GB655557A - Improvements in or relating to the production of aldehydes and to catalysts for use in oxidative processes - Google Patents

Improvements in or relating to the production of aldehydes and to catalysts for use in oxidative processes

Info

Publication number
GB655557A
GB655557A GB24191/47A GB2419147A GB655557A GB 655557 A GB655557 A GB 655557A GB 24191/47 A GB24191/47 A GB 24191/47A GB 2419147 A GB2419147 A GB 2419147A GB 655557 A GB655557 A GB 655557A
Authority
GB
United Kingdom
Prior art keywords
cerium
oxide
molybdenum
molybdenum trioxide
salt
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
GB24191/47A
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.)
Goodrich Corp
Original Assignee
BF Goodrich Corp
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 BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of GB655557A publication Critical patent/GB655557A/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
    • C07C45/37Preparation 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 >C—O—functional groups to >C=O groups
    • C07C45/38Preparation 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 >C—O—functional groups to >C=O groups being a primary hydroxyl group
    • 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
    • B01J23/16Catalysts 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
    • B01J23/24Chromium, molybdenum or tungsten
    • B01J23/28Molybdenum

Landscapes

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

Abstract

Aldehydes are prepared from aliphatic alcohols having up to four carbon atoms by reacting the alcohols and oxygen in vapour phase in the presence of a catalytic body comprising molybdenum trioxide and a lesser amount by weight of cerium oxide or samarium oxide prepared by mixing an aqueous solution of a molybdenum salt and a cerium or samarium salt with a carbonaceous binder or support and calcining the resultant mixture. The preferred catalyst contains 90 to 99 parts molybdenum trioxide and 1 to 10 parts of cerium oxide. Three preparations of a molybdenum trioxide/cerium oxide catalyst are described in detail (see Group III), an aqueous solution of ammonium molybdate or other molybdenum salt is mixed with an aqueous solution of cerium chloride or other cerium salt to form a complex colloidal dispersion to which is added a carbonaceous material supporting agent, e.g. soluble starch, activated charcoal, ammonium alginate, methyl cellulose or polyvinyl alcohol; water is evaporated off to leave a paste which is pelleted or extruded into cylindrical pieces or the paste is dried and then pelleted; finally the particles are calcined. The product normally contains some carbon. A summary is given of a number of conversions of methanol to form aldehyde employing molybdenum trioxide-cerium oxide catalysts in which the oxide ratios are 90 : 10 or 99 : 1 and the supporting agent is carbonized starch or activated charcoal. The general procedure consists of passing metered air through methanol and then directing the air-methanol mixture through a heated chamber, e.g. an aluminium tube, containing the catalyst; the effluent gases are passed through a bubble cap absorption tower countercurrently to water which dissolves out the formaldehyde. The methanol and air or oxygen are preferably anhydrous, and oxidation temperatures within the range of 300 DEG to 500 DEG C. are employed, with a contact time of about 0.3 to 2.0 seconds. Other alcohols mentioned are ethanol, propanol and butanols. The Specification as open to inspection under Sect. 91 relates to the production of aldehydes in general by reacting an alcohol with oxygen at elevated temperature in the presence of a catalytic body comprising molybdenum oxide and a lesser amount of a rare earth metal oxide. Reference is made to inert supporting agents generally for use with the catalysts, e.g. pumice and activated alumina. This subject-matter does not appear in the Specification as accepted.ALSO:Catalytic agents for use in the oxidation to aldehydes of aliphatic alcohols containing up to 4 carbon atoms comprise molybdenum trioxide and a lesser amount by weight of cerium oxide or samarium oxide prepared by mixing an aqueous solution of a molybdenum salt and a cerium or samarium salt with a carbonaceous binder or support and calcining the resultant mixture. In a typical preparation, a solution of ammonium molybdate is mixed with a solution of cerium chloride (obtained by reacting cerium hydrate with concentrated hydrochloric acid), the pH is adjusted to about 5 by addition of ammonium hydroxide and a solution of soluble starch is added to the resulting complex colloidal dispersion. The mixture is concentrated to a thick paste, pelleted, dried and then calcined, yielding a catalyst comprising 99 parts molybdenum trioxide, 1 part cerium oxide and a small proportion of carbonized starch. In place of the starch there may be used activated cocoanut charcoal, ammonium alginate, methyl cellulose or polyvinyl ether. Another catalytic composition described contains 90 parts molybdenum trioxide, 10 parts cerium oxide and about 6 parts of carbon. A summary is given of conversions of methanol to formaldehyde by vapour phase oxidation with air at about 300-500 DEG C. (see Group IV (b). Other alcohols mentioned are ethanol, propanol and butanols. The Specification as open to inspection under Sect. 91 relates to catalytic agents comprising molybdenum oxide and a lesser amount of a rare earth metal oxide for use in the oxidation to aldehydes of alcohols in general. Pumice, activated alumina and other inert supports for the catalysts may be used. This subject-matter does not appear in the Specification as accepted.
GB24191/47A 1946-09-04 1947-09-02 Improvements in or relating to the production of aldehydes and to catalysts for use in oxidative processes Expired GB655557A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US655557XA 1946-09-04 1946-09-04

Publications (1)

Publication Number Publication Date
GB655557A true GB655557A (en) 1951-07-25

Family

ID=22063526

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24191/47A Expired GB655557A (en) 1946-09-04 1947-09-02 Improvements in or relating to the production of aldehydes and to catalysts for use in oxidative processes

Country Status (1)

Country Link
GB (1) GB655557A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1182647B (en) * 1961-11-09 1964-12-03 Eastman Kodak Co Process for the preparation of aldehydes from primary alkanols or alkenols which are branched in the 2-position
DE1211629B (en) * 1962-08-14 1966-03-03 Basf Ag Process for the dehydrogenation of cyclohexanol
CN113816484A (en) * 2021-09-01 2021-12-21 中化环境科技工程有限公司 Method and apparatus for treating wastewater
CN115430437A (en) * 2022-09-19 2022-12-06 陕西科技大学 Molybdenum salt heterogeneous carrier and preparation method and application thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1182647B (en) * 1961-11-09 1964-12-03 Eastman Kodak Co Process for the preparation of aldehydes from primary alkanols or alkenols which are branched in the 2-position
DE1211629B (en) * 1962-08-14 1966-03-03 Basf Ag Process for the dehydrogenation of cyclohexanol
CN113816484A (en) * 2021-09-01 2021-12-21 中化环境科技工程有限公司 Method and apparatus for treating wastewater
CN115430437A (en) * 2022-09-19 2022-12-06 陕西科技大学 Molybdenum salt heterogeneous carrier and preparation method and application thereof
CN115430437B (en) * 2022-09-19 2023-08-22 陕西科技大学 Molybdenum salt heterogeneous carrier and preparation method and application thereof

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