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GB852019A - Improvements in and relating to polymerization - Google Patents

Improvements in and relating to polymerization

Info

Publication number
GB852019A
GB852019A GB20283/58A GB2028358A GB852019A GB 852019 A GB852019 A GB 852019A GB 20283/58 A GB20283/58 A GB 20283/58A GB 2028358 A GB2028358 A GB 2028358A GB 852019 A GB852019 A GB 852019A
Authority
GB
United Kingdom
Prior art keywords
epoxy
methylcyclohexylmethyl
vinyl chloride
polymers
acrylate
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
GB20283/58A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB852019A publication Critical patent/GB852019A/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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F20/32Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals

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

Polymers of unsaturated esters of epoxycyclohexylmethanols of formula: <FORM:0852019/IV(a)/1> where R1 to R6 represent hydrogen or alkyl groups and R represents an alkenyl group having 2 to 4 carbon atoms, may be prepared by reacting the esters with themselves or with one or more unsaturated monomers containing at least one ethylenic double bond and/or acetylenic triple bond. The polymerization may be effected in bulk, in solution, e.g. in acetone, in aqueous suspension, e.g. in the presence of hydroxyethyl cellulose, or in aqueous emulsion, e.g. in the presence of sodium dioctyl sulphosuccinate, in the presence of catalysts, e.g. acetyl peroxide, lauroyl peroxide and potassium persulphate. Many suitable monomers are listed and examples describe the homopolymerization of (12) 3, 4-epoxy-6-methylcyclohexylmethyl crotonate and (13) 3, 4-epoxy-6-methylcyclohexylmethyl acrylate and the copolymerization of 3, 4-epoxy-6-methylcyclohexylmethyl crotonate with (1,2 and 8) vinyl chloride, (3) acrylonitrile, (4) vinyl acetate (5) ethyl acrylate, (6) vinylidene chloride, (7) chlorostyrene, (9) vinylchloride and acrylonitrile, (10) vinyl chloride and vinylidene chloride, and (11) vinyl chloride and vinyl acetate, and of 3, 4-epoxy-6-methylcyclohexylmethyl acrylate with (14 and 15) vinyl chloride, (16) methyl methacrylate and (17) chlorostyrene. The polymers may be cured in the presence of curing agents, e.g. polybasic inorganic and organic acids, polyphenols and polyamines. The polymers may be used in protective coatings, linings, laminates or for impregnating cloth. Films may be cast from solutions, e.g. in benzene, cyclohexanone, dimethyl formamide and methyl isobutyl ketone, containing phosphoric acid, and cured by heating.
GB20283/58A 1957-06-26 1958-06-25 Improvements in and relating to polymerization Expired GB852019A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US852019XA 1957-06-26 1957-06-26

Publications (1)

Publication Number Publication Date
GB852019A true GB852019A (en) 1960-10-19

Family

ID=22190114

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20283/58A Expired GB852019A (en) 1957-06-26 1958-06-25 Improvements in and relating to polymerization

Country Status (2)

Country Link
DE (1) DE1063808B (en)
GB (1) GB852019A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8796350B2 (en) 2010-03-09 2014-08-05 Henkel US IP LLC Cationic UV-crosslinkable acrylic polymers for pressure sensitive adhesives

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5557007A (en) * 1990-09-28 1996-09-17 Union Carbide Chemicals & Plastics Technology Corporation Unsaturated polylactone acrylates and derivatives thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8796350B2 (en) 2010-03-09 2014-08-05 Henkel US IP LLC Cationic UV-crosslinkable acrylic polymers for pressure sensitive adhesives
US9469794B2 (en) 2010-03-09 2016-10-18 Henkel IP & Holding GmbH Cationic UV-crosslinkable acrylic polymers for pressure sensitive adhesives

Also Published As

Publication number Publication date
DE1063808B (en) 1959-08-20

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