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US4281078A Expired / Lapsed US ⏱️ 0.0 years remaining

High-solids polyurethane enamel coating composition

Assignee: EIDP Inc
•
Filing: 1979-11-26
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Granted: 1981-07-28
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Expires: 1999-11-26
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Abstract

Abstract A coating composition of a urethane polymer has film-forming constituents of an organic polyisocyanate, a low molecular weight hydroxyl-functional acrylic copolymer, and a low molecular weight hydroxyl-functional polyester based on branched-chain glycols. The composition can be applied at environmentally-acceptable solids levels and cured at ambient temperatures to form a durable film.

Inventors

  • 👤 Clifford H. Strolle
  • 👤 Glenn D. Thornley

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 10:34
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6216; C08G18/622; C08G18/6225; C08G18/6229; C08G18/4009; C08G18/4063; C08G18/42; C08G18/4205; C08G18/4208; C08G18/4211; C08G18/4219; Y; Y10; Y10S; Y10S525/00; Y10S525/92

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 318 words
A coating composition, capable of curing at ambient temperatures, of a mixture of a polymer blend and a solvent for the polymer blend wherein the blend is 65-90% by weight of the mixture and consists essentially of (a) 25-45% by weight, based on the weight of the blend, of an organic polyisocyanate; (b) 5-25% by weight, based on the weight of the blend, of a copolymer of (1) a hydroxyalkyl ester of acrylic or methacrylic acid wherein the alkyl group has 2-10 carbon atoms and wherein the hydroxyalkyl ester is 25-35% by weight of the copolymer, and (2) at least one other ethylenically unsaturated monomer that is copolymerizable with the hydroxyalkyl ester but that is free of functional groups reactive with the polyisocyanate at ambient temperatures, wherein this monomer is selected from the group consisting of vinyl chloride, vinylidene chloride, ethylene, propylene, vinyl acetate, butadiene, styrene, α-methyl styrene, dibutyl maleate, C 1 -C 12 alkyl esters of acrylic acid, C 1 -C 12 alkyl esters of methacrylic acid, and mixtures of these wherein the copolymer has a hydroxyl content of 2-6% by weight; and (c) 40-60% by weight, based on the weight of the blend, of a saturated polyester polyol that is the reaction product of (1) pentaerythritol and at least one branched-chain glycol wherein the molar ratio of glycol to pentaerythritol is from 2:1 to 6:1, (2) an aromatic or aliphatic monocarboxylic acid selected from the group consisting of benzoic acid, paratertiary butyl-benzoic acid, triethyl benzoic acid, toluic acid, phenylacetic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, pelargonic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, and mixtures of these, and (3) a mixture of an aromatic and a aliphatic dicarboxylic acid wherein the molar ratio of aromatic acid to aliphatic acid is from 2:1 to 6:1, wherein the polyol has a hydroxyl content of 5-9% by weight.
Claim 2
Dependent Claim 318 words
A coating composition, capable of curing at ambient temperatures, of a mixture of a polymer blend and a solvent for the polymer blend wherein the blend is 65-90% by weight of the mixture and consists essentially of (a) 25-45% by weight, based on the weight of the blend, of an organic polyisocyanate; (b) 5-25% by weight, based on the weight of the blend, of a copolymer of (1) a hydroxyalkyl ester of acrylic or methacrylic acid wherein the alkyl group has 2-10 carbon atoms and wherein the hydroxyalkyl ester is 25-35% by weight of the copolymer, and (2) at least one other ethylenically unsaturated monomer that is copolymerizable with the hydroxyalkyl ester but that is free of functional groups reactive with the polyisocyanate at ambient temperatures, wherein this monomer is selected from the group consisting of vinyl chloride, vinylidene chloride, ethylene, propylene, vinyl acetate, butadiene, styrene, α-methyl styrene, dibutyl maleate, C 1 -C 12 alkyl esters of acrylic acid, C 1 -C 12 alkyl esters of methacrylic acid, and mixtures of these wherein the copolymer has a hydroxyl content