US20120117990A1 - Heat transfer process - Google Patents
Heat transfer process Download PDFInfo
- Publication number
- US20120117990A1 US20120117990A1 US13/386,701 US201013386701A US2012117990A1 US 20120117990 A1 US20120117990 A1 US 20120117990A1 US 201013386701 A US201013386701 A US 201013386701A US 2012117990 A1 US2012117990 A1 US 2012117990A1
- Authority
- US
- United States
- Prior art keywords
- refrigerant
- ene
- heat transfer
- trans
- carbon atoms
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 17
- 239000003507 refrigerant Substances 0.000 claims abstract description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 230000006835 compression Effects 0.000 claims abstract description 12
- 238000007906 compression Methods 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 238000001704 evaporation Methods 0.000 claims abstract description 5
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 3
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims abstract description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 18
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 claims description 18
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 10
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims description 9
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims description 9
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical group Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 claims description 9
- NLOLSXYRJFEOTA-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluorobut-2-ene Chemical compound FC(F)(F)C=CC(F)(F)F NLOLSXYRJFEOTA-UHFFFAOYSA-N 0.000 claims description 8
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 7
- 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 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000314 lubricant Substances 0.000 claims description 6
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 5
- 239000001569 carbon dioxide Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 3
- 229920001774 Perfluoroether Polymers 0.000 claims description 2
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- -1 polyol ester Chemical class 0.000 claims description 2
- 229920001289 polyvinyl ether Polymers 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 15
- 230000005494 condensation Effects 0.000 abstract description 8
- 238000009833 condensation Methods 0.000 abstract description 8
- 230000008020 evaporation Effects 0.000 abstract description 4
- 239000012530 fluid Substances 0.000 description 16
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 4
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 description 3
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- 238000004378 air conditioning Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- LDTMPQQAWUMPKS-OWOJBTEDSA-N (e)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C\Cl LDTMPQQAWUMPKS-OWOJBTEDSA-N 0.000 description 2
- FYIRUPZTYPILDH-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)C(F)(F)F FYIRUPZTYPILDH-UHFFFAOYSA-N 0.000 description 2
- CVMVAHSMKGITAV-UHFFFAOYSA-N 1,1,1,4,4,5,5,5-octafluoropent-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)F CVMVAHSMKGITAV-UHFFFAOYSA-N 0.000 description 2
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 description 2
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 2
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000013529 heat transfer fluid Substances 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- ICTYZHTZZOUENE-NSCUHMNNSA-N (e)-1,1,1-trifluorobut-2-ene Chemical compound C\C=C\C(F)(F)F ICTYZHTZZOUENE-NSCUHMNNSA-N 0.000 description 1
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 description 1
- VWDLXSWESRUSTM-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptakis(fluoromethoxy)propane Chemical compound FCOC(OCF)C(OCF)(OCF)C(OCF)(OCF)OCF VWDLXSWESRUSTM-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical compound CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 description 1
- ZDCWZRQSHBQRGN-UHFFFAOYSA-N 1,1,1,2,3-pentafluoropropane Chemical compound FCC(F)C(F)(F)F ZDCWZRQSHBQRGN-UHFFFAOYSA-N 0.000 description 1
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- VKKBJZFVPNUYQL-UHFFFAOYSA-N 1,1,1,4,4-pentafluorobut-2-ene Chemical compound FC(F)C=CC(F)(F)F VKKBJZFVPNUYQL-UHFFFAOYSA-N 0.000 description 1
- AHVCRWLQBFGUKH-UHFFFAOYSA-N 1,1,1,4-tetrafluorobut-2-ene Chemical compound FCC=CC(F)(F)F AHVCRWLQBFGUKH-UHFFFAOYSA-N 0.000 description 1
- QRPMHFKSNFTWQM-UHFFFAOYSA-N 1,1,2,2,3,3-hexafluoro-4-(trifluoromethoxy)butane Chemical compound FC(F)C(F)(F)C(F)(F)COC(F)(F)F QRPMHFKSNFTWQM-UHFFFAOYSA-N 0.000 description 1
- AWTOFSDLNREIFS-UHFFFAOYSA-N 1,1,2,2,3-pentafluoropropane Chemical compound FCC(F)(F)C(F)F AWTOFSDLNREIFS-UHFFFAOYSA-N 0.000 description 1
- YUXNODKRNXNFFO-UHFFFAOYSA-N 1,1,4-trifluorobut-2-ene Chemical compound FCC=CC(F)F YUXNODKRNXNFFO-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- HOMDJHGZAAKUQV-UHFFFAOYSA-N 1-(propoxymethoxy)propane Chemical compound CCCOCOCCC HOMDJHGZAAKUQV-UHFFFAOYSA-N 0.000 description 1
- SLLMGLPBJIHXSR-UHFFFAOYSA-N 1-chloro-1,1-difluorobut-2-ene Chemical compound CC=CC(F)(F)Cl SLLMGLPBJIHXSR-UHFFFAOYSA-N 0.000 description 1
- LDTMPQQAWUMPKS-UHFFFAOYSA-N 1-chloro-3,3,3-trifluoroprop-1-ene Chemical class FC(F)(F)C=CCl LDTMPQQAWUMPKS-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
- HJEORQYOUWYAMR-UHFFFAOYSA-N 2-[(2-butylphenoxy)methyl]oxirane Chemical compound CCCCC1=CC=CC=C1OCC1OC1 HJEORQYOUWYAMR-UHFFFAOYSA-N 0.000 description 1
- HSDVRWZKEDRBAG-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COC(CCCCC)OCC1CO1 HSDVRWZKEDRBAG-UHFFFAOYSA-N 0.000 description 1
- SXYHZEQKWNODPB-UHFFFAOYSA-N 2-[difluoro(methoxy)methyl]-1,1,1,2,3,3,3-heptafluoropropane;1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane Chemical compound COC(F)(F)C(F)(F)C(F)(F)C(F)(F)F.COC(F)(F)C(F)(C(F)(F)F)C(F)(F)F SXYHZEQKWNODPB-UHFFFAOYSA-N 0.000 description 1
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 description 1
- GCOYJVXNTBXPGM-UHFFFAOYSA-N 4-chloro-1,1,1-trifluorobut-2-ene Chemical compound FC(F)(F)C=CCCl GCOYJVXNTBXPGM-UHFFFAOYSA-N 0.000 description 1
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 206010016326 Feeling cold Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 230000000779 depleting effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 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
- 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
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/106—Carbon dioxide
-
- 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
-
- 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
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
-
- 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
- C09K2205/12—Hydrocarbons
- C09K2205/122—Halogenated hydrocarbons
-
- 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
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
- C10M2201/103—Clays; Mica; Zeolites
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
- C10M2203/065—Well-defined aromatic compounds used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
- C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
- C10M2209/043—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
- C10M2209/1023—Polyesters used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/1033—Polyethers, i.e. containing di- or higher polyoxyalkylene groups used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/022—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/055—Particles related characteristics
- C10N2020/06—Particles of special shape or size
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
Definitions
- the present invention relates to a heat transfer process using a composition containing hydrofluoroolefins. It relates more particularly to the use of a composition containing hydrofluoroolefins in heat pumps.
- HFC-134a a chlorofluorocarbon refrigerant
- HFC-134a hydrofluorocarbon refrigerant (1,1,1,2-tetrafluoroethane: HFC-134a)
- GWP global warming potential
- carbon dioxide is nontoxic, nonflammable and has a very low GWP
- it has been suggested as a refrigerant in air conditioning systems as a replacement for HFC-134a.
- the use of carbon dioxide presents several drawbacks, notably connected with the very high pressure when it is employed as refrigerant in existing equipment and technologies.
- compositions comprising at least one fluoroalkene having three or four carbon atoms, notably pentafluoropropene and tetrafluoropropene, preferably having a GWP of at most 150, as heat transfer fluids.
- fluorohaloalkenes having from 3 to 6 carbon atoms notably tetrafluoropropenes, pentafluoropropenes and chlorotrifluoropropenes are described as being usable as heat transfer fluid.
- compositions containing hydrofluoroolefins are quite particularly suitable as heat transfer fluid in heat pumps, especially heat pumps operating at high condensation temperature. Moreover, these compositions have a negligible ODP and a GWP less than that of the existing heat transfer fluids.
- a heat pump is a thermodynamic device enabling heat to be transferred from the coldest medium to the hottest medium.
- the heat pumps employed for heating are said to be of the compression type and operation is based on the principle of a cycle with compression of fluids, called refrigerants. These heat pumps function with compression systems having a single stage or several stages. At a given stage, when the refrigerant is compressed and passes from the gaseous state to the liquid state, an exothermic reaction (condensation) takes place, which produces heat. Conversely, if the fluid is expanded, causing it to pass from the liquid state to the gaseous state, an endothermic reaction (evaporation) takes place, which produces a sensation of cold. Thus, everything is based on the change of state of a fluid used in a closed circuit.
- Each stage of a compression system comprises (i) an evaporation step during which, on contact with calories drawn from the environment, the refrigerant, on account of its low boiling point, passes from the two-phase state (liquid/gas) to the gaseous state, (ii) a compression step during which the gas from the preceding step is raised to high pressure, (iii) a condensation step during which the gas will transfer its heat to the heating circuit (hot environment); the refrigerant, still compressed, becomes liquid again and (iv) an expansion step during which the pressure of the fluid is reduced.
- the fluid is ready for absorbing calories again from the cold environment.
- the present invention relates to a heat transfer process using a compression system having at least one stage comprising successively a step of evaporation of a refrigerant, a compression step, a condensation step of said fluid at a temperature greater than or equal to 70° C. and an expansion step of said fluid, characterized in that the refrigerant comprises at least one hydrofluoroolefin having at least 4 carbon atoms represented by formula (I) R 1 CH ⁇ CHR 2 in which R 1 and R 2 represent, independently, alkyl groups having from 1 to 6 carbon atoms, substituted with at least one fluorine atom, optionally with at least one chlorine atom.
- At least one alkyl group of the hydrofluoroolefin is completely substituted with fluorine atoms.
- the condensation temperature of the refrigerant is between 70 and 150° C., and advantageously between 95 and 140° C.
- hydrofluoroolefins of formula (I) that are particularly advantageous, mention may notably be made of 1,1,1,4,4,4-hexafluorobut-2-ene, 1,1,1,4,4,5,5,5-octafluoro-pent-2-ene, 1,1,1,4-tetrafluorobut-2-ene, 1,1,1,4,4-pentafluorobut-2-ene, 1,1,4-trifluorobut-2-ene, 1,1,1-trifluorobut-2-ene, 4-chloro-1,1,1-trifluorobut-2-ene, 4-chloro-4,4-difluorobut-2-ene.
- the preferred hydrofluoroolefins of formula (I) can be in the cis or trans form or mixture of the two.
- the refrigerant can comprise at least one compound selected from hydrofluorocarbons, hydrocarbons, (hydro)fluoroethers, hydrochlorofluoropropenes, hydrofluoropropenes, ethers, methyl formate, carbon dioxide and trans-1,2-dichloroethylene.
- hydrofluorocarbons mention may notably be made of 1,1,1,3,3-pentafluorobutane, 1,1,1,2-tetrafluoroethane, pentafluoroethane, 1,1,1,3,3-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,3,3,3-hexafluoropropane, 1,1,2,2,3-pentafluoropropane, 1,1,1,3,3-pentafluorobutane, 1,1,1,2,2,3,4,5,5,5-decafluoropentane and 1,1,1,2,3,3,3-heptafluoropropane.
- Hydrocarbons having at least three carbon atoms are preferred. Hydrocarbons with five carbon atoms such as pentane, isopentane, cyclopentane are particularly preferred.
- the preferred hydrochlorofluoropropenes are 2-chloro-3,3,3-trifluoroprop-1-ene, 1-chloro-3,3,3-trifluoroprop-1-ene, in particular trans-1-chloro-3,3,3-trifluoroprop-1-ene.
- hydrofluoroethers are those having from three to six carbon atoms.
- hydrofluoroethers mention may notably be made of heptafluoromethoxypropane, nonafluoromethoxybutane and nonafluoroethoxybutane.
- hydrofluoroether is available in several isomeric forms such as 1,1,1,2,2,3,3,4,4-nonafluoro-ethoxybutane, 1,1,1,2,3,3 -hexafluoro-2-(trifluoromethyl)-3-ethoxybutane, 1,1,1,2,2,3,3,4,4-nonafluoro-methoxybutane, 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-methoxybutane, and 1,1,1,2,2,3,3-heptafluoromethoxypropane.
- the preferred hydrofluoropropenes are trifluoropropenes such as 1,1,1-trifluoropropene, tetrafluoropropenes such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), and 1,3,3,3-tetrafluoropropene (cis and/or trans).
- the ethers can be selected from dimethyl ether, diethyl ether, dimethoxymethane or dipropoxymethane.
- the refrigerant comprises at least one hydrofluoroolefin of formula (I) and at least one hydrofluorocarbon.
- the hydrofluorocarbon selected is advantageously 1,1,1,3,3-pentafluorobutane and 1,1,1,3,3-pentafluoropropane.
- Azeotropic compositions of 1,1,1,4,4,4-hexafluorobut-2-ene or of 1,1,1,4,4,5,5,5-octafluoro-pent-2-ene with methyl formate, pentane, isopentane, cyclopentane or trans-1,2-dichloroethylene may also be suitable.
- the refrigerant comprises at least 10 wt. % of hydrofluoroolefins of formula (I).
- the refrigerant comprises from 40 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 60 wt. % of at least one compound selected from pentane, isopentane, cyclopentane and trans-1,2-dichloroethylene.
- refrigerants that are particularly preferred, mention may be made of those comprising from 60 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 40 wt. % of cyclopentane, pentane, isopentane or trans-1,2-dichloroethylene.
- the refrigerant used in the present invention can comprise a stabilizer of the hydrofluoroolefin.
- the stabilizer represents at most 5 wt. % relative to the total composition of the fluid.
- nitromethane ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butyl hydroquinone, 2,6-di-ter-butyl-4-methylphenol, epoxides (alkyl optionally fluorinated or perfluorinated or alkenyl or aromatic) such as n-butyl glycidyl ether, hexanediol diglycidyl ether, allyl glycidyl ether, butylphenylglycidyl ether, phosphites, phosphates, phosphonates, thiols and lactones.
- nitromethane ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butyl hydro
- the refrigerant used in the process according to the present invention can comprise lubricants such as mineral oil, alkylbenzene, polyalfaolefin, polyalkylene glycol, polyol ester and polyvinyl ether.
- lubricants such as mineral oil, alkylbenzene, polyalfaolefin, polyalkylene glycol, polyol ester and polyvinyl ether.
- the lubricants used with the refrigerant can comprise nanoparticles for improving the thermal conductivity of the fluid as well as its compatibility with the lubricants. As nanoparticles, mention may notably be made of particles of Al 2 O 3 or of TiO 2 .
- the lubricants used with the refrigerant can comprise dehumidifying agents of the zeolite type.
- the zeolites absorb water and thus limit corrosion and deterioration of performance.
- COP coefficient of performance, which is defined, for a heat pump, as the ratio of the useful high-temperature power supplied by the system to the power supplied to or consumed by the system
- CAP volumetric capacity, it is the calorific capacity of heating per unit volume (kJ/m3)
- % CAP or COP is the ratio of the value of CAP or COP of the fluid relative to that obtained with HCFC-114.
- the COP of the various products is calculated as % of the COP of HCFC114 or R114.
- the binary mixtures (H, J) and (C, J) have a COP, a condenser inlet temperature and a compression ratio equivalent to the value of R114 and these products are quasi-azeotropes with values of temperature lapse below 2.2° C.
- Product J and the mixtures (E, J) have a COP 5% higher than the COP of the reference product (R114).
- the COP and CAP of the various products are calculated as % of COP and CAP of R114 respectively.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to a heat transfer process using a composition containing hydro(chloro)fluoroolefins. It more particularly relates to a heat transfer process that successively comprises a step of evaporation of a refrigerant; a step of compression, a step of condensation of said refrigerant at a temperature greater than or equal to 70° C. and a step of expansion of said refrigerant characterized in that the refrigerant comprises at least one hydrofluoroolefin having at least four carbon atoms represented by the formula (I) R1CH═CHR2 in which R1 and R2 independently represent alkyl groups having from 1 to 6 carbon atoms, substituted with at least one fluorine atom, optionally with at least one chlorine atom.
Description
- The present invention relates to a heat transfer process using a composition containing hydrofluoroolefins. It relates more particularly to the use of a composition containing hydrofluoroolefins in heat pumps.
- The problems posed by substances depleting the ozone layer of the atmosphere (having ozone depletion potential, ODP) were discussed in Montreal, where the protocol was signed requiring a reduction of the production and use of chlorofluorocarbons (CFCs). Amendments have been made to this protocol, requiring abandonment of CFCs and extending the controls to other products.
- The refrigeration and air conditioning industry has invested heavily in substitutes for these refrigerants.
- In the automotive industry, the air conditioning systems for vehicles marketed in many countries have changed over from a chlorofluorocarbon refrigerant (CFC-12) to a hydrofluorocarbon refrigerant (1,1,1,2-tetrafluoroethane: HFC-134a), which is less harmful to the ozone layer. However, with regard to the objectives established by the Kyoto protocol, HFC-134a (GWP=1300) is regarded as having a high warming effect. A fluid's contribution to the greenhouse effect is quantified by a criterion, the global warming potential (GWP), which summarizes the warming effect, taking a reference value of 1 for carbon dioxide.
- As carbon dioxide is nontoxic, nonflammable and has a very low GWP, it has been suggested as a refrigerant in air conditioning systems as a replacement for HFC-134a. However, the use of carbon dioxide presents several drawbacks, notably connected with the very high pressure when it is employed as refrigerant in existing equipment and technologies.
- Document JP 4110388 describes the use of hydrofluoropropenes of formula C3HmFn, with m, n representing an integer between 1 and 5 inclusive and m+n=6, as heat transfer fluids, in particular tetrafluoropropene and trifluoropropene.
- Document WO2004/037913 discloses the use of compositions comprising at least one fluoroalkene having three or four carbon atoms, notably pentafluoropropene and tetrafluoropropene, preferably having a GWP of at most 150, as heat transfer fluids.
- In document WO 2007/002625, fluorohaloalkenes having from 3 to 6 carbon atoms, notably tetrafluoropropenes, pentafluoropropenes and chlorotrifluoropropenes are described as being usable as heat transfer fluid.
- Document WO2007/053697 describes heat transfer fluids comprising fluoroolefins having at least 5 carbon atoms.
- In the area of heat pumps, substitutes for dichlorotetrafluoroethane (HCFC-114), used in conditions of high condensation temperature, have been proposed. Thus, document U.S. Pat. No. 6,814,884 describes a composition comprising 1,1,1,3,3-pentafluorobutane (HFC-365mfc) and at least one compound selected from 1,1,1,2-tetrafluoroethane, pentafluoroethane (HFC-125), 1,1,1,3,3-pentafluoropropane (HFC-245fa) and 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea). However, these compounds have a high GWP and have very high compression ratios and temperature lapses relative to HCFC-114.
- Document US 20090049856 describes heat transfer fluids comprising 1,1,1,3,3-pentafluoropropane (HFC-245fa), 1,1,1,2,3,3-hexafluoropropane (HFC-236ea) and tetrafluoroethane (HFC-134a). However, these mixtures have very high temperatures at the condenser inlet (compressor outlet), which means overheating of the mechanical parts and a decrease in overall efficiency of the compressor. Moreover, the critical temperatures of these mixtures (around 110° C.) are below the desired condensation temperature (120 or even 150° C.), so that they cannot be used in high-temperature heat pumps.
- The applicant has now discovered that compositions containing hydrofluoroolefins are quite particularly suitable as heat transfer fluid in heat pumps, especially heat pumps operating at high condensation temperature. Moreover, these compositions have a negligible ODP and a GWP less than that of the existing heat transfer fluids.
- Furthermore, these mixtures have critical temperatures above 150° C., thus permitting their use in high-temperature heat pumps.
- A heat pump is a thermodynamic device enabling heat to be transferred from the coldest medium to the hottest medium. The heat pumps employed for heating are said to be of the compression type and operation is based on the principle of a cycle with compression of fluids, called refrigerants. These heat pumps function with compression systems having a single stage or several stages. At a given stage, when the refrigerant is compressed and passes from the gaseous state to the liquid state, an exothermic reaction (condensation) takes place, which produces heat. Conversely, if the fluid is expanded, causing it to pass from the liquid state to the gaseous state, an endothermic reaction (evaporation) takes place, which produces a sensation of cold. Thus, everything is based on the change of state of a fluid used in a closed circuit.
- Each stage of a compression system comprises (i) an evaporation step during which, on contact with calories drawn from the environment, the refrigerant, on account of its low boiling point, passes from the two-phase state (liquid/gas) to the gaseous state, (ii) a compression step during which the gas from the preceding step is raised to high pressure, (iii) a condensation step during which the gas will transfer its heat to the heating circuit (hot environment); the refrigerant, still compressed, becomes liquid again and (iv) an expansion step during which the pressure of the fluid is reduced. The fluid is ready for absorbing calories again from the cold environment.
- The present invention relates to a heat transfer process using a compression system having at least one stage comprising successively a step of evaporation of a refrigerant, a compression step, a condensation step of said fluid at a temperature greater than or equal to 70° C. and an expansion step of said fluid, characterized in that the refrigerant comprises at least one hydrofluoroolefin having at least 4 carbon atoms represented by formula (I) R1CH═CHR2 in which R1 and R2 represent, independently, alkyl groups having from 1 to 6 carbon atoms, substituted with at least one fluorine atom, optionally with at least one chlorine atom.
- Preferably, at least one alkyl group of the hydrofluoroolefin is completely substituted with fluorine atoms.
- Preferably, the condensation temperature of the refrigerant is between 70 and 150° C., and advantageously between 95 and 140° C.
- As hydrofluoroolefins of formula (I) that are particularly advantageous, mention may notably be made of 1,1,1,4,4,4-hexafluorobut-2-ene, 1,1,1,4,4,5,5,5-octafluoro-pent-2-ene, 1,1,1,4-tetrafluorobut-2-ene, 1,1,1,4,4-pentafluorobut-2-ene, 1,1,4-trifluorobut-2-ene, 1,1,1-trifluorobut-2-ene, 4-chloro-1,1,1-trifluorobut-2-ene, 4-chloro-4,4-difluorobut-2-ene.
- The preferred hydrofluoroolefins of formula (I) can be in the cis or trans form or mixture of the two.
- Besides the hydrofluoroolefin(s) of formula (I), the refrigerant can comprise at least one compound selected from hydrofluorocarbons, hydrocarbons, (hydro)fluoroethers, hydrochlorofluoropropenes, hydrofluoropropenes, ethers, methyl formate, carbon dioxide and trans-1,2-dichloroethylene.
- As hydrofluorocarbons, mention may notably be made of 1,1,1,3,3-pentafluorobutane, 1,1,1,2-tetrafluoroethane, pentafluoroethane, 1,1,1,3,3-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,3,3,3-hexafluoropropane, 1,1,2,2,3-pentafluoropropane, 1,1,1,3,3-pentafluorobutane, 1,1,1,2,2,3,4,5,5,5-decafluoropentane and 1,1,1,2,3,3,3-heptafluoropropane.
- Hydrocarbons having at least three carbon atoms are preferred. Hydrocarbons with five carbon atoms such as pentane, isopentane, cyclopentane are particularly preferred. The preferred hydrochlorofluoropropenes are 2-chloro-3,3,3-trifluoroprop-1-ene, 1-chloro-3,3,3-trifluoroprop-1-ene, in particular trans-1-chloro-3,3,3-trifluoroprop-1-ene.
- The preferred hydrofluoroethers are those having from three to six carbon atoms. As hydrofluoroethers, mention may notably be made of heptafluoromethoxypropane, nonafluoromethoxybutane and nonafluoroethoxybutane. The hydrofluoroether is available in several isomeric forms such as 1,1,1,2,2,3,3,4,4-nonafluoro-ethoxybutane, 1,1,1,2,3,3 -hexafluoro-2-(trifluoromethyl)-3-ethoxybutane, 1,1,1,2,2,3,3,4,4-nonafluoro-methoxybutane, 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-methoxybutane, and 1,1,1,2,2,3,3-heptafluoromethoxypropane.
- The preferred hydrofluoropropenes are trifluoropropenes such as 1,1,1-trifluoropropene, tetrafluoropropenes such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), and 1,3,3,3-tetrafluoropropene (cis and/or trans). The ethers can be selected from dimethyl ether, diethyl ether, dimethoxymethane or dipropoxymethane.
- Preferably, the refrigerant comprises at least one hydrofluoroolefin of formula (I) and at least one hydrofluorocarbon. The hydrofluorocarbon selected is advantageously 1,1,1,3,3-pentafluorobutane and 1,1,1,3,3-pentafluoropropane.
- Azeotropic compositions of 1,1,1,4,4,4-hexafluorobut-2-ene or of 1,1,1,4,4,5,5,5-octafluoro-pent-2-ene with methyl formate, pentane, isopentane, cyclopentane or trans-1,2-dichloroethylene may also be suitable.
- Preferably, the refrigerant comprises at least 10 wt. % of hydrofluoroolefins of formula (I).
- According to one embodiment of the invention, the refrigerant comprises from 40 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 60 wt. % of at least one compound selected from pentane, isopentane, cyclopentane and trans-1,2-dichloroethylene.
- As refrigerants that are particularly preferred, mention may be made of those comprising from 60 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 40 wt. % of cyclopentane, pentane, isopentane or trans-1,2-dichloroethylene.
- The refrigerant used in the present invention can comprise a stabilizer of the hydrofluoroolefin. The stabilizer represents at most 5 wt. % relative to the total composition of the fluid.
- As stabilizers, mention may notably be made of nitromethane, ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butyl hydroquinone, 2,6-di-ter-butyl-4-methylphenol, epoxides (alkyl optionally fluorinated or perfluorinated or alkenyl or aromatic) such as n-butyl glycidyl ether, hexanediol diglycidyl ether, allyl glycidyl ether, butylphenylglycidyl ether, phosphites, phosphates, phosphonates, thiols and lactones.
- The refrigerant used in the process according to the present invention can comprise lubricants such as mineral oil, alkylbenzene, polyalfaolefin, polyalkylene glycol, polyol ester and polyvinyl ether. The lubricants used with the refrigerant can comprise nanoparticles for improving the thermal conductivity of the fluid as well as its compatibility with the lubricants. As nanoparticles, mention may notably be made of particles of Al2O3 or of TiO2.
- The lubricants used with the refrigerant can comprise dehumidifying agents of the zeolite type. The zeolites absorb water and thus limit corrosion and deterioration of performance.
- Hereinafter:
- Evap: evaporator,
- Cond: condenser,
- Temp: temperature,
- Comp: compressor,
- P: pressure,
- Ratio: compression ratio
- COP: coefficient of performance, which is defined, for a heat pump, as the ratio of the useful high-temperature power supplied by the system to the power supplied to or consumed by the system
- CAP: volumetric capacity, it is the calorific capacity of heating per unit volume (kJ/m3)
- % CAP or COP is the ratio of the value of CAP or COP of the fluid relative to that obtained with HCFC-114.
- The performance of the refrigerant in the operating conditions of the heat pump with the temperature at the evaporator maintained at 30° C., at the compressor inlet maintained at 35° C. and at the condenser at 90° C. are given below.
- The COP of the various products is calculated as % of the COP of HCFC114 or R114.
- Isentropic efficiency of the compressor: 59.3%
- C ISOPENTANE
- E trans-1,2-dichloroethylene
- H pentane
- J 1,1,1,4,4,4-hexafluorobut-2-ene
-
Temp Temp evap Temp evap Temp comp T cond expander inlet outlet inlet inlet T cond inlet evap P cond P Ratio Efficiency % (° C.) (° C.) (° C.) (° C.) (° C.) (° C.) (bar) (bar) (p/p) Lapse comp COP HCFC-114 30 30 35 96 90 85 2.5 11.55 4.6 0.0 0.59 100 245fa/236ea/ 30 35 113 90 85 6.0 27.4 4.6 3.28 0.59 99 134a (10/10/80 wt. %) 365mfc/227ea 25 30 35 104 90 85 0.9 7.89 9.1 4.8 0.59 90 75/25 wt. %) J 30 30 35 92 90 85 0.9 5.58 6.2 0.0 0.59 104 H J 5 95 29 30 35 93 90 85 1.0 6.18 6.2 1.5 0.59 100 20 80 29 30 35 90 90 85 1.2 6.78 5.5 1.4 0.59 100 30 70 30 30 35 90 90 85 1.3 6.80 5.2 0.0 0.59 102 40 60 28 30 35 93 90 85 1.2 6.70 5.5 2.1 0.59 100 C J 30 70 29 30 35 90 90 85 1.5 7.49 5.2 1.0 0.59 100 40 60 30 30 35 90 90 85 1.5 7.48 5.0 0.2 0.59 101 E J 5 95 29 30 35 94 90 85 1.0 5.80 6.1 0.5 0.59 104 10 90 29 30 35 96 90 85 1.0 5.94 6.0 0.7 0.59 105 15 85 29 30 35 98 90 85 1.0 6.02 5.8 0.6 0.59 106 20 80 30 30 35 100 90 85 1.1 6.05 5.7 0.2 0.59 108 30 70 29 30 35 106 90 85 1.0 6.02 5.8 0.8 0.59 109 40 60 26 30 35 117 90 85 0.9 5.91 6.5 4.2 0.59 106 - The results show an increase in COP relative to the reference product (R114).
- The binary mixtures (H, J) and (C, J) have a COP, a condenser inlet temperature and a compression ratio equivalent to the value of R114 and these products are quasi-azeotropes with values of temperature lapse below 2.2° C.
- Product J and the mixtures (E, J) have a COP 5% higher than the COP of the reference product (R114).
- The performance of the refrigerant in heat pump operating conditions with temperature at the evaporator maintained at 80° C., at the compressor inlet maintained at 85° C. and at the condenser at 140° C. are given below.
- The COP and CAP of the various products are calculated as % of COP and CAP of R114 respectively.
- Isentropic efficiency of the compressor: 59.3%
- C ISOPENTANE
- E trans-1,2-dichloroethylene
- H pentane
- J 1,1,1,4,4,4-hexafluorobut-2-ene
-
Temp Temp evap Temp evap Temp comp T cond expander inlet outlet inlet inlet T cond inlet evap P cond P Ratio Efficiency % % (° C.) (° C.) (° C.) (° C.) (° C.) (° C.) (bar) (bar) (p/p) Lapse comp CAP COP HCFC-R114 80 80 85 148 140 135 9.3 29.6 3.2 0.0 0.59 100 100 245fa 80 80 85 147 140 135 7.9 28.6 3.6 0.0 0.59 114 118 365mfc 80 80 85 140 140 135 3.5 14.1 4.0 0.0 0.59 71 151 365mfc/227 ea 77 80 85 148 140 135 4.3 20.7 4.8 3.1 0.59 79 123 (75/25 J 80 80 85 140 140 135 4.3 16.6 3.8 0.0 0.59 81 146 H J 5 95 79 80 85 140 140 135 4.6 17.4 3.8 0.7 0.59 82 141 10 90 79 80 85 140 140 135 4.9 18.0 3.7 0.9 0.59 83 137 15 85 79 80 85 140 140 135 5.2 18.3 3.5 0.7 0.59 84 136 20 80 80 80 85 140 140 135 5.3 18.4 3.5 0.3 0.59 85 136 30 70 80 80 85 140 140 135 5.4 18.3 3.45 0.1 0.59 85 137 40 60 79 80 85 141 140 135 5.1 17.9 3.5 1.2 0.59 83 136 C J 5 95 79 80 85 141 140 135 4.7 17.8 3.8 0.9 0.59 82 138 10 90 79 80 85 141 140 135 5.0 18.7 3.7 1.3 0.59 83 134 15 85 79 80 85 141 140 135 5.3 19.3 3.6 1.4 0.59 85 131 20 80 79 80 85 140 140 135 5.6 19.7 3.5 1.0 0.59 86 130 30 70 80 80 85 140 140 135 6.0 19.9 3.3 0.1 0.59 87 130 40 60 80 80 85 140 140 135 5.9 19.7 3.3 0.2 0.59 87 131 E J 5 95 80 80 85 140 140 135 4.5 16.8 3.8 0.2 0.59 85 149 10 90 80 80 85 140 140 135 4.6 17.0 3.7 0.2 0.59 88 151 15 85 80 80 85 141 140 135 4.7 17.1 3.6 0.2 0.59 92 155 20 80 80 80 85 142 140 135 4.8 17.1 3.6 0.0 0.59 95 158 30 70 79 80 85 146 140 135 4.6 16.9 3.6 0.6 0.59 98 163 40 60 77 80 85 154 140 135 4.2 16.5 3.9 3.2 0.59 96 162 - The results show that the COP of the new products is far greater than the COP of the reference (R114).
Claims (11)
1. A heat transfer process employing a compression system having at least one stage comprising successively: evaporating a refrigerant, compressing said refrigerant, condensing said refrigerant at a temperature greater than or equal to 70° C. and expanding said refrigerant, characterized in that the refrigerant comprises at least one hydrofluoroolefin having at least 4 carbon atoms represented by the formula R1CH═CHR2 in which R1 and R2 represent, independently, alkyl groups having from 1 to 6 carbon atoms, substituted with at least one fluorine atom, optionally substituted with at least one chlorine atom.
2. The process as claimed in claim 1 , characterized in that the temperature is between 70 and 150° C.
3. The process as claimed in claim 1 , characterized in that the refrigerant further comprises at least one compound selected from the group consisting of hydrofluorocarbons, hydrocarbons, (hydro)fluoroethers, hydrochlorofluoropropenes, hydrofluoropropenes, ethers, methyl formate, carbon dioxide and trans-1,2-dichloroethylene.
4. The process as claimed in claim 1 , characterized in that the refrigerant comprises at least one hydrofluorocarbon selected from the group consisting of 1,1,1,3,3-pentafluorobutane and 1,1,1,3,3-pentafluoropropane.
5. The process as claimed in claim 1 , characterized in that the refrigerant comprises at least one hydrocarbon selected from the group consisting of pentane, isopentane and cyclopentane.
6. The process as claimed in claim 1 , characterized in that the refrigerant comprises from 40 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 60 wt. % of at least one compound selected from the group consisting of pentane, isopentane, cyclopentane and trans-1,2-dichloroethylene.
7. The process as claimed in claim 1 , characterized in that refrigerant comprises from 60 to 100 wt. % of 1,1,1,4,4,4-hexafluorobut-2-ene and from 0 to 40 wt. % of cyclopentane, pentane, isopentane or trans-1,2-dichloroethylene.
8. The process as claimed in claim 1 , characterized in that the refrigerant further comprises a stabilizer.
9. The process as claimed in 8, characterized in that the refrigerant further comprises a lubricant.
10. The process as claimed in claim 9 , characterized in that the lubricant is polyalkylene glycol, polyol ester or polyvinyl ether.
11. The process as claimed in claim 1 , characterized in that the temperature is between 95 and 140° C.
Applications Claiming Priority (3)
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|---|---|---|---|
| FR0955261 | 2009-07-28 | ||
| FR0955261A FR2948678B1 (en) | 2009-07-28 | 2009-07-28 | HEAT TRANSFER METHOD |
| PCT/FR2010/051279 WO2011015737A1 (en) | 2009-07-28 | 2010-06-23 | Heat transfer process |
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| PCT/FR2010/051279 A-371-Of-International WO2011015737A1 (en) | 2009-07-28 | 2010-06-23 | Heat transfer process |
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| US16/027,602 Continuation US20190040292A1 (en) | 2009-07-28 | 2018-07-05 | Heat transfer process |
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| US17/332,261 Abandoned US20220119694A1 (en) | 2009-07-28 | 2021-05-27 | Heat transfer process |
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| US16/027,602 Abandoned US20190040292A1 (en) | 2009-07-28 | 2018-07-05 | Heat transfer process |
| US17/332,261 Abandoned US20220119694A1 (en) | 2009-07-28 | 2021-05-27 | Heat transfer process |
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| US (3) | US20120117990A1 (en) |
| EP (2) | EP2459667B1 (en) |
| JP (3) | JP6021642B2 (en) |
| CN (1) | CN102471670B (en) |
| ES (1) | ES2619933T3 (en) |
| FR (1) | FR2948678B1 (en) |
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| WO (1) | WO2011015737A1 (en) |
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| WO2018175367A1 (en) * | 2017-03-20 | 2018-09-27 | The Chemours Company Fc, Llc | Compositions and uses of trans-1,1,1,4,4,4-hexafluoro-2-butene |
| US11053420B2 (en) | 2017-09-12 | 2021-07-06 | Arkema France | Composition on the basis of hydrochlorofluoroolefin and mineral oil |
| US12456851B2 (en) * | 2020-10-22 | 2025-10-28 | AGC Inc. | Gas-insulated switching device using C3HCIF4 or C4H2F6 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20190040292A1 (en) | 2019-02-07 |
| FR2948678A1 (en) | 2011-02-04 |
| CN102471670A (en) | 2012-05-23 |
| FR2948678B1 (en) | 2011-10-14 |
| JP2016197007A (en) | 2016-11-24 |
| CN102471670B (en) | 2015-07-01 |
| EP3176239A1 (en) | 2017-06-07 |
| JP6021642B2 (en) | 2016-11-09 |
| PL2459667T3 (en) | 2017-06-30 |
| US20220119694A1 (en) | 2022-04-21 |
| WO2011015737A1 (en) | 2011-02-10 |
| EP2459667B1 (en) | 2017-02-22 |
| JP2019032155A (en) | 2019-02-28 |
| JP2013500373A (en) | 2013-01-07 |
| EP2459667A1 (en) | 2012-06-06 |
| ES2619933T3 (en) | 2017-06-27 |
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| STCB | Information on status: application discontinuation |
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