y Paint dry film thickness (/ m) 80 80 80 80 40 40 40
乾燥 (°C> 10分)  Drying (° C> 10 minutes)
焼付け 80 180 180 80 180 180 180 塗料種 iii 5 iii 塗装方法 SP SP SP 着色ベース塗料 乾燥膜厚( < m) - 80 40 80 乾燥 (°C、10分) 20  Baking 80 180 180 80 180 180 180 Paint type iii 5 iii Painting method SP SP SP Colored base paint Dry film thickness (<m)-80 40 80 Dry (° C, 10 minutes) 20
焼付け 180 180 塗料種 iv 8 8 塗装方法 SP SP SP 上塗リクリヤー塗料 乾燥膜厚 ( i m) 80 80 80 乾燥 (°C、10分)  Baking 180 180 Coating type iv 8 8 Coating method SP SP SP Top-coat clear coating Dry film thickness (im) 80 80 80 Drying (° C, 10 minutes)
焼付け 140 180 180 複層膜数 2 2 2 3 2 3 4 2 2 3 下塗り a a a a a a a a a a 塗装工程膜 中塗り a a  Baking 140 180 180 Number of layers 2 2 2 3 2 3 4 2 2 3 Undercoat a a a a a a a a a a a
膜 a:発明品使用 着色上塗リ b b b b a a a Membrane a: Use of invention product Colored top coat b b b b a a a
b :従来品使用  b: Conventional product used
成 着色ベース b a b クリヤー b a a 焼付け工程 2G2B 2G1 B 2C2B 2G2B 2C2B 3C3B 4G3B 2C1 B 2C2B 3C2B Coloring base b a b Clear b a a Baking process 2G2B 2G1 B 2C2B 2G2B 2C2B 3C3B 4G3B 2C1 B 2C2B 3C2B
5 5 5 5 5 5 5 5 5 5 垂れ性 5 5 5 5 5 5 5 5 5 5 ヮキ性 5 5 5 5 5 5 5 5 5 5 平滑性 5 5 5 5 5 5 5 5 5 5 耐水性 5 5 5 5 5 5 5 5 5 5 表 7 5 5 5 5 5 5 5 5 5 5 Sagging 5 5 5 5 5 5 5 5 5 5 Paint 5 5 5 5 5 5 5 5 5 5 Smoothness 5 5 5 5 5 5 5 5 5 5 Water resistance 5 5 5 5 5 5 5 5 5 5 Table 7
実 施 例  Example
3-1 1 3-12 3-13 3-14 3-15 3-16 3-17 3-18 3-19 3-20 3-1 1 3-12 3-13 3-14 3-15 3-16 3-17 3-18 3-19 3-20
A B C A A A A A A A A B C A A A A A A A
塗料種 4 4 4 2 ii ii ii ii ii ii 塗装方法 SP SP SP SP ED ED ED ED ED ED 乾燥膜厚(/i m) 40 40 40 40 40 40 40 40 40 40 下塗り塗料  Paint type 4 4 4 2 ii ii ii ii ii ii Paint method SP SP SP SP ED ED ED ED ED ED Dry film thickness (/ im) 40 40 40 40 40 40 40 40 40 40 Undercoat paint
乾燥 (。C、10分) 20 20 焼付け条件 180 180 180 1 80 180 180 180 (°C、 20分)  Drying (.C, 10 minutes) 20 20 Baking conditions 180 180 180 1 80 180 180 180 (° C, 20 minutes)
塗料種 1 塗装方法 SP 中塗り塗料 乾燥膜厚 m) 80  Paint type 1 Coating method SP Intermediate paint Dry film thickness m) 80
乾燥 、 10分)  Drying, 10 minutes)
焼付け 180 塗料種 5 5 i 6 6  Baking 180 Paint type 5 5 i 6 6
塗装方法 SP SP SP SP SP  Painting method SP SP SP SP SP
着色上塗 y塗料 乾燥膜厚 ( m) 40 40 80 40 40 Colored top coat y paint Dry film thickness (m) 40 40 80 40 40
乾燥 (。G、10分)  Drying (.G, 10 minutes)
焼付け . 180 180 80 180 180  Baking .180 180 80 180 180
塗料種 5 5 5 5 iii 塗装方法 SP SP SP SP SP 着色ベース塗料 乾燥膜厚( m) 40 40 40 40 80 乾燥 ( 、10分) 20 20 20 20 焼付け 180  Paint type 5 5 5 5 iii Painting method SP SP SP SP SP Colored base paint Dry film thickness (m) 40 40 40 40 80 Dry (, 10 minutes) 20 20 20 20 Bake 180
難 8 8 8 8 8 塗装方法 SP SP SP SP SP 上塗り  Difficult 8 8 8 8 8 Painting method SP SP SP SP SP Top coat
乾燥膜厚 (ju m) 80 80 80 80 80 クリヤー塗料  Dry film thickness (ju m) 80 80 80 80 80 Clear paint
乾燥 ( 、10分)  Drying (, 10 minutes)
焼付け 180 180 180 180 180 複層膜数 3 2 2 2 2 2 3 3 4 3 下塗り a a a a b b b b b b 塗装工程膜 中塗り a 膜 a :発明品使用  Baking 180 180 180 180 180 Number of multilayer films 3 2 2 2 2 2 3 3 4 3 Undercoating a a a a a b b b b b b b Coating process Intermediate coating a Film a: Use of invention
着色上塗り a  Colored topcoat a
構 b :従来品使 a a b a Structure b: Conventional product a a b a
成 用 着色べ一ス a a a a b クリヤー a a a a a 焼付け工程 3C2B 2G2B 2G2B 2C2B 2C2B 2C1 B 3C2B 3C3B 4C2B 3C2B ί乍業性 5 5 5 5 5 5 5 5 5 5 垂れ性 5 5 5 5 5 5 5 5 5 5 結 Application Coloring base a a a a b Clear a a a a a Baking process 3C2B 2G2B 2G2B 2C2B 2C2B 2C1 B 3C2B 3C3B 4C2B 3C2B
ヮキ性 5 5 5 5 5 5 5 5 5 5 果  5 5 5 5 5 5 5 5 5 5 5 Fruit
平滑性 5 5 5 5 5 5 5 5 5 5 耐水性 5 5 5 5 5 5 5 5 5 5 表 8 Smoothness 5 5 5 5 5 5 5 5 5 5 Water resistance 5 5 5 5 5 5 5 5 5 5 Table 8
実 施 例 比 較 例  Example Example Comparative Example
3-21 3-22 3-23 3-24 3-1 3-2 3-3 3-4 3-5 3-6 3-21 3-22 3-23 3-24 3-1 3-2 3-3 3-4 3-5 3-6
A A A A A A A A A A A A A A A A A A A A A
塗料種 ii ii ii ii ii 10 ii ii ii ii 塗装方法 ED ED ED ED ED ED ED ED ED ED 乾燥膜厚( i m) 40 40 40 40 40 40 40 40 40 40 下塗り塗料  Paint type ii ii ii ii ii 10 10 ii ii ii ii Coating method ED ED ED ED ED ED ED ED ED ED Dry film thickness (im) 40 40 40 40 40 40 40 40 40 40 40 Undercoat paint
