GB420386A - Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins - Google Patents

Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins

Info

Publication number
GB420386A
GB420386A GB1837333A GB1837333A GB420386A GB 420386 A GB420386 A GB 420386A GB 1837333 A GB1837333 A GB 1837333A GB 1837333 A GB1837333 A GB 1837333A GB 420386 A GB420386 A GB 420386A
Authority
GB
United Kingdom
Prior art keywords
mixture
plastic
polysulphide
solution
aldehyde
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
GB1837333A
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.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber Co Ltd
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 Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Priority to GB1837333A priority Critical patent/GB420386A/en
Publication of GB420386A publication Critical patent/GB420386A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/14Polysulfides
    • C08G75/16Polysulfides by polycondensation of organic compounds with inorganic polysulfides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/38Block or graft polymers prepared by polycondensation of aldehydes or ketones onto macromolecular compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Plastic compositions of organic polysulphide plastics, of the kind obtained by the reaction of reactive halogenized hydrocarbons with a polysulphide or thiosulphate of an alkali or alkaline earth metal, and synthetic resins of the phenol-aldehyde, polyhydric alcohol-polycarboxylic acid and aldehyde-arylamine types are manufactured by dissolving the organic polysulphide plastic in one of the parent substances for the resin and completing the formation of the latter after the addition of the remaining parent substance or substances. The process may be carried out by dissolving the plastic in an aromatic hydroxy compound or compounds, e.g. phenol, and reacting the solution with an aldehyde, e.g. formaldehyde or acetaldehyde, or a mixture of aldehydes, the aldehyde being, if desired, generated in situ; or by dissolving the plastic in a polybasic acid or anhydride or a mixture thereof, e.g. phthalic anhydride or a mixture thereof with an aliphatic dicarboxylic acid, and treating the solution with one or more polyhydric alcohols, e.g. glycerol or a mixture of glycerol and glycol; or by dissolving the plastic in an aromatic amine, e.g. aniline, or a mixture of amines, and reacting the solution with one or more aldehydes, e.g. acetaldehyde. The polysulphide plastics may be prepared by reacting di- or polyhalogenated saturated or unsaturated hydrocarbons with a polysulphide or thiosulphate of an alkali or alkaline earth metal, and in the latter case removing the metallic radicle by hydrolysis, oxidation or reduction. The products are suitable for addition to rubber for improving its impermeability and oil- and solvent-resistance. In examples: (1) diethylene tetrasulphide (obtained by refluxing a mixture of an alcoholic solution of ethylene dichloride and aqueous sodium thiosulphate and heating the product with hydrogen peroxide) is dissolved in molten phenol and the solution is treated with formalin in the presence of hydrochloric acid; the product may be added to a rubber mix containing sulphur, zinc oxide, mercaptobenzthiazole, stearic acid and carbon black, which is then vulcanized; (2) diethylene tetrasulphide is dissolved in molten phthalic anhydride and the mixture as heated with glycerol and succinic acid; (3) diethylene tetrasulphide is dissolved in molten phenol and the solution is heated with paracetaldehyde in the presence of sulphuric acid; (4) diethylene tetrasulphide is dissolved in hot aniline and the mixture is refluxed with aqueous formaldehyde.ALSO:The impermeability and oil- and solventresistance of rubber are improved by the addition of plastic compositions of organic polysulphide plastics, of the kind obtained by the reaction of reactive halogenized hydrocarbons with a polysulphide or thiosulphate of an alkali or alkaline earth metal, and synthetic resins of the phenol-aldehyde, polyhydric alcohol-polycarboxylic acid and aldehyde-arylamine types, obtained by dissolving the organic polysulphide plastic in one of the parent substances for the resin and completing the formation of the latter after the addition of the remaining parent substance or substances. In an example, a plastic composition produced by dissolving diethylene tetrasulphide in molten phenol and treating the solution with formalin is added to a rubber mix containing sulphur, zinc oxide, mercaptobenzthiazole, stearic acid, and carbon black, which is then vulcanized.
GB1837333A 1933-06-28 1933-06-28 Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins Expired GB420386A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1837333A GB420386A (en) 1933-06-28 1933-06-28 Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1837333A GB420386A (en) 1933-06-28 1933-06-28 Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins

Publications (1)

Publication Number Publication Date
GB420386A true GB420386A (en) 1934-11-30

Family

ID=10111339

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1837333A Expired GB420386A (en) 1933-06-28 1933-06-28 Improvements in or relating to the production of compositions comprising organic polysulphide plastics and synthetic resins

Country Status (1)

Country Link
GB (1) GB420386A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2646415A (en) * 1948-02-11 1953-07-21 Reconstruction Finance Corp Copolymers of polythiols, phenols, and aldehydes
US4211687A (en) 1977-07-27 1980-07-08 Hooker Chemicals & Plastics Corp. Polymer blends with improved flame retardance
EP0055212A1 (en) * 1980-12-13 1982-06-30 Ciba-Geigy Ag Process for preparing dispersions which contain phenol resins, and their use as adhesives

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2646415A (en) * 1948-02-11 1953-07-21 Reconstruction Finance Corp Copolymers of polythiols, phenols, and aldehydes
US4211687A (en) 1977-07-27 1980-07-08 Hooker Chemicals & Plastics Corp. Polymer blends with improved flame retardance
EP0055212A1 (en) * 1980-12-13 1982-06-30 Ciba-Geigy Ag Process for preparing dispersions which contain phenol resins, and their use as adhesives

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