MX2013000065A - Proceso para la manufactura de olefinas fluoradas. - Google Patents
Proceso para la manufactura de olefinas fluoradas.Info
- Publication number
- MX2013000065A MX2013000065A MX2013000065A MX2013000065A MX2013000065A MX 2013000065 A MX2013000065 A MX 2013000065A MX 2013000065 A MX2013000065 A MX 2013000065A MX 2013000065 A MX2013000065 A MX 2013000065A MX 2013000065 A MX2013000065 A MX 2013000065A
- Authority
- MX
- Mexico
- Prior art keywords
- formula
- compound
- metal
- group
- reaction
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 36
- 150000001336 alkenes Chemical class 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 6
- 238000006243 chemical reaction Methods 0.000 claims abstract description 72
- 150000001875 compounds Chemical class 0.000 claims abstract description 64
- 238000006356 dehydrogenation reaction Methods 0.000 claims abstract description 32
- 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 description 11
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000003054 catalyst Substances 0.000 claims description 88
- 229910052751 metal Inorganic materials 0.000 claims description 38
- 239000002184 metal Substances 0.000 claims description 38
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 15
- 239000000047 product Substances 0.000 claims description 11
- 229910052749 magnesium Inorganic materials 0.000 claims description 9
- 229910000510 noble metal Inorganic materials 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 239000012467 final product Substances 0.000 claims description 6
- 150000002222 fluorine compounds Chemical class 0.000 claims description 6
- 239000007800 oxidant agent Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 229910052741 iridium Inorganic materials 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- 229910052703 rhodium Inorganic materials 0.000 claims description 5
- 229910052707 ruthenium Inorganic materials 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 229910052733 gallium Inorganic materials 0.000 claims description 3
- 229910052746 lanthanum Inorganic materials 0.000 claims description 3
- 229910052727 yttrium Inorganic materials 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 abstract description 14
- 150000004812 organic fluorine compounds Chemical class 0.000 abstract description 5
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 15
- 230000003197 catalytic effect Effects 0.000 description 15
- 238000005796 dehydrofluorination reaction Methods 0.000 description 11
- 239000000843 powder Substances 0.000 description 10
- 239000007795 chemical reaction product Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000001354 calcination Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 230000001590 oxidative effect Effects 0.000 description 6
- 150000001335 aliphatic alkanes Chemical class 0.000 description 5
- 239000003518 caustics Substances 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 230000008929 regeneration Effects 0.000 description 4
- 238000011069 regeneration method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZDCWZRQSHBQRGN-UHFFFAOYSA-N 1,1,1,2,3-pentafluoropropane Chemical compound FCC(F)C(F)(F)F ZDCWZRQSHBQRGN-UHFFFAOYSA-N 0.000 description 2
- INEMUVRCEAELBK-UHFFFAOYSA-N 1,1,1,2-tetrafluoropropane Chemical compound CC(F)C(F)(F)F INEMUVRCEAELBK-UHFFFAOYSA-N 0.000 description 2
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- 238000010574 gas phase reaction Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical class CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 description 1
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- PFFGXVGPSGJOBV-UHFFFAOYSA-N 1,1,1,3-tetrafluoropropane Chemical compound FCCC(F)(F)F PFFGXVGPSGJOBV-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 229910000792 Monel Inorganic materials 0.000 description 1
- 229910002666 PdCl2 Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910003455 mixed metal oxide Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/04—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated 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
