GB990639A - Process for the preparation of a saturated compound containing the>c=o grouping - Google Patents
Process for the preparation of a saturated compound containing the>c=o groupingInfo
- Publication number
- GB990639A GB990639A GB3277661A GB3277661A GB990639A GB 990639 A GB990639 A GB 990639A GB 3277661 A GB3277661 A GB 3277661A GB 3277661 A GB3277661 A GB 3277661A GB 990639 A GB990639 A GB 990639A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxygen
- oxide
- olefine
- vanadium
- chosen
- 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
-
- 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
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/28—Molybdenum
-
- 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
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
-
- 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
-
- 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
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
-
- 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
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
A saturated compound containing the >C=O grouping is made by oxidizing an olefine in the vapour phase with oxygen or a gas containing free oxygen, in the presence of steam and a catalytic composition comprising at least one oxide of molybdenum, tungsten or vanadium, with the proviso that if vanadium oxide is chosen it is used in the form of a heteropolyacid or a salt thereof the reaction may be carried out in presence of a diluent e.g. nitrogen or other gases such as carbon oxides and aliphatic hydrocarbons. Preferably, the water/olefine molar ratio is between 1 and 10, the oxygen/olefine molar ratio is between 0.1 and 5, and the reaction temperature is 180 DEG -450 DEG C. with contact times of 0.05-10 seconds, at 1 to 10 atmospheres. If oxygen/olefine ratio is high, the oxygen may be introduced a little at a time at different levels of the reactor. The unreacted gases may be recycled. In examples ethylene is converted to acetaldehyde and acetic acid and propylene is converted to acetone. Ethyl alcohol and carbon oxides are also formed.ALSO:A catalyst composition for use in a process for the preparation of a saturated compound containing the \yRC=O grouping comprises at least one oxide of molybdenum, tungsten or vanadium, with the proviso that if vanadium oxide is chosen it is used in the form of a heteropoly-acid or a salt thereof. The catalyst may contain in addition, at least one oxide or acid of boron, aluminium, silicon, titanium, germanium, zirconium, tin, cerium, phosphorus, arsenic, antimony, bismuth, sulphur, chromium, selenium, tellurium, manganese, iron, cobalt, or nickel; at least one heteropolyacid chosen from phosphomolybdic, silicomolybdic, phosphotungstic, silicotungstic, phosphomolybdotungstic, silicomolybdotungstic, phosphovanadomolybdic, phosphovanadotungstic, chromomolybdic, vanadomolybdic, manganomolybdic or arsenomolybdic acids; or at least one copper, bismuth, iron, nickel, cobalt, manganese, cadmium, zinc, alkali metal, ammonium or alkaline earth metal salt of any of the above heteropolyacids. The catalyst may be unsupported, in pellet form, or suported on e.g. diatomaceous earths, bentonite, alumina, bauxite, silica, or zirconium dioxide, by impregnating these materials with a solution or suspension of the active components on water, alcohols, esters, ethers or dioxan.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1169560 | 1960-07-01 | ||
IT2041960 | 1960-11-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB990639A true GB990639A (en) | 1965-04-28 |
Family
ID=26326436
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3277661A Expired GB990639A (en) | 1960-07-01 | 1961-06-30 | Process for the preparation of a saturated compound containing the>c=o grouping |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE605502A (en) |
DE (1) | DE1443108A1 (en) |
GB (1) | GB990639A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3546139A (en) * | 1969-11-03 | 1970-12-08 | Eastman Kodak Co | Molybdenum,niobium,tantalum,arsenic in catalysts for vapor phase production of alpha,beta-unsaturated acids |
US3948983A (en) * | 1970-12-05 | 1976-04-06 | Chemische Werke Huls Aktiengesellschaft | Process for the preparation of acetic acid by catalytic gas-phase oxidation of butenes |
CN111545228A (en) * | 2020-05-29 | 2020-08-18 | 烟台大学 | Microwave-assisted aged heteropolyacid salt/cerium oxide composite catalyst and preparation method thereof |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3342869A (en) * | 1962-12-26 | 1967-09-19 | Gulf Oil Corp | Novel oxidation catalyst compositions and processes |
BE639083A (en) * | 1962-10-24 | |||
NL299920A (en) * | 1962-10-31 | |||
GB1053582A (en) * | 1962-12-26 | |||
US3293290A (en) * | 1963-03-04 | 1966-12-20 | Union Oil Co | Process for the production of unsaturated aldehydes and acids |
US3301906A (en) * | 1963-06-27 | 1967-01-31 | Petro Tex Chem Corp | Oxidation of isobutylene to methacrolein |
US3274255A (en) * | 1963-06-27 | 1966-09-20 | Petro Tex Chem Corp | Oxidation of isobutylene to methacrolein |
US3271459A (en) * | 1963-06-27 | 1966-09-06 | Petro Tex Chem Corp | Production of methacrolein |
US3260753A (en) * | 1963-10-14 | 1966-07-12 | Eastman Kodak Co | Catalytic process for preparing acrolein |
DE1207367B (en) * | 1964-05-30 | 1965-12-23 | Roehm & Haas Gmbh | Process for the production of acrolein or methacrolein |
US3359309A (en) * | 1964-06-15 | 1967-12-19 | Eastman Kodak Co | Catalytic process for preparing unsaturated aliphatic aldehydes and monocarboxylic acids from olefins |
US3468958A (en) * | 1965-09-30 | 1969-09-23 | Standard Oil Co | Process for oxidation of olefins to unsaturated aldehydes and acids |
US3499038A (en) * | 1966-08-22 | 1970-03-03 | Eastman Kodak Co | Oxidation of ethylenically unsaturated hydrocarbons |
US3417144A (en) * | 1966-12-19 | 1968-12-17 | Gulf Oil Corp | Novel oxidation processes |
US3437690A (en) * | 1967-11-21 | 1969-04-08 | Eastman Kodak Co | Vapor phase process for preparing unsaturated aliphatic aldehydes and monocarboxylic acids |
-
1961
- 1961-06-28 BE BE605502A patent/BE605502A/en unknown
- 1961-06-28 DE DE19611443108 patent/DE1443108A1/de active Pending
- 1961-06-30 GB GB3277661A patent/GB990639A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3546139A (en) * | 1969-11-03 | 1970-12-08 | Eastman Kodak Co | Molybdenum,niobium,tantalum,arsenic in catalysts for vapor phase production of alpha,beta-unsaturated acids |
US3948983A (en) * | 1970-12-05 | 1976-04-06 | Chemische Werke Huls Aktiengesellschaft | Process for the preparation of acetic acid by catalytic gas-phase oxidation of butenes |
CN111545228A (en) * | 2020-05-29 | 2020-08-18 | 烟台大学 | Microwave-assisted aged heteropolyacid salt/cerium oxide composite catalyst and preparation method thereof |
CN111545228B (en) * | 2020-05-29 | 2023-05-23 | 烟台大学 | Microwave-assisted aging heteropolyacid salt/cerium oxide composite catalyst and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
BE605502A (en) | 1961-11-16 |
DE1443108A1 (en) | 1971-12-02 |
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