GB1031496A - Novel graft interpolymers - Google Patents

Novel graft interpolymers

Info

Publication number
GB1031496A
GB1031496A GB4093664A GB4093664A GB1031496A GB 1031496 A GB1031496 A GB 1031496A GB 4093664 A GB4093664 A GB 4093664A GB 4093664 A GB4093664 A GB 4093664A GB 1031496 A GB1031496 A GB 1031496A
Authority
GB
United Kingdom
Prior art keywords
polymerizing
monomer
stage
block copolymer
monovinyl aromatic
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
GB4093664A
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.)
Dart Industries Inc
Original Assignee
Rexall Drug and Chemical 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 Rexall Drug and Chemical Co filed Critical Rexall Drug and Chemical Co
Publication of GB1031496A publication Critical patent/GB1031496A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F287/00Macromolecular compounds obtained by polymerising monomers on to block polymers

Abstract

Graft polymers are made by polymerizing a monovinyl aromatic compound, e.g. styrene, or a mixture thereof with acrylonitrile, methyl methacrylate and/or alpha-methyl styrene, in the presence of a block copolymer prepared from a conjugated diolefine and a monovinyl aromatic monomer, preferably a butadienestyrene block copolymer. The grafting reaction is preferably carried out either by bulk polymerizing the monomer-polymer mixture in a first stage, followed by polymerization in aqueous suspension in a second stage, or by polymerizing a monomer-polymer mixture containing 3 to 30% of ethyl benzene. Also present during polymerization may be perioxide catalysts, e.g. tert.-butyl perbenzoate and benzoyl peroxide.
GB4093664A 1963-10-29 1964-10-07 Novel graft interpolymers Expired GB1031496A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US31968363A 1963-10-29 1963-10-29

Publications (1)

Publication Number Publication Date
GB1031496A true GB1031496A (en) 1966-06-02

Family

ID=23243259

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4093664A Expired GB1031496A (en) 1963-10-29 1964-10-07 Novel graft interpolymers

Country Status (2)

Country Link
DE (1) DE1595215A1 (en)
GB (1) GB1031496A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0021488A1 (en) * 1979-06-18 1981-01-07 Shell Internationale Researchmaatschappij B.V. Improved impact polymers and their preparation
EP0069792A1 (en) * 1981-07-13 1983-01-19 The Dow Chemical Company Transparent impact resin and process for the preparation thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0021488A1 (en) * 1979-06-18 1981-01-07 Shell Internationale Researchmaatschappij B.V. Improved impact polymers and their preparation
EP0069792A1 (en) * 1981-07-13 1983-01-19 The Dow Chemical Company Transparent impact resin and process for the preparation thereof

Also Published As

Publication number Publication date
DE1595215A1 (en) 1972-04-06

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