-
- 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
- C07C17/357—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by dehydrogenation
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)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/822,365 US8513474B2 (en) | 2010-06-24 | 2010-06-24 | Process for the manufacture of fluorinated olefins |
| PCT/US2011/041323 WO2011163285A2 (en) | 2010-06-24 | 2011-06-22 | Process for the manufacture of fluorinated olefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2013000065A true MX2013000065A (es) | 2013-02-15 |
Family
ID=45353142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2013000065A MX2013000065A (es) | 2010-06-24 | 2011-06-22 | Proceso para la manufactura de olefinas fluoradas. |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US8513474B2 (OSRAM) |
| EP (3) | EP3915967A1 (OSRAM) |
| JP (3) | JP5886841B2 (OSRAM) |
| CN (2) | CN105037077B (OSRAM) |
| ES (2) | ES2890024T3 (OSRAM) |
| HR (1) | HRP20211696T1 (OSRAM) |
| HU (1) | HUE056296T2 (OSRAM) |
| MX (1) | MX2013000065A (OSRAM) |
| PL (1) | PL3269698T3 (OSRAM) |
| PT (1) | PT3269698T (OSRAM) |
| SI (1) | SI3269698T1 (OSRAM) |
| WO (1) | WO2011163285A2 (OSRAM) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9187386B2 (en) * | 2013-05-23 | 2015-11-17 | The Chemours Company Fc, Llc | Catalytic process of making 1,3,3,3-tetrafluoropropene |
| US9302962B2 (en) | 2014-08-14 | 2016-04-05 | The Chemours Company Fc, Llc | Dehydrofluorination of 245fa to 1234ze |
| JP6052340B2 (ja) * | 2015-05-29 | 2016-12-27 | ダイキン工業株式会社 | 含フッ素化合物含有組成物の製造方法 |
| CN112811978B (zh) * | 2021-04-22 | 2021-07-16 | 泉州宇极新材料科技有限公司 | Z-1,3,3,3-四氟丙烯的制备方法 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2500920A (en) | 1946-07-16 | 1950-03-21 | Phillips Petroleum Co | Process and catalyst for dehydrogenation of hydrocarbons |
| US2757128A (en) | 1951-04-27 | 1956-07-31 | Exxon Research Engineering Co | Low pressure hydrogenation and hydrogen regeneration of the catalyst |
| US3140925A (en) | 1960-05-19 | 1964-07-14 | California Research Corp | Hydrocarbon conversion catalyst |
| JPH0717550B2 (ja) * | 1986-09-30 | 1995-03-01 | 旭化成工業株式会社 | フルオロベンゼンの製造法 |
| CA2019914C (en) * | 1989-07-06 | 1999-06-08 | Maher Yousef Elsheikh | Dehydrofluorination and dehydrogenation of fluorinated alkanes |
| CA2019913A1 (en) * | 1990-06-08 | 1991-12-08 | Michael S. Bolmer | Production of vinylidene fluoride from 1,1-difluoroethane |
| US5087777A (en) * | 1990-12-04 | 1992-02-11 | Allied-Signal Inc. | Partially fluorinated alkenes having a tertiary structure |
| MY116795A (en) | 1998-05-18 | 2004-03-31 | Nippon Catalytic Chem Ind | Lower alkane oxidative dehydrogenation catalysts and a process for producing olefins |
| US20050124840A1 (en) | 2003-12-05 | 2005-06-09 | Conocophillips Company | Process for the production of olefins from alkanes with carbon monoxide co-feed and/or recycle |
| US7026520B1 (en) | 2004-12-09 | 2006-04-11 | Honeywell International Inc. | Catalytic conversion of hydrofluoroalkanol to hydrofluoroalkene |
| WO2007019358A2 (en) | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 1,1,3,3,3-pentafluoropropene |
| US7560602B2 (en) * | 2005-11-03 | 2009-07-14 | Honeywell International Inc. | Process for manufacture of fluorinated olefins |
| US8766020B2 (en) | 2008-07-31 | 2014-07-01 | Honeywell International Inc. | Process for producing 2,3,3,3-tetrafluoropropene |
| US7335804B2 (en) | 2005-11-03 | 2008-02-26 | Honeywell International Inc. | Direct conversion of HCFC 225ca/cb mixture |
| WO2007145171A1 (ja) | 2006-06-13 | 2007-12-21 | Central Glass Company, Limited | １，３，３，３－テトラフルオロプロペンの製造方法 |
| JP5764291B2 (ja) * | 2006-07-13 | 2015-08-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ | テトラフルオロプロペンおよびペンタフルオロプロペンを製造するための触媒製造方法 |
| US7420094B2 (en) | 2006-09-05 | 2008-09-02 | E.I. Du Pont De Nemours And Company | Catalytic isomerization processes of 1,3,3,3-tetrafluoropropene for making 2,3,3,3-tetrafluoropropene |
| WO2008030440A2 (en) | 2006-09-05 | 2008-03-13 | E. I. Du Pont De Nemours And Company | Process to manufacture 2,3,3,3-tetrafluoropropene |
