JP2007526384A5 - - Google Patents
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- JP2007526384A5 JP2007526384A5 JP2007501773A JP2007501773A JP2007526384A5 JP 2007526384 A5 JP2007526384 A5 JP 2007526384A5 JP 2007501773 A JP2007501773 A JP 2007501773A JP 2007501773 A JP2007501773 A JP 2007501773A JP 2007526384 A5 JP2007526384 A5 JP 2007526384A5
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- JP
- Japan
- Prior art keywords
- cbrf
- ocf
- cbrfc
- cbrfcf
- cbr
- 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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- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims description 49
- 239000000203 mixture Substances 0.000 claims description 43
- GFGAOQYLPGMLRJ-UHFFFAOYSA-N CBrC Chemical compound CBrC GFGAOQYLPGMLRJ-UHFFFAOYSA-N 0.000 claims description 21
- 125000001931 aliphatic group Chemical group 0.000 claims description 13
- 239000013529 heat transfer fluid Substances 0.000 claims description 10
- 239000003507 refrigerant Substances 0.000 claims description 10
- 238000005057 refrigeration Methods 0.000 claims description 9
- MQVIUJVDDOWJRO-UHFFFAOYSA-N 1,1,1,2,2,5,5,5-octafluoro-4-(trifluoromethyl)pentan-3-one Chemical compound FC(F)(F)C(C(F)(F)F)C(=O)C(F)(F)C(F)(F)F MQVIUJVDDOWJRO-UHFFFAOYSA-N 0.000 claims description 7
- SIVXJSMXRSOFRR-UHFFFAOYSA-N 1,1,1,2,4,4,5,5,6,6,6-undecafluoro-2-(trifluoromethyl)hexan-3-one Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F SIVXJSMXRSOFRR-UHFFFAOYSA-N 0.000 claims description 7
- FUXUGMZKQNYLDJ-UHFFFAOYSA-N 1,1,1,2,4,4,5,5-octafluoro-2-(trifluoromethyl)pentan-3-one Chemical compound FC(F)C(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F FUXUGMZKQNYLDJ-UHFFFAOYSA-N 0.000 claims description 7
- UDVYMKMTPUSSLP-UHFFFAOYSA-N 1,1,1,2,4,4,5,5-octafluoro-5-(trifluoromethoxy)-2-(trifluoromethyl)pentan-3-one Chemical compound FC(F)(F)OC(F)(F)C(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F UDVYMKMTPUSSLP-UHFFFAOYSA-N 0.000 claims description 7
- GRVMOMUDALILLH-UHFFFAOYSA-N 1,1,1,2,4,5,5,5-octafluoro-2,4-bis(trifluoromethyl)pentan-3-one Chemical compound FC(F)(F)C(F)(C(F)(F)F)C(=O)C(F)(C(F)(F)F)C(F)(F)F GRVMOMUDALILLH-UHFFFAOYSA-N 0.000 claims description 7
- ABQIAHFCJGVSDJ-UHFFFAOYSA-N 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one Chemical compound FC(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F ABQIAHFCJGVSDJ-UHFFFAOYSA-N 0.000 claims description 7
- AGIDPKBYYVHLOG-UHFFFAOYSA-N 2-chloro-1,1,1,4,4,5,5,5-octafluoro-2-(trifluoromethyl)pentan-3-one Chemical compound FC(F)(F)C(F)(F)C(=O)C(Cl)(C(F)(F)F)C(F)(F)F AGIDPKBYYVHLOG-UHFFFAOYSA-N 0.000 claims description 7
- RMLFHPWPTXWZNJ-UHFFFAOYSA-N novec 1230 Chemical compound FC(F)(F)C(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F RMLFHPWPTXWZNJ-UHFFFAOYSA-N 0.000 claims description 7
- 238000004378 air conditioning Methods 0.000 claims description 5
- 125000002723 alicyclic group Chemical group 0.000 claims description 5
- 125000005283 haloketone group Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- QLOAVXSYZAJECW-UHFFFAOYSA-N methane;molecular fluorine Chemical group C.FF QLOAVXSYZAJECW-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 125000003118 aryl group Chemical group 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
- 239000002904 solvent Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 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
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229920001774 Perfluoroether Polymers 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
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 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
- 125000000743 hydrocarbylene group Chemical group 0.000 description 2
- 150000002431 hydrogen 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
- 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
