CN113801531B - High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof - Google Patents
High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof Download PDFInfo
- Publication number
- CN113801531B CN113801531B CN202111212535.1A CN202111212535A CN113801531B CN 113801531 B CN113801531 B CN 113801531B CN 202111212535 A CN202111212535 A CN 202111212535A CN 113801531 B CN113801531 B CN 113801531B
- Authority
- CN
- China
- Prior art keywords
- agent
- mixed solution
- alkyd resin
- water
- parts
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 78
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 43
- 239000002184 metal Substances 0.000 title claims abstract description 43
- 239000002519 antifouling agent Substances 0.000 title claims abstract description 31
- 238000002360 preparation method Methods 0.000 title claims description 12
- 229920000180 alkyd Polymers 0.000 claims abstract description 54
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 52
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 45
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims abstract description 42
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 36
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 23
- 239000002270 dispersing agent Substances 0.000 claims abstract description 22
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 21
- 238000010276 construction Methods 0.000 claims abstract description 13
- 230000007613 environmental effect Effects 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 7
- 239000011259 mixed solution Substances 0.000 claims description 61
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 48
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 47
- 238000003756 stirring Methods 0.000 claims description 43
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 38
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 37
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 34
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 33
- 238000002156 mixing Methods 0.000 claims description 27
- 238000001816 cooling Methods 0.000 claims description 24
- 239000000080 wetting agent Substances 0.000 claims description 23
- 239000002562 thickening agent Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 21
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 20
- 229960002446 octanoic acid Drugs 0.000 claims description 19
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 claims description 18
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 18
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 17
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 17
- 229910021389 graphene Inorganic materials 0.000 claims description 17
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 17
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 15
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 15
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000008367 deionised water Substances 0.000 claims description 12
- 229910021641 deionized water Inorganic materials 0.000 claims description 12
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 12
- 239000000440 bentonite Substances 0.000 claims description 9
- 229910000278 bentonite Inorganic materials 0.000 claims description 9
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 9
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical group [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 8
- 230000004224 protection Effects 0.000 claims description 8
- 229910017052 cobalt Inorganic materials 0.000 claims description 7
- 239000010941 cobalt Substances 0.000 claims description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 7
- RQINQJTUMGQYOB-UHFFFAOYSA-N 6-methylheptyl dihydrogen phosphate Chemical compound CC(C)CCCCCOP(O)(O)=O RQINQJTUMGQYOB-UHFFFAOYSA-N 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 claims 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 1
- 239000002131 composite material Substances 0.000 claims 1
- 239000004922 lacquer Substances 0.000 claims 1
- 239000003973 paint Substances 0.000 abstract description 21
- 238000000576 coating method Methods 0.000 abstract description 16
- 239000011248 coating agent Substances 0.000 abstract description 12
- 239000000178 monomer Substances 0.000 abstract description 8
- 239000010410 layer Substances 0.000 abstract description 6
- 239000012792 core layer Substances 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 230000002349 favourable effect Effects 0.000 abstract description 3
- 239000011258 core-shell material Substances 0.000 abstract description 2
- 230000009477 glass transition Effects 0.000 abstract description 2
- 230000004048 modification Effects 0.000 abstract description 2
- 238000012986 modification Methods 0.000 abstract description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 239000004408 titanium dioxide Substances 0.000 abstract 1
- 239000004925 Acrylic resin Substances 0.000 description 18
- 229920000178 Acrylic resin Polymers 0.000 description 18
- 239000007788 liquid Substances 0.000 description 11
- 229910019142 PO4 Inorganic materials 0.000 description 8
- 239000010452 phosphate Substances 0.000 description 8
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- -1 phthalate ester Chemical class 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910014314 BYK190 Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- JXASPPWQHFOWPL-UHFFFAOYSA-N Tamarixin Natural products C1=C(O)C(OC)=CC=C1C1=C(OC2C(C(O)C(O)C(CO)O2)O)C(=O)C2=C(O)C=C(O)C=C2O1 JXASPPWQHFOWPL-UHFFFAOYSA-N 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000005028 tinplate Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 229940009868 aluminum magnesium silicate Drugs 0.000 description 1
- WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical group [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/46—Polyesters chemically modified by esterification
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/56—Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds other than from esters thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2237—Oxides; Hydroxides of metals of titanium
- C08K2003/2241—Titanium dioxide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses a high-environmental-protection water-based metal protective paint capable of being constructed outdoors, which comprises the following raw materials: the invention relates to a water-based acrylic modified alkyd resin, a dispersant, nanometer titanium dioxide, a film forming agent, a defoaming agent and the like, wherein acrylic acid and hydroxyethyl acrylate monomers are copolymerized with the alkyd resin, then methyl methacrylate and butyl methacrylate monomers are added for copolymerization modification with the alkyd resin, so that the alkyd resin forms a complex multi-layer core-shell structure, the added acrylic acid and hydroxyethyl acrylate monomers and the alkyd resin copolymer are in a core layer, the methyl methacrylate and butyl methacrylate monomers and the alkyd resin copolymer are in a shell layer, the shell layer is favorable for film formation of a coating, and the core layer structure can improve the glass transition temperature of the coating due to the large polarity of acrylic acid and hydroxyethyl acrylate, so that the metal paint has a low film forming temperature, and the viscosity of the alkyd resin is moderate at a low environmental temperature, and the construction is convenient.