| GB0806422D0 (en) | 2008-04-09 | 2008-05-14 | Ineos Fluor Holdings Ltd | Process |
| US8013194B2 (en) * | 2008-03-14 | 2011-09-06 | Honeywell International Inc. | Process for the manufacture of fluorinated olefins |
| USRE49849E1 (en) | 2006-10-31 | 2024-02-27 | The Chemours Company Fc, Llc | Processes for the production of fluoropropanes and halopropenes |
| CN101796002B (zh) | 2007-09-11 | 2013-04-10 | 大金工业株式会社 | 2,3,3,3-四氟丙烯的制造方法 |
| US8044250B2 (en) | 2007-11-16 | 2011-10-25 | Honeywell International Inc. | Manufacture of 1,1,1,2,3,3-hexafluoropropane and 1,1,1,2-tetrafluoropropane via catalytic hydrogenation |
| GB0801209D0 (en) | 2008-01-23 | 2008-02-27 | Ineos Fluor Holdings Ltd | Process |
| GB0806389D0 (en) | 2008-04-09 | 2008-05-14 | Ineos Fluor Holdings Ltd | Process |
| GB0806419D0 (en) | 2008-04-09 | 2008-05-14 | Ineos Fluor Holdings Ltd | Process |
| AU2009244263B2 (en) | 2008-05-07 | 2014-05-22 | The Chemours Company Fc, Llc. | Compositions comprising 1,1,1,2,3-pentafluoropropane or 2,3,3,3- tetrafluoropropene |
| GB0808836D0 (en) | 2008-05-15 | 2008-06-18 | Ineos Fluor Ltd | Process |
| FR2946644B1 (fr) | 2009-06-12 | 2011-10-14 | Arkema France | Procede de fabrication du pentafluoropropane. |
| FR2948362B1 (fr) | 2009-07-23 | 2012-03-23 | Arkema France | Procede de preparation de composes fluores |
| US8129574B2 (en) | 2009-08-31 | 2012-03-06 | Honeywell International Inc. | Hydrogenation process for fluorocarbons |
| US8158549B2 (en) | 2009-09-04 | 2012-04-17 | Honeywell International Inc. | Catalysts for fluoroolefins hydrogenation |
| US8486293B2 (en) | 2009-10-30 | 2013-07-16 | E I Du Pont De Nemours And Company | Hydrogen fluoride-HFC-254eb azeotrope and its uses |
-
2010
- 2010-06-24 US US12/822,365 patent/US8513474B2/en active Active
-
2011
- 2011-06-22 EP EP21178869.0A patent/EP3915967A1/en active Pending
- 2011-06-22 HR HRP20211696TT patent/HRP20211696T1/hr unknown
- 2011-06-22 PL PL17170975T patent/PL3269698T3/pl unknown
- 2011-06-22 ES ES17170975T patent/ES2890024T3/es active Active
- 2011-06-22 PT PT171709751T patent/PT3269698T/pt unknown
- 2011-06-22 JP JP2013516706A patent/JP5886841B2/ja active Active
- 2011-06-22 WO PCT/US2011/041323 patent/WO2011163285A2/en not_active Ceased
- 2011-06-22 ES ES11798788.3T patent/ES2632189T3/es active Active
- 2011-06-22 CN CN201510355950.0A patent/CN105037077B/zh not_active Expired - Fee Related
- 2011-06-22 HU HUE17170975A patent/HUE056296T2/hu unknown
- 2011-06-22 MX MX2013000065A patent/MX2013000065A/es active IP Right Grant
- 2011-06-22 CN CN201180040537.5A patent/CN103038198B/zh not_active Expired - Fee Related
- 2011-06-22 EP EP11798788.3A patent/EP2585424B1/en not_active Not-in-force
- 2011-06-22 SI SI201132008T patent/SI3269698T1/sl unknown
- 2011-06-22 EP EP17170975.1A patent/EP3269698B1/en active Active
-
2013
- 2013-07-17 US US13/944,207 patent/US8940948B2/en active Active
-
2015
- 2015-11-26 JP JP2015230340A patent/JP2016074702A/ja active Pending
-
2017
- 2017-04-24 JP JP2017085023A patent/JP6367418B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN103038198B (zh) | 2015-11-25 |
| JP2016074702A (ja) | 2016-05-12 |
| EP2585424A4 (en) | 2014-01-08 |
| PL3269698T3 (pl) | 2022-01-17 |
| HRP20211696T1 (hr) | 2022-03-04 |
| EP3269698B1 (en) | 2021-08-04 |
| EP2585424A2 (en) | 2013-05-01 |
| WO2011163285A2 (en) | 2011-12-29 |
| ES2890024T3 (es) | 2022-01-17 |
| WO2011163285A3 (en) | 2012-03-29 |
| US8940948B2 (en) | 2015-01-27 |
| SI3269698T1 (sl) | 2021-11-30 |
| US8513474B2 (en) | 2013-08-20 |
| JP6367418B2 (ja) | 2018-08-01 |
| US20110319674A1 (en) | 2011-12-29 |
| CN105037077A (zh) | 2015-11-11 |
| EP3915967A1 (en) | 2021-12-01 |
| EP3269698A1 (en) | 2018-01-17 |
| JP2017200907A (ja) | 2017-11-09 |
| CN103038198A (zh) | 2013-04-10 |
| EP2585424B1 (en) | 2017-05-17 |
| JP2013529640A (ja) | 2013-07-22 |
| ES2632189T3 (es) | 2017-09-11 |
| CN105037077B (zh) | 2017-12-22 |
| PT3269698T (pt) | 2021-09-08 |
| HUE056296T2 (hu) | 2022-02-28 |
| US20130303808A1 (en) | 2013-11-14 |
| JP5886841B2 (ja) | 2016-03-16 |
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