Foamable polyolefin composition and method for manufacturing foamed polyolefin

Claim 3

A method for manufacturing foamed polyolefin according to claim 1 wherein 0.01 to 3 parts by weight of the crosslinking agent, 0.1 to 30 parts by weight of the blowing agent, and 0.01 to 2 parts by weight of the gas trapping agent are added to 100 parts by weight of the polyolefin.

Claim 4

A method for manufacturing foamed polyolefin according to claim 2 wherein 0.01 to 1.0 part by weight of the gas trapping agent is added to 100 parts by weight of the polyolefin.

Claim 5

A method for manufacturing foamed polyolefin according to claim 2 wherein 0.01 to 0.5 part by weight of the gas trapping agent to added to 100 parts by weight of the polyolefin.

Claim 6

A method for manufacturing foamed polyolefin according to claim 1 wherein the blowing agent evolves gas in a volume of not more than 2 cc per one gram of the blowing agent and not more than 35 cc per one gram of the blowing agent in 2 and 10 minutes, respectively, after heating to 180°C begins in the thermal decomposition test.

Claim 7

A method for manufacturing foamed polyolefin according to claim 1 wherein the heating of the shaped mixture is carried out under normal pressure.

Claim 8

A method for manufacturing foamed polyolefin according to claim 1 wherein the mixture is shaped into sheet form and thereafter heated for forming on a wire-net in a hot-air heating oven.

Claim 9

The method of claim 1 wherein said organic peroxide is selected from the group consisting of dicumyl peroxide; di-tert. butyl peroxide; 1,3-bis (tert. butyl peroxyidopropyl) benzene; 2,5-dimethyl-2,5-di (tert. butylperoxy) hexane and 2,5-dimethyl-2,5-di(tert. butylperoxy) hexyne-3.

Claim 10

The method of claim 1 wherein said azide compound is 1,9-nonane-bis-sulfonazide or 1,7-heptane-bis-sulfonazide.

Claim 11

The method of claim 1 wherein said cross-linking agent is silyl peroxide.

Claim 12

The method of claim 1 wherein said blowing agent is selected from the group consisting of azodicarbonamide, dinitrosopentamethylene tetramine, barium azodicarboxylate, hydroazodicarbonamide, p-toluene sulfonyl semicarbazide and trihydrazine triazine.

Claim 13

The method of claim 1 wherein said ethylene copolymer is selected from the group consisting of ethylenebutene copolymer, ethylene-propylene copolymer and ethylene-vinyl acetate copolymer, said copolymers being composed mainly of ethylene.

Claim 14

A foamable polyolefin composition comprising the following ingredients in the parts by weight specified: a. 100 parts polyolefin selected from the group consisting of ethylene homopolymer, ethylene copolymer, propylene homopolymer and propylene copolymer, said copolymers being composed mostly of said olefin, b. 0.01 to 3 parts of cross-linking agent selected from the group consisting of organic peroxides, azide compounds and silicon-containing peroxides, c. 0.1 to 30 parts of blowing agent which decomposes at a temperature higher than the decomposition temperature of said cross-linking agent to evolve gas in a volume of not more than 2cc per gram of the blowing agent in 2 minutes after heating to 180°C begins in the thermal decomposition test, and d. 0.01 to 2 parts of a gas trapping agent selected from the group consisting of diallyl cyanurate, diallyl isocyanurate, triallyl cyanurate and triallyl isocyanurate acrylic or methacrylic acid with a polyol or polyoxy-benzene containing at least two acrylate or methacrylate groups, 1, 2-polybutadiene and triallyl phosphate.

Claim 15

A foamable polyolefin composition comprising the following ingredients in the parts by weight specified: a. 100 parts polyolefin selected from the group consisting of ethylene homopolymer, ethylene copolymer, propylene homopolymer and propylene copolymer, said copolymers being composed mostly of said olefin, b. 0.01 to 3 parts of cross-linking agent selected from the group consisting of organic peroxides, azide compounds and silicon-containing peroxides, c. 0.1 to 30 parts of blowing agent which decomposes at a temperature higher than the decomposition temperature of said cross-linking agent to evolve gas in a volume of not more than 2cc per gram of the blowing agent in 2 minutes after heating to 180°C begins in the thermal decomposition test, and d. 0.01 to 2 parts of a gas trapping agent selected from the group consisting of diallyl cyanurate, diallyl isocyanurate, triallyl cyanurate and triallyl isocyanurate acrylic or methacrylic acid with a polyol or polyoxy-benzene containing at least two acrylate or methacrylate groups, 1, 2-polybutadiene and triallyl phosphate.

Claim 16

A foamable polyolefin composition according to claim 13 wherein 0.01 to 1.0 part by weight of the gas trapping agent is present on the basis of 100 parts by weight of the polyolefin.

Claim 17

A foamable polyolefin composition according to claim 13 wherein 0.01 to 0.5 part by weight of the gas trapping agent is present on the basis of 100 parts by weight of the polyolefin.

Claim 18

A foamable polyolefin composition according to claim 13 wherein the blowing agent evolves gas in a volume of not more than 2 cc per one gram of the blowing agent and not more than 35 cc per one gram of the blowing agent in 2 and 10 minutes respectively after heating to 180°C begins in the thermal decomposition test.

Claim 19

A foamable polyolefin composition according to claim 13 which comprises 100 parts by weight of a low-density polyethylene, 0.2 to 0.8 part by weight of an organic peroxide as crosslinking agent, 0.1 to 30 parts by weight of a blowing agent evolving gas in a volume of not more than 2 cc per one gram of the blowing agent and not more than 35 cc per one gram of the blowing agent in 2 and 10 minutes respectively after heating to 180°C begins in the thermal decomposition test, and 0.3 to 0.8 part by weight of a gas trapping agent selected from the group consisting of triallyl cyanurate and triallyl isocyanurate.