GB572279A - Soft synthetic rubberlike masses - Google Patents
Soft synthetic rubberlike massesInfo
- Publication number
- GB572279A GB572279A GB376/44A GB37644A GB572279A GB 572279 A GB572279 A GB 572279A GB 376/44 A GB376/44 A GB 376/44A GB 37644 A GB37644 A GB 37644A GB 572279 A GB572279 A GB 572279A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butadiene
- alcohol
- coagulated
- sulphur
- acrylonitrile
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/14—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
- C08F236/16—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen containing halogen
Abstract
A mixture of a butadiene-1,3 hydrocarbon or a halogen derivative thereof and a vinyl cyanide are polymerized in the presence of a minor proportion, e.g. 0.5 to 5 per cent of a drying oil, e.g. tung, linseed, perilla or oiticica oils. Specified components of the mixture are butadiene, isoprene, dimethyl butadiene or chlorobutadiene and acrylonitrile or methacrylonitrile. In examples: (1) butadiene, acrylonitrile, sodium perborate, tung oil, decylbenzene sodium sulphonate and carbon tetrachloride were emulsified in water and heated in a glasslined rocking autoclave at 70 DEG C. for 70 hours. A rubber-like mass was coagulated by alcohol and boiled in an aqueous solution of sodium bisulphite to destroy the catalyst, washed and dried. Compositions containing the copolymer, "Gastex" (Registered Trade Mark), zinc oxide, sulphur, cyclohexylamino - thio - benzthiazole, diphenyl guanidine, stearic acid and dibutyl phthalate were cured by heating; (2) a similar emulsion containing isoprene in place of butadiene and also benzoyl peroxide was heated at 55-60 DEG C. for 72 hours, coagulated with alcohol and the product washed with alcohol and acetone and finally with water. Compositions containing the copolymer, stearic acid, triphenyl phosphate, sulphur, zinc oxide, dibenzothiazyl thiol, dimethyl urea and diphenyl guanidine were similarly cured. U.S.A. Specification 1,973,000 is referred to.ALSO:A mixture of a butadiene-1,3 hydrocarbon or a halogen derivative thereof and a vinyl cyanide are polymerized in the presence of a minor proportion, e.g. 0.5 to 5 per cent, of a drying oil, e.g. tung, linseed, perilla or oiticica oils. Specified components of the mixture are butadiene, isoprene, dimethyl butadiene or chlorobutadiene and acrylonitrile or methacrylonitrile. In examples: (1) butadiene, acrylonitrile, sodium perborate, tung oil, decylbenzene sodium sulphonate and carbon tetrachloride were emulsified in water and heated in a glass-lined rocking autoclave at 70 DEG C. for 70 hours. A rubber-like mass was coagulated by alcohol and boiled in an aqueous solution of sodium bisulphite to destroy the catalyst, washed and dried. Compositions containing the copolymer, "Gastex" (Registered Trade Mark), zinc oxide, sulphur, cyclohexylamino-thio-benzthiazole, diphenyl guanidine, stearic acid and dibutyl phthalate were cured by heating; (2) a similar emulsion containing isoprene in place of butadiene and also benzoyl peroxide was heated at 55-60 DEG C. for 72 hours, coagulated with alcohol and the product washed with alcohol and acetone and finally with water. Compositions containing the copolymer, stearic acid, triphenyl phosphate, sulphur, zinc oxide, dibenzothiazyl thiol, dimethyl urea and diphenyl guanidine were similarly cured. U.S.A. Specification 1,973,000 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US572279XA | 1941-05-01 | 1941-05-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB572279A true GB572279A (en) | 1945-10-01 |
Family
ID=22009289
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5794/42A Expired GB572919A (en) | 1941-05-01 | 1942-04-29 | Soft synthetic rubberlike masses |
GB376/44A Expired GB572279A (en) | 1941-05-01 | 1942-04-29 | Soft synthetic rubberlike masses |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5794/42A Expired GB572919A (en) | 1941-05-01 | 1942-04-29 | Soft synthetic rubberlike masses |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB572919A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1077864B (en) * | 1953-01-14 | 1960-03-17 | Metallgesellschaft Ag | Process for the production of synthetic rubber vulcanizates or regenerates |
-
1942
- 1942-04-29 GB GB5794/42A patent/GB572919A/en not_active Expired
- 1942-04-29 GB GB376/44A patent/GB572279A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB572919A (en) | 1945-10-30 |
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