GB876024A - Process for the manufacture of aldehydes and ketanes - Google Patents
Process for the manufacture of aldehydes and ketanesInfo
- Publication number
- GB876024A GB876024A GB88/58A GB8858A GB876024A GB 876024 A GB876024 A GB 876024A GB 88/58 A GB88/58 A GB 88/58A GB 8858 A GB8858 A GB 8858A GB 876024 A GB876024 A GB 876024A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalysts
- chloride
- palladium
- metals
- compound
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
Abstract
Aldehydes and ketones are produced by passing an olefine and oxygen, or a gas containing oxygen, over a catalyst containing a compound of a transition metal of the 5th to 8th groups or 1st sub-group of the Periodic System, the catalyst containing ions of the transition element and anions of strong acids, in the presence of steam or a substance capable of forming steam under the reaction conditions. Particularly good catalysts are those containing the compounds, especially the halides, of the platinum metals, in particular of palladium and rhodium. It is advantageous to use catalysts that contain, in addition to a compound of one of the platinum metals, compounds of other transition metals particularly those capable of existing in several valency states. Preferably the catalysts are deposited on supports having a large surface, e.g. active carbon, alumina, silica, pumice and silicates. The activity of the catalysts can be enhanced by the addition of acidic substances. The preferred temperature range for carrying out the process is 50-300 DEG C. and the preferred pressure range 0.1-20 atm. gauge. In the examples various catalysts are used for the conversion of ethylene to acetaldehyde, propylene to acetone, butines to methyl ethyl ketone and styrene to acetophenone.ALSO:Catalysts for use in the oxidation of olefines to the corresponding aldehydes or ketones comprise a compound of a transition metal of the 5th to 8th Group or 1st subgroup of the Periodic System, the catalyst containing ions of said transition metals and anions of strong acids. Preferred catalysts are those containing compounds, especially halides, of the platinum metals, particularly palladium and rhodium. It is advantageous to use catalysts that contain, in addition to a compound of one of the platinum metals, compounds of other transition metals, particularly those capable of existing in several valency states. Preferably the catalysts are deposited on supports having a large surface area, e.g. active carbon alumina, silica, pumice and silicates, e.g. montmorillonite. The activity of the catalysts is enhanced by the addition of acidic substances. The metallic salts may be obtained from the metals themselves under the reaction conditions. In the examples supported catalysts are prepared from palladium chloride alone or with one or more of ferric chloride or sulphate, cupric acetate chloride or sulphate manganous chloride, magnesium perchlorate or calcium carbonate or chloride; palladium phosphate with one or more of ferric chloride, manganese sulphate, copper sulphate, cobalt chloride or copper acetate; palladium and cupric bromides and ferric nitrate; cupro-hexaprom platinate; rhodium hydroxide and hydrochloric acid; iridium and hydrochloric acid; ruthenium chloride and ferric chloride; VOSO4 with or without sodium hexahydroxy platinate; chloroauric acid and ferric chloride; ferric chloride alone or with platinum chloride; cupric bromide and chromic chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE876024X | 1957-01-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB876024A true GB876024A (en) | 1961-08-30 |
Family
ID=6817533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB88/58A Expired GB876024A (en) | 1957-01-04 | 1958-01-01 | Process for the manufacture of aldehydes and ketanes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB876024A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3384669A (en) * | 1962-07-25 | 1968-05-21 | Celanese Corp | Process and catalyst for oxidizing olefins to carbonyl compounds |
US3668257A (en) * | 1966-08-08 | 1972-06-06 | Union Oil Co | Oxidation of olefins |
US4528401A (en) * | 1982-09-21 | 1985-07-09 | Exxon Research & Engineering Co. | Catalytic process for the manufacture of ketones |
US4560804A (en) * | 1982-09-21 | 1985-12-24 | Exxon Research & Engineering Co. | Catalytic process for the manufacture of ketones |
US4560803A (en) * | 1982-09-21 | 1985-12-24 | Exxon Research & Engineering Co. | Catalysts and process for oxidation of olefins to ketones |
US4737482A (en) * | 1983-07-25 | 1988-04-12 | Exxon Research & Engineering Co. | Catalysts for oxidation of olefins to ketones |
US4876392A (en) * | 1982-09-21 | 1989-10-24 | Exxon Research & Engineering Company | Process for preparation of keystones by oxidation of secondary alcohols using a trimetallic catalyst comprising molybdenum, rhenium and a group VIII noble metal |
-
1958
- 1958-01-01 GB GB88/58A patent/GB876024A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3384669A (en) * | 1962-07-25 | 1968-05-21 | Celanese Corp | Process and catalyst for oxidizing olefins to carbonyl compounds |
US3668257A (en) * | 1966-08-08 | 1972-06-06 | Union Oil Co | Oxidation of olefins |
US4528401A (en) * | 1982-09-21 | 1985-07-09 | Exxon Research & Engineering Co. | Catalytic process for the manufacture of ketones |
US4560804A (en) * | 1982-09-21 | 1985-12-24 | Exxon Research & Engineering Co. | Catalytic process for the manufacture of ketones |
US4560803A (en) * | 1982-09-21 | 1985-12-24 | Exxon Research & Engineering Co. | Catalysts and process for oxidation of olefins to ketones |
US4876392A (en) * | 1982-09-21 | 1989-10-24 | Exxon Research & Engineering Company | Process for preparation of keystones by oxidation of secondary alcohols using a trimetallic catalyst comprising molybdenum, rhenium and a group VIII noble metal |
US4737482A (en) * | 1983-07-25 | 1988-04-12 | Exxon Research & Engineering Co. | Catalysts for oxidation of olefins to ketones |
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