GB680330A - Improvements in interpolymers of trichloroalkenes - Google Patents

Improvements in interpolymers of trichloroalkenes

Info

Publication number
GB680330A
GB680330A GB667749A GB667749A GB680330A GB 680330 A GB680330 A GB 680330A GB 667749 A GB667749 A GB 667749A GB 667749 A GB667749 A GB 667749A GB 680330 A GB680330 A GB 680330A
Authority
GB
United Kingdom
Prior art keywords
vinyl
methyl
allyl
diallyl
ethyl
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
GB667749A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB667749A priority Critical patent/GB680330A/en
Publication of GB680330A publication Critical patent/GB680330A/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
    • C08F214/00Copolymers 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 halogen
    • C08F214/02Monomers containing chlorine
    • C08F214/14Monomers containing three or more carbon atoms

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  • 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

0.1 to 25 molar equivalents of a trichloroalkene having 3 to 5 carbon atoms per molecule and all the chlorine atoms attached to the same carbon atom are copolymerized with one or more monomeric olefinic compounds containing 1 to 4 ethylenic linkages, but excluding dipropenyl and alkyl and chlorine substituted dipropenyl esters of alpha, beta-unsaturated dicarboxylic acids, by heating in the presence of a peroxidic catalyst. Trichloroalkenes specified are 3,3,3-trichloropropene, 1,1,3-trichloropropene, 4,4,4 - trichloro - 1 - butene, 1,1,1-trichloro - 2 - butene, and 4,4,4 - trichloro - 2-methyl - 1 - butene. Copolymerizable monomers specified are ethylene, propylene, butene-1, isobutylene, styrene, alpha-methyl styrene, para-methyl styrene, divinyl benzene, vinyl naphthalene, para-chlorostyrene, para-fluorostyrene, 2,5-dichlorostyrene, vinyl fluoride, vinyl chloride, vinylidene fluoride, vinylidene chloride, trichloroethylene, allyl chloride, methallyl chloride, 2,3-dichloropropene, 1,3-butadiene, 2-methyl-1,3-butadiene, 1,5-hexadiene, 2-chloro-1,3-butadiene, allyl, methallyl, ethallyl, chloroallyl, crotyl, and cinnamyl alcohols, vinyl ethyl, vinyl butyl, vinyl hexyl, vinyl cyclohexyl, vinyl phenyl, vinyl benzyl, vinyl tolyl, divinyl, methyl isopropenyl, allyl ethyl, methallyl ethyl, methally phenyl, methallyl benzyl, 2-chloroallyl ethyl, allyl 2-naphthyl, diallyl, dimethallyl, and dichloroallyl ethers, betaallyloxyethanol, 1,2-diallyloxyethane, 1,4-diallyloxybenzene, vinyl acetate, chloroacetate, propionate, n-butyrate, and benzoate, divinyl oxalate, divinyl phthalate, isopropenyl acetate, allyl acetate, chloroacetate, glycollate, butyrate, stearate, benzoate, para-chlorobenzoate, and para-methoxy benzoate, methallyl acetate, acrylate, allyl methacrylate, beta-allyloxyethyl acrylate, chloroallyl acrylate, allyl chloroacrylate, allyl ethacrylate, methallyl cinnamate, allyl crotonate, crotyl acrylate, diallyl adipate, triallyl tricarballylate, diallyl, dimethallyl, dichloroallyl, and diallyloxyethyl phthalates, diallyloxyethyl fumarate, dimethallyloxyethyl fumarate, diallyloxyethyl itaconate, triallyl aconitate, diallyl oxalate, diallyl succinate, dichloroallyl adipate, dicrotyl succinate, dimethallyl adipate, diallyloxyethyl adipate, and the polyalkenyl esters of malonic, alpha-methyl malonic, glutaric, pimelic, and azelaic acids, diallyl carbonate, diallyl sulphate, triallyl, trimethallyl, and triallyloxyethyl phosphates, tetraallyl silicate, tetraallyl titanate, tetramethallyl silicate, and tetramethyllyl stannate, vinyl methyl, isopropenyl methyl, allyl methyl, allyl phenyl, and diallyl ketones, mesityl oxide, acrylic, methacrylic, and ethacrylic acids, methyl, beta-chloroethyl, n-butyl, 2-ethylhexyl, n-octyl, vinyl, allyl, phenyl, tolyl, and benzyl acrylates, methyl, 2-ethylhexyl and n-octyl methacrylates, methyl chloroacrylates, ethyl chloroacrylate, methyl ethacrylate, methyl crotonate, acrylamide, N - methylmethacrylamide, N-phenyl acrylamide, N-allyl acrylamide, acrylonitrile, and methacrylonitrile, diethyl, dibutyl, di-2-ethyl hexyl, and di-n-octyl maleates, maleic anhydride, maleimide, N-methyl maleimide, N-butyl maleimide, N-phenyl maleimide, N-benzyl maleimide, diethyl, di-2-ethyl hexyl, di-n-octyl, and diallyloxyethyl fumarates, fumaronitrile, itaconic anhydride, di-2-ethyl hexyl itaconate, dihexyl itaconate, itacononitrile, dimethyl mesaconate and citraconate, 2-vinyl pyridine, 2-vinyl furan, and 2-vinyl thiophen. Peroxidic catalysts specified, which may be added incrementally during the reaction, are acetyl peroxide, benzoyl peroxide, and tert. butyl hydroperoxide. The preferred copolymers are the soluble, unsaturated copolymers of the trichloroalkenes with polyolefinic esters, which may be further polymerized with the aid of heat and catalysts, or dissolved in liquid copolymerizable compounds such as butyl, tolyl, and allyl acrylates, vinyl butyrate, styrene, and diethyl and diallyl fumarates, and further copolymerized. The copolymers may be used in the preparation of rods, blocks, sheets, and coating and laminating compositions.
GB667749A 1949-03-11 1949-03-11 Improvements in interpolymers of trichloroalkenes Expired GB680330A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB667749A GB680330A (en) 1949-03-11 1949-03-11 Improvements in interpolymers of trichloroalkenes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB667749A GB680330A (en) 1949-03-11 1949-03-11 Improvements in interpolymers of trichloroalkenes

Publications (1)

Publication Number Publication Date
GB680330A true GB680330A (en) 1952-10-01

Family

ID=9818786

Family Applications (1)

Application Number Title Priority Date Filing Date
GB667749A Expired GB680330A (en) 1949-03-11 1949-03-11 Improvements in interpolymers of trichloroalkenes

Country Status (1)

Country Link
GB (1) GB680330A (en)

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