JP2007517974A5 - - Google Patents
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- Publication number
- JP2007517974A5 JP2007517974A5 JP2006549684A JP2006549684A JP2007517974A5 JP 2007517974 A5 JP2007517974 A5 JP 2007517974A5 JP 2006549684 A JP2006549684 A JP 2006549684A JP 2006549684 A JP2006549684 A JP 2006549684A JP 2007517974 A5 JP2007517974 A5 JP 2007517974A5
- Authority
- JP
- Japan
- Prior art keywords
- och
- weight percent
- difluoromethoxy
- tetrafluoroethane
- ethoxy
- 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- Withdrawn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
- 239000000203 mixture Substances 0.000 claims description 37
- YKICUSOQECKQRR-UHFFFAOYSA-N 1,1,2-trifluoro-2-methoxyethane Chemical compound COC(F)C(F)F YKICUSOQECKQRR-UHFFFAOYSA-N 0.000 claims description 8
- CRGZRXUKXVTRNO-UHFFFAOYSA-N 1,1-difluoro-2-methoxyethane Chemical compound COCC(F)F CRGZRXUKXVTRNO-UHFFFAOYSA-N 0.000 claims description 8
- HBRLMDFVVMYNFH-UHFFFAOYSA-N 1-ethoxy-1,1,2,2-tetrafluoroethane Chemical compound CCOC(F)(F)C(F)F HBRLMDFVVMYNFH-UHFFFAOYSA-N 0.000 claims description 8
- RPVUQXHGCXIWHO-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1-difluoroethane Chemical compound FC(F)COC(F)F RPVUQXHGCXIWHO-UHFFFAOYSA-N 0.000 claims description 8
- 239000003507 refrigerant Substances 0.000 claims description 7
- 238000005057 refrigeration Methods 0.000 claims description 7
- ZYAMKYAPIQPWQR-UHFFFAOYSA-N 1,1,1,2,2-pentafluoro-3-methoxypropane Chemical compound COCC(F)(F)C(F)(F)F ZYAMKYAPIQPWQR-UHFFFAOYSA-N 0.000 claims description 6
- PKMXTDVNDDDCSY-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoro-3-methoxypropane Chemical compound COC(F)(F)C(F)C(F)(F)F PKMXTDVNDDDCSY-UHFFFAOYSA-N 0.000 claims description 6
- VNXYDFNVQBICRO-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-methoxypropane Chemical compound COC(C(F)(F)F)C(F)(F)F VNXYDFNVQBICRO-UHFFFAOYSA-N 0.000 claims description 6
- YUOXYWMLEGWQLB-UHFFFAOYSA-N 1,1,1-trifluoro-3-methoxypropane Chemical compound COCCC(F)(F)F YUOXYWMLEGWQLB-UHFFFAOYSA-N 0.000 claims description 6
- PYSBCYQDWOCAHY-UHFFFAOYSA-N 1,1,2-trifluoro-1-methoxy-2-(trifluoromethoxy)ethane Chemical compound COC(F)(F)C(F)OC(F)(F)F PYSBCYQDWOCAHY-UHFFFAOYSA-N 0.000 claims description 6
- DEYAWNMYIUDQER-UHFFFAOYSA-N 1-(1,1,2,2-tetrafluoroethoxy)propane Chemical compound CCCOC(F)(F)C(F)F DEYAWNMYIUDQER-UHFFFAOYSA-N 0.000 claims description 6
- KQUULKREOKHZAM-UHFFFAOYSA-N 1-(difluoromethoxy)-1,2,2-trifluoroethane Chemical compound FC(F)OC(F)C(F)F KQUULKREOKHZAM-UHFFFAOYSA-N 0.000 claims description 6
- HNQMKNFMSPECFD-UHFFFAOYSA-N 1-ethoxy-1,1,2,2,3,3,3-heptafluoropropane Chemical compound CCOC(F)(F)C(F)(F)C(F)(F)F HNQMKNFMSPECFD-UHFFFAOYSA-N 0.000 claims description 6
- OMGXRQKWXWMTFU-UHFFFAOYSA-N 2,3-difluoro-4-(trifluoromethyl)oxetane Chemical compound FC1OC(C(F)(F)F)C1F OMGXRQKWXWMTFU-UHFFFAOYSA-N 0.000 claims description 6
- RMFXYVDVYHFRRQ-UHFFFAOYSA-N 2-ethoxy-1,1,1,2,3,3,3-heptafluoropropane Chemical compound CCOC(F)(C(F)(F)F)C(F)(F)F RMFXYVDVYHFRRQ-UHFFFAOYSA-N 0.000 claims description 6
- ISSHBUUZSURRBQ-UHFFFAOYSA-N 2-ethoxy-1,1,1,2-tetrafluoroethane Chemical compound CCOC(F)C(F)(F)F ISSHBUUZSURRBQ-UHFFFAOYSA-N 0.000 claims description 6
