JP2012512991A5 - - Google Patents
Download PDFInfo
- Publication number
- 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.)
- Withdrawn
Links
- 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
- VVMQLAKDFBLCHB-UHFFFAOYSA-N 1,1,1,2,3,4,4,5,5,5-decafluoropent-2-ene Chemical compound FC(F)(F)C(F)=C(F)C(F)(F)C(F)(F)F VVMQLAKDFBLCHB-UHFFFAOYSA-N 0.000 claims description 2
- MRZSIBDWXMHMHF-UHFFFAOYSA-N 1,1,1,2,3,4,4,5,5-nonafluoropent-2-ene Chemical compound FC(F)C(F)(F)C(F)=C(F)C(F)(F)F MRZSIBDWXMHMHF-UHFFFAOYSA-N 0.000 claims description 2
- BLNWTWDBKNPDDJ-UHFFFAOYSA-N 1,1,1,2,3,4,4-heptafluorobut-2-ene Chemical compound FC(F)C(F)=C(F)C(F)(F)F BLNWTWDBKNPDDJ-UHFFFAOYSA-N 0.000 claims description 2
- INDAMBLSEJSSNR-UHFFFAOYSA-N 1,1,1,2,3,4,5,5,5-nonafluoropent-2-ene Chemical compound FC(F)(F)C(F)C(F)=C(F)C(F)(F)F INDAMBLSEJSSNR-UHFFFAOYSA-N 0.000 claims description 2
- JSADPKAWAKXUTE-UHFFFAOYSA-N 1,1,1,2,3,4-hexafluorobut-2-ene Chemical compound FCC(F)=C(F)C(F)(F)F JSADPKAWAKXUTE-UHFFFAOYSA-N 0.000 claims description 2
- HBNXKNOVGAHUNV-UHFFFAOYSA-N 1,1,1,2,3-pentafluorobut-2-ene Chemical compound CC(F)=C(F)C(F)(F)F HBNXKNOVGAHUNV-UHFFFAOYSA-N 0.000 claims description 2
- JBYVVEFBYYDZIM-UHFFFAOYSA-N 1,1,1,2,4,4,4-heptafluoro-3-methylbut-2-ene Chemical compound FC(F)(F)C(C)=C(F)C(F)(F)F JBYVVEFBYYDZIM-UHFFFAOYSA-N 0.000 claims description 2
- QJUQOEDMOXIJDL-UHFFFAOYSA-N 1,1,1,2,4,4,5,5,6,6,7,7,7-tridecafluorohept-2-ene Chemical compound FC(F)(F)C(F)=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)F QJUQOEDMOXIJDL-UHFFFAOYSA-N 0.000 claims description 2
- LTVIWHSKXRWJJN-UHFFFAOYSA-N 1,1,1,2,4,4-hexafluorobut-2-ene Chemical compound FC(F)C=C(F)C(F)(F)F LTVIWHSKXRWJJN-UHFFFAOYSA-N 0.000 claims description 2
- JZSOMBFGZXZIJI-UHFFFAOYSA-N 1,1,1,2,4-pentafluorobut-2-ene Chemical compound FCC=C(F)C(F)(F)F JZSOMBFGZXZIJI-UHFFFAOYSA-N 0.000 claims description 2
- HHDLUXLBJXTFHQ-UHFFFAOYSA-N 1,1,1,2,5,5,5-heptafluoro-4-methylpent-2-ene Chemical compound FC(F)(F)C(C)C=C(F)C(F)(F)F HHDLUXLBJXTFHQ-UHFFFAOYSA-N 0.000 claims description 2
- AQWKMAFGWXOGIG-UHFFFAOYSA-N 1,1,1,2,5,5,6,6,7,7,7-undecafluoro-2-(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)F AQWKMAFGWXOGIG-UHFFFAOYSA-N 0.000 claims description 2
- MOFKZTVDKCOVFH-UHFFFAOYSA-N 1,1,1,2,5,5,6,6,7,7,8,8,8-tridecafluoro-2-(trifluoromethyl)oct-3-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)F MOFKZTVDKCOVFH-UHFFFAOYSA-N 0.000 claims description 2
- POVIEAZAEWOXMC-UHFFFAOYSA-N 1,1,1,2,5,5,6,6,7,7,8,8,9,9,9-pentadecafluoro-2-(trifluoromethyl)non-3-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)F POVIEAZAEWOXMC-UHFFFAOYSA-N 0.000 claims description 2
- MDHZOVDNDIWFOL-UHFFFAOYSA-N 1,1,1,2,5,5,6,6,7,8,8,8-dodecafluoro-2,7-bis(trifluoromethyl)oct-3-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C=CC(F)(F)C(F)(F)C(F)(C(F)(F)F)C(F)(F)F MDHZOVDNDIWFOL-UHFFFAOYSA-N 0.000 claims description 2
- MENIAFHNLVVJPO-UHFFFAOYSA-N 1,1,1,2,5,5,6,7,7,7-decafluoro-2,6-bis(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F MENIAFHNLVVJPO-UHFFFAOYSA-N 0.000 claims description 2
- CGTAZKPCFRZASZ-UHFFFAOYSA-N 1,1,1,2,5,6,6,6-octafluoro-2,5-bis(trifluoromethyl)hex-3-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C=CC(F)(C(F)(F)F)C(F)(F)F CGTAZKPCFRZASZ-UHFFFAOYSA-N 0.000 claims description 2
- SPCJQBWPTGIYJG-UHFFFAOYSA-N 1,1,1,2,5,6,6,7,7,7-decafluoro-2,5-bis(trifluoromethyl)hept-3-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)F SPCJQBWPTGIYJG-UHFFFAOYSA-N 0.000 claims description 2
- GWUOUBDZRNVLJX-UHFFFAOYSA-N 1,1,1,2,6,6,7,7,7-nonafluoro-2,5,5-tris(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(F)C(C(F)(F)F)(C(F)(F)F)C=CC(F)(C(F)(F)F)C(F)(F)F GWUOUBDZRNVLJX-UHFFFAOYSA-N 0.000 claims description 2
- MMJXXOIUVNOFPL-UHFFFAOYSA-N 1,1,1,2-tetrafluorobut-2-ene Chemical compound CC=C(F)C(F)(F)F MMJXXOIUVNOFPL-UHFFFAOYSA-N 0.000 claims description 2
- BSXMAPHRWXFCMC-UHFFFAOYSA-N 1,1,1,3,4,4,5,5,6,6,7,7,7-tridecafluorohept-2-ene Chemical compound FC(F)(F)C=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F BSXMAPHRWXFCMC-UHFFFAOYSA-N 0.000 claims description 2
