GB689392A - Oxidation of olefines - Google Patents

Oxidation of olefines

Info

Publication number
GB689392A
GB689392A GB730150A GB730150A GB689392A GB 689392 A GB689392 A GB 689392A GB 730150 A GB730150 A GB 730150A GB 730150 A GB730150 A GB 730150A GB 689392 A GB689392 A GB 689392A
Authority
GB
United Kingdom
Prior art keywords
heated
propylene
passing
activated alumina
bauxite
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
GB730150A
Inventor
Charles Albin Woodcock
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 GB730150A priority Critical patent/GB689392A/en
Publication of GB689392A publication Critical patent/GB689392A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • B01J23/72Copper
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In a modification of the process for the manufacture of acrolein and methacrolein by the catalytic oxidation of propylene and isobutene respectively with gases containing molecular oxygen at temperatures between 230 DEG and 400 DEG C. by passing the reacting gas mixture in the presence of elementary selenium over a contact material comprising initially copper oxide distributed upon activated alumina, the activated alumina is replaced by natural bauxite. It is desirable to use a bauxite as carrier which contains only a minor amount of iron compounds. Other features of the process are described in the parent Specification and the efficiency of the contact material may be increased by heat treatment at high temperatures. In the example bauxites containing varying proportions of iron are ground, heated and treated with warm aqueous copper nitrate. The liquid is drained off and the residue is dried and heated. The yields of acrolein obtained by passing a stream of propylene in air and selenium over the heated contact materials are compared.
GB730150A 1950-03-23 1950-03-23 Oxidation of olefines Expired GB689392A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB730150A GB689392A (en) 1950-03-23 1950-03-23 Oxidation of olefines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB730150A GB689392A (en) 1950-03-23 1950-03-23 Oxidation of olefines

Publications (1)

Publication Number Publication Date
GB689392A true GB689392A (en) 1953-03-25

Family

ID=9830493

Family Applications (1)

Application Number Title Priority Date Filing Date
GB730150A Expired GB689392A (en) 1950-03-23 1950-03-23 Oxidation of olefines

Country Status (1)

Country Link
GB (1) GB689392A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139480B (en) * 1959-02-17 1962-11-15 Distillers Co Yeast Ltd Process for the production of acrolein and methacrolein
DE1158487B (en) * 1959-04-02 1963-12-05 Distellers Company Ltd Process for the production of acrolein or methacrolein

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139480B (en) * 1959-02-17 1962-11-15 Distillers Co Yeast Ltd Process for the production of acrolein and methacrolein
DE1158487B (en) * 1959-04-02 1963-12-05 Distellers Company Ltd Process for the production of acrolein or methacrolein
DE1158487C2 (en) * 1959-04-02 1974-03-14 Distellers Company Ltd PROCESS FOR MANUFACTURING ACROLEIN OR METHACROLEIN

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