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GB772746A - Styrene polymers - Google Patents

Styrene polymers

Info

Publication number
GB772746A
GB772746A GB25403/54A GB2540354A GB772746A GB 772746 A GB772746 A GB 772746A GB 25403/54 A GB25403/54 A GB 25403/54A GB 2540354 A GB2540354 A GB 2540354A GB 772746 A GB772746 A GB 772746A
Authority
GB
United Kingdom
Prior art keywords
cyclohexyl
ester
acid
esters
methacrylic acid
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
GB25403/54A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB772746A publication Critical patent/GB772746A/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
    • C08F22/00Homopolymers and 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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Copolymers soluble in or compatible with benzine are prepared from (a) one or more esters derived from acrylic or methacrylic acid and a saturated aliphatic or cycloaliphatic alcohol containing more than 8 carbon atoms constituting 20 to 40 per cent by weight of the total monomers; and (b) styrene or nuclear substituted styrene and, optionally, an additional polymerisable vinyl compound. Component (a) may comprise the decyl, dodecyl, cetyl, octadecyl, and cyclohexyl-cyclohexyl esters of acrylic or methacrylic acid and the styrene may be nuclear substituted by alkyl, alkoxy, halogen or aryl residues. In a modification component (a) may include an ester of a polymerizable organic acid other than acrylic or methacrylic acid and a saturated aliphatic or cycloaliphatic alcohol containing more than 8 carbon atoms, e.g. trimethyl cyclohexyl, t.-butyl cyclohexyl and cyclohexyl-cyclohexyl esters and half esters of ethylene-a ,b -dicarboxylic acids such as fumaric or maleic acid. The optional vinyl compound may be vinyl acetate, or an ester derived from a saturated or unsaturated aliphatic alcohol containing not more than 8 carbon atoms and a polymerizable organic acid, e.g. methyl, ethyl and cyclohexyl esters of acrylic, methacrylic, fumaric, and maleic acids or amides thereof or acrolein or methacrolein. Polymerization may be carried out in solution, in bulk or in an aqueous suspension or emulsion using catalysts such as benzoyl peroxide, redox systems, or azo compounds, ultra-violet light and heat, and regulators such as diisopropylxanthogen disulphide. In examples, styrene and the dodecyl or octadecyl ester of methacrylic acid, with or without methyl methacrylate, the cyclohexyl ester of methacrylic acid and the dicyclohexyl ester of fumaric acid, are copolymerized in bulk or in solution in benzine using benzoyl peroxide, or in aqueous dispersion containing polyvinyl alcohol using lauroyl peroxide and diisopropylxanthogen disulphide. Lacquers are formed by the addition of chlorinated diphenyl, linseed oil or phthalic acid resins to a benzine solution of the copolymer. Specification 491,800, [Group IV], is referred to.
GB25403/54A 1953-09-03 1954-09-01 Styrene polymers Expired GB772746A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE772746X 1953-09-03

Publications (1)

Publication Number Publication Date
GB772746A true GB772746A (en) 1957-04-17

Family

ID=6682327

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25403/54A Expired GB772746A (en) 1953-09-03 1954-09-01 Styrene polymers

Country Status (1)

Country Link
GB (1) GB772746A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4388434A (en) 1977-02-07 1983-06-14 Rohm And Haas Company Lithographic ink vehicle containing addition polymer and aliphatic hydrocarbon solvent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4388434A (en) 1977-02-07 1983-06-14 Rohm And Haas Company Lithographic ink vehicle containing addition polymer and aliphatic hydrocarbon solvent

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