JP2012512991A5 - - Google Patents
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- JP2012512991A5 JP2012512991A5 JP2011542417A JP2011542417A JP2012512991A5 JP 2012512991 A5 JP2012512991 A5 JP 2012512991A5 JP 2011542417 A JP2011542417 A JP 2011542417A JP 2011542417 A JP2011542417 A JP 2011542417A JP 2012512991 A5 JP2012512991 A5 JP 2012512991A5
- Authority
- JP
- Japan
- Prior art keywords
- trifluoromethyl
- butene
- ene
- chf
- group
- 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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- 239000012530 fluid Substances 0.000 claims description 63
- 150000001336 alkenes Chemical class 0.000 claims description 28
- 238000010521 absorption reaction Methods 0.000 claims description 23
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 20
- 101150065749 Churc1 gene Proteins 0.000 claims description 20
- 102100038239 Protein Churchill Human genes 0.000 claims description 20
- 150000001924 cycloalkanes Chemical class 0.000 claims description 20
- 229910052731 fluorine Inorganic materials 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- 230000002745 absorbent Effects 0.000 claims description 18
- 239000002250 absorbent Substances 0.000 claims description 18
- 229910052794 bromium Inorganic materials 0.000 claims description 18
- 229910052801 chlorine Inorganic materials 0.000 claims description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 18
- 229910052740 iodine Inorganic materials 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 229910052710 silicon Inorganic materials 0.000 claims description 18
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 239000006096 absorbing agent Substances 0.000 claims description 14
- 238000001704 evaporation Methods 0.000 claims description 12
- 125000003107 substituted aryl group Chemical group 0.000 claims description 12
- 238000001816 cooling Methods 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 8
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 claims description 8
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 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 claims description 5
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 claims description 5
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 4
- HTKQZWCWSRBOKO-UHFFFAOYSA-N 1,1,1,2,2,4,5,5,6,6,7,7,7-tridecafluorohept-3-ene Chemical compound FC(F)(F)C(F)(F)C=C(F)C(F)(F)C(F)(F)C(F)(F)F HTKQZWCWSRBOKO-UHFFFAOYSA-N 0.000 claims description 4
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-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
- ZBKIRWGFFLBFDX-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluoro-2-(trifluoromethyl)but-2-ene Chemical compound FC(F)(F)C=C(C(F)(F)F)C(F)(F)F ZBKIRWGFFLBFDX-UHFFFAOYSA-N 0.000 claims description 4
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 claims description 4
- WXGNWUVNYMJENI-UHFFFAOYSA-N 1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)F WXGNWUVNYMJENI-UHFFFAOYSA-N 0.000 claims description 4
- QAERDLQYXMEHEB-UHFFFAOYSA-N 1,1,3,3,3-pentafluoroprop-1-ene Chemical compound FC(F)=CC(F)(F)F QAERDLQYXMEHEB-UHFFFAOYSA-N 0.000 claims description 4
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims description 4
- ZUAQTIHDWIHCSV-UHFFFAOYSA-N 1,2,3,3-tetrafluoroprop-1-ene Chemical compound FC=C(F)C(F)F ZUAQTIHDWIHCSV-UHFFFAOYSA-N 0.000 claims description 4
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 150000003973 alkyl amines Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 229910052786 argon Inorganic materials 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000002619 bicyclic group Chemical group 0.000 claims description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- -1 cyclic alkene Chemical class 0.000 claims description 4
- 235000019404 dichlorodifluoromethane Nutrition 0.000 claims description 4
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims description 4
- UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 239000002608 ionic liquid Substances 0.000 claims description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 4
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 4
- QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-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
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 4
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 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 claims description 3
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims description 3
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 3
- VKKBJZFVPNUYQL-OWOJBTEDSA-N (E)-1,1,1,4,4-pentafluorobut-2-ene Chemical compound FC(F)\C=C\C(F)(F)F VKKBJZFVPNUYQL-OWOJBTEDSA-N 0.000 claims description 2
- NIJFGUAYRFPTBD-OWOJBTEDSA-N (e)-1,1,1,2,2,3,3,6,6,7,7,8,8,8-tetradecafluorooct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)\C=C\C(F)(F)C(F)(F)C(F)(F)F NIJFGUAYRFPTBD-OWOJBTEDSA-N 0.000 claims description 2
- WSJULBMCKQTTIG-OWOJBTEDSA-N (e)-1,1,1,2,3,4,4,4-octafluorobut-2-ene Chemical compound FC(F)(F)C(/F)=C(\F)C(F)(F)F WSJULBMCKQTTIG-OWOJBTEDSA-N 0.000 claims description 2
- SAPOZTRFWJZUFT-OWOJBTEDSA-N (e)-1,1,1,2,3,4,5,5,5-nonafluoro-4-(trifluoromethyl)pent-2-ene Chemical compound FC(F)(F)C(/F)=C(\F)C(F)(C(F)(F)F)C(F)(F)F SAPOZTRFWJZUFT-OWOJBTEDSA-N 0.000 claims description 2
- PXINDCPNVPPLOD-OWOJBTEDSA-N (e)-1,1,1,5,5,5-hexafluoro-4-(trifluoromethyl)pent-2-ene Chemical compound FC(F)(F)\C=C\C(C(F)(F)F)C(F)(F)F PXINDCPNVPPLOD-OWOJBTEDSA-N 0.000 claims description 2
- FFTOUVYEKNGDCM-OWOJBTEDSA-N (e)-1,3,3-trifluoroprop-1-ene Chemical compound F\C=C\C(F)F FFTOUVYEKNGDCM-OWOJBTEDSA-N 0.000 claims description 2
- HVOUHYGSLBPLGT-NSCUHMNNSA-N (e)-4,4,5,5,6,6,6-heptafluorohex-2-ene Chemical compound C\C=C\C(F)(F)C(F)(F)C(F)(F)F HVOUHYGSLBPLGT-NSCUHMNNSA-N 0.000 claims description 2
- IRUCBBFNLDIMIK-BQYQJAHWSA-N (e)-oct-4-ene Chemical compound CCC\C=C\CCC IRUCBBFNLDIMIK-BQYQJAHWSA-N 0.000 claims description 2
- YIFLMZOLKQBEBO-UPHRSURJSA-N (z)-1,1,1,2,4,4,4-heptafluorobut-2-ene Chemical compound FC(F)(F)C(/F)=C/C(F)(F)F YIFLMZOLKQBEBO-UPHRSURJSA-N 0.000 claims description 2
- DAFSRGHZDWBZKC-UPHRSURJSA-N (z)-1,1,1,2,4,4,5,5,5-nonafluoropent-2-ene Chemical compound FC(F)(F)C(/F)=C/C(F)(F)C(F)(F)F DAFSRGHZDWBZKC-UPHRSURJSA-N 0.000 claims description 2
- MZPZBRBIEBBNIA-UPHRSURJSA-N (z)-1,1,1,3,4,4,5,5,5-nonafluoropent-2-ene Chemical compound FC(F)(F)\C=C(/F)C(F)(F)C(F)(F)F MZPZBRBIEBBNIA-UPHRSURJSA-N 0.000 claims description 2
- DDKFHEFCVPCJKU-UPHRSURJSA-N (z)-1,1,2,4,4-pentafluorobut-2-ene Chemical compound FC(F)\C=C(/F)C(F)F DDKFHEFCVPCJKU-UPHRSURJSA-N 0.000 claims description 2
- DMUPYMORYHFFCT-UPHRSURJSA-N (z)-1,2,3,3,3-pentafluoroprop-1-ene Chemical compound F\C=C(/F)C(F)(F)F DMUPYMORYHFFCT-UPHRSURJSA-N 0.000 claims description 2
- FBYFFPSDVKHUET-UPHRSURJSA-N (z)-1,2,3,3,4,4-hexafluorobut-1-ene Chemical compound F\C=C(/F)C(F)(F)C(F)F FBYFFPSDVKHUET-UPHRSURJSA-N 0.000 claims description 2
- ZUAQTIHDWIHCSV-UPHRSURJSA-N (z)-1,2,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C(/F)C(F)F ZUAQTIHDWIHCSV-UPHRSURJSA-N 0.000 claims description 2
- MQQLAYMCXDAYFW-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,5,6,6,7,7,7-tetradecafluoroheptane Chemical compound FC(F)(F)C(F)(F)C(F)C(F)C(F)(F)C(F)(F)C(F)(F)F MQQLAYMCXDAYFW-UHFFFAOYSA-N 0.000 claims description 2
- AITFZJZHSKYXLQ-UHFFFAOYSA-N 1,1,1,2,2,3,3,6,6,7,7,8,9,9,9-pentadecafluoro-8-(trifluoromethyl)non-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(C(F)(F)F)C(F)(F)F AITFZJZHSKYXLQ-UHFFFAOYSA-N 0.000 claims description 2
- GFAFNBBYWKMUTI-UHFFFAOYSA-N 1,1,1,2,2,3,3,6,7,7,8,8,8-tridecafluoro-6-(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)F GFAFNBBYWKMUTI-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- RFYFRYQYXJPKMF-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,6,6,6-dodecafluorohex-3-ene Chemical compound FC(F)(F)C(F)(F)C(F)=C(F)C(F)(F)C(F)(F)F RFYFRYQYXJPKMF-UHFFFAOYSA-N 0.000 claims description 2
- QAQXDIFHMWHZAL-UHFFFAOYSA-N 1,1,1,2,2,3,4-heptafluorohex-3-ene Chemical compound CCC(F)=C(F)C(F)(F)C(F)(F)F QAQXDIFHMWHZAL-UHFFFAOYSA-N 0.000 claims description 2
- IMFRQXJTPNCKAO-UHFFFAOYSA-N 1,1,1,2,2,3,5,5,6,6,7,7,7-tridecafluorohept-3-ene Chemical compound FC(F)(F)C(F)(F)C(F)=CC(F)(F)C(F)(F)C(F)(F)F IMFRQXJTPNCKAO-UHFFFAOYSA-N 0.000 claims description 2
- HAKDOAXLYMHZSQ-UHFFFAOYSA-N 1,1,1,2,2,3,6,6,7,8,8,8-dodecafluoro-3,7-bis(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(C(F)(F)F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F HAKDOAXLYMHZSQ-UHFFFAOYSA-N 0.000 claims description 2
- LGOQFJQJNHYWHK-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,6-decafluorohex-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)F LGOQFJQJNHYWHK-UHFFFAOYSA-N 0.000 claims description 2
- YWSYXYXSEWRSMA-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,7,7,7-dodecafluorohept-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)F YWSYXYXSEWRSMA-UHFFFAOYSA-N 0.000 claims description 2
- YJSIBKOUPOTQEG-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,7,7,8,8,8-tetradecafluorooct-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)F YJSIBKOUPOTQEG-UHFFFAOYSA-N 0.000 claims description 2
- OEBKCCWRUFDDOM-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,7,7,8,8,9,9,10,10,10-octadecafluorodec-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F OEBKCCWRUFDDOM-UHFFFAOYSA-N 0.000 claims description 2
- IKEULTDRFFGVIG-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,7,7,8,8,9,9,9-hexadecafluoronon-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F IKEULTDRFFGVIG-UHFFFAOYSA-N 0.000 claims description 2
- XHWLRBOAVBXSON-UHFFFAOYSA-N 1,1,1,2,2,5,5,6,6,7,8,8,8-tridecafluoro-7-(trifluoromethyl)oct-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(C(F)(F)F)C(F)(F)F XHWLRBOAVBXSON-UHFFFAOYSA-N 0.000 claims description 2
- NXTXGAQCBDQXMS-UHFFFAOYSA-N 1,1,1,2,2,5,6,6,6-nonafluoro-5-(trifluoromethyl)hex-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)F NXTXGAQCBDQXMS-UHFFFAOYSA-N 0.000 claims description 2
- QQCOPRMGGYUQBE-UHFFFAOYSA-N 1,1,1,2,2,5,6,6,7,7,7-undecafluoro-5-(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)F QQCOPRMGGYUQBE-UHFFFAOYSA-N 0.000 claims description 2
- WGNAKJSYVCANQZ-UHFFFAOYSA-N 1,1,1,2,2,5,6,6,7,7,8,8,9,9,9-pentadecafluoro-5-(trifluoromethyl)non-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F WGNAKJSYVCANQZ-UHFFFAOYSA-N 0.000 claims description 2
