GB1061447A - Dehydrogenation of cycloalkanols - Google Patents

Dehydrogenation of cycloalkanols

Info

Publication number
GB1061447A
GB1061447A GB4969663A GB4969663A GB1061447A GB 1061447 A GB1061447 A GB 1061447A GB 4969663 A GB4969663 A GB 4969663A GB 4969663 A GB4969663 A GB 4969663A GB 1061447 A GB1061447 A GB 1061447A
Authority
GB
United Kingdom
Prior art keywords
zno
annealed
precipitation
salt
compounds
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
GB4969663A
Inventor
Heinrich Sperber
Guenter Poehler
Otto Goehre
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB1061447A publication Critical patent/GB1061447A/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
    • C07C45/002Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by dehydrogenation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • 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
    • B01J23/06Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of zinc, cadmium or mercury

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)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

The gas phase dehydrogenation of cycloalkanols to cycloalkanones is conducted at elevated temperature in presence of a catalyst consisting of at least 80% of ZnO which has been obtained by precipitation from a Zn salt with a basic precipitant, and drying and annealing the ZnO, which has a surface of 5-20 m.2/g. The production of cyclohexanone from cyclohexanol is exemplified; other specified starting materials are 4-methylcyclohexanol, cyclooctanol and cyclododecanol.ALSO:ZnO, intended for use as a dehydrogenation catalyst, is prepared by precipitation from a Zn salt with a basic precipitant, dried and annealed to obtain a surface of 5-20 m2/g. The precipitate may be slowly heated to 400 DEG C. and annealed at between 400 DEG and 600 DEG C. until the desired surface is obtained. An after-treatment with H2 at 300-500 DEG is optional.ALSO:A dehydrogenation catalyst comprises ZnO which has been prepared by precipitation from a Zn salt with a basic precipitant, dried and annealed to obtain a surface of 5-20 m2/g. Ingredients which may be present in an amount of up to 20% are: pumice or other silicates, Cu compounds, alkali or alkaline earth metal salts of mineral acids and rare earth compounds; the Cu compounds may be e.g. oxide, hydroxide, carbonate or nitrate. The ZnO is preferably annealed at 400-600 DEG C. and may be treated with H2 at 300-500 DEG before use. A binding agent such as starch, graphite or stearic acid may be used in making the catalyst.
GB4969663A 1962-12-18 1963-12-17 Dehydrogenation of cycloalkanols Expired GB1061447A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB0070020 1962-12-18

Publications (1)

Publication Number Publication Date
GB1061447A true GB1061447A (en) 1967-03-15

Family

ID=6976509

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4969663A Expired GB1061447A (en) 1962-12-18 1963-12-17 Dehydrogenation of cycloalkanols

Country Status (2)

Country Link
DE (1) DE1443462A1 (en)
GB (1) GB1061447A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5093099A (en) * 1987-11-16 1992-03-03 Kao Corporation Flaky powder of zinc oxide and its composition for external use
DE3900243C2 (en) * 1989-01-05 1993-11-18 Brueggemann L Kg Zinc oxide, zinc carbonate and basic zinc carbonate, process for their preparation and their use
DE19609954A1 (en) * 1996-03-14 1997-09-18 Basf Ag Process for the dehydrogenation of secondary cyclic alcohols
DE19933079A1 (en) * 1999-07-19 2001-01-25 Bayer Ag Dehydrogenation catalysts
DE10055717A1 (en) * 2000-11-10 2002-05-29 Jens Burfeind Transporting and/or storing hydrogen in chemically fixed form for use as fuel comprises using an alcohol as the chemical hydrogen storage medium, and releasing the hydrogen from the alcohol at the consumer site, forming a ketone
WO2007082790A1 (en) * 2006-01-13 2007-07-26 Basf Aktiengesellschaft Process for regenerating a dehydrogenation catalyst

Also Published As

Publication number Publication date
DE1443462C3 (en) 1974-03-28
DE1443462A1 (en) 1969-08-14

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