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AU741972B2 - Oligomeric epoxy/isocyanate systems - Google Patents

Oligomeric epoxy/isocyanate systems Download PDF

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AU741972B2
AU741972B2 AU85092/98A AU8509298A AU741972B2 AU 741972 B2 AU741972 B2 AU 741972B2 AU 85092/98 A AU85092/98 A AU 85092/98A AU 8509298 A AU8509298 A AU 8509298A AU 741972 B2 AU741972 B2 AU 741972B2
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Prior art keywords
hydroxyl
component
composition
epoxy
isocyanate
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AU8509298A (en
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Robert John Barsotti
Lee R. Harper
John David Nordstrom
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EIDP Inc
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EI Du Pont de Nemours and Co
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    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/003—Polymeric products of isocyanates or isothiocyanates with epoxy compounds having no active hydrogen
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4045—Mixtures of compounds of group C08G18/58 with other macromolecular compounds
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/58—Epoxy resins
    • 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
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/08—Polyurethanes from polyethers

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Description

TITLE
OLIGOMERIC EPOXY/ISOCYANATE SYSTEMS BACKGROUND OF THE INVENTION This invention concerns coating systems comprising non-isocyanate and isocyanate components in organic solvents. The non-isocyanate components being an oligomer or blend of oligomers containing at least two functional groups, at least one being epoxy; optionally present is a polyester or oligo-ester or acrylic polymer having at least two hydroxyl groups.
U.S. 5,215,783 discloses a process for coating a substrate with a waterborne basecoat and a clearcoat containing a polymeric epoxy group.
SUMMARY OF THE INVENTION It has now been discovered that oligomeric epoxies will react directly 15 with isocyanates to form well-crosslinked coatings. This reaction occurs rapidly at elevated temperatures but relatively slowly at room temperature. This is in sharp contrast to polymeric acrylic epoxies which react poorly at any temperature.
The room temperature reaction is enhanced significantly by the use of epoxy compounds which also include hydroxyl moieties. These epoxies can be used as diluents in traditional hydroxyl/ isocyanate coatings. This crosslinking system results in coatings with very low volatile organic content (VOC) that are durable and display good etch and mar resistance.
The invention specifically concerns a curable coating composition of a binder in organic solvent comprising A) a non-isocyanate component wherein: i) 5-100% by weight of the non-isocyanate component is an oligomer or blend of oligomers with a weight average molecular weight not exceeding about 3,000, a polydispersity not exceeding 1.7, containing at least two functional groups with at least one being an epoxy group, the remaining being epoxy or hydroxyl; ii) 0-95% by weight of the non-isocyanate component of a polyester, oligo-ester or acrylic polymer each having at least two hydroxyl groups; and B) an oligomeric isocyanate crosslinker containing at least two isocyanate groups; the equivalents of B to A being 0.5 to 3.0 of isocyanate to epoxy or epoxy plus hydroxyl.
Contemplated embodiments of the invention are those wherein component (ii) is absent and cure is accelerated by ambient moisture, and where 1,1 all0955.spc/10/26/01 WO 99/05193 PCT/US98/15230 component (ii) contains at least one hydroxyl group derived from acrylates and/or methacrylates, and at least one epoxy group derived from glycidyl methacrylate and/or glycidyl acrylate.
Also contemplated is the above composition cured at ambient conditions or baked at elevated temperatures. Such composition can include hydroxyl and/or epoxy-functional nonaqueous dispersions, and these optional crosslinkers: aldimines, ketimines, and polyaspartic esters. Catalysts such as tin and tertiary amines (alone or in combination with acetic acid) can be employed.
The disclosed composition is useful in clearcoats and pigmented compositions to coat substrates, preferably vehicle bodies and vehicle body parts.
DETAILS OF THE INVENTION The compositions of this invention show a remarkable combination of wet-properties and film-properties. The combination ofoligomeric epoxies crosslinked by oligomeric isocyanates have shown 1) the potential for extremely low volatile organic content (VOC).