- UXFGSYQYBDJVHJ-UHFFFAOYSA-N 1,1,1,2,2,6,6,6-octafluoro-5,5-bis(trifluoromethyl)hex-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)F UXFGSYQYBDJVHJ-UHFFFAOYSA-N 0.000 claims description 2
- YJSHAZHSJYRKPY-UHFFFAOYSA-N 1,1,1,2,2,6,6,7,7,8,8,8-dodecafluoro-5,5-bis(trifluoromethyl)oct-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F YJSHAZHSJYRKPY-UHFFFAOYSA-N 0.000 claims description 2
- OIYAZAWPPZHMGK-UHFFFAOYSA-N 1,1,1,2,3,3,6,6,7,7,8,8,9,9,9-pentadecafluoro-2-(trifluoromethyl)non-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F OIYAZAWPPZHMGK-UHFFFAOYSA-N 0.000 claims description 2
- WSJULBMCKQTTIG-UHFFFAOYSA-N 1,1,1,2,3,4,4,4-octafluorobut-2-ene Chemical compound FC(F)(F)C(F)=C(F)C(F)(F)F WSJULBMCKQTTIG-UHFFFAOYSA-N 0.000 claims description 2
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- GBZQVGMPGUEDOI-UHFFFAOYSA-N 2,3,4,4,4-pentafluorobut-1-ene Chemical compound FC(=C)C(F)C(F)(F)F GBZQVGMPGUEDOI-UHFFFAOYSA-N 0.000 claims description 2
- NHGSUDHIUKAWHN-UHFFFAOYSA-N 2,4,4,4-tetrafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC(=C)C(C(F)(F)F)C(F)(F)F NHGSUDHIUKAWHN-UHFFFAOYSA-N 0.000 claims description 2
- MMZARORJGNLKAW-UHFFFAOYSA-N 2-(difluoromethyl)-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)C(=C)C(F)(F)F MMZARORJGNLKAW-UHFFFAOYSA-N 0.000 claims description 2
- IYOLYUNUVFIFIE-UHFFFAOYSA-N 2-(difluoromethyl)-3,3-difluoroprop-1-ene Chemical compound FC(F)C(=C)C(F)F IYOLYUNUVFIFIE-UHFFFAOYSA-N 0.000 claims description 2
- QMIWYOZFFSLIAK-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)prop-1-ene Chemical compound FC(F)(F)C(=C)C(F)(F)F QMIWYOZFFSLIAK-UHFFFAOYSA-N 0.000 claims description 2
- NTJPBRSQUATARU-UHFFFAOYSA-N 3,3,4,4,4-pentafluoro-2-(trifluoromethyl)but-1-ene Chemical compound FC(F)(F)C(=C)C(F)(F)C(F)(F)F NTJPBRSQUATARU-UHFFFAOYSA-N 0.000 claims description 2
- IZHPSCJEIFFRLN-UHFFFAOYSA-N 3,3,4,4,4-pentafluorobut-1-ene Chemical compound FC(F)(F)C(F)(F)C=C IZHPSCJEIFFRLN-UHFFFAOYSA-N 0.000 claims description 2
- LQAPOTKKMIZDGP-UHFFFAOYSA-N 3,3,4,4,5,5,5-heptafluoropent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=C LQAPOTKKMIZDGP-UHFFFAOYSA-N 0.000 claims description 2
- GVEUEBXMTMZVSD-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,6-nonafluorohex-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C=C GVEUEBXMTMZVSD-UHFFFAOYSA-N 0.000 claims description 2
- AMSKBEPWWFORCT-UHFFFAOYSA-N 3,3,4,4,5,5,6,6-octafluorohex-1-ene Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)C=C AMSKBEPWWFORCT-UHFFFAOYSA-N 0.000 claims description 2
- BNLLWAALHYCOQM-UHFFFAOYSA-N 3,3,4,4-tetrafluorobut-1-ene Chemical compound FC(F)C(F)(F)C=C BNLLWAALHYCOQM-UHFFFAOYSA-N 0.000 claims description 2
- GHTJJDFBXCKNEO-UHFFFAOYSA-N 3,3,4,4-tetrafluorocyclobutene Chemical compound FC1(F)C=CC1(F)F GHTJJDFBXCKNEO-UHFFFAOYSA-N 0.000 claims description 2
- RBMOVUILDUBRGH-UHFFFAOYSA-N 3,3,4,5,5,5-hexafluoropent-1-ene Chemical compound FC(F)(F)C(F)C(F)(F)C=C RBMOVUILDUBRGH-UHFFFAOYSA-N 0.000 claims description 2
- YOIHZDOLVJDWDY-UHFFFAOYSA-N 3,4,4,4-tetrafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC(F)(F)C(F)(C=C)C(F)(F)F YOIHZDOLVJDWDY-UHFFFAOYSA-N 0.000 claims description 2
- YCJCPOBHORUPPD-UHFFFAOYSA-N 3,4,4,5,5,5-hexafluoropent-2-ene Chemical compound CC=C(F)C(F)(F)C(F)(F)F YCJCPOBHORUPPD-UHFFFAOYSA-N 0.000 claims description 2
- SCFVSGJMZBDUNL-UHFFFAOYSA-N 3,4,4,5,5,6,6,6-octafluorohex-2-ene Chemical compound CC=C(F)C(F)(F)C(F)(F)C(F)(F)F SCFVSGJMZBDUNL-UHFFFAOYSA-N 0.000 claims description 2
- PEKLMCIOHLIAQH-UHFFFAOYSA-N 3-(difluoromethylidene)-1,1,1,5,5,5-hexafluoropentane Chemical compound FC(=C(CC(F)(F)F)CC(F)(F)F)F PEKLMCIOHLIAQH-UHFFFAOYSA-N 0.000 claims description 2
- JIZADPXDLBDMAY-UHFFFAOYSA-N 4,4,4-trifluoro-2-(trifluoromethyl)but-1-ene Chemical compound FC(F)(F)CC(=C)C(F)(F)F JIZADPXDLBDMAY-UHFFFAOYSA-N 0.000 claims description 2
- OMHQNXCLPDUMDM-UHFFFAOYSA-N 4,4,4-trifluoro-3,3-bis(trifluoromethyl)but-1-ene Chemical compound FC(F)(F)C(C=C)(C(F)(F)F)C(F)(F)F OMHQNXCLPDUMDM-UHFFFAOYSA-N 0.000 claims description 2
- QUBWAWBAEZVWFL-UHFFFAOYSA-N 4,4,5,5,5-pentafluoro-2-(trifluoromethyl)pent-1-ene Chemical compound FC(F)(F)C(=C)CC(F)(F)C(F)(F)F QUBWAWBAEZVWFL-UHFFFAOYSA-N 0.000 claims description 2
- VJOOWZFVJAJKPV-UHFFFAOYSA-N 4,4,5,5,6,6,6-heptafluorohex-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)CC=C VJOOWZFVJAJKPV-UHFFFAOYSA-N 0.000 claims description 2
- NVUXCFNCNLOREY-UHFFFAOYSA-N 7,7,7-trifluorohept-3-ene Chemical compound CCC=CCCC(F)(F)F NVUXCFNCNLOREY-UHFFFAOYSA-N 0.000 claims description 2
- IRZZTMWOOGFLBN-UHFFFAOYSA-N 9,9,9-trifluoronon-4-ene Chemical compound CCCC=CCCCC(F)(F)F IRZZTMWOOGFLBN-UHFFFAOYSA-N 0.000 claims description 2
- 229910016467 AlCl 4 Inorganic materials 0.000 claims description 2
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 claims description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims description 2
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910018286 SbF 6 Inorganic materials 0.000 claims description 2
- 239000007983 Tris buffer Substances 0.000 claims description 2
- 239000001273 butane Substances 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- WMIYKQLTONQJES-UHFFFAOYSA-N hexafluoroethane Chemical compound FC(F)(F)C(F)(F)F WMIYKQLTONQJES-UHFFFAOYSA-N 0.000 claims description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 2
- 239000001282 iso-butane Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019407 octafluorocyclobutane Nutrition 0.000 claims description 2
- 229960004065 perflutren Drugs 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 238000005086 pumping Methods 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 claims 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 claims 2
- KQWUAJHKKHLDSO-UHFFFAOYSA-N 1,1,1,2,2,3,3,6,6,7,7,8,8,9,9,10,10,10-octadecafluorodec-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F KQWUAJHKKHLDSO-UHFFFAOYSA-N 0.000 claims 1
- UJFNGAXYSRQBOH-UHFFFAOYSA-N 1,1,1,2,2,3,3,7,7,8,8,8-dodecafluoro-6,6-bis(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)C(F)(F)F UJFNGAXYSRQBOH-UHFFFAOYSA-N 0.000 claims 1
- WJJSBSLCSMLZIR-UHFFFAOYSA-N 1,1,1,2,2,6,6,7,7,7-decafluoro-5,5-bis(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)C(F)(F)F WJJSBSLCSMLZIR-UHFFFAOYSA-N 0.000 claims 1
- HSJSUZZRDOPOCQ-UHFFFAOYSA-N 1,1,1,2,4,4,5,5,5-nonafluoro-3-methylpent-2-ene Chemical compound FC(F)(F)C(F)=C(C)C(F)(F)C(F)(F)F HSJSUZZRDOPOCQ-UHFFFAOYSA-N 0.000 claims 1
- FWOBGHOPUVPBLC-UHFFFAOYSA-N 1,1,1,6,6,6-hexafluoro-2,2,5,5-tetrakis(trifluoromethyl)hex-3-ene Chemical compound FC(F)(F)C(C(F)(F)F)(C(F)(F)F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)F FWOBGHOPUVPBLC-UHFFFAOYSA-N 0.000 claims 1
- YLJDUZGXRKGBJW-UHFFFAOYSA-N 1,1,1-trifluorohex-3-ene Chemical compound CCC=CCC(F)(F)F YLJDUZGXRKGBJW-UHFFFAOYSA-N 0.000 claims 1
- 238000003682 fluorination reaction Methods 0.000 claims 1
- CVMVAHSMKGITAV-OWOJBTEDSA-N (e)-1,1,1,4,4,5,5,5-octafluoropent-2-ene Chemical compound FC(F)(F)\C=C\C(F)(F)C(F)(F)F CVMVAHSMKGITAV-OWOJBTEDSA-N 0.000 description 1
- OPUDNJOIACEIEI-OWOJBTEDSA-N (e)-1,1,1,4,5,5,5-heptafluoro-4-(trifluoromethyl)pent-2-ene Chemical compound FC(F)(F)\C=C\C(F)(C(F)(F)F)C(F)(F)F OPUDNJOIACEIEI-OWOJBTEDSA-N 0.000 description 1
- LDTMPQQAWUMPKS-UPHRSURJSA-N (z)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C/Cl LDTMPQQAWUMPKS-UPHRSURJSA-N 0.000 description 1
- JDSAEJDPKZFUOX-UHFFFAOYSA-N 1,1,1,2,2,3,3,6,6,7,8,8,8-tridecafluoro-7-(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F JDSAEJDPKZFUOX-UHFFFAOYSA-N 0.000 description 1
- DYJSLBOHTCEJEH-UHFFFAOYSA-N 1,1,1,2,2,3,6,6,7,7,8,8,9,9,9-pentadecafluoro-3-(trifluoromethyl)non-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)F DYJSLBOHTCEJEH-UHFFFAOYSA-N 0.000 description 1
- MBSZRYOIDYIQCQ-UHFFFAOYSA-N 1,1,1,2,2,3,6,7,7,8,8,8-dodecafluoro-3,6-bis(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(F)C(F)(C(F)(F)F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)F MBSZRYOIDYIQCQ-UHFFFAOYSA-N 0.000 description 1
- JXCIOROGZZLKPJ-UHFFFAOYSA-N 1,1,1,2,3,3,6,6,7,8,8,8-dodecafluoro-2,7-bis(trifluoromethyl)oct-4-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C(F)(F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F JXCIOROGZZLKPJ-UHFFFAOYSA-N 0.000 description 1
- MQBOTKTYOQSXMC-UHFFFAOYSA-N 1,1,1,2,6,6,6-heptafluoro-2,5,5-tris(trifluoromethyl)hex-3-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)F MQBOTKTYOQSXMC-UHFFFAOYSA-N 0.000 description 1
- BRHMFXVXLONVKC-UHFFFAOYSA-N 1,1,1,4,4,5,5,6,6,6-decafluorohex-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)F BRHMFXVXLONVKC-UHFFFAOYSA-N 0.000 description 1
- SXSREXZPYXYIST-UHFFFAOYSA-N 1,1,1,4,4,5,5,6,6,7,7,8,8,9,9,9-hexadecafluoronon-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SXSREXZPYXYIST-UHFFFAOYSA-N 0.000 description 1
- ZWBUGYHKBYWABL-UHFFFAOYSA-N 1,1,1,5,5,5-hexafluoro-4,4-bis(trifluoromethyl)pent-2-ene Chemical compound FC(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)F ZWBUGYHKBYWABL-UHFFFAOYSA-N 0.000 description 1
- YTODRVVPUGSOKX-UHFFFAOYSA-N 1,4,4,4-tetrafluoro-3-methylbut-1-ene Chemical compound FC=CC(C)C(F)(F)F YTODRVVPUGSOKX-UHFFFAOYSA-N 0.000 description 1
- FHQKLIHFKVAEEP-UHFFFAOYSA-N 3,3,4,4,5,5-hexafluorocyclopentene Chemical compound FC1(F)C=CC(F)(F)C1(F)F FHQKLIHFKVAEEP-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- FSOCDJTVKIHJDC-UHFFFAOYSA-N bis(perfluorobutyl)ethene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)F FSOCDJTVKIHJDC-UHFFFAOYSA-N 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- WZHKDGJSXCTSCK-UHFFFAOYSA-N hept-3-ene Chemical compound CCCC=CCC WZHKDGJSXCTSCK-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical group Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 description 1
Description
結晶化抑制剤としては、2009年11月6日出願の同時係属PCT特許出願第PCT/US09/63599号明細書ならびに2009年3月31日出願の同時係属米国特許仮出願第61/165,089号明細書、第61/165,093号明細書、第61/165,147号明細書、第61/165,155号明細書、第61/165,160号明細書、第61/165,161号明細書、第61/165,166号明細書および第61/165,173号明細書に記載された化合物が挙げられる。
以下に、本発明の好ましい態様を示す。
[1] (a)作動流体を吸収剤に吸収して、吸収剤と作動流体との混合物を形成するための吸収器と、
(b)前記吸収剤および作動流体を前記吸収器から受けて予熱するために、前記吸収器と流体連通して配置された第1の熱交換器と、
(c)前記吸収剤と作動流体との混合物を、前記吸収器から前記第1の熱交換器までポンピングするための液体ポンプと、
(d)前記第1の熱交換器から前記予熱混合物を受け、追加の熱を前記予備混合物に移すことによって前記作動流体の高圧蒸気を放出するための、前記第1の熱交換器と流体連通して配置された発電機発生器と、
(e)前記高圧作動流体から機械仕事を生じさせるために、前記発電機発生器と流体連通して配置された機械仕事を生じさせるためのデバイスと
を含み、前記吸収剤がイオン液体を含む、吸収パワーサイクルシステム。
[2] (a)前記機械仕事を生じさせるためのデバイスから出る前記高圧作動流体を凝縮する凝縮器と、
