JPH033370B2 - - Google Patents
Info
- Publication number
- JPH033370B2 JPH033370B2 JP18004585A JP18004585A JPH033370B2 JP H033370 B2 JPH033370 B2 JP H033370B2 JP 18004585 A JP18004585 A JP 18004585A JP 18004585 A JP18004585 A JP 18004585A JP H033370 B2 JPH033370 B2 JP H033370B2
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic
- aprotic solvent
- electrolyte
- electrolytic solution
- carbon atoms
- 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
- 239000008151 electrolyte solution Substances 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 11
- 239000000010 aprotic solvent Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000003990 capacitor Substances 0.000 claims description 9
- 239000003792 electrolyte Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- -1 tetrafluoroborate salt Chemical class 0.000 claims description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-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
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 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
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-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
- 239000000203 mixture Substances 0.000 claims 1
- ATHHXGZTWNVVOU-VQEHIDDOSA-N n-methylformamide Chemical group CN[13CH]=O ATHHXGZTWNVVOU-VQEHIDDOSA-N 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 6
- 239000002253 acid Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000002334 glycols Chemical class 0.000 description 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 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
- 229940021013 electrolyte solution Drugs 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000000243 solution Substances 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
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 description 1
- CGWWRMKUJFUTPT-UHFFFAOYSA-N 3-methyl-1h-indole Chemical compound C1=CC=C2C(C)=CNC2=C1.C1=CC=C2C(C)=CNC2=C1 CGWWRMKUJFUTPT-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
- 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
- 230000000694 effects Effects 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 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
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
Landscapes
- Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60180045A JPS6240715A (ja) | 1985-08-17 | 1985-08-17 | 電解コンデンサ用電解液 |
| EP86305476A EP0209376B1 (en) | 1985-07-17 | 1986-07-16 | An electrolyte for electrolytic capacitor |
| DE8686305476T DE3686914T2 (de) | 1985-07-17 | 1986-07-16 | Elektrolyt fuer elektrolytkondensator. |
| US06/886,987 US4664830A (en) | 1985-07-17 | 1986-07-16 | Electrolyte for electrolytic capacitor |
| CA000514064A CA1272016A (en) | 1985-07-17 | 1986-07-17 | Electrolyte for electrolytic capacitor |
| KR1019860005841A KR940004942B1 (ko) | 1985-07-17 | 1986-07-18 | 전해콘덴서용 전해액 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60180045A JPS6240715A (ja) | 1985-08-17 | 1985-08-17 | 電解コンデンサ用電解液 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6240715A JPS6240715A (ja) | 1987-02-21 |
| JPH033370B2 true JPH033370B2 (enrdf_load_stackoverflow) | 1991-01-18 |
Family
ID=16076520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60180045A Granted JPS6240715A (ja) | 1985-07-17 | 1985-08-17 | 電解コンデンサ用電解液 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6240715A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10227890A1 (de) | 2002-06-21 | 2004-01-29 | Carl Freudenberg Kg | Flexibles Band- oder Flachkabel |
-
1985
- 1985-08-17 JP JP60180045A patent/JPS6240715A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6240715A (ja) | 1987-02-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0612746B2 (ja) | 電解コンデンサ用電解液 | |
| JPH01194313A (ja) | 電解コンデンサ用電解液 | |
| JPH08298229A (ja) | 電気二重層コンデンサ用電解液 | |
| JPS62219908A (ja) | 電解コンデンサ用電解液 | |
| JPH0340495B2 (enrdf_load_stackoverflow) | ||
| JPH0376775B2 (enrdf_load_stackoverflow) | ||
| JPH033370B2 (enrdf_load_stackoverflow) | ||
| JPH038093B2 (enrdf_load_stackoverflow) | ||
| KR900005559B1 (ko) | 전해콘덴서용 전해액 | |
| US4786428A (en) | Electrolyte for electrolytic capacitor | |
| JPS62145714A (ja) | 電解コンデンサ用電解液 | |
| JPH0376774B2 (enrdf_load_stackoverflow) | ||
| JPS62171110A (ja) | 電解コンデンサ用電解液 | |
| JP2701875B2 (ja) | 電解コンデンサ用電解液 | |
| JP2572021B2 (ja) | 電解コンデンサ用電解液 | |
| JP2004134458A (ja) | 電解コンデンサ駆動用電解液 | |
| JPS6218018A (ja) | 電解コンデンサ用電解液 | |
| JP2925183B2 (ja) | 電解コンデンサ用電解液 | |
| JPH0254919A (ja) | 電解コンデンサ用電解液 | |
| JP2004193435A (ja) | 電解コンデンサ用電解液 | |
| JP2741609B2 (ja) | 電解コンデンサ用電解液 | |
| JP2902686B2 (ja) | 電解コンデンサ用電解液 | |
| JPH0332204B2 (enrdf_load_stackoverflow) | ||
| JPH0810663B2 (ja) | 電解コンデンサ用電解液 | |
| JP2004134655A (ja) | 電解コンデンサ駆動用電解液 |