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GB1040287A - Improvements in or relating to the manufacture of synthetic rubber compositions - Google Patents

Improvements in or relating to the manufacture of synthetic rubber compositions

Info

Publication number
GB1040287A
GB1040287A GB3227563A GB3227563A GB1040287A GB 1040287 A GB1040287 A GB 1040287A GB 3227563 A GB3227563 A GB 3227563A GB 3227563 A GB3227563 A GB 3227563A GB 1040287 A GB1040287 A GB 1040287A
Authority
GB
United Kingdom
Prior art keywords
mixture
acrylonitrile
styrene
copolymer
initiator
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
GB3227563A
Inventor
Zygmunt Kromolicki
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.)
Sterling Moulding Materials Ltd
Original Assignee
Sterling Moulding Materials 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 Sterling Moulding Materials Ltd filed Critical Sterling Moulding Materials Ltd
Priority to GB3227563A priority Critical patent/GB1040287A/en
Publication of GB1040287A publication Critical patent/GB1040287A/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
    • 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
    • C08L25/08Copolymers of styrene
    • C08L25/12Copolymers of styrene with unsaturated nitriles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

Moulding materials are made by forming a graft copolymer by reacting a mixture of 95-60% of a styrene and 5-40% of acrylonitrile with a synthetic rubber latex of polybutadiene or a copolymer of butadiene and styrene and/or acrylonitrile, 90-30 parts of monomer mixture being used per 10-70 parts of latex solids, coagulating and drying the graft polymer so produced and blending it with a particulate copolymer of acrylonitrile and a styrene containing 90-60% of the latter which has an intrinsic viscosity of less than 1 and has been prepared by suspension polymerization in the presence of an initiator and a chain transfer agent. The examples describe: (1) (a) grafting styrene and acrylonitrile in a polybutadiene latex in the presence of lauryl mercaptan, p-menthane hydroperoxide, ferrous sulphate and water, (b) copolymerizing styrene and acrylonitrile in aqueous suspension in the presence of a mixture of lauryl peroxide ditertiary butyl peroxide and diisopropyl percarbonate as initiator and a mixture of 1,4-dihydronaphthalene, alpha-methylstyrene dimer and dodecyl mercaptan as chain transfer agent, and (c) blending polymers (a) and (b); (3) as in (1) but using a styrene-acrylonitrile copolymer made in the presence of a mixture of lauryl, tertiary butyl and ditertiary butyl peroxides as initiator and a mixture of 1,4-dihydronaphthalene, dodecyl mercaptan and 1,1-diphenylethylene as chain transfer agent, and (5) the preparation of an acrylonitrile-styrene-alpha-methylstyrene copolymer in aqueous suspension in the presence of a mixture of lauryl, tert.-butyl and ditert.-butyl peroxides as initiator and a mixture of 1,4-dihydronaphthalene, dodecyl mercaptan and 1,1-diphenylethylene as a chain transfer agent.
GB3227563A 1963-08-15 1963-08-15 Improvements in or relating to the manufacture of synthetic rubber compositions Expired GB1040287A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3227563A GB1040287A (en) 1963-08-15 1963-08-15 Improvements in or relating to the manufacture of synthetic rubber compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3227563A GB1040287A (en) 1963-08-15 1963-08-15 Improvements in or relating to the manufacture of synthetic rubber compositions

Publications (1)

Publication Number Publication Date
GB1040287A true GB1040287A (en) 1966-08-24

Family

ID=10336079

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3227563A Expired GB1040287A (en) 1963-08-15 1963-08-15 Improvements in or relating to the manufacture of synthetic rubber compositions

Country Status (1)

Country Link
GB (1) GB1040287A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187221A (en) * 1984-12-28 1993-02-16 Chemische Werke Huels Aktiengesellschaft Styrene/butadiene graft copolymer latex and heat-vulcanizable composition, containing the latter as reinforcing latex, for the production of latex foam
FR2778185A1 (en) * 1998-04-30 1999-11-05 Rhodia Chimie Sa GRAFT COPOLYMER USEFUL FOR PREPARING PRESSURE-SENSITIVE ADHESIVE COMPOSITIONS
US20180179373A1 (en) * 2016-12-23 2018-06-28 Lotte Advanced Materials Co., Ltd. Ionizing Radiation Resistant Thermoplastic Resin Composition and Article Comprising the Same
US10472510B2 (en) 2016-12-30 2019-11-12 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article manufactured using the same
US10472490B2 (en) 2016-10-25 2019-11-12 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article produced thereform
US10544278B2 (en) 2016-11-02 2020-01-28 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article produced therefrom
US10787532B2 (en) 2016-12-22 2020-09-29 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article manufactured using the same
US11124643B2 (en) 2016-12-27 2021-09-21 Lotte Chemical Corporation Thermoplastic resin composition and molded article manufactured therefrom
US11365304B2 (en) 2016-12-23 2022-06-21 Lotte Chemical Corporation Foaming resin composition, preparation method therefor, and foam using same
US11505674B2 (en) 2017-11-08 2022-11-22 Lotte Chemical Corporation Thermoplastic resin composition and molded article produced from same
US12084569B2 (en) 2018-11-30 2024-09-10 Lotte Chemical Corporation Thermoplastic resin composition and molded article formed therefrom

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187221A (en) * 1984-12-28 1993-02-16 Chemische Werke Huels Aktiengesellschaft Styrene/butadiene graft copolymer latex and heat-vulcanizable composition, containing the latter as reinforcing latex, for the production of latex foam
FR2778185A1 (en) * 1998-04-30 1999-11-05 Rhodia Chimie Sa GRAFT COPOLYMER USEFUL FOR PREPARING PRESSURE-SENSITIVE ADHESIVE COMPOSITIONS
WO1999057167A1 (en) * 1998-04-30 1999-11-11 Rhodia Chimie Grafted copolymer useful for preparing pressure-sensitive adhesive compositions
US10472490B2 (en) 2016-10-25 2019-11-12 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article produced thereform
US10544278B2 (en) 2016-11-02 2020-01-28 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article produced therefrom
US10787532B2 (en) 2016-12-22 2020-09-29 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article manufactured using the same
US20180179373A1 (en) * 2016-12-23 2018-06-28 Lotte Advanced Materials Co., Ltd. Ionizing Radiation Resistant Thermoplastic Resin Composition and Article Comprising the Same
US10815368B2 (en) * 2016-12-23 2020-10-27 Lotte Advanced Materials Co., Ltd. Ionizing radiation resistant thermoplastic resin composition and article comprising the same
US11365304B2 (en) 2016-12-23 2022-06-21 Lotte Chemical Corporation Foaming resin composition, preparation method therefor, and foam using same
US11124643B2 (en) 2016-12-27 2021-09-21 Lotte Chemical Corporation Thermoplastic resin composition and molded article manufactured therefrom
US10472510B2 (en) 2016-12-30 2019-11-12 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and article manufactured using the same
US11505674B2 (en) 2017-11-08 2022-11-22 Lotte Chemical Corporation Thermoplastic resin composition and molded article produced from same
US12084569B2 (en) 2018-11-30 2024-09-10 Lotte Chemical Corporation Thermoplastic resin composition and molded article formed therefrom

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