VOC's below 2.0 lbs/gallon, (0.24 kg/liter) and in some cases (with only epoxy/isocyanate) approaching 1.0 (0.12 kg/liter) VOC, have been successfully sprayed with excellent appearance and cure; 2) the etch resistance of these coatings is superior to standard hydroxyl/isocyanate systems of similar film Tg (glass transition temperature).
This results in coatings with a superior etch/mar balance which is critical to today's finishes; 3) the fracture properties of these systems, as measured by singleindentor testing, is superior to standard hydroxyl/isocyanate systems; and 4) excellent durability exceeding 7000 hours of acccelerated QUV exposure (using an FS-40 bulb) has been seen with these coatings.
These epoxy or epoxy/hydroxyl-functional oligomers can be used to improve the spray solids or film properties of standard polymeric isocyanatecrosslinked systems.
Binder Components Representative binder components of these systems include epoxyfunctional oligomers, epoxy/hydroxyl-functional oligomers and isocyanatefunctional oligomers. Other functional oligomers and polymers can also be included in the formulations of this invention.
Component A(i) The oligomeric component contains at least two functional groups and should have a molecular weight of less than about 3000. Typical epoxy WO 99/05193 PCT/US98/15230 components containing a hydroxy functionality or (OH) group include, among others, sorbitol polyglycidyl ether, mannitol polyglycidyl ether, pentaerythritol polyglycidyl ether, glycerol polyglycidyl ether, low molecular weight epoxy resins such as epoxy resins of epichlorohydrin and bisphenol-A, and polyglycidyl ethers of isocyanurates, for example, "Denecol" EX301 from Nagase and DCE-358® sorbitol polyglycidyl ether from Dixie Chemical. These types ofoligomers are preferred for ambient cure, but are also useful for baked systems.
Epoxy components which typically do not contain significant hydroxy functionality include, among others, di- and polyglycidyl esters of polycarboxylic acids, and di- and polyglycidyl esters of acids, such as Araldite CY-184® from Ciba-Geigy, or XU-71950 from Dow Chemical are preferred since they form high quality finishes. Cycloaliphatic epoxies can also be used, such as ERL-4221 from Union Carbide. These oligomers are primarily used in baked systems, but can be used at low levels in ambient cured systems.
Component B The composition also contains an organic isocyanate crosslinking agent in the amount of 0.5 to 3.0 equivalents of isocyanate per equivalent of epoxy or epoxy/hydroxyl. Optimum film properties are achieved when one epoxy group reacts with two isocyanate groups. However, it was determined that a broad latitude in stoichiometry of isocyanate to epoxy can sometimes be useful depending on final wet- and dry-coating properties desired. Any of the conventional aromatic, aliphatic, or cycloaliphatic isocyanates; trifunctional isocyanates and isocyanate functional adducts of a polyol and a diisocyanate can be used. Typically useful diisocyanates are 1,6-hexamethylene diisocyanate, isophorone diisocyanate, 4,4'-biphenylene diisocyanate, toluene diisocyanate, bis-cyclohexyl diisocyanate, tetramethylene xylene diisocyanate, ethyl ethylene diisocyanate, 2,3-dimethyl ethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-phenylene diisocyanate, 1,5-napthalene diisocyanate, bis-(4-isocyanatocyclohexyl)-methane, 4,4'-diisocyanatodiphenyl ether and the like.
Typical trifunctional isocyanates that can be used are triphenylmethane triisocyanate, 1,3,5-benzene triisocyanate, 2,4,6-toluene triisocyanate and the like, Trimers of diisocyanates also can be used such as the trimer of hexamethylene diisocyanate which is sold under the tradename "Desmodur"® N-3390 and the trimer of isophorone diisocyanate. Trifunctional adducts of triols and diisocyanates can be used.
Optional Ingredients The present coating composition can further comprise a functional amount of catalyst, generally about 0.1 to 5 weight percent, based on the weight of WO 99/05193 PCT/US98/15230 solids in the formulation. A wide variety of catalysts can be used, such as dibutyl tin dilaurate or tertiary amines such as triethylenediamine. These catalysts can be used alone or in conjunction with carboxylic acids such as acetic acid. It is preferred that a catalyst be employed.
The coating compositions of the present invention are formulated into high solids coating systems dissolved in at least one solvent. The solvent is usually organic. Preferred solvents include aromatic hydrocarbons such as petroleum naphtha or xylenes; ketones such as methyl amyl ketone, methyl isobutyl ketone, methyl ethyl ketone or acetone; esters such as butyl acetate or hexyl acetate; and glycol ether esters such as propylene glycol monomethyl ether acetate. It is preferred to employ solvent.