- JVLWJKWBKARHRQ-UHFFFAOYSA-N 1,1,1,3,4,4-hexafluorobut-2-ene Chemical compound FC(F)C(F)=CC(F)(F)F JVLWJKWBKARHRQ-UHFFFAOYSA-N 0.000 claims description 2
- RGYWQQYKFBYEHS-UHFFFAOYSA-N 1,1,1,3,4,5,5,5-octafluoro-4-(trifluoromethyl)pent-2-ene Chemical compound FC(F)(F)C=C(F)C(F)(C(F)(F)F)C(F)(F)F RGYWQQYKFBYEHS-UHFFFAOYSA-N 0.000 claims description 2
- YCBCLGNNEUTCEC-UHFFFAOYSA-N 1,1,1,3,4-pentafluorobut-2-ene Chemical compound FCC(F)=CC(F)(F)F YCBCLGNNEUTCEC-UHFFFAOYSA-N 0.000 claims description 2
- CGLWHABLUPITJQ-UHFFFAOYSA-N 1,1,1,3-tetrafluoro-2-(trifluoromethyl)but-2-ene Chemical compound CC(F)=C(C(F)(F)F)C(F)(F)F CGLWHABLUPITJQ-UHFFFAOYSA-N 0.000 claims description 2
- LRUCMYWNQPGVEL-UHFFFAOYSA-N 1,1,1,3-tetrafluoro-2-(trifluoromethyl)pent-2-ene Chemical compound CCC(F)=C(C(F)(F)F)C(F)(F)F LRUCMYWNQPGVEL-UHFFFAOYSA-N 0.000 claims description 2
- CUKJWRYRLCTJNJ-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl)but-2-ene Chemical compound FC(F)(F)C(C(F)(F)F)=C(C(F)(F)F)C(F)(F)F CUKJWRYRLCTJNJ-UHFFFAOYSA-N 0.000 claims description 2
- FOLBRSGQGGTARP-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluoro-2-methyl-3-(trifluoromethyl)but-2-ene Chemical compound FC(F)(F)C(C)=C(C(F)(F)F)C(F)(F)F FOLBRSGQGGTARP-UHFFFAOYSA-N 0.000 claims description 2
- NLOLSXYRJFEOTA-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluorobut-2-ene Chemical compound FC(F)(F)C=CC(F)(F)F NLOLSXYRJFEOTA-UHFFFAOYSA-N 0.000 claims description 2
- CVMVAHSMKGITAV-UHFFFAOYSA-N 1,1,1,4,4,5,5,5-octafluoropent-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)F CVMVAHSMKGITAV-UHFFFAOYSA-N 0.000 claims description 2
- JSQOTUOXUHPDPI-UHFFFAOYSA-N 1,1,1,4,4,5,5,6,6,7,7,7-dodecafluorohept-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)F JSQOTUOXUHPDPI-UHFFFAOYSA-N 0.000 claims description 2
- JYJDYPJOQLXHAY-UHFFFAOYSA-N 1,1,1,4,4,5,5,6,6,7,7,8,8,8-tetradecafluorooct-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F JYJDYPJOQLXHAY-UHFFFAOYSA-N 0.000 claims description 2
- HBRPTBHEGLRYCI-UHFFFAOYSA-N 1,1,1,4,4,5,5,6,7,7,7-undecafluoro-6-(trifluoromethyl)hept-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(F)C(F)(C(F)(F)F)C(F)(F)F HBRPTBHEGLRYCI-UHFFFAOYSA-N 0.000 claims description 2
- JSHNCPXULRISNM-UHFFFAOYSA-N 1,1,1,4,4,5,6,6,6-nonafluoro-5-(trifluoromethyl)hex-2-ene Chemical compound FC(F)(F)C=CC(F)(F)C(F)(C(F)(F)F)C(F)(F)F JSHNCPXULRISNM-UHFFFAOYSA-N 0.000 claims description 2
- JBKYCTFEBKECDW-UHFFFAOYSA-N 1,1,1,4,4-pentafluoro-2-(trifluoromethyl)pent-2-ene Chemical compound CC(F)(F)C=C(C(F)(F)F)C(F)(F)F JBKYCTFEBKECDW-UHFFFAOYSA-N 0.000 claims description 2
- DBSLQKROKPOBHG-UHFFFAOYSA-N 1,1,1,4,5,5,6,6,6-nonafluoro-4-(trifluoromethyl)hex-2-ene Chemical compound FC(F)(F)C=CC(F)(C(F)(F)F)C(F)(F)C(F)(F)F DBSLQKROKPOBHG-UHFFFAOYSA-N 0.000 claims description 2
- FQJHHXBFDDKSEP-UHFFFAOYSA-N 1,1,1,4-tetrafluoro-2-(trifluoromethyl)but-2-ene Chemical compound FCC=C(C(F)(F)F)C(F)(F)F FQJHHXBFDDKSEP-UHFFFAOYSA-N 0.000 claims description 2
- VXZOROPSQKWUGE-UHFFFAOYSA-N 1,1,1,5,5,6,6,6-octafluoro-4,4-bis(trifluoromethyl)hex-2-ene Chemical compound FC(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)C(F)(F)F VXZOROPSQKWUGE-UHFFFAOYSA-N 0.000 claims description 2
- YBUBKYDEBDTCPO-UHFFFAOYSA-N 1,1,1,5,5,6,6,7,7,7-decafluoro-2,2-bis(trifluoromethyl)hept-3-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)F YBUBKYDEBDTCPO-UHFFFAOYSA-N 0.000 claims description 2
- RYSQTCRDEZOZHM-UHFFFAOYSA-N 1,1,1,5,5,6,7,7,7-nonafluoro-2,2,6-tris(trifluoromethyl)hept-3-ene Chemical compound FC(F)(F)C(F)(C(F)(F)F)C(F)(F)C=CC(C(F)(F)F)(C(F)(F)F)C(F)(F)F RYSQTCRDEZOZHM-UHFFFAOYSA-N 0.000 claims description 2
- QQXUXJCUYPLLIK-UHFFFAOYSA-N 1,1,1-trifluoro-2-(trifluoromethyl)but-2-ene Chemical compound CC=C(C(F)(F)F)C(F)(F)F QQXUXJCUYPLLIK-UHFFFAOYSA-N 0.000 claims description 2
- DRZKCOVBPOESIK-UHFFFAOYSA-N 1,1,1-trifluoronon-4-ene Chemical compound CCCCC=CCCC(F)(F)F DRZKCOVBPOESIK-UHFFFAOYSA-N 0.000 claims description 2
