Process for preparation of polyolefin graft copolymers

Claim 2

A process for preparing a polyolefin graft copolymer, which comprises subjecting a copolymer selected from the group consisting of copolymers of ethylene with diolefins and copolymers of C 3 to C 8 α-olefins with diolefins and containing 2 to 40 double bond per 1000 monomeric units therein and a monomer radical graft-copolymerizable onto said copolymer to a suspension graft copolymerization in the presence of a radical initiator in an inert organic solvent capable of dissolving said radical-polymerizable monomer but incapable of dissolving said graft copolymer and of reacting therewith, at a temperature at which said copolymer is not melted.

Claim 3

The process of claim 1 wherein said radical graft-copolymerizable monomer is a vinyl monomer selected from the group consisting of acrylic acid, C 1 to C 8 alkyl esters thereof, methacrylic acid, C 1 to C 8 alkyl esters thereof, glycidyl acrylate, glycidyl methacrylate, acrylamide, methacrylamide, N,N-dimethyl acrylamide, N,N-dimethyl methacrylamide, acrylonitrile, methacrylonitrile and styrene.

Claim 4

The process of claim 1 wherein said radical graft-copolymerizable monomer is a carboxylic acid or its derivative selected from the group consisting of maleic acid, maleic anhydride, C 1 to C 8 alkyl monoesters of maleic acid, C 1 to C 8 alkyl diesters of maleic acid, maleimide, maleic acid monoamide, maleic acid diamide, citraconic anhydride and 5-norbornene-2,3-dicarboxylic anhydride.

Claim 5

The process of claim 1 wherein said inert organic solvent is a member selected from the group consisting of aromatic hydrocarbons, halogenated aromatic hydrocarbons, aliphatic carboxylic acids, aliphatic carboxylic anhydrides, C 1 to C 8 alkyl esters of aliphatic carboxylic acids and alicyclic hydrocarbons.

Claim 6

The process of claim 1 wherein said diolefin is butadiene.

Claim 7

The process of claim 1 wherein said copolymer is obtained by copolymerizing an α-olefin with a diolefin using a catalyst composed of an organoaluminum compound and a halogen compound of a transition metal supported on a carrier of a magnesium-containing compound.

Claim 8

The process of claim 1 wherein said copolymer contains from 4-40 double bonds per 1,000 monomeric units.

Claim 9

The process of claim 1 wherein said copolymer is selected from copolymers of α-olefins with 3 to 8 carbon atoms with diolefins wherein said α-olefins are selected from the group consisting of propylene, butene-1 and 4-methyl-1-pentene, and said diolefin is butadiene.

Claim 10

The process of claim 1 wherein said copolymer has a viscosity average molecular weight of about 10,000 to about 1,000,000, an apparent density of about 0.20 to about 0.32 g/cm 3 , and a melt index of about 3 to about 5.

Claim 11

The process of claim 1 wherein said radical graft-copolymerizable monomer is a vinyl monomer selected from acrylic acid, C 1 to C 8 alkyl esters thereof, methacrylic acid, C 1 to C 8 alkyl esters thereof, glycidyl acrylate, glycidyl methacrylate, acrylamide, methacrylamide, N,N-dimethyl acrylamide and N,N-dimethyl methacrylamide, or a carboxylic acid or its derivative selected from the group consisting of maleic anhydride, citraconic anhydride and 5-norbornene-2,3-dicarboxylic anhydride.

Claim 12

The process of claim 4 wherein said inert organic solvent is selected from the group consisting of glacial acetic acid, acetic anhydride, methyl acetate, ethyl acetate, butyl acetate, benzene, toluene, xylene, chlorobenzene, cyclohexane, methyl cyclohexane, and chlorocyclohexane.

Claim 13

The process of claim 1 wherein said radical initiator is an organic peroxide selected from the group consisting of diisopropyl peroxide, ditertiary butyl peroxide, tertiary butyl hydroperoxide, dicumyl peroxide, dibenzoyl peroxide, cumyl hydroperoxide, tertiary butyl peracetate, tertiary butyl peroxy laurate, tertiary butyl perbenzoate, ditertiary butyl perphthalate, methylethylketone peroxide, octanol peroxide, and diisopropyl peroxycarbonate.

Claim 14

The process of claim 1 wherein said radical initiator is an azonitrile selected from the group consisting of azobisisopropionitrile and azobisisobutyronitrile.

Claim 15

The process of claim 12 wherein the amount of said radical initiator is about 0.02 to about 5% by weight based on the starting olefin copolymer.

Claim 16

The process of claim 13 wherein the amount of said radical initiator is about 0.02 to about 5% by weight based on the starting olefin copolymer.

Claim 17

The process for preparing a polyolefin graft copolymer according to claim 1 which comprises subjecting about 100 parts by weight of said copolymer with about 1 to about 100 parts by weight of said monomer radical graft-copolymerizable onto said copolymer to a suspension graft copolymerization in the presence of a radical initiator in about 200 to about 500 parts by volume per 100 parts by weight of the starting copolymer of said inert organic solvent at a temperature of about 60° to about 90° C.

Claim 18

The process of claim 16 wherein said diolefin is butadiene, said α-olefins with 3 to 8 carbon atoms are selected from the group consisting of propylene, butene-1 and 4-methyl-1-pentene, said copolymer contains 4-40 double bonds per 1,000 monomeric units, and has a viscosity average molecular weight of about 10,000 to about 1,000,000, and an apparent density of about 0.20 to about 0.32 g/cm 3 , and a melt index of about 3 to about 5, said monomer radical graft-copolymerizable onto said copolymer is a vinyl monomer selected from the group consisting of acrylic acid, C 1 to C 8 alkyl esters thereof, methacrylic acid, C 1 to C 8 alkyl esters thereof, glycidyl acrylate, glycidyl methacrylate, acrylamide, methacrylamide, N,N-dimethyl acrylamide and N,N-dimethyl methacrylamide, or a carboxylic acid or its derivative selected from the group consisting of maleic anhydride, citraconic anhydride and 5-norbornene-2,3-dicarboxylic anhydride, said inert organic solvent is selected from the group consisting of glacial acetic acid, acetic anhydride, methyl acetate, ethyl acetate, butyl acetate, benzene, toluene, xylene, chlorobenzene, cyclohexane, methyl cyclohexane, and chlorocyclohexane, and the radical initiator is an organic peroxide selected from the group consisting of diisopropyl peroxide, ditertiary butyl peroxide, tertiary butyl hydroperoxide, dicumyl peroxide, dibenzoyl peroxide, cumyl hydroperoxide, tertiary butyl peracetate, tertiary butyl peroxy laurate, tertiary butyl perbenzoate, ditertiary butyl perphthalate, methylethylketone peroxide, octanol peroxide, and diisopropyl peroxycarbonate or an azonitrile selected from the group consisting of azobisisopropionitrile and azobisisobutyronitrile, and is used in an amount of from about 0.02 to about 5% by weight, based on the starting olefin copolymer.