乾燥 (。C、10分) 20 20 焼付け条件 180 180 180 180 180 180 180 180 ( 、 20分)  Drying (.C, 10 minutes) 20 20 Baking conditions 180 180 180 180 180 180 180 180 (, 20 minutes)
塗料種 vii 1 vii vii vii 塗装方法 SP SP SP SP SP 中塗り塗料 乾燥膜厚 (jU m) 80 80 80 80 80 乾燥 (°C、10分)  Paint type vii 1 vii vii vii Coating method SP SP SP SP SP Intermediate paint Dry film thickness (jU m) 80 80 80 80 80 Dry (° C, 10 minutes)
焼付け 180 180 180 180 180 塗料種 6 11 11  Baking 180 180 180 180 180 Paint type 6 11 11
塗装方法 SP SP SP  Painting method SP SP SP
着色上塗り塗料 乾燥膜厚 ( m) 40 80 80  Colored top coat Dry film thickness (m) 40 80 80
乾燥 (°C、10分)  Drying (° C, 10 minutes)
焼付け 180 180 180  Baking 180 180 180
塗料種 iii iii Hi 9 9 9 9 塗装方法 SP SP SP SP SP SP SP 着色ベース塗料 乾燥膜厚( m) 80 80 80 80 80 80 80 乾燥 (°C、10分) 20 . 20  Paint type iii iii Hi 9 9 9 9 Coating method SP SP SP SP SP SP SP SP Colored base paint Dry film thickness (m) 80 80 80 80 80 80 80 Dry (° C, 10 minutes) 20.20
焼付け 180 180 180 180 180 塗料種 8 8 IV IV iv iv 塗装方法 SP SP SP SP SP SP 上塗 yクリヤー塗料乾燥膜厚 ( m) 80 80 80 80 80 80 乾燥 ( 、10分)  Baking 180 180 180 180 180 Coating type 8 8 IV IV iv iv Coating method SP SP SP SP SP SP Top coat y Clear coating dry film thickness (m) 80 80 80 80 80 80 Drying (, 10 minutes)
焼付け 180 180 140 140 140 140 複層膜数 3 3 3 4 2 2 3 3 4 下塗り b b b b b b b b b b 中塗り b a b b b 膜 塗装工程膜  Baking 180 180 140 140 140 140 Number of layers 3 3 3 4 2 2 3 3 4 Undercoat b b b b b b b b b b Intercoat b a b b b Coating coating
a:発明品使用 着色上塗り a b b  a: Use of invention product Colored top coat a b b
構 b:従来品使用 Structure b: Conventional product used
成 着色ベース b b b b b b. b クリヤー a a b b b b 焼付け工程 3C3B 3C3B 3G3B 4C4B 2C1 B 2C2B 3C2B 3C3B 4C2B 4G4B 乍業性 5 5 5 5 3 4 3 5 3 ' 垂れ性 5 5 5 5 3 3 3 3 3 4 ヮキ性 5 5 5 5 3 3 3 4 3 4 果 Colored base bbbbb b.b clear aabbbb baking process 5 5 5 5 3 3 3 4 3 4 Fruit
平滑性 5 5 5 5 3 3 3 5 3 4 耐水性 5 5 5 5 3 3 4 5 4 5 実施例 4 [調色方法] Smoothness 5 5 5 5 3 3 3 5 3 4 Water resistance 5 5 5 5 3 3 4 5 4 5 Example 4 [Color matching method]
A)ベース塗料の調製  A) Preparation of base paint
A- 1)粗粉碎物の製造  A- 1) Manufacture of coarse powder
原料を下記配合 1 に示す比率で使用し、 高速ミキサーで均一に混 合した後、 溶融押出機を用いて溶融混練すると共に、 厚さ約 l mm のシート状に押出して冷却固化させる。 このシート状物を破碎機に 通して粗粉砕した後、 篩目が 1. 0 mmのフィル夕一に通して粗粉 砕物を得る。  The raw materials are used in the ratio shown in Formulation 1 below, mixed uniformly with a high-speed mixer, melt-kneaded using a melt extruder, and extruded into a sheet with a thickness of about 1 mm to be cooled and solidified. This sheet material is coarsely crushed through a crusher, and then passed through a filter having a sieve of 1.0 mm to obtain a coarsely crushed material.
配合 1 :  Formula 1:
「ファインディ ック M— 8 0 2 0」 5 4 9 (部) “FINEDIC M—800 200” 5 4 9 (parts)
「クレラン V P L S 2 2 5 6」 8 2 `` Cleran V P L S 2 2 5 6 '' 8 2
ベンゾィン 0 4  Benzoin 0 4
「 A E R 6 0 0 2」 3 0  `` A E R 6 0 0 2 '' 3 0
「ァクロナール 4 F」 0 5  `` Acronal 4 F '' 0 5
「酸化チタン C R 9 7」 3 2 0  `` Titanium oxide C R 9 7 '' 3 2 0
「Hostaperm Yellow H4G N」 1 0  “Hostaperm Yellow H4G N” 1 0
A- 2)ベース塗料の製造  A-2) Production of base paint
下記配合 2 に示す比率で用いた原料配合物 1 0 k gを、 ディスパ —によって撹拌しながら混合し、 この混合物を冷却機構内蔵型の湿 式循環型ピーズミル [分散メディア ; 直径 1. 0 mmのニツカ ト一 社製ジルコ二アポ一ル 「 Y T Z」 を、 ベッセル容積に対して 8 0 % 装入したもの] に連結した循環槽に投入し、 アジテーターディスク を周速 1 0 mZ秒の速度で回転させながら、 循環流量 2 リ ッ トル Z 分で 6 0分間循環させることによって微粉砕処理を行う。 次いで、 篩目 5 0 mのフィル夕一に通して濾過することにより、 ベ一ス色 の水分散型粉体塗料 (ベース塗料 : A1) を得る。 得られたベース塗 料 (A1) の性状 · 特性を表 9 に示す。  10 kg of the raw material mixture used in the ratio shown in the following formula 2 is mixed with a disperser while stirring, and this mixture is a wet circulation type peas mill with a built-in cooling mechanism. [Dispersion media: Niska with a diameter of 1.0 mm The Zirconia applicator “YTZ” manufactured by Toshiba Corporation was charged to a circulation tank connected to a vessel with 80% of the vessel volume], and the agitator disc was rotated at a peripheral speed of 10 mZ seconds. While circulating at a circulating flow rate of 2 liters Z minutes for 60 minutes, the pulverization process is performed. Then, the mixture is filtered through a 50-m sieve filter to obtain a base color water-dispersible powder coating material (base coating material: A1). Table 9 shows the properties and characteristics of the obtained base coating (A1).
