GB1303308A - - Google Patents

Info

Publication number
GB1303308A
GB1303308A GB5383070A GB5383070A GB1303308A GB 1303308 A GB1303308 A GB 1303308A GB 5383070 A GB5383070 A GB 5383070A GB 5383070 A GB5383070 A GB 5383070A GB 1303308 A GB1303308 A GB 1303308A
Authority
GB
United Kingdom
Prior art keywords
polymer
styrene
butadiene
polystyrene
methyl
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
GB5383070A
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 filed Critical
Publication of GB1303308A publication Critical patent/GB1303308A/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
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes

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

1303308 Craft polymers POLYMER CORP Ltd 12 Nov 1970 [24 Dec 1969] 53830/70 Heading C3G A process of preparing ABS and MBS resins comprises: (1) dissolving a mixture of preformed rubbery polymer A and preformed polymer B in a mixture of grafting monomers, (2) prepolymerizing with agitation the mixture so formed to a conversion of grafting monomers of from 10 to 40% preferably 20-40%, whereby a dispersion is formed of a solution of said preformed polymers, in a solution of a polymer of said grafting monomers, said solutions being solutions in the residual grafting monomers, (3) continuing the polymerization of the residual grafting to at least 50% conversion, said continued polymerization being carried out in bulk or in aqueous suspension under suspension conditions, and (4) recovering the thermoplastic resin so formed, wherein polymer A is a polydiolefin having a 1,4-content of at least 85%, and polymer B is a polymer of butadiene-1,3 having at least 50% of butadiene units in the 1,2- configuration, and said grafting monomers comprise a mixture of styrene or a polymerizable homologue of styrene with one or more of acrylonitrile, polymerizable homologues of acrylonitrile, methyl methacrylate and polymerizable homologues of methyl methacrylate. Polymer A is preferably a polybutadiene, such as a cis-polybutadiene, or a polyisoprene. Polymer B may be a hcmopolymer of butadiene such as a polybutadiene having a 1,2-content of at least 80%, or a copolymer of butadiene with less than 50% by weight of a copolymerisable monomer such as styrene, α-methyl styrene, acrylonitrile, methacrylonitrile and methyl methacrylate, or a block copolymer of an alkenyl aromatic hydrocarbon and butadiene-1,3 such as polystyrene-polybutadiene-polystyrene, polystyrene - butadiene/styrene copolymer, polystyrene - butadiene / styrene copolymer - polystyrene, polystyrene - polybutadiene - poly α-methyl styrene, and poly α-methyl styrenepolybutadiene-poly α-methyl styrene. The weight ratio of polymer A to polymer B is preferably greater than 1 : 1, more preferably 10 : 1-1À5 : 1. The continued polymerization is preferably carried out in aqueous suspension medium comprising an aqueous solution of polyvinyl alcohol. The pre-polymerization in bulk is preferably carried out at 50-120‹ C. and the continued polymerization, if still in bulk, is preferably carried out at 30-200‹ C. The polymer produced by the process comprises 15-75% by weight of polymerized styrene and/or its polymerizable homologues, 12-30% by weight of polymerized acrylonitrile, methyl methacylate and/or their polymerizable homologue and 5-30% by weight of the rubber.
GB5383070A 1969-12-24 1970-11-12 Expired GB1303308A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA70816 1969-12-24

Publications (1)

Publication Number Publication Date
GB1303308A true GB1303308A (en) 1973-01-17

Family

ID=4086105

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5383070A Expired GB1303308A (en) 1969-12-24 1970-11-12

Country Status (6)

Country Link
JP (1) JPS4917432B1 (en)
CA (1) CA910533A (en)
DE (1) DE2063291A1 (en)
FR (1) FR2074228A5 (en)
GB (1) GB1303308A (en)
NL (1) NL7017810A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1452478A (en) * 1972-11-22 1976-10-13 Agfa Gevaert Process for homogeneously dispersing polymer particles in aqueous medium
US4524180A (en) * 1982-05-21 1985-06-18 The Dow Chemical Company Rubber-modified, impact-resistant polymeric compositions
JPH0246820U (en) * 1988-09-22 1990-03-30
JPH036427U (en) * 1989-06-08 1991-01-22

Also Published As

Publication number Publication date
NL7017810A (en) 1971-06-28
FR2074228A5 (en) 1971-10-01
DE2063291A1 (en) 1972-06-15
CA910533A (en) 1972-09-19
JPS4917432B1 (en) 1974-04-30

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee