GB493884A - Improvements in the manufacture of higher alcohols - Google Patents
Improvements in the manufacture of higher alcoholsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C07C11/08—Alkenes with four carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/03—Preparation 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
- C07C29/04—Preparation 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.
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)
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 |
-
1937
- 1937-04-21 GB GB11364/37A patent/GB493884A/en not_active Expired
Cited By (4)
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 |
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