Thermosetting coating composition

Claim 2

An organic solvent based thermosetting composition comprising: (A) crosslinkable hydroxy functional epoxy ester resin having a number average molecular weight (Mn) between about 1,000 and about 5,000, said resin comprising the reaction product of diepoxide reactant (i) in chain extension reaction substantially simultaneously with dicarboxylic acid and diphenol, and (ii) in chain termination reaction with acid component comprising hydroxy functional acid; and (B) polyfunctional, hydroxy-reactive crosslinking agent selected from aminoplast crosslinking agent, blocked polyisocyanate crosslinking agent comprising at least two isocyanate groups blocked by reaction with an active hydrogen bearing blocking agent, and a compatible mixture of any of them, said crosslinking agent being included in an amount such that at the cure temperature of the composition said crosslinking agent will provide between about 0.5 and about 1.6 hydroxy reactive groups per hydroxy group contributed by said epoxy ester resin.

Claim 3

The solvent based thermosetting composition in accordance with claim 1, wherein said hydroxy functional epoxy ester resin comprises the reaction product of said acid component with said diepoxide reactant previously chain extended with diphenol and dicarboxylic acid.

Claim 4

The solvent based thermosetting composition in accordance with claim 1, wherein said hydroxy functional epoxy ester resin comprises the reaction product of said diepoxide reactant substantially simultaneously with diphenol, dicarboxylic acid and said acid component.

Claim 5

A solvent based, thermosetting composition in accordance with claim 1, wherein said diepoxide is selected from the group consisting of bisphenol-A epichlorohydrin epoxy resin, hydantoin epoxy resin, cyclic and acyclic aliphatic diepoxides, and a compatible mixture of any of them.

Claim 6

A solvent based thermosetting composition in accordance with claim 1, wherein said diphenol reactant has the general formula: ##STR6## wherein R is a divalent, organic, linking moiety substantially unreactive with said diepoxide and with said acid component.

Claim 7

A solvent based thermosetting composition in accordance with claim 5, wherein said diphenol reactant is selected from the group consisting of bisphenol-A, bisphenol-B and a compatible mixture thereof.

Claim 8

A solvent based thermosetting composition in accordance with claim 1, wherein said dicarboxylic acid used to chain extend said diepoxide is selected from the group consisting of saturated or unsaturated, cyclic or acyclic, aliphatic or aromatic dicaboxylic acids and mixtures thereof.

Claim 9

A solvent based thermosetting composition in accordance with claim 7, wherein said dicarboxylic acid is of the general formula: HOOC--R"'--COOH wherein R"' is a divalent, linking moiety substantially unreactive with the epoxy functionality of said diepoxide.

Claim 10

A solvent based thermosetting composition in accordance with claim 8, wherein R"' is selected from the group consisting of straight and branched alkylene or alkylidene moieties of about 4 to about 42 carbons.

Claim 11

The solvent based thermosetting composition of claim 1, wherein said hydroxy functional acid is selected from C 3 -C 26 acids bearing a single carboxyl group, at least one primary hydroxyl group, and no additional functionality which would react substantially with said chain extension reactants or the reaction product thereof.

Claim 12

The solvent based thermosetting composition of claim 1, wherein said hydroxy functional acid is selected from those of the general formula: ##STR7## wherein n is 0 to 20; R 1 , R 2 , R 3 and R 4 are the same or different and each is C 1 -C 4 alkylene; and Z and Z' are selected independently from H, OH, nitrile ester, halogen and amide.

Claim 13

The solvent based thermosetting composition of claim 11, wherein at least one of Z and Z' bears an hydroxyl group.

Claim 14

The solvent based thermosetting composition of claim 1, wherein said hydroxy functional acid is selected from the group consisting of dimethylolpropionic acid, bis(hydroxy ethyl)propionic acid, bis(hydroxy propyl)propionic acid, and a compatible mixture of any of them.

Claim 15

The solvent based thermosetting composition of claim 1, wherein said acid component further comprises fatty acid, said hydroxy functional acid and said fatty acid being in molar ratio of from 1:0 to about 1:1, respectively.

Claim 16

The solvent based thermosetting composition of claim 14, wherein said fatty acid is selected from the group consisting of Soya fatty acid, butyric, lauric, palmitic and stearic fatty acid and a compatible mixture of any of them.

Claim 17

A solvent based, thermosetting composition in accordance with claim 1, wherein said crosslinking agent consists essentially of blocked polyisocyanate.

Claim 18

A solvent based, thermosetting composition in accordance with claim 16, wherein said blocked polyisocyanate is selected from blocked aliphatic, aromatic, cycloalkylene, aliphatic aromatic and nuclear substituted aromatic polyisocyanates.

Claim 19

A solvent based, thermosetting composition in accordance with claim 1, wherein said blocked polyisocyanate crosslinking agent comprises blocked polymethylene polyphenol isocyanate which prior to blocking has the formula: ##STR8## wherein x equals 1 to 3.

Claim 20

A solvent based, thermosetting composition in accordance with claim 1, wherein blocked polyisocyanate crosslinking agent is employed which comprises the reaction product of an active hydrogen-bearing blocking agent with polyisocyanate comprising isocyanurate ring-bearing polyisocyanate prepared by cyclotrimerization of diisocyanate.

