Polyetherene-polyacrylic polymerizable compositions

Claim 2

A composition of matter comprising: A. a polyetherene represented by the structure: ##STR5## where R 1 is a radical of molecular weight less than about 2000 obtained by removal of active hydrogen from an active hydrogen compound selected from the group consisting of water, alcohols, thiols, carboxylic acids, carboxylic amides and amines, where the functionality of R 1 is n and is in the range of 1 to 10, where the E units are represented by the structure ##STR6## and are derived from allyl glycidyl ether, where R 2 is selected from the group consisting of hydrogen and C 2 to C 10 organic radicals, where the product of m and n is at least 4 and not more than about 60 and where the allyloxy equivalent of the polyetherene is less than about 250; B. a non-air-curing polyacrylyl monomer represented by the structure: ##STR7## where R 3 is selected from the group consisting of H, methyl or ethyl, p is an integer in the range of 2 to 10, and R 4 is the residue of a polyol, a polycarboxylic acid, a polyamine, a polyepoxide or a polyisocyanate of molecular weight less than about 2000, containing a hydrocarbon, polyester, polyamide, polyether or polyurethane backbone; and C. a metallic drier: wherein the weight ratio of polyetherene to non-air-curing polyacrylyl monomer is in the range of from 1:19 to 1:1.

Claim 3

The composition of claim 1 wherein the allyloxy equivalent is less than about 150.

Claim 4

The composition of claim 1 wherein the weight ratio of polyetherene to non-air-curing ethylenically unsaturated monomer is in the range of 1:9 to 1:2.

Claim 5

The composition of claim 1 wherein R 1 is hydroxyl, or the radical obtained from a monohydric or polyhydric alcohol, R 2 is hydrogen, the product of m and n is less than about 40 and the allyloxy equivalent is less than about 120.

Claim 6

The composition of claim 1 wherein the radicals R 1 and R 4 are both hydrocarbon or polyester or polyamide or polyether or polyurethane.

Claim 7

The composition of claim 1 wherein the radicals R 1 and R 4 are both neopentyl glycol polyester.

Claim 8

The composition of claim 1 wherein the non-air-curing polyacrylyl monomer contains up to 50 weight percent of a mono-ethylenically unsaturated monomer.

Claim 9

The composition of claim 1 wherein the non-air-curing polyacrylyl monomer contains from about 0.5 to about 10 weight percent of acrylic acid or methacrylic acid.

Claim 10

The composition of claim 1 containing from 0.1 to 1% by weight of the metallic drier.

Claim 11

The composition of claim 1 containing up to 5% by weight of a free radical initiator.

Claim 12

The composition of claim 4 containing from 0.1 to 1% by weight of the metallic drier.

Claim 13

The composition of claim 4 containing up to 5% by weight of a free radical initiator.

Claim 14

A process of polymerizing a composition comprising a polyetherene and a non-air-curing polyacrylyl monomer which comprises adding up to 1% of a metal drier and exposing the composition to an oxygen containing atmosphere at a temperature in the range of about 25° to about 120° C.; wherein the polyetherene is represented by the structure: ##STR8## wherein R 1 is a radical of molecular weight less than about 2000 obtained by removal of active hydrogen from an active hydrogen compound selected from the group consisting of water, alcohols, thiols, carboxylic acids, carboxylic amides and amines, where the functionality of R 1 is n and is in the range of 1 to 10, where the E units are represented by the structure ##STR9## and are derived from allyl glycidyl ether, where R 2 is selected from the group consisting of hydrogen and C 1 to C 10 organic radicals, where the product of m and n is at least 4 and not more than about 60 and where the allyloxy equivalent of the polyetherene is less than about 250; wherein the non-air-curing ethylenically unsaturated monomer is represented by the structure: ##STR10## where R 3 is selected from the group consisting of H, methyl or ethyl, p is an integer in the range of 2 to 10, and R 4 is the residue of a polyol, a polycarboxylic acid, a polyamine, a polyepoxide or a polyisocyanate of molecular weight less than about 2000, containing a hydrocarbon, polyester, polyamide, polyether or polyurethane backbone; and wherein the weight ratio of polyetherene to non-air-curing ethylenically unsaturated monomer is in the range of from 1:19 to 1:1.

Claim 15

A process of polymerizing a composition comprising a polyetherene and a non-air-curing polyacrylyl monomer which comprises adding up to 1% of a metal drier and exposing the composition to an oxygen containing atmosphere at a temperature in the range of about 25° to about 120° C.; wherein the polyetherene is represented by the structure: ##STR8## wherein R 1 is a radical of molecular weight less than about 2000 obtained by removal of active hydrogen from an active hydrogen compound selected from the group consisting of water, alcohols, thiols, carboxylic acids, carboxylic amides and amines, where the functionality of R 1 is n and is in the range of 1 to 10, where the E units are represented by the structure ##STR9## and are derived from allyl glycidyl ether, where R 2 is selected from the group consisting of hydrogen and C 1 to C 10 organic radicals, where the product of m and n is at least 4 and not more than about 60 and where the allyloxy equivalent of the polyetherene is less than about 250; wherein the non-air-curing ethylenically unsaturated monomer is represented by the structure: ##STR10## where R 3 is selected from the group consisting of H, methyl or ethyl, p is an integer in the range of 2 to 10, and R 4 is the residue of a polyol, a polycarboxylic acid, a polyamine, a polyepoxide or a polyisocyanate of molecular weight less than about 2000, containing a hydrocarbon, polyester, polyamide, polyether or polyurethane backbone; and wherein the weight ratio of polyetherene to non-air-curing ethylenically unsaturated monomer is in the range of from 1:19 to 1:1.

Claim 16

The process of claim 13 wherein the allyloxy equivalent is less than about 150.

Claim 17

The process of claim 13 wherein the weight ratio of polyetherene to non-air-curing ethylenically unsaturated monomer is in the range of 1:9 to 1:2.

Claim 18

The process of claim 13 wherein R 1 is hydroxyl, or the radical obtained from a monohydric or polyhydric alcohol, R 2 is hydrogen, the product of m and n is less than about 40, and the allyloxy equivalent is less than about 120.

Claim 19

The process of claim 13 wherein the radicals R 1 and R 4 are both hydrocarbon or polyester or polyamide or polyether or polyurethane.

Claim 20

The process of claim 13 wherein the radicals R 1 and R 4 are both neopentyl glycol polyester.

Claim 21

The process of claim 13 wherein the non-air-curing polyacrylyl monomer contains up to 50 weight percent of a mono-ethylenically unsaturated monomer.

Claim 22

The process of claim 13 wherein the non-air-curing polyacrylyl monomer contains from about 0.5 to about 10 weight percent of acrylic or methacrylic acid.

Claim 23

The process of claim 13 wherein up to 5% by weight of a free radical initiator is added to the polymerizable composition.

Claim 24

The process of claim 16 wherein up to 5% by weight of a free radical initiator is added to the polymerizable composition.

Claim 25

The polymerized product of claim 1.

Claim 26

The polymerized product of claim 4.

Claim 27

The polymerized product of claim 5.

Claim 28

The polymerized product of claim 6.

Claim 29

The polymerized product of claim 7.

Claim 30

The polymerized product of claim 8.

Claim 31

The composition of claim 1 containing from 0.01 to 5% by weight of an organic hydroperoxide.

Claim 32

The process of claim 13 wherein from 0.01 to 5% by weight of an organic hydroperoxide is added to the polymerizable composition.

Claim 33

The polymerized product of claim 29.