JP2007517973A5 - - Google Patents
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- Publication number
- JP2007517973A5 JP2007517973A5 JP2006549683A JP2006549683A JP2007517973A5 JP 2007517973 A5 JP2007517973 A5 JP 2007517973A5 JP 2006549683 A JP2006549683 A JP 2006549683A JP 2006549683 A JP2006549683 A JP 2006549683A JP 2007517973 A5 JP2007517973 A5 JP 2007517973A5
- Authority
- JP
- Japan
- Prior art keywords
- weight percent
- difluorobutane
- och
- difluoropentane
- trifluoromethyl
- 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- Withdrawn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 36
- XRKOOHTZZDPJNE-UHFFFAOYSA-N 1,1,1-trifluorohexane Chemical compound CCCCCC(F)(F)F XRKOOHTZZDPJNE-UHFFFAOYSA-N 0.000 claims description 8
- AKQMZZOTFNLAQJ-UHFFFAOYSA-N 1,1,2,2-tetrafluorocyclobutane Chemical compound FC1(F)CCC1(F)F AKQMZZOTFNLAQJ-UHFFFAOYSA-N 0.000 claims description 8
- GQSMEOJGQJMOHA-UHFFFAOYSA-N 1,1,3-trifluoropropane Chemical compound FCCC(F)F GQSMEOJGQJMOHA-UHFFFAOYSA-N 0.000 claims description 8
- JFGBHUQZXJIATI-UHFFFAOYSA-N 1,3-difluorobutane Chemical compound CC(F)CCF JFGBHUQZXJIATI-UHFFFAOYSA-N 0.000 claims description 8
- QSWGSLWFQDIXSH-UHFFFAOYSA-N 2,2-difluoropentane Chemical compound CCCC(C)(F)F QSWGSLWFQDIXSH-UHFFFAOYSA-N 0.000 claims description 8
- 239000003507 refrigerant Substances 0.000 claims description 7
- 238000005057 refrigeration Methods 0.000 claims description 7
- 239000013529 heat transfer fluid Substances 0.000 claims description 6
- XJSRKJAHJGCPGC-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F XJSRKJAHJGCPGC-UHFFFAOYSA-N 0.000 claims description 4
- WXFBZGUXZMEPIR-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5-undecafluoropentane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F WXFBZGUXZMEPIR-UHFFFAOYSA-N 0.000 claims description 4
- CFDFPRUMKAXRIO-UHFFFAOYSA-N 1,1,1,2,2,3,3,5,5,5-decafluoropentane Chemical compound FC(F)(F)CC(F)(F)C(F)(F)C(F)(F)F CFDFPRUMKAXRIO-UHFFFAOYSA-N 0.000 claims description 4
- RIQRGMUSBYGDBL-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,5-decafluoropentane Chemical compound FC(F)(F)C(F)C(F)C(F)(F)C(F)(F)F RIQRGMUSBYGDBL-UHFFFAOYSA-N 0.000 claims description 4
- KSUHRWWSNHJRMY-UHFFFAOYSA-N 1,1,1,2,2,4-hexafluorobutane Chemical compound FCCC(F)(F)C(F)(F)F KSUHRWWSNHJRMY-UHFFFAOYSA-N 0.000 claims description 4
- HOPIMNPCVOTFDN-UHFFFAOYSA-N 1,1,1,2,2,5,5,5-octafluoro-4-(trifluoromethyl)pentane Chemical compound FC(F)(F)C(C(F)(F)F)CC(F)(F)C(F)(F)F HOPIMNPCVOTFDN-UHFFFAOYSA-N 0.000 claims description 4
- OYHDMNJHLNLQAR-UHFFFAOYSA-N 1,1,1,2,3,3,4,4-octafluoro-2-(trifluoromethyl)butane Chemical compound FC(F)C(F)(F)C(F)(C(F)(F)F)C(F)(F)F OYHDMNJHLNLQAR-UHFFFAOYSA-N 0.000 claims description 4
- WZLFPVPRZGTCKP-UHFFFAOYSA-N 1,1,1,3,3-pentafluorobutane Chemical compound CC(F)(F)CC(F)(F)F WZLFPVPRZGTCKP-UHFFFAOYSA-N 0.000 claims description 4
- ZLLFAXODNBYNCI-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluoro-2-(trifluoromethyl)butane Chemical compound FC(F)(F)CC(C(F)(F)F)C(F)(F)F ZLLFAXODNBYNCI-UHFFFAOYSA-N 0.000 claims description 4
- CONTVCYXDSFGMN-UHFFFAOYSA-N 1,1,1-trifluoro-3-methylbutane Chemical compound CC(C)CC(F)(F)F CONTVCYXDSFGMN-UHFFFAOYSA-N 0.000 claims description 4
- GENRYAJRHIWOJI-UHFFFAOYSA-N 1,1,1-trifluoropentane Chemical compound CCCCC(F)(F)F GENRYAJRHIWOJI-UHFFFAOYSA-N 0.000 claims description 4
- LKLFXAVIFCLZQS-UHFFFAOYSA-N 1,1,2,2,3,3,4,4-octafluorobutane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)F LKLFXAVIFCLZQS-UHFFFAOYSA-N 0.000 claims description 4
- AWTOFSDLNREIFS-UHFFFAOYSA-N 1,1,2,2,3-pentafluoropropane Chemical compound FCC(F)(F)C(F)F AWTOFSDLNREIFS-UHFFFAOYSA-N 0.000 claims description 4
