GB360331A - Process for absorbing isobutylene in strong acids - Google Patents

Process for absorbing isobutylene in strong acids

Info

Publication number
GB360331A
GB360331A GB9413/31A GB941331A GB360331A GB 360331 A GB360331 A GB 360331A GB 9413/31 A GB9413/31 A GB 9413/31A GB 941331 A GB941331 A GB 941331A GB 360331 A GB360331 A GB 360331A
Authority
GB
United Kingdom
Prior art keywords
isobutylene
acid
distillation
absorbed
sulphuric
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
GB9413/31A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB360331A publication Critical patent/GB360331A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/03Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
    • C07C29/04Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
    • C07C29/05Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds with formation of absorption products in mineral acids and their hydrolysis
    • C07C29/06Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds with formation of absorption products in mineral acids and their hydrolysis the acid being sulfuric acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In the process of absorbing isobutylene in strong acids, e.g sulphuric, phosphoric, and toluene sulphonic acids, more molecular proportions of isobutylene are absorbed per molecule of acid than correspond to the basicity of the acid. The acid liquors obtained may be worked up into polymers of isobutylene, mainly di- and tri-isobutylene, by heating, preferably under pressure, with or without previous dilution; or tertiary butyl alcohol may be obtained by distillation. If the distillation is effected in such a manner as to obtain a quick removal of the vapours, e.g. by distillation with steam or under reduced pressure, or both, it is unnecessary first to neutralize the acid liquor, but it is preferred to have during the distillation an acid concentration of less than 40 per cent when sulphuric acid is employed. The best yield of the alcohol from the isobutylene absorbed is obtained with not more than 3 molecules of isobutylene per molecule of sulphuric acid. In examples (1) isobutylene is absorbed in sulphuric acid. (2) Isobutylene is absorbed in isopropyl sulphuric acid, and the mass is then neutralized with ammonia, and steam distilled. The alcohols are salted out and dried. (3) The alcohols are distilled off under reduced pressure. (4) The process is similar to that of Example 2. (5) The acid liquor is diluted slightly and heated in a closed tube to produce di-and tri-isobutylene. (6) The acid liquor is heated without dilution, whereby the proportion of tri-isobutylene is increased slightly.
GB9413/31A 1930-04-28 1931-03-27 Process for absorbing isobutylene in strong acids Expired GB360331A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL360331X 1930-04-28

Publications (1)

Publication Number Publication Date
GB360331A true GB360331A (en) 1931-11-05

Family

ID=19785375

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9413/31A Expired GB360331A (en) 1930-04-28 1931-03-27 Process for absorbing isobutylene in strong acids

Country Status (1)

Country Link
GB (1) GB360331A (en)

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