ES2461343T5 - Procedimientos para la síntesis de olefinas fluoradas - Google Patents
Procedimientos para la síntesis de olefinas fluoradas Download PDFInfo
- Publication number
- ES2461343T5 ES2461343T5 ES08840751T ES08840751T ES2461343T5 ES 2461343 T5 ES2461343 T5 ES 2461343T5 ES 08840751 T ES08840751 T ES 08840751T ES 08840751 T ES08840751 T ES 08840751T ES 2461343 T5 ES2461343 T5 ES 2461343T5
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- Spain
- Prior art keywords
- compound
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- formula
- iiib
- chfch
- 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.)
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- 238000000034 method Methods 0.000 title claims description 24
- 230000015572 biosynthetic process Effects 0.000 title claims description 9
- 238000003786 synthesis reaction Methods 0.000 title claims description 9
- 150000001336 alkenes Chemical class 0.000 title description 8
- 238000006243 chemical reaction Methods 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 38
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 12
- 239000007791 liquid phase Substances 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 239000007795 chemical reaction product Substances 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- 238000006555 catalytic reaction Methods 0.000 claims description 5
- 150000003983 crown ethers Chemical class 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 239000012808 vapor phase Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 19
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 18
- 239000007789 gas Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 8
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 7
- 239000012071 phase Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- ZDCWZRQSHBQRGN-UHFFFAOYSA-N 1,1,1,2,3-pentafluoropropane Chemical compound FCC(F)C(F)(F)F ZDCWZRQSHBQRGN-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910000792 Monel Inorganic materials 0.000 description 4
- 238000005796 dehydrofluorination reaction Methods 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 235000011089 carbon dioxide Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 239000011269 tar Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 238000010574 gas phase reaction Methods 0.000 description 2
- -1 heat transfer media Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 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 1
- SHXHPUAKLCCLDV-UHFFFAOYSA-N 1,1,1-trifluoropentane-2,4-dione Chemical compound CC(=O)CC(=O)C(F)(F)F SHXHPUAKLCCLDV-UHFFFAOYSA-N 0.000 description 1
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 1
- PLTIOZOVDUUXDQ-UHFFFAOYSA-N 3,3-dichloro-1,1,1-trifluoropropane Chemical compound FC(F)(F)CC(Cl)Cl PLTIOZOVDUUXDQ-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical class CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000000110 cooling liquid Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 150000005828 hydrofluoroalkanes Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000003206 sterilizing agent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- 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
- C07C17/21—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/23—Preparation of halogenated hydrocarbons by dehalogenation
-
- 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
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US249958 | 1988-09-27 | ||
| US6850907P | 2007-10-15 | 2007-10-15 | |
| US68509 | 2007-10-15 | ||
| US12/249,958 US9079818B2 (en) | 2007-10-15 | 2008-10-12 | Process for synthesis of fluorinated olefins |
| PCT/US2008/079759 WO2009052064A2 (en) | 2007-10-15 | 2008-10-14 | Processes for synthesis of fluorinated olefins |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2461343T3 ES2461343T3 (es) | 2014-05-19 |