- ZKNHDJMXIUOHLX-UHFFFAOYSA-N 2-ethoxy-1,1,1-trifluoroethane Chemical compound CCOCC(F)(F)F ZKNHDJMXIUOHLX-UHFFFAOYSA-N 0.000 claims description 6
- NKEBKUGEYSHGKA-UHFFFAOYSA-N 3-(difluoromethoxy)-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)OCC(F)(F)C(F)(F)F NKEBKUGEYSHGKA-UHFFFAOYSA-N 0.000 claims description 6
- 239000013529 heat transfer fluid Substances 0.000 claims description 6
- CUTPKDUMZWIJKT-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-(1,2,2,2-tetrafluoroethoxy)propane Chemical compound FC(F)(F)C(F)OC(F)(F)C(F)(F)C(F)(F)F CUTPKDUMZWIJKT-UHFFFAOYSA-N 0.000 claims description 4
- NOPJRYAFUXTDLX-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-methoxypropane Chemical compound COC(F)(F)C(F)(F)C(F)(F)F NOPJRYAFUXTDLX-UHFFFAOYSA-N 0.000 claims description 4
- GCDWNCOAODIANN-UHFFFAOYSA-N 1,1,1,2,2-pentafluoro-2-methoxyethane Chemical compound COC(F)(F)C(F)(F)F GCDWNCOAODIANN-UHFFFAOYSA-N 0.000 claims description 4
- PQRIAFIOMWFFPM-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoro-3-(1,1,2,2,2-pentafluoroethoxy)propane Chemical compound FC(F)(F)C(F)C(F)(F)OC(F)(F)C(F)(F)F PQRIAFIOMWFFPM-UHFFFAOYSA-N 0.000 claims description 4
- UDKWMTKIRQSDHF-UHFFFAOYSA-N 1,1,1,2-tetrafluoro-2-(trifluoromethoxy)ethane Chemical compound FC(F)(F)C(F)OC(F)(F)F UDKWMTKIRQSDHF-UHFFFAOYSA-N 0.000 claims description 4
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 4
- OHLVGBXMHDWRRX-UHFFFAOYSA-N 1,1,1-trifluoro-2-methoxyethane Chemical compound COCC(F)(F)F OHLVGBXMHDWRRX-UHFFFAOYSA-N 0.000 claims description 4
- KVRDTYTVCCKIMF-UHFFFAOYSA-N 1,1,1-trifluoro-2-methoxypropane Chemical compound COC(C)C(F)(F)F KVRDTYTVCCKIMF-UHFFFAOYSA-N 0.000 claims description 4
- CMRJNALMNDBXQC-UHFFFAOYSA-N 1,1,2,2,3,3-hexafluoro-1-methoxypropane Chemical compound COC(F)(F)C(F)(F)C(F)F CMRJNALMNDBXQC-UHFFFAOYSA-N 0.000 claims description 4
- CWIFAKBLLXGZIC-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-1-(2,2,2-trifluoroethoxy)ethane Chemical compound FC(F)C(F)(F)OCC(F)(F)F CWIFAKBLLXGZIC-UHFFFAOYSA-N 0.000 claims description 4
- YQQHEHMVPLLOKE-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-1-methoxyethane Chemical compound COC(F)(F)C(F)F YQQHEHMVPLLOKE-UHFFFAOYSA-N 0.000 claims description 4
- XLJTWSJIJSUZLQ-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-3-(trifluoromethoxy)propane Chemical compound FC(F)C(F)(F)COC(F)(F)F XLJTWSJIJSUZLQ-UHFFFAOYSA-N 0.000 claims description 4
- KHQLHXUKGLATEO-UHFFFAOYSA-N 1,1,3,3-tetrafluoro-1-(trifluoromethoxy)propane Chemical compound FC(F)CC(F)(F)OC(F)(F)F KHQLHXUKGLATEO-UHFFFAOYSA-N 0.000 claims description 4
- SFNHUVOCGCQZEG-UHFFFAOYSA-N 1,1-difluoro-2-(trifluoromethoxy)ethane Chemical compound FC(F)COC(F)(F)F SFNHUVOCGCQZEG-UHFFFAOYSA-N 0.000 claims description 4
- KJZMPIUWBKMUQY-UHFFFAOYSA-N 1-(1,1-difluoroethoxy)-1,1,2,2-tetrafluoroethane Chemical compound CC(F)(F)OC(F)(F)C(F)F KJZMPIUWBKMUQY-UHFFFAOYSA-N 0.000 claims description 4
- BFPGPHGEDKDBCN-UHFFFAOYSA-N 1-(2,2-difluoroethoxy)-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)COC(F)(F)C(F)(F)F BFPGPHGEDKDBCN-UHFFFAOYSA-N 0.000 claims description 4
- SLSZYCUCKFSOCN-UHFFFAOYSA-N 1-(difluoromethoxy)-1,1,2,2-tetrafluoroethane Chemical compound FC(F)OC(F)(F)C(F)F SLSZYCUCKFSOCN-UHFFFAOYSA-N 0.000 claims description 4
