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GB1000485A - Improvements in or relating to the fluorination of halo-olefines - Google Patents

Improvements in or relating to the fluorination of halo-olefines

Info

Publication number
GB1000485A
GB1000485A GB4797/62A GB479762A GB1000485A GB 1000485 A GB1000485 A GB 1000485A GB 4797/62 A GB4797/62 A GB 4797/62A GB 479762 A GB479762 A GB 479762A GB 1000485 A GB1000485 A GB 1000485A
Authority
GB
United Kingdom
Prior art keywords
ccl2
gives
alumina
halides
solution
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
GB4797/62A
Inventor
Andrea Scipioni
Gian Paolo Gambaretto
Dominico Zanon
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.)
Sicedison SpA
Original Assignee
Sicedison SpA
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 Sicedison SpA filed Critical Sicedison SpA
Priority to GB4797/62A priority Critical patent/GB1000485A/en
Publication of GB1000485A publication Critical patent/GB1000485A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • C07C17/21Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
    • 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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Organic fluorine compounds are obtained by passing a mixture of a halo-olefine and hydrogen fluoride in the gaseous phase at elevated temperature, e.g. 200-400 DEG C., over a catalyst consisting essentially of partially fluorinated activated alumina, which may be activated by impregnation with a solution of one or more polyvalent metal halides, e.g. halides of chromium, cobalt, nickel or manganese. In examples (1) CHCl:CCl2 gives CF3CH2Cl; (2) vinyl chloride gives CH3CHF2, CH2:CHF and CH3CHFCl; (3) CH2:CCl2 gives CH3CF3; and (4) CCl2:CCl2 gives CF3CHCl2. Other products are also obtained in small amounts. Other specified reactions are of CCl2:CHCH3 to CH3CH2CF3, and of CH2:CCl.CH2Cl to CH2ClCF2CH3, through various intermediates. Reference has been directed by the Comptroller to Specification 770,640.ALSO:Fluorination catalysts (see Division C2) consist of partially fluorinated activated alumina, e.g. activated by impregnation with a solution of one or more polyvalent metal halides, such as halides of chromium, cobalt, nickel or manganese. Alumina may be impregnated with a solution as defined, heated in air at 500-650 DEG C., and then treated with HF at 250-300 DEG C., preferably to 70-80% fluorination of the alumina. The catalyst may form a fixed, mobile or fluid bed. Used catalyst may be regenerated by treatment with air and steam at 500-700 DEG C. Reference has been directed by the Comptroller to Specification 770,640.
GB4797/62A 1962-02-07 1962-02-07 Improvements in or relating to the fluorination of halo-olefines Expired GB1000485A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4797/62A GB1000485A (en) 1962-02-07 1962-02-07 Improvements in or relating to the fluorination of halo-olefines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4797/62A GB1000485A (en) 1962-02-07 1962-02-07 Improvements in or relating to the fluorination of halo-olefines

Publications (1)

Publication Number Publication Date
GB1000485A true GB1000485A (en) 1965-08-04

Family

ID=9783977

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4797/62A Expired GB1000485A (en) 1962-02-07 1962-02-07 Improvements in or relating to the fluorination of halo-olefines

Country Status (1)

Country Link
GB (1) GB1000485A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4766259A (en) * 1987-08-13 1988-08-23 E. I. Du Pont De Nemours And Company Gas-phase fluorination process
US4766260A (en) * 1987-07-07 1988-08-23 E. I. Du Pont De Nemours And Company Gas-phase fluorination process
US4843181A (en) * 1987-10-22 1989-06-27 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,1,1-trifluorodichloroethane and 1,1,1,2-tetrafluorochloroethane
US4967023A (en) * 1987-03-09 1990-10-30 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination in the presence of catalysts
US5185482A (en) * 1989-02-03 1993-02-09 E. I. Du Pont De Nemours And Company Manufacture of 1,1,1,2-tetrafluoroethane
US5276224A (en) * 1987-03-09 1994-01-04 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination in the presence of catalysts
US5300710A (en) * 1991-03-20 1994-04-05 E. I. Du Pont De Nemours And Company Process for the manufacture of 2-chloro-1,1,1,2-tetrafluoroethane and pentafluoroethane
US5300711A (en) * 1991-03-20 1994-04-05 E. I. Du Pont De Nemours And Company Process for the manufacture of 2,2-dichloro-1,1,1-trifluoroethane, 2-chloro-1,1,1,2-tetrafluoroethane and pentafluoroethane
US5319147A (en) * 1991-12-23 1994-06-07 Ausimont S.P.A. Process for the neutralization of perfluoropolyoxyalkylenes
US5321170A (en) * 1991-03-20 1994-06-14 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,1,1,2-tetrafluoroethane
US5463151A (en) * 1989-07-12 1995-10-31 Ausimont S.R.L. Process for preparing 1,1,1,2-tetrafluoroethane
US5959166A (en) * 1994-07-04 1999-09-28 Korea Institute Of Science And Technology Method for concurrently producing different hydrofluoro carbons
US6040486A (en) * 1991-03-20 2000-03-21 E. I. Du Pont De Nemours And Company Process for the manufacture of 2-chloro-1,1,1-trifluoroethane
US6187280B1 (en) 1997-05-22 2001-02-13 Ausimont S.P.A. Process for the preparation of aluminum fluoride
US6307114B1 (en) 1992-08-14 2001-10-23 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2-chloroethane

