GB912686A - A process for the oxidation of olefinic hydrocarbons - Google Patents
A process for the oxidation of olefinic hydrocarbonsInfo
- Publication number
- GB912686A GB912686A GB3730860A GB3730860A GB912686A GB 912686 A GB912686 A GB 912686A GB 3730860 A GB3730860 A GB 3730860A GB 3730860 A GB3730860 A GB 3730860A GB 912686 A GB912686 A GB 912686A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalyst
- methyl
- pentene
- molybdenum
- copper
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Unsaturated aldehydes and ketones are produced by passing a molecular oxygen-containing gas and steam through a fluidised bed of a heavy metal-containing oxidation catalyst, thereby entraining the catalyst in suspended form in the gas leaving the catalyst bed, adding an olefinic hydrocarbon having at least 3 carbon atoms per molecule to the suspension, passing the mixture through an externally cooled elongated reaction zone maintained at 250-750 DEG C. while maintaining the catalyst in suspended state, separating the catalyst from the effluent from the reaction zone, and obtaining an a .b -unsaturated aldehyde or ketone from the effluent. Suitable catalysts are, for example, tellurium oxide alone or in combination with an oxide of molybdenum, tungsten or uranium; copper oxide in combination with a metal of the palladium-platinum group or with Group VIII elements of the fourth series; selenites and tellurites of silver, lead, iron, cobalt, nickel or cadmium; copper and silica gel with cadmium, cobalt, molybdenum, thorium, manganese, calcium or titanium; and selenium in combination with an oxide of copper, vanadium, tellurium, chromium, molybdenum, tungsten, uranium, or tin, or with copper aluminate or silicate. The preferred catalysts are those containing oxides of molybdenum and bismuth, e.g. bismuth molybdate, and, if desired, these catalysts may be modified by the addition of phosphorus or phosphorus compounds. The catalyst may be, for example, bismuth phosphomolybdate. The catalysts may be used with conventional supports. The catalyst separated from the reactor effluent may be passed into a catalyst cooling zone through which oxygen is passed thereby forming the suspension, the catalyst being cooled by indirect heat exchange with water so that steam is formed. The olefine used as starting material may be mixed with one or more saturated hydrocarbons. Suitable starting olefins are, for example, propylene, butene-1-ol-2, isobutylene, pentene-1-ol-2, 3-methyl-pentene-1, 2-methyl-butene - 1, hexene - 1, hexene - 2, 4 - methyl-pentene-1, 3,3 - dimethyl - butene-1, 4-methyl-pentene-1, octene-1, cyclopentene, cyclohexene and 3-methyl-cyclohexene. Specification 912,687 is referred to. Reference has been directed by the Comptroller to Specification 821,999.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85047859A | 1959-11-02 | 1959-11-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB912686A true GB912686A (en) | 1962-12-12 |
Family
ID=25308225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3730860A Expired GB912686A (en) | 1959-11-02 | 1960-10-31 | A process for the oxidation of olefinic hydrocarbons |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1149704B (en) |
GB (1) | GB912686A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2827380A1 (en) * | 1978-06-22 | 1980-01-10 | Hoechst Ag | METHOD FOR PRODUCING ACETALDEHYDE |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1065835B (en) * | 1959-09-24 | Esso Research And Engineering Company, Elizabeth, N. J. (V. St. A.) | Process for the dehydrogenation of two or more hydrocarbons | |
DE938844C (en) * | 1951-06-08 | 1956-02-09 | Standard Oil Dev Co | Process for the conversion of hydrocarbon residue oils |
-
1960
- 1960-10-31 DE DES71080A patent/DE1149704B/en active Pending
- 1960-10-31 GB GB3730860A patent/GB912686A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1149704B (en) | 1963-06-06 |
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