Description
Technical Field
The invention relates to the technical field of coatings, in particular to a high-environmental-protection water-based metal protective paint capable of being constructed outdoors and a preparation method thereof.
Background
The metal is easily affected by illumination, rain wash, cold and hot stimulation and the like after being exposed in the external environment for a long time, is very easy to rust, and affects the service life of metal products. The most effective way to solve this problem is to apply a protective paint to the metal surface. Most of the traditional metallic paints are solvent-based metallic paints, which contain a large amount of organic solvents, and the organic solvents volatilize when in use, thereby causing serious pollution to the environment. In recent years, waterborne coatings have gradually replaced traditional solvent-based coatings, and the yield of solvent-based coatings in many developed countries has exceeded 50% of the total coating yield.
The traditional water-based alkyd resin has the advantages of low price and good molding property, and is widely applied to the preparation of water-based metal paint. However, the conventional alkyd resin contains a large amount of ester groups and is easily decomposed in water, resulting in reduced product performance, reduced viscosity and poor film-forming property. In addition, the coating film has poor weather resistance, is not easy to form a film under high temperature conditions during outdoor construction, and is easy to deteriorate, embrittle and fall off outdoors. In addition, when the temperature is lower (-10 ℃), the viscosity of the alkyd resin is too high, which affects the outdoor spraying construction in some areas. In addition, the existing water-based paint for metal devices or equipment has high requirement on the flatness of the equipment before spraying, and uneven spraying is easy to occur on the convex or concave parts of irregular devices, so that the use of the water-based alkyd resin is limited.
Therefore, the development of the high-adaptability water-based alkyd resin which can be constructed under the severe outdoor conditions of high temperature or low temperature and can be quickly dried to form a film is urgently needed; meanwhile, the paint has excellent adhesive force and uniform dispersity on irregular parts of metal device equipment, and can best play a role in protecting metal by the waterborne alkyd resin.
Disclosure of Invention
In order to solve the problems, the invention aims to provide a metal protective paint which can be constructed outdoors and has high environmental protection and water resistance and a preparation method thereof.
In order to achieve the purpose, the invention is realized by the following technical scheme:
the high-environmental-protection water-based metal protective paint capable of being constructed outdoors comprises the following raw materials in parts by weight: 30-40 parts of water-based acrylic acid modified alkyd resin, 1-2 parts of dispersant, 10-16 parts of nano titanium dioxide, 2-3 parts of film forming agent, 0.3-0.8 part of defoaming agent, 5-10 parts of talcum powder, 0.1-0.5 part of wetting agent, 0.3-0.5 part of thickening agent, 1-2 parts of isooctyl alcohol phosphate, 0.1-0.3 part of flatting agent, 0.2-0.6 part of silane coupling agent, 0.4-0.6 part of drier and 25-35 parts of deionized water;
the dispersant is
Or BYK190;
the film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
The mass ratio of FX 511 to ethylene glycol is 2-5: 5;
the defoaming agent is TEGO-901W or TEGO-810;
the wetting agent is TEGO-245 or TEGO-270 or TEGO-280;
the thickening agent is magnesium aluminum silicate or/and bentonite;
the leveling agent is
NO.77 or POLYFLOW NO.77;
the drier is a ZHV-10 drier or cobalt naphthanate;
the waterborne acrylic modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 180-230 ℃, stirring for reaction for 3-6 hours, carrying out reduced pressure distillation to remove dimethylbenzene, cooling a reaction system to 170-190 ℃, adding maleic anhydride, stirring for reaction for 1-3 hours, cooling to 100-130 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 0.5-1.5 hours, and cooling to 70-90 ℃ to obtain aqueous acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:10 to 15:20 to 23:18 to 22:13 to 15:5 to 9:2 to 5:45 to 60 percent;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:22 to 25:1 to 5:4 to 6:0.5 to 2;
(3) adding the first mixed solution obtained in the step (2) into the waterborne acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 0.5-1 hour at 70-90 ℃, then adding the second mixed solution obtained in the step (2), stirring for 2-3 hours at 70-90 ℃, adjusting the pH value of a reaction system to be 8-9 by using ammonia water, and dispersing for 0.5-1.5 hours at a high speed to obtain a waterborne acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1 to 2:1 to 2;
the mass concentration of the ammonia water is 15-25%.
