KR20100039361A - 하이드로플루오로올레핀의 제조 공정 - Google Patents
하이드로플루오로올레핀의 제조 공정 Download PDFInfo
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- KR20100039361A KR20100039361A KR1020107001917A KR20107001917A KR20100039361A KR 20100039361 A KR20100039361 A KR 20100039361A KR 1020107001917 A KR1020107001917 A KR 1020107001917A KR 20107001917 A KR20107001917 A KR 20107001917A KR 20100039361 A KR20100039361 A KR 20100039361A
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- catalyst
- hydrochlorofluoroolefin
- hydrochloroolefin
- coproduct
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- 238000000034 method Methods 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title abstract description 5
- 238000003682 fluorination reaction Methods 0.000 claims abstract description 20
- 239000003054 catalyst Substances 0.000 claims description 25
- 239000007789 gas Substances 0.000 claims description 14
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 239000011651 chromium Substances 0.000 claims description 11
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims description 9
- SMCNZLDHTZESTK-UHFFFAOYSA-N 2-chloro-1,1,1,2-tetrafluoropropane Chemical compound CC(F)(Cl)C(F)(F)F SMCNZLDHTZESTK-UHFFFAOYSA-N 0.000 claims description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 9
- 229910052804 chromium Inorganic materials 0.000 claims description 9
- UMGQVBVEWTXECF-UHFFFAOYSA-N 1,1,2,3-tetrachloroprop-1-ene Chemical compound ClCC(Cl)=C(Cl)Cl UMGQVBVEWTXECF-UHFFFAOYSA-N 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 claims description 5
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims 4
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims 4
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical compound CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 claims 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 239000011572 manganese Substances 0.000 claims 1
- 238000004064 recycling Methods 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 abstract description 11
- 239000007791 liquid phase Substances 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- WAIPAZQMEIHHTJ-UHFFFAOYSA-N [Cr].[Co] Chemical compound [Cr].[Co] WAIPAZQMEIHHTJ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910000423 chromium oxide Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010574 gas phase reaction Methods 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- OWXJKYNZGFSVRC-NSCUHMNNSA-N (e)-1-chloroprop-1-ene Chemical compound C\C=C\Cl OWXJKYNZGFSVRC-NSCUHMNNSA-N 0.000 description 1
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
- VJGCZWVJDRIHNC-UHFFFAOYSA-N 1-fluoroprop-1-ene Chemical compound CC=CF VJGCZWVJDRIHNC-UHFFFAOYSA-N 0.000 description 1
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- 238000001994 activation Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229940095564 anhydrous calcium sulfate Drugs 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000003541 multi-stage reaction Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000013215 result calculation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
-
- 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
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)
Abstract
Description
Claims (22)
- a) 촉매의 부재하에, 하이드로클로로올레핀을 액체상 불소화하여 화학식 C3F3H(a+x-1)Cl4-(a+x)의 하이드로클로로플루오로올레핀과 HCl과 제 1 공생성물을 형성하는 단계; 및 후속으로
b) 적합한 촉매의 존재하에, 하이드로클로로플루오로올레핀을 기체상 불소화하여 화학식 C3H(a+x-1) F7-(a+x)의 하이드로플루오로올레핀과 제 2 공생성물을 형성하는 단계
를 포함하는, 화학식 C3H(a+x-1)F7-(a+x)(식에서, a = 0, 1, 2, 3 또는 4이고, x = 0, 1, 2 또는 3이며, (a+x)는 1 이상임)의 하이드로플루오로올레핀을 제조하는 공정. - 제1항에 있어서, 촉매의 부재하에 하이드로클로로올레핀을 액체상 불소화하는 a) 단계는 하이드로클로로올레핀을 불화수소와 접촉시키는 것을 포함하는 것인 공정.
- 제1항에 있어서, 하이드로클로로플루오로올레핀을 불소화하기 이전에, 상기 하이드로클로로플루오로올레핀과 HCl과 제 1 공생성물로부터 HCl를 분리시키는 단계를 더 포함하는 공정.
- 제1항에 있어서, 상기 제 1 공생성물은 펜타플루오로프로판과 클로로테트라플루오로프로판을 포함하는 것인 공정.
- 제4항에 있어서, 상기 펜타플루오로프로판은 HFC-245cb를 포함하고, 상기 클로로테트라플루오로프로판은 HCFC-244bb를 포함하는 것인 공정.