of 2-6% by weight; and (c) 40-60% by weight, based on the weight of the blend, of a saturated polyester polyol that is the reaction product of (1) pentaerythritol and at least one branched-chain glycol wherein the molar ratio of glycol to pentaerythritol is from 2:1 to 6:1, (2) an aromatic or aliphatic monocarboxylic acid selected from the group consisting of benzoic acid, paratertiary butyl-benzoic acid, triethyl benzoic acid, toluic acid, phenylacetic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, pelargonic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, and mixtures of these, and (3) a mixture of an aromatic and a aliphatic dicarboxylic acid wherein the molar ratio of aromatic acid to aliphatic acid is from 2:1 to 6:1, wherein the polyol has a hydroxyl content of 5-9% by weight.
Claim 3
Dependent Claim 31 words
The coating composition of claim 1 in which the organic polyisocyanate is selected from the group consisting of aliphatic diisocyanates, cycloaliphatic diisocyanates, alkaryl diisocyanates, aralkyl diisocyanates, heterocyclic diisocyanates, and aryl diisocyanates.
Claim 4
Dependent Claim 29 words
The coating composition of claim 1 in which the organic polyisocyanate has the formula ##STR3## wherein R 2 is aromatic or an aliphatic hydrocarbon radical having 1-12 carbon atoms.
Claim 5
Dependent Claim 21 words
The coating composition of claim 3 wherein the copolymer is of hydroxyethyl acrylate, styrene, and at least one other alkyl methacrylate.
Claim 6
Dependent Claim 22 words
The coating composition of claim 3 wherein the copolymer is of hydroxyethyl acrylate, lauryl methacrylate, and at least one other alkyl methacrylate.
Claim 7
Dependent Claim 81 words
The coating composition of claim 4 or 5 wherein the branched-chain glycol is neopentyl glycol; the monocarboxylic acid is selected from the group consisting of benzoic acid, lauric acid, pelargonic acid, and mixtures of these; and the aromatic dicarboxylic acid is selected from the group consisting of phthalic acid, isophthalic acid, terephthalic acid, and mixtures of these, and the aliphatic dicarboxylic acid is selected from the group consisting of succinic acid, glutaric acid, adipic acid, pimelic acid, and mixtures of these.
Claim 8
Dependent Claim 40 words
The coating composition of claim 3 wherein the copolymer is of hydroxyethyl acrylate, methyl methacrylate, and lauryl methacrylate and wherein the polyester polyol is the reaction product of pentaerythritol, neopentyl glycol, benzoic acid, isophthalic acid, phthalic acid, and adipic acid.
Claim 9
Dependent Claim 41 words
The coating composition of claim 3 wherein the copolymer is of hydroxyethyl acrylate, lauryl methacrylate, ethyl methacrylate, and styrene, and wherein the polyester polyol is the reaction product of pentaerythritol, neopentyl glycol, lauric acid, isophthalic acid, phthalic acid, and adipic acid.
Claim 10
Dependent Claim 14 words
The coating composition of claims 3, 4, 5, 7, or 8 additionally containing pigment.
Claim 11
Dependent Claim 20 words
The coating composition of claim 3, 4, 5, 7, or 8 additionally containing an ultraviolet light stabilizer and an oxidant.
Claim 12
Dependent Claim 37 words
A substrate coated with a first cured coating composition according to claim 3 overlaid with a second cured coating composition according to claim 3 wherein the first composition contains pigment and wherein the second composition is unpigmented.
Claim 13
Dependent Claim 17 words
The substrate of claim 11 wherein the first cured coating composition additionally contains a ultraviolet light stabilizer.
Claim 14
Dependent Claim 15 words
The substrate of claim 12 wherein the first cured coating composition additionally contains an antioxidant.
Claim 15
Dependent Claim 19 words
The substrate of claim 13 wherein the second cured coating composition additionally contains and ultraviolet light stabilizer and antioxidant.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-07-27 1985-01-26 1985-07-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-07-27 1989-01-26 1989-07-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-07-27 1993-01-26 1993-07-28 $7700.00 Window Closed / Lapsed

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