Preferably, the silane coupling agent is KH-561 or Mp200.
Preferably, the dispersant is
Preferably, the defoaming agent is TEGO-901W.
Preferably, the wetting agent is TEGO-270.
Preferably, the thickening agent is magnesium aluminum silicate and bentonite according to a mass ratio of 2: 1.
Preferably, the leveling agent is
NO.77。
Preferably, the drier is cobalt naphthanate
Preferably, the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:24:4:5:1.5.
preferably, the mass ratio of the caprylic acid to the capric acid to the trimethylolpropane to the phthalic acid to the xylene to the maleic anhydride to the graphene oxide to the ethylene glycol monobutyl ether is 20:12:22:20:14:7:3:50.
the invention also discloses a preparation method of the metal protective paint with high environmental protection and water resistance, which can be used for outdoor construction and comprises the following steps:
uniformly mixing 10-16 parts of nano titanium dioxide, 0.2-0.6 part of silane coupling agent and 25-35 parts of deionized water in parts by weight to obtain a third mixed solution;
30-40 parts of water-based acrylic acid modified alkyd resin, 1-2 parts of a dispersing agent, 2-3 parts of a film forming agent, 0.3-0.8 part of a defoaming agent, 5-10 parts of talcum powder, 0.1-0.5 part of a wetting agent, 0.3-0.5 part of a thickening agent, 1-2 parts of isooctyl alcohol phosphate, 0.1-0.3 part of a leveling agent and 0.4-0.6 part of a drier are stirred and mixed, the third mixed liquid obtained in the step is added into the mixture, the mixture is stirred and mixed uniformly, and the mixture is ground to a fineness of less than 50 microns, so that the metal protective paint which can be constructed outdoors and has high environmental protection water resistance is obtained;
the dispersant is
Or BYK190;
the film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
Of FX 511 and ethylene glycolThe mass ratio is 2-5: 5;
the defoaming agent is TEGO-901W or TEGO-810;
the wetting agent is TEGO-245 or TEGO-270 or TEGO-280;
the thickening agent is magnesium aluminum silicate or/and bentonite;
the leveling agent is
NO.77 or POLYFLOW NO.77;
the drier is a ZHV-10 drier or cobalt naphthanate;
the water-based acrylic acid modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 180-230 ℃, stirring for reaction for 3-6 hours, carrying out reduced pressure distillation to remove dimethylbenzene, cooling a reaction system to 170-190 ℃, adding maleic anhydride, stirring for reaction for 1-3 hours, cooling to 100-130 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 0.5-1.5 hours, and cooling to 70-90 ℃ to obtain aqueous acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20: 10-15: 20 to 23:18 to 22:13 to 15:5 to 9:2 to 5:45 to 60 percent;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:22 to 25:1 to 5:4 to 6:0.5 to 2;
(3) adding the first mixed solution obtained in the step (2) into the waterborne acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 0.5-1 hour at 70-90 ℃, then adding the second mixed solution obtained in the step (2), stirring for 2-3 hours at 70-90 ℃, adjusting the pH value of a reaction system to be 8-9 by using ammonia water, and dispersing for 0.5-1.5 hours at a high speed to obtain a waterborne acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1 to 2: 1-2;
the mass concentration of the ammonia water is 15-25%.
Compared with the prior art, the invention has the following advantages:
the high-environmental-protection water-based metal protective paint capable of being constructed outdoors adopts short-chain fatty acid caprylic acid and capric acid modified water-based alkyd resin, has higher reaction activity due to the short carbon chains of the caprylic acid and the capric acid under the high-temperature condition, and can participate in the esterification reaction of trimethylolpropane. The obtained product contains short fatty chains, on one hand, the short fatty chains and benzene rings have hydrophobicity and are easier to approach in molecules, so that ester groups of phthalate ester and the like can be protected and hydrolysis is prevented, and on the other hand, the introduction of the short fatty chains enables the molecules to have amphipathy and better compatibility with moisture, a film forming agent, a wetting agent, a defoaming agent and the like in the coating, so that the coating system is more uniform, and the coating is more favorable for the adhesion and film formation of the coating on the metal surface.
