GB572919A - Soft synthetic rubberlike masses - Google Patents
Soft synthetic rubberlike massesInfo
- Publication number
- GB572919A GB572919A GB5794/42A GB579442A GB572919A GB 572919 A GB572919 A GB 572919A GB 5794/42 A GB5794/42 A GB 5794/42A GB 579442 A GB579442 A GB 579442A GB 572919 A GB572919 A GB 572919A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butadiene
- styrene
- benzene
- hydrocarbon
- per cent
- 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 butadiene-1 : 3 hydrocarbon or a halogen derivative thereof and a vinyl benzene are copolymerized in the presence of a minor proportion, e.g. 0.5 per cent to 5 per cent of a drying oil, e.g. tung, perilla, linseed or oiticica oils. The butadiene hydrocarbon may be butadiene itself, isoprene, dimethyl butadiene or chlor-butadiene. The vinyl benzenes are those described in U.S.A. Specification 1,938,731, e.g. styrene itself, divinyl benzene and a -methyl styrene. The polymerization may be conducted in aqueous emulsion containing a stabilizing agent, a catalyst and a promoter. In an example, water, sodium perborate, decyl benzene sodium sulphonate, styrene, benzoyl peroxide, butadiene, carbon tetrachloride and tung oil were charged into a rotating iron autoclave and heated at 70 DEG C. for 3 days, after which the emulsion was coagulated by addition of alcohol. A vulcanizable composition may be prepared from the product by the addition of zinc oxide, whiting, sulphur, dibenzothiazyl-thiol-dimethylurea, diphenyl-guanidine and stearic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US572279XA | 1941-05-01 | 1941-05-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB572919A true GB572919A (en) | 1945-10-30 |
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 After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB376/44A Expired GB572279A (en) | 1941-05-01 | 1942-04-29 | Soft synthetic rubberlike masses |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB572919A (en) |
Cited By (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
Cited By (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 |
Also Published As
Publication number | Publication date |
---|---|
GB572279A (en) | 1945-10-01 |
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