(b)前記圧力を減じ、前記作動流体を部分的に蒸発させるための膨張デバイスと、
(c)前記作動流体を完全に蒸発させて、冷却を行うための蒸発器と
をさらに含む、[1]に記載の吸収パワーサイクルシステム。
[3] 前記イオン液体が、カチオンとアニオンとを含み、前記カチオンが、リチウム、ナトリウム、カリウム、セシウム、および以下の式
式中、R1、R2、R3、R4、R5、R6、R12およびR13は、
(i)H、
(ii)ハロゲン、
(iii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iv)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(v)C6〜C20非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25非置換ヘテロアリール、および
(vi) C6〜C25置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25置換ヘテロアリールであって、前記置換アリールまたは置換ヘテロアリールが、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有するもの
からなる群から独立して選択され、
R7、R8、R9およびR10は、
(i)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(ii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iii)C6〜C25非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25非置換ヘテロアリール、および
(iv)C6〜C25置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25置換ヘテロアリールであって、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有する置換アリールまたは置換ヘテロアリール
からなる群から独立して選択され、
任意選択的に、R1、R2、R3、R4、R5、R6、R7、R8、R9およびR10の少なくとも2つが一緒になって、環状または二環式のアルカニルまたはアルケニル基を形成することができ、
前記アニオンが、
[CH3CO2]-、[HSO4]-、[CH3OSO3]-、[C2H5OSO3]-、[AlCl4]-、[CO3]2-、[HCO3]-、[NO2]-、[NO3]-、[SO4]2-、[PO3]3-、[HPO3]2-、[H2PO3]1-、[PO4]3-、[HPO4]2-、[H2PO4]-、[HSO3]-、[CuCl2]-、Cl-、Br-、I-、SCN-、BR1R2R3R4、BOR1OR2OR3OR4、任意選択的にアルキルまたは置換アルキルで置換されたカーボレート(1−カルバドデカボレート(1−))、任意選択的にアルキルアミン、置換アルキルアミン、アルキルまたは置換アルキルで置換されたカーボラン(ジカルバドデカボレート(1−))、[BF4]-、[PF6]-、[SbF6]-、[CF3SO3]-、[HCF2CF2SO3]-、[CF3HFCCF2SO3]-、[HCClFCF2SO3]-、[(CF3SO2)2N]-、[(CF3CF2SO2)2N]-、[(CF3SO2)3C]-、[CF3CO2]-、[CF3OCFHCF2SO3]-、[CF3CF2OCFHCF2SO3]-、[CF3CFHOCF2CF2SO3]-、[CF2HCF2OCF2CF2SO3]-、[CF2ICF2OCF2CF2SO3]-、[CF3CF2OCF2CF2SO3]-、[(CF2HCF2SO2)2N]-、[(CF3CFHCF2SO2)2N]-、F-および式
(式中、R11は、
(i)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(ii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iii)C6〜C10非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C10非置換ヘテロアリール、および
(iv)C6〜C10置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C10置換ヘテロアリールであって、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有する置換アリールまたは置換ヘテロアリール
からなる群から独立して選択され、
任意選択的により、R1、R2、R3、R4、R5、R6、R7、R8、R9およびR10の少なくとも2つが一緒になって、環状または二環式のアルカニルまたはアルケニル基を形成することができる)
[1]に記載の吸収パワーサイクルシステム。
[4] 前記作動流体が水またはアンモニアを含む、[1]に記載の吸収パワーサイクルシステム。
[5] 前記作動流体が、ヒドロフルオロカーボン、ヒドロクロロフルオロカーボン、クロロフルオロカーボン、フルオロカーボン、窒素(N2)、酸素(O2)、二酸化炭素(CO2)、アルゴン(Ar)、水素(H2)、フッ素化されていないヒドロカーボン、メタノールおよび前述したもののいずれかの混合物からなる群から選択される作動流体を含む、[1]に記載の吸収パワーサイクルシステム。
[6] 前記フッ素化されていないヒドロカーボンは、C1〜C7の直鎖状、分枝状または環状のアルカンおよびC1〜C7の直鎖状、分枝状または環状のアルケンからなる群から選択される、[5]に記載の吸収パワーサイクルシステム。
[7] 前記作動流体が、
(i)式E−R1CH=CHR2またはZ−R1CH=CHR2(式中、R1およびR2は、独立に、C1〜C6パーフルオロアルキル基である)のフルオロオレフィン、
(ii)式シクロ−[CX=CY(CZW)n−](式中、X、Y、ZおよびWは、独立に、HまたはFであり、nは2〜5の整数である)の環状フルオロオレフィン、および
(iii)テトラフルオロエチレン(CF2=CF2)、ヘキサフルオロプロペン(CF3CF=CF2)、1,2,3,3,3−ペンタフルオロ−1−プロペン(CHF=CFCF3)、1,1,3,3,3−ペンタフルオロ−1−プロペン(CF2=CHCF3)、1,1,2,3,3−ペンタフルオロ−1−プロペン(CF2=CFCHF2)、1,2,3,3−テトラフルオロ−1−プロペン(CHF=CFCHF2)、2,3,3,3−テトラフルオロ−1−プロペン(CH2=CFCF3)、1,3,3,3−テトラフルオロ−1−プロペン(CHF=CHCF3)、1,1,2,3−テトラフルオロ−1−プロペン(CF2=CFCH2F)、1,1,3,3−テトラフルオロ−1−プロペン(CF2=CHCHF2)、1,2,3,3−テトラフルオロ−1−プロペン(CHF=CFCHF2)、3,3,3−トリフルオロ−1−プロペン(CH2=CHCF3)、2,3,3−トリフルオロ−1−プロペン(CHF2CF=CH2)、1,1,2−トリフルオロ−1−プロペン(CH3CF=CF2)、1,2,3−トリフルオロ−1−プロペン(CH2FCF=CF2)、1,1,3−トリフルオロ−1−プロペン(CH2FCH=CF2)、1,3,3−トリフルオロ−1−プロペン(CHF2CH=CHF)、1,1,1,2,3,4,4,4−オクタフルオロ−2−ブテン(CF3CF=CFCF3)、1,1,2,3,3,4,4,4−オクタフルオロ−1−ブテン(CF3CF2CF=CF2)、1,1,1,2,4,4,4−ヘプタフルオロ−2−ブテン(CF3CF=CHCF3)、1,2,3,3,4,4,4−ヘプタフルオロ−1−ブテン(CHF=CFCF2CF3)、1,1,1,2,3,4,4−ヘプタフルオロ−2−ブテン(CHF2CF=CFCF3)、1,3,3,3−テトラフルオロ−2−(トリフルオロメチル)−1−プロペン((CF3)2C=CHF)、1,1,3,3,4,4,4−ヘプタフルオロ−1−ブテン(CF2=CHCF2CF3)、1,1,2,3,4,4,4−ヘプタフルオロ−1−ブテン(CF2=CFCHFCF3)、1,1,2,3,3,4,4−ヘプタフルオロ−1−ブテン(CF2=CFCF2CHF2)、2,3,3,4,4,4−ヘキサフルオロ−1−ブテン(CF3CF2CF=CH2)、1,3,3,4,4,4−ヘキサフルオロ−1−ブテン(CHF=CHCF2CF3)、1,2,3,4,4,4−ヘキサフルオロ−1−ブテン(CHF=CFCHFCF3)、1,2,3,3,4,4−ヘキサフルオロ−1−ブテン(CHF=CFCF2CHF2)、1,1,2,3,4,4−ヘキサフルオロ−2−ブテン(CHF2CF=CFCHF2)、1,1,1,2,3,4−ヘキサフルオロ−2−ブテン(CH2FCF=CFCF3)、1,1,1,2,4,4−ヘキサフルオロ−2−ブテン(CHF2CH=CFCF3)、1,1,1,3,4,4−ヘキサフルオロ−2−ブテン(CF3CH=CFCHF2)、1,1,2,3,3,4−ヘキサフルオロ−1−ブテン(CF2=CFCF2CH2F)、1,1,2,3,4,4−ヘキサフルオロ−1−ブテン(CF2=CFCHFCHF2)、3,3,3−トリフルオロ−2−(トリフルオロメチル)−1−プロペン(CH2=C(CF3)2)、1,1,1,2,4−ペンタフルオロ−2−ブテン(CH2FCH=CFCF3)、1,1,1,3,4−ペンタフルオロ−2−ブテン(CF3CH=CFCH2F)、3,3,4,4,4−ペンタフルオロ−1−ブテン(CF3CF2CH=CH2)、1,1,1,4,4−ペンタフルオロ−2−ブテン(CHF2CH=CHCF3)、1,1,1,2,3−ペンタフルオロ−2−ブテン(CH3CF=CFCF3)、2,3,3,4,4−ペンタフルオロ−1−ブテン(CH2=CFCF2CHF2)、1,1,2,4,4−ペンタフルオロ−2−ブテン(CHF2CF=CHCHF2)、1,1,2,3,3−ペンタフルオロ−1−ブテン(CH3CF2CF=CF2)、1,1,2,3,4−ペンタフルオロ−2−ブテン(CH2FCF=CFCHF2)、1,1,3,3,3−ペンタフルオロ−2−メチル−1−プロペン(CF2=C(CF3)(CH3))、2−(ジフルオロメチル)−3,3,3−トリフルオロ−1−プロペン(CH2=C(CHF2)(CF3))、2,3,4,4,4−ペンタフルオロ−1−ブテン(CH2=CFCHFCF3)、1,2,4,4,4−ペンタフルオロ−1−ブテン(CHF=CFCH2CF3)、1,3,4,4,4−ペンタフルオロ−1−ブテン(CHF=CHCHFCF3)、1,3,3,4,4−ペンタフルオロ−1−ブテン(CHF=CHCF2CHF2)、1,2,3,4,4−ペンタフルオロ−1−ブテン(CHF=CFCHFCHF2)、3,3,4,4−テトラフルオロ−1−ブテン(CH2=CHCF2CHF2)、1,1−ジフルオロ−2−(ジフルオロメチル)−1−プロペン(CF2=C(CHF2)(CH3))、1,3,3,3−テトラフルオロ−2−メチル−1−プロペン(CHF=C(CF3)(CH3))、3,3−ジフルオロ−2−(ジフルオロメチル)−1−プロペン(CH2=C(CHF2)2)、1,1,1,2−テトラフルオロ−2−ブテン(CF3CF=CHCH3)、1,1,1,3−テトラフルオロ−2−ブテン(CH3CF=CHCF3)、1,1,1,2,3,4,4,5,5,5−デカフルオロ−2−ペンテン(CF3CF=CFCF2CF3)、1,1,2,3,3,4,4,5,5,5−デカフルオロ−1−ペンテン(CF2=CFCF2CF2CF3)、1,1,1,4,4,4−ヘキサフルオロ−2−(トリフルオロメチル)−2−ブテン((CF3)2C=CHCF3)、1,1,1,2,4,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CF=CHCF2CF3)、1,1,1,3,4,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CH=CFCF2CF3)、1,2,3,3,4,4,5,5,5−ノナフルオロ−1−ペンテン(CHF=CFCF2CF2CF3)、1,1,3,3,4,4,5,5,5−ノナフルオロ−1−ペンテン(CF2=CHCF2CF2CF3)、1,1,2,3,3,4,4,5,5−ノナフルオロ−1−ペンテン(CF2=CFCF2CF2CHF2)、1,1,2,3,4,4,5,5,5−ノナフルオロ−2−ペンテン(CHF2CF=CFCF2CF3)、1,1,1,2,3,4,4,5,5−ノナフルオロ−2−ペンテン(CF3CF=CFCF2CHF2)、1,1,1,2,3,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CF=CFCHFCF3)、1,2,3,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CFCF(CF3)2)、1,1,2,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CFCH(CF3)2)、1,1,1,4,4,4−ヘキサフルオロ−2−(トリフルオロメチル)−2−ブテン(CF3CH=C(CF3)2)、1,1,3,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CHCF(CF3)2)、2,3,3,4,4,5,5,5−オクタフルオロ−1−ペンテン(CH2=CFCF2CF2CF3)、1,2,3,3,4,4,5,5−オクタフルオロ−1−ペンテン(CHF=CFCF2CF2CHF2)、3,3,4,4,4−ペンタフルオロ−2−(トリフルオロメチル)−1−ブテン(CH2=C(CF3)CF2CF3)、1,1,4,4,4−ペンタフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CHCH(CF3)2)、1,3,4,4,4−ペンタフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CHCF(CF3)2)、1,1,4,4,4−ペンタフルオロ−2−(トリフルオロメチル)−1−ブテン(CF2=C(CF3)CH2CF3)、3,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン((CF3)2CFCH=CH2)、3,3,4,4,5,5,5−ヘプタフルオロ−1−ペンテン(CF3CF2CF2CH=CH2)、2,3,3,4,4,5,5−ヘプタフルオロ−1−ペンテン(CH2=CFCF2CF2CHF2)、1,1,3,3,5,5,5−ヘプタフルオロ−1−ブテン(CF2=CHCF2CH2CF3)、1,1,1,2,4,4,4−ヘプタフルオロ−3−メチル−2−ブテン(CF3CF=C(CF3)(CH3))、2,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン(CH2=CFCH(CF3)2)、1,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CHCH(CF3)2)、1,1,1,4−テトラフルオロ−2−(トリフルオロメチル)−2−ブテン(CH2FCH=C(CF3)2)、1,1,1,3−テトラフルオロ−2−(トリフルオロメチル)−2−ブテン(CH3CF=C(CF3)2)、1,1,1−トリフルオロ−2−(トリフルオロメチル)−2−ブテン((CF3)2C=CHCH3)、3,4,4,5,5,5−ヘキサフルオロ−2−ペンテン(CF3CF2CF=CHCH3)、1,1,1,4,4,4−ヘキサフルオロ−2−メチル−2−ブテン(CF3C(CH3)=CHCF3)、3,3,4,5,5,5−ヘキサフルオロ−1−ペンテン(CH
2=CHCF2CHFCF3)、4,4,4−トリフルオロ−2−(トリフルオロメチル)−1−ブテン(CH2=C(CF3)CH2CF3)、1,1,2,3,3,4,4,5,5,6,6,6−ドデカフルオロ−1−ヘキセン(CF3(CF2)3CF=CF2)、1,1,1,2,2,3,4,5,5,6,6,6−ドデカフルオロ−3−ヘキセン(CF3CF2CF=CFCF2CF3)、1,1,1,4,4,4−ヘキサフルオロ−2,3−ビス(トリフルオロメチル)−2−ブテン((CF3)2C=C(CF3)2)、1,1,1,2,3,4,5,5,5−ノナフルオロ−4−(トリフルオロメチル)−2−ペンテン((CF3)2CFCF=CFCF3)、1,1,1,4,4,5,5,5−オクタフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CHC2F5)、1,1,1,3,4,5,5,5−オクタフルオロ−4−(トリフルオロメチル)−2−ペンテン((CF3)2CFCF=CHCF3)、3,3,4,4,5,5,6,6,6−ノナフルオロ−1−ヘキセン(CF3CF2CF2CF2CH=CH2)、4,4,4−トリフルオロ−3,3−ビス(トリフルオロメチル)−1−ブテン(CH2=CHC(CF3)3)、1,1,1,4,4,4−ヘキサフルオロ−3−メチル−2−(トリフルオロメチル)−2−ブテン((CF3)2C=C(CH3)(CF3))、2,3,3,5,5,5−ヘキサフルオロ−4−(トリフルオロメチル)−1−ペンテン(CH2=CFCF2CH(CF3)2)、1,1,1,2,4,4,5,5,5−ノナフルオロ−3−メチル−2−ペンテン(CF3CF=C(CH3)CF2CF3)、1,1,1,5,5,5−ヘキサフルオロ−4−(トリフルオロメチル)−2−ペンテン(CF3CH=CHCH(CF3)2)、3,4,4,5,5,6,6,6−オクタフルオロ−2−ヘキセン(CF3CF2CF2CF=CHCH3)、3,3,4,4,5,5,6,6−オクタフルオロ1−ヘキセン(CH2=CHCF2CF2CF2CHF2)、1,1,1,4,4−ペンタフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CHCF2CH3)、4,4,5,5,5−ペンタフルオロ−2−(トリフルオロメチル)−1−ペンテン(CH2=C(CF3)CH2C2F5)、3,3,4,4,5,5,5−ヘプタフルオロ−2−メチル−1−ペンテン(CF3CF2CF2C(CH3)=CH2)、4,4,5,5,6,6,6−ヘプタフルオロ−2−ヘキセン(CF3CF2CF2CH=CHCH3)、4,4,5,5,6,6,6−ヘプタフルオロ−1−ヘキセン(CH2=CHCH2CF2C2F5)、1,1,1,2,2,3,4−ヘプタフルオロ−3−ヘキセン(CF3CF2CF=CFC2H5)、4,5,5,5−テトラフルオロ−4−(トリフルオロメチル)−1−ペンテン(CH2=CHCH2CF(CF3)2)、1,1,1,2,5,5,5−ヘプタフルオロ−4−メチル−2−ペンテン(CF3CF=CHCH(CF3)(CH3))、1,1,1,3−テトラフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CFC2H5)、1,1,1,2,3,4,4,5,5,6,6,7,7,7−テトラデカフルオロ−2−ヘプテン(CF3CF=CFCF2CF2C2F5)、1,1,1,2,2,3,4,5,5,6,6,7,7,7−テトラデカフルオロ−3−ヘプテン(CF3CF2CF=CFCF2C2F5)、1,1,1,3,4,4,5,5,6,6,7,7,7−トリデカフルオロ−2−ヘプテン(CF3CH=CFCF2CF2C2F5)、1,1,1,2,4,4,5,5,6,6,7,7,7−トリデカフルオロ−2−ヘプテン(CF3CF=CHCF2CF2C2F5)、1,1,1,2,2,4,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(CF3CF2CH=CFCF2C2F5)および1,1,1,2,2,3,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(CF3CF2CF=CHCF2C2F5)からなる群から選択されるフルオロオレフィンからなる群から選択される少なくとも1つのヒドロフルオロカーボンまたはフルオロカーボンを含む、[5]に記載の吸収パワーサイクルシステム。
[8] 前記フルオロオレフィンが、1,1,1,4,4,4−ヘキサフルオロブタ−2−エン、1,1,1,4,4,5,5,5−オクタフルオロペンタ−2−エン、1,1,1,4,4,5,5,6,6,6−デカフルオロヘキサ−2−エン、1,1,1,4,5,5,5−ヘプタフルオロ−4−(トリフルオロメチル)ペンタ−2−エン、1,1,1,2,2,5,5,6,6,6−デカフルオロヘキサ−3−エン、1,1,1,4,4,5,5,6,6,7,7,7−ドデカフルオロヘプタ−2−エン、1,1,1,4,4,5,6,6,6−ノナフルオロ−5−(トリフルオロメチル)ヘキサ−2−エン、1,1,1,4,5,5,6,6,6−ノンフルオロ−4−(トリフルオロメチル)ヘキサ−2−エン、1,1,1,5,5,5−ヘキサフルオロ−4,4−ビス(トリフルオロメチル)ペンタ−2−エン、1,1,1,2,2,5,5,6,6,7,7,7−ドデカフルオロヘプタ−3−エン、1,1,1,2,2,5,6,6,6−ノナフルオロ−5−(トリフルオロメチル)ヘキサ−3−エン、1,1,1,4,4,5,5,6,6,7,7,8,8,8−テトラデカフルオロオクタ−2−エン、1,1,1,4,4,5,5,6,7,7,7−ウンデカフルオロ−6−(トリフルオロメチル)ヘプタ−2−エン、1,1,1,5,5,6,6,6−オクタフルオロ−4,4−ビス(トリフルオロメチル)ヘキサ−2−エン、1,1,1,2,2,5,5,6,6,7,7,8,8,8−テトラデカフルオロオクタ−3−エン、1,1,1,2,2,5,5,6,7,7,7−ウンデカフルオロ−6−(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,2,5,6,6,7,7,7−ウンデカフルオロ−5−(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,2,6,6,6−オクタフルオロ−5,5−ビス(トリフルオロメチル)ヘキサ−3−エン、1,1,1,2,2,3,3,6,6,7,7,8,8,8−テトラデカフルオロオクタ−4−エン、1,1,1,2,5,6,6,6−オクタフルオロ−2,5−ビス(トリフルオロメチル)ヘキサ−3−エン、1,1,1,2,5,5,6,6,7,7,7−ウンデカフルオロ−2−(トリフルオロメチル)ヘプタ−3−エン、1,1,1,4,4,5,5,6,6,7,7,8,8,9,9,9−ヘキサデカフルオロノナ−2−エン、1,1,1,4,5,5,6,6,7,7,8,8,8−トリデカフルオロ−4−(トリフルオロメチル)ヘプタ−2−エン、1,1,1,6,6,6−オクタフルオロ−4,4−ビス(トリフルオロメチル)ヘプタ−2−エン、1,1,1,2,2,5,5,6,6,7,7,8,8,9,9,9−ヘキサデカフルオロノナ−3−エン、1,1,1,2,2,5,5,6,6,7,8,8,8−トリデカフルオロ−7−(トリフルオロメチル)オクタ−3−エン、1,1,1,2,2,6,6,7,7,7−デカフルオロ−5,5−ビス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,2,3,3,6,6,7,7,8,8,9,9,9−ヘキサデカフルオロノナ−4−エン、1,1,1,2,2,3,3,6,6,7,8,8,8−トリデカフルオロ−7−(トリフルオロメチル)オクタ−4−エン、1,1,1,2,2,3,3,6,7,7,8,8,8−トリデカフルオロ−6−(トリフルオロメチル)オクタ−4−エン、1,1,1,5,5,6,6,7,7,7−デカフルオロ−2,2−ビス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,5,5,6,6,7,7,8,8,8−トリデカフルオロ−2(トリフルオロメチル)オクタ−3−エン、1,1,1,2,5,5,6,7,7,7−デカフルオロ−2,6−ビス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,5,6,6,7,7,7−デカフルオロ−2,5−ビス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,6,6,6−ヘプタフルオロ−2,5,5−トリス(トリフルオロメチル)ヘキサ−3−エン、1,1,1,2,2,5,5,6,6,7,7,8,8,9,9,10,10,10−オクタデカフルオロデカ−3−エン、1,1,1,2,2,5,6,6,7,7,8,8,9,9,9−ペンタデカフルオロ−5−(トリフルオロメチル)ノナ−3−エン、1,1,1,2,2,6,6,7,7,8,8,8−ドデカフルオロ−5,5−ビス(トリフルオロメチル)オクタ−3−エン、1,1,1,2,2,3,3,6,6,7,7,8,8,9,9,10,10,10−オクタデカフルオロデカ−4−エン、1,1,1,2,2,3,3,6,6,7,7,8,9,9,9−ペンタデカフルオロ−8−(トリフルオロメチル)ノナ−4−エン、1,1,1,2,2,3,3,7,7,8,8,8−ドデカフルオロ−6,6−ビス(トリフルオロメチル)オクタ−4−エン、1,1,1,2,5,5,6,6,7,7,8,8,9,9,9−ペンタデカフルオロ−2−(トリフルオロメチル)ノナ−3−エン、1,1,1,2,5,5,6,6,7,8,8,8−ドデカフルオロ−2,7−ビス(トリフルオロメチル)オクタ−3−エン、1,1,1,2,6,6,7,7,7−ノナフルオロ−2,5,5−トリス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,2,3,3,4,4,7,7,8,8,9,9,10,10,10−オクタデカフルオロデカ−5−エン、1,1,1,2,3,3,6,6,7,7,8,8,9,9,9−ペンタデカフルオロ−2−(トリフルオロメチル)ノナ−4−エン、1,1,1,2,2,3,6,6,7,7,8,8,9,9,9−ペンタデカフルオロ−3−(トリフルオロメチル)ノナ−4−エン、1,1,1,5,5,6,6,7,7,8,8,8−ドデカフルオロ−2,2,−ビス(トリフルオロメチル)オクタ−3−エン、1,1,1,2,3,3,6,6,7,8,8,8−ドデカフルオロ−2,7−ビス(トリフルオロメチル)オクタ−4−エン、1,1,1,2,3,3,6,7,7,8,8,8−ドデカフルオロ−2,6−ビス(トリフルオロメチル)オクタ−4−エン、1,1,1,5,5,6,7,7,7−ノナフルオロ−2,2,6−トリス(トリフルオロメチル)ヘプタ−3−エン、1,1,1,2,2,3,6,7,7,8,8,8−ドデカフルオロ−3,6−ビス(トリフルオロメチル)オクタ−4−エン、1,1,1,2,2,3,6,7,7,8,8,8−ドデカフルオロ−3,6−ビス(トリフルオロメチル)オクタ−4−エン、1,1,1,5,6,6,7,7,7−ノナフルオロ−2,2,5−トリス(トリフルオロメチル)ヘプタ−3−エンおよび1,1,1,6,6,6−ヘキサフルオロ−2,2,5,5−テトラキス(トリフルオロメチル)ヘキサ−3−エンからなる群から選択される、[7]に記載の吸収パワーサイクルシステム。