Acrylic acid and hydroxyethyl acrylate monomers are copolymerized with alkyd resin, and then methyl methacrylate and butyl methacrylate monomers are added to be copolymerized with the alkyd resin for modification, so that the alkyd resin forms a complex multi-layer core-shell structure, the acrylic acid and hydroxyethyl acrylate monomers which are added first and the alkyd resin copolymer are in a core layer, the methyl methacrylate and butyl methacrylate monomers and the alkyd resin copolymer are in a shell layer, the shell layer structure is favorable for film formation of the coating, the core layer structure has higher polarity of acrylic acid and hydroxyethyl acrylate, the structure can improve the glass transition temperature of the coating, and the metal paint is ensured to have low film forming temperature, so that the viscosity of the alkyd resin is moderate at low environmental temperature, and the construction is convenient;
the invention adopts
FX 511 and ethylene glycol are compounded to form a film forming agent, so that the performance of the film can be obviously improved, the film forming temperature is reduced, and the adhesion between the film and metal is firmer;
according to the preparation method, the silane coupling agent is firstly adopted to treat the nano titanium dioxide, so that on one hand, the nano titanium dioxide has excellent ultraviolet resistance and weather resistance and can enable a paint film to be more stable, and on the other hand, the treated nano titanium dioxide can improve the covering power and the adhesive force of the paint film, so that the paint film is easy to form at high and low temperatures, and the paint film has stable properties and cannot be embrittled and fall off.
Detailed Description
The invention aims to provide a high-environmental-protection water-based metal protective paint capable of being constructed outdoors, which is realized by the following technical scheme, and the invention is further described by combining with specific embodiments.
Example 1
The high-environmental-protection water-based metal protective paint capable of being constructed outdoors comprises the following raw materials: 30kg of water-based acrylic acid modified alkyd resin, 1kg of dispersing agent, 10kg of nano titanium dioxide, 2kg of film forming agent, 0.3kg of defoaming agent, 5kg of talcum powder, 0.1kg of wetting agent, 0.3kg of thickening agent, 1kg of isooctyl alcohol phosphate, 0.1kg of flatting agent, 0.2kg of silane coupling agent, 0.4kg of drier and 25kg of deionized water;
the silane coupling agent is Mp200;
the dispersant is
The film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
The mass ratio of FX 511 to ethylene glycol is 2:5;
the defoaming agent is TEGO-901W;
the wetting agent is TEGO-245;
the thickening agent is aluminum magnesium silicate;
the leveling agent is
NO.77；
The drier is a ZHV-10 drier;
the water-based acrylic acid modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 180 ℃, stirring for reaction for 3 hours, carrying out reduced pressure distillation to remove dimethylbenzene, cooling a reaction system to 170 ℃, adding maleic anhydride, stirring for reaction for 1 hour, cooling to 100 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 0.5 hour, and cooling to 70 ℃ to obtain aqueous acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:10:20:18:13:5:2:45, a first step of;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:22:1:4:0.5;
(3) adding the first mixed solution obtained in the step (2) into the waterborne acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 0.5 hour at 70-90 ℃, then adding the second mixed solution obtained in the step (2), stirring for 2 hours at 70-90 ℃, adjusting the pH value of a reaction system to be 8 by using ammonia water, and dispersing at high speed for 0.5 hour to obtain a waterborne acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1:2;
the mass concentration of the ammonia water is 15%.
Embodiment 1 the preparation method of the outdoor-construction-applicable high-environmental-protection water-based metal protective paint comprises the following steps:
uniformly mixing 10kg of nano titanium dioxide, 0.2kg of silane coupling agent and 25kg of deionized water in parts by weight to obtain a third mixed solution;
the preparation method comprises the following steps of mixing 30kg of waterborne acrylic modified alkyd resin, 1kg of dispersing agent, 2kg of film-forming agent, 0.3kg of defoaming agent, 5kg of talcum powder, 0.1kg of wetting agent, 0.3kg of thickening agent, 1kg of isooctyl alcohol phosphate ester, 0.1kg of leveling agent and 0.4kg of drier through stirring, adding the third mixed liquid obtained in the step into the mixture, stirring and mixing uniformly, grinding the mixture until the fineness is smaller than 50 mu m, and obtaining the high-environmental-protection water-based metal protective paint capable of being constructed outdoors.
Example 2
The outdoor-construction high-environmental-protection water-based metal protective paint is composed of the following raw materials: 40kg of water-based acrylic acid modified alkyd resin, 2kg of dispersing agent, 16kg of nano titanium dioxide, 3kg of film forming agent, 0.8kg of defoaming agent, 10kg of talcum powder, 0.5kg of wetting agent, 0.5kg of thickening agent, 2kg of isooctyl alcohol phosphate ester, 0.3kg of flatting agent, 0.6kg of silane coupling agent, 0.6kg of drier and 35kg of deionized water;
the dispersant is BYK190;
the film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
The mass ratio of FX 511 to ethylene glycol is 1:1;
the defoaming agent is TEGO-810;
the wetting agent is TEGO-270;
the thickening agent is bentonite;
the flatting agent is POLYFLOW NO.77;
the drier is cobalt naphthanate;
the silane coupling agent is KH-561;
the water-based acrylic acid modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 230 ℃, stirring for reaction for 6 hours, carrying out reduced pressure distillation to remove dimethylbenzene, cooling a reaction system to 190 ℃, adding maleic anhydride, stirring for reaction for 3 hours, cooling to 130 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 1.5 hours, and cooling to 90 ℃ to obtain aqueous acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:15:23:22:15:9:5:60;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:25:5:6:2;
(3) adding the first mixed solution obtained in the step (2) into the water-based acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 1 hour at the temperature of 80-90 ℃, then adding the second mixed solution obtained in the step (2), stirring for 3 hours at the temperature of 80-90 ℃, adjusting the pH value of a reaction system to be 9 by using ammonia water, and dispersing at a high speed for 1.5 hours to obtain the water-based acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:2:2;
the mass concentration of the ammonia water is 25%.