配合 2 :  Formula 2:
粗粉碎物(注) 5 0. 0 (部) Coarse powder (Note) 50.0 (parts)
「サ一フイ ノ一ル 4 4 0」 0. 2 「Disperbyk— 1 9 0 J 0 2 「アデ力ノール UH— 5 4 0」 0 4 「ラスミン MK— 9」 ( 1 0 %水溶液) 0 2 ィオン交換水 4 9 0“Saving number 4 4 0” 0.2 “Disperbyk— 1900 J02” “Adder power UH—540” 0 4 “Rasmin MK—9” (10% aqueous solution) 0 2 Dion exchange water 4 9 0
(注)上記配合 1 によって得た粗粉碎物 表 9
Figure imgf000065_0001
(Note) Coarse powder obtained by the above formulation 1
Figure imgf000065_0001
B)調色用塗料の調製 B) Preparation of paint for toning
B- 1)調色用ホワイ ト塗料の調製  B-1) Preparation of white paint for toning
下記配合 3 を採用した以外は前記と同様 して粗粉砕物を得る。 配合 3 :  A coarsely pulverized product is obtained in the same manner as above except that the following formulation 3 is used. Formula 3:
「ファイ ンディ ック M— 8 0 2 0 J 5 4 9 (部) “Findick M—820 0 J 54 9 (parts)
「クレラン V P L S 2 2 5 6」 8 2 `` Cleran V P L S 2 2 5 6 '' 8 2
ベンゾィン 0 4  Benzoin 0 4
「 A E R 6 0 0 2」 3 0  `` A E R 6 0 0 2 '' 3 0
「ァクロナール 4 F」 0 5  `` Acronal 4 F '' 0 5
「酸化チタン C R 9 7」 3 3 0  `` Titanium oxide C R 9 7 '' 3 3 0
次いで、 下記配合 4に示す比率で配合した原料配合物 1 0 k gを デイスパーによって撹拌しながら混合し、 この混合物を冷却機構内 蔵型の湿式循環型ビーズミル [分散メディ ァ ; 直径 1 . O mmの二 ッカ ト一社製ジルコニァポール 「Y T Z」 ] を、 ベッセル容積に対 して 8 0 %装入したもの] に連結した循環槽に投入し、 アジテ一夕 一ディスクを周速 1 0 m/秒の速度で回転させながら、 循環流量 2 リ ッ トル Z分で 1 0 0分間循環させることによって微粉碎処理を行 う。 次いで、 篩目 5 Ο ΠΙのフィルタ一を通して濾過する ことによ り、 調色用ホワイ ト塗料(B1)を得る。 得られた調色用ホワイ ト塗料 (Bl)の性状 · 特性を表 1 0 に示す。 Next, 10 kg of the raw material mixture blended in the ratio shown in the following formulation 4 was mixed with a disperser while stirring, and the mixture was cooled with a wet circulation type bead mill with a built-in cooling mechanism [dispersion media; 1.0 mm in diameter. Zirconia pole "YTZ" manufactured by Nikkatsu Co., Ltd.] is charged into a circulation tank connected to a vessel with 80% of the vessel volume], and a disk of Agite is set at a peripheral speed of 10 m. The powder is crushed by circulating at a circulation flow rate of 2 liters Z for 100 minutes while rotating at a speed of 1 / sec. Subsequently, the mixture is filtered through a filter having a sieve of 5 mm to obtain a toning white paint (B1). Obtained white paint for toning Table 10 shows the properties and characteristics of (Bl).
配合 4 ; '  Formula 4;
粗粉碎物(注) 3 0. 0 (部) Coarse powder (Note) 30.0 (parts)
「サ一フィ ノール 4 4 0」 0. 2“Safinol 4 4 0” 0.2
「Disperbyk— 1 9 0」 0. 2“Disperbyk—1 9 0” 0.2
「アデ力ノール UH— 5 4 0」 0. 4“Ade Force Knoll UH—5 4 0” 0.4
「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 2 イオン交換水 6 9. 0 "Rasmin MK-9" (10% aqueous solution) 0.2 Deionized water 69.0
(注)上記で得た粗粉碎物  (Note) Coarse powder obtained above
B-2)調色用ブラック塗料の調製 B-2) Preparation of black paint for toning
前記配合 3 における 「酸化チタン C R 9 7 」 に代えて、 「三菱力 一ボンブラック MA— 1 0 0」 (三菱化学社製) を 「フアインディ ック M— 8 0 2 0」 5 4. 9部に対し 0. 8部使用した以外は前記 と同様にして粗粉砕物を得る。 次いで、 上記と同様にして前記配合 4と同じ原料配合でディスパ一 (同前) により混合し、 以下も同様 にして冷却機構内蔵型湿式循環型ビーズミルを用いた微粉碎処理お よび濾過を行う ことにより、 調色用ブラック塗料(B2)を得る。 得ら れた調色法ブラック塗料(B2)の性状 · 特性を表 1 0に示す。  In place of "Titanium oxide CR97" in Formulation 3, "Mitsubishi Rikibon Black MA-100" (manufactured by Mitsubishi Chemical Corporation) was replaced with "Finick M-82002" 54.9 parts. To obtain a coarsely pulverized product in the same manner as above except that 0.8 part was used. Next, in the same manner as described above, the same raw material composition as in the above-mentioned composition 4 is mixed by a disperser (same as above), and thereafter, the fine pulverization treatment and filtration using a wet circulation type bead mill with a built-in cooling mechanism are performed in the same manner. As a result, a toning black paint (B2) is obtained. Table 10 shows the properties and characteristics of the toning black paint (B2) obtained.
B-3)調色用レッ ド塗料の調製 B-3) Preparation of red paint for toning
前記配合 3 にお ける 「酸化チタ ン C R 9' 7 」 に代えて、 「Novoperm Red F3RK70」 (Clariant 社製の C. I. Pigment Red 170) を 「ファイ ンディ ック M— 8 0 2 0」 5 4. 9部に対し 4. 0部使用した以外は、 前記と同様にして粗粉砕物を得、 次いで、 上 記と同様に前記配合 4 と同じ原料配合でデイスパー (同前) により 混合し、 以下も同様にして冷却機構内蔵型湿式循環型ビーズミルを 用いた微粉碎処理および濾過を行う ことにより、 調色用レツ ド塗料. (B3)を得る。 得られた調色用レツ ド塗料(B3)の性状 · 特性を表 1 0 に示す。 B-4)調色用イェロー塗料の調製 "Novoperm Red F3RK70" (CI Pigment Red 170 manufactured by Clariant) was replaced with "Findick M-820 0" in place of "Titanium oxide CR 9'7" in Formulation 3 above. A coarsely pulverized product was obtained in the same manner as described above except that 4.0 parts was used for 9 parts, and then mixed with a disperser (same as above) in the same raw material composition as in the above-mentioned composition 4 in the same manner as above. In the same manner, by performing fine powder treatment and filtration using a wet circulation type bead mill with a built-in cooling mechanism, a toning red paint (B3) is obtained. Table 10 shows the properties and characteristics of the toning red paint (B3). B-4) Preparation of yellow paint for toning
前記配合 3 にお ける 「酸化チタ ン C R 9 7 」 に代えて、 「Hostaperm Yellow H4G Nj ( Clariant 社製の C. I. Pigment Yellow 151) を 「ファイ ンディ ック M— 8 0 2 0」 5 4. 9部に 対し 5. 0部使用した以外は、 前記と同様にして粗粉碎物を得、 次 いで、 上記と同様に前記配合 4 と同じ原料配合でデイスパー (同 前) により混合し、 以下も同様にして冷却機構内蔵型湿式循環型ビ ーズミルを用いた微粉碎処理および濾過を行う ことにより、 調色用 イェロー塗料(B4)を得る。 得られた調色用イェロー塗料(B4)の性 状 · 特性を表 1 0 に示す。  "Hostaperm Yellow H4G Nj (CI Pigment Yellow 151 manufactured by Clariant)" was used instead of "Titanium Oxide CR97" in Formulation 3 above. Parts, except that 5.0 parts was used, to obtain a coarsely crushed material in the same manner as above, and then mixed with the same raw material composition as in the above-mentioned composition 4 using a disperser (the same as above). Then, fine grinding and filtration using a wet circulation type bead mill with a built-in cooling mechanism are performed to obtain a toning yellow paint (B4). Table 10 shows the properties and characteristics of the obtained toning yellow paint (B4).
