GB743353A - Polystyrene rubber compositions - Google Patents

Polystyrene rubber compositions

Info

Publication number
GB743353A
GB743353A GB1483853A GB1483853A GB743353A GB 743353 A GB743353 A GB 743353A GB 1483853 A GB1483853 A GB 1483853A GB 1483853 A GB1483853 A GB 1483853A GB 743353 A GB743353 A GB 743353A
Authority
GB
United Kingdom
Prior art keywords
rubber
polystyrene
parts
composition
vulcanizing
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
GB1483853A
Inventor
Stanley Maurice Ardley
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.)
British Resin Products Ltd
Original Assignee
British Resin Products 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 British Resin Products Ltd filed Critical British Resin Products Ltd
Priority to GB1483853A priority Critical patent/GB743353A/en
Publication of GB743353A publication Critical patent/GB743353A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00Compositions of unspecified rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene

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 vulcanized composition of polystyrene or copolymers thereof, with a major proportion of rubber and 5 to 25 parts per 100 parts of styrene of an ester plasticizer such as dibutyl and dioctyl phthalates and tricresyl phosphate is prepared by mixing part of the rubber with the other ingredients at an elevated temperature and compounding the product with more rubber and vulcanizing agents, and finally vulcanizing. The products, of increased hardness and elasticity, may be used for shoe soleing, flooring, extrusion, insulating and translucent materials.ALSO:An ester plasticizer such as dibutyl phthalate, dioctyl phthalate or tricresyl phosphate is incorporated in a mix of polystyrene and rubber to make them compatible, the mix containing a major proportion of rubber to allow of its being vulcanized and containing 5 to 25 parts by weight of ester to 100 parts of polystrene. The mix is preferably made by mixing polystyrene with the plasticizer and some of the rubber to give a homogeneous intermediate product containing 1 to 3 parts of polystyrene to 1 part of rubber, which is then mixed with the remainder of the rubber and the vulcanizing and compounding agents. The polystyrene may be wholly or in part replaced by a copolymer of styrene containing a major proportion of styrene units in its molecular structure. In an example the initial composition was, in parts by weight, pale crepe rubber 100, polystyrene 200, dibutyl phthalate 10. The rubber was masticated for 3 minutes at a temperature of 35-40 DEG C. and mixed with powdered polystyrene and plasticizer. The mixture was then heated to 150 DEG C. to gell the polystyrene and was further milled for 5 minutes. The resulting composition was then mixed with rubber and vulcanizing ingredients to give a final composition, in parts by weight, pale crepe rubber 90 or 80, polystyrene/rubber/composition 30 or 60, zinc oxides 5, sulphur 3, stearic acid 2, cyclohexyl benzthiazyl sulphonamide 1. An alternative method of preparing the intermediate composition and a further example using an initial composition of 100 parts crepe rubber, 100 parts polystyrene and 10 parts dibutyl phthalate, are given.
GB1483853A 1953-05-28 1953-05-28 Polystyrene rubber compositions Expired GB743353A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1483853A GB743353A (en) 1953-05-28 1953-05-28 Polystyrene rubber compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1483853A GB743353A (en) 1953-05-28 1953-05-28 Polystyrene rubber compositions

Publications (1)

Publication Number Publication Date
GB743353A true GB743353A (en) 1956-01-11

Family

ID=10048365

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1483853A Expired GB743353A (en) 1953-05-28 1953-05-28 Polystyrene rubber compositions

Country Status (1)

Country Link
GB (1) GB743353A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1211385B (en) * 1957-06-18 1966-02-24 Montedison Spa Process for vulcanizing elastomer mixtures

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1211385B (en) * 1957-06-18 1966-02-24 Montedison Spa Process for vulcanizing elastomer mixtures

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