| ES2461343T5 true ES2461343T5 (es) | 2022-03-24 |
Family
ID=40534878
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08840751T Active ES2461343T5 (es) | 2007-10-15 | 2008-10-14 | Procedimientos para la síntesis de olefinas fluoradas |
Country Status (8)
| Country | Link |
|---|---|
| US (5) | US9079818B2 (enExample) |
| EP (1) | EP2203402B2 (enExample) |
| JP (1) | JP5615179B2 (enExample) |
| KR (1) | KR101579788B1 (enExample) |
| CN (2) | CN101868435B (enExample) |
| ES (1) | ES2461343T5 (enExample) |
| MX (1) | MX2010004005A (enExample) |
| WO (1) | WO2009052064A2 (enExample) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8084653B2 (en) | 2004-04-29 | 2011-12-27 | Honeywell International, Inc. | Method for producing fluorinated organic compounds |
| CN103553871A (zh) | 2006-10-31 | 2014-02-05 | 纳幕尔杜邦公司 | 氟丙烷、卤代丙烯以及2-氯-3,3,3-三氟-1-丙烯与hf的共沸组合物和1,1,1,2,2-五氟丙烷与hf的共沸组合物的制备方法 |
| US9079818B2 (en) * | 2007-10-15 | 2015-07-14 | Honeywell International Inc. | Process for synthesis of fluorinated olefins |
| JP5370479B2 (ja) | 2008-08-26 | 2013-12-18 | ダイキン工業株式会社 | 共沸又は共沸様組成物、及び２，３，３，３−テトラフルオロプロペンの製造方法 |
| KR20110086037A (ko) * | 2008-10-13 | 2011-07-27 | 다우 글로벌 테크놀로지스 엘엘씨 | 염화된 및/또는 불화된 프로펜의 제조 방법 |
| FR2948362B1 (fr) * | 2009-07-23 | 2012-03-23 | Arkema France | Procede de preparation de composes fluores |
| CN102686544B (zh) * | 2009-10-09 | 2017-02-15 | 蓝立方知识产权公司 | 用于生产氯化和/或氟化丙烯和高级烯烃的方法 |
| WO2011044447A2 (en) * | 2009-10-09 | 2011-04-14 | Dow Global Technologies, Inc | Process for the production of chlorinated and/or fluorinated propenes |
| KR20120091192A (ko) | 2009-10-09 | 2012-08-17 | 다우 글로벌 테크놀로지스 엘엘씨 | 등온 다중튜브 반응기 및 이를 도입한 방법 |
| BR112012007913A2 (pt) | 2009-10-09 | 2019-09-24 | Dow Global Technologies Llc | reator adiabático de fluxo pistonado, processo para produzir um prpeno clorado ou fluorado, processo para preparar um produto a jusante e processo para preparar 2,3,3,3-tetrafluoroprop-1-eno (hfo-123yf) ou 1,3,3,3-tetrafluoroprop-1-eno (hfo-123ze) |
| US8618340B2 (en) * | 2009-11-03 | 2013-12-31 | Honeywell International Inc. | Integrated process for fluoro-olefin production |
| WO2011102538A2 (en) * | 2010-02-19 | 2011-08-25 | Daikin Industries, Ltd. | Process for producing 2-chloro-3,3,3-trifluoropropene |
| US8927791B2 (en) | 2010-04-29 | 2015-01-06 | Honeywell International Inc. | Method for producing tetrafluoropropenes |
| US20110269999A1 (en) | 2010-04-29 | 2011-11-03 | Honeywell International Inc. | Process for dehydrohalogenation of halogenated alkanes |
| EP2586762B1 (en) * | 2010-06-23 | 2019-08-07 | AGC Inc. | Production method for 1,1-dichloro-2,3,3,3-tetra-fluoropropene and 2,3,3,3-tetrafluoropropene |
| US8907149B2 (en) | 2011-05-31 | 2014-12-09 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
| WO2012166394A1 (en) | 2011-05-31 | 2012-12-06 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| WO2012170239A1 (en) | 2011-06-08 | 2012-12-13 | Dow Agrosciences, Llc | Process for the production of chlorinated and/or fluorinated propenes |
| US8907148B2 (en) | 2011-08-07 | 2014-12-09 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
| CN103717557A (zh) | 2011-08-07 | 2014-04-09 | 陶氏环球技术有限责任公司 | 生产氯化的丙烯的方法 |
| JP6050372B2 (ja) | 2011-11-21 | 2016-12-21 | ブルー キューブ アイピー エルエルシー | クロロアルカンの製造方法 |
| CA2856717A1 (en) | 2011-12-02 | 2013-06-06 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
| US9199899B2 (en) | 2011-12-02 | 2015-12-01 | Blue Cube Ip Llc | Process for the production of chlorinated alkanes |
| JP6170068B2 (ja) | 2011-12-13 | 2017-07-26 | ブルー キューブ アイピー エルエルシー | 塩素化プロパン及びプロペンの製造方法 |
| CN104011000A (zh) | 2011-12-22 | 2014-08-27 | 陶氏环球技术有限责任公司 | 生产四氯甲烷的方法 |
| EP2794521B1 (en) | 2011-12-23 | 2016-09-21 | Dow Global Technologies LLC | Process for the production of alkenes and/or aromatic compounds |
| EP4098644A1 (en) * | 2012-02-29 | 2022-12-07 | Honeywell International Inc. | Process for producing 2,3,3,3-tetrafluoropropene |
| US9598334B2 (en) | 2012-09-20 | 2017-03-21 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| US9321707B2 (en) | 2012-09-20 | 2016-04-26 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| EP2900364B1 (en) | 2012-09-30 | 2018-06-13 | Blue Cube IP LLC | Weir quench and processes incorporating the same |
| CA2887559A1 (en) | 2012-10-26 | 2014-05-01 | Dow Global Technologies Llc | Mixer and reactor and process incorporating the same |
| WO2014100066A1 (en) | 2012-12-18 | 2014-06-26 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| US9475740B2 (en) | 2012-12-19 | 2016-10-25 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| EP2961722A2 (en) | 2013-02-27 | 2016-01-06 | Blue Cube IP LLC | Process for the production of chlorinated propenes |
| US9403741B2 (en) | 2013-03-09 | 2016-08-02 | Blue Cube Ip Llc | Process for the production of chlorinated alkanes |
| US10005705B2 (en) | 2015-11-12 | 2018-06-26 | Honeywell International Inc. | Process for the production of fluorinated cyclobutane |
| US9790151B2 (en) | 2015-11-12 | 2017-10-17 | Honeywell International Inc. | Process for making 2,3,3,3-tetrafluoropropene and/or vinylidine fluoride |
| US9856193B2 (en) | 2015-11-12 | 2018-01-02 | Honeywell International Inc. | Process for the production of fluorinated cyclobutane |
| FR3049599B1 (fr) * | 2016-04-04 | 2018-03-16 | Arkema France | Procede de preparation de l'hexafluorobutadiene. |
| EP3455322B1 (en) * | 2016-05-09 | 2021-03-03 | 3M Innovative Properties Company | Hydrofluoroolefins and methods of using same |
| MX2019005161A (es) | 2016-11-08 | 2019-08-12 | Honeywell Int Inc | Proceso para la produccion de ciclobutano fluorado. |
| GB201701099D0 (en) | 2017-01-23 | 2017-03-08 | Mexichem Fluor Sa De Cv | Process |
| CN119118781A (zh) | 2018-06-06 | 2024-12-13 | 霍尼韦尔国际公司 | 用于HCFC-244bb的脱氯化氢以制备HFO-1234yf的方法 |
| EP3841081A4 (en) | 2018-08-24 | 2022-05-18 | Honeywell International Inc. | Processes for producing trifluoroiodomethane and trifluoroacetyl iodide |
| US11209196B2 (en) | 2018-10-26 | 2021-12-28 | The Chemours Company Fc, Llc | HFO-1234ZE, HFO-1225ZC and HFO-1234YF compositions and processes for producing and using the compositions |
| BR112021022059A2 (pt) | 2018-10-26 | 2021-12-28 | Chemours Co Fc Llc | Composições de fluoropropeno, métodos de produção de uma mistura e de resfriamento, processos para transferência de calor, para tratamento de uma superfície e para formação de uma composição, sistema de refrigeração, aparelhos de refrigeração, uso da composição de fluoropropeno e método para substituição de um refrigerante |
| KR102892009B1 (ko) * | 2018-10-26 | 2025-11-28 | 더 케무어스 컴퍼니 에프씨, 엘엘씨 | Hfo-1234ze 및 hfo-1234yf 조성물, 및 조성물의 제조 및 사용 방법 |
| CN113796173B (zh) | 2018-12-21 | 2025-04-08 | 霍尼韦尔国际公司 | 热传递方法、系统和流体 |
| US11554956B2 (en) | 2019-04-16 | 2023-01-17 | Honeywell International Inc. | Integrated process and catalysts for manufacturing hydrogen iodide from hydrogen and iodine |
| MX2022005113A (es) * | 2019-12-09 | 2022-05-30 | Chemours Co Fc Llc | Sintesis catalizada de alquenos fluorados y composiciones de alquenos fluorados. |
| CN112592254B (zh) * | 2020-12-21 | 2023-12-26 | 江苏三美化工有限公司 | 一种制备2，3，3，3-四氟丙烯的系统及其制备方法 |
| JP7749693B2 (ja) | 2021-04-15 | 2025-10-06 | ジョージアン リサーチ インスティテュート オブ ケミカル インダストリー カンパニー，リミテッド | ２，３，３，３－テトラフルオロプロペンを製造する方法 |
| US20240377504A1 (en) | 2023-05-12 | 2024-11-14 | Nxp B.V. | Time-based correction technique for multistatic radar system |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2931840A (en) | 1958-11-25 | 1960-04-05 | Du Pont | Process for preparing 2, 3, 3, 3-tetrafluoropropene |
| JPH01207250A (ja) | 1988-02-12 | 1989-08-21 | Daikin Ind Ltd | 含フツ素オレフインの製造方法 |
| US5162594A (en) | 1990-10-11 | 1992-11-10 | E. I. Du Pont De Nemours And Company | Process for production of polyfluoroolefins |
| US5986151A (en) | 1997-02-05 | 1999-11-16 | Alliedsignal Inc. | Fluorinated propenes from pentafluoropropane |
| US6124510A (en) | 1998-07-21 | 2000-09-26 | Elf Atochem North America, Inc. | 1234ze preparation |
| DE60140425D1 (de) * | 2000-02-02 | 2009-12-24 | Daikin Ind Ltd | Produktionsverfahren von fluorkohlenwasserstoffen |
| US6548719B1 (en) | 2001-09-25 | 2003-04-15 | Honeywell International | Process for producing fluoroolefins |
| US7674939B2 (en) * | 2004-04-29 | 2010-03-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| 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 |
| US8084653B2 (en) | 2004-04-29 | 2011-12-27 | Honeywell International, Inc. | Method for producing fluorinated organic compounds |
| US7678949B2 (en) | 2005-08-05 | 2010-03-16 | E.I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 2,3,3,3-tetrafluoropropene |
| US7476771B2 (en) | 2005-11-01 | 2009-01-13 | E.I. Du Pont De Nemours + Company | Azeotrope compositions comprising 2,3,3,3-tetrafluoropropene and hydrogen fluoride and uses thereof |
| ES2400732T3 (es) * | 2005-11-03 | 2013-04-11 | Honeywell International Inc. | Método para la producción de compuestos orgánicos fluorados |
| US8071825B2 (en) * | 2006-01-03 | 2011-12-06 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| EP3336074B1 (en) * | 2006-01-03 | 2025-07-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US9035111B2 (en) | 2007-08-22 | 2015-05-19 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US9079818B2 (en) * | 2007-10-15 | 2015-07-14 | Honeywell International Inc. | Process for synthesis of fluorinated olefins |
-
2008
- 2008-10-12 US US12/249,958 patent/US9079818B2/en active Active
- 2008-10-14 MX MX2010004005A patent/MX2010004005A/es active IP Right Grant
- 2008-10-14 CN CN200880111631.3A patent/CN101868435B/zh active Active
- 2008-10-14 KR KR1020107010675A patent/KR101579788B1/ko not_active Expired - Fee Related
- 2008-10-14 EP EP08840751.5A patent/EP2203402B2/en active Active
- 2008-10-14 WO PCT/US2008/079759 patent/WO2009052064A2/en not_active Ceased
- 2008-10-14 CN CN201410158373.1A patent/CN103992205A/zh active Pending
- 2008-10-14 ES ES08840751T patent/ES2461343T5/es active Active
- 2008-10-14 JP JP2010530051A patent/JP5615179B2/ja active Active
-
2015
- 2015-07-13 US US14/797,699 patent/US20160145176A1/en not_active Abandoned
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2018
- 2018-05-23 US US15/987,463 patent/US20180265434A1/en not_active Abandoned
-
2020
- 2020-10-30 US US17/085,331 patent/US20210047251A1/en not_active Abandoned
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2023
- 2023-04-04 US US18/130,439 patent/US20230234902A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP2203402A2 (en) | 2010-07-07 |
| MX2010004005A (es) | 2010-04-30 |
| US20180265434A1 (en) | 2018-09-20 |
| JP5615179B2 (ja) | 2014-10-29 |
| JP2011500695A (ja) | 2011-01-06 |
| US20230234902A1 (en) | 2023-07-27 |
| EP2203402B2 (en) | 2021-10-20 |
| CN101868435A (zh) | 2010-10-20 |
| CN103992205A (zh) | 2014-08-20 |
| CN101868435B (zh) | 2014-06-04 |
| US20090099396A1 (en) | 2009-04-16 |
| EP2203402B1 (en) | 2014-03-05 |
| US20210047251A1 (en) | 2021-02-18 |
| EP2203402A4 (en) | 2011-02-09 |
| KR20100094465A (ko) | 2010-08-26 |
| ES2461343T3 (es) | 2014-05-19 |
| WO2009052064A3 (en) | 2009-06-11 |
| US9079818B2 (en) | 2015-07-14 |
| US20160145176A1 (en) | 2016-05-26 |
| KR101579788B1 (ko) | 2015-12-24 |
| WO2009052064A2 (en) | 2009-04-23 |
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