Embodiment 2 the preparation method of the outdoor-construction-applicable high-environmental-protection water-based metal protective paint includes the following steps:
uniformly mixing 16kg of nano titanium dioxide, 0.6kg of silane coupling agent and 35kg of deionized water in parts by weight to obtain a third mixed solution;
40kg of waterborne acrylic modified alkyd resin, 2kg of dispersing agent, 3kg of film-forming agent, 0.8kg of defoaming agent, 10kg of talcum powder, 0.5kg of wetting agent, 0.5kg of thickening agent, 2kg of isooctanol phosphate ester, 0.3kg of leveling agent and 0.6kg of drier are stirred and mixed, the third mixed liquid obtained in the step is added into the third mixed liquid, the third mixed liquid is stirred and mixed uniformly, and the third mixed liquid is ground until the fineness is smaller than 50 mu m, so that the environment-friendly water-based metal protective paint capable of being constructed outdoors is obtained.
Example 3
The outdoor-construction high-environmental-protection water-based metal protective paint is composed of the following raw materials: 38kg of water-based acrylic acid modified alkyd resin, 1.4kg of dispersing agent, 12kg of nano titanium dioxide, 2.2kg of film forming agent, 0.4kg of defoaming agent, 6kg of talcum powder, 0.2kg of wetting agent, 0.4kg of thickening agent, 1.4kg of isooctyl alcohol phosphate, 0.15kg of flatting agent, 0.3kg of silane coupling agent, 0.45kg of drier and 32kg of deionized water;
the dispersant is
The film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
The mass ratio of FX 511 to ethylene glycol is 3:5;
the defoaming agent is TEGO-901W;
the wetting agent is TEGO-280;
the thickening agent is prepared from magnesium aluminum silicate and bentonite according to a mass ratio of 1:3 mixing to obtain;
the leveling agent is
NO.77；
The drier is a ZHV-10 drier;
the silane coupling agent is Mp200;
the waterborne acrylic modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 220 ℃, stirring for reaction for 5 hours, distilling under reduced pressure to remove dimethylbenzene, cooling the reaction system to 175 ℃, adding maleic anhydride, stirring for reaction for 1.5 hours, cooling to 110 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 1 hour, and cooling to 85 ℃ to obtain water-based acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:12:21:19:14:8:4:55;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:24:2:4.5:1.5;
(3) adding the first mixed solution obtained in the step (2) into the waterborne acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 45 minutes at 75-85 ℃, then adding the second mixed solution obtained in the step (2), stirring for 2.5 hours at 75-85 ℃, adjusting the pH value of a reaction system to be 8.5 by using ammonia water, and dispersing at high speed for 1.2 hours to obtain a waterborne acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1:2;
the mass concentration of the ammonia water is 18%.
Embodiment 3 provides a method for preparing an outdoor-workable, high-environmental-protection, water-based metal protective paint, comprising the steps of:
uniformly mixing 12kg of nano titanium dioxide, 0.3kg of silane coupling agent and 32kg of deionized water in parts by weight to obtain a third mixed solution;
38kg of water-based acrylic acid modified alkyd resin, 1.4kg of dispersing agent, 2.2kg of film-forming agent, 0.4kg of defoaming agent, 6kg of talcum powder, 0.2kg of wetting agent, 0.4kg of thickening agent, 1.4kg of isooctyl alcohol phosphate, 0.15kg of flatting agent and 0.45kg of drier are stirred and mixed, the third mixed liquid obtained in the step is added into the mixture, the mixture is stirred and mixed uniformly, and the mixture is ground until the fineness is smaller than 50 microns, so that the high-environmental-protection water-based metal protective paint capable of being constructed outdoors is obtained.
