JP6184475B2 - 誘電性気体としてのフッ素化ニトリル - Google Patents
誘電性気体としてのフッ素化ニトリル Download PDFInfo
- Publication number
- JP6184475B2 JP6184475B2 JP2015504592A JP2015504592A JP6184475B2 JP 6184475 B2 JP6184475 B2 JP 6184475B2 JP 2015504592 A JP2015504592 A JP 2015504592A JP 2015504592 A JP2015504592 A JP 2015504592A JP 6184475 B2 JP6184475 B2 JP 6184475B2
- Authority
- JP
- Japan
- Prior art keywords
- dielectric
- tetrafluoro
- trifluoromethoxy
- propanenitrile
- heptafluoroisobutyronitrile
- 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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- 239000007789 gas Substances 0.000 title description 44
- 150000002825 nitriles Chemical class 0.000 title description 10
- 239000012530 fluid Substances 0.000 claims description 37
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 239000003989 dielectric material Substances 0.000 claims description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 239000001307 helium Substances 0.000 claims description 5
- 229910052734 helium Inorganic materials 0.000 claims description 5
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 239000011261 inert gas Substances 0.000 claims description 4
- 239000003570 air Substances 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 3
- 239000001272 nitrous oxide Substances 0.000 claims description 3
- UWNGUOVHDOXBPJ-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethoxy)propanenitrile Chemical compound FC(F)(F)OC(F)(C#N)C(F)(F)F UWNGUOVHDOXBPJ-UHFFFAOYSA-N 0.000 description 46
- AASDJASZOZGYMM-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanenitrile Chemical compound FC(F)(F)C(F)(C#N)C(F)(F)F AASDJASZOZGYMM-UHFFFAOYSA-N 0.000 description 43
- 239000007788 liquid Substances 0.000 description 29
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 239000003990 capacitor Substances 0.000 description 14
- 238000010792 warming Methods 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- 150000001408 amides Chemical class 0.000 description 8
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 8
- 230000005540 biological transmission Effects 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 235000011089 carbon dioxide Nutrition 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 6
- 238000004821 distillation Methods 0.000 description 6
- 231100000419 toxicity Toxicity 0.000 description 6
- 230000001988 toxicity Effects 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 150000003071 polychlorinated biphenyls Chemical class 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- -1 (CF3) 2CFCN Chemical compound 0.000 description 4
- DEYAKVNIRRRJGO-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanamide Chemical compound NC(=O)C(F)(C(F)(F)F)C(F)(F)F DEYAKVNIRRRJGO-UHFFFAOYSA-N 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000003682 fluorination reaction Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000002826 nitrites Chemical class 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000000769 gas chromatography-flame ionisation detection Methods 0.000 description 2
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- LSACYLWPPQLVSM-UHFFFAOYSA-N isobutyric acid anhydride Chemical compound CC(C)C(=O)OC(=O)C(C)C LSACYLWPPQLVSM-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- CAWRUEZRLRNISR-UHFFFAOYSA-N methyl 2,3,3,3-tetrafluoro-2-methoxypropanoate Chemical compound COC(=O)C(F)(OC)C(F)(F)F CAWRUEZRLRNISR-UHFFFAOYSA-N 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000002390 rotary evaporation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 2