- CPLSOYONVLSMGL-UHFFFAOYSA-N 1,1-difluorobutane Chemical compound CCCC(F)F CPLSOYONVLSMGL-UHFFFAOYSA-N 0.000 claims description 4
- PSSHQAXMSKKIBE-UHFFFAOYSA-N 1,1-difluoropentane Chemical compound CCCCC(F)F PSSHQAXMSKKIBE-UHFFFAOYSA-N 0.000 claims description 4
- MBPIQXLEEJZOMY-UHFFFAOYSA-N 1,2-difluoro-2-methylpropane Chemical compound CC(C)(F)CF MBPIQXLEEJZOMY-UHFFFAOYSA-N 0.000 claims description 4
- VHJOGNLCVJAXFE-UHFFFAOYSA-N 1,2-difluorobutane Chemical compound CCC(F)CF VHJOGNLCVJAXFE-UHFFFAOYSA-N 0.000 claims description 4
- JKYLNUHIUDXCMN-UHFFFAOYSA-N 1,2-difluoropentane Chemical compound CCCC(F)CF JKYLNUHIUDXCMN-UHFFFAOYSA-N 0.000 claims description 4
- OLURRGJWZJYRIM-UHFFFAOYSA-N 1,3-difluoro-2-methylpropane Chemical compound FCC(C)CF OLURRGJWZJYRIM-UHFFFAOYSA-N 0.000 claims description 4
- OOLOYCGJRJFTPM-UHFFFAOYSA-N 1,3-difluoropropane Chemical compound FCCCF OOLOYCGJRJFTPM-UHFFFAOYSA-N 0.000 claims description 4
- CXHPKSYTQFAXIN-UHFFFAOYSA-N 1,4-difluorobutane Chemical compound FCCCCF CXHPKSYTQFAXIN-UHFFFAOYSA-N 0.000 claims description 4
- GRELHMBELDGGLT-UHFFFAOYSA-N 2,3-difluorobutane Chemical compound CC(F)C(C)F GRELHMBELDGGLT-UHFFFAOYSA-N 0.000 claims description 4
- JHNVZNKTGCNIRI-UHFFFAOYSA-N 2-(difluoromethyl)-1,1,1,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)(C(F)F)C(F)(F)F JHNVZNKTGCNIRI-UHFFFAOYSA-N 0.000 claims description 4
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims description 4
- 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
- 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 | |
| US11/014,438 US20050151112A1 (en) | 2004-01-14 | 2004-12-16 | 1,1,1,2,2,3,3,4,4-Nonafluoro-4-methoxybutane refrigerant compositions comprising hydrofluorocarbon, and uses thereof |
| PCT/US2005/001507 WO2005067557A2 (en) | 2004-01-14 | 2005-01-12 | 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane refrigerant compositions comprising hydrofluorocarbon, and uses thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007517973A JP2007517973A (ja) | 2007-07-05 |
| JP2007517973A5 true JP2007517973A5 (https=) | 2008-02-28 |
Family
ID=34797985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006549683A Withdrawn JP2007517973A (ja) | 2004-01-14 | 2005-01-12 | ヒドロフルオロカーボンを含む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) | EP1723211A2 (https=) |
| JP (1) | JP2007517973A (https=) |
| KR (1) | KR20060122923A (https=) |
| AR (1) | AR048146A1 (https=) |
| AU (1) | AU2005204954A1 (https=) |
| BR (1) | BRPI0506517A (https=) |
| CA (1) | CA2552625A1 (https=) |
| NO (1) | NO20063645L (https=) |
| RU (1) | RU2006129275A (https=) |
| WO (1) | WO2005067557A2 (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5417871A (en) * | 1994-03-11 | 1995-05-23 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
| US5580906A (en) * | 1995-05-19 | 1996-12-03 | E. I. Du Pont De Nemours And Company | Ternary azeotropic compositions |
-
2005
- 2005-01-12 KR KR1020067016228A patent/KR20060122923A/ko not_active Withdrawn
- 2005-01-12 WO PCT/US2005/001507 patent/WO2005067557A2/en not_active Ceased
- 2005-01-12 JP JP2006549683A patent/JP2007517973A/ja not_active Withdrawn
- 2005-01-12 BR BRPI0506517-8A patent/BRPI0506517A/pt not_active Application Discontinuation
- 2005-01-12 AU AU2005204954A patent/AU2005204954A1/en not_active Abandoned
- 2005-01-12 CA CA002552625A patent/CA2552625A1/en not_active Abandoned
- 2005-01-12 RU RU2006129275/04A patent/RU2006129275A/ru not_active Application Discontinuation
- 2005-01-12 EP EP05711558A patent/EP1723211A2/en not_active Withdrawn
- 2005-01-14 AR ARP050100133A patent/AR048146A1/es unknown
-
2006
- 2006-08-11 NO NO20063645A patent/NO20063645L/no not_active Application Discontinuation
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