GB830791A - Sulphur-vulcanizable rubber compositions - Google Patents

Sulphur-vulcanizable rubber compositions

Info

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
Application number
GB3847156A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bridgestone Firestone Inc
Original Assignee
Firestone Tire and Rubber Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Firestone Tire and Rubber Co filed Critical Firestone Tire and Rubber Co
Priority to GB3847156A priority Critical patent/GB830791A/en
Publication of GB830791A publication Critical patent/GB830791A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/43Compounds 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.
GB3847156A 1956-12-17 1956-12-17 Sulphur-vulcanizable rubber compositions Expired GB830791A (en)

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)

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