GB709674A - Oxidation of hydrocarbons - Google Patents
Oxidation of hydrocarbonsInfo
- Publication number
- GB709674A GB709674A GB10472/52A GB1047252A GB709674A GB 709674 A GB709674 A GB 709674A GB 10472/52 A GB10472/52 A GB 10472/52A GB 1047252 A GB1047252 A GB 1047252A GB 709674 A GB709674 A GB 709674A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxygen
- reaction mixture
- preferred
- reaction
- acetic
- 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
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Liquid hydrocarbons containing less than 6 carbon atoms are oxidized in the liquid phase in a solvent medium containing an oxidation catalyst by means of gaseous oxygen with removal of water from the reaction mixture substantially as it is formed. Preferably a portion of the reaction mixture is allowed to distil over during reaction, condensed to allow of water removal by separation into phases, and the hydrocarbon phase returned to the reaction zone. The aqueous phase may be treated for recovery of water-soluble products. Reaction temperatures of 125-225 DEG C. and pressures of 200-2000 p.s.i. are preferred. Air or oxygen may be used as oxidizing gas. A ratio of 0.5-10 mols. of oxygen to each mol. of fresh hydrocarbon introduced is preferred. Recycled hydrocarbon may range from 5-50 parts per part of fresh hydrocarbon introduced. Preferably the oxygen is completely consumed. Metal salts, especially of cobalt, nickel, copper or manganese with acetic, propionic, benzoic or naphthenic acids are preferred; 0.1-1.5 per cent by weight of catalyst based on solvent is used. Specified solvents are acetic-acid, acetone, benzene and methyl or ethyl acetate. The partial distillation may be assisted by the use of inert stripping gases. The condenser is preferably maintained at -7 DEG -+25 DEG C. In an example, n-butane in acetic acid with cobalt acetate is treated with air, a portion of the reaction mixture being distilled as above described, and mainly acetic acid recovered with some acetate esters and methyl ethyl ketone.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US709674XA | 1951-04-28 | 1951-04-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB709674A true GB709674A (en) | 1954-06-02 |
Family
ID=22098439
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10472/52A Expired GB709674A (en) | 1951-04-28 | 1952-04-25 | Oxidation of hydrocarbons |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB709674A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4032570A (en) * | 1971-11-08 | 1977-06-28 | Gulf Research & Development Company | Process for converting butane to acetic acid |
US4131742A (en) * | 1975-11-03 | 1978-12-26 | Bp Chemicals Limited | Cobalt-catalyzed oxidation of hydrocarbons |
FR2478626A1 (en) * | 1980-03-20 | 1981-09-25 | Union Carbide Corp | CONTINUOUS CATALYTIC PROCESS FOR LIQUID PHASE OXIDATION OF ACETIC ACID BUTANE |
EP1806331A2 (en) * | 2006-01-10 | 2007-07-11 | Rohm and Haas Company | Liquid-phase (Amm)oxidation process |
-
1952
- 1952-04-25 GB GB10472/52A patent/GB709674A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4032570A (en) * | 1971-11-08 | 1977-06-28 | Gulf Research & Development Company | Process for converting butane to acetic acid |
US4131742A (en) * | 1975-11-03 | 1978-12-26 | Bp Chemicals Limited | Cobalt-catalyzed oxidation of hydrocarbons |
FR2478626A1 (en) * | 1980-03-20 | 1981-09-25 | Union Carbide Corp | CONTINUOUS CATALYTIC PROCESS FOR LIQUID PHASE OXIDATION OF ACETIC ACID BUTANE |
EP1806331A2 (en) * | 2006-01-10 | 2007-07-11 | Rohm and Haas Company | Liquid-phase (Amm)oxidation process |
EP1806331A3 (en) * | 2006-01-10 | 2007-07-18 | Rohm and Haas Company | Liquid-phase (Amm)oxidation process |
US7456313B2 (en) | 2006-01-10 | 2008-11-25 | Rohm And Haas Company | Liquid-phase (AMM)oxidation process |
KR100880857B1 (en) * | 2006-01-10 | 2009-01-30 | 롬 앤드 하아스 컴패니 | Liquid-phase Ammoxidation process |
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