- MENFQHLOYXZCGV-UHFFFAOYSA-N 1,1,1-trifluorooct-3-ene Chemical compound CCCCC=CCC(F)(F)F MENFQHLOYXZCGV-UHFFFAOYSA-N 0.000 claims description 2
- ZVJOQYFQSQJDDX-UHFFFAOYSA-N 1,1,2,3,3,4,4,4-octafluorobut-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)F ZVJOQYFQSQJDDX-UHFFFAOYSA-N 0.000 claims description 2
- PBWHQPOHADDEFU-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,5-decafluoropent-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F PBWHQPOHADDEFU-UHFFFAOYSA-N 0.000 claims description 2
- RMHCWMIZBMGHKV-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,6,6,6-dodecafluorohex-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RMHCWMIZBMGHKV-UHFFFAOYSA-N 0.000 claims description 2
- XIHZPMIIUZSVFY-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5-nonafluoropent-1-ene Chemical compound FC(F)C(F)(F)C(F)(F)C(F)=C(F)F XIHZPMIIUZSVFY-UHFFFAOYSA-N 0.000 claims description 2
- SXKNYNUXUHCUHX-UHFFFAOYSA-N 1,1,2,3,3,4-hexafluorobut-1-ene Chemical compound FCC(F)(F)C(F)=C(F)F SXKNYNUXUHCUHX-UHFFFAOYSA-N 0.000 claims description 2
- HQMMBTYEDVZZOA-UHFFFAOYSA-N 1,1,2,3,3-pentafluorobut-1-ene Chemical compound CC(F)(F)C(F)=C(F)F HQMMBTYEDVZZOA-UHFFFAOYSA-N 0.000 claims description 2
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 claims description 2
- PKOMSEMCHKPPOC-UHFFFAOYSA-N 1,1,2,3,4,4,4-heptafluorobut-1-ene Chemical compound FC(F)(F)C(F)C(F)=C(F)F PKOMSEMCHKPPOC-UHFFFAOYSA-N 0.000 claims description 2
- CCHWGPNQONFKSV-UHFFFAOYSA-N 1,1,2,3,4,4,5,5,5-nonafluoropent-2-ene Chemical compound FC(F)C(F)=C(F)C(F)(F)C(F)(F)F CCHWGPNQONFKSV-UHFFFAOYSA-N 0.000 claims description 2
- PJJZTZMNFKVNPA-UHFFFAOYSA-N 1,1,2,3,4,4-hexafluorobut-1-ene Chemical compound FC(F)C(F)C(F)=C(F)F PJJZTZMNFKVNPA-UHFFFAOYSA-N 0.000 claims description 2
- CCESOERWJBCZBO-UHFFFAOYSA-N 1,1,2,3,4,4-hexafluorobut-2-ene Chemical compound FC(F)C(F)=C(F)C(F)F CCESOERWJBCZBO-UHFFFAOYSA-N 0.000 claims description 2
- PNVHHLZXQBHKNX-UHFFFAOYSA-N 1,1,2,3,4-pentafluorobut-2-ene Chemical compound FCC(F)=C(F)C(F)F PNVHHLZXQBHKNX-UHFFFAOYSA-N 0.000 claims description 2
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 claims description 2
- HSHAILBKIPODRY-UHFFFAOYSA-N 1,1,2,4,4,4-hexafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC(F)=C(F)C(C(F)(F)F)C(F)(F)F HSHAILBKIPODRY-UHFFFAOYSA-N 0.000 claims description 2
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 claims description 2
- LNGDLROYEAUMEQ-UHFFFAOYSA-N 1,1,2-trifluoroprop-1-ene Chemical compound CC(F)=C(F)F LNGDLROYEAUMEQ-UHFFFAOYSA-N 0.000 claims description 2
- WEYCUBLCUXRXRQ-UHFFFAOYSA-N 1,1,3,3,3-pentafluoro-2-methylprop-1-ene Chemical compound FC(F)=C(C)C(F)(F)F WEYCUBLCUXRXRQ-UHFFFAOYSA-N 0.000 claims description 2
- GCNWWRIQEJNUIF-UHFFFAOYSA-N 1,1,3,3,4,4,4-heptafluorobut-1-ene Chemical compound FC(F)=CC(F)(F)C(F)(F)F GCNWWRIQEJNUIF-UHFFFAOYSA-N 0.000 claims description 2
- BNYODXFAOQCIIO-UHFFFAOYSA-N 1,1,3,3-tetrafluoroprop-1-ene Chemical compound FC(F)C=C(F)F BNYODXFAOQCIIO-UHFFFAOYSA-N 0.000 claims description 2
- UDLSJLBLIOSNHV-UHFFFAOYSA-N 1,1,3,4,4,4-hexafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC(F)=CC(F)(C(F)(F)F)C(F)(F)F UDLSJLBLIOSNHV-UHFFFAOYSA-N 0.000 claims description 2
- URZZGOOCQOQVOC-UHFFFAOYSA-N 1,1,3-trifluoroprop-1-ene Chemical compound FCC=C(F)F URZZGOOCQOQVOC-UHFFFAOYSA-N 0.000 claims description 2
- DMUPYMORYHFFCT-UHFFFAOYSA-N 1,2,3,3,3-pentafluoroprop-1-ene Chemical compound FC=C(F)C(F)(F)F DMUPYMORYHFFCT-UHFFFAOYSA-N 0.000 claims description 2
- PVYYRPAHXQUHAW-UHFFFAOYSA-N 1,2,3,3,4,4,4-heptafluorobut-1-ene Chemical compound FC=C(F)C(F)(F)C(F)(F)F PVYYRPAHXQUHAW-UHFFFAOYSA-N 0.000 claims description 2
- YAQXNCHHASYLCA-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoropent-1-ene Chemical compound FC=C(F)C(F)(F)C(F)(F)C(F)(F)F YAQXNCHHASYLCA-UHFFFAOYSA-N 0.000 claims description 2
- ZFFLXJVVPHACEG-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,6,6-decafluorocyclohexene Chemical compound FC1=C(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F ZFFLXJVVPHACEG-UHFFFAOYSA-N 0.000 claims description 2
