PT97608A - Processo para a preparacao de 1,1,1,2-tetrafluoro-cloroetano e de pentafluoroetano - Google Patents
Processo para a preparacao de 1,1,1,2-tetrafluoro-cloroetano e de pentafluoroetano Download PDFInfo
- Publication number
- PT97608A PT97608A PT97608A PT9760891A PT97608A PT 97608 A PT97608 A PT 97608A PT 97608 A PT97608 A PT 97608A PT 9760891 A PT9760891 A PT 9760891A PT 97608 A PT97608 A PT 97608A
- Authority
- PT
- Portugal
- Prior art keywords
- chromium
- catalyst
- pentahalogenoethane
- chloroethane
- tetrafluoro
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 21
- BOUGCJDAQLKBQH-UHFFFAOYSA-N 1-chloro-1,2,2,2-tetrafluoroethane Chemical compound FC(Cl)C(F)(F)F BOUGCJDAQLKBQH-UHFFFAOYSA-N 0.000 title claims abstract description 6
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 title claims abstract description 6
- 238000002360 preparation method Methods 0.000 title claims description 9
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000003682 fluorination reaction Methods 0.000 claims abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 19
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 12
- 239000011651 chromium Substances 0.000 claims abstract description 12
- 230000003197 catalytic effect Effects 0.000 claims abstract description 11
- 239000000460 chlorine Substances 0.000 claims abstract description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 230000003647 oxidation Effects 0.000 claims abstract description 3
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- JQZFYIGAYWLRCC-UHFFFAOYSA-N 1-chloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)(F)Cl JQZFYIGAYWLRCC-UHFFFAOYSA-N 0.000 claims description 3
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims description 3
- YMRMDGSNYHCUCL-UHFFFAOYSA-N 1,2-dichloro-1,1,2-trifluoroethane Chemical compound FC(Cl)C(F)(F)Cl YMRMDGSNYHCUCL-UHFFFAOYSA-N 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 claims 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 claims 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- GRWVQDDAKZFPFI-UHFFFAOYSA-H chromium(III) sulfate Chemical compound [Cr+3].[Cr+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRWVQDDAKZFPFI-UHFFFAOYSA-H 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- -1 oxyhalide Chemical compound 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 230000004913 activation Effects 0.000 description 7
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical group O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229940117975 chromium trioxide Drugs 0.000 description 3
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 3
- 229910001026 inconel Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 229950011008 tetrachloroethylene Drugs 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910000423 chromium oxide Inorganic materials 0.000 description 2
- BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical compound [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- AFTSHZRGGNMLHC-UHFFFAOYSA-N 1,1-dichloro-1,2,2-trifluoroethane Chemical compound FC(F)C(F)(Cl)Cl AFTSHZRGGNMLHC-UHFFFAOYSA-N 0.000 description 1
- NYQYILNIBHLSAX-UHFFFAOYSA-N 1-chloropent-3-en-2-one Chemical compound CC=CC(=O)CCl NYQYILNIBHLSAX-UHFFFAOYSA-N 0.000 description 1
- YUQQQYGEDJGUCI-UHFFFAOYSA-N 2,2-dibromo-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Br)Br YUQQQYGEDJGUCI-UHFFFAOYSA-N 0.000 description 1
- 229910016569 AlF 3 Inorganic materials 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 108010081348 HRT1 protein Hairy Proteins 0.000 description 1
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 description 1
- 102100039990 Hairy/enhancer-of-split related with YRPW motif protein 2 Human genes 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 101100170590 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) DMA1 gene Proteins 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 101150061866 hey2 gene Proteins 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/206—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/26—Chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Developing Agents For Electrophotography (AREA)
- Pyrrole Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9005908A FR2661906B1 (fr) | 1990-05-11 | 1990-05-11 | Procede de fabrication du 1,1,1,2-tetrafluoro-chloroethane et du pentafluoroethane. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT97608A true PT97608A (pt) | 1992-01-31 |
Family
ID=9396524
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97608A PT97608A (pt) | 1990-05-11 | 1991-05-08 | Processo para a preparacao de 1,1,1,2-tetrafluoro-cloroetano e de pentafluoroetano |
Country Status (15)
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9007029D0 (en) * | 1990-03-29 | 1990-05-30 | Ici Plc | Chemical process |
| FR2669022B1 (fr) * | 1990-11-13 | 1992-12-31 | Atochem | Procede de fabrication du tetrafluoro-1,1,1,2-ethane. |
| ES2128354T3 (es) * | 1991-05-06 | 1999-05-16 | Du Pont | Procedimiento para la preparacion de pentafluoroetano. |
| ZA923274B (en) * | 1991-05-06 | 1993-11-08 | Du Pont | Process for the manufacture of pentafluoroethane |
| DK0513823T3 (da) * | 1991-05-17 | 1996-02-05 | Hoechst Ag | Fremgangsmåde til fremstilling af pentafluorethan (R 125) |
| FR2684567B1 (fr) * | 1991-12-09 | 1994-11-04 | Atochem | Catalyseurs massiques a base d'oxydes de chrome et de nickel, et leur application a la fluoration d'hydrocarbures halogenes. |
| GB9311742D0 (en) * | 1992-06-10 | 1993-07-21 | Ici Plc | Production of hydrofluoroalkanes |
| US5395999A (en) * | 1992-11-06 | 1995-03-07 | E. I. Du Pont De Nemours And Company | Catalytic chlorofluorination process for producing CHClFCF3 and CHF2 CF3 |
| EP0687660B2 (en) † | 1993-03-05 | 2006-05-17 | Daikin Industries, Limited | Process for producing 1,1,1,2,2-pentafluoroethane, process for producing 2,2-dichloro-1,1,1-trifluoroethane, and method of purifying 1,1,1,2,2-pentafluoroethane |
| GB9325756D0 (en) * | 1993-12-16 | 1994-02-16 | Ici Plc | Production of pentafluoroethane |
| US5475167A (en) * | 1995-02-17 | 1995-12-12 | E. I. Du Pont De Nemours And Company | Process for the manufacture of pentafluoroethane |
| CA2213579C (en) * | 1995-02-24 | 2007-04-17 | Daikin Industries Ltd. | Process for producing pentafluoroethane and tetrafluorochloroethane |
| JP3853397B2 (ja) * | 1995-05-11 | 2006-12-06 | イネオス フラウアー ホールデイングス リミテッド | ペンタフルオロエタンの製造方法及びペンタフルオロエタンに転化するのに適当な組成物 |
| FR2754815B1 (fr) * | 1996-10-18 | 1998-12-04 | Atochem Elf Sa | Purification du pentafluoroethane |
| FR2764883B1 (fr) * | 1997-06-18 | 1999-07-16 | Atochem Elf Sa | Procede de fabrication d'hydrofluoroalcanes |
| JP4378779B2 (ja) † | 1998-07-17 | 2009-12-09 | ダイキン工業株式会社 | 含フッ素エタンの製造方法 |
| RU2179885C1 (ru) * | 2001-04-24 | 2002-02-27 | Открытое акционерное общество "Галоген" | Катализатор для синтеза хладонов |
| FR2828193B1 (fr) | 2001-08-03 | 2004-04-02 | Atofina | Nouveau procede de preparation du 1,1,1,-trifluoro-2,2-dichloroethane |
| US20070191652A1 (en) * | 2004-03-29 | 2007-08-16 | Hiromoto Ohno | Process for production of 1,1,1,2- tetrafluoroethane and/or pentafluorethane and applications of the same |
| GB0525701D0 (en) | 2005-12-17 | 2006-01-25 | Ineos Fluor Holdings Ltd | Process |
| GB0525699D0 (en) | 2005-12-17 | 2006-01-25 | Ineos Fluor Holdings Ltd | Process |
| GB0525700D0 (en) | 2005-12-17 | 2006-01-25 | Ineos Fluor Holdings Ltd | Process |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB468447A (en) * | 1936-01-03 | 1937-07-05 | Fred Davison Leicester | Improvements in or relating to the manufacture of fluorine derivatives of aliphatic hydrocarbons |
| GB745818A (en) * | 1952-06-12 | 1956-03-07 | Nat Smelting Co Ltd | Improvements in or relating to a process for producing fluorohalo-derivatives of saturated aliphatic hydrocarbons |
| DE1568614A1 (de) * | 1962-01-13 | 1970-03-05 | Hoechst Ag | Verfahren zur Herstellung fluorhaltiger aliphatischer Verbindungen |
| CA931978A (en) * | 1968-01-24 | 1973-08-14 | Frank J. Christoph, Jr. | Process for preparing trichlorotrifluoroethane and dichlorotetrafluoroethane |
| US3632834A (en) * | 1968-10-23 | 1972-01-04 | Du Pont | Process for preparing trichlorotrifluoroethane and dichlorotetrafluoroethane |
| US4129603A (en) * | 1978-02-07 | 1978-12-12 | Imperial Chemical Industries Limited | Manufacture of halogenated compounds |
| JPS6012910B2 (ja) * | 1979-08-04 | 1985-04-04 | ダイキン工業株式会社 | フツ素化触媒 |
| JPS59225131A (ja) * | 1983-06-06 | 1984-12-18 | Showa Denko Kk | ジフルオロメタンの製造方法 |
| 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 |
| IN171977B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1988-06-29 | 1993-02-27 | Du Pont | |
| FR2669022B1 (fr) * | 1990-11-13 | 1992-12-31 | Atochem | Procede de fabrication du tetrafluoro-1,1,1,2-ethane. |
-
1990
- 1990-05-11 FR FR9005908A patent/FR2661906B1/fr not_active Expired - Fee Related
-
1991
- 1991-04-03 CA CA002039646A patent/CA2039646C/fr not_active Expired - Fee Related
- 1991-04-12 NO NO911442A patent/NO172796C/no unknown
- 1991-04-29 DE DE69101025T patent/DE69101025T2/de not_active Expired - Fee Related
- 1991-04-29 EP EP91401136A patent/EP0456552B1/fr not_active Expired - Lifetime
- 1991-04-29 AT AT91401136T patent/ATE100430T1/de not_active IP Right Cessation
- 1991-04-29 ES ES91401136T patent/ES2048569T3/es not_active Expired - Lifetime
- 1991-04-29 AU AU76053/91A patent/AU630807B2/en not_active Ceased
- 1991-05-07 KR KR1019910007372A patent/KR930010404B1/ko not_active Expired - Fee Related
- 1991-05-08 PT PT97608A patent/PT97608A/pt not_active Application Discontinuation
- 1991-05-09 TW TW080103611A patent/TW258725B/zh active
- 1991-05-10 IE IE161591A patent/IE911615A1/en unknown
- 1991-05-10 FI FI912296A patent/FI912296A7/fi not_active Application Discontinuation
- 1991-05-10 JP JP3106017A patent/JPH06102631B2/ja not_active Expired - Lifetime
-
1993
- 1993-05-24 US US08/065,422 patent/US5354928A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04226927A (ja) | 1992-08-17 |
| TW258725B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1995-10-01 |
| US5354928A (en) | 1994-10-11 |
| KR930010404B1 (ko) | 1993-10-23 |
| FR2661906A1 (fr) | 1991-11-15 |
| AU7605391A (en) | 1991-11-14 |
| NO172796B (no) | 1993-06-01 |
| FI912296A0 (fi) | 1991-05-10 |
| ES2048569T3 (es) | 1994-03-16 |
| EP0456552A1 (fr) | 1991-11-13 |
| FI912296L (fi) | 1991-11-12 |
| CA2039646A1 (fr) | 1991-11-12 |
| DE69101025D1 (de) | 1994-03-03 |
| FI912296A7 (fi) | 1991-11-12 |
| NO172796C (no) | 1993-09-08 |
| EP0456552B1 (fr) | 1994-01-19 |
| NO911442L (no) | 1991-11-12 |
| FR2661906B1 (fr) | 1993-10-01 |
| DE69101025T2 (de) | 1994-07-28 |
| ATE100430T1 (de) | 1994-02-15 |
| KR910019941A (ko) | 1991-12-19 |
| IE911615A1 (en) | 1991-11-20 |
| AU630807B2 (en) | 1992-11-05 |
| JPH06102631B2 (ja) | 1994-12-14 |
| CA2039646C (fr) | 1996-10-22 |
| NO911442D0 (no) | 1991-04-12 |
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