B-5)調色用ブルー塗料の調製 B-5) Preparation of blue paint for toning
前記配合 3 における 「酸化チタン C R 9 7」 に代えて、 「シァ二 ンブルー 4 9 5 0 」 (大日精化工業社製の C. I. Pigment Blue 15:4) を 「ファインデイ ツク M— 8 0 2 0」 5 4. 9部に対し 4. 0部使用した以外は、 前記と同様にして粗;^砕物を得、 次いで、 上 記と同様に前記配合 4と同じ原料配合でデイスパー (同前) により 混合し、 以下も同様にして冷却機構内蔵型湿式循環型ビーズミルを 用いた微粉碎処理および濾過を行う ことにより、 調色用ブル一塗料 (B5)を得る。 得られた調色用ブルー塗料(B5)の性状 · 特性を表 1 0 に示す。 表 1 0  In place of "Titanium oxide CR97" in Formulation 3, "Cyan Blue 495" (CI Pigment Blue 15: 4 manufactured by Dainichi Seika Kogyo Co., Ltd.) A crude product was obtained in the same manner as described above, except that 4.0 parts was used for 54.9 parts. The mixture is mixed, and thereafter, finely pulverized and filtered using a wet-circulation type bead mill with a built-in cooling mechanism in the same manner to obtain a toning blue paint (B5). Table 10 shows the properties and characteristics of the obtained toning blue paint (B5). Table 10
粒径 10jW m超の 固形分濃度 粘度  Solids concentration of particle size more than 10jW m Viscosity
符号 色調 D50( n m)  Code Color tone D50 (n m)
含有割合(maSS%) ( m a s s % ) (mPa-s) Content ratio (ma SS %) (mass%) (mPa-s)
B1 ホワイト 4.5 0 30.5 3700  B1 White 4.5 0 30.5 3700
B2 ブラック 4.2 0 30.5 3700  B2 Black 4.2 0 30.5 3700
B3 レッド、 4.4 0 30.5 3700  B3 red, 4.4 0 30.5 3700
B4 イエロ一 4.4 0 30.5 3700  B4 Yellow 1 4.4 0 30.5 3700
B5 ブル一 4.3 0 30.5 3700 c)艷調整剤の製造 B5 Bull 1 4.3 0 30.5 3700 c) Manufacture of gloss regulator
下記配合 5に示す比率で各原料を配合し、 デイスパーを用いてデ イスク周速 1 0 mZ秒で混合することにより艷調整剤を製造する。 配合 5 (艷調整剤)  Each raw material is blended in the ratio shown in the following formula 5, and mixed with a disperser at a disk peripheral speed of 10 mZ seconds to produce an gloss adjusting agent. Formula 5 (glossy adjuster)
「A C E MA TT H K 4 6 0 J 1 5. 0 (部) “A C E MA TT H K 46 0 J 15.0 (parts)
「サーフィ ノール 4 4 0」 0. 2 "Surfinol 4 4 0" 0.2
イオン交換水 8 4. 8 比較例  Deionized water 84.8 Comparative example
a - 1)比較べース塗料①の調製  a-1) Preparation of comparative base paint ①
前記配合 1 に示したのと同様の原料配合で粗粉碎物を得、 これを 前記配合 2 と同様の配合比率で使用し、 微粉砕処理のための循環時 間を 3 0分に短縮した以外は前記実施例と同様にして比較ベース塗 料(al)を得た。 該ベース塗料(al)の性状 · 特性を下記表 1 1 に示す a-2)比較べ—ス塗料②の調製  A coarse powdered material was obtained by the same raw material blend as shown in the above-mentioned blend 1, and this was used in the same blend ratio as in the above-mentioned blend 2, except that the circulation time for the fine grinding treatment was reduced to 30 minutes. In the same manner as in the above example, a comparative base coating (al) was obtained. The properties and properties of the base paint (al) are shown in Table 11 below. A-2) Preparation of comparative base paint
刖記配合 1 に示したのと同様の原料配合で粗粉碎物を得、 これを 前記配合 2 と同様の配合比率で使用し、 微粉砕化処理のための循環 時間を 1 2 0分に延長した以外は前記実施例と同様にして比較べ一 ス塗料(a2)を得た。 該比較ベース塗料(a2)の性状 · 特性を下記表 1 1 に示す。  粗 Coarse ground material was obtained with the same raw material composition as shown in Formulation 1, and this was used in the same composition ratio as in Formulation 2 above, and the circulation time for fine pulverization was extended to 120 minutes. A comparative base paint (a2) was obtained in the same manner as in the above example, except for the above. The properties and characteristics of the comparative base paint (a2) are shown in Table 11 below.
Figure imgf000068_0001
b)調色用比較塗料の調製
Figure imgf000068_0001
b) Preparation of comparative paint for toning
b - 1)調色用比較ブラック塗料の調製 前記実施例の「調色用ブラック塗料の調製」において、 微粉碎処理 のための循環を 6 0分に短縮した以外は前記 B- 1)と同様にして、 下記表 1 2 に示す性状 · 特性の調色用ブラック塗料(bl)を得た。 b- 2)調色用ブル一塗料の調製 b-1) Preparation of comparative black paint for toning In "Preparation of black paint for toning" of the above example, the properties and properties shown in Table 12 below were obtained in the same manner as in B-1) except that the circulation for the fine powder was shortened to 60 minutes. To obtain a black paint (bl) for toning. b-2) Preparation of blue paint for toning
前記実施例の「調色用ブルー塗料の調製」において、 微粉砕処理の ための循環を 6 0分に短縮した以外は前記 B-4)と同様にして、 下 L 2 に示す性状 · 特性の調色用ブル一塗料(b2)を得る。 表 1 2  In the “Preparation of blue paint for toning” of the above example, the properties and properties shown in L 2 below were the same as in B-4) except that the circulation for the fine pulverization treatment was shortened to 60 minutes. A toning blue paint (b2) is obtained. Table 1 2
Figure imgf000069_0001
b_3)調色用参考ブラック塗料の調製
Figure imgf000069_0001
b_3) Preparation of reference black paint for toning
下記配合 6 に示す比率で原料を配合し、 高速ミキサ一で均一に混 合した後、 溶融押出機を用いて加熱溶融混練すると共にシート状に 押出し、 冷却固化させることにより、 厚さ約 l mmのシー 1、状物を 得る。 こ のシート状物を破碎機に通して破碎した後、 篩目 1. 0 m mのフィルタ一に通し、 平均粒径が約 0. 5 m mのクリァー粗粉砕 物を得る。  The raw materials are blended in the ratio shown in the following Formulation 6, uniformly mixed by a high-speed mixer, heated and kneaded using a melt extruder, extruded into a sheet shape, and cooled and solidified to obtain a thickness of about lmm. Sea 1, get a thing. After the sheet material is crushed by a crusher, it is passed through a filter having a sieve of 1.0 mm to obtain a coarsely ground clear material having an average particle size of about 0.5 mm.