The coating compositions of the present invention can also contain up to 40% of total binder of a dispersed acrylic component which is a polymer particle dispersed in an organic media, which particle is stabilized by what is known as steric stabilization. Hereafter, the dispersed phase or particle, sheathed by a steric barrier, will be referred to as the "macromolecular polymer" or "core". The stabilizer forming the steric barrier, attached to this core, will be referred to as the "macromonomer chains" or "arms".
The dispersed polymer contains about 10 to 90%, preferably 50 to 80%, by weight, based on the weight of the dispersed polymer, of a high molecular weight core having a weight average molecular weight of about 50,000 to 500,000. The preferred average particle size is 0.1 to 0.5 microns. The arms, attached to the core, make up about 10 to 90%, preferably 10 to 59%, by weight of the dispersed polymer, and have a weight average molecular weight of about 1,000 to 30,000, preferably 1,000 to 10,000.
The macromolecular core of the dispersed polymer is comprised of polymerized acrylic monomer(s) optionally copolymerized with ethylenically unsaturated monomer(s). Suitable monomers include styrene, alkyl acrylate or methacrylate, ethylenically unsaturated monocarboxylic acid, and/or silanecontaining monomers. Such monomers as methyl methacrylate contribute to a high Tg (glass transition temperature) dispersed polymer, whereas such "softening" monomers as butyl acrylate or 2-ethylhexylacrylate contribute to a low Tg dispersed polymer. Other optional monomers are hydroxyalkyl acrylates or methacrylates or acrylonitrile. Optionally, the macromolecular core can be crosslinked through the use ofdiacrylates or dimethacrylates such as allyl methacrylate or post reaction of hydroxyl moieties with polyfunctional isocyanates.
The macromonomer arms attached to the core can contain polymerized monomers of alkyl methacrylate, alkyl acrylate, each having 1 to 12 WO 99/05193 PCT/US98/15230 carbon atoms in the alkyl group, as well as glycidyl acrylate or glycidyl methacrylate or ethylenically unsaturated monocarboxylic acid for anchoring and/or crosslinking. Typically useful hydroxy-containing monomers are hydroxy alkyl acrylates or methacrylates as described above.
Additional crosslinkers can be included in this formula such as aldemine, including the reaction product of isobutyraldehyde with diamines such as isophorone diamine and the like; ketimines such as the reaction product of methyl isobutyl ketone with diamines such as isophorone diamine; and polyaspartic esters.
The coating compositions of the present invention can also contain conventional additives such as pigments, stabilizers, ultraviolet light stabilizers, antioxidants, rheology control agents, flow agents, toughening agents and fillers.
Such additional additives will, of course, depend on the intended use of the coating composition. Fillers, pigments, and other additives that would adversely effect the clarity of the cured coating will not be included if the composition is intended as a clear coating.
Component A(ii): The coating compositions of the present invention can also an acrylic polymer of weight average molecular weight greater than 3,000, or a conventional polyester such as SCD® 1040 from Etna Product Inc. for improved properties and appearance, sag resistance, flow and leveling and such. The acrylic polymer can be composed of typical monomers such as acrylates, methacrylates, styrene and the like and functional monomers such as hydroxy ethyl acrylate, glycidyl methacrylate, or the like.
Representative hydroxyl-functional oligomers that can be employed as component A(ii) include the reaction product of multifunctional alcohols such as pentaerythritol, hexanediol, trimethylol propane, and the like, with cyclic monomeric anhydrides such as hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, and the like, said reaction product further extended by reaction with monofunctional epoxies such as butylene oxide, propylene oxide, and the like to form hydroxyl oligomers.
Non-alicyclic oligomers (linear or aromatic) can include succinic anhydride- or phthalic anhydride-derived moieites such as described above.
Caprolactone oligomers which can be made by reacting caprolactone with a cycloaliphatic, aliphatic or aromatic polyol can also be used. Particulary useful caprolactone oligomers are described in columns 4 to 5 of U.S. Patent 5,286,782.
Preferred oligomers A(ii) have weight average molecular weights not exceeding about 3,000 with a polydispersity not exceeding about 1.7; more preferred oligomers have molecular weights not exceeding about 2,500 and WO 99/05193 PCT/US98/15230 polydispersity not exceeding about 1.4; most preferred oligomers have molecular weights not exceeding about 2,200, and polydisperity not exceeding about 1.25.