- MFNUKMQUVGMCEW-UHFFFAOYSA-N 1-(difluoromethoxy)-1,1,2-trifluoroethane Chemical compound FCC(F)(F)OC(F)F MFNUKMQUVGMCEW-UHFFFAOYSA-N 0.000 claims description 4
- ZNPNIRDITDQGKG-UHFFFAOYSA-N 1-(trifluoromethoxy)propane Chemical compound CCCOC(F)(F)F ZNPNIRDITDQGKG-UHFFFAOYSA-N 0.000 claims description 4
- UUXWSQGUZUAECB-UHFFFAOYSA-N 1-ethoxy-1,2,2-trifluoroethane Chemical compound CCOC(F)C(F)F UUXWSQGUZUAECB-UHFFFAOYSA-N 0.000 claims description 4
- AIPBKZUVKDTCOC-UHFFFAOYSA-N 2-(1,1,2,2-tetrafluoroethoxy)propane Chemical compound CC(C)OC(F)(F)C(F)F AIPBKZUVKDTCOC-UHFFFAOYSA-N 0.000 claims description 4
- UNIYHTKWMKXESF-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)OC(C(F)(F)F)C(F)(F)F UNIYHTKWMKXESF-UHFFFAOYSA-N 0.000 claims description 4
- ZASBKNPRLPFSCA-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1,1-trifluoroethane Chemical compound FC(F)OCC(F)(F)F ZASBKNPRLPFSCA-UHFFFAOYSA-N 0.000 claims description 4
- UQGJBCKUPBIEDQ-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1,1-trifluoropropane Chemical compound FC(F)(F)C(C)OC(F)F UQGJBCKUPBIEDQ-UHFFFAOYSA-N 0.000 claims description 4
- JYFWUMLHFWQKFF-UHFFFAOYSA-N 2-ethoxy-1,1,1,3,3,3-hexafluoropropane Chemical compound CCOC(C(F)(F)F)C(F)(F)F JYFWUMLHFWQKFF-UHFFFAOYSA-N 0.000 claims description 4
- LTRUYHVIVWXQMY-UHFFFAOYSA-N 3-(difluoromethoxy)-1,1,1,2,2,3-hexafluoropropane Chemical compound FC(F)OC(F)C(F)(F)C(F)(F)F LTRUYHVIVWXQMY-UHFFFAOYSA-N 0.000 claims description 4
- PCTQNZRJAGLDPD-UHFFFAOYSA-N 3-(difluoromethoxy)-1,1,2,2-tetrafluoropropane Chemical compound FC(F)OCC(F)(F)C(F)F PCTQNZRJAGLDPD-UHFFFAOYSA-N 0.000 claims description 4
- RWZITMOKDXSASG-UHFFFAOYSA-N 3-ethoxy-1,1,2,2-tetrafluoropropane Chemical compound CCOCC(F)(F)C(F)F RWZITMOKDXSASG-UHFFFAOYSA-N 0.000 claims description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 4
- DPYMFVXJLLWWEU-UHFFFAOYSA-N desflurane Chemical compound FC(F)OC(F)C(F)(F)F DPYMFVXJLLWWEU-UHFFFAOYSA-N 0.000 claims description 4
- DFEYYRMXOJXZRJ-UHFFFAOYSA-N sevoflurane Chemical compound FCOC(C(F)(F)F)C(F)(F)F DFEYYRMXOJXZRJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims description 4
- XDFJJLSCPQLSBD-UHFFFAOYSA-N 1,1,1,2-tetrafluoro-2-(fluoromethoxy)ethane Chemical compound FCOC(F)C(F)(F)F XDFJJLSCPQLSBD-UHFFFAOYSA-N 0.000 claims description 2
- AJJGOHRUWOHVIZ-UHFFFAOYSA-N 1-methoxy-2-(trifluoromethoxy)ethane Chemical compound COCCOC(F)(F)F AJJGOHRUWOHVIZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 2
- VNKYTQGIUYNRMY-UHFFFAOYSA-N methoxypropane Chemical compound CCCOC VNKYTQGIUYNRMY-UHFFFAOYSA-N 0.000 claims description 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 125000002723 alicyclic group Chemical group 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000007850 fluorescent dye Substances 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- 238000004378 air conditioning Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 2
- VWCLQNINSPFHFV-UHFFFAOYSA-N 10-oxapentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2(11),4,6,8,12,15,17,19,21-decaene Chemical compound C1=CC=C2C3=CC=C4OC5=CC=CC=C5CC4=C3C=CC2=C1 VWCLQNINSPFHFV-UHFFFAOYSA-N 0.000 description 2
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 2
- PQJUJGAVDBINPI-UHFFFAOYSA-N 9H-thioxanthene Chemical compound C1=CC=C2CC3=CC=CC=C3SC2=C1 PQJUJGAVDBINPI-UHFFFAOYSA-N 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000000743 hydrocarbylene group Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008378 aryl ethers Chemical class 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- -1 carbon atoms Aryl ethers Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LYGJENNIWJXYER-BJUDXGSMSA-N nitromethane Chemical group [11CH3][N+]([O-])=O LYGJENNIWJXYER-BJUDXGSMSA-N 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53681904P | 2004-01-14 | 2004-01-14 | |
US11/014,334 US7220363B2 (en) | 2004-01-14 | 2004-12-16 | 1,1,1,2,2,3,3,4,4-Nonafluoro-4-methoxybutane refrigerant compositions comprising a fluoroether and uses thereof |
PCT/US2005/001508 WO2005068579A1 (en) | 2004-01-14 | 2005-01-12 | 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane refrigerant compositions comprising a fluoroether and uses thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2007517974A JP2007517974A (ja) | 2007-07-05 |
JP2007517974A5 true JP2007517974A5 (ru) | 2008-02-28 |
Family
ID=34797982
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006549684A Withdrawn JP2007517974A (ja) | 2004-01-14 | 2005-01-12 | フルオロエーテルを含む1,1,1,2,2,3,3,4,4−ノナフルオロ−4−メトキシブタン冷媒組成物およびその使用 |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1704199A1 (ru) |
JP (1) | JP2007517974A (ru) |
KR (1) | KR20060122924A (ru) |
AR (1) | AR049612A1 (ru) |
AU (1) | AU2005205600A1 (ru) |
BR (1) | BRPI0506540A (ru) |
CA (1) | CA2552832A1 (ru) |
NO (1) | NO20063643L (ru) |
RU (1) | RU2006129311A (ru) |
WO (1) | WO2005068579A1 (ru) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100972141B1 (ko) * | 2008-01-15 | 2010-07-23 | 주식회사 웰라이트 | 가로등 |
JP2010185048A (ja) * | 2009-02-13 | 2010-08-26 | Daikin Ind Ltd | 熱伝達装置および熱伝達方法、ならびにそれに用いる熱伝達流体 |
JP5987497B2 (ja) * | 2012-06-27 | 2016-09-07 | セントラル硝子株式会社 | フッ素化エーテルを含む熱伝達作動媒体 |
FR3057272B1 (fr) | 2016-10-10 | 2020-05-08 | Arkema France | Compositions azeotropiques a base de tetrafluoropropene |
FR3057271B1 (fr) | 2016-10-10 | 2020-01-17 | Arkema France | Utilisation de compositions a base de tetrafluoropropene |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5578137A (en) * | 1993-08-31 | 1996-11-26 | E. I. Du Pont De Nemours And Company | Azeotropic or azeotrope-like compositions including 1,1,1,2,3,4,4,5,5,5-decafluoropentane |
-
2005
- 2005-01-12 CA CA002552832A patent/CA2552832A1/en not_active Abandoned
- 2005-01-12 KR KR1020067016229A patent/KR20060122924A/ko not_active Application Discontinuation
- 2005-01-12 BR BRPI0506540-2A patent/BRPI0506540A/pt not_active Application Discontinuation
- 2005-01-12 RU RU2006129311/04A patent/RU2006129311A/ru not_active Application Discontinuation
- 2005-01-12 WO PCT/US2005/001508 patent/WO2005068579A1/en active Application Filing
- 2005-01-12 AU AU2005205600A patent/AU2005205600A1/en not_active Abandoned
- 2005-01-12 JP JP2006549684A patent/JP2007517974A/ja not_active Withdrawn
- 2005-01-12 EP EP05705842A patent/EP1704199A1/en not_active Withdrawn
- 2005-01-14 AR ARP050100136A patent/AR049612A1/es unknown
-
2006
- 2006-08-11 NO NO20063643A patent/NO20063643L/no not_active Application Discontinuation
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