GB497841A - Improvements in the manufacture and production of interpolymerisation products - Google Patents
Improvements in the manufacture and production of interpolymerisation productsInfo
- Publication number
- GB497841A GB497841A GB1760137A GB1760137A GB497841A GB 497841 A GB497841 A GB 497841A GB 1760137 A GB1760137 A GB 1760137A GB 1760137 A GB1760137 A GB 1760137A GB 497841 A GB497841 A GB 497841A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethinyl
- vinyl
- heated
- carbinol
- beta
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A rubber-like product is obtained by treating a mixture of butadiene, or an alkyl, aryl, or chlorsubstitution product thereof, and a vinyl ethinyl carbinol. Specified ingredients are butadiene, isoprene, 2.3-dimethylbutadiene, 2-phenylbutadiene, monochlor- and dichlor-butadienes, vinyl ethinyl dimethyl carbinol, 1-vinyl-ethinyl-cyclohexane-1-ol, vinyl ethinyl ethyl methyl carbinol and vinyl ethinyl-di-isopropyl carbinol. The polymerization may be carried out by heating the mixture of the monomers in the presence of per-compounds, and if desired under pressure, or in aqueous emulsion. The interpolymers are practically insoluble in organic solvents, may be mixed with fillers or dyestuffs, and may be vulcanized, after the addition of vulcanizing agents, vulcanization accelerators and, if desired, agents protecting against ageing, to form articles similar to soft or hard rubber. In examples: (1) butadiene and vinyl ethinyl dimethyl carbinol are heated in a closed vessel in the presence of benzoyl peroxide; (2) beta-chlorbutadiene and vinyl ethinyl dimethyl carbinol are heated in a closed vessel with benzoyl peroxide; the interpolymer produced is mixed with colophony, a softener obtained by extracting lignite low temperature carbonization tar with ethyl alcohol, gas carbon, zinc oxide, magnesium oxide, sulphur and N-phenyl-, beta-naphthylamine and treated to form a product resembling hard or soft rubber depending upon the proportions of the ingredients used to form the interpolymer; (3) beta-chlorbutadiene and vinyl ethinyl dimethyl carbinol are emulsified with water, ammonia, oleic acid and benzoyl peroxide, and the emulsion heated; the interpolymer is heated in the mixture described in example 2 to yield a product similar to hard rubber; (4) beta-chlorbutadiene and 1-vinyl-ethinyl-cyclohexane-1-ol are heated in a closed vessel with benzoyl peroxide; and (5) butadiene and vinyl ethinyl dimethyl carbinol are emulsified with an aqueous solution of sodium oleate, ammonium persulphate is added, and the mixture heated in a closed vessel; a small amount of phenyl beta-naphthyl amine dissolved in benzene or dispersed in water is then added and the interpolymer coagulated by the addition of sodium chloride and acetic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1760137A GB497841A (en) | 1937-06-24 | 1937-06-24 | Improvements in the manufacture and production of interpolymerisation products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1760137A GB497841A (en) | 1937-06-24 | 1937-06-24 | Improvements in the manufacture and production of interpolymerisation products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB497841A true GB497841A (en) | 1938-12-28 |
Family
ID=10098008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1760137A Expired GB497841A (en) | 1937-06-24 | 1937-06-24 | Improvements in the manufacture and production of interpolymerisation products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB497841A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2424182A (en) * | 1944-02-12 | 1947-07-15 | Du Pont | Synthetic rubberlike butadiene-acrylonitrile-aliphatic vinylethinyl carbinol material |
US2426560A (en) * | 1944-04-18 | 1947-08-26 | Du Pont | Copolymers of fluoro-1,3-butadiene and an alkenylethinyl carbinol |
US2520711A (en) * | 1947-03-11 | 1950-08-29 | Du Pont | Composition of crotyl cellulose and compatible butadiene copolymer |
-
1937
- 1937-06-24 GB GB1760137A patent/GB497841A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2424182A (en) * | 1944-02-12 | 1947-07-15 | Du Pont | Synthetic rubberlike butadiene-acrylonitrile-aliphatic vinylethinyl carbinol material |
US2426560A (en) * | 1944-04-18 | 1947-08-26 | Du Pont | Copolymers of fluoro-1,3-butadiene and an alkenylethinyl carbinol |
US2520711A (en) * | 1947-03-11 | 1950-08-29 | Du Pont | Composition of crotyl cellulose and compatible butadiene copolymer |
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