Claim 21

A solvent based, thermosetting composition in accordance with claim 19, wherein said blocked polyisocyanate crosslinking agent consists essentially of blocked trifunctional isocyanurate represented by the formula: ##STR9## wherein each L is selected independently from the group consisting of aliphatic, cycloaliphatic and aromatic divalent radicals and B is the residue of said active hydrogen bearing blocking agent.

Claim 22

A solvent based, thermosetting composition in accordance with claim 1, wherein said polyisocyanate employed in the preparation of said blocked polyisocyanate crosslinking agent comprises an isocyanate terminated prepolymer prepared by reacting polyol with an excess of polyisocyanate.

Claim 23

A solvent based, thermosetting composition in accordance with claim 1, wherein said crosslinking agent consists of blocked polyisocyanate prepared by (A) reacting (i) organic diisocyanate represented by the formula OCN--L'--NCO wherein L' is selected from the group consisting of aliphatic, cycloaliphatic and aromatic radicals and combinations thereof and wherein one of the isocyanate groups thereof is substantially more reactive than the other, and (ii) sufficient active hydrogen bearing blocking agent to react with substantially all of said more reactive isocyanate groups; and (B) reacting the reaction product of (A) with sufficient polyol to react with the remaining isocyanate groups.

Claim 24

A solvent based, thermosetting composition in accordance with claim 22, wherein said polyol is selected from oligoester diols and triols which (i) have a number average molecular weight (Mn) between about 150 and about 3,000 and (ii) are the product of esterification reaction between carboxylic acid reactant and epoxide reactant, said esterification reaction product being selected from the group consisting of the esterification reaction product of: (a) polycarboxylic acid and monoepoxide; (b) polyepoxide and monocarboxylic acid containing no ethylenical unsaturation and bearing no hydroxy functionality; (c) hydroxy functional carboxylic acid and monoepoxide; (d) monocarboxylic acid and hydroxy functional monoepoxide; and (e) mixtures of (a)-(d).

Claim 25

The solvent based, thermosetting composition of claim 1, wherein said crosslinking agent consists of hexa(methoxymethyl)melamine.

Claim 26

An organic solvent based, thermosetting composition comprising: (A) crosslinkable hydroxy functional epoxy ester resin having a number average molecular weight (Mn) between about 1,000 and about 5,000, said resin comprising the reaction product of diepoxide reactant selected from the group consisting of bisphenol-A epichlorohydrin epoxy resin, hydantoin epoxy resin, cyclic and acyclic aliphatic diepoxide and a compatible mixture of any of them, (i) in chain extension reaction substantially simultaneously with diphenol reactant selected from the group consisting of Bisphenol-A, Bisphenol-B and a compatible mixture thereof, and dicarboxylic acid reactant selected from the group consisting of substantially saturated, acyclic aliphatic dimer acids of about 4-42 carbons and a compatible mixture thereof, and (ii) primary hydroxy functional organic acid selected from the group consisting of dimethylolpropionic acid, bis(hydroxy ethyl)propionic acid, bis(hydroxy propyl)propionic acid and a compatible mixture of any of them; and (B) blocked polyisocyanate crosslinking agent comprising at least two isocyanate groups which have been blocked by reaction with an active hydrogen bearing blocking agent, said blocked polyisocyanate being selected from blocked aliphatic, aromatic, cycloalkylene, aliphatic aromatic, and nuclear substituted aromatic polyisocyanates and being included in said composition in an amount such that upon de-blocking of the blocked isocyanate groups thereof at the cure temperature of the composition, said crosslinking agent will provide between about 0.5 and about 1.6 reactive isocyanate groups per reactive hydroxy group of said epoxy ester resin.

Claim 27

An organic solvent based, thermosetting composition comprising: (A) crosslinkable hydroxy functional epoxy ester resin having a number average molecular weight (Mn) between about 1,000 and about 5,000, said resin comprising the reaction product of diepoxide reactant selected from the group consisting of bisphenol-A epichlorohydrin epoxy resin, hydantoin epoxy resin, cyclic and acyclic aliphatic diepoxide and a compatible mixture of any of them, (i) in chain extension reaction substantially simultaneously with diphenol reactant selected from the group consisting of Bisphenol-A, Bisphenol-B and a compatible mixture thereof, and dicarboxylic acid reactant selected from the group consisting of substantially saturated, acyclic aliphatic dimer acids of about 4-42 carbons and a compatible mixture thereof, and (ii) primary hydroxy functional organic acid selected from the group consisting of dimethylolpropionic acid, bis(hydroxy ethyl)propionic acid, bis(hydroxy propyl)propionic acid and a compatible mixture of any of them; and (B) blocked polyisocyanate crosslinking agent comprising at least two isocyanate groups which have been blocked by reaction with an active hydrogen bearing blocking agent, said blocked polyisocyanate being selected from blocked aliphatic, aromatic, cycloalkylene, aliphatic aromatic, and nuclear substituted aromatic polyisocyanates and being included in said composition in an amount such that upon de-blocking of the blocked isocyanate groups thereof at the cure temperature of the composition, said crosslinking agent will provide between about 0.5 and about 1.6 reactive isocyanate groups per reactive hydroxy group of said epoxy ester resin.