Thermoplastic copolymers and preparation thereof

Claim 2

A process for preparing an organic solvent soluble copolymer having at least one unreacted epoxy radical and at least one unreacted carboxyl radical per molecule, said process comprising a first step of reacting an epoxy resin of the formula: ##STR5## where n = 0 to 6, with an α, β-ethylenically unsaturated carboxylic acid or an acid anhydride while heating at 120° to 200° C. until the epoxy resin is reacted to such an extent that there is a decrease in acid value between the start of the first step and the conclusion of the first step of at least 26.8% and up to about 64%; and a second step of copolymerizing in solution 0.1 to 31.7 parts by weight of the resulting reaction product with 68.3 to 99.9 parts by weight of at least one other copolymerizable monomer at a temperature lower than the heating temperature of the first step to form a resin, such that in said first step: (a) said epoxy resin has an epoxide equivalent of 180-195 and said acid is acrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.81 to 1.95; or (b) said epoxy resin has an epoxide equivalent of 425-550 and said acid is methacrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.64 to 2.12; or (c) said epoxy resin has an epoxide equivalent of 425-550 and said anhydride is maleic anhydride in a ratio of equivalents of epoxy to equivalents of anhydride of 1.61 to 2.08.

Claim 3

Process according to claim 1 wherein said first step reaction is carried out by heating at 140° to 160° C.

Claim 4

Process according to claim 2 wherein a polymerization inhibitor is employed in said first step to prevent polymerization of acrylic acid and methacrylic acid.

Claim 5

Process according to claim 3 wherein said polymerization inhibitor is selected from the group consisting of benzoquinone, hydroquinone, dinitrobenzene and α,α-diphenyl-β-picryl hydrazyl.

Claim 6

Process according to claim 3 wherein said polymerization inhibitor comprises 200 ppm hydroquinone relative to acrylic acid or methacrylic acid.

Claim 7

Process according to claim 1 wherein a chain transfer agent is employed in said second step.

Claim 8

Process according to claim 6 wherein said chain transfer agent is lauryl mercaptan, n-octyl mercaptan, thiophenol, carbon tetrachloride, or triethyl amine.

Claim 9

Process according to claim 1, which comprises either heating a mixture of (1) epoxy resin, (2) α,β-ethylenic unsaturated acid, and (3) polymerizable monomers, thereby to effect the reactions of (1) with (2), and (2) with (3), simultaneously, or first copolymerizing (2) and (3), and thereafter reacting the resulting copolymer with (1).

Claim 10

Process according to claim 1 wherein said other copolymerizable monomer is at least one monomer selected from the group consisting of methyl methacrylate, ethyl acrylate, styrene, acrylamide and acrylonitrile.

Claim 11

Process according to claim 1 wherein a polymerization solvent is employed in said second step, said solvent selected from the group consisting of benzene, toluene, xylene, methyl acetate, ethyl acetate, butyl acetate, methyl ethyl ketone, methyl isobutyl ketone, acetone, methanol, ethanol, propanol, butanol, dioxane and acetonitrile.

Claim 12

Process according to claim 1 wherein: (a) said acid is acrylic acid, said decrease in acid value is 31.2 to 64% and said other copolymerizable monomer is methyl methacrylate, ethyl acrylate, styrene, acrylamide, acrylonitrile or mixtures thereof; or (b) said acid is methacrylic acid, said decrease in acid value is 26.8 to 51.3% and said other copolymerizable monomers are methyl methacrylate and ethyl acrylate; or (c) said anhydride is maleic anhydride, said reduction in acid number is 42% and said other copolymerizable monomers are methyl methacrylate, ethyl acrylate and styrene.

Claim 13

An organic solvent soluble copolymer having at least one unreacted epoxy radical and at least one unreacted carboxyl radical per molecule, said copolymer comprising the reaction product from a first step of reacting an epoxy resin of the formula: ##STR6## where n = 0 to 6, with an α,β-ethylenically unsaturated carboxylic acid or an acid anhydride while heating at 120° to 200° C. until the epoxy resin is reacted to such an extent that there is a decrease in acid value between the start of the first step and the conclusion of the first step of at least 26.8% and up to about 64%; and a second step of copolymerizing in solution 0.1 to 31.7 parts by weight of the reaction product from the first step with 68.3 to 99.9 parts by weight of at least one other copolymerizable monomer at a temperature lower than the heating temperature of the first step to form said copolymer; such that in said first step: (a) said epoxy resin has an epoxide equivalent of 180-195 and said acid is acrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.81 to 1.95; or (b) said epoxy resin has an epoxide equivalent of 425-550 and said acid is methacrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.64 to 2.12; or (c) said epoxy resin has an epoxide equivalent of 425-550 and said anhydride is maleic anhydride in a ratio of equivalents of epoxy to equivalents of anhydride of 1.61 to 2.08.

Claim 14

An organic solvent soluble copolymer having at least one unreacted epoxy radical and at least one unreacted carboxyl radical per molecule, said copolymer comprising the reaction product from a first step of reacting an epoxy resin of the formula: ##STR6## where n = 0 to 6, with an α,β-ethylenically unsaturated carboxylic acid or an acid anhydride while heating at 120° to 200° C. until the epoxy resin is reacted to such an extent that there is a decrease in acid value between the start of the first step and the conclusion of the first step of at least 26.8% and up to about 64%; and a second step of copolymerizing in solution 0.1 to 31.7 parts by weight of the reaction product from the first step with 68.3 to 99.9 parts by weight of at least one other copolymerizable monomer at a temperature lower than the heating temperature of the first step to form said copolymer; such that in said first step: (a) said epoxy resin has an epoxide equivalent of 180-195 and said acid is acrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.81 to 1.95; or (b) said epoxy resin has an epoxide equivalent of 425-550 and said acid is methacrylic acid in a ratio of equivalents of epoxy to equivalents of acid of 1.64 to 2.12; or (c) said epoxy resin has an epoxide equivalent of 425-550 and said anhydride is maleic anhydride in a ratio of equivalents of epoxy to equivalents of anhydride of 1.61 to 2.08.

Claim 15

Copolymer according to claim 1 wherein: (a) said acid is acrylic acid, said decrease in acid value is 31.2 to 64% and said other copolymerizable monomer is methyl methacrylate, ethyl acrylate, styrene, acrylamide, acrylonitrile or mixtures thereof; or (b) said acid is methacrylic acid, said decrease in acid value is 26.8 to 51.3% and said other copolymerizable monomers are methyl methacrylate and ethyl acrylate; or (c) said anhydride is maleic anhydride, said reduction in acid number is 42% and said other copolymerizable monomers are methyl methacrylate, ethyl acrylate and styrene.

Claim 16

Copolymer composition comprising an organic solvent, copolymers according to claim 12 and, if necessary, pigments.

Claim 17

Copolymer composition comprising an organic solvent, copolymers according to claim 13 and, if necessary, pigments.

Claim 18

Copolymer comprising the material obtained by drying the copolymer of claim 12 at a temperature of from room temperature to 160° C.