- YBMDPYAEZDJWNY-UHFFFAOYSA-N 1,2,3,3,4,4,5,5-octafluorocyclopentene Chemical compound FC1=C(F)C(F)(F)C(F)(F)C1(F)F YBMDPYAEZDJWNY-UHFFFAOYSA-N 0.000 claims description 2
- OUXZWOASPZPWJQ-UHFFFAOYSA-N 1,2,3,3,4,4,5,5-octafluoropent-1-ene Chemical compound FC=C(F)C(F)(F)C(F)(F)C(F)F OUXZWOASPZPWJQ-UHFFFAOYSA-N 0.000 claims description 2
- QVHWOZCZUNPZPW-UHFFFAOYSA-N 1,2,3,3,4,4-hexafluorocyclobutene Chemical compound FC1=C(F)C(F)(F)C1(F)F QVHWOZCZUNPZPW-UHFFFAOYSA-N 0.000 claims description 2
- DQXNKOLPOICZKZ-UHFFFAOYSA-N 1,2,3,4,4,4-hexafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC=C(F)C(F)(C(F)(F)F)C(F)(F)F DQXNKOLPOICZKZ-UHFFFAOYSA-N 0.000 claims description 2
- ZEDVIYBBMGBWDN-UHFFFAOYSA-N 1,2,3,4,4,4-hexafluorobut-1-ene Chemical compound FC=C(F)C(F)C(F)(F)F ZEDVIYBBMGBWDN-UHFFFAOYSA-N 0.000 claims description 2
- PPPRDNQESONMRT-UHFFFAOYSA-N 1,2,3,4,4-pentafluorobut-1-ene Chemical compound FC=C(F)C(F)C(F)F PPPRDNQESONMRT-UHFFFAOYSA-N 0.000 claims description 2
- TXHNVFGQJAAUNB-UHFFFAOYSA-N 1,2,3-trifluoroprop-1-ene Chemical compound FCC(F)=CF TXHNVFGQJAAUNB-UHFFFAOYSA-N 0.000 claims description 2
- GKHWFTRRRKPLGU-UHFFFAOYSA-N 1,2,4,4,4-pentafluorobut-1-ene Chemical compound FC=C(F)CC(F)(F)F GKHWFTRRRKPLGU-UHFFFAOYSA-N 0.000 claims description 2
- FYDLLXJLGCDGFH-UHFFFAOYSA-N 1,3,3,3-tetrafluoro-2-(trifluoromethyl)prop-1-ene Chemical compound FC=C(C(F)(F)F)C(F)(F)F FYDLLXJLGCDGFH-UHFFFAOYSA-N 0.000 claims description 2
- FPWXPJYOCIDGEH-UHFFFAOYSA-N 1,3,3,3-tetrafluoro-2-methylprop-1-ene Chemical compound FC=C(C)C(F)(F)F FPWXPJYOCIDGEH-UHFFFAOYSA-N 0.000 claims description 2
- CDOOAUSHHFGWSA-UHFFFAOYSA-N 1,3,3,3-tetrafluoropropene Chemical compound FC=CC(F)(F)F CDOOAUSHHFGWSA-UHFFFAOYSA-N 0.000 claims description 2
- LYSWMVUQFULFQU-UHFFFAOYSA-N 1,3,3,4,4,4-hexafluorobut-1-ene Chemical compound FC=CC(F)(F)C(F)(F)F LYSWMVUQFULFQU-UHFFFAOYSA-N 0.000 claims description 2
- XVHNAYYMRHUCFJ-UHFFFAOYSA-N 1,3,3,4,4-pentafluorobut-1-ene Chemical compound FC=CC(F)(F)C(F)F XVHNAYYMRHUCFJ-UHFFFAOYSA-N 0.000 claims description 2
- FVLJAHBUWGQLBO-UHFFFAOYSA-N 1,3,4,4,4-pentafluorobut-1-ene Chemical compound FC=CC(F)C(F)(F)F FVLJAHBUWGQLBO-UHFFFAOYSA-N 0.000 claims description 2
- FHKSBNVLMZMYCI-UHFFFAOYSA-N 1,4,4,4-tetrafluoro-3-(trifluoromethyl)but-1-ene Chemical compound FC=CC(C(F)(F)F)C(F)(F)F FHKSBNVLMZMYCI-UHFFFAOYSA-N 0.000 claims description 2
- FAOACLKUNWKVPH-UHFFFAOYSA-N 2,3,3,4,4,4-hexafluorobut-1-ene Chemical compound FC(=C)C(F)(F)C(F)(F)F FAOACLKUNWKVPH-UHFFFAOYSA-N 0.000 claims description 2
- ZHKVUSSHABANQG-UHFFFAOYSA-N 2,3,3,4,4,5,5-heptafluoropent-1-ene Chemical compound FC(F)C(F)(F)C(F)(F)C(F)=C ZHKVUSSHABANQG-UHFFFAOYSA-N 0.000 claims description 2
- RDIZQSPNUCXZQY-UHFFFAOYSA-N 2,3,3,5,5,5-hexafluoro-4-(trifluoromethyl)pent-1-ene Chemical compound FC(=C)C(F)(F)C(C(F)(F)F)C(F)(F)F RDIZQSPNUCXZQY-UHFFFAOYSA-N 0.000 claims description 2
- JMRIJKGIVGYIAD-UHFFFAOYSA-N 2,3,3-trifluoroprop-1-ene Chemical compound FC(F)C(F)=C JMRIJKGIVGYIAD-UHFFFAOYSA-N 0.000 claims description 2
- 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
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| 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 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012512991A JP2012512991A (ja) | 2012-06-07 |
| JP2012512991A5 true JP2012512991A5 (https=) | 2013-01-24 |
Family
ID=42264102
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011542417A Withdrawn JP2012512991A (ja) | 2008-12-19 | 2009-12-17 | 吸収パワーサイクルシステム |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20100154419A1 (https=) |
| EP (1) | EP2359076A2 (https=) |
| JP (1) | JP2012512991A (https=) |
| KR (1) | KR20110111413A (https=) |
| CN (1) | CN102257334A (https=) |
| AU (1) | AU2009335807A1 (https=) |
| BR (1) | BRPI0917780A2 (https=) |
| WO (1) | WO2010080467A2 (https=) |
Families Citing this family (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY160614A (en) * | 2006-02-28 | 2017-03-15 | Du Pont | Azeotropic compositions comprising fluorinated compounds for cleaning applications |