The coating compositions are typically applied to a substrate by conventional techniques such as spraying, electrostatic spraying, roller coating, dipping or brushing. The present formulations are particularly useful as a clear coating for outdoor articles, such as automobile and other vehicle body parts. The substrate is generally prepared with a primer and/or a color coat or other surface preparation prior to coating with the present compositions.
After application to a substrate, the present compositions can be cured by heating to a temperature of about 1200 to 150 0 C for a period of about 15 to minutes or with the proper formulation can be cured at ambient conditions (about 600 to 110 0 F, depending on the geographical location, usually 650 to 90 0
F).
The performance characteristics of the final cured coating composition are excellent, providing a combination of excellent gloss and durability to abrasion, sunlight and acidic rain. At the same time, the compositions provide low volatile organic content and ease of handling. The ability to apply the present compositions by spraying techniques with the unusually low VOC content is surprising.
The present invention is further illustrated by the following specific examples, in which parts and percentages are by weight unless otherwise indicated.
EXAMPLES
KEY FOR EXAMPLES Tradename or identifier Chemical Description Tinuvin®384 (UVA) substituted benzotriazole (Ciba-Geigy) Tinuvin®292 (HALS) hindered amine derivative (Ciba-Geigy) BYK®306 silane flow additive (BYK-Chemie) Tolonate®HDT or HDT-LV isocyanurate oligomers of hexamethylene diisocyanate (Rhone-Poulenc) Procedure 1 TETRAHYDROXY-FUNCTIONAL OLIGOMER Preparation of Acid Oligomer To a 12-liter flask fitted with an agitator, condenser, heating mantle, nitrogen inlet, thermocouple and an addition port was added 2447.2 gms of propylene glycol monomethylether acetate, 792.4 gms of pentaerythritol and 1.36 gms of triethylamine. The reaction mixture was agitated and heated to 140 0
C
under a nitrogen blanket at which time 3759 gms of methyl hexahydrophthalic WO 99/05193 PCT/US98/15230 anhydride was added over 6 hrs. The reaction mixture was then held at 140°C until no anhydride bands were observed on an infrared spectroscopic trace.
Preparation ofHydroxy Oligomer To a 5-liter flask fitted with an agitator, condenser, heating mantle, nitrogen inlet, thermocouple and an addition port was added 2798.4 gms of acid oligomer prepared above and 2.76 gms of triethylamine. The mixture was agitated and heated to 60 0 C under nitrogen. Then, 696.9 gms of 1,2-epoxy butane was added over 120 mins, after which the temperature was raised to 105 0 C and held at that temperature until the acid number dropped to about 10 or less. Percent weight solids were 71.5, Gardner viscosity V, number average molecular weight 895 and weight average molecular weight 1022 as determined by GPC (polystyrene standard).
Procedure 2 The hydroxy-functional acrylic component was made as follows: a stirred, heated reactor is charged with I Methyl amyl ketone 148.05 parts This mixture was heated to reflux (about 150-155 0
C)
The following feed was then added simultaneously with part Il uniformly over 5 hours while maintaining reflux: II Isobutyl methacrylate monomer 182.56 2-ethylhexyl methacrylate monomer 237.37 2-hydroxyethyl methacrylate 129.16 The following feed was fed simultaneously with part II over 150 minutes. When addition is complete cool reactor to 130 0
C.
Im Methyl amyl ketone 58.64 t-butyl peroxyacetate 70% soln 26.51 After the previous feed the following was added over 30 minutes while maintaining reflux (hold temperature at 130 0 C. Cool and fill sample IV Methyl amyl ketone 14.81 t-butyl peroxyacetate initiator 6.55 The batch was then cooled and filled out.
Total -804.00 Solids 68.0% Viscosity W to Y Gardner-Holdt Gallon Weight =8.04 Example 1 Two-Component Oligomeric Epoxy/Isocyanate clear bake system Component (i) WO 99/05193 PCT/US98/15230 Diglycidyl ester of 1,2 cyclohexane dicarboxylic acid 189.78 Tinuvin®384 (UV Screener from Ciba-Geigy) 11.01 Tinuvin®292 (Hindered Amine Light Stabilizer from Ciba-Geigy) 8.26 10% BYK-301® (flow additive from BYK Chemie) in Propylene Glycol Monomethyl ether acetate 2.76 DiButyl Tin Dilaurate (DBTDL) in Butyl Acetate 1.38 Butyl Acetate Component B Tolonate HDT-LV® (Isocyanurate trimer of hexamethylene diisocyanate from Rhone-Poulenc) 361.06 Components and are mixed, the clear is then thinned to a Zahn #2 viscosity of 30 seconds with butyl acetate. The clear is spray-applied over a black solvent-borne basecoat which has already been baked for 30 minutes at 130 0 C (265 0 The coating is cured for 30 minutes at 141 0 C (285 0 This coating exhibits excellent cure, hardness, and appearance.
