GB694354A - Oxidation of olefines - Google Patents

Oxidation of olefines

Info

Publication number
GB694354A
GB694354A GB9573/49A GB957349A GB694354A GB 694354 A GB694354 A GB 694354A GB 9573/49 A GB9573/49 A GB 9573/49A GB 957349 A GB957349 A GB 957349A GB 694354 A GB694354 A GB 694354A
Authority
GB
United Kingdom
Prior art keywords
copper
contact material
selenium
olefine
examples
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
Application number
GB9573/49A
Inventor
David James Hadley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB9573/49A priority Critical patent/GB694354A/en
Publication of GB694354A publication Critical patent/GB694354A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/21Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C47/22Acryaldehyde; Methacryaldehyde
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation 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
    • C07C45/34Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation 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
    • C07C45/34Preparation 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
    • C07C45/35Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/21Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation

Abstract

In a process for the manufacture of unsaturated aldehydes olefines of the general formula <FORM:0694354/IV (b)/1> in which R is a hydrogen atom or alkyl group, are passed with molecular oxygen, with or without the admixture of inert gases, at temperatures of 180 DEG to 400 DEG C. in the presence in the reaction zone of elementary selenium over a contact material comprising the chromate, molybdate, sulphate, tungstate or vanadate of copper. The copper compounds may be distributed on a carrier such as pumice, asbestos, silica gel and alumina or may be formed into pellets. The elementary selenium may be added to the mixture of gaseous reactants as vapour, e.g. part or the whole of the olefine or olefine-oxygen mixture may be passed over heated selenium or it may be generated in situ by the decomposition of selenides, such as selenides of silver, antimony and cobalt, added to the contact mass containing the copper compounds. Alternatively elementary selenium may be mixed with the contact material before use. The molecular oxygen may be pure or commercial oxygen or air and the amount of olefine in the gas mixtures should be less than that corresponding to the lower explosion limit. Inert gases may be added such as carbon dioxide and steam and these may be removed by scrubbing with alkali or condensation respectively from the reaction mixture when it is desired to recycle unreacted olefine. In some cases the contact material may be given a preliminary heat treatment. The process may be carried out in a single pass or continuously when part of the gas is vented and the remainder is recirculated after replenishing the olefine and molecular oxygen. Unsaturated aldehydes produced by the process are recovered from the reaction mixture, e.g. by scrubbing with water. In examples propylene mixed with air is passed over heated selenium and then through a tube containing heated contact material which consists of (1) copper sulphate on alumina, (2) copper vanadate, (3) copper tungstate, (4) copper chromate and (5) copper molybdate, the material being formed into pellets in examples 2-5, graphite being added as lubricant in examples 2 and 3. By replacing propylene by isobutene or any other olefine of the defined structure the corresponding unsaturated aldehyde is obtained. Specifications 625,330, 648,386 and 655,210 are referred to.ALSO:In a process for the manufacture of unsaturated aldehydes by passing olefines of the general formula <FORM:0694354/III/1> in which R is a hydrogen atom or alkyl group, with molecular oxygen, with or without the admixture of inert gases, at temperatures of 180 DEG to 400 DEG C in the presence in the reaction zone of elementary selenium over a contact material comprising the chromate, molybdate, sulphate, tungstate or vanadate of copper. The copper compounds may be distributed on carriers such as pumice, asbestos, silica gel and alumina or where this presents difficulties, e.g. with the tungstate, vanadate or molybdate the copper compound may be made into pellets. Elementary selenium may be introduced into the reaction zone, e.g. by passing part or the whole of the mixed reactants or the olefine over heated selenium and thence to the reactor, it may be generated in situ by the addition of decomposable selenides, e.g. the selenides of silver, antimony and cobalt, to the contact material or elementary selenium may be added to the contact material. Heat treatment of the solid contact material may be employed when this can be applied without decomposition of the contact material. In examples: (1) activated alumina is treated with aqueous copper sulphate and dried (2) ammonium vanadate and copper sulphate are reacted in aqueous solution (3) copper tungstate is obtained from aqueous solutions of sodium tungstate and copper nitrate (4) copper chromate is obtained by adding copper carbonate to aqueous chromium trioxide and refluxing (5) copper molybdate is obtained from aqueous solutions of sodium molybdate and copper sulphate. The precipitate in examples (2)-(5) is washed, dried and after addition of graphite as lubricant in examples (2) and (3) is made into tablets or pellets. Propylene is mixed with air and the mixture passed over heated selenium and the heated contact materials in the examples to obtain acrolein. Isobutene and other olefines of the defined configuration are stated to be similarly oxidized to the corresponding unsaturated aldehydes (see Group IV(b)). Specifications 625,330, 648,386 and 655,210 are referred to.
GB9573/49A 1949-04-08 1949-04-08 Oxidation of olefines Expired GB694354A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB9573/49A GB694354A (en) 1949-04-08 1949-04-08 Oxidation of olefines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9573/49A GB694354A (en) 1949-04-08 1949-04-08 Oxidation of olefines

Publications (1)

Publication Number Publication Date
GB694354A true GB694354A (en) 1953-07-22

Family

ID=9874593

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9573/49A Expired GB694354A (en) 1949-04-08 1949-04-08 Oxidation of olefines

Country Status (1)

Country Link
GB (1) GB694354A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3159680A (en) * 1964-12-01 kister
US3177257A (en) * 1965-04-06 Oxidative hydrocarbon conversion
EP0668104B1 (en) * 1994-02-22 1999-05-19 BASF Aktiengesellschaft Multimetal oxide masses

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3159680A (en) * 1964-12-01 kister
US3177257A (en) * 1965-04-06 Oxidative hydrocarbon conversion
EP0668104B1 (en) * 1994-02-22 1999-05-19 BASF Aktiengesellschaft Multimetal oxide masses

Similar Documents

Publication Publication Date Title
US3057915A (en) Process for oxidizing olefins to aldehydes, ketones and acids
US3833638A (en) Ammoxidation of saturated hydrocarbons
US3522299A (en) Process for the oxidation of olefins to aldehydes and acids and catalyst therefor
US3086041A (en) Production of aliphatic nitriles from olefins
GB901297A (en) Process for the production of pentafluoroethane
US2367169A (en) Process for treatment of olefins
US4046823A (en) Process for producing 1,2-dichloroethane
GB694354A (en) Oxidation of olefines
US2670380A (en) Oxidation of olefins
GB976883A (en) Improvements in or relating to the manufacture of organic flourine compounds
US3232991A (en) Preparation of formaldehyde
US2670379A (en) Office
US2974173A (en) Acetaldehyde manufacture
GB1039369A (en) Catalytic conversion of ethane to vinyl chloride
US2593437A (en) Manufacture of unsaturated aldehydes
US2338805A (en) Production of organic compounds
US3794668A (en) Vapor phase oxidation of phenols
US2828325A (en) Production of benzonitrile
US3119883A (en) Dehydrogenation of ethane
US3894091A (en) Process for production of acrolein
US2087038A (en) Process for the dehydrogenation of higher alcohols
GB678557A (en) Manufacture of aldehydes
US3862236A (en) Production of propionaldehyde
US3309395A (en) Production of acrylonitrile or methacrylonitrile
US3280182A (en) Oxidation of acrolein or methacrolein over antimony molybdate, cobalt molybdate or tin molybdate in the presence of arsenic or arsenic oxide