[9] 前記フルオロオレフィンが、1,2,3,3,4,4−ヘキサフルオロシクロブテン、3,3,4,4−テトラフルオロシクロブテン、3,3,4,4,5,5,−ヘキサフルオロシクロペンテン、1,2,3,3,4,4,5,5−オクタフルオロシクロペンテンおよび1,2,3,3,4,4,5,5,6,6−デカフルオロシクロヘキセンからなる群から選択される、[7]に記載の吸収パワーサイクルシステム。
[10] 前記作動流体が、ジフルオロメタン(HFC−32)、ペンタフルオロエタン(HFC−125)、1,1,2,2−テトラフルオロエタン(HFC−134)、1,1,1,2−テトラフルオロエタン(HFC−134a)、1,1,1−トリフルオロエタン(HFC−143a)、1,1−ジフルオロエタン(HFC−152a)、フルオロエタン(HFC−161)、1,1,1,3,3−ペンタフルオロプロパン(HFC−245fa)、1,1,1,3,3,3−ヘキサフルオロプロパン(HFC−236fa)、1,1,1,2,3,3,3−ヘプタフルオロプロパン(HFC−227ea)、1,1,1,3,3−ペンタフルオロブタン(HFC−365mfc)、1,1,1,2,3,4,4,5,5,5−デカフルオロペンタン(HFC−43−10mee)、1,1,1,2,2,3,4,5,5,6,6,7,7,7−テトラデカフルオロヘプタン(HFC−63−14mcee)、2,3,3,3−テトラフルオロプロペン(HFO−1234yf)、1,3,3,3−テトラフルオロプロペン(HFO−1234ze)、1,2,3,3−テトラフルオロプロペン(HFO−1234ye)、3,3,3−トリフルオロプロペン(HFO−1243zf)、1,2,3,3,3−ペンタフルオロプロペン(HFO−1225ye)、1,1,1,3,3−ペンタフルオロプロペン(HFO−1225zc)、1,1,1,2,2,4,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(HFO−162−13mczy)および1,1,1,2,2,3,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(HFO−162−13mcyz)、ジクロロジフルオロメタン(CFC−12)、フルオロトリクロロメタン(CFC−11)、1,1,2−トリクロロ−1,2,2−トリフルオロエタン(CFC−113)、1,2−ジクロロ−1,1,2,2−テトラフルオロエタン(CFC−114)、クロロジフルオロメタン(HCFC−22)、2−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233xf)、1−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233zd)、パーフルオロメタン(FC−14)、パーフルオロエタン(FC−116)、パーフルオロプロパン(FC−218)、パーフルオロシクロブタン(FC−C318)、オクタフルオロ−2−ブテン(FO−1318my)、メタン、エタン、エチレン、プロパン、シクロプロパン、プロピレン、n−ブタン、ブタン、イソブタン、シクロブタン、n−ペンタン、イソペンタン、n−ヘキサン、シクロヘキサン、n−ヘプタン、窒素(N2)、酸素(O2)、二酸化炭素(CO2)、アンモニア(NH3)、アルゴン(Ar)、水素(H2)およびこれらの混合物からなる群から選択される少なくとも1つの作動流体を含む、[5]に記載の吸収パワーサイクルシステム。
[11] 前記発電機発生器と前記第1の熱交換器の間、および前記第1の熱交換器と前記吸収器の間に、前記吸収剤と作動流体との混合物を、前記吸収器に戻して再循環するための再循環ラインをさらに含む、[1]に記載の吸収パワーサイクルシステム。
[12] 前記作動流体が、2−クロロ−3,3,3−トリフルオロプロペン、シス−またはトランス−1−クロロ−3,3,3−トリフルオロプロペン、3,4,4,4−テトラフルオロ−3−トリフルオロメチル−1−ブテン、シス−またはトランス−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンおよびこれらの組み合わせからなる群から選択される少なくとも1つの作動流体を含む、[1]に記載の吸収パワーサイクルシステム。
[13] 前記作動流体が、
約51重量パーセント〜約70重量パーセントのシス−HFO−1336mzzおよび約49重量パーセント〜約30重量パーセントのイソペンタン、
約62重量パーセント〜約78重量パーセントのシス−HFO−1336mzzおよび約38重量パーセント〜約22重量パーセントのn−ペンタン、
約75重量パーセント〜約88重量パーセントのシス−HFO−1336mzzおよび約25重量パーセント〜約12重量パーセントのシクロペンタン、
約25重量パーセント〜約35重量パーセントのシス−HFO−1336mzzおよび約75重量パーセント〜約65重量パーセントのHCFC−123、
約67重量パーセント〜約87重量パーセントのシス−HFO−1336mzzおよび約33重量パーセント〜約13重量パーセントのトランス−1,2−ジクロロエチレン、ならびに
約61重量パーセント〜約78重量パーセントのトランス−HFO−1438mzzおよび約39重量パーセント〜約22重量パーセントのイソペンタン
からなる群から選択される少なくとも1つの共沸または共沸様組成物を含む、[1]に記載の吸収パワーサイクルシステム。
[14] (a)吸収器において吸収剤/作動流体混合物を形成する工程と、
(b)前記吸収剤/作動流体混合物を加熱して、作動流体蒸気を放出する工程と、
(c)前記作動流体蒸気を機械仕事を生じさせるためのデバイスに送る工程と、
(d)前記加熱された吸収剤/作動流体混合物を改良再形成する工程と
を含む機械仕事を生じさせる方法。
[15] 工程(c)と(d)の間に、
(c−i)凝縮器において前記作動流体を凝縮する工程と、
(c−ii)膨張デバイスにおいて前記作動流体を部分的に蒸発させる工程と、
(c−iii)蒸発器において前記作動流体を完全に蒸発させて、冷却を行う工程と
をさらに含む、[14]に記載の方法。
[16] 工程(c)と(d)の間に、
(c−i)凝縮器において前記作動流体を凝縮して熱を生成する工程と、
(c−ii)膨張デバイスにおいて前記作動流体を部分的に蒸発させる工程と、
(c−iii)蒸発器において前記作動流体を完全に蒸発させる工程と
をさらに含む、[14]に記載の方法。
[17] 工程(c)と(d)の間に、冷却するストリームからの熱を第2の熱交換器で吸収して、前記冷却するストリームを冷却する工程をさらに含む、[14]に記載の方法。
Crystallization inhibitors include copending PCT patent application PCT / US09 / 63599 filed on Nov. 6, 2009 and co-pending US provisional application 61 / 165,089 filed Mar. 31, 2009. No. 61 / 165,093, 61 / 165,147, 61 / 165,155, 61 / 165,160, 61 / 165,161 No. 61 / 165,166 and 61 / 165,173.
Below, the preferable aspect of this invention is shown.
[1] (a) an absorber for absorbing the working fluid into the absorbent to form a mixture of the absorbent and the working fluid;
(B) a first heat exchanger disposed in fluid communication with the absorber to receive and preheat the absorbent and working fluid from the absorber;
(C) a liquid pump for pumping the mixture of absorbent and working fluid from the absorber to the first heat exchanger;
(D) fluid communication with the first heat exchanger for receiving the preheated mixture from the first heat exchanger and releasing high pressure steam of the working fluid by transferring additional heat to the premix; Generator generator arranged in a
(E) a device for generating mechanical work disposed in fluid communication with the generator generator to generate mechanical work from the high pressure working fluid, and the absorbent comprises an ionic liquid; Absorption power cycle system.
[2] (a) a condenser that condenses the high pressure working fluid exiting the device for generating mechanical work;
(B) an expansion device for reducing the pressure and partially evaporating the working fluid;
(C) The absorption power cycle system according to [1], further including an evaporator for completely evaporating the working fluid and performing cooling.
[3] The ionic liquid includes a cation and an anion, and the cation is lithium, sodium, potassium, cesium, and the following formula:
Wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 12 and R 13 are
(I) H,
(Ii) halogen,
(Iii) optionally Cl, Br, F, I, OH, substituted with at least one element selected from the group consisting of NH 2 and SH, -CH 3, -C 2 H 5 or C 3 ~ A C 25 linear, branched or cyclic alkane or alkene,
(Iv) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 25 linear, branched or cyclic alkane or alkene that,
(V) C 6 ~C 20 unsubstituted aryl or O, N, C 3 ~C 25 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (vi) C 6 ~C 25 substituted aryl, or O, N, a C 3 -C 25 substituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, The substituted aryl or substituted heteroaryl is
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of those having 1 to 3 substituents independently selected from the group consisting of
R 7 , R 8 , R 9 and R 10 are
(I) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(Ii) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 25 linear, branched or cyclic alkane or alkene that,
(Iii) C 6 ~C 25 unsubstituted aryl or O, N, C 3 ~C 25 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (iv) C 6 ~C 25 substituted aryl, or O, N, a C 3 -C 25 substituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,,
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of substituted aryl or substituted heteroaryl having 1 to 3 substituents independently selected from the group consisting of
Optionally, at least two of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are taken together to form a cyclic or bicyclic alkanyl Or an alkenyl group can be formed,
The anion is
[CH 3 CO 2 ] − , [HSO 4 ] − , [CH 3 OSO 3 ] − , [C 2 H 5 OSO 3 ] − , [AlCl 4 ] − , [CO 3 ] 2− , [HCO 3 ] − , [NO 2 ] − , [NO 3 ] − , [SO 4 ] 2− , [PO 3 ] 3− , [HPO 3 ] 2− , [H 2 PO 3 ] 1− , [PO 4 ] 3− , [HPO 4 ] 2− , [H 2 PO 4 ] − , [HSO 3 ] − , [CuCl 2 ] − , Cl − , Br − , I − , SCN − , BR 1 R 2 R 3 R 4 , BOR 1 OR 2 OR 3 OR 4 , a carboxylate (1-carbadodecaborate (1-)) optionally substituted with alkyl or substituted alkyl, optionally substituted with alkylamine, substituted alkylamine, alkyl or substituted alkyl Carborane (dicarbadodecaborate (1-)), [BF 4 ] − , [PF 6 ] − , [SbF 6 ] − , [C F 3 SO 3 ] − , [HCF 2 CF 2 SO 3 ] − , [CF 3 HFCCF 2 SO 3 ] − , [HCClFCF 2 SO 3 ] − , [(CF 3 SO 2 ) 2 N] − , [(CF 3 CF 2 SO 2 ) 2 N] − , [(CF 3 SO 2 ) 3 C] − , [CF 3 CO 2 ] − , [CF 3 OCHFHCF 2 SO 3 ] − , [CF 3 CF 2 OCFHCCF 2 SO 3 ] -, [CF 3 CFHOCF 2 CF 2 SO 3] -, [CF 2 HCF 2 OCF 2 CF 2 SO 3] -, [CF 2 ICF 2 OCF 2 CF 2 SO 3] -, [CF 3 CF 2 OCF 2 CF 2 SO 3 ] − , [(CF 2 HCF 2 SO 2 ) 2 N] − , [(CF 3 CFHCF 2 SO 2 ) 2 N] − , F − and the formula
(Wherein R 11 is
(I) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 10 linear, branched or cyclic alkane or alkene,
(Ii) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 10 linear, branched or cyclic alkane or alkene that,
(Iii) C 6 ~C 10 unsubstituted aryl or O, N, C 3 ~C 10 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (Iv) C 6 -C 10 substituted aryl, or C 3 -C 10 substituted heteroaryl having 1 to 3 heteroatoms independently selected from the group consisting of O, N, Si and S,
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 10 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of substituted aryl or substituted heteroaryl having 1 to 3 substituents independently selected from the group consisting of
Optionally, at least two of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are taken together to form a cyclic or bicyclic alkanyl Or an alkenyl group can be formed)
The absorption power cycle system according to [1].
[4] The absorption power cycle system according to [1], wherein the working fluid includes water or ammonia.
[5] The working fluid is hydrofluorocarbon, hydrochlorofluorocarbon, chlorofluorocarbon, fluorocarbon, nitrogen (N 2 ), oxygen (O 2 ), carbon dioxide (CO 2 ), argon (Ar), hydrogen (H 2 ), The absorption power cycle system of [1], comprising a working fluid selected from the group consisting of non-fluorinated hydrocarbons, methanol and mixtures of any of the foregoing.
[6] hydro carbon is not the fluorinated consists C 1 -C 7 linear, branched or cyclic alkanes and C 1 -C 7 linear, branched or cyclic alkene The absorption power cycle system according to [5], which is selected from the group.
[7] The working fluid is
(I) a fluoroolefin of the formula E—R 1 CH═CHR 2 or Z—R 1 CH═CHR 2 where R 1 and R 2 are independently a C 1 -C 6 perfluoroalkyl group ,
(Ii) cyclic of the formula cyclo- [CX = CY (CZW) n- ], wherein X, Y, Z and W are independently H or F and n is an integer of 2-5. fluoroolefin, and (iii) tetrafluoroethylene (CF 2 = CF 2), hexafluoropropene (CF 3 CF = CF 2) , 1,2,3,3,3- pentafluoro-1-propene (CHF = CFCF 3 ), 1,1,3,3,3-pentafluoro-1-propene (CF 2 = CHCF 3 ), 1,1,2,3,3-pentafluoro-1-propene (CF 2 = CFCHF 2 ) , 1,2,3,3-tetrafluoro-1-propene (CHF = CFCHF 2), 2,3,3,3- tetrafluoro-1-propene (CH 2 = CFCF 3), 1,3,3, 3-tetrafluoro-1-propene (CHF = HCF 3), 1,1,2,3-tetrafluoro-1-propene (CF 2 = CFCH 2 F) , 1,1,3,3- tetrafluoro-1-propene (CF 2 = CHCHF 2), 1 , 2,3,3-tetrafluoro-1-propene (CHF = CFCHF 2), 3,3,3- trifluoro-1-propene (CH 2 = CHCF 3), 2,3,3- trifluoro -1 - propene (CHF 2 CF = CH 2) , 1,1,2- trifluoro-1-propene (CH 3 CF = CF 2) , 1,2,3- trifluoro-1-propene (CH 2 FCF = CF 2 ), 1,1,3-trifluoro-1-propene (CH 2 FCH═CF 2 ), 1,3,3-trifluoro-1-propene (CHF 2 CH═CHF), 1,1,1, 2,3,4,4,4-octafluoro-2-butene (C 3 CF = CFCF 3), 1,1,2,3,3,4,4,4- octafluoro-1-butene (CF 3 CF 2 CF = CF 2), 1,1,1,2,4, 4,4-heptafluoro-2-butene (CF 3 CF═CHCF 3 ), 1,2,3,3,4,4,4-heptafluoro-1-butene (CHF═CFCF 2 CF 3 ), 1, 1,1,2,3,4,4-heptafluoro-2-butene (CHF 2 CF═CFCF 3 ), 1,3,3,3-tetrafluoro-2- (trifluoromethyl) -1-propene ( (CF 3 ) 2 C═CHF), 1,1,3,3,4,4,4-heptafluoro-1-butene (CF 2 ═CHCF 2 CF 3 ), 1,1,2,3,4, 4,4-heptafluoro-1-butene (CF 2 = CFCHFCF 3 ), 1,1,2,3,3,4,4-heptaful Oro-1-butene (CF 2 = CFCF 2 CHF 2 ), 2,3,3,4,4,4-hexafluoro-1-butene (CF 3 CF 2 CF═CH 2 ), 1,3,3, 4,4,4-hexafluoro-1-butene (CHF = CHCF 2 CF 3 ), 1,2,3,4,4,4-hexafluoro-1-butene (CHF = CFCHFCF 3 ), 1,2, 3,3,4,4-hexafluoro-1-butene (CHF═CFCF 2 CHF 2 ), 1,1,2,3,4,4-hexafluoro-2-butene (CHF 2 CF═CFCHF 2 ), 1,1,1,2,3,4-hexafluoro-2-butene (CH 2 FCF═CFCF 3 ), 1,1,1,2,4,4-hexafluoro-2-butene (CHF 2 CH═ CFCF 3), 1,1,1,3,4,4- hexafluoro-2-butene (C 3 CH = CFCHF 2), 1,1,2,3,3,4- hexafluoro-1-butene (CF 2 = CFCF 2 CH 2 F), 1,1,2,3,4,4- hexafluoro 1-butene (CF 2 = CFCHFCHF 2), 3,3,3- trifluoro-2- (trifluoromethyl) -1-propene (CH 2 = C (CF 3 ) 2), 1,1,1, 2,4-pentafluoro-2-butene (CH 2 FCH═CFCF 3 ), 1,1,1,3,4-pentafluoro-2-butene (CF 3 CH═CFCH 2 F), 3,3,4 , 4,4-pentafluoro-1-butene (CF 3 CF 2 CH═CH 2 ), 1,1,1,4,4-pentafluoro-2-butene (CHF 2 CH═CHCF 3 ), 1,1 , 1,2,3-pentafluoro-2-butene (CH 3 CF = CFCF 3) , 2, , 3,4,4-pentafluoro-1-butene (CH 2 = CFCF 2 CHF 2 ), 1,1,2,4,4- pentafluoro-2-butene (CHF 2 CF = CHCHF 2) , 1, 1,2,3,3-pentafluoro-1-butene (CH 3 CF 2 CF = CF 2), 1,1,2,3,4- pentafluoro-2-butene (CH 2 FCF = CFCHF 2) , 1,1,3,3,3-pentafluoro-2-methyl-1-propene (CF 2 ═C (CF 3 ) (CH 3 )), 2- (difluoromethyl) -3,3,3-trifluoro 1-propene (CH 2 = C (CHF 2 ) (CF 3)), 2,3,4,4,4- pentafluoro-1-butene (CH 2 = CFCHFCF 3), 1,2,4,4 , 4-Pentafluoro-1-butene (CHF = CFCH 2 CF 3 ), 1,3,4, 4,4-pentafluoro-1-butene (CHF = CHCHFCF 3 ), 1,3,3,4,4-pentafluoro-1-butene (CHF = CHCF 2 CHF 2 ), 1,2,3,4, 4-pentafluoro-1-butene (CHF = CFCHFCHF 2 ), 3,3,4,4-tetrafluoro-1-butene (CH 2 = CHCF 2 CHF 2 ), 1,1-difluoro-2- (difluoromethyl) ) -1-propene (CF 2 ═C (CHF 2 ) (CH 3 )), 1,3,3,3-tetrafluoro-2-methyl-1-propene (CHF═C (CF 3 ) (CH 3 )) ), 3,3-difluoro-2- (difluoromethyl) -1-propene (CH 2 ═C (CHF 2 ) 2 ), 1,1,1,2-tetrafluoro-2-butene (CF 3 CF═CHCH) 3), 1,1,1,3-Tetorafuru B-2-butene (CH 3 CF = CHCF 3) , 1,1,1,2,3,4,4,5,5,5- decafluoro-2-pentene (CF 3 CF = CFCF 2 CF 3) , 1,1,2,3,3,4,4,5,5,5- decafluoro-1-pentene (CF 2 = CFCF 2 CF 2 CF 3), 1,1,1,4,4,4 - hexafluoro-2- (trifluoromethyl) -2-butene ((CF 3) 2 C = CHCF 3), 1,1,1,2,4,4,5,5,5- nonafluoro-2-pentene (CF 3 CF═CHCF 2 CF 3 ), 1,1,1,3,4,4,5,5,5-nonafluoro-2-pentene (CF 3 CH═CFCF 2 CF 3 ), 1,2,3 , 3,4,4,5,5,5- nonafluoro-1-pentene (CHF = CFCF 2 CF 2 CF 3), 1,1,3,3,4, , 5,5,5-nonafluoro-1-pentene (CF 2 = CHCF 2 CF 2 CF 3), 1,1,2,3,3,4,4,5,5- nonafluoro-1-pentene (CF 2 = CFCF 2 CF 2 CHF 2) , 1,1,2,3,4,4,5,5,5- nonafluoro-2-pentene (CHF 2 CF = CFCF 2 CF 3), 1,1,1,2 , 3,4,4,5,5-nonafluoro-2-pentene (CF 3 CF═CFCF 2 CHF 2 ), 1,1,1,2,3,4,5,5,5-nonafluoro-2-pentene (CF 3 CF═CFCHFCF 3 ), 1,2,3,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CHF═CFCF (CF 3 ) 2 ), 1,1, 2,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CFCH (CF 3 ) 2 ), 1,1,1,4,4,4-hexafluoro-2- (trifluoromethyl) -2-butene (CF 3 CH═C (CF 3 ) 2 ), 1, 1,3,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CHCF (CF 3 ) 2 ), 2,3,3,4,4,5,5 5-octafluoro-1-pentene (CH 2 = CFCF 2 CF 2 CF 3), 1,2,3,3,4,4,5,5- octafluoro-1-pentene (CHF = CFCF 2 CF 2 CHF 2 ), 3,3,4,4,4-pentafluoro-2- (trifluoromethyl) -1-butene (CH 2 ═C (CF 3 ) CF 2 CF 3 ), 1,1,4,4 4-pentafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CHCH (CF 3 ) 2), 1, 4,4,4-pentafluoro-3- (trifluoromethyl) -1-butene (CHF = CHCF (CF 3) 2), 1,1,4,4,4- pentafluoro-2- (trifluoromethyl methyl) -1-butene (CF 2 = C (CF 3 ) CH 2 CF 3), 3,4,4,4- tetrafluoro-3- (trifluoromethyl) -1-butene ((CF 3) 2 CFCH = CH 2), 3,3,4,4,5,5,5- heptafluoro-1-pentene (CF 3 CF 2 CF 2 CH = CH 2), 2,3,3,4,4,5, 5-heptafluoro-1-pentene (CH 2 = CFCF 2 CF 2 CHF 2), 1,1,3,3,5,5,5- heptafluoro-1-butene (CF 2 = CHCF 2 CH 2 CF 3 ), 1,1,1,2,4,4,4-heptafluoro-3-methyl-2-butene (C 3 CF = C (CF 3) (CH 3)), 2,4,4,4- tetrafluoro-3- (trifluoromethyl) -1-butene (CH 2 = CFCH (CF 3 ) 2), 1, 4,4,4-tetrafluoro-3- (trifluoromethyl) -1-butene (CHF = CHCH (CF 3 ) 2 ), 1,1,1,4-tetrafluoro-2- (trifluoromethyl)- 2-butene (CH 2 FCH═C (CF 3 ) 2 ), 1,1,1,3-tetrafluoro-2- (trifluoromethyl) -2-butene (CH 3 CF═C (CF 3 ) 2 ) 1,1,1-trifluoro-2- (trifluoromethyl) -2-butene ((CF 3 ) 2 C═CHCH 3 ), 3,4,4,5,5,5-hexafluoro-2- Pentene (CF 3 CF 2 CF═CHCH 3 ), 1,1,1,4,4,4-hexafluoro Ro-2-methyl-2-butene (CF 3 C (CH 3 ) ═CHCF 3 ), 3,3,4,5,5,5-hexafluoro-1-pentene (CH
2 = CHCF 2 CHFCF 3 ), 4,4,4-trifluoro-2- (trifluoromethyl) -1-butene (CH 2 ═C (CF 3 ) CH 2 CF 3 ), 1,1,2,3 , 3,4,4,5,5,6,6,6- dodecafluoro-1-hexene (CF 3 (CF 2) 3 CF = CF 2), 1,1,1,2,2,3,4 , 5,5,6,6,6- dodecafluoro-3- hexene (CF 3 CF 2 CF = CFCF 2 CF 3), 1,1,1,4,4,4- hexafluoro-2,3-bis (Trifluoromethyl) -2-butene ((CF 3 ) 2 C═C (CF 3 ) 2 ), 1,1,1,2,3,4,5,5,5-nonafluoro-4- (trifluoro methyl) -2-pentene ((CF 3) 2 CFCF = CFCF 3), 1,1,1,4,4,5,5,5- octafluoro-2- (g Fluoromethyl) -2-pentene ((CF 3) 2 C = CHC 2 F 5), 1,1,1,3,4,5,5,5- octafluoro-4- (trifluoromethyl) -2 Pentene ((CF 3 ) 2 CFCF═CHCF 3 ), 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene (CF 3 CF 2 CF 2 CF 2 CH═CH 2 ) , 4,4,4-trifluoro-3,3-bis (trifluoromethyl) -1-butene (CH 2 = CHC (CF 3 ) 3), 1,1,1,4,4,4- hexafluoro -3-methyl-2- (trifluoromethyl) -2-butene ((CF 3) 2 C = C (CH 3) (CF 3)), 2,3,3,5,5,5- hexafluoro - 4- (trifluoromethyl) -1-pentene (CH 2 = CFCF 2 CH ( CF 3) 2), 1,1,1,2 , 4,4,5,5,5-nonafluoro-3-methyl-2-pentene (CF 3 CF = C (CH 3) CF 2 CF 3), 1,1,1,5,5,5- hexafluoro 4- (trifluoromethyl) -2-pentene (CF 3 CH = CHCH (CF 3) 2), 3,4,4,5,5,6,6,6- octafluoro-2-hexene (CF 3 CF 2 CF 2 CF═CHCH 3 ), 3,3,4,4,5,5,6,6-octafluoro 1-hexene (CH 2 ═CHCF 2 CF 2 CF 2 CHF 2 ), 1,1,1 , 4,4-pentafluoro-2- (trifluoromethyl) -2-pentene ((CF 3 ) 2 C═CHCF 2 CH 3 ), 4,4,5,5,5-pentafluoro-2- (tri fluoromethyl) -1-pentene (CH 2 = C (CF 3 ) CH 2 C 2 F 5), 3,3,4,4 5,5,5-heptafluoro-2-methyl-1-pentene (CF 3 CF 2 CF 2 C (CH 3) = CH 2), 4,4,5,5,6,6,6- heptafluoro - 2- hexene (CF 3 CF 2 CF 2 CH = CHCH 3), 4,4,5,5,6,6,6- heptafluoro-1-hexene (CH 2 = CHCH 2 CF 2 C 2 F 5), 1,1,1,2,2,3,4-heptafluoro-3-hexene (CF 3 CF 2 CF═CFC 2 H 5 ), 4,5,5,5-tetrafluoro-4- (trifluoromethyl) ) 1-pentene (CH 2 = CHCH 2 CF ( CF 3) 2), 1,1,1,2,5,5,5- heptafluoro-4-methyl-2-pentene (CF 3 CF = CHCH ( CF 3) (CH 3)) , 1,1,1,3- tetrafluoro-2- (trifluoromethyl) - - pentene ((CF 3) 2 C = CFC 2 H 5), 1,1,1,2,3,4,4,5,5,6,6,7,7,7- tetradecanoyl-fluoro-2- heptene (CF 3 CF = CFCF 2 CF 2 C 2 F 5), 1,1,1,2,2,3,4,5,5,6,6,7,7,7- tetradecanoyl-fluoro-3- Heptene (CF 3 CF 2 CF═CFCF 2 C 2 F 5 ), 1,1,1,3,4,4,5,5,6,6,7,7,7-tridecafluoro-2-heptene ( CF 3 CH═CFCF 2 CF 2 C 2 F 5 ), 1,1,1,2,4,4,5,5,6,6,7,7,7-tridecafluoro-2-heptene (CF 3 CF = CHCF 2 CF 2 C 2 F 5 ), 1,1,1,2,2,4,5,5,6,6,7,7,7-tridecafluoro-3-heptene (CF 3 CF 2 CH = CFCF 2 C 2 F 5 ) and 1,1,1,2,2,3,5,5,6,6,7,7,7-tridecafluoro-3-heptene (CF 3 CF 2 CF═CHCF 2 C 2 F The absorption power cycle system according to [5], comprising at least one hydrofluorocarbon or fluorocarbon selected from the group consisting of fluoroolefins selected from the group consisting of 5 ).
[8] The fluoroolefin is 1,1,1,4,4,4-hexafluorobut-2-ene, 1,1,1,4,4,5,5,5-octafluoropent-2-ene. Ene, 1,1,1,4,4,5,5,6,6,6-decafluorohex-2-ene, 1,1,1,4,5,5,5-heptafluoro-4- ( Trifluoromethyl) pent-2-ene, 1,1,1,2,2,5,5,6,6,6-decafluorohex-3-ene, 1,1,1,4,4,5, 5,6,6,7,7,7-dodecafluorohept-2-ene, 1,1,1,4,4,5,6,6,6-nonafluoro-5- (trifluoromethyl) hexa-2 -Ene, 1,1,1,4,5,5,6,6,6-nonfluoro-4- (trifluoromethyl) hex-2-ene, 1,1,1,5,5, 5-Hexafluoro-4,4-bis (trifluoromethyl) pent-2-ene, 1,1,1,2,2,5,5,6,6,7,7,7-dodecafluorohepta-3 -Ene, 1,1,1,2,2,5,6,6,6-nonafluoro-5- (trifluoromethyl) hex-3-ene, 1,1,1,4,4,5,5, 6,6,7,7,8,8,8-tetradecafluorooct-2-ene, 1,1,1,4,4,5,5,6,7,7,7-undecafluoro-6 -(Trifluoromethyl) hept-2-ene, 1,1,1,5,5,6,6,6-octafluoro-4,4-bis (trifluoromethyl) hex-2-ene, 1,1 , 1,2,2,5,5,6,6,7,7,8,8,8-tetradecafluorooct-3-ene, 1,1,1,2,2,5,5,6 7,7,7-undecafluoro-6- (trifluoromethyl) hept-3-ene, 1,1,1,2,2,5,6,6,7,7,7-undecafluoro-5 -(Trifluoromethyl) hept-3-ene, 1,1,1,2,2,6,6,6-octafluoro-5,5-bis (trifluoromethyl) hex-3-ene, 1,1 , 1,2,2,3,3,6,6,7,7,8,8,8-tetradecafluorooct-4-ene, 1,1,1,2,5,6,6,6- Octafluoro-2,5-bis (trifluoromethyl) hex-3-ene, 1,1,1,2,5,5,6,6,7,7,7-undecafluoro-2- (trifluoro Methyl) hept-3-ene, 1,1,1,4,4,5,5,6,6,7,7,8,8,9,9,9-hexadecafluoronona 2-ene, 1,1,1,4,5,5,6,6,7,7,8,8,8-tridecafluoro-4- (trifluoromethyl) hept-2-ene, 1,1 , 1,6,6,6-octafluoro-4,4-bis (trifluoromethyl) hept-2-ene, 1,1,1,2,2,5,5,6,6,7,7, 8,8,9,9,9-hexadecafluoronon-3-ene, 1,1,1,2,2,5,5,6,6,7,8,8,8-tridecafluoro-7 -(Trifluoromethyl) oct-3-ene, 1,1,1,2,2,6,6,7,7,7-decafluoro-5,5-bis (trifluoromethyl) hept-3-ene 1,1,1,2,2,3,3,6,6,7,7,8,8,9,9,9-hexadecafluoronon-4-ene, 1,1,1,2, 2, 3, 3, 6, 6 , 7,8,8,8-tridecafluoro-7- (trifluoromethyl) oct-4-ene, 1,1,1,2,2,3,3,6,7,7,8,8, 8-Tridecafluoro-6- (trifluoromethyl) oct-4-ene, 1,1,1,5,5,6,6,7,7,7-decafluoro-2,2-bis (trifluoro Methyl) hept-3-ene, 1,1,1,2,5,5,6,6,7,7,8,8,8-tridecafluoro-2 (trifluoromethyl) oct-3-ene, 1,1,1,2,5,5,6,7,7,7-decafluoro-2,6-bis (trifluoromethyl) hept-3-ene, 1,1,1,2,5,6 , 6,7,7,7-decafluoro-2,5-bis (trifluoromethyl) hept-3-ene, 1,1,1,2,6,6,6-heptafluoro 2,5,5-tris (trifluoromethyl) hex-3-ene, 1,1,1,2,2,5,5,6,6,7,7,8,8,9,9,10, 10,10-octadecafluorodec-3-ene, 1,1,1,2,2,5,6,6,7,7,8,8,9,9,9-pentadecafluoro-5- ( Trifluoromethyl) non-3-ene, 1,1,1,2,2,6,6,7,7,8,8,8-dodecafluoro-5,5-bis (trifluoromethyl) octa-3 -Ene, 1,1,1,2,2,3,3,6,7,7,8,8,9,9,10,10,10-octadecafluorodec-4-ene, 1, 1,1,2,2,3,3,6,6,7,7,8,9,9,9-pentadecafluoro-8- (trifluoromethyl) non-4-ene, 1,1,1 , 2,2,3 3,7,7,8,8,8-dodecafluoro-6,6-bis (trifluoromethyl) oct-4-ene, 1,1,1,2,5,5,6,6,7,7 , 8,8,9,9,9-pentadecafluoro-2- (trifluoromethyl) non-3-ene, 1,1,1,2,5,5,6,6,7,8,8, 8-dodecafluoro-2,7-bis (trifluoromethyl) oct-3-ene, 1,1,1,2,6,6,7,7,7-nonafluoro-2,5,5-tris (tri Fluoromethyl) hept-3-ene, 1,1,1,2,2,3,3,4,4,7,7,8,8,9,9,10,10,10-octadecafluorodeca- 5-ene, 1,1,1,2,3,3,6,6,7,7,8,8,9,9,9-pentadecafluoro-2- (trifluoromethyl) non-4- Ene, 1,1,1,2,2,3,6,6,7,7,8,8,9,9,9-pentadecafluoro-3- (trifluoromethyl) non-4-ene, 1,1,5,5,6,6,7,7,8,8,8-dodecafluoro-2,2, -bis (trifluoromethyl) oct-3-ene, 1,1,1,2 , 3,3,6,6,7,8,8,8-dodecafluoro-2,7-bis (trifluoromethyl) oct-4-ene, 1,1,1,2,3,3,6, 7,7,8,8,8-dodecafluoro-2,6-bis (trifluoromethyl) oct-4-ene, 1,1,1,5,5,6,7,7,7-nonafluoro-2 , 2,6-Tris (trifluoromethyl) hept-3-ene, 1,1,1,2,2,3,6,7,7,8,8,8-dodecafluoro-3,6-bis ( G Fluoromethyl) oct-4-ene, 1,1,1,2,2,3,6,7,7,8,8,8-dodecafluoro-3,6-bis (trifluoromethyl) oct-4- Ene, 1,1,1,5,6,6,7,7,7-nonafluoro-2,2,5-tris (trifluoromethyl) hept-3-ene and 1,1,1,6,6 The absorption power cycle system according to [7], which is selected from the group consisting of 6-hexafluoro-2,2,5,5-tetrakis (trifluoromethyl) hex-3-ene.
[9] The fluoroolefin is 1,2,3,3,4,4-hexafluorocyclobutene, 3,3,4,4-tetrafluorocyclobutene, 3,3,4,4,5,5, -Consisting of hexafluorocyclopentene, 1,2,3,3,4,4,5,5-octafluorocyclopentene and 1,2,3,3,4,4,5,5,6,6-decafluorocyclohexene The absorption power cycle system according to [7], which is selected from the group.
[10] The working fluid is difluoromethane (HFC-32), pentafluoroethane (HFC-125), 1,1,2,2-tetrafluoroethane (HFC-134), 1,1,1,2- Tetrafluoroethane (HFC-134a), 1,1,1-trifluoroethane (HFC-143a), 1,1-difluoroethane (HFC-152a), fluoroethane (HFC-161), 1,1,1,3 , 3-pentafluoropropane (HFC-245fa), 1,1,1,3,3,3-hexafluoropropane (HFC-236fa), 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea), 1,1,1,3,3-pentafluorobutane (HFC-365mfc), 1,1,1,2,3,4,4,5,5,5-decuff Luopentane (HFC-43-10mee), 1,1,1,2,2,3,4,5,5,6,6,7,7,7-tetradecafluoroheptane (HFC-63-14mce), 2 , 3,3,3-tetrafluoropropene (HFO-1234yf), 1,3,3,3-tetrafluoropropene (HFO-1234ze), 1,2,3,3-tetrafluoropropene (HFO-1234ye), 3,3,3-trifluoropropene (HFO-1243zf), 1,2,3,3,3-pentafluoropropene (HFO-1225ye), 1,1,1,3,3-pentafluoropropene (HFO- 1225zc), 1,1,1,2,2,4,5,5,6,6,7,7,7-tridecafluoro-3-heptene (HFO-162-13mczy) and 1 1,1,2,2,3,5,5,6,6,7,7,7-tridecafluoro-3-heptene (HFO-162-13mcyz), dichlorodifluoromethane (CFC-12), fluorotrichloro Methane (CFC-11), 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113), 1,2-dichloro-1,1,2,2-tetrafluoroethane (CFC- 114), chlorodifluoromethane (HCFC-22), 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf), 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd), Perfluoromethane (FC-14), perfluoroethane (FC-116), perfluoropropane (FC-218), perfluorocyclobutane ( C-C318), octafluoro-2-butene (FO-1318my), methane, ethane, ethylene, propane, cyclopropane, propylene, n-butane, butane, isobutane, cyclobutane, n-pentane, isopentane, n-hexane, Selected from the group consisting of cyclohexane, n-heptane, nitrogen (N 2 ), oxygen (O 2 ), carbon dioxide (CO 2 ), ammonia (NH 3 ), argon (Ar), hydrogen (H 2 ) and mixtures thereof The absorption power cycle system according to [5], including at least one working fluid.
[11] A mixture of the absorbent and the working fluid is placed in the absorber between the generator generator and the first heat exchanger and between the first heat exchanger and the absorber. The absorption power cycle system according to [1], further including a recirculation line for returning and recirculating.
[12] The working fluid is 2-chloro-3,3,3-trifluoropropene, cis- or trans-1-chloro-3,3,3-trifluoropropene, 3,4,4,4-tetra Selected from the group consisting of fluoro-3-trifluoromethyl-1-butene, cis- or trans-1,1,1,4,4,5,5,5-octafluoro-2-pentene and combinations thereof The absorption power cycle system according to [1], comprising at least one working fluid.
[13] The working fluid is
From about 51 weight percent to about 70 weight percent cis-HFO-1336mzz and from about 49 weight percent to about 30 weight percent isopentane;
From about 62 weight percent to about 78 weight percent cis-HFO-1336mzz and from about 38 weight percent to about 22 weight percent n-pentane;
From about 75 weight percent to about 88 weight percent cis-HFO-1336mzz and from about 25 weight percent to about 12 weight percent cyclopentane;
From about 25 weight percent to about 35 weight percent cis-HFO-1336mzz and from about 75 weight percent to about 65 weight percent HCFC-123;
About 67 weight percent to about 87 weight percent cis-HFO-1336mzz and about 33 weight percent to about 13 weight percent trans-1,2-dichloroethylene, and about 61 weight percent to about 78 weight percent trans-HFO-1438 mzz. And at least one azeotropic or azeotrope-like composition selected from the group consisting of about 39 weight percent to about 22 weight percent isopentane.
[14] (a) forming an absorbent / working fluid mixture in the absorber;
(B) heating the absorbent / working fluid mixture to release working fluid vapor;
(C) sending the working fluid vapor to a device for generating mechanical work;
(D) reforming the heated absorbent / working fluid mixture to produce mechanical work.
[15] Between steps (c) and (d),
(Ci) condensing the working fluid in a condenser;
(C-ii) partially evaporating the working fluid in an expansion device;
(C-iii) The method according to [14], further comprising: evaporating the working fluid completely in an evaporator and performing cooling.
[16] Between steps (c) and (d),
(Ci) condensing the working fluid in a condenser to generate heat;
(C-ii) partially evaporating the working fluid in an expansion device;
(C-iii) The method according to [14], further comprising: completely evaporating the working fluid in an evaporator.
[17] The method according to [14], further comprising a step of absorbing heat from the cooling stream in a second heat exchanger between the steps (c) and (d), and cooling the cooling stream. the method of.
Claims (15)
(b)前記吸収剤と作動流体との混合物を前記吸収器から受容および予熱するための前記吸収器と流体連通して配置された第1の熱交換器と、
(c)前記吸収剤と作動流体との混合物を、前記吸収器から、前記第1の熱交換器へポンピングするための液体ポンプと、
(d)前記第1の熱交換器から予熱混合物を受容し、追加の熱を前記予備混合物に移すことによって作動流体の高圧蒸気を放出するための前記第1の熱交換器と流体連通して配置された発生器と、
(e)高圧作動流体から機械仕事を生じさせるために、前記発生器と流体連通して配置された機械仕事を生じさせるためのデバイスと
を含み、
前記吸収剤がイオン液体を含むことを特徴とする吸収パワーサイクルシステム。 (A) an absorber for absorbing the working fluid into the absorbent to form a mixture of the absorbent and the working fluid;
(B) a first heat exchanger disposed in fluid communication with the absorber for receiving and preheating the mixture of absorbent and working fluid from the absorber;
(C) a liquid pump for pumping the mixture of absorbent and working fluid from the absorber to the first heat exchanger;
(D) in fluid communication with the first heat exchanger for receiving a preheated mixture from the first heat exchanger and releasing high pressure steam of a working fluid by transferring additional heat to the premix; A deployed generator; and
(E) a device for generating mechanical work disposed in fluid communication with the generator to generate mechanical work from the high pressure working fluid;
The absorption power cycle system, wherein the absorbent contains an ionic liquid.
(b)圧力を減じて、前記作動流体を部分的に蒸発させるための膨張デバイスと、
(c)前記作動流体を完全に蒸発させて、冷却を行うための蒸発器と
をさらに含むことを特徴とする請求項1に記載の吸収パワーサイクルシステム。 (A) a condenser that condenses the high-pressure working fluid exiting the device for producing the mechanical work;
(B) an expansion device for reducing pressure and partially evaporating the working fluid;
The absorption power cycle system according to claim 1, further comprising: (c) an evaporator for completely evaporating the working fluid and performing cooling.
式中、R1、R2、R3、R4、R5、R6、R12およびR13は、
(i)H、
(ii)ハロゲン、
(iii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iv)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(v)C6〜C20非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25非置換ヘテロアリール、および
(vi)C6〜C25置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25置換ヘテロアリールであって、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有する置換アリールまたは置換ヘテロアリール
からなる群から独立して選択され、
R7、R8、R9およびR10は、
(i)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(ii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iii)C6〜C25非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25非置換ヘテロアリール、および
(iv)C6〜C25置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C25置換ヘテロアリールであって、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C25の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有する置換アリールまたは置換ヘテロアリール
からなる群から独立して選択され、
任意選択的に、R1、R2、R3、R4、R5、R6、R7、R8、R9およびR10の少なくとも2つが一緒になって、環状または二環式のアルカニルまたはアルケニル基を形成することができ、
前記アニオンが、
[CH3CO2]-、[HSO4]-、[CH3OSO3]-、[C2H5OSO3]-、[AlCl4]-、[CO3]2-、[HCO3]-、[NO2]-、[NO3]-、[SO4]2-、[PO3]3-、[HPO3]2-、[H2PO3]1-、[PO4]3-、[HPO4]2-、[H2PO4]-、[HSO3]-、[CuCl2]-、Cl-、Br-、I-、SCN-、BR1R2R3R4、BOR1OR2OR3OR4、任意選択的にアルキルまたは置換アルキルで置換されたカーボレート(1−カルバドデカボレート(1−))、任意選択的にアルキルアミン、置換アルキルアミン、アルキルまたは置換アルキルで置換されたカーボラン(ジカルバドデカボレート(1−))、[BF4]-、[PF6]-、[SbF6]-、[CF3SO3]-、[HCF2CF2SO3]-、[CF3HFCCF2SO3]-、[HCClFCF2SO3]-、[(CF3SO2)2N]-、[(CF3CF2SO2)2N]-、[(CF3SO2)3C]-、[CF3CO2]-、[CF3OCFHCF2SO3]-、[CF3CF2OCFHCF2SO3]-、[CF3CFHOCF2CF2SO3]-、[CF2HCF2OCF2CF2SO3]-、[CF2ICF2OCF2CF2SO3]-、[CF3CF2OCF2CF2SO3]-、[(CF2HCF2SO2)2N]-、[(CF3CFHCF2SO2)2N]-、F-および式
(式中、R11は、
(i)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(ii)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、O、N、SiおよびSからなる群から選択される1〜3個のヘテロ原子を含む−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(iii)C6〜C10非置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C10非置換ヘテロアリール、および
(iv)C6〜C10置換アリール、またはO、N、SiおよびSからなる群から独立して選択される1〜3個のヘテロ原子を有するC3〜C10置換ヘテロアリールであって、
(1)任意選択的にCl、Br、F、I、OH、NH2およびSHからなる群から選択される少なくとも1つの要素で置換された、−CH3、−C2H5またはC3〜C10の直鎖状、分枝状または環状のアルカンまたはアルケン、
(2)OH、
(3)NH2および
(4)SH
からなる群から独立して選択される1〜3個の置換基を有する置換アリールまたは置換ヘテロアリール
からなる群から独立して選択され、
任意選択的に、R1、R2、R3、R4、R5、R6、R7、R8、R9およびR10の少なくとも2つが一緒になって、環状または二環式のアルカニルまたはアルケニル基を形成することができる)
ことを特徴とする請求項1に記載の吸収パワーサイクルシステム。 The ionic liquid contains a cation and an anion, and the cation is lithium, sodium, potassium, cesium, and the following formula:
Wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 12 and R 13 are
(I) H,
(Ii) halogen,
(Iii) optionally Cl, Br, F, I, OH, substituted with at least one element selected from the group consisting of NH 2 and SH, -CH 3, -C 2 H 5 or C 3 ~ A C 25 linear, branched or cyclic alkane or alkene,
(Iv) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 25 linear, branched or cyclic alkane or alkene that,
(V) C 6 ~C 20 unsubstituted aryl or O, N, C 3 ~C 25 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (vi) C 6 ~C 25 substituted aryl, or O, N, a C 3 -C 25 substituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,,
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of substituted aryl or substituted heteroaryl having 1 to 3 substituents independently selected from the group consisting of
R 7 , R 8 , R 9 and R 10 are
(I) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(Ii) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 25 linear, branched or cyclic alkane or alkene that,
(Iii) C 6 ~C 25 unsubstituted aryl or O, N, C 3 ~C 25 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (iv) C 6 ~C 25 substituted aryl, or O, N, a C 3 -C 25 substituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,,
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 25 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of substituted aryl or substituted heteroaryl having 1 to 3 substituents independently selected from the group consisting of
Optionally, at least two of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are taken together to form a cyclic or bicyclic alkanyl Or an alkenyl group can be formed,
The anion is
[CH 3 CO 2 ] − , [HSO 4 ] − , [CH 3 OSO 3 ] − , [C 2 H 5 OSO 3 ] − , [AlCl 4 ] − , [CO 3 ] 2− , [HCO 3 ] − , [NO 2 ] − , [NO 3 ] − , [SO 4 ] 2− , [PO 3 ] 3− , [HPO 3 ] 2− , [H 2 PO 3 ] 1− , [PO 4 ] 3− , [HPO 4 ] 2− , [H 2 PO 4 ] − , [HSO 3 ] − , [CuCl 2 ] − , Cl − , Br − , I − , SCN − , BR 1 R 2 R 3 R 4 , BOR 1 OR 2 OR 3 OR 4 , a carboxylate (1-carbadodecaborate (1-)) optionally substituted with alkyl or substituted alkyl, optionally substituted with alkylamine, substituted alkylamine, alkyl or substituted alkyl Carborane (dicarbadodecaborate (1-)), [BF 4 ] − , [PF 6 ] − , [SbF 6 ] − , [C F 3 SO 3 ] − , [HCF 2 CF 2 SO 3 ] − , [CF 3 HFCCF 2 SO 3 ] − , [HCClFCF 2 SO 3 ] − , [(CF 3 SO 2 ) 2 N] − , [(CF 3 CF 2 SO 2 ) 2 N] − , [(CF 3 SO 2 ) 3 C] − , [CF 3 CO 2 ] − , [CF 3 OCHFHCF 2 SO 3 ] − , [CF 3 CF 2 OCFHCCF 2 SO 3 ] -, [CF 3 CFHOCF 2 CF 2 SO 3] -, [CF 2 HCF 2 OCF 2 CF 2 SO 3] -, [CF 2 ICF 2 OCF 2 CF 2 SO 3] -, [CF 3 CF 2 OCF 2 CF 2 SO 3 ] − , [(CF 2 HCF 2 SO 2 ) 2 N] − , [(CF 3 CFHCF 2 SO 2 ) 2 N] − , F − and the formula
(I) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 10 linear, branched or cyclic alkane or alkene,
(Ii) selected from the group consisting of O, N, Si and S, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH 1-3 -CH 3 containing a hetero atom, -C 2 H 5 or C 3 -C 10 linear, branched or cyclic alkane or alkene that,
(Iii) C 6 ~C 10 unsubstituted aryl or O, N, C 3 ~C 10 unsubstituted heteroaryl having 1-3 heteroatoms independently selected from the group consisting of Si and S,, and (Iv) C 6 -C 10 substituted aryl, or C 3 -C 10 substituted heteroaryl having 1 to 3 heteroatoms independently selected from the group consisting of O, N, Si and S,
(1) —CH 3 , —C 2 H 5 or C 3 —, optionally substituted with at least one element selected from the group consisting of Cl, Br, F, I, OH, NH 2 and SH A C 10 linear, branched or cyclic alkane or alkene,
(2) OH,
(3) NH 2 and (4) SH
Independently selected from the group consisting of substituted aryl or substituted heteroaryl having 1 to 3 substituents independently selected from the group consisting of
Optionally, at least two of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are taken together to form a cyclic or bicyclic alkanyl Or an alkenyl group can be formed)
The absorption power cycle system according to claim 1.