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000008378 aryl ethers Chemical class 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 125000004428 fluoroalkoxy group Chemical group 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- -1 hydrocarbon radicals Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 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 |
|---|---|---|---|
| US54997804P | 2004-03-04 | 2004-03-04 | |
| US11/014,006 US7501074B2 (en) | 2004-03-04 | 2004-12-16 | Haloketone refrigerant compositions and uses thereof |
| PCT/US2005/001511 WO2005094395A2 (en) | 2004-03-04 | 2005-01-12 | Haloketone refrigerant compositions and uses thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007526384A JP2007526384A (ja) | 2007-09-13 |
| JP2007526384A5 true JP2007526384A5 (https=) | 2008-02-28 |
Family
ID=35064349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007501773A Withdrawn JP2007526384A (ja) | 2004-03-04 | 2005-01-12 | ハロケトン冷媒組成物およびその使用 |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1720953A2 (https=) |
| JP (1) | JP2007526384A (https=) |
| KR (1) | KR20060128041A (https=) |
| AR (1) | AR048079A1 (https=) |
| AU (1) | AU2005227844A1 (https=) |
| BR (1) | BRPI0508143A (https=) |
| CA (1) | CA2557874A1 (https=) |
| NO (1) | NO20064479L (https=) |
| RU (1) | RU2006134980A (https=) |
| SG (1) | SG135205A1 (https=) |
| WO (1) | WO2005094395A2 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008027594A2 (en) | 2006-09-01 | 2008-03-06 | E. I. Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
| CN104017544B (zh) | 2006-09-01 | 2017-04-12 | 纳幕尔杜邦公司 | 氟烯烃用的环氧化物和氟化环氧化物稳定剂 |
| CN101517032B (zh) | 2006-09-01 | 2013-04-24 | 纳幕尔杜邦公司 | 氟烯烃用的抗坏血酸、对苯二甲酸酯或硝基甲烷稳定剂 |
| WO2008042066A1 (en) | 2006-09-01 | 2008-04-10 | E.I. Du Pont De Nemours And Company | Amine stabilizers for fluoroolefins |
| EP2057246A1 (en) | 2006-09-01 | 2009-05-13 | E.I. Du Pont De Nemours And Company | Thiol and thioether stabilizers for fluoroolefins |
| WO2008027514A1 (en) | 2006-09-01 | 2008-03-06 | E. I. Du Pont De Nemours And Company | Terpene, terpenoid, and fullerene stabilizers for fluoroolefins |
| ES2705488T3 (es) | 2006-09-01 | 2019-03-25 | Chemours Co Fc Llc | Estabilizadores que contienen fósforo para fluoroolefinas |
| CN105505323A (zh) * | 2008-03-07 | 2016-04-20 | 阿科玛股份有限公司 | 具有改进的油返回的卤代烯热传输组合物 |
| EP2250144A4 (en) | 2008-03-07 | 2014-06-04 | Arkema Inc | FORMULATED AND STABLE SYSTEMS CONTAINING CHLORO-3,3,3-TRIFLUOROPROPENE |
| FR2930019B1 (fr) * | 2008-04-09 | 2012-12-07 | Airbus France | Procede de refroidissement d'un element confine au moyen d'un fluide caloporteur |
| DE102017203043A1 (de) * | 2017-02-24 | 2018-08-30 | Siemens Aktiengesellschaft | Wärmepumpenanordnung und Verfahren zum Betrieb einer Wärmepumpenanordnung |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000024814A1 (en) * | 1998-10-26 | 2000-05-04 | 3M Innovative Properties Company | Process for preparation of polymeric foam using fluorinated ketones as blowing agents |
| ES2230125T5 (es) * | 1999-07-20 | 2016-10-04 | 3M Innovative Properties Company | Uso de cetonas fluoradas en composiciones extintoras de incendios |
| US6423673B1 (en) * | 2001-09-07 | 2002-07-23 | 3M Innovation Properties Company | Azeotrope-like compositions and their use |
-
2005
- 2005-01-12 WO PCT/US2005/001511 patent/WO2005094395A2/en not_active Ceased
- 2005-01-12 RU RU2006134980/04A patent/RU2006134980A/ru unknown
- 2005-01-12 JP JP2007501773A patent/JP2007526384A/ja not_active Withdrawn
- 2005-01-12 KR KR1020067020556A patent/KR20060128041A/ko not_active Withdrawn
- 2005-01-12 BR BRPI0508143-2A patent/BRPI0508143A/pt not_active Application Discontinuation
- 2005-01-12 SG SG200706291-2A patent/SG135205A1/en unknown
- 2005-01-12 EP EP05722453A patent/EP1720953A2/en not_active Withdrawn
- 2005-01-12 CA CA002557874A patent/CA2557874A1/en not_active Abandoned
- 2005-01-12 AU AU2005227844A patent/AU2005227844A1/en not_active Abandoned
- 2005-03-04 AR ARP050100849A patent/AR048079A1/es unknown
-
2006
- 2006-10-03 NO NO20064479A patent/NO20064479L/no not_active Application Discontinuation
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