GB1202711A - Catalyst regeneration process - Google Patents

Catalyst regeneration process

Info

Publication number
GB1202711A
GB1202711A GB3064/67A GB306467A GB1202711A GB 1202711 A GB1202711 A GB 1202711A GB 3064/67 A GB3064/67 A GB 3064/67A GB 306467 A GB306467 A GB 306467A GB 1202711 A GB1202711 A GB 1202711A
Authority
GB
United Kingdom
Prior art keywords
solution
catalyst
jan
regeneration process
catalyst regeneration
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
GB3064/67A
Inventor
David Cyril Marshall
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB3064/67A priority Critical patent/GB1202711A/en
Publication of GB1202711A publication Critical patent/GB1202711A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C07D213/22Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing two or more pyridine rings directly linked together, e.g. bipyridyl
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J25/00Catalysts of the Raney type
    • B01J25/04Regeneration or reactivation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/48Liquid treating or treating in liquid phase, e.g. dissolved or suspended
    • B01J38/64Liquid treating or treating in liquid phase, e.g. dissolved or suspended using alkaline material; using salts
    • 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)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pyridine Compounds (AREA)

Abstract

1,202,711. Regenerating Raney nickel. IMPERIAL CHEMICAL INDUSTRIES Ltd. 15 Jan., 1968 [20 Jan., 1967], No. 3064/67. Heading B1E. Raney nickel catalysts which have lost activity in use as contact agents in the conversion of pyridines to 2:2'-dipyridyls are reregenerated by contact with an alcoholic solution of an alkali metal hydroxide. The solution may be passed through a bed of catalyst or the latter suspended in an agitated solution. An example describes the revivification of a Raney Ni catalyst using an ethanolic solution of KOH.
GB3064/67A 1967-01-20 1967-01-20 Catalyst regeneration process Expired GB1202711A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3064/67A GB1202711A (en) 1967-01-20 1967-01-20 Catalyst regeneration process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3064/67A GB1202711A (en) 1967-01-20 1967-01-20 Catalyst regeneration process

Publications (1)

Publication Number Publication Date
GB1202711A true GB1202711A (en) 1970-08-19

Family

ID=9751311

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3064/67A Expired GB1202711A (en) 1967-01-20 1967-01-20 Catalyst regeneration process

Country Status (1)

Country Link
GB (1) GB1202711A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2211287A1 (en) * 1972-12-25 1974-07-19 Toyo Soda Mfg Co Ltd
US4966972A (en) * 1989-01-19 1990-10-30 Reilly Industries, Inc. Process and catalyst for the preparation of 2,2'-bipyridyls
US5221747A (en) * 1989-01-19 1993-06-22 Reilly Industries, Inc. Improved process and catalyst for the preparation of 2,2' bipyridyls
CN102580766A (en) * 2012-01-13 2012-07-18 浙江龙华精细化工有限公司 Regeneration method of recycled Raney-Ni catalyst for EHA (2-ethylhexyl 4-(dimethylamino)benzoate)
CN105130883A (en) * 2015-08-10 2015-12-09 安徽国星生物化学有限公司 2,2'-bipyridine, catalytic coupling synthesis method and applications thereof
GB202106814D0 (en) 2020-05-14 2021-06-30 Johnson Matthey Plc Catalyst for biaryl production

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2211287A1 (en) * 1972-12-25 1974-07-19 Toyo Soda Mfg Co Ltd
US4966972A (en) * 1989-01-19 1990-10-30 Reilly Industries, Inc. Process and catalyst for the preparation of 2,2'-bipyridyls
US5221747A (en) * 1989-01-19 1993-06-22 Reilly Industries, Inc. Improved process and catalyst for the preparation of 2,2' bipyridyls
CN102580766A (en) * 2012-01-13 2012-07-18 浙江龙华精细化工有限公司 Regeneration method of recycled Raney-Ni catalyst for EHA (2-ethylhexyl 4-(dimethylamino)benzoate)
CN102580766B (en) * 2012-01-13 2013-08-28 浙江优创材料科技股份有限公司 Regeneration method of recycled Raney-Ni catalyst for EHA (2-ethylhexyl 4-(dimethylamino)benzoate)
CN105130883A (en) * 2015-08-10 2015-12-09 安徽国星生物化学有限公司 2,2'-bipyridine, catalytic coupling synthesis method and applications thereof
GB202106814D0 (en) 2020-05-14 2021-06-30 Johnson Matthey Plc Catalyst for biaryl production
WO2021229227A1 (en) 2020-05-14 2021-11-18 Johnson Matthey Public Limited Company Catalyst for biaryl production
GB2599981A (en) 2020-05-14 2022-04-20 Johnson Matthey Plc Catalyst for biaryl production

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee