RU2006129311A - Композиции хладагента на основе 1, 1, 1, 2, 2, 3, 3, 4, 4-нонафтор-4-метоксибутана, включающие простой фторсодержащий эфир, и их применение - Google Patents
Композиции хладагента на основе 1, 1, 1, 2, 2, 3, 3, 4, 4-нонафтор-4-метоксибутана, включающие простой фторсодержащий эфир, и их применение Download PDFInfo
- Publication number
- RU2006129311A RU2006129311A RU2006129311/04A RU2006129311A RU2006129311A RU 2006129311 A RU2006129311 A RU 2006129311A RU 2006129311/04 A RU2006129311/04 A RU 2006129311/04A RU 2006129311 A RU2006129311 A RU 2006129311A RU 2006129311 A RU2006129311 A RU 2006129311A
- Authority
- RU
- Russia
- Prior art keywords
- och
- weight
- difluoromethoxy
- composition
- tetrafluoroethane
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 31
- 239000003507 refrigerant Substances 0.000 title claims 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 title 1
- 229910052731 fluorine Inorganic materials 0.000 title 1
- 239000011737 fluorine Substances 0.000 title 1
- -1 phenanthracenes Chemical class 0.000 claims 17
- 125000004432 carbon atom Chemical group C* 0.000 claims 13
- 229930195733 hydrocarbon Natural products 0.000 claims 10
- 239000004215 Carbon black (E152) Substances 0.000 claims 9
- 238000000034 method Methods 0.000 claims 9
- 125000001931 aliphatic group Chemical group 0.000 claims 7
- 238000001816 cooling Methods 0.000 claims 6
- 238000004378 air conditioning Methods 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 5
- 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 4
- YUOXYWMLEGWQLB-UHFFFAOYSA-N 1,1,1-trifluoro-3-methoxypropane Chemical compound COCCC(F)(F)F YUOXYWMLEGWQLB-UHFFFAOYSA-N 0.000 claims 4
- 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 4
- YKICUSOQECKQRR-UHFFFAOYSA-N 1,1,2-trifluoro-2-methoxyethane Chemical compound COC(F)C(F)F YKICUSOQECKQRR-UHFFFAOYSA-N 0.000 claims 4
- CRGZRXUKXVTRNO-UHFFFAOYSA-N 1,1-difluoro-2-methoxyethane Chemical compound COCC(F)F CRGZRXUKXVTRNO-UHFFFAOYSA-N 0.000 claims 4
- KQUULKREOKHZAM-UHFFFAOYSA-N 1-(difluoromethoxy)-1,2,2-trifluoroethane Chemical compound FC(F)OC(F)C(F)F KQUULKREOKHZAM-UHFFFAOYSA-N 0.000 claims 4
- HBRLMDFVVMYNFH-UHFFFAOYSA-N 1-ethoxy-1,1,2,2-tetrafluoroethane Chemical compound CCOC(F)(F)C(F)F HBRLMDFVVMYNFH-UHFFFAOYSA-N 0.000 claims 4
- OMGXRQKWXWMTFU-UHFFFAOYSA-N 2,3-difluoro-4-(trifluoromethyl)oxetane Chemical compound FC1OC(C(F)(F)F)C1F OMGXRQKWXWMTFU-UHFFFAOYSA-N 0.000 claims 4
- RPVUQXHGCXIWHO-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1-difluoroethane Chemical compound FC(F)COC(F)F RPVUQXHGCXIWHO-UHFFFAOYSA-N 0.000 claims 4
- ISSHBUUZSURRBQ-UHFFFAOYSA-N 2-ethoxy-1,1,1,2-tetrafluoroethane Chemical compound CCOC(F)C(F)(F)F ISSHBUUZSURRBQ-UHFFFAOYSA-N 0.000 claims 4
- 239000007850 fluorescent dye Substances 0.000 claims 4
- 150000003254 radicals Chemical class 0.000 claims 4
- 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 3
- 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 3
- 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 3
- DEYAWNMYIUDQER-UHFFFAOYSA-N 1-(1,1,2,2-tetrafluoroethoxy)propane Chemical compound CCCOC(F)(F)C(F)F DEYAWNMYIUDQER-UHFFFAOYSA-N 0.000 claims 3
- 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 3
- 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 3
- ZKNHDJMXIUOHLX-UHFFFAOYSA-N 2-ethoxy-1,1,1-trifluoroethane Chemical compound CCOCC(F)(F)F ZKNHDJMXIUOHLX-UHFFFAOYSA-N 0.000 claims 3
- 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 3
- 150000001408 amides Chemical class 0.000 claims 3
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 claims 3
- 230000006835 compression Effects 0.000 claims 3
- 238000007906 compression Methods 0.000 claims 3
- 239000002826 coolant Substances 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 3
- 229940052303 ethers for general anesthesia Drugs 0.000 claims 3
- 238000001704 evaporation Methods 0.000 claims 3
- 150000002576 ketones Chemical class 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- 150000002825 nitriles Chemical class 0.000 claims 3
- 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 2
- 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 2
- 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 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims 2
- OHLVGBXMHDWRRX-UHFFFAOYSA-N 1,1,1-trifluoro-2-methoxyethane Chemical compound COCC(F)(F)F OHLVGBXMHDWRRX-UHFFFAOYSA-N 0.000 claims 2
- KVRDTYTVCCKIMF-UHFFFAOYSA-N 1,1,1-trifluoro-2-methoxypropane Chemical compound COC(C)C(F)(F)F KVRDTYTVCCKIMF-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- YQQHEHMVPLLOKE-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-1-methoxyethane Chemical compound COC(F)(F)C(F)F YQQHEHMVPLLOKE-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- SFNHUVOCGCQZEG-UHFFFAOYSA-N 1,1-difluoro-2-(trifluoromethoxy)ethane Chemical compound FC(F)COC(F)(F)F SFNHUVOCGCQZEG-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- 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 2
- MFNUKMQUVGMCEW-UHFFFAOYSA-N 1-(difluoromethoxy)-1,1,2-trifluoroethane Chemical compound FCC(F)(F)OC(F)F MFNUKMQUVGMCEW-UHFFFAOYSA-N 0.000 claims 2
- ZNPNIRDITDQGKG-UHFFFAOYSA-N 1-(trifluoromethoxy)propane Chemical compound CCCOC(F)(F)F ZNPNIRDITDQGKG-UHFFFAOYSA-N 0.000 claims 2
- UUXWSQGUZUAECB-UHFFFAOYSA-N 1-ethoxy-1,2,2-trifluoroethane Chemical compound CCOC(F)C(F)F UUXWSQGUZUAECB-UHFFFAOYSA-N 0.000 claims 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 class C1=CC=C2C3=CC=C4OC5=CC=CC=C5CC4=C3C=CC2=C1 VWCLQNINSPFHFV-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- ZASBKNPRLPFSCA-UHFFFAOYSA-N 2-(difluoromethoxy)-1,1,1-trifluoroethane Chemical compound FC(F)OCC(F)(F)F ZASBKNPRLPFSCA-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- OALHHIHQOFIMEF-UHFFFAOYSA-N 3',6'-dihydroxy-2',4',5',7'-tetraiodo-3h-spiro[2-benzofuran-1,9'-xanthene]-3-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 OALHHIHQOFIMEF-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- RWZITMOKDXSASG-UHFFFAOYSA-N 3-ethoxy-1,1,2,2-tetrafluoropropane Chemical compound CCOCC(F)(F)C(F)F RWZITMOKDXSASG-UHFFFAOYSA-N 0.000 claims 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims 2
- 125000002723 alicyclic group Chemical group 0.000 claims 2
- 150000001454 anthracenes Chemical class 0.000 claims 2
- 150000008378 aryl ethers Chemical class 0.000 claims 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims 2
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 235000001671 coumarin Nutrition 0.000 claims 2
- 125000000332 coumarinyl group Chemical class O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- DPYMFVXJLLWWEU-UHFFFAOYSA-N desflurane Chemical compound FC(F)OC(F)C(F)(F)F DPYMFVXJLLWWEU-UHFFFAOYSA-N 0.000 claims 2
- 239000000975 dye Substances 0.000 claims 2
- 150000002170 ethers Chemical class 0.000 claims 2
- 150000002334 glycols Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 150000002596 lactones Chemical class 0.000 claims 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims 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 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- DFEYYRMXOJXZRJ-UHFFFAOYSA-N sevoflurane Chemical compound FCOC(C(F)(F)F)C(F)(F)F DFEYYRMXOJXZRJ-UHFFFAOYSA-N 0.000 claims 2
- 150000005075 thioxanthenes Chemical class 0.000 claims 2
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 2
- 150000003732 xanthenes Chemical class 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 150000007860 aryl ester derivatives Chemical class 0.000 claims 1
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000003750 conditioning effect Effects 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 230000008020 evaporation Effects 0.000 claims 1
- 239000012760 heat stabilizer Substances 0.000 claims 1
- 239000013529 heat transfer fluid Substances 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 230000000873 masking effect Effects 0.000 claims 1
- LYGJENNIWJXYER-BJUDXGSMSA-N nitromethane Chemical group [11CH3][N+]([O-])=O LYGJENNIWJXYER-BJUDXGSMSA-N 0.000 claims 1
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
- 239000003017 thermal stabilizer Substances 0.000 claims 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 1
- 230000008016 vaporization Effects 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/11—Ethers
- C09K2205/112—Halogenated ethers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/22—All components of a mixture being fluoro compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/24—Only one single fluoro component present
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53681904P | 2004-01-14 | 2004-01-14 | |
| US60/536,819 | 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 |
| US11/014,334 | 2004-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2006129311A true RU2006129311A (ru) | 2008-02-20 |
Family
ID=34797982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006129311/04A RU2006129311A (ru) | 2004-01-14 | 2005-01-12 | Композиции хладагента на основе 1, 1, 1, 2, 2, 3, 3, 4, 4-нонафтор-4-метоксибутана, включающие простой фторсодержащий эфир, и их применение |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1704199A1 (https=) |
| JP (1) | JP2007517974A (https=) |
| KR (1) | KR20060122924A (https=) |
| AR (1) | AR049612A1 (https=) |
| AU (1) | AU2005205600A1 (https=) |
| BR (1) | BRPI0506540A (https=) |
| CA (1) | CA2552832A1 (https=) |
| NO (1) | NO20063643L (https=) |
| RU (1) | RU2006129311A (https=) |
| WO (1) | WO2005068579A1 (https=) |
Families Citing this family (6)
| 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 |
| CA3153966A1 (en) * | 2019-10-28 | 2021-05-06 | The Chemours Company Fc, Llc | Heat transfer fluids for use in low temperature chiller applications |
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 RU RU2006129311/04A patent/RU2006129311A/ru not_active Application Discontinuation
- 2005-01-12 CA CA002552832A patent/CA2552832A1/en not_active Abandoned
- 2005-01-12 WO PCT/US2005/001508 patent/WO2005068579A1/en not_active Ceased
- 2005-01-12 JP JP2006549684A patent/JP2007517974A/ja not_active Withdrawn
- 2005-01-12 EP EP05705842A patent/EP1704199A1/en not_active Withdrawn
- 2005-01-12 KR KR1020067016229A patent/KR20060122924A/ko not_active Withdrawn
- 2005-01-12 BR BRPI0506540-2A patent/BRPI0506540A/pt not_active Application Discontinuation
- 2005-01-12 AU AU2005205600A patent/AU2005205600A1/en not_active Abandoned
- 2005-01-14 AR ARP050100136A patent/AR049612A1/es unknown
-
2006
- 2006-08-11 NO NO20063643A patent/NO20063643L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20060122924A (ko) | 2006-11-30 |
| WO2005068579A1 (en) | 2005-07-28 |
| AU2005205600A1 (en) | 2005-07-28 |
| NO20063643L (no) | 2006-10-04 |
| JP2007517974A (ja) | 2007-07-05 |
| AR049612A1 (es) | 2006-08-23 |
| CA2552832A1 (en) | 2005-07-28 |
| EP1704199A1 (en) | 2006-09-27 |
| BRPI0506540A (pt) | 2007-02-27 |
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| Date | Code | Title | Description |
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| FA93 | Acknowledgement of application withdrawn (no request for examination) |
Effective date: 20080229 |