GB642050A - Improvements in or relating to isobutylene copolymers - Google Patents
Improvements in or relating to isobutylene copolymersInfo
- Publication number
- GB642050A GB642050A GB8880/48A GB888048A GB642050A GB 642050 A GB642050 A GB 642050A GB 8880/48 A GB8880/48 A GB 8880/48A GB 888048 A GB888048 A GB 888048A GB 642050 A GB642050 A GB 642050A
- Authority
- GB
- United Kingdom
- Prior art keywords
- divinyl
- copolymers
- butadiene
- specified
- methyl
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/08—Butenes
- C08F210/10—Isobutene
- C08F210/12—Isobutene with conjugated diolefins, e.g. butyl rubber
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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
Copolymers are made by copolymerizing a mixture of a major proportion of isobutylene, a minor proportion of a multi-olefin having from 4 to 14 carbon atoms per molecule and from 0.1 to 5 per cent by weight of the total mixture, of a divinyl aromatic compound at a temperature between - 40 DEG and - 160 DEG C. in the presence of a Friedel-Craft catalyst. Specified multi-olefins are butadiene, piperylene, dimethyl butadiene, myrcene, allo-ocymene, 2-methyl-3-butyl butadiene-1,3 and 2-methyl-4-nonyl butadiene-1,3. Specified divinyl aromatic compounds are ortho-, para- and metadivinyl benzene, divinyl-naphthyl compounds, divinyl-toluenes, divinyl-xylenes, and di-isopropenyl benzene. The Friedel-Crafts catalyst is employed as a solution in a low-freezing non-complex-forming solvent. The reduced temperature may be obtained by adding to the polymerization mixture liquid propane, ethane, ethylene, fluorochlor organic compounds or solid carbon dioxide. The polymerization may be effected in bulk or in the presence of a diluent, e.g. methyl or ethyl chloride, methylene or ethylene dichloride, chloroform, ethyl trichloride or carbon bisulphide. The diluents may be solvents for the catalyst; other specified solvents are sulphuryl chloride, heptane and hexanes. Specified catalysts are aluminium chloride or bromide, titanium tetrachloride and boron trifluoride. The copolymers may be compounded with plasticizers, e.g. hydrocarbons, dioctylphthalate; curing agents, e.g. sulphur, paraquinone dioxime, or dinitroso benzene; zinc oxide or stearic acid, carbon black, tetramethyl thiuram disulphide, 2-mercapto-benzothiazole, and copolymers of isobutylene and a multi-olefin. The copolymers may be extruded and made into inner tubes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US642050XA | 1947-06-06 | 1947-06-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB642050A true GB642050A (en) | 1950-08-23 |
Family
ID=22054273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8880/48A Expired GB642050A (en) | 1947-06-06 | 1948-03-25 | Improvements in or relating to isobutylene copolymers |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE815844C (en) |
GB (1) | GB642050A (en) |
NL (1) | NL69305C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2781334A (en) * | 1952-05-01 | 1957-02-12 | Exxon Research Engineering Co | Divinyl aromatic modified isoolefinmultiolefin copolymers |
US2906725A (en) * | 1955-10-12 | 1959-09-29 | Exxon Research Engineering Co | Synthetic polymer compositions with improved physical properties from mixtures of rubbery polymers |
EP1505083A1 (en) * | 2003-08-05 | 2005-02-09 | Bayer Inc. | Method of improving reversion resistance |
EP1566392A1 (en) * | 2004-02-23 | 2005-08-24 | Lanxess Inc. | Butyl-type rubber with high hardness |
-
0
- NL NL69305D patent/NL69305C/xx active
-
1948
- 1948-03-25 GB GB8880/48A patent/GB642050A/en not_active Expired
-
1950
- 1950-05-03 DE DEST997A patent/DE815844C/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2781334A (en) * | 1952-05-01 | 1957-02-12 | Exxon Research Engineering Co | Divinyl aromatic modified isoolefinmultiolefin copolymers |
US2906725A (en) * | 1955-10-12 | 1959-09-29 | Exxon Research Engineering Co | Synthetic polymer compositions with improved physical properties from mixtures of rubbery polymers |
EP1505083A1 (en) * | 2003-08-05 | 2005-02-09 | Bayer Inc. | Method of improving reversion resistance |
EP1566392A1 (en) * | 2004-02-23 | 2005-08-24 | Lanxess Inc. | Butyl-type rubber with high hardness |
Also Published As
Publication number | Publication date |
---|---|
DE815844C (en) | 1951-10-04 |
NL69305C (en) |
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