配合 6  Formula 6
「ファインディ ック M— 8 0 2 0」 5 4 9 (部) 「クレラン V P L S 2 2 5 6」 8 2 ベンゾィン 0 4  “FINEDIC M—800 2 0” 5 4 9 (parts) “Cleran V P L S 2 2 5 6” 8 2 Benzoin 0 4
「A E R 6 0 0 2」 3 0 「ァクロナ一ル 4 F」 ' 0 5 上記で得たク リア一粗粉砕物を使用し、 下記配合 7に示す比率で 用いた原料配合物 1 0 k gをディス.パー (同前) によつて混合し、 この混合物を冷却機構内蔵型の湿式循環型ビーズミル [分散メディ ァ ; 直径 1 . 0 mmのニツカ ト -社製ジルコ二アポ一ル 「 Y T Z (商品名) 」 を、 ベッセル容積に対して 8 0 %装入したもの] に連 結した循環槽に投入し、 アジテーターディスクを周速 1 O mZ秒の 速度で回転させながら、 循環流量 2 リ ッ トルノ分で 6 0分間循環さ せることによって微粉砕処理を行う。 次いで、 篩目 5 0 /z mのフィ ル夕一を通して濾過することにより、 下記表 1 3 に示す性状 · 特性 の調色用参考ブラック塗料(b3)を得る。 “AER 600 2” 30 0 “Acronal 4F” '05 Use the coarsely crushed clear product obtained above, and dissolve 10 kg of the raw material formulation used in the ratio shown in Formulation 7 below. The mixture is mixed by a par (same as above), and this mixture is dispersed in a wet circulation type bead mill with a built-in cooling mechanism. A: A 1.0 mm diameter Nitkat-Zirconia applicator "YTZ (trade name)" was charged at 80% of the vessel volume] into a circulation tank connected to The fine grinding process is performed by circulating the agitator disk at a peripheral speed of 1 OmZ seconds for 60 minutes at a circulation flow rate of 2 liters. Subsequently, the mixture is filtered through a filter having a sieve of 50 / zm to obtain a reference black paint (b3) for toning having properties and characteristics shown in Table 13 below.
配合 7 :  Formula 7:
前記配合 6で得た粗粉碎物 3 0. 0 (部) 「サ一フィ ノール 4 4 0」 0. 2 「アデ力ノール UH— 5 4 0」 0. 4 「Disperbyk— 1 9 0」 0 2 「ラスミン MK— 9」 ( 1 0 %水溶液) 0. 2 イオン交換水 6 9. 0 30.0 (parts) “Safinol 4440” 0.2 “Adekinol UH—540” 0.4 0.4 “Disperbyk—190” 0 2 "Rasmin MK-9" (10% aqueous solution) 0.2 Deionized water 69.0
「三菱カーボンブラック MA— 0 0」 0. 4 b-4)調色用参考ブル一塗料の調 "Mitsubishi Carbon Black MA-0 0" 0.4 b-4) Tone of reference paint for toning
前記調色用参考ブラック塗料の調製において、 前記配合 7 の 「三 菱カーボンブラック MA— 1 0 0」 ( 0. 4部) に代えて 「シァ二 ンブル一 4 9 5 0」 ( 1. 7 % ) を使用した以外は前記と全く同様 にして、 下記表 1 3に示す性状 · 特性の調色用参考ブル一塗料(b4) を調製した。 表 1 3  In the preparation of the reference black paint for toning, in place of "Mitsubishi Carbon Black MA-100" (0.4 parts) in the above-mentioned Formulation 7, "Shimbble 495" (1.7%) ) Was used in the same manner as described above to prepare a reference blue paint (b4) for toning having properties and characteristics shown in Table 13 below. Table 13
Figure imgf000070_0001
上記表 1 3 に示した調色用参考ブラック塗料(b3)および調色用参 考ブル一塗料(b4)は、 前述の如く塗料ベースとなるクリア一樹脂粉 末と着色顔料を粉末状態で混合したもので、 ミク口的には樹脂粉末 と顔料粉末が個別に分散混合したものであり、 着色顔料を樹脂と溶 融混合してから微粉砕し、 樹脂と顔料が一体となった本発明の調色 用塗料とは異なる。
Figure imgf000070_0001
The reference black paint for color matching (b3) and the reference paint for color matching (b4) shown in Table 13 above were used as the paint base as described above. Powder and color pigment are mixed in a powder state.Mikuguchi is a mixture of resin powder and pigment powder separately dispersed and mixed.The color pigment is melt-mixed with the resin, then finely pulverized, and mixed with the resin. This is different from the toning paint of the present invention in which the pigment is integrated.
b-5, 6)調色用ブラック塗料およびブルー塗料 (市販水系顔料分散 液)  b-5, 6) Toning black paint and blue paint (commercially available aqueous pigment dispersion)
下記表 1 4 に示す市販の水系塗料向け顔料分散液を調色用塗料 (b5)、 (b6)として使用した。 これらの顔料分散液は、 極めて微細な 顔料粉末を水系媒体に分散させたものであり、 やはり、 着色顔料を ベース樹脂と溶融混合してから微粉砕し、 樹脂と顔料が一体となつ た本発明の調色用塗料とは異なる。 表 1 4  Commercially available pigment dispersions for aqueous paints shown in Table 14 below were used as toning paints (b5) and (b6). These pigment dispersions are obtained by dispersing an extremely fine pigment powder in an aqueous medium, and the color pigment is melt-mixed with a base resin and then finely pulverized to form the resin and pigment of the present invention. Is different from the toning paint. Table 14
Figure imgf000071_0001
性能評価試験 ;
Figure imgf000071_0001
Performance evaluation test;
上記で得た各べ一ス塗料と調色用塗料を様々の配合比率と組合せ で使用し、 ディスパ一で均一に混合することにより調色して調色塗 料を調製し、 塗装作業性や塗膜性能を調べた。 結果を表 1 5および 表 1 6, 1 7 に示す。 なお、 塗装にはァネス ト岩田社製のスプレー ガン 「W— 1 0 0」 (ノズル口径 1. 3 mm) を使用し、 S P C C 鋼板 (同前) に 3回塗りでスプレー塗装し、 次いで熱風乾燥機に装 入し 1 9 0 °Cで 2 0分間焼付処理してから塗膜性能を評価した。 表 1 5 塗料の調色配合 塗料諸元 .塗料特性 塗膜特性 The base paint and toning paint obtained above are used in various mixing ratios and combinations, and the toning is prepared by uniformly mixing with a disperser to prepare a toning paint. The coating performance was examined. The results are shown in Table 15 and Tables 16 and 17. Spray gun “W-100” (nozzle diameter: 1.3 mm) manufactured by Annest Iwata Co., Ltd. was used for spray painting, and the SPCC steel plate (same before) was spray-painted three times and then hot-air dried. The film was loaded into the machine and baked at 190 ° C for 20 minutes, and then the coating film performance was evaluated. Table 1-5 Toning composition of paint
符号へ'-ス塗料 調色塗料 ぺ' -ス塗料 調色塗料 粒径比 貯蔵 膜厚 色 表 E$fl度 To sign '-paint paint Toning paint ぺ' -paint paint Toning paint Particle size ratio Storage Film thickness Color table E $ fl degree
タレ 光 Sauce light