Example 4
The outdoor-construction high-environmental-protection water-based metal protective paint is composed of the following raw materials: 35kg of water-based acrylic acid modified alkyd resin, 1.5kg of dispersing agent, 15kg of nano titanium dioxide, 2.5kg of film forming agent, 0.4kg of defoaming agent, 6kg of talcum powder, 0.3kg of wetting agent, 0.4kg of thickening agent, 1.5kg of isooctyl alcohol phosphate ester, 0.2kg of flatting agent, 0.5kg of silane coupling agent, 0.5kg of drier and 30kg of deionized water;
the dispersant is
The film-forming agent is
Mixture of FX 511 and ethylene glycol, wherein
The mass ratio of FX 511 to ethylene glycol is 2-5: 5;
the defoaming agent is TEGO-901W;
the wetting agent is TEGO-270;
the thickening agent is prepared from magnesium aluminum silicate and bentonite according to a mass ratio of 2:1, preparing a composition;
the leveling agent is
NO.77；
The drier is cobalt naphthanate;
the silane coupling agent is KH-561;
the water-based acrylic acid modified alkyd resin is prepared by the following steps:
(1) adding caprylic acid, capric acid, trimethylolpropane and phthalic acid into dimethylbenzene, heating to 200 ℃, stirring for reaction for 4 hours, carrying out reduced pressure distillation to remove dimethylbenzene, cooling a reaction system to 180 ℃, adding maleic anhydride, stirring for reaction for 1-3 hours, cooling to 120 ℃, adding graphene oxide and ethylene glycol monobutyl ether, stirring for 1 hour, and cooling to 80 ℃ to obtain aqueous acrylic resin;
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:12:22:20:14:7:3:50;
(2) uniformly mixing acrylic acid, hydroxyethyl acrylate and azobisisobutyronitrile to obtain a first mixed solution for later use;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:24:4:5:1.5;
(3) adding the first mixed solution obtained in the step (2) into the waterborne acrylic resin obtained in the step (1), controlling the temperature not to exceed 90 ℃ when the addition is finished, stirring for 1 hour at 70-80 ℃, then adding the second mixed solution obtained in the step (2), stirring for 2.5 hours at 80-90 ℃, adjusting the pH value of a reaction system to be 8.5 by using ammonia water, and dispersing at high speed for 1 hour to obtain a waterborne acrylic modified alkyd resin;
wherein the mass ratio of the water-based acrylic resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:2:1;
the mass concentration of the ammonia water is 20%.
Embodiment 4 the preparation method of the outdoor-construction-applicable high-environmental-protection water-based metal protective paint includes the following steps:
uniformly mixing 15kg of nano titanium dioxide, 0.5kg of silane coupling agent and 30kg of deionized water in parts by weight to obtain a third mixed solution;
35kg of waterborne acrylic modified alkyd resin, 1.5kg of dispersing agent, 2.5kg of film-forming agent, 0.4kg of defoaming agent, 6kg of talcum powder, 0.3kg of wetting agent, 0.4kg of thickening agent, 1.5kg of isooctanol phosphate, 0.2kg of flatting agent and 0.5kg of drier are stirred and mixed, the third mixed liquid obtained in the step is added into the third mixed liquid, the third mixed liquid is stirred and mixed uniformly, and the third mixed liquid is ground until the fineness is smaller than 50 mu m, so that the metal protective paint capable of being constructed outdoors and having high environmental protection and water resistance is obtained.
The outdoor construction-applicable high-environmental-protection water-based metal protective paint obtained in the embodiments 1 to 4 of the invention is coated on the surface of standard tinplate to form a paint film with the thickness of 25 to 30 microns, the surface drying time and the actual drying time of the paint film are determined according to GB/T1728-89, the adhesive force grade of the paint film is determined according to GB/T9286-1998, the hardness of the paint film is determined according to GB/T6936-2006, and the weather resistance is determined according to GB/T9276-96. The results are shown in Table 1.
TABLE 1 results of basic Properties of the paint films
The high-environmental-protection water-based metal protective paint which can be constructed outdoors and is obtained in the embodiments 1 to 4 of the invention is coated on the surface of standard tinplate at a low temperature of 0 to 5 ℃ and a high temperature of 50 to 55 ℃ respectively to form a paint film with a thickness of 25 to 30 mu m, the surface drying time and the actual drying time of the paint film are measured by referring to GB/T1728-89 (the test temperature is adjusted to be 0 to 5 ℃ and 50 to 55 ℃), the adhesion level of the paint film is measured by referring to GB/T9286-1998 (the test temperature is adjusted to be 0 to 5 ℃ and 50 to 55 ℃), the hardness of the paint film is measured by referring to GB/T6936-2006 (the test temperature is adjusted to be 0 to 5 ℃ and 50 to 55 ℃), and the results are shown in Table 2.
TABLE 2 Performance test results at Low and high temperatures for outdoor-workable, high environmental water-based metal protective paints
As can be seen from the comparison of the data in tables 1 and 2, the metal protective paint which can be constructed outdoors and has high environmental protection and water resistance has good coating performance under high-temperature and low-temperature environments, has little influence on the hardness and adhesive force of a coating film, is flat in the experimental test, has no flowing, falling and cracking phenomena, and has good service performance.
