JPS6144418A - 電解コンデンサ駆動用電解液 - Google Patents

Info

Publication number

JPS6144418A

JPS6144418A JP16620084A JP16620084A JPS6144418A JP S6144418 A JPS6144418 A JP S6144418A JP 16620084 A JP16620084 A JP 16620084A JP 16620084 A JP16620084 A JP 16620084A JP S6144418 A JPS6144418 A JP S6144418A

Authority

JP

Japan

Prior art keywords

acid

group

carboxylic acid

electrolyte

integer

Prior art date

1984-08-08

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

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• Global Dossier
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• 239000003792 electrolyte Substances 0.000 title description 9
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 30
• 239000003990 capacitor Substances 0.000 claims description 18
• 239000008151 electrolyte solution Substances 0.000 claims description 13
• 150000003839 salts Chemical class 0.000 claims description 11
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
• 239000002904 solvent Substances 0.000 claims description 7
• 239000000126 substance Substances 0.000 claims description 2
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
• 239000002253 acid Substances 0.000 description 36
• 150000001875 compounds Chemical class 0.000 description 17
• -1 2,2-dimethyl-3-propyl-3-carboxyvaleric acid Chemical compound 0.000 description 8
• 150000001735 carboxylic acids Chemical class 0.000 description 6
• 229920006395 saturated elastomer Polymers 0.000 description 6
• 150000001991 dicarboxylic acids Chemical class 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 3
• 150000003863 ammonium salts Chemical class 0.000 description 3
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
• 239000004327 boric acid Substances 0.000 description 3
• CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 3
• OWCLRJQYKBAMOL-UHFFFAOYSA-N 2-butyloctanedioic acid Chemical compound CCCCC(C(O)=O)CCCCCC(O)=O OWCLRJQYKBAMOL-UHFFFAOYSA-N 0.000 description 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
• XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
• 229910052782 aluminium Inorganic materials 0.000 description 2
• 150000008064 anhydrides Chemical class 0.000 description 2
• 230000006866 deterioration Effects 0.000 description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
• BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
• 239000000243 solution Substances 0.000 description 2
• 238000009736 wetting Methods 0.000 description 2
• IJPLBEKFHCNADU-UHFFFAOYSA-N 2-ethyl-2-propylbutanedioic acid Chemical compound CCCC(CC)(C(O)=O)CC(O)=O IJPLBEKFHCNADU-UHFFFAOYSA-N 0.000 description 1
• VKZYRCUVDRFYEZ-UHFFFAOYSA-N 2-icosylpropanedioic acid Chemical compound CCCCCCCCCCCCCCCCCCCCC(C(O)=O)C(O)=O VKZYRCUVDRFYEZ-UHFFFAOYSA-N 0.000 description 1
• MBQUPZUNFWWORX-UHFFFAOYSA-N 2-nonadecylbutanedioic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(C(O)=O)CC(O)=O MBQUPZUNFWWORX-UHFFFAOYSA-N 0.000 description 1
• HLWLFKQBSHRRCB-UHFFFAOYSA-N 2-nonylbutanedioic acid Chemical compound CCCCCCCCCC(C(O)=O)CC(O)=O HLWLFKQBSHRRCB-UHFFFAOYSA-N 0.000 description 1
• FPOGSOBFOIGXPR-UHFFFAOYSA-N 2-octylbutanedioic acid Chemical compound CCCCCCCCC(C(O)=O)CC(O)=O FPOGSOBFOIGXPR-UHFFFAOYSA-N 0.000 description 1
• FNZSVEHJZREFPF-UHFFFAOYSA-N 2-pentylbutanedioic acid Chemical compound CCCCCC(C(O)=O)CC(O)=O FNZSVEHJZREFPF-UHFFFAOYSA-N 0.000 description 1
• MWTDCUHMQIAYDT-UHFFFAOYSA-N 2-tetradecylbutanedioic acid Chemical compound CCCCCCCCCCCCCCC(C(O)=O)CC(O)=O MWTDCUHMQIAYDT-UHFFFAOYSA-N 0.000 description 1
• KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
• 229940126062 Compound A Drugs 0.000 description 1
• VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
• 239000005977 Ethylene Substances 0.000 description 1
• NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
• 150000008065 acid anhydrides Chemical class 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 125000003342 alkenyl group Chemical group 0.000 description 1
• 125000000217 alkyl group Chemical group 0.000 description 1
• 125000003277 amino group Chemical group 0.000 description 1
• 238000007664 blowing Methods 0.000 description 1
• QUJSFPXBUIZZAC-UHFFFAOYSA-N boric acid;ethane-1,2-diol Chemical compound OCCO.OB(O)O QUJSFPXBUIZZAC-UHFFFAOYSA-N 0.000 description 1
• 229910052799 carbon Inorganic materials 0.000 description 1
• 150000001721 carbon Chemical class 0.000 description 1
• 125000004432 carbon atom Chemical group C* 0.000 description 1
• 150000001734 carboxylic acid salts Chemical class 0.000 description 1
• 239000003795 chemical substances by application Substances 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 238000000354 decomposition reaction Methods 0.000 description 1
• RVIXKDRPFPUUOO-UHFFFAOYSA-N dimethylselenide Chemical compound C[Se]C RVIXKDRPFPUUOO-UHFFFAOYSA-N 0.000 description 1
• 238000005886 esterification reaction Methods 0.000 description 1
• 239000011888 foil Substances 0.000 description 1
• 239000007789 gas Substances 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
• 230000002269 spontaneous effect Effects 0.000 description 1

Cited By (2)