CA2527802A1 - Synthese de sels de lithium d'imides anhydres contenant un substituant fluorosulfonyle ou fluorophosphoryle - Google Patents
Synthese de sels de lithium d'imides anhydres contenant un substituant fluorosulfonyle ou fluorophosphoryle Download PDFInfo
- Publication number
- CA2527802A1 CA2527802A1 CA 2527802 CA2527802A CA2527802A1 CA 2527802 A1 CA2527802 A1 CA 2527802A1 CA 2527802 CA2527802 CA 2527802 CA 2527802 A CA2527802 A CA 2527802A CA 2527802 A1 CA2527802 A1 CA 2527802A1
- Authority
- CA
- Canada
- Prior art keywords
- process according
- reaction
- electroattractor
- radical
- anhydrous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- -1 imides lithium salts Chemical class 0.000 title claims abstract description 32
- 229910003002 lithium salt Inorganic materials 0.000 title claims description 15
- 230000015572 biosynthetic process Effects 0.000 title abstract description 9
- 238000003786 synthesis reaction Methods 0.000 title abstract description 6
- 238000000034 method Methods 0.000 claims abstract description 58
- 239000002253 acid Substances 0.000 claims abstract description 25
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims description 35
- 159000000002 lithium salts Chemical class 0.000 claims description 12
- 150000003949 imides Chemical class 0.000 claims description 11
- 239000000460 chlorine Substances 0.000 claims description 10
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 7
- 229910005143 FSO2 Inorganic materials 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical group [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 6
- 125000004437 phosphorous atom Chemical group 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 4
- VBKNTGMWIPUCRF-UHFFFAOYSA-M potassium;fluoride;hydrofluoride Chemical compound F.[F-].[K+] VBKNTGMWIPUCRF-UHFFFAOYSA-M 0.000 claims description 3
- 239000012429 reaction media Substances 0.000 claims description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims 3
- 229910020364 ClSO2 Inorganic materials 0.000 claims 2
- 239000007792 gaseous phase Substances 0.000 claims 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims 2
- 229910018926 (FSO2)2NLi Inorganic materials 0.000 abstract description 5
- VDVLPSWVDYJFRW-UHFFFAOYSA-N lithium;bis(fluorosulfonyl)azanide Chemical compound [Li+].FS(=O)(=O)[N-]S(F)(=O)=O VDVLPSWVDYJFRW-UHFFFAOYSA-N 0.000 description 16
- 238000002360 preparation method Methods 0.000 description 15
- 229910010941 LiFSI Inorganic materials 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 229910013131 LiN Inorganic materials 0.000 description 6
- 229910001290 LiPF6 Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 238000004293 19F NMR spectroscopy Methods 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 3
- 229910006095 SO2F Inorganic materials 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 3
- 229910001416 lithium ion Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910017050 AsF3 Inorganic materials 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 229910019256 POF3 Inorganic materials 0.000 description 2
- 101100408805 Schizosaccharomyces pombe (strain 972 / ATCC 24843) pof3 gene Proteins 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000000010 aprotic solvent Substances 0.000 description 2
- JCMGUODNZMETBM-UHFFFAOYSA-N arsenic trifluoride Chemical compound F[As](F)F JCMGUODNZMETBM-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- CTIKAHQFRQTTAY-UHFFFAOYSA-N fluoro(trimethyl)silane Chemical compound C[Si](C)(C)F CTIKAHQFRQTTAY-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000006138 lithiation reaction Methods 0.000 description 2
- 229940006487 lithium cation Drugs 0.000 description 2
- KTQDYGVEEFGIIL-UHFFFAOYSA-N n-fluorosulfonylsulfamoyl fluoride Chemical compound FS(=O)(=O)NS(F)(=O)=O KTQDYGVEEFGIIL-UHFFFAOYSA-N 0.000 description 2
- FFUQCRZBKUBHQT-UHFFFAOYSA-N phosphoryl fluoride Chemical compound FP(F)(F)=O FFUQCRZBKUBHQT-UHFFFAOYSA-N 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 229910018928 (FSO2)2N Inorganic materials 0.000 description 1
- 238000006677 Appel reaction Methods 0.000 description 1
- 229910001558 CF3SO3Li Inorganic materials 0.000 description 1
- 241001517013 Calidris pugnax Species 0.000 description 1
- 229910005185 FSO3H Inorganic materials 0.000 description 1
- 229910005187 FSO3Li Inorganic materials 0.000 description 1
- 101000928408 Homo sapiens Protein diaphanous homolog 2 Proteins 0.000 description 1
- 229910013528 LiN(SO2 CF3)2 Inorganic materials 0.000 description 1
- 229910013406 LiN(SO2CF3)2 Inorganic materials 0.000 description 1
- 229910019188 POF2 Inorganic materials 0.000 description 1
- 102100036469 Protein diaphanous homolog 2 Human genes 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- WEVYAHXRMPXWCK-FIBGUPNXSA-N acetonitrile-d3 Chemical compound [2H]C([2H])([2H])C#N WEVYAHXRMPXWCK-FIBGUPNXSA-N 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 1
- QSZMZKBZAYQGRS-UHFFFAOYSA-N lithium;bis(trifluoromethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F QSZMZKBZAYQGRS-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GGYPIUANQNUBOE-UHFFFAOYSA-N n-(trifluoromethylsulfonyl)sulfamoyl fluoride Chemical compound FC(F)(F)S(=O)(=O)NS(F)(=O)=O GGYPIUANQNUBOE-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- MHEBVKPOSBNNAC-UHFFFAOYSA-N potassium;bis(fluorosulfonyl)azanide Chemical compound [K+].FS(=O)(=O)[N-]S(F)(=O)=O MHEBVKPOSBNNAC-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D15/00—Lithium compounds
- C01D15/04—Halides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2527802 CA2527802A1 (fr) | 2005-12-12 | 2005-12-12 | Synthese de sels de lithium d'imides anhydres contenant un substituant fluorosulfonyle ou fluorophosphoryle |
| US12/097,148 US7919629B2 (en) | 2005-12-12 | 2006-12-12 | Sulphonyl-1,2,4-triazole salts |
| PCT/FR2006/002712 WO2007068822A2 (fr) | 2005-12-12 | 2006-12-12 | Sels de sulfonyl-1, 2, 4-triazole |
| US13/079,476 US20110178306A1 (en) | 2005-12-12 | 2011-04-04 | Sulphonyl-1,2,4-Triazole Salts |
| US13/478,728 US20120232285A1 (en) | 2005-12-12 | 2012-05-23 | Sulfonyl-1,2,4-triazole salts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2527802 CA2527802A1 (fr) | 2005-12-12 | 2005-12-12 | Synthese de sels de lithium d'imides anhydres contenant un substituant fluorosulfonyle ou fluorophosphoryle |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2527802A1 true CA2527802A1 (fr) | 2007-06-12 |
Family
ID=38162328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2527802 Abandoned CA2527802A1 (fr) | 2005-12-12 | 2005-12-12 | Synthese de sels de lithium d'imides anhydres contenant un substituant fluorosulfonyle ou fluorophosphoryle |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2527802A1 (fr) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2975684A1 (fr) * | 2011-05-24 | 2012-11-30 | Arkema France | Procede de preparation de bis(fluorosulfonyl)imidure de lithium ou sodium |
| WO2014036814A1 (fr) * | 2012-09-10 | 2014-03-13 | 江苏华盛精化工股份有限公司 | Procédé de préparation de bis(fluorosulfonyl)imide |
| WO2015012897A1 (fr) | 2013-07-26 | 2015-01-29 | Boulder Ionics Corporation | Synthèse de bis(fluorosulfonyl)imide d'hydrogène |
| JP2016204218A (ja) * | 2015-04-24 | 2016-12-08 | ステラケミファ株式会社 | フルオロスルホニルイミド化合物の製造方法 |
| WO2017080831A1 (fr) * | 2015-11-13 | 2017-05-18 | Lonza Ltd | Procédé de préparation de bis(fluorosulfonyl)imide et de ses sels |
| JP2018035060A (ja) * | 2016-08-30 | 2018-03-08 | 森田化学工業株式会社 | リチウムビス（フルオロスルホニル）イミド組成物 |
| JP2018035054A (ja) * | 2016-05-26 | 2018-03-08 | 森田化学工業株式会社 | ビス（フルオロスルホニル）イミドアルカリ金属塩の製造方法ならびにビス（フルオロスルホニル）イミドアルカリ金属塩組成物 |
| JP2018035059A (ja) * | 2016-08-30 | 2018-03-08 | 森田化学工業株式会社 | リチウムビス（フルオロスルホニル）イミド組成物 |
| US9947967B2 (en) | 2009-11-27 | 2018-04-17 | Nippon Shokubai Co., Ltd. | Fluorosulfonyl imide salt and method for producing fluorosulfonyl imide salt |
| KR20190003708A (ko) * | 2016-05-27 | 2019-01-09 | 가부시기가이샤 닛뽕쇼꾸바이 | 비스(플루오로설포닐)이미드 알칼리 금속염의 제조방법 |
| KR20190003710A (ko) | 2016-05-27 | 2019-01-09 | 가부시기가이샤 닛뽕쇼꾸바이 | 비스(플루오로설포닐)이미드 알칼리 금속염의 제조방법 및 비수계 전해액의 제조방법 |
| KR20190006524A (ko) | 2017-02-08 | 2019-01-18 | 모리타 가가쿠 고교 가부시키가이샤 | 비스(플루오로술포닐)이미드 금속염 및 해당 금속염의 제조 방법 |
| US20190161356A1 (en) * | 2017-11-28 | 2019-05-30 | Nippon Shokubai Co., Ltd. | Lithium bis(fluorosulfonyl)imide composition |
| EP3782982A1 (fr) | 2019-08-22 | 2021-02-24 | Fujian Yongjing Technology Co., Ltd. | Procédé pour la synthèse de sels conducteurs fluorés pour batteries au lithium-ion |
| WO2021171948A1 (fr) | 2020-02-27 | 2021-09-02 | 株式会社日本触媒 | Composition, matériau de solution électrolytique et solution électrolytique |
| WO2023169843A1 (fr) | 2022-03-07 | 2023-09-14 | Specialty Operations France | Procédé de production de sels de lithium fluorosulfonyl imide |
| WO2023169842A1 (fr) | 2022-03-07 | 2023-09-14 | Specialty Operations France | Procédé de production de sels sulfonyl imide alcalins |
| WO2024002897A1 (fr) | 2022-07-01 | 2024-01-04 | Specialty Operations France | Procédé de fluoration de bis(chlorosulfonyl)imide d'hydrogène en phase gazeuse |
| WO2024061956A1 (fr) | 2022-09-22 | 2024-03-28 | Specialty Operations France | Procédé de production de sels d'imide de sulfonyle alcalin |
| WO2025132313A1 (fr) | 2023-12-20 | 2025-06-26 | Specialty Operations France | Procédé de fluoration d'hydrogène bis(chlorosulfonyl)imide en phase gazeuse |
-
2005
- 2005-12-12 CA CA 2527802 patent/CA2527802A1/fr not_active Abandoned
Cited By (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9947967B2 (en) | 2009-11-27 | 2018-04-17 | Nippon Shokubai Co., Ltd. | Fluorosulfonyl imide salt and method for producing fluorosulfonyl imide salt |
| EP2505551B1 (fr) | 2009-11-27 | 2018-07-25 | Nippon Shokubai Co., Ltd. | Sel d'imide de fluorosulfonyle et procédé de production d'un sel d'imide de fluorosulfonyle |
| EP2505551B2 (fr) † | 2009-11-27 | 2022-03-09 | Nippon Shokubai Co., Ltd. | Sel d'imide de fluorosulfonyle et procédé de production d'un sel d'imide de fluorosulfonyle |
| US10547084B2 (en) | 2011-05-24 | 2020-01-28 | Arkema France | Process for the preparation of lithium or sodium bis(fluorosulphonyl)imide |
| WO2012160280A3 (fr) * | 2011-05-24 | 2013-02-28 | Arkema France | Procede de preparation de bis(fluorosulfonyl)imidure de lithium ou sodium |
| FR2975684A1 (fr) * | 2011-05-24 | 2012-11-30 | Arkema France | Procede de preparation de bis(fluorosulfonyl)imidure de lithium ou sodium |
| US9394172B2 (en) | 2011-05-24 | 2016-07-19 | Arkema France | Process for the preparation of lithium or sodium bis(fluorosulphonyl)imide |
| US9440852B2 (en) | 2011-05-24 | 2016-09-13 | Arkema France | Method for producing lithium or sodium bis(fluorosulfonyl)imide |
| EP3620433A1 (fr) * | 2011-05-24 | 2020-03-11 | Arkema France | Bis(fluorosulfonyl)imidure de lithium |
| CN103663393A (zh) * | 2012-09-10 | 2014-03-26 | 江苏华盛精化工股份有限公司 | 双氟代磺酰亚胺锂的制备方法 |
| CN103663393B (zh) * | 2012-09-10 | 2015-09-30 | 江苏华盛精化工股份有限公司 | 双氟代磺酰亚胺锂的制备方法 |
| WO2014036814A1 (fr) * | 2012-09-10 | 2014-03-13 | 江苏华盛精化工股份有限公司 | Procédé de préparation de bis(fluorosulfonyl)imide |
| EP3024779A4 (fr) * | 2013-07-26 | 2017-03-15 | Coorstek Fluorochemicals, Inc. | Synthèse de bis(fluorosulfonyl)imide d'hydrogène |
| EP3024779B1 (fr) | 2013-07-26 | 2019-07-17 | Coorstek Fluorochemicals, Inc. | Synthèse de bis(fluorosulfonyl)imide d'hydrogène |
| WO2015012897A1 (fr) | 2013-07-26 | 2015-01-29 | Boulder Ionics Corporation | Synthèse de bis(fluorosulfonyl)imide d'hydrogène |
| JP2016204218A (ja) * | 2015-04-24 | 2016-12-08 | ステラケミファ株式会社 | フルオロスルホニルイミド化合物の製造方法 |
| WO2017080831A1 (fr) * | 2015-11-13 | 2017-05-18 | Lonza Ltd | Procédé de préparation de bis(fluorosulfonyl)imide et de ses sels |
| CN109311669A (zh) * | 2016-05-26 | 2019-02-05 | 森田化学工业株式会社 | 双氟磺酰亚胺碱金属盐的制造方法和双氟磺酰亚胺碱金属盐组合物 |
| EP3466871A4 (fr) * | 2016-05-26 | 2019-10-23 | Nippon Shokubai Co., Ltd. | Procédé de fabrication de sel de métal alcalin de bis(fluorosulfonyl)imide, et composition de sel de métal alcalin de bis(fluorosulfonyl)imide |
| CN109311669B (zh) * | 2016-05-26 | 2022-04-19 | 株式会社日本触媒 | 双氟磺酰亚胺碱金属盐的制造方法和双氟磺酰亚胺碱金属盐组合物 |
| KR20190002543A (ko) | 2016-05-26 | 2019-01-08 | 모리타 가가쿠 고교 가부시키가이샤 | 비스(플루오로술포닐)이미드 알칼리 금속염의 제조 방법 및 비스(플루오로술포닐)이미드 알칼리 금속염 조성물 |
| KR102328454B1 (ko) * | 2016-05-26 | 2021-11-18 | 가부시키가이샤 닛폰 쇼쿠바이 | 비스(플루오로술포닐)이미드 알칼리 금속염의 제조 방법 및 비스(플루오로술포닐)이미드 알칼리 금속염 조성물 |
| JP2018035054A (ja) * | 2016-05-26 | 2018-03-08 | 森田化学工業株式会社 | ビス（フルオロスルホニル）イミドアルカリ金属塩の製造方法ならびにビス（フルオロスルホニル）イミドアルカリ金属塩組成物 |
| CN109415209A (zh) * | 2016-05-27 | 2019-03-01 | 株式会社日本触媒 | 二(氟磺酰基)亚胺碱金属盐的制备方法 |
| EP3466872A4 (fr) * | 2016-05-27 | 2019-10-30 | Nippon Shokubai Co., Ltd. | Procédé de production d'un sel de métal alcalin de bis(fluorosulfonyl)imide et procédé de production d'une solution électrolytique non aqueuse |
| CN109415209B (zh) * | 2016-05-27 | 2022-09-27 | 株式会社日本触媒 | 二(氟磺酰基)亚胺碱金属盐的制备方法 |
| KR20190003710A (ko) | 2016-05-27 | 2019-01-09 | 가부시기가이샤 닛뽕쇼꾸바이 | 비스(플루오로설포닐)이미드 알칼리 금속염의 제조방법 및 비수계 전해액의 제조방법 |
| JPWO2017204303A1 (ja) * | 2016-05-27 | 2019-03-22 | 株式会社日本触媒 | ビス（フルオロスルホニル）イミドアルカリ金属塩の製造方法 |
| KR20190003708A (ko) * | 2016-05-27 | 2019-01-09 | 가부시기가이샤 닛뽕쇼꾸바이 | 비스(플루오로설포닐)이미드 알칼리 금속염의 제조방법 |
| EP3466873A4 (fr) * | 2016-05-27 | 2019-10-23 | Nippon Shokubai Co., Ltd. | Procédé de production de sel de métal alcalin bis(fluorosulfonyl)imide |
| US10829377B2 (en) | 2016-05-27 | 2020-11-10 | Nippon Shokubai Co., Ltd. | Method for producing bis(fluorosulfonyl)imide alkali metal salt and method for producing non aqueous electrolytic solution |
| KR102208181B1 (ko) * | 2016-05-27 | 2021-01-28 | 가부시기가이샤 닛뽕쇼꾸바이 | 비스(플루오로설포닐)이미드 알칼리 금속염의 제조방법 |
| JP2018035060A (ja) * | 2016-08-30 | 2018-03-08 | 森田化学工業株式会社 | リチウムビス（フルオロスルホニル）イミド組成物 |
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| US11097949B2 (en) | 2017-02-08 | 2021-08-24 | Morita Chemical Industries Co., Ltd. | Bis(fluorosulfonyl) imide metal salt and method for preparing same |
| KR20190006524A (ko) | 2017-02-08 | 2019-01-18 | 모리타 가가쿠 고교 가부시키가이샤 | 비스(플루오로술포닐)이미드 금속염 및 해당 금속염의 제조 방법 |
| US20190161356A1 (en) * | 2017-11-28 | 2019-05-30 | Nippon Shokubai Co., Ltd. | Lithium bis(fluorosulfonyl)imide composition |
| EP3782982A1 (fr) | 2019-08-22 | 2021-02-24 | Fujian Yongjing Technology Co., Ltd. | Procédé pour la synthèse de sels conducteurs fluorés pour batteries au lithium-ion |
| WO2021171948A1 (fr) | 2020-02-27 | 2021-09-02 | 株式会社日本触媒 | Composition, matériau de solution électrolytique et solution électrolytique |
| WO2023169843A1 (fr) | 2022-03-07 | 2023-09-14 | Specialty Operations France | Procédé de production de sels de lithium fluorosulfonyl imide |
| WO2023169842A1 (fr) | 2022-03-07 | 2023-09-14 | Specialty Operations France | Procédé de production de sels sulfonyl imide alcalins |
| WO2024002897A1 (fr) | 2022-07-01 | 2024-01-04 | Specialty Operations France | Procédé de fluoration de bis(chlorosulfonyl)imide d'hydrogène en phase gazeuse |
| WO2024061956A1 (fr) | 2022-09-22 | 2024-03-28 | Specialty Operations France | Procédé de production de sels d'imide de sulfonyle alcalin |
| WO2025132313A1 (fr) | 2023-12-20 | 2025-06-26 | Specialty Operations France | Procédé de fluoration d'hydrogène bis(chlorosulfonyl)imide en phase gazeuse |
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