GB578846A - Manufacture of polymeric materials from butadiene or its homologues - Google Patents

Manufacture of polymeric materials from butadiene or its homologues

Info

Publication number
GB578846A
GB578846A GB245543A GB245543A GB578846A GB 578846 A GB578846 A GB 578846A GB 245543 A GB245543 A GB 245543A GB 245543 A GB245543 A GB 245543A GB 578846 A GB578846 A GB 578846A
Authority
GB
United Kingdom
Prior art keywords
butadiene
acid
sodium
soluble
saponifiable
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
GB245543A
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.)
DENIS BERTRAM KELLY
Imperial Chemical Industries Ltd
Original Assignee
DENIS BERTRAM KELLY
Imperial Chemical Industries Ltd
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 DENIS BERTRAM KELLY, Imperial Chemical Industries Ltd filed Critical DENIS BERTRAM KELLY
Priority to GB245543A priority Critical patent/GB578846A/en
Priority to FR930136D priority patent/FR930136A/en
Publication of GB578846A publication Critical patent/GB578846A/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
    • C08F4/00Polymerisation catalysts
    • C08F4/28Oxygen or compounds releasing free oxygen
    • 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
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F36/04Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated

Landscapes

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

Abstract

Rubber-like products are obtained by polymerizing an aqueous mixture comprising (a) one or more saponifiable derivatives of acrylic acid, methacrylic acid or a -chloracrylic acid; (b) butadiene-1 : 3 or its homologues or mixtures thereof; (c) persulphuric acid or a water-soluble persulphate; and (d) a water-soluble salt of an oxyacid of sulphur having reducing properties. The saponifiable derivatives referred to are the esters, amides and nitriles of the said acids. In examples, butadiene is polymerized with acrylonitrile, methylmethacrylate and ethylacrylate in the presence of sodium hydrosulphite, sodium thiosulphate or sodium sulphite and ammonium persulphate. Phenyl-b -naphthylamine is used as an anti-oxidant and the sodium salts of sulphated sperm oil alcohols are used as emulsifying agent. Disodium hydrogen phosphate and citric acid or sodium acetate and acetic acid are also added. The polymers are coagulated with alcohol and brine and are washed and dried. In another example, 2 : 3-dimethylbutadiene is polymerized with acrylonitrile. Other salts of oxyacids of sulphur mentioned are alkali metal and ammonium pyrosulphites, bisulphites and sulphoxylates and addition compounds with aldehydes and ketones. 2-Methyl butadiene-1 : 3 is specified as a butadiene homologue. Soaps, sulphonated fats and oils and soluble cellulose ethers may be used as emulsifying agents.
GB245543A 1943-02-15 1943-02-15 Manufacture of polymeric materials from butadiene or its homologues Expired GB578846A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB245543A GB578846A (en) 1943-02-15 1943-02-15 Manufacture of polymeric materials from butadiene or its homologues
FR930136D FR930136A (en) 1943-02-15 1946-07-02 Manufacture of polymeric materials from butadiene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB245543A GB578846A (en) 1943-02-15 1943-02-15 Manufacture of polymeric materials from butadiene or its homologues

Publications (1)

Publication Number Publication Date
GB578846A true GB578846A (en) 1946-07-15

Family

ID=9739876

Family Applications (1)

Application Number Title Priority Date Filing Date
GB245543A Expired GB578846A (en) 1943-02-15 1943-02-15 Manufacture of polymeric materials from butadiene or its homologues

Country Status (2)

Country Link
FR (1) FR930136A (en)
GB (1) GB578846A (en)

Also Published As

Publication number Publication date
FR930136A (en) 1948-01-16

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