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GB283841A - Improvements in and relating to the manufacture of synthetic rubber - Google Patents

Improvements in and relating to the manufacture of synthetic rubber

Info

Publication number
GB283841A
GB283841A GB1446/28A GB144628A GB283841A GB 283841 A GB283841 A GB 283841A GB 1446/28 A GB1446/28 A GB 1446/28A GB 144628 A GB144628 A GB 144628A GB 283841 A GB283841 A GB 283841A
Authority
GB
United Kingdom
Prior art keywords
isoprene
sodium
carbon dioxide
polymerized
hydroxy compound
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
GB1446/28A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB283841A publication Critical patent/GB283841A/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
    • 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)
  • Compositions Of Macromolecular Compounds (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

283,841. I. G. Farbenindustrie Akt.- Ges. Jan. 15, 1927, [Convention date]. Caoutchouc, synthetic.-Hydrocarbons suitable for the manufacture of synthetic rubber, such as butadiene, isoprene, and dimethylbutadiene, are polymerized by treatment with an alkali metal, such as sodium or potassium, in an atmosphere of hydrogen, nitrogen, or carbon dioxide and in the presence of an organic hydroxy compound or ether; the quantity of organic hydroxy compound employed should not be sufficient to react with all the alkali metal present. It is preferred to use an organic hydroxy compound or ether of high molecular weight, such as starch, cellulose, a cellulose ether, or superficially oxidized rubber. The reaction mixture may include an inorganic hydroxy compound, the presence of which in the mixture may be ensured by using superficially oxidized sodium or by treating the hydrocarbon in a moist state. The reaction mixture mav include also an inert solvent, such as a hydrocarbon, which may be removed from the product to any desired extent. The polymerization may be effected in the cold or at a raised temperature, and the mass may be in motion or at rest. According to the examples, (1) isoprene, glycerine, and sodium wire are agitated together at 60‹ C. in an atmosphere of carbon dioxide until a polymerized product is obtained; (2) dried isoprene is mixed with starch and sodium and the mixture is treated as in example 1; (3) isoprene previously saturated with hydrogen is mixed with ethyl cellulose and superficially oxidized sodium and is polymerized at 40-50‹ C. in an atmosphene of hydrogen; (4) imperfectly dried isoprene containing isoprene alcohol as an impurity is treated with sodium, solid caustic soda, and benzene, and, after the mixture has been saturated with carbon dioxide, is polymerized at 60-70‹ C. in an atmosphere of carbon dioxide.
GB1446/28A 1968-06-28 1928-01-16 Improvements in and relating to the manufacture of synthetic rubber Expired GB283841A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE283841X 1968-06-28

Publications (1)

Publication Number Publication Date
GB283841A true GB283841A (en) 1929-04-16

Family

ID=6048581

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1446/28A Expired GB283841A (en) 1968-06-28 1928-01-16 Improvements in and relating to the manufacture of synthetic rubber

Country Status (1)

Country Link
GB (1) GB283841A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2692255A (en) * 1952-01-19 1954-10-19 Goodrich Co B F Modification of alkali metal catalyzed polymerization of conjugated diene hydrocarbons

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2692255A (en) * 1952-01-19 1954-10-19 Goodrich Co B F Modification of alkali metal catalyzed polymerization of conjugated diene hydrocarbons

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