GB817622A - Improvements in or relating to catalytic processes for preparing ketones from secondary alcohols - Google Patents

Improvements in or relating to catalytic processes for preparing ketones from secondary alcohols

Info

Publication number
GB817622A
GB817622A GB712557A GB712557A GB817622A GB 817622 A GB817622 A GB 817622A GB 712557 A GB712557 A GB 712557A GB 712557 A GB712557 A GB 712557A GB 817622 A GB817622 A GB 817622A
Authority
GB
United Kingdom
Prior art keywords
catalyst
activation
secondary alcohol
compound
decompose
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
GB712557A
Inventor
William Edyvean
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 Research Ltd
Original Assignee
Shell Research Ltd
Filing date
Publication date
Application filed by Shell Research Ltd filed Critical Shell Research Ltd
Publication of GB817622A publication Critical patent/GB817622A/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
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts

Landscapes

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

Abstract

The catalyst in a continuous vapour phase catalytic dehydrogenation process for the preparation of a ketone from a secondary alcohol is activated or regenerated by contacting it with the secondary alcohol in liquid state and containing at least one metal compound which will decompose to form a catalytically active deposit on the catalyst. Suitable catalysts may contain one or more metals such as copper, silver, chromium, manganese, nickel, tungsten, cobalt, iron, cadmium, uranium, tin and zinc, either as such or as the oxides or hydroxides. They may be supported on carriers such as kieselguhr, pumice, majolica or porcelain. The compound contained in the secondary alcohol during the activation is preferably a salt or salts (advantageously of an organic acid such as acetic acid) of one or more of the catalyst metals which will decompose to form a catalytically active compound, usually the oxide, of the metal(s) on the catalyst. The total amount of activating compound(s) may be between 1 and 10 pounds per ton of catalyst. The activation process is usually repeated during the operation of the plant, e.g. at periodic intervals of between 500 and 1000 hours. The activation may be effected by passing the liquid feed through the catalyst while gradually heating to reaction temperature (e.g. 300-500 DEG C.). The catalyst may be in a fixed bed or fluidized. In an example a catalyst comprising brass spelter previously pickled in mineral acid is activated by adding aqueous zinc acetate to the liquid feed during the warming-up stage and used for preparing acetone from isopropanol/water azeotrope.ALSO:The catalyst in a continuous vapour phase catalytic dehydrogenation process for the preparation of a ketone from a secondary alcohol is activated or regenerated by contacting it with the secondary alcohol in liquid state and containing at least one metal compound which will decompose to form a catalytically active deposit on the catalyst. Suitable catalysts may contain one or more metals such as copper, silver, chromium, manganese, nickel, tungsten, cobalt, iron, cadmium, uranium, tin and zinc, either as such or as the oxides or hydroxides. They may be supported on carriers such as kieselguhr, pumice, majolica or porcelain. The compound contained in the secondary alcohol during the activation is preferably a salt or salts (advantageously of an organic acid such as acetic acid) of one or more of the catalyst metals which will decompose to form a catalytically active compound, usually the oxide, of the metal(s) on the catalyst. The total amount of activating compound(s) may be between 1 and 10 pounds per ton of catalyst. The activation process is usually repeated during the operation of the plant, e.g. at periodic intervals of between 500 and 1000 hours. The activation may be effected by passing the liquid feed through the catalyst while gradually heating to reaction temperature (e.g. 300-500 DEG C.). The process is particularly suitable in the production of ketones from secondary alcohols containing up to about four carbon atoms. The alcohol may be anhydrous or admixed with water, e.g. as the azeotrope. The catalyst may be in a fixed bed or fluidized. In an example a catalyst comprising brass spelter previously pickled in mineral acid is activated by adding aqueous zinc acetate to the liquid feed during the warming-up stage and used for preparing acetone from isopropanol/water azeotrope.
GB712557A 1957-03-04 Improvements in or relating to catalytic processes for preparing ketones from secondary alcohols Expired GB817622A (en)

Publications (1)

Publication Number Publication Date
GB817622A true GB817622A (en) 1959-08-06

Family

ID=1628864

Family Applications (1)

Application Number Title Priority Date Filing Date
GB712557A Expired GB817622A (en) 1957-03-04 Improvements in or relating to catalytic processes for preparing ketones from secondary alcohols

Country Status (1)

Country Link
GB (1) GB817622A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4421933A (en) * 1982-07-02 1983-12-20 Shell Oil Company Process for the co-production of ketones and mono-olefins
US4453015A (en) * 1981-10-16 1984-06-05 Shell Oil Company Methyl ethyl ketone process
US4472593A (en) * 1981-10-16 1984-09-18 Shell Oil Company Conversion of isopropyl alcohol to acetone
US6794331B2 (en) 2000-02-18 2004-09-21 Degussa Ag Raney copper

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4453015A (en) * 1981-10-16 1984-06-05 Shell Oil Company Methyl ethyl ketone process
US4472593A (en) * 1981-10-16 1984-09-18 Shell Oil Company Conversion of isopropyl alcohol to acetone
US4421933A (en) * 1982-07-02 1983-12-20 Shell Oil Company Process for the co-production of ketones and mono-olefins
US6794331B2 (en) 2000-02-18 2004-09-21 Degussa Ag Raney copper
US7632967B2 (en) 2000-02-18 2009-12-15 Degussa Ag Raney copper

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