A1 B1 B2 B3 B4 B5 整剤 粒径 ( m) 粒径 ( ) 安定性 作業性 ( ju m)混じり 平滑性 Ra(ju m)A1 B1 B2 B3 B4 B5 Control agent Particle size (m) Particle size () Stability Workability (jum) Blended Smoothness Ra (jum)
1 100 20 10.5 4.5 2.3 5 5 5 40 5 5 0.04 91 100 20 10.5 4.5 2.3 5 5 5 40 5 5 0.04 9
2 100 20 10.5 4.2 2.5 5 5 5 40 5 5 0.04 92 100 20 10.5 4.2 2.5 5 5 5 40 5 5 0.04 9
3 100 20 10.5 4.4 2.4 5 5 5 40 5 5 0.04 93 100 20 10.5 4.4 2.4 5 5 5 40 5 5 0.04 9
4 100 20 10.5 4.4 2.4 5 5 5 40 5 5 0.04 94 100 20 10.5 4.4 2.4 5 5 5 40 5 5 0.04 9
5 100 20 10.5 4.3 2.4 5 5 5 40 5 5 0.04 95 100 20 10.5 4.3 2.4 5 5 5 40 5 5 0.04 9
6 100 10 10 10 10.5 4.4 2.4 5 5 5 40 5 5 0.05 6 6 100 10 10 10 10.5 4.4 2.4 5 5 5 40 5 5 0.05 6
表 1 6 塗料の調色配合 塗料諸元 Table 16 6 Toning composition of paint
符号 へ' -ス塗料 調色塗料 へ'ース塗料の 調色塗料の  Sign To '-paint Toning paint Tooth paint-Toning paint
粒径比 Particle size ratio
Al al al B2 Bo b 41 bZ b3 b4 bo bo 粒径( m) ¾i径( m)Al al al B2 Bo b 41 bZ b3 b4 bo bo Particle size (m) ¾i size (m)
7 Af\ 7 Af \
4U 10.5 4.2 2.5 4U 10.5 4.2 2.5
8 100 40 1U.0 4.4 2.4 y 100 20 10.5 9.2 1.18 100 40 1U.0 4.4 2.4 y 100 20 10.5 9.2 1.1
10 100 20 10.5 9.3 1.110 100 20 10.5 9.3 1.1
1 1 100 20 17 4.2 4.01 1 100 20 17 4.2 4.0
12 100 20 17 9.2 1.812 100 20 17 9.2 1.8
13 100 20 3.6 4.2 0.913 100 20 3.6 4.2 0.9
14 100 20 3.6 9.2 0.414 100 20 3.6 9.2 0.4
15 100 20 10.5 4.5 2.315 100 20 10.5 4.5 2.3
16 100 20 10.5 4.5 2.316 100 20 10.5 4.5 2.3
17 100 0.4 10.5 17 100 0.4 10.5
18 100 0.9 10.5 18 100 0.9 10.5
表 1 7 Table 17
Figure imgf000074_0001
上記表 1 5は、 本発明で定める好ましい要件を全て満たす実施例 であり、 いずれの例でも、 塗装作業性が良好で且つ塗膜特性 (色混 じりや平滑性) も非常に優れていることが分かる。 なおこれらの例 では、 調色用塗料の配合量を 1 0部または 2 0部に特定した例を示 したが、 実際に調色を行う際には、 目標とするベース塗料の色調に 応じて調色用塗料の配合量が適正に調整されることは当然であり、 また 2種以上の調色用塗料を併用して微妙な色合せを行うことも勿 論可能である。
Figure imgf000074_0001
Table 15 above is an example that satisfies all of the preferable requirements defined in the present invention. In each of the examples, the coating workability is good and the coating film properties (color mixing and smoothness) are also extremely excellent. I understand. In these examples, examples were given in which the blending amount of the toning paint was specified to be 10 parts or 20 parts.However, when actually performing the toning, the toning was performed according to the target color tone of the base paint. It is natural that the blending amount of the toning paint is properly adjusted, and it is of course possible to perform delicate color matching using two or more kinds of toning paints.
これらに対し、 表 1 6 , 1 7 に示した符号 7 , 8は、 ベース塗料 と調色用塗料の粒度構成はいずれも適正であるが、 調色用塗料の配 合量がやや多過ぎる参考例であり、 若干の色混じりが観察される。 また符合 9 , 1 0は、 ベース塗料の粒度構成は適切であるが調色用 塗料の粒度構成が規定要件を外れる比較例であり、 明らかな色混じ りが観察される。 On the other hand, reference numerals 7 and 8 shown in Tables 16 and 17 indicate that the particle size composition of the base paint and the toning paint is both appropriate, but the amount of the toning paint is too large. This is an example, and slight color mixing is observed. Reference numerals 9, 10 are comparative examples in which the particle size composition of the base paint is appropriate but the particle size composition of the toning paint does not satisfy the specified requirements, and clear color mixing is observed.
符号 1 1は、 ベ一ス塗料の平均粒径が粗すぎる比較例、 符号 1 2 は、 ベース塗料と調色用塗料の平均粒径が粗すぎる比較例であり、 何れも明らかに色混じ りが観察される他、 塗膜性能 (平滑性ゃタ レ) が悪い。  Reference numeral 11 is a comparative example in which the average particle size of the base paint is too coarse, and reference numeral 12 is a comparative example in which the average particle size of the base paint and the toning paint is too coarse. Are observed and the coating film performance (smoothness sagging) is poor.
符号 1 3 , 1 4は、 ベース塗料の平均粒径が小さ過ぎる比較例で あり、 調色用塗料の如何を問わず塗装作業性が劣悪で塗装不可能で める。  Reference numerals 13 and 14 are comparative examples in which the average particle size of the base paint is too small, and the paint workability is poor irrespective of the toning paint, making it impossible to paint.
符号 1 5, 1 6および符号 1 7 , 1 8は、 粒度構成の適切なベー ス塗料に対して、 調色用塗料としてクリァ一樹脂粉末と微細な顔料 粉末の混合分散液を使用した例であり、 ベース塗料の粒度構成が適 切であることから塗装作業性、 塗膜の平滑性ゃタレは良好であるが 超微粒子状の顔料粉末が単独で存在することにより、 仕上り塗膜面 が顔料粉末による色浮き状態となり、 光沢も低下する。 また、 貯蔵 中に顔料成分とベース塗料が相分離を生じる。  Reference numerals 15 and 16 and reference numerals 17 and 18 are examples in which a mixed dispersion of clear resin powder and fine pigment powder was used as a toning coating for a base coating with an appropriate particle size composition. Yes, the workability of coating and the smoothness of the coating film are good due to the appropriate particle size composition of the base paint, but the finished coating film surface is pigmented by the presence of ultrafine pigment powder alone. The color is floated by the powder, and the gloss is reduced. During storage, the pigment component and the base paint undergo phase separation.
産業上の利用可能性 本発明は、 以上の様に構成されており、 以下に示す多く に利点を 享受できる。 INDUSTRIAL APPLICABILITY The present invention is configured as described above, and can enjoy many advantages described below.
