GB830791A - Sulphur-vulcanizable rubber compositions - Google Patents
Sulphur-vulcanizable rubber compositionsInfo
- Publication number
- GB830791A GB830791A GB3847156A GB3847156A GB830791A GB 830791 A GB830791 A GB 830791A GB 3847156 A GB3847156 A GB 3847156A GB 3847156 A GB3847156 A GB 3847156A GB 830791 A GB830791 A GB 830791A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amine
- bis
- sulphur
- hexathio
- butadiene
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/43—Compounds containing sulfur bound to nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A hexathio-bis-secondary amine produced from a water-soluble secondary aliphatic or cycloaliphatic amine containing only carbon, hydrogen, and nitrogen, and further containing 2 to 12 inclusive carbon atoms per molecule of amine, is prepared from an initially produced amine di-, tri-, or tetra-sulphide by reaction with sulphur, or by reacting the amine with a sulphur chloride and sulphur in the presence of an alkali and in an aqueous medium. Specified amines for use as starting materials are dimethyl-, methylethyl-, diethyl-, di-n-propyl-, di-isopropyl-, dibutyl-, diamyl-, dihexyl-, dicyclopentyl-, and dicyclohexyl-amines. A slightly soluble amine is dissolved in water for the reaction, and the amount dissolved may be increased by adding a chemically inert watermiscible organic liquid, e.g. dioxane-1,4. Examples describe the preparation of hexathiobis-dimethylamine and hexathio-bis-diethylamine.ALSO:A sulphur-vulcanizable natural or synthetic rubber composition containing no free sulphur contains 0.1 to 2 parts by weight per 100 parts rubber of a hexathio-bis-secondary amine produced from a water-soluble secondary aliphatic or cycloaliphatic amine containing only carbon, hydrogen and nitrogen and further containing 2 to 12 carbon atoms per molecule. The hexathio-bis-secondary amine is prepared from an initially produced amine di-, tri-, or tetrasulphide by reaction with sulphur, or by reacting the amine with a sulphur chloride and sulphur in the presence of an alkali and in an aqueous medium. Specified amines for use as starting materials are dimethyl-, methylethyl-, diethyl-, di-n-propyl-, di-isopropyl-, dibutyl-, diamyl-, dihexyl-, dicyclopentyl-, and dicyclohexyl-amines. The vulcanizable composition may contain a known accelerator, e.g. cyclohexyl benzothiazyl sulphenamide, mercaptobenzothiazole, dithio - bis - benzothiazole, diphenyl guanidine, an aldehyde amine, a dithiocarbamate, a thiuram sulphide, or a xanthate. The specified synthetic rubbers are copolymers of butadiene and styrene or acrylontrile, or of isobutene and isoprene or butadiene, polybutadienes, and polyisoprenes. Reclaimed natural and/or synthetic rubber may also be used in the composition. The hexathio-bis-secondary amine may be incorporated in the composition by milling or by adding an aqueous dispersion thereof to a latex of natural and/or synthetic rubber. Alternatively it may be added directly or in a compatible solvent to a rubber solution to be used as a cement. Examples are specified of vulcanizable compositions including (a) natural rubber and hexa-thio-bis-dimethylamine, (b) butadiene-styrene copolymer and hexa-thio-bis-dimethylamine, and (c) butadiene-styrene copolymer and hexa-thio-bis-diethylamine, respectively.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3847156A GB830791A (en) | 1956-12-17 | 1956-12-17 | Sulphur-vulcanizable rubber compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3847156A GB830791A (en) | 1956-12-17 | 1956-12-17 | Sulphur-vulcanizable rubber compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB830791A true GB830791A (en) | 1960-03-23 |
Family
ID=10403667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3847156A Expired GB830791A (en) | 1956-12-17 | 1956-12-17 | Sulphur-vulcanizable rubber compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB830791A (en) |
-
1956
- 1956-12-17 GB GB3847156A patent/GB830791A/en not_active Expired
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