Example 2 Oligomeric Epoxy/Oligomeric Hydroxyl/Isocyanate clear bake system Components and (ii) Diglycidyl ester of 1,2 cyclohexane dicarboxylic acid 102.6 Tetra Hydroxyl functional oligomer (from Procedure 141.71 Tinuvin®384 (UV Screener from Ciba-Geigy) 10.82 Tinuvin®292 (Hindered Amine Light Stabilizer from Ciba-Geigy) 8.12 BYK-301® (flow additive from BYK Chemie) in Propylene Glycol Monomethyl ether acetate 2.16 DiButyl Tin Dilaurate in Butyl Acetate 1.35 Butyl Acetate 67 WO 99/05193 PCT/US98/15230 Component (B) Tolonate HDT-LV® (Isocyanurate trimer of hexamethylene diisocyanate from Rhone-Poulenc) 335.92 The components are mixed, the clear is then thinned to a Zahn #2 viscosity of 30 seconds with butyl acetate. The clear is spray-applied over a black water-borne basecoat which has already received a warm air flash of 5 minutes at 82 0 C (180°F). The coating is cured for 30 minutes at 141 0 C (285 0 This coating exhibits excellent cure, hardness, and appearance.
Example 3 Oligomeric Epoxy/Aldimine/Isocyanate clear bake system Component (i) ERL 4299 (cycloaliphatic epoxy from Union Carbide) 101.5 Desmophen® XP-7069 (Aldimine from Bayer) 101.5 Tinuvin®384 (UV Screener from Ciba-Geigy) 10.64 Tinuvin®292 (Hindered Amine Light Stabilizer from Ciba-Geigy) 7.98 BYK-301® (flow additive from BYK Chemie) in Propylene Glycol Monomethyl ether acetate 2.13 10% Octanoic acid in Propylene Glycol Monomethylester acetate 3.73 Butyl Acetate 92 Component (B) Tolonate HDT® (Isocyanurate trimer of hexamethylene diisocyanate from Rhone-Poulenc) 340.04 Components and are mixed, the clear is then thinned to a Zahn #2 viscosity of 30 seconds with butyl acetate. The clear is spray-applied over a black water-borne basecoat which has already received a warm air flash of minutes at 85 0 C (180 0 The coating is cured for 30 minutes at 141 0 C (285 0
F).
This coating exhibits excellent cure, hardness, and appearance.
WO 99/05193 PCT/US98/15230 Example 4 Oligomeric Epoxy/Hydroxyl with Isocyanate Clearcoat bake/ambient system Component (i) DC E 358® Sorbitol ether epoxy/hydroxyl compound from Dixie Chemical 12.86 BYK-301® (flow additive from BYK Chemie) in Propylene Glycol Monomethyl ether acetate 0.49 1% DiButyl Tin Dilaurate in Methyl Ethyl Ketone 2.45 Butyl Acetate 18.06 Component (B) Tolonate HDT® (Isocyanurate trimer of hexamethylene diisocyanate from Rhone-Poulenc) 36.14 Components and are mixed. The clear is drawn down over primed steel panels and TEDLAR® to a thickness of about 2 mils. The coating is cured for 30 minutes at 141 0 C (285 0 This coating exhibits excellent cure, hardness, mar resistance, and appearance. The percent gel fraction as measured by boiling the free film of this coating in acetone for 6 hours is 97.7%, which is excellent.
This same coating was cured at ambient conditions and found to give good hardness, appearance and cure. The gel fraction on the air dried system after days of room temperature aging was 94.7%. The "surface dry time" as measured by a BK dry time tester was 260 minutes.
Example Oligomeric Epoxy/Isocyanate clearcoat bake system Component (i) ERL 4221 (cycloaliphatic epoxy from Union Carbide) 13.14 BYK-301® (flow additive from BYK Chemie) in Propylene Glycol Monomethyl ether acetate 0.49 1% DiButyl Tin Dilaurate in Methyl Ethyl Ketone 2.45 Butyl Acetate 18.06 Component (B) Tolonate HDT® (Isocyanurate trimer of hexamethylene diisocyanate from Rhone-Poulenc) 35.86 Components and are mixed. The clear is drawn down over primed steel panels and TEDLAR® to a thickness of about 2 mils. The coating is cured for 30 minutes at 141 0 C (285 0 This coating exhibits excellent cure, WO 99/05193 WO 9905193PCTIUS98/15230 hardness, and appearance. The gel fraction as measured by boiling the free film of this coating in acetone for 6 hours is 96.2%.
Examples 6 and 7 Inredient Weight W!eiht(7) IBMAIEHMlAIHEMA Resin 96.93 114.98 (Procedure 2) XUGY-358' 6.58 6.95 MEK 43.46 26.38 Tinuvin TM 1130 UV screener 3.31 3.39 Tinuvin Tm 123 hindered amine light 2.21 2.26 stabilizer
BYK
T m 306 flow additive (silane) 1.60 1.60 DBTDL in MEK 0.44 0.45 acetic acid 1.00 1.00 Tolonate HDT TM 32.16 30.79 xene 12.32 12.19 viscosity-initial (Zahn #2 cup) 19 sec; 28 sec viscosity 4 hours 32 sec; Zahn) 41 sec; Zahn) BK dry time #2 2 1.00 hour 0.875 hour BK dry time 32 1.25 hours 1.50 hours VOC 0.42 kg/liter 0.43 kg/lite Tukon hardness (Knoop) 2.95 7.70 1 Sorbitol Ether Epoxy-hydroxyl from Dixie Chemical 2 0 3 -Surface dry time using BK dry time tester r' 11a- Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.
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Claims (16)

