KR950701896A - 1,1,1,2,3-펜타플루오로프로펜의 제조방법 및 1,1,1,2,3-펜타플루오로프로판의 제조방법 - Google Patents
1,1,1,2,3-펜타플루오로프로펜의 제조방법 및 1,1,1,2,3-펜타플루오로프로판의 제조방법Info
- Publication number
- KR950701896A KR950701896A KR1019940704439A KR19940704439A KR950701896A KR 950701896 A KR950701896 A KR 950701896A KR 1019940704439 A KR1019940704439 A KR 1019940704439A KR 19940704439 A KR19940704439 A KR 19940704439A KR 950701896 A KR950701896 A KR 950701896A
- Authority
- KR
- South Korea
- Prior art keywords
- pentafluoropropane
- producing
- pentafluoropropene
- activated carbon
- catalyst
- 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.)
- Withdrawn
Links
- ZDCWZRQSHBQRGN-UHFFFAOYSA-N 1,1,1,2,3-pentafluoropropane Chemical compound FCC(F)C(F)(F)F ZDCWZRQSHBQRGN-UHFFFAOYSA-N 0.000 title claims abstract 15
- DMUPYMORYHFFCT-UHFFFAOYSA-N 1,2,3,3,3-pentafluoroprop-1-ene Chemical compound FC=C(F)C(F)(F)F DMUPYMORYHFFCT-UHFFFAOYSA-N 0.000 title claims abstract 10
- 238000000034 method Methods 0.000 title claims 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 24
- 239000003054 catalyst Substances 0.000 claims abstract 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims abstract 10
- 238000004519 manufacturing process Methods 0.000 claims abstract 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract 8
- 229910052804 chromium Inorganic materials 0.000 claims abstract 8
- 239000011651 chromium Substances 0.000 claims abstract 8
- 229910052751 metal Inorganic materials 0.000 claims abstract 7
- 239000002184 metal Substances 0.000 claims abstract 7
- 239000002253 acid Substances 0.000 claims abstract 6
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract 5
- 239000001257 hydrogen Substances 0.000 claims abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 5
- 229910052763 palladium Inorganic materials 0.000 claims abstract 5
- 229910052725 zinc Inorganic materials 0.000 claims abstract 5
- 239000011701 zinc Substances 0.000 claims abstract 5
- FYIRUPZTYPILDH-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)C(F)(F)F FYIRUPZTYPILDH-UHFFFAOYSA-N 0.000 claims abstract 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract 4
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims abstract 4
- 229910052737 gold Inorganic materials 0.000 claims abstract 4
- 239000010931 gold Substances 0.000 claims abstract 4
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract 4
- 239000011733 molybdenum Substances 0.000 claims abstract 4
- 229910052703 rhodium Inorganic materials 0.000 claims abstract 4
- 239000010948 rhodium Substances 0.000 claims abstract 4
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims abstract 4
- 229910052714 tellurium Inorganic materials 0.000 claims abstract 4
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims abstract 4
- 229910052716 thallium Inorganic materials 0.000 claims abstract 4
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 claims abstract 4
- 150000003839 salts Chemical class 0.000 claims abstract 3
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000002739 metals Chemical class 0.000 claims abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 claims 4
- 229910052802 copper Inorganic materials 0.000 claims 4
- 239000010949 copper Substances 0.000 claims 4
- 239000007789 gas Substances 0.000 claims 4
- 229910052709 silver Inorganic materials 0.000 claims 4
- 239000004332 silver Substances 0.000 claims 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 2
- 239000000956 alloy Substances 0.000 claims 2
- 229910045601 alloy Inorganic materials 0.000 claims 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 2
- 239000000741 silica gel Substances 0.000 claims 2
- 229910002027 silica gel Inorganic materials 0.000 claims 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- MWDWMQNTNBHJEI-UHFFFAOYSA-N 1,1,2,3,3-pentafluoropropane Chemical compound FC(F)C(F)C(F)F MWDWMQNTNBHJEI-UHFFFAOYSA-N 0.000 claims 1
- VJGCZWVJDRIHNC-UHFFFAOYSA-N 1-fluoroprop-1-ene Chemical compound CC=CF VJGCZWVJDRIHNC-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- NEIHULKJZQTQKJ-UHFFFAOYSA-N [Cu].[Ag] Chemical compound [Cu].[Ag] NEIHULKJZQTQKJ-UHFFFAOYSA-N 0.000 abstract 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
-
- 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
-
- 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
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/132—Halogens; Compounds thereof with chromium, molybdenum, tungsten or polonium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/354—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by hydrogenation
-
- 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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
-
- 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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/60—Platinum group metals with zinc, cadmium or mercury
-
- 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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/652—Chromium, molybdenum or tungsten
-
- 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
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
- B01J23/8926—Copper and noble metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP92-171949 | 1992-06-05 | ||
| JP17194992 | 1992-06-05 | ||
| JP17910692 | 1992-06-12 | ||
| JP92-179106 | 1992-06-12 | ||
| JP92-262866 | 1992-09-04 | ||
| JP26286592 | 1992-09-04 | ||
| JP26286692 | 1992-09-04 | ||
| JP92-262865 | 1992-09-04 | ||
| JP92-360966 | 1992-12-29 | ||
| JP36096692 | 1992-12-29 | ||
| PCT/JP1993/000661 WO1993025510A1 (fr) | 1992-06-05 | 1993-05-19 | Procedes d'obtention de 1,1,1,2,3-pentafluoro-propene et de 1,1,1,2,3-pentafluoro-propane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR950701896A true KR950701896A (ko) | 1995-05-17 |
Family
ID=27528535
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019940704439A Withdrawn KR950701896A (ko) | 1992-06-05 | 1993-05-19 | 1,1,1,2,3-펜타플루오로프로펜의 제조방법 및 1,1,1,2,3-펜타플루오로프로판의 제조방법 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5679875A (enExample) |
| EP (2) | EP0644173A1 (enExample) |
| JP (1) | JP3158440B2 (enExample) |
| KR (1) | KR950701896A (enExample) |
| CN (1) | CN1083040A (enExample) |
| AU (1) | AU664753B2 (enExample) |
| BR (1) | BR9306493A (enExample) |
| CA (1) | CA2137279C (enExample) |
| RU (1) | RU94046237A (enExample) |
| WO (1) | WO1993025510A1 (enExample) |
Families Citing this family (119)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3369604B2 (ja) * | 1992-09-04 | 2003-01-20 | ダイキン工業株式会社 | 1,1,1,2,3,3−ヘキサフルオロプロパンの製造方法及びテトラフルオロクロロプロペンの製造方法 |
| US5396000A (en) * | 1993-05-24 | 1995-03-07 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,1,1,2,3,-pentafluoropropane |
| JP3500617B2 (ja) * | 1993-08-27 | 2004-02-23 | ダイキン工業株式会社 | ヘキサフルオロシクロブタンの製造方法 |
| JP3543863B2 (ja) * | 1994-12-16 | 2004-07-21 | ダイキン工業株式会社 | 1,1,1,2,3,3−ヘキサフルオロプロパンの製造方法 |
| DE69715244T2 (de) | 1996-11-21 | 2003-09-18 | E.I. Du Pont De Nemours And Co., Wilmington | Katalytische herstellung von vinylfluorid |
| EP0958265B1 (en) * | 1997-01-31 | 2003-04-02 | E.I. Du Pont De Nemours And Company | The catalytic manufacture of pentafluoropropenes |
| US5945573A (en) * | 1997-01-31 | 1999-08-31 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,1,1,3,3-pentafluoropropane |
| JP4186253B2 (ja) * | 1998-03-31 | 2008-11-26 | 日本ゼオン株式会社 | フッ素化飽和炭化水素の製造方法 |
| US20080292564A1 (en) * | 2002-10-25 | 2008-11-27 | Honeywell International, Inc. | Aerosol compositions containing fluorine substituted olefins and methods and systems using same |
| US20090253820A1 (en) * | 2006-03-21 | 2009-10-08 | Honeywell International Inc. | Foaming agents and compositions containing fluorine sustituted olefins and methods of foaming |
| US7279451B2 (en) * | 2002-10-25 | 2007-10-09 | Honeywell International Inc. | Compositions containing fluorine substituted olefins |
| US8033120B2 (en) | 2002-10-25 | 2011-10-11 | Honeywell International Inc. | Compositions and methods containing fluorine substituted olefins |
| US7230146B2 (en) * | 2003-10-27 | 2007-06-12 | Honeywell International Inc. | Process for producing fluoropropenes |
| US20040089839A1 (en) | 2002-10-25 | 2004-05-13 | Honeywell International, Inc. | Fluorinated alkene refrigerant compositions |
| CN106634852A (zh) * | 2002-10-25 | 2017-05-10 | 霍尼韦尔国际公司 | 含有氟取代烯烃的组合物 |
| US9796848B2 (en) * | 2002-10-25 | 2017-10-24 | Honeywell International Inc. | Foaming agents and compositions containing fluorine substituted olefins and methods of foaming |
| US9005467B2 (en) * | 2003-10-27 | 2015-04-14 | Honeywell International Inc. | Methods of replacing heat transfer fluids |
| RU2248844C1 (ru) * | 2003-06-25 | 2005-03-27 | Институт элементоорганических соединений им. А.Н. Несмеянова РАН | Композиция в качестве катализатора деиодирования для получения гексафтор-1,2,3,4-тетрахлорбутана и способ получения гексафтор-1,2,3,4-тетрахлорбутана |
| US9255046B2 (en) | 2003-07-25 | 2016-02-09 | Honeywell International Inc. | Manufacturing process for HFO-1234ze |
| US7563936B2 (en) * | 2006-10-27 | 2009-07-21 | Honeywell International Inc | Processes for geometric isomerization of halogenated olefins |
| US7880040B2 (en) | 2004-04-29 | 2011-02-01 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US8530708B2 (en) * | 2003-07-25 | 2013-09-10 | Honeywell International Inc. | Processes for selective dehydrohalogenation of halogenated alkanes |
| US20050038302A1 (en) * | 2003-08-13 | 2005-02-17 | Hedrick Vicki E. | Systems and methods for producing fluorocarbons |
| US7091388B2 (en) * | 2003-09-26 | 2006-08-15 | Honeywell International Inc. | Method of making 1,1,3,3,3-pentafluoropropene |
| US7655610B2 (en) * | 2004-04-29 | 2010-02-02 | Honeywell International Inc. | Blowing agent compositions comprising fluorinated olefins and carbon dioxide |
| US9308199B2 (en) | 2004-04-29 | 2016-04-12 | Honeywell International Inc. | Medicament formulations |
| US20180161076A1 (en) | 2003-10-27 | 2018-06-14 | Honeywell International Inc. | Foaming agents and compositions containing fluorine substituted olefins, and methods of foaming |
| US9499729B2 (en) * | 2006-06-26 | 2016-11-22 | Honeywell International Inc. | Compositions and methods containing fluorine substituted olefins |
| US7605117B2 (en) * | 2004-04-16 | 2009-10-20 | Honeywell International Inc. | Methods of replacing refrigerant |
| JP4864879B2 (ja) * | 2004-04-29 | 2012-02-01 | ハネウェル・インターナショナル・インコーポレーテッド | 1,3,3,3−テトラフルオロプロペンの合成方法 |
| CA2564991C (en) * | 2004-04-29 | 2013-03-19 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene and 2,3,3,3-tetrafluoropropene |
| US9102579B2 (en) * | 2004-04-29 | 2015-08-11 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US8383867B2 (en) * | 2004-04-29 | 2013-02-26 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US7951982B2 (en) * | 2004-04-29 | 2011-05-31 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US9024092B2 (en) * | 2006-01-03 | 2015-05-05 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US7659434B2 (en) * | 2004-04-29 | 2010-02-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US7674939B2 (en) * | 2004-04-29 | 2010-03-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US8084653B2 (en) | 2004-04-29 | 2011-12-27 | Honeywell International, Inc. | Method for producing fluorinated organic compounds |
| WO2005118134A1 (ja) * | 2004-06-04 | 2005-12-15 | Mitsubishi Rayon Co., Ltd. | パラジウム含有触媒およびその製造方法 |
| US7897823B2 (en) * | 2004-10-29 | 2011-03-01 | E. I. Du Pont De Nemours And Company | Process for production of azeotrope compositions comprising hydrofluoroolefin and hydrogen fluoride and uses of said azeotrope compositions in separation processes |
| US7569170B2 (en) | 2005-03-04 | 2009-08-04 | E.I. Du Pont De Nemours And Company | Compositions comprising a fluoroolefin |
| US20220389297A1 (en) | 2005-03-04 | 2022-12-08 | The Chemours Company Fc, Llc | Compositions comprising a fluoroolefin |
| AU2016200229B2 (en) * | 2005-03-04 | 2017-03-09 | The Chemours Company Fc, Llc. | Compositions comprising a fluoroolefin |
| US8420706B2 (en) * | 2005-06-24 | 2013-04-16 | Honeywell International Inc. | Foaming agents, foamable compositions, foams and articles containing halogen substituted olefins, and methods of making same |
| US8574451B2 (en) * | 2005-06-24 | 2013-11-05 | Honeywell International Inc. | Trans-chloro-3,3,3-trifluoropropene for use in chiller applications |
| US7388117B2 (en) * | 2005-11-01 | 2008-06-17 | E.I. Du Pont De Nemours And Company | Azeotrope compositions comprising 1,2,3,3,3-pentafluoropropene and hydrogen fluoride and uses thereof |
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| CN111003786B (zh) * | 2019-12-18 | 2022-09-13 | 鲁东大学 | 一种高效降解芳香氟代物的催化还原脱氟处理方法 |
| WO2023149559A1 (ja) * | 2022-02-04 | 2023-08-10 | エヌ・イーケムキャット株式会社 | 水素化反応用触媒およびその製造方法、ならびに水素化有機化合物の製造方法 |
| FR3137845B1 (fr) | 2022-07-12 | 2025-07-18 | Arkema France | Procédé de purification du 1,1,1,2,3,3-hexafluoropropane |
| TW202430495A (zh) * | 2022-10-03 | 2024-08-01 | 日商關東電化工業股份有限公司 | 氟烯烴之製造方法 |
| CN116041217B (zh) * | 2023-02-09 | 2025-10-10 | 国网安徽省电力有限公司电力科学研究院 | 一种利用消去反应去除七氟异丁腈中1,1,1,2,3,3,3-七氟丙烷的方法 |
| CN118108570A (zh) * | 2024-01-24 | 2024-05-31 | 浙江衢化氟化学有限公司 | 一种由1,1,2,3,3,3-六氟丙烯生产2,3,3,3-四氟丙烯的方法 |
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| US2599631A (en) * | 1945-12-06 | 1952-06-10 | Du Pont | Preparation of vinyl fluoride |
| US2461523A (en) * | 1946-12-04 | 1949-02-15 | Du Pont | Dehydrofluorination of polyfluoroalkanes |
| US2695320A (en) * | 1950-08-28 | 1954-11-23 | Monsanto Chemicals | Vinyl fluoride preparation from 1, 2-difluoroethane |
| US2912470A (en) * | 1956-01-04 | 1959-11-10 | Detrex Chem Ind | Method of dehydrohalogenating halogenated hydrocarbons |
| US3432562A (en) * | 1965-09-24 | 1969-03-11 | Phillips Petroleum Co | Dehydrofluorination process and products |
| US3636172A (en) * | 1969-10-29 | 1972-01-18 | Phillips Petroleum Co | Dehalogenation of fluorohalocarbons |
| JPS607975B2 (ja) * | 1978-03-30 | 1985-02-28 | ダイキン工業株式会社 | フツ化ビニリデンの製造法 |
| ES8706398A1 (es) * | 1986-02-24 | 1987-07-01 | Pescanova Sa | Proceso de fabricacion de calamar reconstituido |
| IT1221776B (it) * | 1988-01-15 | 1990-07-12 | Ausimont Spa | Processo per la preparazione di 1,2 difluoroetano e di 1,1,2 trifluoroetano |
| JP2638154B2 (ja) * | 1988-11-08 | 1997-08-06 | 旭硝子株式会社 | 1,1,2,2―テトラフルオロエタンの製造方法 |
-
1993
- 1993-05-19 BR BR9306493A patent/BR9306493A/pt not_active Application Discontinuation
- 1993-05-19 US US08/338,528 patent/US5679875A/en not_active Expired - Lifetime
- 1993-05-19 WO PCT/JP1993/000661 patent/WO1993025510A1/ja not_active Ceased
- 1993-05-19 KR KR1019940704439A patent/KR950701896A/ko not_active Withdrawn
- 1993-05-19 AU AU40888/93A patent/AU664753B2/en not_active Ceased
- 1993-05-19 EP EP93910362A patent/EP0644173A1/en not_active Withdrawn
- 1993-05-19 JP JP50132794A patent/JP3158440B2/ja not_active Expired - Fee Related
- 1993-05-19 CA CA002137279A patent/CA2137279C/en not_active Expired - Fee Related
- 1993-05-19 EP EP96105492A patent/EP0726243A1/en not_active Withdrawn
- 1993-05-19 RU RU94046237/04A patent/RU94046237A/ru unknown
- 1993-06-05 CN CN93106544A patent/CN1083040A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA2137279C (en) | 2001-08-21 |
| BR9306493A (pt) | 1998-09-15 |
| JP3158440B2 (ja) | 2001-04-23 |
| CA2137279A1 (en) | 1993-12-23 |
| RU94046237A (ru) | 1996-10-27 |
| EP0644173A1 (en) | 1995-03-22 |
| CN1083040A (zh) | 1994-03-02 |
| AU664753B2 (en) | 1995-11-30 |
| WO1993025510A1 (fr) | 1993-12-23 |
| AU4088893A (en) | 1994-01-04 |
| EP0644173A4 (enExample) | 1995-04-05 |
| EP0726243A1 (en) | 1996-08-14 |
| US5679875A (en) | 1997-10-21 |
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