Claims (5)
1. The utility model provides a but outdoor construction, high environmental protection waterborne metal protection lacquer which characterized in that: the composite material comprises the following raw materials in parts by weight: 30-40 parts of waterborne acrylic modified alkyd resin, 1-2 parts of dispersant, 10-16 parts of nano titanium dioxide, 2-3 parts of film forming agent, 0.3-0.8 part of defoaming agent, 5-10 parts of talcum powder, 0.1-0.5 part of wetting agent, 0.3-0.5 part of thickening agent, 1-2 parts of isooctanol phosphate, 0.1-0.3 part of flatting agent, 0.2-0.6 part of silane coupling agent, 0.4-0.6 part of drier and 25-35 parts of deionized water;
the dispersant is Dispersago ^ -9610W;
the film forming agent is a mixture of DAPRO FX 511 and ethylene glycol, wherein the mass ratio of DAPRO FX 511 to ethylene glycol is 2 to 5:5;
the defoaming agent is TEGO-901W;
the wetting agent is TEGO-245 or TEGO-270 or TEGO-280;
the thickening agent is magnesium aluminum silicate or/and bentonite;
the flatting agent is VOK-FL NO.77 or POLYFLOW NO.77;
the drier is a ZHV-10 drier or cobalt naphthanate;
the silane coupling agent is KH-561 or Mp200;
the waterborne acrylic modified alkyd resin is prepared by the following steps:
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:10 to 15:20 to 23:18 to 22:13 to 15:5 to 9:2 to 5:45 to 60 percent;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:22 to 25:1 to 5:4 to 6:0.5 to 2;
wherein the mass ratio of the water-based alkyd resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1 to 2:1 to 2;
the mass concentration of the ammonia water is 15-25%.
2. The outdoor-construction high-environmental-protection water-based metal protective paint according to claim 1, characterized in that: the wetting agent is TEGO-270.
3. The outdoor-construction high-environmental-protection water-based metal protective paint according to claim 1, characterized in that: the thickening agent is prepared from magnesium aluminum silicate and bentonite according to a mass ratio of 2: 1.
4. The outdoor-construction high-environmental-protection water-based metal protective paint according to claim 1, characterized in that: the flatting agent is VOK-FL NO.77.
5. The preparation method of the outdoor-construction high-environmental-protection water-based metal protective paint of claim 1, which is characterized in that: the method comprises the following steps:
the dispersant is Disppersago-9610W;
the film forming agent is a mixture of DAPRO FX 511 and ethylene glycol, wherein the mass ratio of DAPRO FX 511 to ethylene glycol is 2 to 5:5;
the defoaming agent is TEGO-901W;
the wetting agent is TEGO-245 or TEGO-270 or TEGO-280;
the thickening agent is magnesium aluminum silicate or/and bentonite;
the flatting agent is VOK-FL NO.77 or POLYFLOW NO.77;
the drier is a ZHV-10 drier or cobalt naphthanate;
the silane coupling agent is KH-561 or Mp200;
the waterborne acrylic modified alkyd resin is prepared by the following steps:
wherein the mass ratio of caprylic acid, capric acid, trimethylolpropane, phthalic acid, dimethylbenzene, maleic anhydride, graphene oxide and ethylene glycol monobutyl ether is 20:10 to 15:20 to 23:18 to 22:13 to 15:5 to 9:2 to 5:45 to 60 percent;
uniformly mixing methyl methacrylate and butyl methacrylate to obtain a second mixed solution for later use;
wherein the mass ratio of acrylic acid, methyl methacrylate, hydroxyethyl acrylate, butyl methacrylate and azobisisobutyronitrile is 5:22 to 25:1 to 5:4 to 6:0.5 to 2;
wherein the mass ratio of the water-based alkyd resin obtained in the step (1) to the first mixed solution to the second mixed solution is 10:1 to 2:1 to 2;
the mass concentration of the ammonia water is 15-25%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202111212535.1A CN113801531B (en) | 2021-10-19 | 2021-10-19 | High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202111212535.1A CN113801531B (en) | 2021-10-19 | 2021-10-19 | High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN113801531A CN113801531A (en) | 2021-12-17 |
| CN113801531B true CN113801531B (en) | 2023-03-10 |
Family
ID=78897852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202111212535.1A Active CN113801531B (en) | 2021-10-19 | 2021-10-19 | High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN113801531B (en) |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101591500A (en) * | 2009-06-23 | 2009-12-02 | 常州光辉化工有限公司 | Waterborne normal-temperature self-crosslinking acrylic acid modified alkyd antirust paint |