( 1 )水分散型粉体塗料における粉体の平均粒径 (D 5 0 ) や粒度 分布、 更には固形分濃度を特定することによって、 塗料としての分 離安定性やスプレーガンを用いた塗装作業性、 廃液処理などの問題 を生じることなく、 表面がきめ細かで凹凸が少なく優れた塗膜外観 を与える水分散型粉体塗料を提供できる。  (1) By specifying the average particle size (D50), particle size distribution, and solid content of the powder in the water-dispersed powder coating, the separation stability as a coating and coating using a spray gun It is possible to provide a water-dispersed powder coating material that has a fine surface, has little unevenness, and provides an excellent coating appearance without causing problems such as workability and waste liquid treatment.
(2)本発明で好ましく使用されるスチレン · マレイ ン酸共重合体 のアルキレンォキサイ ド付加物は、 飽和炭化水素結合で構成されて いるので、 薬品、 熱、 光などの外的因子に対して主鎖が切断される 恐れがなく、 耐水性、 耐候性などに優れた塗膜を与える。 (2) The alkylene oxide adduct of the styrene / maleic acid copolymer preferably used in the present invention is composed of a saturated hydrocarbon bond. As a result, there is no danger of the main chain being cut by external factors such as chemicals, heat, and light, and a coating film with excellent water resistance and weather resistance is provided.
しかもマレイン酸に由来する力ルポキシル基は極性が高いので、 プラスチック類、 金属類、 無機材類などを含めて殆どの被塗物に対 する付着性に優れている。 またアルキレンオキサイ ド付加物は、 ス チレン · マレイン酸共重合体主鎖から離れた親水性の側鎖として分 子中に存在するので、 主鎖との立体障害などが少なく親水基として の機能が十分に発揮される。 そのため、 例えば本発明で定める塗料 を被塗物に塗装した直後の塗膜は、 塗料粒子の表面が該親水基によ つて保護され焼付工程でも粒子表面で急激な水の蒸発が起こらない ので、 ヮキゃピンホールなどの塗膜欠陥を生じ難い。  In addition, since the olepoxyl group derived from maleic acid has a high polarity, it has excellent adhesion to almost any object to be coated, including plastics, metals, and inorganic materials. In addition, the alkylene oxide adduct is present in the molecule as a hydrophilic side chain away from the main chain of the styrene / maleic acid copolymer, so it has little steric hindrance to the main chain and functions as a hydrophilic group. Is fully demonstrated. Therefore, for example, in a coating film immediately after applying the coating material specified in the present invention to the object to be coated, the surface of the coating particles is protected by the hydrophilic group, and rapid water evaporation does not occur on the particle surface even in the baking process. Less coating film defects such as pinholes.
更に、 本発明で好ましく使用するスチレン · マレイン酸共重合体 のアルキレンォキサイ ド付加物は、 疎水性と親水性とのバランスが よいので、 安定して優れた塗膜性能を発揮する。  Furthermore, the alkylene oxide adduct of a styrene / maleic acid copolymer preferably used in the present invention has a good balance between hydrophobicity and hydrophilicity, and thus exhibits excellent coating performance stably.
( 3 )本発明の製法によれば、 塗料用樹脂又はこれと顔料を溶融混 合し、 好ましくはシート状に加工してから粗粉砕した後、 循環型ビ ーズミルを用いて微粉砕することによって、 上記平均粒径 (D 5 0 ) や粒度分布の要件を満たす水分散型粉体塗料を容易に製造でき る。  (3) According to the production method of the present invention, a coating resin or a pigment and a pigment are melt-mixed, preferably processed into a sheet, coarsely pulverized, and then finely pulverized using a circulation type bead mill. A water-dispersed powder coating material satisfying the requirements of the above average particle size (D50) and particle size distribution can be easily produced.
( 4 )本発明の調色方法によれば、 水分散型粉体塗料における樹脂 粉体の平均粒径と粒度分布、 更には固形分濃度の特定されたベース 塗料に使用すると共に、 特に固形成分の粒度構成が特定された水分 散型の調色用粉体塗料を使用することによって、 水分散型粉体塗料 では困難であるベース塗料の微妙な色合せや塗装現楊などでの調色 を簡単に実施できる。  (4) According to the toning method of the present invention, the average particle size and the particle size distribution of the resin powder in the water-dispersed powder coating material, and further, the solid component concentration is used for the specified base coating material, By using a water-dispersed toning powder coating with a specified particle size composition, it is possible to adjust the delicate color matching of the base coating and toning with a paint sprayer, which is difficult with a water-dispersed powder coating. Easy to implement.

Claims

請求の範囲 The scope of the claims
1 . 塗料用樹脂を含み、 平均粒径 (D 5 0 ) が 1〜 3 0 mで ある粉体が水に分散されたものであることを特徴とする水分散型粉 体塗料。 1. A water-dispersed powder coating comprising a resin for coating and having an average particle diameter (D50) of 1 to 30 m dispersed in water.
2 . 前記粉体の平均粒径 (D 5 0 ) が 5〜 1 5 mである請求 項 1 に記載の水分散型粉体塗料。 2. The water-dispersed powder coating according to claim 1, wherein the powder has an average particle size (D50) of 5 to 15 m.
3 . 前記粉体は、 粒径が 5 0 m以上である粒子の占める比率が 1 0 %質量以下であり、 且つ粒径が 0 . 5 /z m以下である粒子の占 める比率が 1 0質量%以下である請求項 1 または 2 に記載の水分散 型粉体塗料。 3. In the powder, the ratio of particles having a particle size of 50 m or more is 10% by mass or less, and the ratio of particles having a particle size of 0.5 / zm or less is 10% or less. The water-dispersed powder coating according to claim 1, which is not more than mass%.
4 . 前記粉体は、 2 0 /2 m以上の粒子の占める比率が 1 0質 量%以下、 3 m以下の粒子の占める比率が 1 0質量%以下である 請求項 3 に記載の水分散型粉体塗料。 4. The aqueous dispersion according to claim 3, wherein in the powder, a ratio of particles occupying 20/2 m or more is 10% by mass or less, and a ratio of particles occupying 3 m or less is 10% by mass or less. Mold powder paint.
5 . 前記塗料用樹脂を含む粉体が、 スチレン · マレイン酸共重 合体のアルキレンォキサイ ド付加物と界面活性剤の共存下に、 水に 分散されたものである請求項 1 〜 4のいずれかに記載の水分散型粉 体塗料。 5. The powder according to any one of claims 1 to 4, wherein the powder containing the coating resin is dispersed in water in the presence of an alkylene oxide adduct of a styrene / maleic acid copolymer and a surfactant. A water-dispersible powder paint according to the above item.
6 . 前記スチレン · マレイン酸共重合体のアルキレンォキサイ ド付加物が、 エチレンオキサイ ドとプロピレンオキサイ ドとの共付 加物である請求項 5に記載の水分散型粉体塗料。 6. The water-dispersed powder coating composition according to claim 5, wherein the alkylene oxide adduct of the styrene / maleic acid copolymer is a co-addition product of ethylene oxide and propylene oxide.
7 . 前記界面活性剤が非イオン系界面活性剤である請求項 5ま たは 6に記載の水分散型粉体塗料。 7. The water-dispersed powder coating according to claim 5, wherein the surfactant is a nonionic surfactant.
