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GB606080A - Improvement in unsaturated polymeric materials - Google Patents

Improvement in unsaturated polymeric materials

Info

Publication number
GB606080A
GB606080A GB898/46A GB89846A GB606080A GB 606080 A GB606080 A GB 606080A GB 898/46 A GB898/46 A GB 898/46A GB 89846 A GB89846 A GB 89846A GB 606080 A GB606080 A GB 606080A
Authority
GB
United Kingdom
Prior art keywords
acetone
product
allyl
fumarate
alcohol
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
GB898/46A
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
Priority claimed from US788958A external-priority patent/US2526434A/en
Publication of GB606080A publication Critical patent/GB606080A/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
    • C08F212/00Copolymers 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 an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
    • 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)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Acetone-soluble, fusible, ternary interpolymers are made by heating in the presence of peroxide catalysts a mixture of (a) styrene or p-chloro- or p-methyl-styrene; (b) diallyl or dimethallyl fumarate and (c) allyl or methallyl alcohol and halting the reaction by cooling, if desired adding an inhibitor such as hydroquinone, before gelation occurs. The proportion of the alcohol is at least 10 per cent of the fumarate. Excess of the alcohol may be used as a solvent. Catalysts specified are acetyl, benzoyl, acetyl-benzoyl and succinyl peroxides and tert-butyl hydrogen peroxide. Modifiers such as carbon tetrachloride may be present. The product may be purified by solution in acetone and precipitation with gasoline. The interpolymers may be modified by reaction with alkyl, allyl and acyl halides and dihalides, organic acids and anhydrides, e.g. polycarboxylic acids and chloracetic anhydride, aldehydes or organic isocyanates, isothiocyanates and diisocyanates. Dyes, pigments, e.g. titanium dioxide, fillers, plasticisers and solvents, e.g. acetone, cyclohexanone, carbitol acetate and xylene may be incorporated into the product, which may be further heated, if desired with addition of catalyst, to the insoluble, infusible stage. The product may also be dissolved in methyl or allyl acrylates, vinyl acetate or diallyl fumarate and further polymerized.
GB898/46A 1945-03-01 1946-01-10 Improvement in unsaturated polymeric materials Expired GB606080A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US606080XA 1945-03-01 1945-03-01
US788958A US2526434A (en) 1947-11-29 1947-11-29 Interpolymers of styrene, an allylic fumarate, and an allylic alcohol

Publications (1)

Publication Number Publication Date
GB606080A true GB606080A (en) 1948-08-05

Family

ID=26740107

Family Applications (2)

Application Number Title Priority Date Filing Date
GB898/46A Expired GB606080A (en) 1945-03-01 1946-01-10 Improvement in unsaturated polymeric materials
GB24763/48A Expired GB665269A (en) 1945-03-01 1948-09-22 Improvements in interpolymers of a styrene, an allylic fumarate and an allylic alcohol

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB24763/48A Expired GB665269A (en) 1945-03-01 1948-09-22 Improvements in interpolymers of a styrene, an allylic fumarate and an allylic alcohol

Country Status (2)

Country Link
FR (2) FR973454A (en)
GB (2) GB606080A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2617787A (en) * 1949-10-27 1952-11-11 Us Rubber Co Quaternary interpolymers of (a) certain 2-alkenyl esters of alpha-olefinic polycarboxylic acids, (b) certain monovinyl benzenes, (c) certain monoolefinic carboxylic esters, and (d) certain 2-alkenyl alcohols, chlorides, ethers, or esters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2617787A (en) * 1949-10-27 1952-11-11 Us Rubber Co Quaternary interpolymers of (a) certain 2-alkenyl esters of alpha-olefinic polycarboxylic acids, (b) certain monovinyl benzenes, (c) certain monoolefinic carboxylic esters, and (d) certain 2-alkenyl alcohols, chlorides, ethers, or esters

Also Published As

Publication number Publication date
GB665269A (en) 1952-01-23
FR962260A (en) 1950-06-07
FR973454A (en) 1951-02-12

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