JPWO2020246519A5 - - Google Patents
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- Publication number
- JPWO2020246519A5 JPWO2020246519A5 JP2021524884A JP2021524884A JPWO2020246519A5 JP WO2020246519 A5 JPWO2020246519 A5 JP WO2020246519A5 JP 2021524884 A JP2021524884 A JP 2021524884A JP 2021524884 A JP2021524884 A JP 2021524884A JP WO2020246519 A5 JPWO2020246519 A5 JP WO2020246519A5
- Authority
- JP
- Japan
- Prior art keywords
- lithium
- bis
- anion
- imide
- fluoride
- 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.)
- Granted
Links
- -1 hexafluorophosphate anions Chemical class 0.000 description 28
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 14
- 229910052744 lithium Inorganic materials 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 10
- 229910019142 PO4 Inorganic materials 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 7
- 239000010452 phosphate Substances 0.000 description 7
- 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 description 6
- 229910003002 lithium salt Inorganic materials 0.000 description 6
- 159000000002 lithium salts Chemical class 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid group Chemical group C(C(=O)O)(=O)O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 229910052700 potassium Inorganic materials 0.000 description 5
- 239000011591 potassium Substances 0.000 description 5
- 150000001450 anions Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010828 elution Methods 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 4
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- KGCSOBYKHTVXLK-UHFFFAOYSA-M lithium ethyl fluoro phosphate Chemical compound P(=O)(OF)(OCC)[O-].[Li+] KGCSOBYKHTVXLK-UHFFFAOYSA-M 0.000 description 3
- KNWQLFOXPQZGPX-UHFFFAOYSA-N methanesulfonyl fluoride Chemical compound CS(F)(=O)=O KNWQLFOXPQZGPX-UHFFFAOYSA-N 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- CHHOPPGAFVFXFS-UHFFFAOYSA-M [Li+].[O-]S(F)(=O)=O Chemical compound [Li+].[O-]S(F)(=O)=O CHHOPPGAFVFXFS-UHFFFAOYSA-M 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000001351 cycling effect Effects 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- BYPHZHGVWNKAFC-UHFFFAOYSA-N ethenesulfonyl fluoride Chemical compound FS(=O)(=O)C=C BYPHZHGVWNKAFC-UHFFFAOYSA-N 0.000 description 2
- UQSQSQZYBQSBJZ-UHFFFAOYSA-M fluorosulfonate Chemical compound [O-]S(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-M 0.000 description 2
- IGILRSKEFZLPKG-UHFFFAOYSA-M lithium;difluorophosphinate Chemical compound [Li+].[O-]P(F)(F)=O IGILRSKEFZLPKG-UHFFFAOYSA-M 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
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
- SLVAEVYIJHDKRO-UHFFFAOYSA-N trifluoromethanesulfonyl fluoride Chemical compound FC(F)(F)S(F)(=O)=O SLVAEVYIJHDKRO-UHFFFAOYSA-N 0.000 description 2
- ZXMGHDIOOHOAAE-UHFFFAOYSA-N 1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical compound FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F ZXMGHDIOOHOAAE-UHFFFAOYSA-N 0.000 description 1
- RDOGTTNFVLSBKG-UHFFFAOYSA-N 1,2-difluoro-3-methoxybenzene Chemical compound COC1=CC=CC(F)=C1F RDOGTTNFVLSBKG-UHFFFAOYSA-N 0.000 description 1
- VAYTZRYEBVHVLE-UHFFFAOYSA-N 1,3-dioxol-2-one Chemical compound O=C1OC=CO1 VAYTZRYEBVHVLE-UHFFFAOYSA-N 0.000 description 1
- GWAOOGWHPITOEY-UHFFFAOYSA-N 1,5,2,4-dioxadithiane 2,2,4,4-tetraoxide Chemical compound O=S1(=O)CS(=O)(=O)OCO1 GWAOOGWHPITOEY-UHFFFAOYSA-N 0.000 description 1
- RYIRMSRYCSMGJA-UHFFFAOYSA-N 1,5,2,4-dioxadithiepane 2,2,4,4-tetraoxide Chemical compound O=S1(=O)CS(=O)(=O)OCCO1 RYIRMSRYCSMGJA-UHFFFAOYSA-N 0.000 description 1
- APPZESCOGKWYIH-UHFFFAOYSA-N 1,5,2,4-dioxadithiocane 2,2,4,4-tetraoxide Chemical compound O=S1(=O)CS(=O)(=O)OCCCO1 APPZESCOGKWYIH-UHFFFAOYSA-N 0.000 description 1
- GUYHXQLLIISBQF-UHFFFAOYSA-N 1-cyclohexyl-2-fluorobenzene Chemical compound FC1=CC=CC=C1C1CCCCC1 GUYHXQLLIISBQF-UHFFFAOYSA-N 0.000 description 1
- MMZYCBHLNZVROM-UHFFFAOYSA-N 1-fluoro-2-methylbenzene Chemical compound CC1=CC=CC=C1F MMZYCBHLNZVROM-UHFFFAOYSA-N 0.000 description 1
- KLECYOQFQXJYBC-UHFFFAOYSA-N 1-fluoro-2-phenylbenzene Chemical group FC1=CC=CC=C1C1=CC=CC=C1 KLECYOQFQXJYBC-UHFFFAOYSA-N 0.000 description 1
- AUNWZUQPAFGHFZ-UHFFFAOYSA-N 1-fluorosulfonyloxypropane Chemical compound CCCOS(F)(=O)=O AUNWZUQPAFGHFZ-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- SAERAINFZWAKGQ-UHFFFAOYSA-N 2-methylbenzenesulfonyl fluoride Chemical compound CC1=CC=CC=C1S(F)(=O)=O SAERAINFZWAKGQ-UHFFFAOYSA-N 0.000 description 1
- QHTJSSMHBLGUHV-UHFFFAOYSA-N 2-methylbutan-2-ylbenzene Chemical compound CCC(C)(C)C1=CC=CC=C1 QHTJSSMHBLGUHV-UHFFFAOYSA-N 0.000 description 1
- QYIOFABFKUOIBV-UHFFFAOYSA-N 4,5-dimethyl-1,3-dioxol-2-one Chemical compound CC=1OC(=O)OC=1C QYIOFABFKUOIBV-UHFFFAOYSA-N 0.000 description 1
- BZRKPSSBFPFUNX-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)benzenesulfonyl fluoride Chemical compound CCC(C)(C)c1ccc(cc1)S(F)(=O)=O BZRKPSSBFPFUNX-UHFFFAOYSA-N 0.000 description 1
- BJWMSGRKJIOCNR-UHFFFAOYSA-N 4-ethenyl-1,3-dioxolan-2-one Chemical compound C=CC1COC(=O)O1 BJWMSGRKJIOCNR-UHFFFAOYSA-N 0.000 description 1
- SBLRHMKNNHXPHG-UHFFFAOYSA-N 4-fluoro-1,3-dioxolan-2-one Chemical compound FC1COC(=O)O1 SBLRHMKNNHXPHG-UHFFFAOYSA-N 0.000 description 1
- YMGHXAOUCWPSDV-UHFFFAOYSA-N 4-tert-butylbenzenesulfonyl fluoride Chemical compound CC(C)(C)C1=CC=C(S(F)(=O)=O)C=C1 YMGHXAOUCWPSDV-UHFFFAOYSA-N 0.000 description 1
- AWRWNHWSKXUBKP-UHFFFAOYSA-M C(CC)OP(=O)([O-])F.[Li+] Chemical compound C(CC)OP(=O)([O-])F.[Li+] AWRWNHWSKXUBKP-UHFFFAOYSA-M 0.000 description 1
- LTFGXQCYRGEYGB-UHFFFAOYSA-N CCC(C#C)OC(O)=O Chemical compound CCC(C#C)OC(O)=O LTFGXQCYRGEYGB-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- IDIPWEYIBKUDNY-UHFFFAOYSA-N benzenesulfonyl fluoride Chemical compound FS(=O)(=O)C1=CC=CC=C1 IDIPWEYIBKUDNY-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- YRIJPMBUGWOQCC-UHFFFAOYSA-N bis(prop-2-ynyl) carbonate Chemical compound C#CCOC(=O)OCC#C YRIJPMBUGWOQCC-UHFFFAOYSA-N 0.000 description 1
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 description 1
- YRLQYTUFYPUCAE-UHFFFAOYSA-N difluorophosphoryloxybenzene Chemical compound FP(F)(=O)OC1=CC=CC=C1 YRLQYTUFYPUCAE-UHFFFAOYSA-N 0.000 description 1
- SXWUDUINABFBMK-UHFFFAOYSA-L dilithium;fluoro-dioxido-oxo-$l^{5}-phosphane Chemical compound [Li+].[Li+].[O-]P([O-])(F)=O SXWUDUINABFBMK-UHFFFAOYSA-L 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- BDIBYQORZHGDIR-UHFFFAOYSA-N fluorosulfonyloxybenzene Chemical compound FS(=O)(=O)OC1=CC=CC=C1 BDIBYQORZHGDIR-UHFFFAOYSA-N 0.000 description 1
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- MBABOKRGFJTBAE-UHFFFAOYSA-N methyl methanesulfonate Chemical compound COS(C)(=O)=O MBABOKRGFJTBAE-UHFFFAOYSA-N 0.000 description 1
- AUUBCQYRIBDKHO-UHFFFAOYSA-N methyl prop-2-ynyl carbonate Chemical compound COC(=O)OCC#C AUUBCQYRIBDKHO-UHFFFAOYSA-N 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 239000011255 nonaqueous electrolyte Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002633 protecting effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019105458 | 2019-06-05 | ||
| JP2019105458 | 2019-06-05 | ||
| PCT/JP2020/022011 WO2020246519A1 (ja) | 2019-06-05 | 2020-06-03 | 非水電解液用容器、及び非水電解液の保存方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2020246519A1 JPWO2020246519A1 (https=) | 2020-12-10 |
| JPWO2020246519A5 true JPWO2020246519A5 (https=) | 2023-06-06 |
| JP7606102B2 JP7606102B2 (ja) | 2024-12-25 |
Family
ID=73653217
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021524884A Active JP7606102B2 (ja) | 2019-06-05 | 2020-06-03 | 非水電解液用容器、及び非水電解液の保存方法 |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP7606102B2 (https=) |
| KR (1) | KR20220017406A (https=) |
| CN (1) | CN113994027A (https=) |
| PL (1) | PL439719A1 (https=) |
| WO (1) | WO2020246519A1 (https=) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20240387873A1 (en) * | 2021-09-17 | 2024-11-21 | Central Glass Co., Ltd. | Nonaqueous solution, holding method, and nonaqueous battery |
| WO2025135049A1 (ja) * | 2023-12-18 | 2025-06-26 | 三井化学株式会社 | 非水電解液及び非水電解質二次電池 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3439085B2 (ja) * | 1997-08-21 | 2003-08-25 | 三洋電機株式会社 | 非水系電解液二次電池 |
| JP2001131765A (ja) | 1999-11-01 | 2001-05-15 | Nisshin Steel Co Ltd | 鉄イオンの溶出を抑制した不動体皮膜を有するステンレス鋼の製造方法 |
| JP2001143667A (ja) * | 1999-11-11 | 2001-05-25 | Toyota Central Res & Dev Lab Inc | 非水系電池 |
| JP2005108531A (ja) | 2003-09-29 | 2005-04-21 | Mitsubishi Chemicals Corp | 非水電解液の調合装置及び非水電解液の製造方法 |
| JP2007087704A (ja) * | 2005-09-21 | 2007-04-05 | Hitachi Vehicle Energy Ltd | 非水電解液二次電池 |
| JP4933182B2 (ja) * | 2006-07-21 | 2012-05-16 | フジテクノ株式会社 | 飲料用ステンレス容器の製造方法 |
| JP5250466B2 (ja) * | 2009-03-31 | 2013-07-31 | 日立ビークルエナジー株式会社 | 非水電解液二次電池及びリチウム二次電池 |
| JP5440362B2 (ja) * | 2010-04-27 | 2014-03-12 | 新日鐵住金株式会社 | リチウムイオン電池用負極ケースの製造方法 |
| US9040199B2 (en) | 2010-09-27 | 2015-05-26 | Panasonic intellectual property Management co., Ltd | Positive electrode active material particles for lithium ion secondary batteries, positive electrode using the same, and lithium ion secondary battery |
| JP2013075692A (ja) * | 2011-09-30 | 2013-04-25 | Nisshin Steel Co Ltd | 液体用容器 |
| JP6086708B2 (ja) | 2012-11-21 | 2017-03-01 | 日新製鋼株式会社 | ステンレス鋼製液体用容器 |
| JP6489770B2 (ja) * | 2013-09-26 | 2019-03-27 | 日新製鋼株式会社 | 非水電解液環境での溶出量の少ないステンレス鋼板およびその製造方法ならびに非水電解液二次電池の外装部材 |
| JP6243695B2 (ja) | 2013-10-08 | 2017-12-06 | 日新製鋼株式会社 | リチウムイオン二次電池電解液保管容器用フェライト系ステンレス鋼および該ステンレス鋼を用いたリチウムイオン二次電池電解液保管容器 |
| CN105745779B (zh) * | 2013-12-25 | 2021-02-05 | 旭化成株式会社 | 含有含甲硅烷基化合物的用于添加于电解液中的组合物、电解液以及锂离子二次电池 |
| EP3146588B1 (en) * | 2014-05-23 | 2018-07-25 | Solvay Sa | Nonaqueous electrolyte compositions comprising cyclic sulfates and lithium borates |
| JP6593659B2 (ja) * | 2015-11-13 | 2019-10-23 | パナソニックIpマネジメント株式会社 | 非水電解質電池および非水電解質電池用部材 |
| KR102148895B1 (ko) * | 2016-07-01 | 2020-08-27 | 샌트랄 글래스 컴퍼니 리미티드 | 비수계 전해액, 및 비수계 전해액 이차전지 |
-
2020
- 2020-06-03 WO PCT/JP2020/022011 patent/WO2020246519A1/ja not_active Ceased
- 2020-06-03 JP JP2021524884A patent/JP7606102B2/ja active Active
- 2020-06-03 CN CN202080040955.3A patent/CN113994027A/zh active Pending
- 2020-06-03 PL PL439719A patent/PL439719A1/pl unknown
- 2020-06-03 KR KR1020217039804A patent/KR20220017406A/ko active Pending
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