| US7641808B2 (en) * | 2007-08-23 | 2010-01-05 | E.I. Du Pont De Nemours And Company | Azeotropic compositions comprising fluorinated olefins for cleaning applications |
| CA2742522C (en) | 2008-11-06 | 2019-02-12 | Michael Hoey | Systems and methods for treatment of prostatic tissue |
| BRPI0914356A2 (pt) * | 2008-11-07 | 2015-10-20 | Du Pont | "composições, aparelho para ajuste de temperatura e processo para ajustar a temperatura de um objeto, meio ou um espaço" |
| US9833277B2 (en) | 2009-04-27 | 2017-12-05 | Nxthera, Inc. | Systems and methods for prostate treatment |
| FR2948679B1 (fr) | 2009-07-28 | 2011-08-19 | Arkema France | Procede de transfert de chaleur |
| US20110144216A1 (en) * | 2009-12-16 | 2011-06-16 | Honeywell International Inc. | Compositions and uses of cis-1,1,1,4,4,4-hexafluoro-2-butene |
| HUE047698T2 (hu) * | 2009-12-22 | 2020-05-28 | Chemours Co Fc Llc | 2,3,3,3-tetrafluorpropént és 2,3-diklór-3,3-difluorpropént tartalmazó kompozíciók |
| WO2011103560A2 (en) * | 2010-02-22 | 2011-08-25 | University Of South Florida | Method and system for generating power from low- and mid- temperature heat sources |
| CN103026149B (zh) * | 2010-04-01 | 2015-08-19 | 埃内尔谋申公司 | 用于存储热能以作为车辆中辅助能源的系统和方法 |
| US8961812B2 (en) * | 2010-04-15 | 2015-02-24 | E I Du Pont De Nemours And Company | Compositions comprising Z-1,2-difluoroethylene and uses thereof |
| US8961811B2 (en) * | 2010-04-15 | 2015-02-24 | E I Du Pont De Nemours And Company | Compositions comprising E-1,2-difluoroethylene and uses thereof |
| CA2841429C (en) * | 2010-08-26 | 2019-04-16 | Michael Joseph Timlin, Iii | A binary condensing thermal power cycle |
| US20120090808A1 (en) * | 2010-10-18 | 2012-04-19 | Alcatel-Lucent Usa, Incorporated | Liquid cooling of remote or off-grid electronic enclosures |
| US20120102996A1 (en) * | 2010-10-29 | 2012-05-03 | General Electric Company | Rankine cycle integrated with absorption chiller |
| FR2968009B1 (fr) | 2010-11-25 | 2012-11-16 | Arkema France | Fluides frigorigenes contenant du (e)-1,1,1,4,4,4-hexafluorobut-2-ene |
| EP3543311B1 (en) * | 2010-11-25 | 2022-11-09 | Arkema France | Use of compositions of chloro-trifluoropropene and hexafluorobutene |
| FR2968310B1 (fr) | 2010-12-03 | 2012-12-07 | Arkema France | Compositions a base de 1,1,1,4,4,4-hexafluorobut-2-ene et de 3,3,4,4,4-pentafluorobut-1-ene |
| IT1406472B1 (it) * | 2010-12-22 | 2014-02-28 | Nuovo Pignone Spa | Prova per similitudine di prestazione di compressore |
| WO2012116174A1 (en) * | 2011-02-23 | 2012-08-30 | Jianguo Xu | Thermally activated pressure booster for heat pumping and power generation |
| US9429046B2 (en) | 2011-03-22 | 2016-08-30 | Climeon Ab | Method for conversion of low temperature heat to electricity and cooling, and system therefore |
| FR2973805B1 (fr) * | 2011-04-08 | 2013-04-12 | Arkema France | Compositions comprenant du 3,3,3-trifluoropropene et de l'ammoniac |
| FR2977256B1 (fr) | 2011-07-01 | 2013-06-21 | Arkema France | Compositions de 2,4,4,4-tetrafluorobut-1-ene et de cis-1,1,1,4,4,4-hexafluorobut-2-ene |
| CN102305110B (zh) * | 2011-07-29 | 2013-06-19 | 中国科学院广州能源研究所 | 利用地热和余热转化为动力循环及供热或暖的装置 |
| ES2989330T3 (es) | 2011-08-19 | 2024-11-26 | Chemours Co Fc Llc | Proceso de ciclos de Rankine orgánicos para generar energía mecánica a partir de calor |
| DK2755614T3 (en) | 2011-09-13 | 2017-12-04 | Nxthera Inc | PROSTATE TREATMENT SYSTEMS |
| WO2013086092A1 (en) * | 2011-12-08 | 2013-06-13 | Paya Diaz Gaspar Pablo | Thermal energy conversion plant |
| EP2812569B1 (en) * | 2011-12-08 | 2016-05-18 | Paya Diaz, Gaspar, Pablo | Thermal energy conversion plant |
| EP2794805A1 (en) * | 2011-12-21 | 2014-10-29 | E. I. Du Pont de Nemours and Company | Use of compositions comprising e-1,1,1,4,4,5,5,5-octafluoro-2-pentene and optionally, 1,1,1,2,3-pentafluoropropane in power cycles |
| AT511823B1 (de) * | 2012-02-03 | 2013-03-15 | Georg Dr Beckmann | Verfahren und einrichtung zur erzeugung von kälte und/oder nutzwärme sowie mechanischer bzw. elektrischer energie mittels eines absorptionskreislaufes |
