JPS62171109A - 電解コンデンサ用電解液 - Google Patents
電解コンデンサ用電解液Info
- Publication number
- JPS62171109A JPS62171109A JP1204886A JP1204886A JPS62171109A JP S62171109 A JPS62171109 A JP S62171109A JP 1204886 A JP1204886 A JP 1204886A JP 1204886 A JP1204886 A JP 1204886A JP S62171109 A JPS62171109 A JP S62171109A
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic capacitor
- electrolytic solution
- piperidine
- acid
- electrolyte
- 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
- 239000003990 capacitor Substances 0.000 title claims description 11
- 239000003792 electrolyte Substances 0.000 title claims description 10
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 16
- 239000008151 electrolyte solution Substances 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 12
- 239000000010 aprotic solvent Substances 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 9
- 150000003053 piperidines Chemical class 0.000 claims description 8
- 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
- PMDCZENCAXMSOU-UHFFFAOYSA-N N-ethylacetamide Chemical compound CCNC(C)=O PMDCZENCAXMSOU-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- ATHHXGZTWNVVOU-UHFFFAOYSA-N monomethyl-formamide Natural products CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 claims description 3
- 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 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
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical group 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
- 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
- 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
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 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
- 239000000126 substance Substances 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 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
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 150000002334 glycols Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-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
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- MWUISCCBFHLWLY-UHFFFAOYSA-N 1,2-dimethylpiperidine Chemical compound CC1CCCCN1C MWUISCCBFHLWLY-UHFFFAOYSA-N 0.000 description 1
- 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
- LLSKXGRDUPMXLC-UHFFFAOYSA-N 1-phenylpiperidine Chemical compound C1CCCCN1C1=CC=CC=C1 LLSKXGRDUPMXLC-UHFFFAOYSA-N 0.000 description 1
- SOSXWJGSWVOLFB-UHFFFAOYSA-N 2-methylpiperidine;3-methylpiperidine Chemical compound CC1CCCNC1.CC1CCCCN1 SOSXWJGSWVOLFB-UHFFFAOYSA-N 0.000 description 1
- WGIAUTGOUJDVEI-UHFFFAOYSA-N 2-phenylpiperidine Chemical compound N1CCCCC1C1=CC=CC=C1 WGIAUTGOUJDVEI-UHFFFAOYSA-N 0.000 description 1
- NZYBILDYPCVNMU-UHFFFAOYSA-N 3-phenylpiperidine Chemical compound C1CCNCC1C1=CC=CC=C1 NZYBILDYPCVNMU-UHFFFAOYSA-N 0.000 description 1
- UZOFELREXGAFOI-UHFFFAOYSA-N 4-methylpiperidine Chemical compound CC1CCNCC1 UZOFELREXGAFOI-UHFFFAOYSA-N 0.000 description 1
- UTBULQCHEUWJNV-UHFFFAOYSA-N 4-phenylpiperidine Chemical compound C1CNCCC1C1=CC=CC=C1 UTBULQCHEUWJNV-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
- XOFNHZHCGBPVGJ-UHFFFAOYSA-N 5-ethyl-2-methylpiperidine Chemical compound CCC1CCC(C)NC1 XOFNHZHCGBPVGJ-UHFFFAOYSA-N 0.000 description 1
- 239000001741 Ammonium adipate Substances 0.000 description 1
- 125000003277 amino group Chemical group 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
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 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 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- -1 organic acid salts Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Primary Cells (AREA)
- Glass Compositions (AREA)
- Hydrogenated Pyridines (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1204886A JPS62171109A (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 |
| DE8787300637T DE3770649D1 (de) | 1986-01-24 | 1987-01-26 | Elektrolyt fuer elektrolytischen kondensator. |
| EP87300637A EP0231114B1 (en) | 1986-01-24 | 1987-01-26 | An electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1204886A JPS62171109A (ja) | 1986-01-24 | 1986-01-24 | 電解コンデンサ用電解液 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62171109A true JPS62171109A (ja) | 1987-07-28 |
| JPH0426774B2 JPH0426774B2 (enrdf_load_stackoverflow) | 1992-05-08 |
Family
ID=11794714
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1204886A Granted JPS62171109A (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) | JPS62171109A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63115876A (ja) * | 1986-10-31 | 1988-05-20 | Mitsubishi Petrochem Co Ltd | 電解液 |
| JP2001291642A (ja) * | 2000-04-10 | 2001-10-19 | Sanyo Chem Ind Ltd | 電解コンデンサ用電解液およびそれを用いた電解コンデンサ用素子 |
-
1986
- 1986-01-24 JP JP1204886A patent/JPS62171109A/ja active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63115876A (ja) * | 1986-10-31 | 1988-05-20 | Mitsubishi Petrochem Co Ltd | 電解液 |
| JP2001291642A (ja) * | 2000-04-10 | 2001-10-19 | Sanyo Chem Ind Ltd | 電解コンデンサ用電解液およびそれを用いた電解コンデンサ用素子 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0426774B2 (enrdf_load_stackoverflow) | 1992-05-08 |
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