GB971952A - Process for the production of alpha,beta-unsaturated aldehydes - Google Patents

Process for the production of alpha,beta-unsaturated aldehydes

Info

Publication number
GB971952A
GB971952A GB20424/62A GB2042462A GB971952A GB 971952 A GB971952 A GB 971952A GB 20424/62 A GB20424/62 A GB 20424/62A GB 2042462 A GB2042462 A GB 2042462A GB 971952 A GB971952 A GB 971952A
Authority
GB
United Kingdom
Prior art keywords
reaction zone
catalyst
oxygen
copper
olefinic hydrocarbon
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
GB20424/62A
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of GB971952A publication Critical patent/GB971952A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/002Mixed oxides other than spinels, e.g. perovskite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • B01J23/88Molybdenum
    • B01J23/887Molybdenum containing in addition other metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/8876Arsenic, antimony or bismuth
    • 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
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • C07C51/252Preparation 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • B01J2523/50Constitutive chemical elements of heterogeneous catalysts of Group V (VA or VB) of the Periodic Table
    • B01J2523/54Bismuth
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • B01J2523/60Constitutive chemical elements of heterogeneous catalysts of Group VI (VIA or VIB) of the Periodic Table
    • B01J2523/68Molybdenum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • B01J2523/80Constitutive chemical elements of heterogeneous catalysts of Group VIII of the Periodic Table
    • B01J2523/84Metals of the iron group
    • B01J2523/842Iron
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • B01J2523/80Constitutive chemical elements of heterogeneous catalysts of Group VIII of the Periodic Table
    • B01J2523/84Metals of the iron group
    • B01J2523/845Cobalt

Abstract

a , b -Unsaturated aliphatic aldehydes are prepared by contacting a mixture of a olefinic hydrocarbon having 3-10 carbon atoms and a gas containing molecular oxygen having a mol ratio of oxygen to olefinic hydrocarbon below 1, with a copper-containing catalyst at a temperature between 275 and 400 DEG C. in a first reaction zone, adding a gas-containing molecular oxygen to the effluence from said first reaction zone so that an admixture having a mol ratio of oxygen to olefinic hydrocarbon above 1 is formed, and contacting the resulting admixture with a catalyst comprising (a) bismuth, cobalt or nickel, (b) a metal from the left-hand column of Group VI of the Periodic Table, and (c) oxygen, in a second reaction zone at a temperature above that maintained in said first reaction zone and being in the range between 375 and 500 DEG C. Preferably, the catalyst in the first reaction zone contains elemental copper and/or one or more oxides of copper and component (b) of the catalyst in the second reaction zone comprises tungsten or molybdenum. Examples describe the preparation of acrolein and methacrolein. Specification 798,564 is referred to.
GB20424/62A 1961-05-29 1962-05-28 Process for the production of alpha,beta-unsaturated aldehydes Expired GB971952A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11323361A 1961-05-29 1961-05-29

Publications (1)

Publication Number Publication Date
GB971952A true GB971952A (en) 1964-10-07

Family

ID=22348310

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20424/62A Expired GB971952A (en) 1961-05-29 1962-05-28 Process for the production of alpha,beta-unsaturated aldehydes

Country Status (2)

Country Link
BE (1) BE618223A (en)
GB (1) GB971952A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL302703A (en) * 1963-03-29
GB991085A (en) * 1963-06-11 1965-05-05 Distillers Co Yeast Ltd Improvements in or relating to the production of unsaturated aliphatic aldehydes
GB1086523A (en) * 1963-09-30 1967-10-11 Mitsubishi Rayon Co Method for producing unsaturated aldehydes and acids
DE1207367B (en) * 1964-05-30 1965-12-23 Roehm & Haas Gmbh Process for the production of acrolein or methacrolein

Also Published As

Publication number Publication date
BE618223A (en) 1962-11-28

Similar Documents

Publication Publication Date Title
JPS5223589A (en) Catalyst for producing alpha,beta-unsaturaded carboxylic acid
ES453887A1 (en) Preparation of acrylic acid and methacrylic acid
GB1087987A (en) Catalysts useful in effecting the shift reaction
ES404686A1 (en) Process for the recovery of rhenium and molybdenum values from molybdenite concentrate
GB971952A (en) Process for the production of alpha,beta-unsaturated aldehydes
GB1157117A (en) Production of Maleic Anhydride
US3686294A (en) Process for the production of methacrylic acid
GB973375A (en) A process for the production of acrolein and methacrolein
US3161671A (en) Process for preparing acrylonitrile
US3624146A (en) Process for the production of acrylic acid from propylene
GB873712A (en) Production of unsaturated aliphatic aldehydes
GB1331423A (en) Process for the production and use of an oxidation catalyst
ES305863A1 (en) A procedure to prepare dimethyl furan. (Machine-translation by Google Translate, not legally binding)
ES316484A1 (en) Procedure for the preparation of olefin oxides. (Machine-translation by Google Translate, not legally binding)
GB998465A (en) Process for preparing ª‡ú¼ª‰-unsaturated aldehydes and ketones from olefines containing at least three carbon atoms
ES403865A1 (en) Catalysts and their use in catalytic processes for producing acrolein
GB908655A (en) Process for the manufacture of unsaturated aldehydes or ketones
ES385428A1 (en) Process for the preparation of alkanones from olefins
GB1064520A (en) Oxidation of hydrocarbons
ES317291A1 (en) Procedure for catalytic oxidation of olefins. (Machine-translation by Google Translate, not legally binding)
GB1354153A (en) Production of unsaturated aldehydes
ES308316A1 (en) Procedure for obtaining oxygenated products from monoolephines and catalyst for its realization. (Machine-translation by Google Translate, not legally binding)
ES381656A1 (en) A procedure to produce acrilonitril and metacrilonitril. (Machine-translation by Google Translate, not legally binding)
JPS55358A (en) Production of unsaturated carboxylic acid
ES442499A1 (en) Preparation of aldehydes and unsaturated carboxylic acids by catalytic oxidation of the corresponding olefines