(i)式E−R1CH=CHR2またはZ−R1CH=CHR2(式中、R1およびR2は、独立に、C1〜C6パーフルオロアルキル基である)のフルオロオレフィン、
(ii)式シクロ−[CX=CY(CZW)n−](式中、X、Y、ZおよびWは、独立に、HまたはFであり、nは2〜5の整数である)の環状フルオロオレフィン、および
(iii)テトラフルオロエチレン(CF2=CF2)、ヘキサフルオロプロペン(CF3CF=CF2)、1,2,3,3,3−ペンタフルオロ−1−プロペン(CHF=CFCF3)、1,1,3,3,3−ペンタフルオロ−1−プロペン(CF2=CHCF3)、1,1,2,3,3−ペンタフルオロ−1−プロペン(CF2=CFCHF2)、1,2,3,3−テトラフルオロ−1−プロペン(CHF=CFCHF2)、2,3,3,3−テトラフルオロ−1−プロペン(CH2=CFCF3)、1,3,3,3−テトラフルオロ−1−プロペン(CHF=CHCF3)、1,1,2,3−テトラフルオロ−1−プロペン(CF2=CFCH2F)、1,1,3,3−テトラフルオロ−1−プロペン(CF2=CHCHF2)、1,2,3,3−テトラフルオロ−1−プロペン(CHF=CFCHF2)、3,3,3−トリフルオロ−1−プロペン(CH2=CHCF3)、2,3,3−トリフルオロ−1−プロペン(CHF2CF=CH2)、1,1,2−トリフルオロ−1−プロペン(CH3CF=CF2)、1,2,3−トリフルオロ−1−プロペン(CH2FCF=CF2)、1,1,3−トリフルオロ−1−プロペン(CH2FCH=CF2)、1,3,3−トリフルオロ−1−プロペン(CHF2CH=CHF)、1,1,1,2,3,4,4,4−オクタフルオロ−2−ブテン(CF3CF=CFCF3)、1,1,2,3,3,4,4,4−オクタフルオロ−1−ブテン(CF3CF2CF=CF2)、1,1,1,2,4,4,4−ヘプタフルオロ−2−ブテン(CF3CF=CHCF3)、1,2,3,3,4,4,4−ヘプタフルオロ−1−ブテン(CHF=CFCF2CF3)、1,1,1,2,3,4,4−ヘプタフルオロ−2−ブテン(CHF2CF=CFCF3)、1,3,3,3−テトラフルオロ−2−(トリフルオロメチル)−1−プロペン((CF3)2C=CHF)、1,1,3,3,4,4,4−ヘプタフルオロ−1−ブテン(CF2=CHCF2CF3)、1,1,2,3,4,4,4−ヘプタフルオロ−1−ブテン(CF2=CFCHFCF3)、1,1,2,3,3,4,4−ヘプタフルオロ−1−ブテン(CF2=CFCF2CHF2)、2,3,3,4,4,4−ヘキサフルオロ−1−ブテン(CF3CF2CF=CH2)、1,3,3,4,4,4−ヘキサフルオロ−1−ブテン(CHF=CHCF2CF3)、1,2,3,4,4,4−ヘキサフルオロ−1−ブテン(CHF=CFCHFCF3)、1,2,3,3,4,4−ヘキサフルオロ−1−ブテン(CHF=CFCF2CHF2)、1,1,2,3,4,4−ヘキサフルオロ−2−ブテン(CHF2CF=CFCHF2)、1,1,1,2,3,4−ヘキサフルオロ−2−ブテン(CH2FCF=CFCF3)、1,1,1,2,4,4−ヘキサフルオロ−2−ブテン(CHF2CH=CFCF3)、1,1,1,3,4,4−ヘキサフルオロ−2−ブテン(CF3CH=CFCHF2)、1,1,2,3,3,4−ヘキサフルオロ−1−ブテン(CF2=CFCF2CH2F)、1,1,2,3,4,4−ヘキサフルオロ−1−ブテン(CF2=CFCHFCHF2)、3,3,3−トリフルオロ−2−(トリフルオロメチル)−1−プロペン(CH2=C(CF3)2)、1,1,1,2,4−ペンタフルオロ−2−ブテン(CH2FCH=CFCF3)、1,1,1,3,4−ペンタフルオロ−2−ブテン(CF3CH=CFCH2F)、3,3,4,4,4−ペンタフルオロ−1−ブテン(CF3CF2CH=CH2)、1,1,1,4,4−ペンタフルオロ−2−ブテン(CHF2CH=CHCF3)、1,1,1,2,3−ペンタフルオロ−2−ブテン(CH3CF=CFCF3)、2,3,3,4,4−ペンタフルオロ−1−ブテン(CH2=CFCF2CHF2)、1,1,2,4,4−ペンタフルオロ−2−ブテン(CHF2CF=CHCHF2)、1,1,2,3,3−ペンタフルオロ−1−ブテン(CH3CF2CF=CF2)、1,1,2,3,4−ペンタフルオロ−2−ブテン(CH2FCF=CFCHF2)、1,1,3,3,3−ペンタフルオロ−2−メチル−1−プロペン(CF2=C(CF3)(CH3))、2−(ジフルオロメチル)−3,3,3−トリフルオロ−1−プロペン(CH2=C(CHF2)(CF3))、2,3,4,4,4−ペンタフルオロ−1−ブテン(CH2=CFCHFCF3)、1,2,4,4,4−ペンタフルオロ−1−ブテン(CHF=CFCH2CF3)、1,3,4,4,4−ペンタフルオロ−1−ブテン(CHF=CHCHFCF3)、1,3,3,4,4−ペンタフルオロ−1−ブテン(CHF=CHCF2CHF2)、1,2,3,4,4−ペンタフルオロ−1−ブテン(CHF=CFCHFCHF2)、3,3,4,4−テトラフルオロ−1−ブテン(CH2=CHCF2CHF2)、1,1−ジフルオロ−2−(ジフルオロメチル)−1−プロペン(CF2=C(CHF2)(CH3))、1,3,3,3−テトラフルオロ−2−メチル−1−プロペン(CHF=C(CF3)(CH3))、3,3−ジフルオロ−2−(ジフルオロメチル)−1−プロペン(CH2=C(CHF2)2)、1,1,1,2−テトラフルオロ−2−ブテン(CF3CF=CHCH3)、1,1,1,3−テトラフルオロ−2−ブテン(CH3CF=CHCF3)、1,1,1,2,3,4,4,5,5,5−デカフルオロ−2−ペンテン(CF3CF=CFCF2CF3)、1,1,2,3,3,4,4,5,5,5−デカフルオロ−1−ペンテン(CF2=CFCF2CF2CF3)、1,1,1,4,4,4−ヘキサフルオロ−2−(トリフルオロメチル)−2−ブテン((CF3)2C=CHCF3)、1,1,1,2,4,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CF=CHCF2CF3)、1,1,1,3,4,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CH=CFCF2CF3)、1,2,3,3,4,4,5,5,5−ノナフルオロ−1−ペンテン(CHF=CFCF2CF2CF3)、1,1,3,3,4,4,5,5,5−ノナフルオロ−1−ペンテン(CF2=CHCF2CF2CF3)、1,1,2,3,3,4,4,5,5−ノナフルオロ−1−ペンテン(CF2=CFCF2CF2CHF2)、1,1,2,3,4,4,5,5,5−ノナフルオロ−2−ペンテン(CHF2CF=CFCF2CF3)、1,1,1,2,3,4,4,5,5−ノナフルオロ−2−ペンテン(CF3CF=CFCF2CHF2)、1,1,1,2,3,4,5,5,5−ノナフルオロ−2−ペンテン(CF3CF=CFCHFCF3)、1,2,3,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CFCF(CF3)2)、1,1,2,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CFCH(CF3)2)、1,1,1,4,4,4−ヘキサフルオロ−2−(トリフルオロメチル)−2−ブテン(CF3CH=C(CF3)2)、1,1,3,4,4,4−ヘキサフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CHCF(CF3)2)、2,3,3,4,4,5,5,5−オクタフルオロ−1−ペンテン(CH2=CFCF2CF2CF3)、1,2,3,3,4,4,5,5−オクタフルオロ−1−ペンテン(CHF=CFCF2CF2CHF2)、3,3,4,4,4−ペンタフルオロ−2−(トリフルオロメチル)−1−ブテン(CH2=C(CF3)CF2CF3)、1,1,4,4,4−ペンタフルオロ−3−(トリフルオロメチル)−1−ブテン(CF2=CHCH(CF3)2)、1,3,4,4,4−ペンタフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CHCF(CF3)2)、1,1,4,4,4−ペンタフルオロ−2−(トリフルオロメチル)−1−ブテン(CF2=C(CF3)CH2CF3)、3,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン((CF3)2CFCH=CH2)、3,3,4,4,5,5,5−ヘプタフルオロ−1−ペンテン(CF3CF2CF2CH=CH2)、2,3,3,4,4,5,5−ヘプタフルオロ−1−ペンテン(CH2=CFCF2CF2CHF2)、1,1,3,3,5,5,5−ヘプタフルオロ−1−ブテン(CF2=CHCF2CH2CF3)、1,1,1,2,4,4,4−ヘプタフルオロ−3−メチル−2−ブテン(CF3CF=C(CF3)(CH3))、2,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン(CH2=CFCH(CF3)2)、1,4,4,4−テトラフルオロ−3−(トリフルオロメチル)−1−ブテン(CHF=CHCH(CF3)2)、1,1,1,4−テトラフルオロ−2−(トリフルオロメチル)−2−ブテン(CH2FCH=C(CF3)2)、1,1,1,3−テトラフルオロ−2−(トリフルオロメチル)−2−ブテン(CH3CF=C(CF3)2)、1,1,1−トリフルオロ−2−(トリフルオロメチル)−2−ブテン((CF3)2C=CHCH3)、3,4,4,5,5,5−ヘキサフルオロ−2−ペンテン(CF3CF2CF=CHCH3)、1,1,1,4,4,4−ヘキサフルオロ−2−メチル−2−ブテン(CF3C(CH3)=CHCF3)、3,3,4,5,5,5−ヘキサフルオロ−1−ペンテン(CH
2=CHCF2CHFCF3)、4,4,4−トリフルオロ−2−(トリフルオロメチル)−1−ブテン(CH2=C(CF3)CH2CF3)、1,1,2,3,3,4,4,5,5,6,6,6−ドデカフルオロ−1−ヘキセン(CF3(CF2)3CF=CF2)、1,1,1,2,2,3,4,5,5,6,6,6−ドデカフルオロ−3−ヘキセン(CF3CF2CF=CFCF2CF3)、1,1,1,4,4,4−ヘキサフルオロ−2,3−ビス(トリフルオロメチル)−2−ブテン((CF3)2C=C(CF3)2)、1,1,1,2,3,4,5,5,5−ノナフルオロ−4−(トリフルオロメチル)−2−ペンテン((CF3)2CFCF=CFCF3)、1,1,1,4,4,5,5,5−オクタフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CHC2F5)、1,1,1,3,4,5,5,5−オクタフルオロ−4−(トリフルオロメチル)−2−ペンテン((CF3)2CFCF=CHCF3)、3,3,4,4,5,5,6,6,6−ノナフルオロ−1−ヘキセン(CF3CF2CF2CF2CH=CH2)、4,4,4−トリフルオロ−3,3−ビス(トリフルオロメチル)−1−ブテン(CH2=CHC(CF3)3)、1,1,1,4,4,4−ヘキサフルオロ−3−メチル−2−(トリフルオロメチル)−2−ブテン((CF3)2C=C(CH3)(CF3))、2,3,3,5,5,5−ヘキサフルオロ−4−(トリフルオロメチル)−1−ペンテン(CH2=CFCF2CH(CF3)2)、1,1,1,2,4,4,5,5,5−ノナフルオロ−3−メチル−2−ペンテン(CF3CF=C(CH3)CF2CF3)、1,1,1,5,5,5−ヘキサフルオロ−4−(トリフルオロメチル)−2−ペンテン(CF3CH=CHCH(CF3)2)、3,4,4,5,5,6,6,6−オクタフルオロ−2−ヘキセン(CF3CF2CF2CF=CHCH3)、3,3,4,4,5,5,6,6−オクタフルオロ1−ヘキセン(CH2=CHCF2CF2CF2CHF2)、1,1,1,4,4−ペンタフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CHCF2CH3)、4,4,5,5,5−ペンタフルオロ−2−(トリフルオロメチル)−1−ペンテン(CH2=C(CF3)CH2C2F5)、3,3,4,4,5,5,5−ヘプタフルオロ−2−メチル−1−ペンテン(CF3CF2CF2C(CH3)=CH2)、4,4,5,5,6,6,6−ヘプタフルオロ−2−ヘキセン(CF3CF2CF2CH=CHCH3)、4,4,5,5,6,6,6−ヘプタフルオロ−1−ヘキセン(CH2=CHCH2CF2C2F5)、1,1,1,2,2,3,4−ヘプタフルオロ−3−ヘキセン(CF3CF2CF=CFC2H5)、4,5,5,5−テトラフルオロ−4−(トリフルオロメチル)−1−ペンテン(CH2=CHCH2CF(CF3)2)、1,1,1,2,5,5,5−ヘプタフルオロ−4−メチル−2−ペンテン(CF3CF=CHCH(CF3)(CH3))、1,1,1,3−テトラフルオロ−2−(トリフルオロメチル)−2−ペンテン((CF3)2C=CFC2H5)、1,1,1,2,3,4,4,5,5,6,6,7,7,7−テトラデカフルオロ−2−ヘプテン(CF3CF=CFCF2CF2C2F5)、1,1,1,2,2,3,4,5,5,6,6,7,7,7−テトラデカフルオロ−3−ヘプテン(CF3CF2CF=CFCF2C2F5)、1,1,1,3,4,4,5,5,6,6,7,7,7−トリデカフルオロ−2−ヘプテン(CF3CH=CFCF2CF2C2F5)、1,1,1,2,4,4,5,5,6,6,7,7,7−トリデカフルオロ−2−ヘプテン(CF3CF=CHCF2CF2C2F5)、1,1,1,2,2,4,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(CF3CF2CH=CFCF2C2F5)および1,1,1,2,2,3,5,5,6,6,7,7,7−トリデカフルオロ−3−ヘプテン(CF3CF2CF=CHCF2C2F5)からなる群から選択されるフルオロオレフィン
からなる群から選択される少なくとも1つのヒドロフルオロカーボンまたはフルオロカーボンを含むことを特徴とする請求項5に記載の吸収パワーサイクルシステム。 The working fluid is
(I) a fluoroolefin of the formula E—R 1 CH═CHR 2 or Z—R 1 CH═CHR 2 where R 1 and R 2 are independently a C 1 -C 6 perfluoroalkyl group ,
(Ii) cyclic of the formula cyclo- [CX = CY (CZW) n- ], wherein X, Y, Z and W are independently H or F and n is an integer of 2-5. fluoroolefin, and (iii) tetrafluoroethylene (CF 2 = CF 2), hexafluoropropene (CF 3 CF = CF 2) , 1,2,3,3,3- pentafluoro-1-propene (CHF = CFCF 3 ), 1,1,3,3,3-pentafluoro-1-propene (CF 2 = CHCF 3 ), 1,1,2,3,3-pentafluoro-1-propene (CF 2 = CFCHF 2 ) , 1,2,3,3-tetrafluoro-1-propene (CHF = CFCHF 2), 2,3,3,3- tetrafluoro-1-propene (CH 2 = CFCF 3), 1,3,3, 3-tetrafluoro-1-propene (CHF = HCF 3), 1,1,2,3-tetrafluoro-1-propene (CF 2 = CFCH 2 F) , 1,1,3,3- tetrafluoro-1-propene (CF 2 = CHCHF 2), 1 , 2,3,3-tetrafluoro-1-propene (CHF = CFCHF 2), 3,3,3- trifluoro-1-propene (CH 2 = CHCF 3), 2,3,3- trifluoro -1 - propene (CHF 2 CF = CH 2) , 1,1,2- trifluoro-1-propene (CH 3 CF = CF 2) , 1,2,3- trifluoro-1-propene (CH 2 FCF = CF 2 ), 1,1,3-trifluoro-1-propene (CH 2 FCH═CF 2 ), 1,3,3-trifluoro-1-propene (CHF 2 CH═CHF), 1,1,1, 2,3,4,4,4-octafluoro-2-butene (C 3 CF = CFCF 3), 1,1,2,3,3,4,4,4- octafluoro-1-butene (CF 3 CF 2 CF = CF 2), 1,1,1,2,4, 4,4-heptafluoro-2-butene (CF 3 CF═CHCF 3 ), 1,2,3,3,4,4,4-heptafluoro-1-butene (CHF═CFCF 2 CF 3 ), 1, 1,1,2,3,4,4-heptafluoro-2-butene (CHF 2 CF═CFCF 3 ), 1,3,3,3-tetrafluoro-2- (trifluoromethyl) -1-propene ( (CF 3 ) 2 C═CHF), 1,1,3,3,4,4,4-heptafluoro-1-butene (CF 2 ═CHCF 2 CF 3 ), 1,1,2,3,4, 4,4-heptafluoro-1-butene (CF 2 = CFCHFCF 3 ), 1,1,2,3,3,4,4-heptaful Oro-1-butene (CF 2 = CFCF 2 CHF 2 ), 2,3,3,4,4,4-hexafluoro-1-butene (CF 3 CF 2 CF═CH 2 ), 1,3,3, 4,4,4-hexafluoro-1-butene (CHF = CHCF 2 CF 3 ), 1,2,3,4,4,4-hexafluoro-1-butene (CHF = CFCHFCF 3 ), 1,2, 3,3,4,4-hexafluoro-1-butene (CHF═CFCF 2 CHF 2 ), 1,1,2,3,4,4-hexafluoro-2-butene (CHF 2 CF═CFCHF 2 ), 1,1,1,2,3,4-hexafluoro-2-butene (CH 2 FCF═CFCF 3 ), 1,1,1,2,4,4-hexafluoro-2-butene (CHF 2 CH═ CFCF 3), 1,1,1,3,4,4- hexafluoro-2-butene (C 3 CH = CFCHF 2), 1,1,2,3,3,4- hexafluoro-1-butene (CF 2 = CFCF 2 CH 2 F), 1,1,2,3,4,4- hexafluoro 1-butene (CF 2 = CFCHFCHF 2), 3,3,3- trifluoro-2- (trifluoromethyl) -1-propene (CH 2 = C (CF 3 ) 2), 1,1,1, 2,4-pentafluoro-2-butene (CH 2 FCH═CFCF 3 ), 1,1,1,3,4-pentafluoro-2-butene (CF 3 CH═CFCH 2 F), 3,3,4 , 4,4-pentafluoro-1-butene (CF 3 CF 2 CH═CH 2 ), 1,1,1,4,4-pentafluoro-2-butene (CHF 2 CH═CHCF 3 ), 1,1 , 1,2,3-pentafluoro-2-butene (CH 3 CF = CFCF 3) , 2, , 3,4,4-pentafluoro-1-butene (CH 2 = CFCF 2 CHF 2 ), 1,1,2,4,4- pentafluoro-2-butene (CHF 2 CF = CHCHF 2) , 1, 1,2,3,3-pentafluoro-1-butene (CH 3 CF 2 CF = CF 2), 1,1,2,3,4- pentafluoro-2-butene (CH 2 FCF = CFCHF 2) , 1,1,3,3,3-pentafluoro-2-methyl-1-propene (CF 2 ═C (CF 3 ) (CH 3 )), 2- (difluoromethyl) -3,3,3-trifluoro 1-propene (CH 2 = C (CHF 2 ) (CF 3)), 2,3,4,4,4- pentafluoro-1-butene (CH 2 = CFCHFCF 3), 1,2,4,4 , 4-Pentafluoro-1-butene (CHF = CFCH 2 CF 3 ), 1,3,4, 4,4-pentafluoro-1-butene (CHF = CHCHFCF 3 ), 1,3,3,4,4-pentafluoro-1-butene (CHF = CHCF 2 CHF 2 ), 1,2,3,4, 4-pentafluoro-1-butene (CHF = CFCHFCHF 2 ), 3,3,4,4-tetrafluoro-1-butene (CH 2 = CHCF 2 CHF 2 ), 1,1-difluoro-2- (difluoromethyl) ) -1-propene (CF 2 ═C (CHF 2 ) (CH 3 )), 1,3,3,3-tetrafluoro-2-methyl-1-propene (CHF═C (CF 3 ) (CH 3 )) ), 3,3-difluoro-2- (difluoromethyl) -1-propene (CH 2 ═C (CHF 2 ) 2 ), 1,1,1,2-tetrafluoro-2-butene (CF 3 CF═CHCH) 3), 1,1,1,3-Tetorafuru B-2-butene (CH 3 CF = CHCF 3) , 1,1,1,2,3,4,4,5,5,5- decafluoro-2-pentene (CF 3 CF = CFCF 2 CF 3) , 1,1,2,3,3,4,4,5,5,5- decafluoro-1-pentene (CF 2 = CFCF 2 CF 2 CF 3), 1,1,1,4,4,4 - hexafluoro-2- (trifluoromethyl) -2-butene ((CF 3) 2 C = CHCF 3), 1,1,1,2,4,4,5,5,5- nonafluoro-2-pentene (CF 3 CF═CHCF 2 CF 3 ), 1,1,1,3,4,4,5,5,5-nonafluoro-2-pentene (CF 3 CH═CFCF 2 CF 3 ), 1,2,3 , 3,4,4,5,5,5- nonafluoro-1-pentene (CHF = CFCF 2 CF 2 CF 3), 1,1,3,3,4, , 5,5,5-nonafluoro-1-pentene (CF 2 = CHCF 2 CF 2 CF 3), 1,1,2,3,3,4,4,5,5- nonafluoro-1-pentene (CF 2 = CFCF 2 CF 2 CHF 2) , 1,1,2,3,4,4,5,5,5- nonafluoro-2-pentene (CHF 2 CF = CFCF 2 CF 3), 1,1,1,2 , 3,4,4,5,5-nonafluoro-2-pentene (CF 3 CF═CFCF 2 CHF 2 ), 1,1,1,2,3,4,5,5,5-nonafluoro-2-pentene (CF 3 CF═CFCHFCF 3 ), 1,2,3,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CHF═CFCF (CF 3 ) 2 ), 1,1, 2,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CFCH (CF 3 ) 2 ), 1,1,1,4,4,4-hexafluoro-2- (trifluoromethyl) -2-butene (CF 3 CH═C (CF 3 ) 2 ), 1, 1,3,4,4,4-hexafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CHCF (CF 3 ) 2 ), 2,3,3,4,4,5,5 5-octafluoro-1-pentene (CH 2 = CFCF 2 CF 2 CF 3), 1,2,3,3,4,4,5,5- octafluoro-1-pentene (CHF = CFCF 2 CF 2 CHF 2 ), 3,3,4,4,4-pentafluoro-2- (trifluoromethyl) -1-butene (CH 2 ═C (CF 3 ) CF 2 CF 3 ), 1,1,4,4 4-pentafluoro-3- (trifluoromethyl) -1-butene (CF 2 = CHCH (CF 3 ) 2), 1, 4,4,4-pentafluoro-3- (trifluoromethyl) -1-butene (CHF = CHCF (CF 3) 2), 1,1,4,4,4- pentafluoro-2- (trifluoromethyl methyl) -1-butene (CF 2 = C (CF 3 ) CH 2 CF 3), 3,4,4,4- tetrafluoro-3- (trifluoromethyl) -1-butene ((CF 3) 2 CFCH = CH 2), 3,3,4,4,5,5,5- heptafluoro-1-pentene (CF 3 CF 2 CF 2 CH = CH 2), 2,3,3,4,4,5, 5-heptafluoro-1-pentene (CH 2 = CFCF 2 CF 2 CHF 2), 1,1,3,3,5,5,5- heptafluoro-1-butene (CF 2 = CHCF 2 CH 2 CF 3 ), 1,1,1,2,4,4,4-heptafluoro-3-methyl-2-butene (C 3 CF = C (CF 3) (CH 3)), 2,4,4,4- tetrafluoro-3- (trifluoromethyl) -1-butene (CH 2 = CFCH (CF 3 ) 2), 1, 4,4,4-tetrafluoro-3- (trifluoromethyl) -1-butene (CHF = CHCH (CF 3 ) 2 ), 1,1,1,4-tetrafluoro-2- (trifluoromethyl)- 2-butene (CH 2 FCH═C (CF 3 ) 2 ), 1,1,1,3-tetrafluoro-2- (trifluoromethyl) -2-butene (CH 3 CF═C (CF 3 ) 2 ) 1,1,1-trifluoro-2- (trifluoromethyl) -2-butene ((CF 3 ) 2 C═CHCH 3 ), 3,4,4,5,5,5-hexafluoro-2- Pentene (CF 3 CF 2 CF═CHCH 3 ), 1,1,1,4,4,4-hexafluoro Ro-2-methyl-2-butene (CF 3 C (CH 3 ) ═CHCF 3 ), 3,3,4,5,5,5-hexafluoro-1-pentene (CH
2 = CHCF 2 CHFCF 3 ), 4,4,4-trifluoro-2- (trifluoromethyl) -1-butene (CH 2 ═C (CF 3 ) CH 2 CF 3 ), 1,1,2,3 , 3,4,4,5,5,6,6,6- dodecafluoro-1-hexene (CF 3 (CF 2) 3 CF = CF 2), 1,1,1,2,2,3,4 , 5,5,6,6,6- dodecafluoro-3- hexene (CF 3 CF 2 CF = CFCF 2 CF 3), 1,1,1,4,4,4- hexafluoro-2,3-bis (Trifluoromethyl) -2-butene ((CF 3 ) 2 C═C (CF 3 ) 2 ), 1,1,1,2,3,4,5,5,5-nonafluoro-4- (trifluoro methyl) -2-pentene ((CF 3) 2 CFCF = CFCF 3), 1,1,1,4,4,5,5,5- octafluoro-2- (g Fluoromethyl) -2-pentene ((CF 3) 2 C = CHC 2 F 5), 1,1,1,3,4,5,5,5- octafluoro-4- (trifluoromethyl) -2 Pentene ((CF 3 ) 2 CFCF═CHCF 3 ), 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene (CF 3 CF 2 CF 2 CF 2 CH═CH 2 ) , 4,4,4-trifluoro-3,3-bis (trifluoromethyl) -1-butene (CH 2 = CHC (CF 3 ) 3), 1,1,1,4,4,4- hexafluoro -3-methyl-2- (trifluoromethyl) -2-butene ((CF 3) 2 C = C (CH 3) (CF 3)), 2,3,3,5,5,5- hexafluoro - 4- (trifluoromethyl) -1-pentene (CH 2 = CFCF 2 CH ( CF 3) 2), 1,1,1,2 , 4,4,5,5,5-nonafluoro-3-methyl-2-pentene (CF 3 CF = C (CH 3) CF 2 CF 3), 1,1,1,5,5,5- hexafluoro 4- (trifluoromethyl) -2-pentene (CF 3 CH = CHCH (CF 3) 2), 3,4,4,5,5,6,6,6- octafluoro-2-hexene (CF 3 CF 2 CF 2 CF═CHCH 3 ), 3,3,4,4,5,5,6,6-octafluoro 1-hexene (CH 2 ═CHCF 2 CF 2 CF 2 CHF 2 ), 1,1,1 , 4,4-pentafluoro-2- (trifluoromethyl) -2-pentene ((CF 3 ) 2 C═CHCF 2 CH 3 ), 4,4,5,5,5-pentafluoro-2- (tri fluoromethyl) -1-pentene (CH 2 = C (CF 3 ) CH 2 C 2 F 5), 3,3,4,4 5,5,5-heptafluoro-2-methyl-1-pentene (CF 3 CF 2 CF 2 C (CH 3) = CH 2), 4,4,5,5,6,6,6- heptafluoro - 2- hexene (CF 3 CF 2 CF 2 CH = CHCH 3), 4,4,5,5,6,6,6- heptafluoro-1-hexene (CH 2 = CHCH 2 CF 2 C 2 F 5), 1,1,1,2,2,3,4-heptafluoro-3-hexene (CF 3 CF 2 CF═CFC 2 H 5 ), 4,5,5,5-tetrafluoro-4- (trifluoromethyl) ) 1-pentene (CH 2 = CHCH 2 CF ( CF 3) 2), 1,1,1,2,5,5,5- heptafluoro-4-methyl-2-pentene (CF 3 CF = CHCH ( CF 3) (CH 3)) , 1,1,1,3- tetrafluoro-2- (trifluoromethyl) - - pentene ((CF 3) 2 C = CFC 2 H 5), 1,1,1,2,3,4,4,5,5,6,6,7,7,7- tetradecanoyl-fluoro-2- heptene (CF 3 CF = CFCF 2 CF 2 C 2 F 5), 1,1,1,2,2,3,4,5,5,6,6,7,7,7- tetradecanoyl-fluoro-3- Heptene (CF 3 CF 2 CF═CFCF 2 C 2 F 5 ), 1,1,1,3,4,4,5,5,6,6,7,7,7-tridecafluoro-2-heptene ( CF 3 CH═CFCF 2 CF 2 C 2 F 5 ), 1,1,1,2,4,4,5,5,6,6,7,7,7-tridecafluoro-2-heptene (CF 3 CF = CHCF 2 CF 2 C 2 F 5 ), 1,1,1,2,2,4,5,5,6,6,7,7,7-tridecafluoro-3-heptene (CF 3 CF 2 CH = CFCF 2 C 2 F 5 ) and 1,1,1,2,2,3,5,5,6,6,7,7,7-tridecafluoro-3-heptene (CF 3 CF 2 CF═CHCF 2 C 2 F The absorption power cycle system according to claim 5, comprising at least one hydrofluorocarbon or fluorocarbon selected from the group consisting of fluoroolefins selected from the group consisting of 5 ).
(b)前吸収剤/作動流体混合物を加熱して、作動流体蒸気を放出する工程と、
(c)前記作動流体蒸気を機械仕事を生じさせるためのデバイスに送る工程と、
(d)加熱された吸収剤/作動流体混合物を再形成する工程と
を含むことを特徴とする機械仕事を生じさせる方法。 (A) forming an absorbent / working fluid mixture in the absorber;
(B) heating the pre-absorbent / working fluid mixture to release working fluid vapor;
(C) sending the working fluid vapor to a device for generating mechanical work;
(D) reshaping the heated absorbent / working fluid mixture.
(c−i)凝縮器において前記作動流体を凝縮する工程と、
(c−ii)膨張デバイスにおいて前記作動流体を部分的に蒸発させる工程と、
(c−iii)蒸発器において前記作動流体を完全に蒸発させて、冷却を行う工程と
をさらに含むことを特徴とする請求項12に記載の方法。 Between steps (c) and (d),
(Ci) condensing the working fluid in a condenser;
(C-ii) partially evaporating the working fluid in an expansion device;
The method according to claim 12, further comprising: (c-iii) completely evaporating the working fluid in an evaporator and performing cooling.
(c−i)凝縮器において前記作動流体を凝縮して熱を生成する工程と、
(c−ii)膨張デバイスにおいて前記作動流体を部分的に蒸発させる工程と、
(c−iii)蒸発器において前記作動流体を完全に蒸発させる工程と
をさらに含むことを特徴とする請求項12に記載の方法。 Between steps (c) and (d),
(Ci) condensing the working fluid in a condenser to generate heat;
(C-ii) partially evaporating the working fluid in an expansion device;
The method of claim 12, further comprising: (c-iii) completely evaporating the working fluid in an evaporator.
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| US13918008P | 2008-12-19 | 2008-12-19 | |
| US61/139,180 | 2008-12-19 | ||
| PCT/US2009/068380 WO2010080467A2 (en) | 2008-12-19 | 2009-12-17 | Absorption power cycle system |
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- 2009-12-17 EP EP09775491A patent/EP2359076A2/en not_active Withdrawn
- 2009-12-17 WO PCT/US2009/068380 patent/WO2010080467A2/en not_active Ceased
- 2009-12-17 JP JP2011542417A patent/JP2012512991A/en not_active Withdrawn
- 2009-12-17 KR KR1020117016679A patent/KR20110111413A/en not_active Withdrawn
- 2009-12-17 BR BRPI0917780A patent/BRPI0917780A2/en not_active IP Right Cessation
- 2009-12-17 CN CN200980151129XA patent/CN102257334A/en active Pending
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