8- 前記界面活性剤が、 H L B : 4〜 1 3の界面活性剤である 請求項 5〜 7のいずれかに記載の水分散型粉体塗料。 8- The water-dispersed powder coating material according to any one of claims 5 to 7, wherein the surfactant is a surfactant having an HLB of 4 to 13.
9. 前記界面活性剤が、 アルキンジオールのアルキレンォキサ ィ ド付加物からなり、 重量平均分子量が 3 0 0〜 3 0 0 0である請 求項 5〜 8のいずれかに記載の水分散型粉体塗料。 9. The aqueous dispersion according to any one of claims 5 to 8, wherein the surfactant comprises an alkyne diol alkylene oxide adduct, and has a weight average molecular weight of 300 to 300,000. Powder paint.
1 0. 前記アルキンジオールのアルキレンォキサイ ド付加物が テトラメチルデシンジオールのエチレンォキサイ ド付加物である請 求項 9 に記載の水分散型粉体塗料。 10. The water-dispersed powder coating composition according to claim 9, wherein the alkylene oxide adduct of alkyne diol is an ethylene oxide adduct of tetramethyldecine diol.
1 1. 固形分濃度が 3 0〜 6 0質量%である請求項 1〜 1 0の いずれかに記載の水分散型粉体塗料。 11. The water-dispersed powder coating according to any one of claims 1 to 10, wherein the solid content concentration is 30 to 60% by mass.
1 2. 2 3 °Cにおける水分散体の粘度が 1 0 0〜 5 0 0 0 m P a · sである請求項 1〜 1 1 のいずれかに記載の水分散型粉体塗料 The water-dispersed powder coating according to any one of claims 1 to 11, wherein the viscosity of the aqueous dispersion at 12.3 ° C is 100 to 500 mPas.
1 3. 前記粉体のガラス転移温度が 3 0〜 8 0 °Cである請求項 1〜 1 2のいずれかに記載の水分散型粉体塗料。 13. The water-dispersed powder coating according to claim 1, wherein the glass transition temperature of the powder is 30 to 80 ° C.
1 4. 前記塗料用樹脂がエポキシ系樹脂、 ポリエステル系樹脂 アクリル系樹脂よりなる群から選択される少なく とも 1種である請 求項 1〜 1 3のいずれかに記載の水分散型粉体塗料。 14. The water-dispersed powder coating according to any one of claims 1 to 13, wherein the coating resin is at least one selected from the group consisting of an epoxy resin, a polyester resin, and an acrylic resin. .
1 5. 前記粉体が、 塗料用樹脂と共に顔料を含むものである請 求項 1〜 1 4のいずれかに記載の水分散型粉体塗料。 15. The water-dispersed powder coating according to any one of claims 1 to 14, wherein the powder contains a pigment together with a coating resin.
1 6. 水分散型粉体塗料を製造する方法であって、 塗料用樹脂 を含む塗料用原料成分を溶融混合し、 これを冷却してから粗粉碎し た後、 該粗粉砕物を 0. Ί〜 2. 3倍量の水に分散させた状態で循 環型ビーズミルにより処理し、 固形成分の平均粒径 (D 5 0 ) が 5 〜 1 5 u rn, 2 0 m以上の粒子の占める比率が 1 0質量%以下、 3 m以下の粒子の占める比率が 1 0質量%以下となる様に微粉碎 することを特徴とする水分散型粉体塗料の製法。 1 6. A method for producing a water-dispersed powder coating, in which the raw material components for coating, including the resin for coating, are melted and mixed, cooled and then coarsely ground. After that, the coarsely pulverized product is dispersed in 0.3 to 2.3 times the amount of water and treated with a circulating bead mill, and the average particle size (D50) of the solid component is 5 to 15 u. rn, water-dispersed powder coating characterized by being finely ground so that the ratio of particles of 20 m or more occupies 10 mass% or less and the particle of 3 m or less occupies 10 mass% or less. Recipe.
1 7. 塗料用樹脂と顔料を一体として含む粉体が水に分散され た水分散型粉体塗料からなり、 前記粉体の平均粒径 (D 5 0 ) が 5 〜 1 5 mで、 且つ 2 0 m以上の粒子の占める比率が 1 0質量% 以下、 3 m以下の粒子の占める比率が 1 0質量%以下で、 固形分 濃度が 3 0〜 6 0質量%であるベース塗料の色彩及び/又は明度を 微調整する方法であって、 1 7. A water-dispersed powder coating material in which a powder containing a coating resin and a pigment as one body is dispersed in water. The powder has an average particle size (D50) of 5 to 15 m, and The color of the base paint having a particle size of 20 m or more occupying 10% by mass or less, a particle occupying 3 m or less occupying 10% by mass or less, and a solid content concentration of 30 to 60% by mass. And / or a method of fine-tuning the brightness,
前記塗料用樹脂と同一もしくは異種の塗料用樹脂を顔料と一体と して含む粉体が水に分散された水分散型粉体塗料からなり、 該粉体 の平均粒径 (D 5 0 ) が 5 m以下 (但し、 粒径が 1 0 /2 mを超え る粗粒物を実質的に含まない) で、 且つ白、 黒.、 赤、 青または黄色 系の顔料を含む少なく とも 1種の調色用塗料を準備じておき、 前記ベース塗料の明度及び/又は色彩に応じて、 前記調色用塗料 の少なく とも 1種を前記べ一ス塗料に適量配合することによって、 該ベース塗料の明度及び Z又は色彩を微調整することを特徴とする 水分散型粉体塗料の調色方法。  It is composed of a water-dispersible powder coating material in which a powder containing the same or different coating resin as the above-mentioned coating resin and a pigment is integrated with water, and the powder has an average particle diameter (D 50). 5 m or less (substantially free of coarse particles having a particle size of more than 10/2 m) and at least one pigment containing white, black, red, blue or yellow pigments A toning paint is prepared in advance, and at least one of the toning paints is added to the base paint in an appropriate amount according to the lightness and / or color of the base paint. A method for toning a water-dispersed powder coating, which comprises finely adjusting brightness, Z or color.
1 8 . 前記ベース塗料に含まれる粉体の平均粒径 (D 5 0 ) (A)と、 前記調色用塗料に含まれる粉体の平均粒径 (D 5 0 ) (B)と の比(AZB)を 1以上、 5以下とする請求項 1 7 に記載の調色方法。 18. The ratio of the average particle size (D 50) (A) of the powder contained in the base paint to the average particle size (D 50) (B) of the powder contained in the toning paint The method of claim 17, wherein (AZB) is 1 or more and 5 or less.
1 9. 前記ベース塗料に対する調色用塗料の配合量を、 固形分 基準で 0. 1質量%以上、 2 0質量%以下とする請求項 1 7 または 1 8 に記載の調色方法。 19. The toning method according to claim 17, wherein the blending amount of the toning paint with respect to the base paint is 0.1% by mass or more and 20% by mass or less on a solid content basis.
2 0 . 前記調色用塗料を配合する前または後に、 艷調整剤を添 加して艷の調整を行う請求項 1 7〜 1 9のいずれかに記載の調色方 法。 20. The method for toning according to any one of claims 17 to 19, wherein the gloss is adjusted by adding an gloss adjusting agent before or after compounding the toning paint.
PCT/JP2003/004677 2002-04-15 2003-04-14 Water-dispersed powder coating, process for the production thereof, and color matching method WO2003087248A1 (en)

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