- 제1항에 있어서, 상기 제 2 공생성물을 상기 하이드로플루오로올레핀으로부터 분리시키는 단계를 더 포함하는 공정.
- 제6항에 있어서, 상기 분리된 제 2 공생성물을 a) 단계로 재순환시키는 단계를 더 포함하는 공정.
- 제1항에 있어서, 상기 제 2 공생성물은 펜타플루오로프로판과 클로로테트라플루오로프로판을 포함하는 것인 공정.
- 제8항에 있어서, 상기 펜타플루오로프로판은 HFC-245cb를 포함하고, 상기 클로로테트라플루오로프로판은 HCFC-244bb를 포함하는 것인 공정.
- 제2항에 있어서, 하이드로클로로올레핀 대 불화수소의 비가 약 3:1 내지 약 500:1의 범위에 속하는 것인 공정.
- 제2항에 있어서, 하이드로클로로올레핀 대 불화수소의 비가 약 10:1 내지 약 200:1의 범위에 속하는 것인 공정.
- 제2항에 있어서, 온도가 약 20℃ 내지 약 300℃의 범위에 속하는 것인 공정.
- 제2항에 있어서, 온도가 약 50℃ 내지 약 150℃의 범위에 속하는 것인 공정.
- 제2항에 있어서, 압력이 약 100 내지 900 psig의 범위에 속하는 것인 공정.
- 제2항에 있어서, 압력이 약 250 내지 700 psig의 범위에 속하는 것인 공정.
- 제1항에 있어서, 적합한 촉매의 존재하에 하이드로클로로플루오로올레핀을 기체상 불소화하는 b) 단계는 적합한 촉매의 존재하에 상기 하이드로클로로플루오로올레핀을 불화수소와 접촉시키는 것을 포함하는 것인 공정.
- 제16항에 있어서, 상기 촉매는 담지되거나 또는 담지되지 않은 크로뮴 촉매인 것인 공정.
- 제16항에 있어서, 상기 촉매는 보조촉매를 더 포함하는 것인 공정.
- 제18항에 있어서, 상기 보조촉매는 니켈, 아연, 코발트 및 망간 중에서 선택되는 것인 공정.
- 제17항에 있어서, 상기 촉매는 사용되기 전에 활성화되는 것인 공정.
- 제20항에 있어서, 상기 촉매는, 사용되기 전에, 약 150 psi를 초과하는 압력에서 활성화되는 것인 공정.
- 제1항에 있어서, 상기 하이드로클로로올레핀은 1,1,2,3-테트라클로로-1-프로펜이고, 상기 하이드로클로로플루오로올레핀은 2-클로로-3,3,3-트리플루오로-1-프로펜이며, 상기 하이드로플루오로올레핀은 2,3,3,3-테트라플루오로-1-프로펜인 공정.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94640607P | 2007-06-27 | 2007-06-27 | |
| US60/946,406 | 2007-06-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100039361A true KR20100039361A (ko) | 2010-04-15 |
| KR101550250B1 KR101550250B1 (ko) | 2015-09-04 |
Family
ID=40186030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107001917A Active KR101550250B1 (ko) | 2007-06-27 | 2008-06-26 | 하이드로플루오로올레핀의 제조 방법 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US8076521B2 (ko) |
| EP (1) | EP2170785B1 (ko) |
| JP (1) | JP5337799B2 (ko) |
| KR (1) | KR101550250B1 (ko) |
| CN (1) | CN101687731B (ko) |
| PL (1) | PL2170785T3 (ko) |
| WO (1) | WO2009003084A1 (ko) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20130136491A (ko) * | 2010-12-01 | 2013-12-12 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 1,1,3-트리클로로-1-프로펜의 합성 |
| KR20180030669A (ko) * | 2015-07-17 | 2018-03-23 | 멕시켐 플루어 소시에다드 아노니마 데 카피탈 바리아블레 | 하이드로(클로로)플루오로올레핀을 건조시키는 방법 |
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| US8058486B2 (en) * | 2004-04-29 | 2011-11-15 | Honeywell International Inc. | Integrated process to produce 2,3,3,3-tetrafluoropropene |
| US8664455B2 (en) | 2008-08-08 | 2014-03-04 | Honeywell International Inc. | Process to manufacture 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
| US8952208B2 (en) * | 2006-01-03 | 2015-02-10 | Honeywell International Inc. | Method for prolonging a catalyst's life during hydrofluorination |
| US8034251B2 (en) | 2007-01-03 | 2011-10-11 | Honeywell International Inc. | Azeotropic compositions of 2-chloro-3,3,3-trifluoropropene (HCFC-1233xf), 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb), and hydrogen fluoride (HF) |
| WO2013067350A1 (en) * | 2011-11-04 | 2013-05-10 | Selma Bektesevic | Process for producing 2,3,3,3-tetrafluoropropene |
| US8563789B2 (en) * | 2007-06-27 | 2013-10-22 | Arkema Inc. | Process for the manufacture of hydrofluoroolefins |
| CN101687731B (zh) * | 2007-06-27 | 2013-09-04 | 阿科玛股份有限公司 | 用于制造氢氟烯烃的方法 |
| US8546624B2 (en) | 2008-03-06 | 2013-10-01 | Honeywell International Inc. | Azeotrope-like composition of 2-chloro-3,3,3-trifluoropropene (HCFC-1233xf) and hydrogen fluoride (HF) |
| US7803283B2 (en) | 2008-03-31 | 2010-09-28 | Honeywell Internationl Inc. | Azeotrope-like compositions of 2-chloro-3,3,3-trifluoropropene (HCFC-1233xf) and 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
| US8071826B2 (en) | 2008-04-04 | 2011-12-06 | Honeywell International Inc. | Process for the preparation of 2,3,3,3-tetrafluoropropene (HFO-1234yf) |
| US8845921B2 (en) | 2008-04-09 | 2014-09-30 | Honeywell International Inc. | Separation of close boiling compounds by addition of a third compound |
| DK2634231T3 (da) | 2008-05-07 | 2022-09-19 | Chemours Co Fc Llc | Sammensætninger |
| US8168837B2 (en) * | 2008-05-15 | 2012-05-01 | Honeywell International Inc. | Process for separating hydrogen fluoride from organic feedstocks |
| US8916733B2 (en) | 2008-06-17 | 2014-12-23 | Honeywell International Inc. | Processes for hydrofluorination of 2-chloro-3,3,3-trifluoropropene to 2-chloro-1,1,1,2-tetrafluoropropane |
| TWI365185B (en) | 2008-07-24 | 2012-06-01 | Lilly Co Eli | Amidophenoxyindazoles useful as inhibitors of c-met |
| WO2010045104A2 (en) | 2008-10-13 | 2010-04-22 | Dow Global Technologies, Inc. | Process for the production of chlorinated and/or fluorinated propenes |
| US8008243B2 (en) * | 2008-10-31 | 2011-08-30 | Honeywell International Inc. | Azeotrope-like compositions of 1,1,2,3-tetrachloropropene and hydrogen fluoride |
| CN102405203B (zh) * | 2009-04-23 | 2015-04-08 | 大金工业株式会社 | 制备2,3,3,3-四氟丙烯的方法 |
| KR101392589B1 (ko) * | 2009-04-23 | 2014-05-21 | 다이킨 고교 가부시키가이샤 | 2-클로로-3,3,3-트리플루오로프로펜의 제조 방법 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| KR20130136491A (ko) * | 2010-12-01 | 2013-12-12 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 1,1,3-트리클로로-1-프로펜의 합성 |
| KR20180030669A (ko) * | 2015-07-17 | 2018-03-23 | 멕시켐 플루어 소시에다드 아노니마 데 카피탈 바리아블레 | 하이드로(클로로)플루오로올레핀을 건조시키는 방법 |
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| PL2170785T3 (pl) | 2018-12-31 |
| KR101550250B1 (ko) | 2015-09-04 |
| EP2170785A1 (en) | 2010-04-07 |
| EP2170785A4 (en) | 2015-04-15 |
| CN101687731A (zh) | 2010-03-31 |
| CN101687731B (zh) | 2013-09-04 |
| JP2010531895A (ja) | 2010-09-30 |
| JP5337799B2 (ja) | 2013-11-06 |
| WO2009003084A1 (en) | 2008-12-31 |
| US20120059202A1 (en) | 2012-03-08 |
| EP2170785B1 (en) | 2018-09-12 |
| US8076521B2 (en) | 2011-12-13 |
| US20100185030A1 (en) | 2010-07-22 |
| US8618338B2 (en) | 2013-12-31 |
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