- LOJJTTDNNWYSGX-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-(1,1,2,2,3,3,4,4,4-nonafluorobutoxy)butane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)C(F)(F)C(F)(F)F LOJJTTDNNWYSGX-UHFFFAOYSA-N 0.000 description 1
- DGORQBFRUVZRPD-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoro-n,n-bis(1,1,1,2,3,3,3-heptafluoropropan-2-yl)propan-2-amine Chemical compound FC(F)(F)C(F)(C(F)(F)F)N(C(F)(C(F)(F)F)C(F)(F)F)C(F)(C(F)(F)F)C(F)(F)F DGORQBFRUVZRPD-UHFFFAOYSA-N 0.000 description 1
- GRVMOMUDALILLH-UHFFFAOYSA-N 1,1,1,2,4,5,5,5-octafluoro-2,4-bis(trifluoromethyl)pentan-3-one Chemical compound FC(F)(F)C(F)(C(F)(F)F)C(=O)C(F)(C(F)(F)F)C(F)(F)F GRVMOMUDALILLH-UHFFFAOYSA-N 0.000 description 1
- ABQIAHFCJGVSDJ-UHFFFAOYSA-N 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one Chemical group FC(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F ABQIAHFCJGVSDJ-UHFFFAOYSA-N 0.000 description 1
- CBEFDCMSEZEGCX-UHFFFAOYSA-N 1,1,2,2,2-pentafluoro-n,n-bis(1,1,2,2,2-pentafluoroethyl)ethanamine Chemical compound FC(F)(F)C(F)(F)N(C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)F CBEFDCMSEZEGCX-UHFFFAOYSA-N 0.000 description 1
- AKQMZZOTFNLAQJ-UHFFFAOYSA-N 1,1,2,2-tetrafluorocyclobutane Chemical compound FC1(F)CCC1(F)F AKQMZZOTFNLAQJ-UHFFFAOYSA-N 0.000 description 1
- BMPMIPFMFUBMNZ-UHFFFAOYSA-N 2,2,3,3,5,5,6,6-octafluoro-4-(1,1,2,2,2-pentafluoroethyl)morpholine Chemical compound FC(F)(F)C(F)(F)N1C(F)(F)C(F)(F)OC(F)(F)C1(F)F BMPMIPFMFUBMNZ-UHFFFAOYSA-N 0.000 description 1
- PQMAKJUXOOVROI-UHFFFAOYSA-N 2,2,3,3,5,5,6,6-octafluoro-4-(trifluoromethyl)morpholine Chemical compound FC(F)(F)N1C(F)(F)C(F)(F)OC(F)(F)C1(F)F PQMAKJUXOOVROI-UHFFFAOYSA-N 0.000 description 1
- RODHNODFUBONAV-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethoxy)propanamide Chemical compound NC(=O)C(F)(C(F)(F)F)OC(F)(F)F RODHNODFUBONAV-UHFFFAOYSA-N 0.000 description 1
- GAKSVIQMUADMSK-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethoxy)propanoyl fluoride Chemical compound FC(=O)C(F)(C(F)(F)F)OC(F)(F)F GAKSVIQMUADMSK-UHFFFAOYSA-N 0.000 description 1
- KJKKAZOJAFQLTQ-UHFFFAOYSA-N 2-(trifluoromethoxy)propanenitrile Chemical compound FC(OC(C#N)C)(F)F KJKKAZOJAFQLTQ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 241000256683 Peregrinus Species 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- 238000004617 QSAR study Methods 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 229910018503 SF6 Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001265 acyl fluorides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000004177 carbon cycle Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010616 electrical installation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 231100000171 higher toxicity Toxicity 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 231100000225 lethality Toxicity 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- PHYUPJDVBMIYFO-UHFFFAOYSA-N methyl 2,3,3,3-tetrafluoro-2-(trifluoromethoxy)propanoate Chemical compound COC(=O)C(F)(C(F)(F)F)OC(F)(F)F PHYUPJDVBMIYFO-UHFFFAOYSA-N 0.000 description 1
- CGMUKBZUGMXXEF-UHFFFAOYSA-N methyl 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanoate Chemical compound COC(=O)C(F)(C(F)(F)F)C(F)(F)F CGMUKBZUGMXXEF-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical class FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 description 1
- 229960004692 perflenapent Drugs 0.000 description 1
- 229960004624 perflexane Drugs 0.000 description 1
- 229950011087 perflunafene Drugs 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- UWEYRJFJVCLAGH-IJWZVTFUSA-N perfluorodecalin Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(F)[C@@]2(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)[C@@]21F UWEYRJFJVCLAGH-IJWZVTFUSA-N 0.000 description 1
- LGUZHRODIJCVOC-UHFFFAOYSA-N perfluoroheptane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F LGUZHRODIJCVOC-UHFFFAOYSA-N 0.000 description 1
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 description 1
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- YVBBRRALBYAZBM-UHFFFAOYSA-N perfluorooctane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YVBBRRALBYAZBM-UHFFFAOYSA-N 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- NJCBUSHGCBERSK-UHFFFAOYSA-N perfluoropentane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F NJCBUSHGCBERSK-UHFFFAOYSA-N 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 1
- AQZYBQIAUSKCCS-UHFFFAOYSA-N perfluorotripentylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F AQZYBQIAUSKCCS-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- SFZCNBIFKDRMGX-UHFFFAOYSA-N sulfur hexafluoride Chemical compound FS(F)(F)(F)(F)F SFZCNBIFKDRMGX-UHFFFAOYSA-N 0.000 description 1
- 229960000909 sulfur hexafluoride Drugs 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/56—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances gases
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/16—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances gases
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
- H01B3/24—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils containing halogen in the molecules, e.g. halogenated oils
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Organic Insulating Materials (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Gas-Insulated Switchgears (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261620192P | 2012-04-04 | 2012-04-04 | |
| US61/620,192 | 2012-04-04 | ||
| PCT/US2013/031854 WO2013151741A1 (en) | 2012-04-04 | 2013-03-15 | Fluorinated nitriles as dielectric gases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015515102A JP2015515102A (ja) | 2015-05-21 |
| JP2015515102A5 JP2015515102A5 (enExample) | 2016-04-21 |
| JP6184475B2 true JP6184475B2 (ja) | 2017-08-23 |
Family
ID=48087699
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015504592A Active JP6184475B2 (ja) | 2012-04-04 | 2013-03-15 | 誘電性気体としてのフッ素化ニトリル |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US20150083979A1 (enExample) |
| EP (1) | EP2834818B2 (enExample) |
| JP (1) | JP6184475B2 (enExample) |
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| WO (1) | WO2013151741A1 (enExample) |
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| US20150083979A1 (en) * | 2012-04-04 | 2015-03-26 | 3M Innovative Properties Company | Fluorinated Nitriles as Dielectric Gases |
| FR2995462B1 (fr) * | 2012-09-10 | 2014-09-05 | Alstom Technology Ltd | Appareil electrique moyenne ou haute tension a faible impact environnemental et a isolation hybride |
| FR3011138B1 (fr) | 2013-09-20 | 2015-10-30 | Alstom Technology Ltd | Appareil electrique moyenne ou haute tension a isolation gazeuse comprenant du dioxyde de carbone, de l'oxygene et de l'heptafluoroisobutyronitrile |
| FR3016746B1 (fr) * | 2014-01-21 | 2017-12-15 | Alstom Technology Ltd | Appareil electrique moyenne ou haute tension a isolation gazeuse comprenant de l'hexafluorure de soufre et un autre compose fluore |
| CA2949581A1 (en) | 2014-05-20 | 2015-11-26 | Abb Schweiz Ag | Electrical apparatus for the generation, transmission, distribution and/or usage of electrical energy and method for recovering a substance from an insulation medium of such an apparatus |
| WO2016032739A1 (en) | 2014-08-27 | 2016-03-03 | 3M Innovative Properties Company | Novel polyfluoroalkylated alkenes and silicon compounds prepared therefrom |
| US9938380B2 (en) | 2014-08-27 | 2018-04-10 | 3M Innovative Properties Company | Polyfluoroalkylated alkenes and silicone compounds prepared therefrom |
| US9938307B2 (en) | 2014-08-27 | 2018-04-10 | 3M Innovative Properties Company | Polyfluoroalkylated alkenes and silane compounds prepared therefrom |
| WO2016064585A1 (en) * | 2014-10-24 | 2016-04-28 | 3M Innovative Properties Company | Segregated fluorinated esters |
| FR3028678B1 (fr) | 2014-11-19 | 2016-12-30 | Schneider Electric Ind Sas | Appareil electrique a isolation electrique et extinction d'arcs electriques ameliorees et procede associe |
| PL3249656T3 (pl) | 2015-01-20 | 2020-08-10 | Ormazabal Corporate Technology, A.I.E. | System izolacji elektrycznej dla rozdzielnic elektrycznych średniego i wysokiego napięcia |
| FR3032828B1 (fr) * | 2015-02-13 | 2017-03-17 | Alstom Technology Ltd | Appareil electrique moyenne ou haute tension a isolation gazeuse comprenant de l'heptafluoroisobutyronitrile et du tetrafluoromethane |
| EP3104391A1 (fr) * | 2015-06-10 | 2016-12-14 | General Electric Technology GmbH | Appareillage electrique a isolation gazeuse rempli d'un gaz dielectrique |
| ES2794631T3 (es) * | 2015-12-04 | 2020-11-18 | Solvay | Métodos para aislar dieléctricamente partes eléctricas activas |
| EP3188196B1 (fr) * | 2015-12-28 | 2020-03-04 | General Electric Technology GmbH | Appareil électrique moyenne ou haute tension à isolation hybride de faible épaisseur |
| DE102016212963A1 (de) * | 2016-07-15 | 2018-01-18 | Siemens Aktiengesellschaft | Elektroenergieübertragungseinrichtung |
| CN109641819B (zh) | 2016-08-22 | 2022-01-07 | 3M创新有限公司 | 丙烯基胺及其制备和使用方法 |
| CN106946669B (zh) * | 2017-03-21 | 2020-09-15 | 国家电网公司 | 一种环保绝缘气体联产工艺及工业化生产装置 |
| DE102017105982B4 (de) | 2017-03-21 | 2022-03-03 | Fritz Driescher KG Spezialfabrik für Elektrizitätswerksbedarf GmbH & Co. | Dielektrisches Medium und damit befüllte gasisolierte Schaltanlage |
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| US11673861B2 (en) | 2017-12-13 | 2023-06-13 | 3M Innovative Properties Company | Perfluorinated 1-alkoxypropenes, compositions, and methods and apparatuses for using same |
| JP7295858B2 (ja) | 2017-12-13 | 2023-06-21 | スリーエム イノベイティブ プロパティズ カンパニー | ハイドロフルオロオレフィンエーテル、組成物、これらを使用するための装置及び方法 |
| WO2019116264A1 (en) | 2017-12-13 | 2019-06-20 | 3M Innovative Properties Company | Perfluorinated 1-alkoxypropenes in dielectric fluids and electrical devices |
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| CN109237304A (zh) * | 2018-06-04 | 2019-01-18 | 国网安徽省电力有限公司电力科学研究院 | 电气设备混合绝缘气体配制灌充系统 |
| CN109180525A (zh) * | 2018-09-11 | 2019-01-11 | 广东电网有限责任公司 | 一种全氟腈类化合物的制备方法 |
| CN109503423A (zh) * | 2018-11-30 | 2019-03-22 | 天津市长芦化工新材料有限公司 | 六氟丙烯二聚体制备全氟异丁腈的方法及全氟异丁腈和应用 |
| EP3898797A4 (en) | 2018-12-21 | 2022-11-02 | Honeywell International Inc. | EXPANSION AGENT COMPOSITIONS CONTAINING 1,2,2-TRIFLUORO-1-TRIFLUOROMETHYLCYCLOBUTANE, AND METHODS OF EXPANSION |
| CN111349019A (zh) * | 2018-12-24 | 2020-06-30 | 浙江蓝天环保高科技股份有限公司 | 一种七氟异丁腈的制备方法 |
| CN111205197A (zh) * | 2020-01-02 | 2020-05-29 | 黎明化工研究设计院有限责任公司 | 一种连续化制备七氟异丁酰胺的方法及其装置 |
| CN111205200A (zh) * | 2020-01-02 | 2020-05-29 | 黎明化工研究设计院有限责任公司 | 一种制备七氟异丁腈的方法及其装置 |
| DE102020202688A1 (de) * | 2020-03-03 | 2021-09-09 | Siemens Aktiengesellschaft | Isolationsmedium für eine Elektroenergieübertragungseinrichtung |
| EP3923301B1 (en) * | 2020-06-11 | 2022-09-07 | General Electric Technology GmbH | Gas-insulated electrical apparatus comprising carbon dioxide, heptafluoroisobutyronitrile and a high content of oxygen |
| CN111817198A (zh) * | 2020-07-10 | 2020-10-23 | 云南电网有限责任公司丽江供电局 | 一种环保型绝缘环网柜 |
| CN111995540A (zh) * | 2020-07-30 | 2020-11-27 | 武汉轻工大学 | 一种七氟异丁酰胺的制备方法 |
| EP3982377B1 (en) | 2020-10-09 | 2023-11-29 | Hitachi Energy Ltd | Method for re-establishing an electrical apparatus of medium or high voltage |
| CN116348968A (zh) * | 2020-10-22 | 2023-06-27 | Agc株式会社 | 电气设备 |
| WO2022107020A1 (en) | 2020-11-23 | 2022-05-27 | 3M Innovative Properties Company | Coating composition comprising a curable fluoropolymer and a hydrofluorochloropropene and fluoroelastomers therefrom |
| JP7705938B2 (ja) | 2020-12-04 | 2025-07-10 | ヒタチ・エナジー・リミテッド | 電気スイッチング装置 |
| WO2022123391A1 (en) | 2020-12-09 | 2022-06-16 | 3M Innovative Properties Company | A coatable curable fluoropolymer and fluoroelastomers therefrom |
| GB202110043D0 (en) | 2021-07-13 | 2021-08-25 | Rolls Royce Plc | Insulating gas composition |
| EP4120292A1 (en) | 2021-07-13 | 2023-01-18 | Hitachi Energy Switzerland AG | Container for storing and transporting a dielectric insulation medium |
| CN113851995A (zh) * | 2021-09-06 | 2021-12-28 | 化学与精细化工广东省实验室 | 一种绝缘气体及应用 |
| US20230368938A1 (en) * | 2022-04-28 | 2023-11-16 | Eaton Intelligent Power Limited | Gas mixture including a fluorinated nitrile for gas-insulated switchgear |
| CN117941014A (zh) | 2022-08-09 | 2024-04-26 | 日立能源有限公司 | 用于产生、传输和/或分配电能的电气设备 |
| CN118056809A (zh) * | 2022-11-18 | 2024-05-21 | 浙江省化工研究院有限公司 | 一种气相催化制备七氟异丁腈的方法 |
| CN115819277B (zh) * | 2022-12-22 | 2024-09-17 | 浙江诺亚氟化工有限公司 | 一种全氟异丁腈的制备方法 |
| WO2024205069A1 (ko) * | 2023-03-24 | 2024-10-03 | 엘에스전선 주식회사 | 전기 절연에 사용되는 절연용 가스 및 이를 이용한 전기 장치 |
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| US8270943B2 (en) | 2010-07-12 | 2012-09-18 | Alcatel Lucent | Method and apparatus for reliable transmission of charging detail records |
| EP2668653A1 (en) | 2011-01-25 | 2013-12-04 | 3M Innovative Properties Company | Fluorinated oxiranes as dielectric fluids |
| FR2975821B1 (fr) | 2011-05-24 | 2013-07-05 | Alstom Grid Sas | Melange de decafluoro-2-methylbutan-3-one et d'un gaz vecteur comme milieu d'isolation electrique et/ou d'extinction des arcs electriques en haute tension |
| US20150083979A1 (en) * | 2012-04-04 | 2015-03-26 | 3M Innovative Properties Company | Fluorinated Nitriles as Dielectric Gases |
| FR2995462B1 (fr) * | 2012-09-10 | 2014-09-05 | Alstom Technology Ltd | Appareil electrique moyenne ou haute tension a faible impact environnemental et a isolation hybride |
| CA2949581A1 (en) * | 2014-05-20 | 2015-11-26 | Abb Schweiz Ag | Electrical apparatus for the generation, transmission, distribution and/or usage of electrical energy and method for recovering a substance from an insulation medium of such an apparatus |
-
2013
- 2013-03-15 US US14/388,301 patent/US20150083979A1/en not_active Abandoned
- 2013-03-15 EP EP13715802.8A patent/EP2834818B2/en not_active Revoked
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| WO2013151741A1 (en) | 2013-10-10 |
| US20150083979A1 (en) | 2015-03-26 |
| EP2834818A1 (en) | 2015-02-11 |
| JP2015515102A (ja) | 2015-05-21 |
| US10573426B2 (en) | 2020-02-25 |
| KR20150005942A (ko) | 2015-01-15 |
| CN108831587A (zh) | 2018-11-16 |
| EP2834818B1 (en) | 2018-06-06 |
| KR102067020B1 (ko) | 2020-01-17 |
| TWI630626B (zh) | 2018-07-21 |
| US20180286530A1 (en) | 2018-10-04 |
| CN104662617A (zh) | 2015-05-27 |
| TW201344708A (zh) | 2013-11-01 |
| EP2834818B2 (en) | 2022-05-18 |
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