1. A curable coating composition of a binder in organicsolvent comprising: A) a non-isocyanate component wherein: i) 5-100% by weight of the non-isocyanate component is an oligomer or blend of oligomers with a weight average molecular weight not exceeding about 3,000, a polydispersity not exceeding 1.7, containing at least two functional groups with at least one being an epoxy group, the remaining being epoxy or hydroxyl; ii) 0-95% by weight of the non-isocyanate component of a polyester, oligo-ester or acrylic polymer each having at least two hydroxyl groups; and B) an oligomeric isocyanate crosslinker containing at least two isocyanate groups; the equivalents of B to A being 0.5 to 3.0 of isocyanate to 15 epoxy or epoxy plus hydroxyl. So
2. A composition according to Claim 1 comprising and and i not (ii).
3. A composition of Claim 1 wherein the functionality of component is epoxy.
4. A composition according to Claim 1 wherein component (ii) contains at least one hydroxyl group derived from a member selected from the 25 group of hydroxyl acrylates and hydroxyl methacrylates and at least one epoxy group derived from a member selected from glycidyl acrylate and glycidyl methacrylate.
A composition of Claim 1 wherein component (ii) is an acrylic polymer having a weight average molecular weight of at least 3000 and at least two hydroxyl groups selected from a member of the group hydroxyl acrylate and hydroxyl methacrylate.
6. A composition of Claim 1 wherein component (ii) is a hydroxyl- functional polyester with a weight average molecular weight of at least 1500.
7. A composition of Claim 1 wherein component (ii) is selected from a linear or branched cycloaliphatic moiety-containing oligomer or blend of 12 al10955.spc/10/26/01 WO 99/05193 PCT/US98/15230 oligomers with a weight average molecular weight not exceeding about 3,000, a polydispersity not exceeding about 1.7, and hydroxyl functionality.
8. A composition of Claim 1 wherein component (ii) is a non- alicyclic oligomer with a weight average molecular weight not exceeding about 3,000, a polydispersity not exceeding about 1.7, and hydroxyl functionality.
9. A composition according to Claim 1 which contains up to percent by weight of total binder of an acrylic component comprising a core of acrylic polymer and, grafted thereto, a plurality of substantially linear stabilizer components, this component containing at least about 2 percent of ethylenically unsaturated monomer with functionality capable of reacting with B, the core being substantially insoluble and the stabilizer components being soluble in the solvent medium.
A composition according to Claim 1 comprising one or more additional crosslinkers selected from the group consisting of aldimine, ketimine and polyaspartic ester.
11. A composition according to Claim 1 comprising a catalyst selected from the group of tin and tertiary amine.
12. An ambient temperature-cured coating of the composition of Claim 1.
13. A bake-cured coating of the composition of Claim 1.
14. A composition according to Claim 1 additionally containing up to 200 parts by weight of pigment, based on 100 parts of binder.
A method for coating a substrate comprising applying thereto a composition according to Claim 1 and curing the composition.
16. A substrate coated with the composition of Claim 1.
AU85092/98A 1997-07-24 1998-07-23 Oligomeric epoxy/isocyanate systems Ceased AU741972B2 (en)

