GB767642A - Production of styrene-type polymers - Google Patents

Production of styrene-type polymers

Info

Publication number
GB767642A
GB767642A GB4624/55A GB462455A GB767642A GB 767642 A GB767642 A GB 767642A GB 4624/55 A GB4624/55 A GB 4624/55A GB 462455 A GB462455 A GB 462455A GB 767642 A GB767642 A GB 767642A
Authority
GB
United Kingdom
Prior art keywords
styrene
methyl
catalyst
butyl
diazoaminobenzene
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
GB4624/55A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto 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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB767642A publication Critical patent/GB767642A/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

Styrene, with or without compounds such as a -methyl styrene, vinyl toluene, acrylonitrile, ethyl and butyl acrylates, and methyl acrylate, is polymerized in the presence of an oily, unsaturated polymer of one or more conjugated diolefines having 4 to 6 carbon atoms, or copolymers with a lesser amount of mono-olefinic monomer. The oily polymers may be prepared from butadiene, isoprene, piperylene, dimethylbutadienes, methyl pentadienes, and chloroprene or mixtures thereof with minor proportions of styrene, a - and p-methyl styrenes, mono- and dichlorostyrenes, ethyl fumarate and maleate, methyl acrylate and methacrylate, methacrylonitrile and vinylidene chloride or with maleic anhydride, butadiene and styrene in a hydrocarbon solvent or diluent, e.g. benzene or heptane using an alkali metal catalyst, e.g. sodium; in aqueous emulsion in the presence of a sulphur-containing modifier, e.g. dodecyl mercaptan; in solution in heptane using hydrogen fluoride as catalyst; or in a diluent using cumene hydroperoxide as catalyst and carbon tetrachloride or di-isopropyl xanthogen disulphide as modifiers. The liquid polymer may be dissolved in the styrene and polymerized, en masse, if desired using catalysts such as hydrogen, benzoyl, t.-butyl and diacetyl peroxides, t.-butyl and cumene hydroperoxides, diethylperoxycarbonate, potassium persulphate, perborates, and a ,a 1 - azodiisobutyronitrile, p - bromobenzenediazonium fluoborate, N-nitrosoparabromoacetanilide, azomethane, phenyldiazonium halides, diazoaminobenzene, p-bromobenzenediazonium hydroxide and p-tolyl-diazoaminobenzene; in aqueous suspension using tricalcium phosphate or vinyl acetate-maleic anhydride as suspending agent; or in aqueous emulsion using a water-soluble salt of a sulphonated long-chain alkyl compound and conventional persulphate or redox catalyst systems. Interpolymerization to form a graft polymer may occur. Plasticisers, stabilizers, fillers, dyes, pigments or other polymers may be added to the products or may be present during the polymerization to give moulding compositions of increased toughness. U.S.A. Specifications 2,550,695, 2,581,094, 2,586,594 and 2,652,342 are referred to.
GB4624/55A 1954-02-16 1955-02-16 Production of styrene-type polymers Expired GB767642A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US767642XA 1954-02-16 1954-02-16

Publications (1)

Publication Number Publication Date
GB767642A true GB767642A (en) 1957-02-06

Family

ID=22134039

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4624/55A Expired GB767642A (en) 1954-02-16 1955-02-16 Production of styrene-type polymers

Country Status (1)

Country Link
GB (1) GB767642A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1082051B (en) * 1957-11-20 1960-05-19 Basf Ag Process for the production of impact-resistant, thermoplastic copolymers
US2994683A (en) * 1959-12-30 1961-08-01 Borg Warner Graft copolymers of an acrylic acid ester/butadiene copolymer, styrene and acrylonitrile
US3047533A (en) * 1959-08-03 1962-07-31 William C Calvert Vinylchloride polymer blends with graft copolymers of a conjugated diene/alkyl acrylate copolymer, an unsaturated hydrocarbon, and an unsaturated nitrile
US3099293A (en) * 1959-10-28 1963-07-30 Exxon Research Engineering Co Reinforced plastic from an open cure technique with a graft polymer
US3185659A (en) * 1961-01-03 1965-05-25 Exxon Research Engineering Co Process for preparing a graft polymer
US3264375A (en) * 1963-01-16 1966-08-02 Monsanto Co Process for the graft polymerization of styrene on alkyl lithium catalyzed polybutadiene using a peroxide catalyst
US3264374A (en) * 1963-01-02 1966-08-02 Monsanto Co Graft copolymer formed by polymerizing butadiene in styrene with an alkylli catalyst, deactivating the catalyst and adding an organic peroxide
DE1224486B (en) * 1959-04-24 1966-09-08 Monsanto Co Molding compositions from mixtures of graft copolymers and copolymers of styrene
EP1251143A1 (en) * 2001-04-17 2002-10-23 Fina Technology, Inc. Monovinylaromatic polymer with improved stress crack resistance

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1082051B (en) * 1957-11-20 1960-05-19 Basf Ag Process for the production of impact-resistant, thermoplastic copolymers
DE1224486B (en) * 1959-04-24 1966-09-08 Monsanto Co Molding compositions from mixtures of graft copolymers and copolymers of styrene
US3047533A (en) * 1959-08-03 1962-07-31 William C Calvert Vinylchloride polymer blends with graft copolymers of a conjugated diene/alkyl acrylate copolymer, an unsaturated hydrocarbon, and an unsaturated nitrile
US3099293A (en) * 1959-10-28 1963-07-30 Exxon Research Engineering Co Reinforced plastic from an open cure technique with a graft polymer
US2994683A (en) * 1959-12-30 1961-08-01 Borg Warner Graft copolymers of an acrylic acid ester/butadiene copolymer, styrene and acrylonitrile
US3185659A (en) * 1961-01-03 1965-05-25 Exxon Research Engineering Co Process for preparing a graft polymer
US3264374A (en) * 1963-01-02 1966-08-02 Monsanto Co Graft copolymer formed by polymerizing butadiene in styrene with an alkylli catalyst, deactivating the catalyst and adding an organic peroxide
US3264375A (en) * 1963-01-16 1966-08-02 Monsanto Co Process for the graft polymerization of styrene on alkyl lithium catalyzed polybutadiene using a peroxide catalyst
US6822046B2 (en) 2000-04-10 2004-11-23 Fina Technology, Inc. Monovinylaromatic polymer with improved stress crack resistance
EP1251143A1 (en) * 2001-04-17 2002-10-23 Fina Technology, Inc. Monovinylaromatic polymer with improved stress crack resistance

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