GB589353A - Process for the production of rubber-like polymers - Google Patents

Process for the production of rubber-like polymers

Info

Publication number
GB589353A
GB589353A GB22874/44A GB2287444A GB589353A GB 589353 A GB589353 A GB 589353A GB 22874/44 A GB22874/44 A GB 22874/44A GB 2287444 A GB2287444 A GB 2287444A GB 589353 A GB589353 A GB 589353A
Authority
GB
United Kingdom
Prior art keywords
alkyl halide
residue
iso
distilled
halide
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
GB22874/44A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development 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 Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to GB22874/44A priority Critical patent/GB589353A/en
Publication of GB589353A publication Critical patent/GB589353A/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
    • C08F210/00Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/04Monomers containing three or four carbon atoms
    • C08F210/08Butenes
    • C08F210/10Isobutene
    • C08F210/12Isobutene with conjugated diolefins, e.g. butyl rubber
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In the low temperature polymerization of iso-olefines having up to 8 carbon atoms with or without a minor proportion of a diolefine having up to 14 carbon atoms, in an alkyl halide diluent having less than 5 carbon atoms at temperatures below -40 DEG C. in the presence of a Friedel-Crafts catalyst dissolved in the same alkyl halide, the reaction slurry is passed into warm water in a flasking zone and its volatile components vaporized and withdrawn, cooled, compressed and dried. The volatile components are then fractionated to give substantially pure alkyl halide (which is used for the preparation of catalyst solution), a mixture of iso-olefine and alkyl halide which is recycled to the feed, and a residue of hydrocarbon by-products which is discarded. The residue may be further fractionated to separate any unreacted diolefine present which is recycled to the feed. Where the alkyl halide is very volatile, e.g. methyl chloride, the pure halide is withdrawn in a first distillation and the mixture of alkyl halide and iso-olefine distilled from the residue, but where a less volatile halide is used, e.g. ethyl chloride, the mixture is removed first and pure alkyl halide distilled from the residue. The alkyl halide recovered may be purified by scrubbing with sulphuric acid, passed over dry caustic soda and redistilled before using to prepare catalyst solution. Isobutylene is the preferred iso-olefine and diolefines specified include butadiene, isoprene, dimethyl butadiene, piperylene, myrcene and dimethylallene. Isobutylene for the feed may be distilled twice, first to remove water and again to remove isobutane, normal butylenes and C5 and heavier hydrocarbons. The diolefine used may be first purified by washing with water and distilled after addition of inhibitor, e.g. tert-butyl catechol or hydroquinone. Specifications 432,196, 483,453, 561,324 and 565,974 are referred to.
GB22874/44A 1944-11-17 1944-11-17 Process for the production of rubber-like polymers Expired GB589353A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB22874/44A GB589353A (en) 1944-11-17 1944-11-17 Process for the production of rubber-like polymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB22874/44A GB589353A (en) 1944-11-17 1944-11-17 Process for the production of rubber-like polymers

Publications (1)

Publication Number Publication Date
GB589353A true GB589353A (en) 1947-06-18

Family

ID=10186422

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22874/44A Expired GB589353A (en) 1944-11-17 1944-11-17 Process for the production of rubber-like polymers

Country Status (1)

Country Link
GB (1) GB589353A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3217049A (en) * 1963-03-04 1965-11-09 Exxon Research Engineering Co Recovery of methyl chloride

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3217049A (en) * 1963-03-04 1965-11-09 Exxon Research Engineering Co Recovery of methyl chloride

Similar Documents

Publication Publication Date Title
US2139179A (en) Purification of alcohols
US2479120A (en) Production of relatively straight chain alkyl aromatic hydrocarbons
GB589353A (en) Process for the production of rubber-like polymers
US2805258A (en) Process for the preparation of hydroperoxides from diisopropylbenzenes
US2560362A (en) Acid extraction of mixed olefin hydrocarbons
US2379731A (en) Olefin isomerization process
GB682022A (en) A process for the production of organic hydroperoxides and the organic hydroperoxides so produced
US2393132A (en) Production of alkenylpyrroles
US2385300A (en) Conversion of hydrocarbons
US2472908A (en) Process for treating a hydrocarbon mixture which is contaminated by small amounts oforganic fluorine compounds
GB664179A (en) Removal of catalyst from olefin polymer products
US2420749A (en) Treatment of monocyclic olefinic hydrocarbons
US2370494A (en) Manufacture of alkanoic acids
US2438211A (en) Process using aluminum bromide-hydrocarbon complex to promote alkylation of aromatic hydrocarbons by olefins of more than two carbon atoms per molecule
US2563050A (en) Treatment of olefins with liquid anhydrous hydrogen bromide
US2397495A (en) Conversion of alkylated aromatic hydrocarbons
US2848512A (en) Preparation of hydrindacenes
US2810771A (en) Tertiary alkylation of impurities in crude diisopropylbenzene mixtures
GB590613A (en) Improvements in or relating to the production and separation of tertiary olefins
US2396844A (en) Alkylation of paraffin hydrocarbons
US2166981A (en) Process for esterifying polymerized olefines
Bobroff et al. Peroxy Esters. meso-Di-t-butylperoxy 2, 3-Diphenylsuccinate
US2385705A (en) Production of butadiene
US2431756A (en) Treatment of terpenic hydrocarbons
US2347667A (en) Isomerization of conjugated diolefins