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US5355697P 1997-07-24 1997-07-24
US60/053556 1997-07-24
PCT/US1998/015230 WO1999005193A1 (en) 1997-07-24 1998-07-23 Oligomeric epoxy/isocyanate systems

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AU (1) AU741972B2 (en)
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CA (1) CA2297808A1 (en)
IL (1) IL133924A (en)
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US7144526B2 (en) * 2003-02-04 2006-12-05 E.I. Du Pont De Nemours And Company Conductive primer composition for ambient cure
US7737243B2 (en) 2006-05-16 2010-06-15 E. I. Du Pont De Nemours And Company Highly productive coating composition for automotive refinishing

Citations (1)

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US4749743A (en) * 1986-10-06 1988-06-07 Ppg Industries, Inc. Epoxy-functional polyurethanes and high solids thermosetting coating compositions thereof

Family Cites Families (3)

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US4169825A (en) * 1975-05-15 1979-10-02 The Sherwin-Williams Company High solids coating compositions
US4409381A (en) * 1981-12-28 1983-10-11 Ford Motor Company Novel diblocked diisocyanate urea urethane oligomers and coating compositions comprising same
JPS6465179A (en) * 1987-09-04 1989-03-10 Nippon Paint Co Ltd Coatings composition for rustpreventive steel sheet having thin coating film

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4749743A (en) * 1986-10-06 1988-06-07 Ppg Industries, Inc. Epoxy-functional polyurethanes and high solids thermosetting coating compositions thereof

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BR9810777A (en) 2000-09-19
KR20010022142A (en) 2001-03-15
TWI239966B (en) 2005-09-21
AU8509298A (en) 1999-02-16
WO1999005193A1 (en) 1999-02-04
NZ502717A (en) 2002-05-31
IL133924A (en) 2004-12-15
JP2001510867A (en) 2001-08-07
CA2297808A1 (en) 1999-02-04
IL133924A0 (en) 2001-04-30

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