| CN103145961A (en) * | 2013-02-22 | 2013-06-12 | 嘉宝莉化工集团股份有限公司 | Modified alkyd resin, preparation method thereof and two-component glossy varnish |
| CN104559708A (en) * | 2015-02-04 | 2015-04-29 | 浙江天女集团制漆有限公司 | Water-borne acrylic modified alkyd enamel and preparation method thereof |
| CN104610535A (en) * | 2013-11-05 | 2015-05-13 | 上海富臣化工有限公司 | Mixed fatty acid modified smell eliminating matt alkyd resin and preparation method thereof |
| CN106833248A (en) * | 2016-12-19 | 2017-06-13 | 广东科迪新材料科技有限公司 | A kind of modified fluorine alkyd resin water-based anticorrosive paint of Graphene |
| CN111073438A (en) * | 2020-01-13 | 2020-04-28 | 浙江天女集团制漆有限公司 | Special water-based acrylic acid modified alkyd anticorrosive paint for steel structure and preparation method thereof |
-
2021
- 2021-10-19 CN CN202111212535.1A patent/CN113801531B/en active Active
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101591500A (en) * | 2009-06-23 | 2009-12-02 | 常州光辉化工有限公司 | Waterborne normal-temperature self-crosslinking acrylic acid modified alkyd antirust paint |
| CN103145961A (en) * | 2013-02-22 | 2013-06-12 | 嘉宝莉化工集团股份有限公司 | Modified alkyd resin, preparation method thereof and two-component glossy varnish |
| CN104610535A (en) * | 2013-11-05 | 2015-05-13 | 上海富臣化工有限公司 | Mixed fatty acid modified smell eliminating matt alkyd resin and preparation method thereof |
| CN104559708A (en) * | 2015-02-04 | 2015-04-29 | 浙江天女集团制漆有限公司 | Water-borne acrylic modified alkyd enamel and preparation method thereof |
| CN106833248A (en) * | 2016-12-19 | 2017-06-13 | 广东科迪新材料科技有限公司 | A kind of modified fluorine alkyd resin water-based anticorrosive paint of Graphene |
| CN111073438A (en) * | 2020-01-13 | 2020-04-28 | 浙江天女集团制漆有限公司 | Special water-based acrylic acid modified alkyd anticorrosive paint for steel structure and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN113801531A (en) | 2021-12-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103965776B (en) | A kind of high temperature resistant heat insulation anticorrosive coating | |
| CN109181486B (en) | Low-VOC epoxy primer and preparation method thereof | |
| CN102504668A (en) | Water-based primer-topcoat synthetic anti-corrosive paint for coating automobile spare parts and preparation method thereof | |
| CN111117426A (en) | High-corrosion-resistance flash-rust-resistant waterborne epoxy primer and preparation method thereof | |
| CN109251661B (en) | Ultrahigh-performance epoxy primer and preparation method thereof | |
| CN108329793B (en) | Graphene modified anti-rust pigment anti-corrosion primer and preparation method thereof | |
| CN114181616B (en) | Chromium-free low-temperature curing water-based zinc-aluminum coating and preparation method and application thereof | |
| CN103305101A (en) | Quick-drying anticorrosive and anti-rust primer and preparation method thereof | |
| CN112521834A (en) | Water-based graphene static-conducting anticorrosive paint and preparation method thereof | |
| CN109593469B (en) | Water-based marking paint and preparation method thereof | |
| WO2022088114A1 (en) | Water-based paint special for glass substrates and preparation method therefor | |
| CN112048238A (en) | Two-component isocyanate coating | |
| CN103342939A (en) | Water-soluble epoxy ester antirust paint | |
| CN113801531B (en) | High-environmental-protection water-based metal protective paint capable of being constructed outdoors and preparation method thereof | |
| CN104004429B (en) | Based on the normal temperature solidified composite coating and preparation method thereof of modification 107 silicon rubber | |
| CN117467315B (en) | Fluorocarbon weather-resistant resin powder coating and preparation method thereof | |
| CN113527984A (en) | High-salt-spray-resistance water-based smooth coating and preparation method thereof | |
| CN110903745B (en) | Anti-corrosion wear-resistant polyester resin and preparation method thereof | |
| CN104945974A (en) | UV-curable rust-proof environment-friendly coating | |
| CN107936713A (en) | A kind of environmental protection equipment antirust corrosion-proof coating | |
| CN108504260B (en) | Radiation-resistant strong acid-resistant dual-curing heavy-duty anticorrosive coating | |
| CN109504222B (en) | Adding nano SiO2Water-based acrylic coating of hollow microspheres | |
| CN110643275A (en) | Plastic UV polyurethane acrylate coating and preparation method thereof | |
| CN114479583B (en) | Preparation method of coating composition | |
| CN110437740B (en) | High-decoration acrylic polysiloxane coating and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |