GB640468A - Improvements in copolymers of dipropenyl esters - Google Patents

Improvements in copolymers of dipropenyl esters

Info

Publication number
GB640468A
GB640468A GB22895/47A GB2289547A GB640468A GB 640468 A GB640468 A GB 640468A GB 22895/47 A GB22895/47 A GB 22895/47A GB 2289547 A GB2289547 A GB 2289547A GB 640468 A GB640468 A GB 640468A
Authority
GB
United Kingdom
Prior art keywords
copolymers
esters
fumaric
dissolving
solvent
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
GB22895/47A
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.)
Uniroyal Inc
Original Assignee
United States Rubber 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 United States Rubber Co filed Critical United States Rubber Co
Publication of GB640468A publication Critical patent/GB640468A/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
    • C08F22/10Esters
    • C08F22/26Esters of unsaturated alcohols
    • C08F22/28Diallyl maleate

Landscapes

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

Abstract

Soluble unsaturated resins capable of ultimate conversion to a solvent and heat resistant state are prepared by copolymerizing a mixture of a dipropenyl ester of an alpha-beta unsaturated dicarboxylic acid and an omega trichloralkene. The preferred esters are those of acids having the general formula Cn H2n-2(COOH)2, where n is from 2 to 6 and include allyl, 2-alkyl- and 2-chloro-allyl esters of maleic, fumaric, itaconic, citraconic and mesaconic acids. Esters of ethyl-fumaric, ethyl-maleic, propyl-fumaric and a -hydromuconic acids are also mentioned. The preferred omega-trichlor-alkenes are those also containing a terminal ethylene linkage, e.g. 3,3,3-trichloropropene-1, 4,4,4-trichlorobutene-1 and 4,4,4 - trichloro - 2 - methylbutene - 1. Polymerization is effected at 25-120 DEG C. in the presence of a peroxidic catalyst such as benzoyl peroxide, acetyl benzoyl peroxide, tert.-butyl hydroperoxide, succinyl peroxide and tert.-butyl perbenzoate. The products which are soluble in acetone, benzene, chloroform, carbon tetrachloride, ethyl acetate and xylene may be purified by repeated solution in a solvent and precipitation with a non-solvent, e.g. n-hexane, or may be dissolved without isolation. Dyes, pigments, fillers, plasticizers and resins may be incorporated before curing the copolymers by the application of heat. The copolymers may be interpolymerized with ethylenic compounds, e.g. butyl methacrylate, allyl acrylate, vinyl acetate and styrene, by dissolving them in these monomers and heating in the presence of a catalyst to the infusible state. An example is also given of dissolving the copolymer in diethyl fumarate and curing in a mould. The copolymers which are non-dissolving and fire-retardant, may be cast and moulded into rods, blocks and sheets or used for impregnating or coating furnishings.
GB22895/47A 1946-11-02 1947-08-18 Improvements in copolymers of dipropenyl esters Expired GB640468A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US640468XA 1946-11-02 1946-11-02

Publications (1)

Publication Number Publication Date
GB640468A true GB640468A (en) 1950-07-19

Family

ID=22053218

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22895/47A Expired GB640468A (en) 1946-11-02 1947-08-18 Improvements in copolymers of dipropenyl esters

Country Status (1)

Country Link
GB (1) GB640468A (en)

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