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4967023A (en) * 1987-03-09 1990-10-30 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination in the presence of catalysts
US5091601A (en) * 1987-03-09 1992-02-25 Austimont S.P.A. Process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination in the presence of catalysts
US5276224A (en) * 1987-03-09 1994-01-04 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination in the presence of catalysts
US4766260A (en) * 1987-07-07 1988-08-23 E. I. Du Pont De Nemours And Company Gas-phase fluorination process
EP0298662A1 (en) * 1987-07-07 1989-01-11 E.I. Du Pont De Nemours And Company Gas-phase fluorination process
US4766259A (en) * 1987-08-13 1988-08-23 E. I. Du Pont De Nemours And Company Gas-phase fluorination process
US4843181A (en) * 1987-10-22 1989-06-27 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,1,1-trifluorodichloroethane and 1,1,1,2-tetrafluorochloroethane
US5345016A (en) * 1989-02-03 1994-09-06 E. I. Du Pont De Nemours And Company Manufacture of 1,1,1,2-tetrafluoroethane
US5185482A (en) * 1989-02-03 1993-02-09 E. I. Du Pont De Nemours And Company Manufacture of 1,1,1,2-tetrafluoroethane
US5880316A (en) * 1989-07-12 1999-03-09 Ausimont S.P.A. Process for preparing 1,1,1,2-tetrafluoroethane
US5463151A (en) * 1989-07-12 1995-10-31 Ausimont S.R.L. Process for preparing 1,1,1,2-tetrafluoroethane
US5608125A (en) * 1989-07-12 1997-03-04 Ausimont S.P.A. Process for preparing 1,1,1,2-tetrafluoroethane
US6037508A (en) * 1989-07-12 2000-03-14 Ausimont S.P.A. Process for preparing 1,1,1,2-tetrafluoroethane
US5321170A (en) * 1991-03-20 1994-06-14 E. I. Du Pont De Nemours And Company Process for the manufacture of 1,1,1,2-tetrafluoroethane
US5300711A (en) * 1991-03-20 1994-04-05 E. I. Du Pont De Nemours And Company Process for the manufacture of 2,2-dichloro-1,1,1-trifluoroethane, 2-chloro-1,1,1,2-tetrafluoroethane and pentafluoroethane
US5300710A (en) * 1991-03-20 1994-04-05 E. I. Du Pont De Nemours And Company Process for the manufacture of 2-chloro-1,1,1,2-tetrafluoroethane and pentafluoroethane
US6040486A (en) * 1991-03-20 2000-03-21 E. I. Du Pont De Nemours And Company Process for the manufacture of 2-chloro-1,1,1-trifluoroethane
US5319147A (en) * 1991-12-23 1994-06-07 Ausimont S.P.A. Process for the neutralization of perfluoropolyoxyalkylenes
US6307114B1 (en) 1992-08-14 2001-10-23 Ausimont S.P.A. Process for preparing 1,1,1-trifluoro-2-chloroethane
US5959166A (en) * 1994-07-04 1999-09-28 Korea Institute Of Science And Technology Method for concurrently producing different hydrofluoro carbons
US6187280B1 (en) 1997-05-22 2001-02-13 Ausimont S.P.A. Process for the preparation of aluminum fluoride

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