| US9039923B2 (en) | 2012-02-14 | 2015-05-26 | United Technologies Corporation | Composition of zeotropic mixtures having predefined temperature glide |
| HK1206961A1 (en) | 2012-04-03 | 2016-01-22 | Nxthera, Inc. | Induction coil vapor generator |
| FR2989084B1 (fr) | 2012-04-04 | 2015-04-10 | Arkema France | Compositions a base de 2,3,3,4,4,4-hexafluorobut-1-ene |
| CN102748894A (zh) * | 2012-07-31 | 2012-10-24 | 苟仲武 | 一种内置发电装置的吸收式制冷系统 |
| US10053374B2 (en) | 2012-08-16 | 2018-08-21 | University Of South Florida | Systems and methods for water desalination and power generation |
| KR102142738B1 (ko) * | 2012-10-08 | 2020-08-07 | 가스파르 파블로 파야 디아즈 | 열 에너지 변환 발전 플랜트 |
| CN103776194B (zh) * | 2012-10-22 | 2016-12-21 | 中国科学院理化技术研究所 | 一种太阳能驱动的co2吸收式制冷机 |
| US11885561B2 (en) | 2012-12-04 | 2024-01-30 | Conocophillips Company | Low global-warming refrigerants in LNG processing |
| EP2967503A4 (en) | 2013-03-14 | 2017-01-18 | Nxthera, Inc. | Systems and methods for treating prostate cancer |
| US20140260252A1 (en) * | 2013-03-15 | 2014-09-18 | Honeywell International Inc. | Stabilized hfo and hcfo compositions for use in high temperature heat transfer applications |
| CN103175246B (zh) * | 2013-04-22 | 2015-08-12 | 赵向龙 | 热力站热能动力循环系统 |
| FR3009203B1 (fr) * | 2013-07-31 | 2017-01-27 | Ifp Energies Now | Procede de captation d'un metal lourd contenu dans un gaz humide integrant une pompe a chaleur pour chauffer le gaz introduit dans une masse de captation |
| EP3042135A4 (en) * | 2013-09-04 | 2017-07-05 | Climeon AB | A method for the conversion of energy using a thermodynamic cycle with a desorber and an absorber |
| US10385251B2 (en) * | 2013-09-30 | 2019-08-20 | University Of Notre Dame Du Lac | Compounds, complexes, compositions, methods and systems for heating and cooling |
| BR112016007564A2 (pt) * | 2013-10-08 | 2017-08-01 | Chemours Co Fc Llc | composição e processos para produzir uma espuma termoplástica ou termorrígida, para produzir refrigeração, para produzir um produto de aerossol e para extinguir ou suprimir um fogo |
| WO2015089190A1 (en) | 2013-12-10 | 2015-06-18 | Nxthera, Inc. | Vapor ablation systems and methods |
| US9968395B2 (en) | 2013-12-10 | 2018-05-15 | Nxthera, Inc. | Systems and methods for treating the prostate |
| SE1400492A1 (sv) | 2014-01-22 | 2015-07-23 | Climeon Ab | An improved thermodynamic cycle operating at low pressure using a radial turbine |
| CN103806967A (zh) * | 2014-02-20 | 2014-05-21 | 贾东明 | 一种基于低温热源的动力循环系统 |
| JP6519909B2 (ja) * | 2014-07-18 | 2019-05-29 | 出光興産株式会社 | 冷凍機油組成物、及び冷凍装置 |
| CA2960174C (en) | 2014-09-23 | 2024-03-12 | The Chemours Company Fc, Llc | Use of (2e)-1,1,1,4,5,5,5-heptafluoro-4-(trifluoromethyl)pent-2-ene in high temperature heat pumps |
| JP6641364B2 (ja) * | 2014-10-30 | 2020-02-05 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | 動力サイクルにおける(2e)−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−エンの使用 |
| CA2972819C (en) | 2015-01-29 | 2023-09-12 | Nxthera, Inc. | Vapor ablation systems and methods |
| CN107530564B (zh) * | 2015-03-02 | 2021-10-29 | 科慕埃弗西有限公司 | Z-1-氯-3,3,3-三氟丙烯的共沸和类共沸组合物 |
| AU2016260529B2 (en) | 2015-05-13 | 2021-02-25 | Boston Scientific Scimed, Inc. | Systems and methods for treating the bladder with condensable vapor |
| WO2016187507A1 (en) | 2015-05-21 | 2016-11-24 | The Chemours Company Fc, Llc | HYDROFLUORINATION OF 1233xf TO 244bb BY SbF5 |
| CN104877636A (zh) * | 2015-05-26 | 2015-09-02 | 安徽中科都菱商用电器股份有限公司 | 一种混合制冷剂 |
| CN104877637A (zh) * | 2015-05-26 | 2015-09-02 | 安徽中科都菱商用电器股份有限公司 | 一种混合制冷剂 |
| CN107923266A (zh) * | 2015-07-28 | 2018-04-17 | 科慕埃弗西有限公司 | 1,3,3,4,4,4‑六氟‑1‑丁烯在动力循环中的用途 |
| BE1023904B1 (nl) * | 2015-09-08 | 2017-09-08 | Atlas Copco Airpower Naamloze Vennootschap | ORC voor het omvormen van afvalwarmte van een warmtebron in mechanische energie en compressorinstallatie die gebruik maakt van een dergelijke ORC. |
| CN105505324A (zh) * | 2015-12-15 | 2016-04-20 | 芜湖源一节能科技有限公司 | 制冷剂及其制备方法和应用 |
| BR112018012199A2 (pt) * | 2015-12-18 | 2018-11-27 | Nxthera Inc | dispositivo para tratamento de próstata, método para tratamento de tecido de próstata, gerador de vapor indutivo, e, kit. |
| WO2017147400A1 (en) * | 2016-02-25 | 2017-08-31 | The Chemours Company Fc, Llc | Use of perfluoroheptenes in power cycle systems |
| US10961874B2 (en) * | 2016-03-06 | 2021-03-30 | Husham Al-Ghizzy | Enhanced thermoutilizer |
| KR101689528B1 (ko) * | 2016-04-29 | 2016-12-26 | 한국화학연구원 | 기체 및 이온성 액체를 이용한 냉난방장치 |
| WO2018039795A1 (en) | 2016-08-31 | 2018-03-08 | University Of Ottawa | Process for catalytic hydrodefluorodimerization of fluoroölefins |
| AU2017382873B2 (en) | 2016-12-21 | 2023-06-01 | Boston Scientific Scimed, Inc. | Vapor ablation systems and methods |
| AU2018205314B2 (en) | 2017-01-06 | 2023-06-15 | Boston Scientific Scimed, Inc. | Transperineal vapor ablation systems and methods |
| KR101890896B1 (ko) * | 2017-04-28 | 2018-08-22 | 주식회사 엔바이온 | 기체 및 이온성 액체를 이용한 냉난방장치 |
| CN107165689A (zh) * | 2017-05-11 | 2017-09-15 | 中国科学院力学研究所 | 一种吸收式co2动力循环系统 |
| CN109280541B (zh) * | 2017-07-19 | 2021-02-12 | 浙江省化工研究院有限公司 | 一种环保型组合物 |
| CN108362033A (zh) * | 2018-01-11 | 2018-08-03 | 中山大学 | 一种氨基离子液体水溶液吸收式制冷工质系统及应用方法 |
| CN108335759B (zh) * | 2018-02-06 | 2019-11-12 | 华中科技大学 | 基于蒸发冷却原理的用于托卡马克装置偏滤器的冷却系统 |
| JP6450896B1 (ja) * | 2018-06-13 | 2019-01-09 | 日立ジョンソンコントロールズ空調株式会社 | 冷媒組成物及びこれを用いた冷凍サイクル装置 |
| WO2020142650A1 (en) * | 2019-01-04 | 2020-07-09 | The Chemours Company Fc, Llc | Quaternary azeotrope and azeotrope-like compositions for solvent and cleaning applications |
| EP3910041A4 (en) * | 2019-01-11 | 2022-10-19 | Daikin Industries, Ltd. | Composition containing trans-1,2-difluoroethylene |
| WO2020150437A1 (en) * | 2019-01-17 | 2020-07-23 | The Chemours Company Fc, Llc | Azeotrope and azeotrope-like compositions comprising (e)-1,1,1,4,4,4-hexafluorobut-2-ene |
| US20220213369A1 (en) * | 2019-04-18 | 2022-07-07 | The Chemours Company Fc, Llc | Fluorinated alkene systems |
| CN109971434A (zh) * | 2019-05-16 | 2019-07-05 | 青岛营上电器有限公司 | 一种低温混合制冷剂 |
| CN110257012B (zh) * | 2019-07-03 | 2021-02-19 | 北京建筑大学 | 适于270℃热源的有机朗肯循环五氟丁烷/环己烷工质 |
| CN110317574B (zh) * | 2019-07-19 | 2020-10-09 | 珠海格力电器股份有限公司 | 混合制冷剂 |
| CN110845997B (zh) * | 2019-10-16 | 2020-12-22 | 珠海格力电器股份有限公司 | 一种热传递介质及适用于冷却器的组合物 |
| CN110822762A (zh) * | 2019-10-31 | 2020-02-21 | 西安交通大学 | 一种适用于低温制冷的吸收式制冷工质对及制冷系统和方法 |
| CN110905618A (zh) * | 2019-11-18 | 2020-03-24 | 天津大学 | 适用于分布式能源系统的内燃机热电联产余热回收系统 |
| JP7617924B2 (ja) * | 2019-12-09 | 2025-01-20 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | フッ素化アルケンの触媒合成及びフッ素化アルケン組成物 |
| CN111981727A (zh) * | 2020-08-06 | 2020-11-24 | 浙大宁波理工学院 | 含有HFO-1336mzz(Z)的溶液在吸收器中制热的方法 |
| CN111981728A (zh) * | 2020-08-06 | 2020-11-24 | 浙大宁波理工学院 | 含有HCFO-1233zd(E)的溶液在吸收器中制热的方法 |
| CN112923596B (zh) * | 2020-11-04 | 2023-01-13 | 张学文 | 单一热源的热机动力循环方法 |
| JP7620418B2 (ja) * | 2020-11-30 | 2025-01-23 | 三井・ケマーズ フロロプロダクツ株式会社 | フッ素系溶剤組成物 |
| CN112984861B (zh) * | 2021-03-11 | 2022-06-17 | 北京科技大学 | 一种太阳能驱动双级吸收式热能系统 |
| CN113882921A (zh) * | 2021-11-12 | 2022-01-04 | 中国石油大学(北京) | 一种以二氧化碳气体为工质的低温循环发电系统和方法 |
| TW202511232A (zh) * | 2023-08-29 | 2025-03-16 | 美商科慕Fc有限責任公司 | 包含雙(全氟烷基)乙烯的共沸組成物及其用途 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041853A (en) * | 1955-11-25 | 1962-07-03 | Harwich Stanley | Refrigerating process and apparatus for the same |
| US3854301A (en) * | 1971-06-11 | 1974-12-17 | E Cytryn | Cryogenic absorption cycles |
| JPH062508A (ja) * | 1992-06-22 | 1994-01-11 | Tsukishima Kikai Co Ltd | 吸収式発電装置 |
| ES2161862T3 (es) * | 1993-12-14 | 2001-12-16 | Du Pont | Proceso para la produccion de butanos perhalofluorados. |
| US7350372B2 (en) * | 2003-10-27 | 2008-04-01 | Wells David N | System and method for selective heating and cooling |
| DE102004024967A1 (de) | 2004-05-21 | 2005-12-08 | Basf Ag | Neue Absorptionsmedien für Absorptionswärmepumpen, Absorptionskältemaschinen und Wärmetransformatoren |
| US7428816B2 (en) * | 2004-07-16 | 2008-09-30 | Honeywell International Inc. | Working fluids for thermal energy conversion of waste heat from fuel cells using Rankine cycle systems |
| US20080111100A1 (en) * | 2006-11-14 | 2008-05-15 | Thomas Raymond H | Use of low gwp refrigerants comprising cf3i with stable lubricants |
| US7313926B2 (en) * | 2005-01-18 | 2008-01-01 | Rexorce Thermionics, Inc. | High efficiency absorption heat pump and methods of use |
| US8715521B2 (en) * | 2005-02-04 | 2014-05-06 | E I Du Pont De Nemours And Company | Absorption cycle utilizing ionic liquid as working fluid |
| RU2007146973A (ru) * | 2005-05-18 | 2009-06-27 | Е.И.Дюпон де Немур энд Компани (US) | Гибридный парокомпрессионно-абсорбционный цикл |
| AR058054A1 (es) * | 2005-09-22 | 2008-01-23 | Du Pont | Utilizacion de liquidos ionicos para la separacion de hidrofluorocarburos |
| BRPI0619713B1 (pt) * | 2005-11-01 | 2018-02-06 | E. I. Du Pont De Nemours And Company | Método de produção de aquecimento ou resfriamento e método de substituição de composição refrigerante ou fluido de transferência de calor original |
| US8506839B2 (en) * | 2005-12-14 | 2013-08-13 | E I Du Pont De Nemours And Company | Absorption cycle utilizing ionic liquids and water as working fluids |
| CN101454420B (zh) * | 2006-05-31 | 2012-07-11 | 纳幕尔杜邦公司 | 利用离子液体作为压缩机润滑剂的蒸汽压缩 |
| US20080111099A1 (en) * | 2006-11-14 | 2008-05-15 | Singh Rajiv R | Heat transfer compositions with a hydrofluoroalkene, an iodocarbon and additives |
| US20080153697A1 (en) * | 2006-12-22 | 2008-06-26 | E. I. Dupont De Nemours And Company | Mixtures of ammonia and ionic liquids |
| US8075777B2 (en) * | 2007-05-16 | 2011-12-13 | E. I. Du Pont De Nemours And Company | Process for the separation of diastereomers |
| US7964760B2 (en) * | 2007-05-25 | 2011-06-21 | E.I. Du Pont De Nemours And Company | Process for the separation of fluorocarbons using ionic liquids |
| EP2190488A1 (en) * | 2007-09-28 | 2010-06-02 | E. I. du Pont de Nemours and Company | Ionic liquid stabilizer compositions |
-
2009
- 2009-12-16 US US12/639,401 patent/US20100154419A1/en not_active Abandoned
- 2009-12-17 CN CN200980151129XA patent/CN102257334A/zh active Pending
- 2009-12-17 EP EP09775491A patent/EP2359076A2/en not_active Withdrawn
- 2009-12-17 BR BRPI0917780A patent/BRPI0917780A2/pt not_active IP Right Cessation
- 2009-12-17 KR KR1020117016679A patent/KR20110111413A/ko not_active Withdrawn
- 2009-12-17 WO PCT/US2009/068380 patent/WO2010080467A2/en not_active Ceased
- 2009-12-17 AU AU2009335807A patent/AU2009335807A1/en not_active Abandoned
- 2009-12-17 JP JP2011542417A patent/JP2012512991A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2012512991A5 (https=) | ||
| JP2012512991A (ja) | 吸収パワーサイクルシステム | |
| JP2012510042A5 (https=) | ||
| JP2011527720A (ja) | イオン性液体およびフルオロオレフィンを含む組成物、ならびに、吸収サイクルシステムにおけるその使用 | |
| CN101573316B (zh) | 通过液-液萃取法分离氟烯烃与hf的方法 | |
| US10968378B2 (en) | Haloolefin-based composition | |
| CN101541715B (zh) | 通过共沸蒸馏将氟代烯烃与氟化氢分离的方法 | |
| JP5905897B2 (ja) | (e)−1,1,1,4,4,4−ヘキサフルオロブテ−2−エンを含む冷凍剤 | |
| AU2009319848A1 (en) | Absorption cycle system having dual absorption circuits | |
| US7728183B2 (en) | Selectively reacting olefins having a terminal CF2 group in a mixture | |
| US9909045B2 (en) | Compositions based on 2,3,3,4,4,4-hexafluorobut-1-ene | |
| JP2008530275A5 (https=) | ||
| CN105164228A (zh) | 热循环用工作介质 | |
| JP2009543787A5 (https=) | ||
| RU2008121877A (ru) | Композиции, содержащие фторолефины, и их применение | |
| KR20120102673A (ko) | 플루오로올레핀 냉매를 갖는 캐스케이드 냉동 시스템 | |
| JP2010501579A5 (https=) | ||
| ES2655418T3 (es) | Composiciones de 2,4,4,4-tetrafluorobut-1-eno y cis-1,1,1,4,4,4-hexafluorobut-2-eno | |
| US20120304686A1 (en) | Absorption cycle system having dual absorption circuits | |
| US20120304682A1 (en) | Absorption Cycle System Having Dual Absorption Circuits | |
| HK1158676A (en) | Compositions comprising ionic liquids and fluoroolefins and use thereof in absorption cycle systems | |
| HK1165539A (en) | Absorption cycle system having dual absorption circuits |