GB338152A - Improvements in the manufacture and production of valuable condensation products from diolefines - Google Patents

Improvements in the manufacture and production of valuable condensation products from diolefines

Info

Publication number
GB338152A
GB338152A GB1505729A GB1505729A GB338152A GB 338152 A GB338152 A GB 338152A GB 1505729 A GB1505729 A GB 1505729A GB 1505729 A GB1505729 A GB 1505729A GB 338152 A GB338152 A GB 338152A
Authority
GB
United Kingdom
Prior art keywords
acid
products
butadiene
reaction
benzene
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
GB1505729A
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
Priority to GB1505729A priority Critical patent/GB338152A/en
Publication of GB338152A publication Critical patent/GB338152A/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)
  • Reinforced Plastic Materials (AREA)

Abstract

338,152. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). May 14, 1929. Caoutchouc, synthetic.-The polymerization of diolefines is effected with at least 30 per cent of an inorganic oxygen-containing acid or an organic derivative of such an acid, and no other substance influencing the reaction is supplied. Suitable agents are sulphuric acid, phosphoric acid. benzene sulphonic acid, toluene sulphonic acid, ptoluene sulphochloride, benzene sulphochloride, or the like. Products of varying character are produced according to the conditions of the reaction: thus, with low temperature, short time of reaction or low concentration of the acid, only or semi-solid products are generally obtained, while by longer or more energetic action harder products are produced. The process may be effected below 0‹ C. and elevated pressures may be em. ployed. The products may be used as adhesives, as additions to paints and lacquers, as additions in the manufacture of rubber-like products for the manufacture of artificial materials such as films, threads. foils, bands, and moulded articles. In the examples (1) butadiene is added slowly to 68 per cent aqueous sulphuric acid at -10‹ C., the mixture being stirred at -7‹ C. until the whole is soluble in water and contains no butadiene; the reaction mixture is' then poured on to ice and volatile matter is removed by steam; the brown mass remaining is dissolved in a solvent such as cyclohexane and washed with water and dilute sodium carbonate solution; after distilling off the solvent a viscous oil is left which distills at 150-300‹ C., leaving as residue a clear resin which softens at 60‹ C, and is soluble in many solvents such as benzene, toluene, xylene, chloroform, and carbon tetrachloride, (2) butadiene is heated in a pressure vessel with aqueous solution of benzene sulphonic acid for 20 hours at 100‹ C. ; on cooling the brown viscous product is treated with steam to remove volatile matter, the viscous dark oil remaining being washed with sodiumcarbonate solution and water and dissolved in ether; the ether is evaporated and a small proportion of an oil is distilled off at 25 m.m. pressure and up to 200‹ C. the residue being a resin similar to that obtained in the first example; (3) butadiene is heated with 89 per cent phosphoric acid, the rest of the process being similar to that of the previous example.
GB1505729A 1929-05-14 1929-05-14 Improvements in the manufacture and production of valuable condensation products from diolefines Expired GB338152A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1505729A GB338152A (en) 1929-05-14 1929-05-14 Improvements in the manufacture and production of valuable condensation products from diolefines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1505729A GB338152A (en) 1929-05-14 1929-05-14 Improvements in the manufacture and production of valuable condensation products from diolefines

Publications (1)

Publication Number Publication Date
GB338152A true GB338152A (en) 1930-11-14

Family

ID=10052267

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1505729A Expired GB338152A (en) 1929-05-14 1929-05-14 Improvements in the manufacture and production of valuable condensation products from diolefines

Country Status (1)

Country Link
GB (1) GB338152A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2440494A (en) * 1941-10-11 1948-04-27 Standard Oil Dev Co Low-temperature polymerization of butadiene in the presence of methallyl chloride
US2579095A (en) * 1947-11-10 1951-12-18 Alexander H Kerr & Co Photopolymerization process and photopolymerizable compositions of matter

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2440494A (en) * 1941-10-11 1948-04-27 Standard Oil Dev Co Low-temperature polymerization of butadiene in the presence of methallyl chloride
US2579095A (en) * 1947-11-10 1951-12-18 Alexander H Kerr & Co Photopolymerization process and photopolymerizable compositions of matter

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