GB493884A - Improvements in the manufacture of higher alcohols - Google Patents

Improvements in the manufacture of higher alcohols

Info

Publication number
GB493884A
GB493884A GB11364/37A GB1136437A GB493884A GB 493884 A GB493884 A GB 493884A GB 11364/37 A GB11364/37 A GB 11364/37A GB 1136437 A GB1136437 A GB 1136437A GB 493884 A GB493884 A GB 493884A
Authority
GB
United Kingdom
Prior art keywords
per cent
solvent
liquid
per
olefines
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
GB11364/37A
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 ALCOHOL CO
Original Assignee
STANDARD ALCOHOL 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 ALCOHOL CO filed Critical STANDARD ALCOHOL CO
Publication of GB493884A publication Critical patent/GB493884A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C11/00Aliphatic unsaturated hydrocarbons
    • C07C11/02Alkenes
    • C07C11/08Alkenes with four carbon atoms
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Alcohols of four carbon atoms or more are obtained by mixing the corresponding olefine, in direct contact with a saturated hydrocarbon, normally liquid or liquid under the reaction conditions and capable of functioning as a solvent for the alcohols produced, with a catalyst consisting of one of the following aqueous solutions: 5-55 per cent sulphuric or phosphoric acid, 0,5-15 per cent hydrochloric acid, 0,5-15 per cent zinc, aluminium or cadmium chloride, or 1-40 per cent ammonium chloride, at a temperature of from 30 DEG C. to below 300 DEG C., suitably 150 DEG C., and a pressure not exceeding 300 lb. per sq. in., e.g. 50 lb. per sq. in., separating the catalyst layer from the solvent layer, and removing the alcohol formed from the solvent. When mixtures normally containing olefines and saturated hydrocarbons are used, e.g. the C4 cut, there may be no need to add extra saturated hydrocarbon. When liquid solvents are added, <PICT:0493884/IV/1> the volume is normally from 50 to 95 per cent of that of the starting material in liquid form. As shown, the reaction mixture, in which the olefine may be in gaseous or preferably liquid form, is fed through line 1 to heating coil 3, the saturated hydrocarbon when added passing in by line 2. The heated mixture of olefines and saturated hydrocarbons passes up tower 4 fitted with plates 5 each carrying a pool of, say, sulphuric acid and to which water is introduced by pipe 7. A heating jacket or coils may be provided. The reaction material passes into drum 9, gases separating through pipe 10. The liquid flows through heating coil 12 to distillation tower 13. Steam may be passed in through pipe 14, a condensing coil 15 being provided. The distillate flows through condenser 16 to vessel 17. The hydrocarbon solvent is recirculated by pump 19. If, say, a light naphtha is used as the solvent, it is distilled from the alcohol, the latter being recovered at the base of the tower 13. Pure olefines such as butylene or amylene, or mixtures obtained by cracking hydrocarbon oils, may be used. Examples relate to the treatment of C4 hydrocarbons containing 11 per cent isobutylene. Specification 453,147 is referred to. The Specification as open to inspection under Sect. 91 refers also to the use of 10 per cent acetic acid solution as a catalyst. This subject-matter does not appear in the Specification as accepted.
GB11364/37A 1936-06-06 1937-04-21 Improvements in the manufacture of higher alcohols Expired GB493884A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US493884XA 1936-06-06 1936-06-06

Publications (1)

Publication Number Publication Date
GB493884A true GB493884A (en) 1938-10-17

Family

ID=21959554

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11364/37A Expired GB493884A (en) 1936-06-06 1937-04-21 Improvements in the manufacture of higher alcohols

Country Status (1)

Country Link
GB (1) GB493884A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3527829A (en) * 1966-05-12 1970-09-08 Nippon Oil Co Ltd Process for producing high-purity isobutylene
EP0175443A2 (en) * 1984-09-17 1986-03-26 Exxon Research And Engineering Company Improved alcohol recovery process
EP0219229A1 (en) * 1985-09-16 1987-04-22 Exxon Research And Engineering Company Improved process for recovery of alcohols from acid streams

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3527829A (en) * 1966-05-12 1970-09-08 Nippon Oil Co Ltd Process for producing high-purity isobutylene
EP0175443A2 (en) * 1984-09-17 1986-03-26 Exxon Research And Engineering Company Improved alcohol recovery process
EP0175443A3 (en) * 1984-09-17 1986-07-02 Exxon Research And Engineering Company Improved alcohol recovery process
EP0219229A1 (en) * 1985-09-16 1987-04-22 Exxon Research And Engineering Company Improved process for recovery of alcohols from acid streams

Similar Documents

Publication Publication Date Title
US2581102A (en) Removal of oxygenated organic compounds from hydrocarbons
GB2043640A (en) Process for isolating methyl t-butylether from the reaction products of methanol with a c hydrocarbon cut containing isobutene
US2659453A (en) Separation of acetylene from gaseous mixtures by glycolonitrile
GB493884A (en) Improvements in the manufacture of higher alcohols
US1847597A (en) Treatment of crude pyroligneous acid
GB534856A (en) An improved catalytic cracking process
Mabery et al. On the composition of certain petroleum oils, and of refining residues
US2130669A (en) Process for producing valuable products from hydrocarbon gases
US1704732A (en) Manufacture of valuable organic products
Calingaert The Mechanism of Thermal Decomposition of the Pentanes
US2300817A (en) Formation of polymers from mixed olefins and iso-olefins
US1536544A (en) Process of purifying ethers
US1688731A (en) Dehydration of alcohols
US2591699A (en) Vapor phase treatment of combined gasoline and water phases of synthesis product with a basic compound
US1790523A (en) Process for the manufacture of secondary amyl alcohol
GB499398A (en) An improved manufacture of secondary alcohols from olefins
US2066461A (en) Process of separating and recovering hydrocarbons and alkyl esters from mixtures thereof
US1919618A (en) Process of making ethyl alcohol
US1988083A (en) Process for refining hydrocarbon oil
US1490520A (en) Process of drying alcohol
US2514291A (en) Production of secondary butyl alcohol
Clarke METHYL ETHYL ISOBUTYL METHANE.
US1844211A (en) Setts
US2038357A (en) Method of dehydrating alcohol
US1790522A (en) Olefine containing pkoduct