GB870462A - Improvements in or relating to the production of acetonitrile - Google Patents

Improvements in or relating to the production of acetonitrile

Info

Publication number
GB870462A
GB870462A GB7260/58A GB726058A GB870462A GB 870462 A GB870462 A GB 870462A GB 7260/58 A GB7260/58 A GB 7260/58A GB 726058 A GB726058 A GB 726058A GB 870462 A GB870462 A GB 870462A
Authority
GB
United Kingdom
Prior art keywords
alkali
alumina
bed
catalyst
ammonia
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
GB7260/58A
Inventor
Kiyoshi Morikawa
Tadao Shiba
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.)
STATE OF JAPAN
Original Assignee
STATE OF JAPAN
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 STATE OF JAPAN filed Critical STATE OF JAPAN
Priority to GB7260/58A priority Critical patent/GB870462A/en
Publication of GB870462A publication Critical patent/GB870462A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/18Preparation of carboxylic acid nitriles by reaction of ammonia or amines with compounds containing carbon-to-carbon multiple bonds other than in six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/32Separation; Purification; Stabilisation; Use of additives
    • C07C253/34Separation; Purification
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

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

Abstract

Acetonitrile is prepared by reacting acetylene and ammonia at 500-650 DEG C. under atmospheric or super-atmospheric pressure in the presence of a catalyst comprising alumina and at least one alkali metal hydroxide, or at least one inorganic salt of an alkali or alkaline earth metal, or at least one organic salt which gives an alkali metal carbonate or thermal decomposition; the ammonia being present in excess of the stoichiometric quantity, and the steam partial pressure in the gases being maintained at 2-50 mm. Hg. The starting gases may also contain hydrogen and carbon monoxide. Suitable salts are NaCl, KCl, LiCl, CaCl2, BaCl2 and alkali metal carbonates. The process may be carried out in fixed or fluidised beds.ALSO:Catalysts suitable for the reaction of acetylene and ammonia to produce acetonitrile (see Group IV(b)) comprise alumina and at least one alkali-metal hydroxide, or at least one inorganic salt of an alkali or alkaline-earth metal, or at least one organic salt which gives an alkali-metal carbonate on thermal decomposition; preferred salts are the chlorides and alkali-metal carbonates. The catalysts may be prepared by adding the hydroxide(s) or salt(s) as an aqueous solution to aluminium hydroxide gel or alumina hydrate, drying the resulting pasty mixture, and roasting at 500-700 DEG C.; or by roasting the alumina and then adding the aqueous solution to the roasted alumina. Carbonaceous matter deposited on the catalyst during use may be removed by heating with an oxygen-containing gas at 500-650 DEG C. The catalyst may be used in fixed-bed or fluidised-bed operation; in the latter case, suitable apparatus comprises a synthesis tower and a smaller regeneration tower, the catalyst circulating continuously. The larger bed may have at the inlet a packed bed comprising a plurality of layers of small inert solid grains (e.g. of silica) with a grid having spaces of a few centimetres embedded in the uppermost layer; the grain size decreases from the bottom layer to the top layer. The uppermost layer may be covered by a fine mesh wire net. The fluidised bed may also contain one or more horizontal wire nets or porous plates.
GB7260/58A 1958-03-06 1958-03-06 Improvements in or relating to the production of acetonitrile Expired GB870462A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB7260/58A GB870462A (en) 1958-03-06 1958-03-06 Improvements in or relating to the production of acetonitrile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB7260/58A GB870462A (en) 1958-03-06 1958-03-06 Improvements in or relating to the production of acetonitrile

Publications (1)

Publication Number Publication Date
GB870462A true GB870462A (en) 1961-06-14

Family

ID=9829697

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7260/58A Expired GB870462A (en) 1958-03-06 1958-03-06 Improvements in or relating to the production of acetonitrile

Country Status (1)

Country Link
GB (1) GB870462A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113620836A (en) * 2021-08-13 2021-11-09 山东达民化工股份有限公司 Preparation method of acetonitrile

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113620836A (en) * 2021-08-13 2021-11-09 山东达民化工股份有限公司 Preparation method of acetonitrile

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