JPH0329286B2 - - Google Patents
Info
- Publication number
- JPH0329286B2 JPH0329286B2 JP1204986A JP1204986A JPH0329286B2 JP H0329286 B2 JPH0329286 B2 JP H0329286B2 JP 1204986 A JP1204986 A JP 1204986A JP 1204986 A JP1204986 A JP 1204986A JP H0329286 B2 JPH0329286 B2 JP H0329286B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- electrolytic
- electrolytic solution
- pyrrolidine
- aprotic solvent
- 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.)
- Expired
Links
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 20
- -1 methylpyrrolidine compound Chemical class 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 11
- 239000000010 aprotic solvent Substances 0.000 claims description 11
- 239000008151 electrolyte solution Substances 0.000 claims description 11
- 239000003990 capacitor Substances 0.000 claims description 10
- 239000003792 electrolyte Substances 0.000 claims description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 4
- PMDCZENCAXMSOU-UHFFFAOYSA-N N-ethylacetamide Chemical compound CCNC(C)=O PMDCZENCAXMSOU-UHFFFAOYSA-N 0.000 claims description 4
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- ATHHXGZTWNVVOU-UHFFFAOYSA-N monomethyl-formamide Natural products CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 claims description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 claims description 2
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001412 amines Chemical group 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 claims description 2
- KERBAAIBDHEFDD-UHFFFAOYSA-N n-ethylformamide Chemical compound CCNC=O KERBAAIBDHEFDD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 2
- PNGLEYLFMHGIQO-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methoxyanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(OC)=C1 PNGLEYLFMHGIQO-UHFFFAOYSA-M 0.000 claims description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- ATHHXGZTWNVVOU-VQEHIDDOSA-N n-methylformamide Chemical group CN[13CH]=O ATHHXGZTWNVVOU-VQEHIDDOSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 4
- 150000002334 glycols Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical class CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- PYHOAVRCHOFKHR-UHFFFAOYSA-N n,n,3,4,5,6-hexamethylphosphinine-2-carboxamide Chemical compound CN(C)C(=O)C1=PC(C)=C(C)C(C)=C1C PYHOAVRCHOFKHR-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- ZIKIUDJDOOCMAN-UHFFFAOYSA-N 1,3-dioxolan-2-one 1-methylpyrrolidin-2-one Chemical compound C1(OCCO1)=O.CN1C(CCC1)=O ZIKIUDJDOOCMAN-UHFFFAOYSA-N 0.000 description 1
- FLDCSPABIQBYKP-UHFFFAOYSA-N 5-chloro-1,2-dimethylbenzimidazole Chemical compound ClC1=CC=C2N(C)C(C)=NC2=C1 FLDCSPABIQBYKP-UHFFFAOYSA-N 0.000 description 1
- 239000001741 Ammonium adipate Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019293 ammonium adipate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Primary Cells (AREA)
- Glass Compositions (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1204986A JPS62171110A (ja) | 1986-01-24 | 1986-01-24 | 電解コンデンサ用電解液 |
| US07/005,759 US4710310A (en) | 1986-01-24 | 1987-01-21 | Electrolyte for electrolytic capacitor |
| CA000528039A CA1301447C (en) | 1986-01-24 | 1987-01-23 | Electrolyte for electrolytic capacitor |
| KR1019870000576A KR940010062B1 (ko) | 1986-01-24 | 1987-01-24 | 전해(電解) 콘덴서용 전해액 |
| EP87300637A EP0231114B1 (en) | 1986-01-24 | 1987-01-26 | An electrolyte for electrolytic capacitor |
| DE8787300637T DE3770649D1 (de) | 1986-01-24 | 1987-01-26 | Elektrolyt fuer elektrolytischen kondensator. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1204986A JPS62171110A (ja) | 1986-01-24 | 1986-01-24 | 電解コンデンサ用電解液 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62171110A JPS62171110A (ja) | 1987-07-28 |
| JPH0329286B2 true JPH0329286B2 (ko) | 1991-04-23 |
Family
ID=11794743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1204986A Granted JPS62171110A (ja) | 1986-01-24 | 1986-01-24 | 電解コンデンサ用電解液 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62171110A (ko) |
-
1986
- 1986-01-24 JP JP1204986A patent/JPS62171110A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62171110A (ja) | 1987-07-28 |
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