GB764298A - Improvements in the polymerisation of acrylonitrile - Google Patents

Improvements in the polymerisation of acrylonitrile

Info

Publication number
GB764298A
GB764298A GB2742852A GB2742852A GB764298A GB 764298 A GB764298 A GB 764298A GB 2742852 A GB2742852 A GB 2742852A GB 2742852 A GB2742852 A GB 2742852A GB 764298 A GB764298 A GB 764298A
Authority
GB
United Kingdom
Prior art keywords
ethyl
methyl
sodium
acrylonitrile
vinyl
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
GB2742852A
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.)
HARRY WESLEY COOVER JNR
Eastman Kodak Co
Original Assignee
HARRY WESLEY COOVER JNR
Eastman Kodak 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 HARRY WESLEY COOVER JNR, Eastman Kodak Co filed Critical HARRY WESLEY COOVER JNR
Priority to GB2742852A priority Critical patent/GB764298A/en
Publication of GB764298A publication Critical patent/GB764298A/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
    • C08F291/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00

Landscapes

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

Abstract

Graft polymers are prepared by polymerizing acrylonitrile as the sole monomeric material in the presence of a preformed interpolymer of monomers containing ethenoid unsaturation which has not been separated from its polymerization medium before the addition of acrylonitrile. Preferred monomers from which the interpolymers are formed are acrylamide and methacrylamide and their N-methyl, -ethyl, -n-propyl, -isopropyl, -n-butyl and -isobutyl substitution products, the methyl, ethyl, n-propyl and isopropyl esters of acrylic, methacrylic, acylaminoacrylic and carbalkoxyaminoacrylic acids, itaconamide and citraconamide and their N-methyl or -ethyl substitution products, vinyl acetate, propionate and butyrates, isopropenyl acetate, styrene, alpha-methylstyrene, para-acetaminostyrene, alpha-acetoxystyrene, ethylene, vinyl and vinylidene chlorides, ethyl and isopropyl vinyl ethers, methyl and ethy isopropenyl ketones, methyl and ethyl vinyl ketones, dimethyl, diethyl and diisopropyl maleates and fumarates, acrylic and methacrylic acids, fumaronitrile, acrylonitrile, methacrylonitrile, N-vinylphthalimide, and butadiene. Polymerization may be carried out in an aqueous medium or in solution in a solvent such as acetonitrile or aqueous acetone in the presence of catalysts such as organic peroxides, e.g. benzoyl, acetyl, acetyl benzoyl, lauryl, oleoyl, triacetone and urea peroxides, tert.-butyl hydroperoxide, alkyl percarbonates, sodium and potassium perborates, alkali metal and ammonium persulphates, ketazines and azines; the oxidizing catalysts may be used together with reducing agents such as potassium and sodium bisulphites. Aqueous media may contain emulsifiers such as sodium lauryl sulphate, sodium isobutyl naphthalene sulphonate, sodium 7-ethyl-2-methylundecan-4-sulphonate, sulphonated ethers, alkali metal or amine addition salts of sulphosuccinic acid esters, alkali metal salts of fatty acids containing from 12 to 20 carbon atoms, sulphonated fatty acid amides and sulphonated esters. Polymerization may also be carried out in the presence of hexyl, octyl, lauryl, dodecyl, and myristyl mercaptans as chain regulators. The graft polymers produced may be used in the preparation of dyeable fibres from solution in dimethyl formamide, either alone or in admixture with polyacrylonitrile. Specifications 358,534, [Group IV], 690,937 and 764,297 are referred to.
GB2742852A 1952-10-31 1952-10-31 Improvements in the polymerisation of acrylonitrile Expired GB764298A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2742852A GB764298A (en) 1952-10-31 1952-10-31 Improvements in the polymerisation of acrylonitrile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2742852A GB764298A (en) 1952-10-31 1952-10-31 Improvements in the polymerisation of acrylonitrile

Publications (1)

Publication Number Publication Date
GB764298A true GB764298A (en) 1956-12-28

Family

ID=10259428

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2742852A Expired GB764298A (en) 1952-10-31 1952-10-31 Improvements in the polymerisation of acrylonitrile

Country Status (1)

Country Link
GB (1) GB764298A (en)

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