GB1198882A - Oxidation of Olefins - Google Patents
Oxidation of OlefinsInfo
- Publication number
- GB1198882A GB1198882A GB2250468A GB2250468A GB1198882A GB 1198882 A GB1198882 A GB 1198882A GB 2250468 A GB2250468 A GB 2250468A GB 2250468 A GB2250468 A GB 2250468A GB 1198882 A GB1198882 A GB 1198882A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tellurium
- metal
- oxygen
- methacrolein
- acrolein
- 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
-
- 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
- B01J23/32—Manganese, technetium or rhenium
- B01J23/34—Manganese
-
- 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
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/057—Selenium or tellurium; Compounds thereof
- B01J27/0576—Tellurium; Compounds thereof
-
- 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)
Abstract
1,198,882. Acrolein; methacrolein; acrylic acid; methacrylic acid. MONTECATINI EDISON S.p.A. 13 May, 1968 [16 May, 1967], No. 22504/68. Heading C2C. [Also in Division B1] Acrolein and/or acrylic acid, or methacrolein and/or methacrylic acid, is prepared by the vapour phase oxidation of propylene and/or acrolein, or of isobutylene and/or methacrolein, with oxygen in the presence of a catalyst composition comprising (A) a mono-phase system based on molybdenum trioxide, the crystal lattice of which has been altered by inclusion of atoms of a substituent metal Ms in an amount such that the atomic ratio of Ms to Mo is 1 to 9, the metal Ms being manganese, cobalt or nickel, and (B) tellurium, present either as the metal or as a compound thereof in an amount such as to provide from 0À1 to 10% by weight of tellurium metal with respect to the total weight of the mono-phase system and the tellurium metal or tellurium compound. The catalyst composition, which may be in the form either of a fixed bed or of a fluidized bed, optionally may include a small quantity of a salt or oxide of an alkali metal and/or may be supported on a carrier material, for example silica, carborundum or pumice stone. The alkali metal may result from the use of sodium telluride or potassium telluride as the (or part of the) source of tellurium; alternatively, the tellurium may be provided by another telluride, for example Ag 2 Te, Cu 2 Te, Bi 2 Te 3 , MoTe 2 , CoTe 2 , NiTe 2 , AgBiTe 2 or NiMoTe 4 . The oxidation is carried out either at atmospheric pressure or at elevated pressure, for example at from 2 to 10 atmospheres, at a temperature preferably of from 300‹ to 550‹ C. and with a contact time preferably of from 0À05 to 5 seconds, the molar ratio of propylene and/or acrolein, or of isobutylene and/or methacrolein, to oxygen preferably being between 1 to 0À5 and 1 to 3. The oxygen may be supplied in the form of air, pure oxygen or a mixture of air and oxygen. The oxidation may be carried out in the presence of a halogen-containing organic compound, for example allyl chloride or allyl bromide, and/or in the presence of an inert gaseous diluent, for example steam, nitrogen, carbon dioxide, a saturated hydrocarbon such as for example propane, or the oxidation reaction products after removal therefrom of product aldehyde and/or product acid; product aldehyde may be recycled in order to be oxidized further to the corresponding acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT796268 | 1967-05-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1198882A true GB1198882A (en) | 1970-07-15 |
Family
ID=11125603
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2250468A Expired GB1198882A (en) | 1967-05-16 | 1968-05-13 | Oxidation of Olefins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1198882A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113813989A (en) * | 2020-06-18 | 2021-12-21 | 中国石油天然气股份有限公司 | Process for the preparation of acrolein |
-
1968
- 1968-05-13 GB GB2250468A patent/GB1198882A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113813989A (en) * | 2020-06-18 | 2021-12-21 | 中国石油天然气股份有限公司 | Process for the preparation of acrolein |
CN113813989B (en) * | 2020-06-18 | 2023-05-26 | 中国石油天然气股份有限公司 | Process for preparing acrolein |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |