JP2017069537A - 電解コンデンサ - Google Patents
電解コンデンサ Download PDFInfo
- Publication number
- JP2017069537A JP2017069537A JP2016108190A JP2016108190A JP2017069537A JP 2017069537 A JP2017069537 A JP 2017069537A JP 2016108190 A JP2016108190 A JP 2016108190A JP 2016108190 A JP2016108190 A JP 2016108190A JP 2017069537 A JP2017069537 A JP 2017069537A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- cation
- electrolytic capacitor
- component
- phosphate
- 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 abstract description 86
- 239000002253 acid Substances 0.000 claims abstract description 49
- 239000003792 electrolyte Substances 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 17
- 239000002184 metal Substances 0.000 claims abstract description 17
- 239000003960 organic solvent Substances 0.000 claims abstract description 17
- 239000002019 doping agent Substances 0.000 claims abstract description 14
- 150000003839 salts Chemical class 0.000 claims abstract description 12
- 239000011888 foil Substances 0.000 claims abstract description 11
- 229920000123 polythiophene Polymers 0.000 claims abstract description 11
- -1 phosphoric acid compound Chemical class 0.000 claims description 192
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 22
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 21
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000008151 electrolyte solution Substances 0.000 claims description 18
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 12
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims description 11
- JVYDLYGCSIHCMR-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butanoic acid Chemical compound CCC(CO)(CO)C(O)=O JVYDLYGCSIHCMR-UHFFFAOYSA-N 0.000 claims description 11
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 11
- 239000011976 maleic acid Substances 0.000 claims description 11
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 11
- 229960004889 salicylic acid Drugs 0.000 claims description 11
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 claims description 11
- UHAMPPWFPNXLIU-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)pentanoic acid Chemical compound CCCC(CO)(CO)C(O)=O UHAMPPWFPNXLIU-UHFFFAOYSA-N 0.000 claims description 10
- 239000005711 Benzoic acid Substances 0.000 claims description 10
- 235000010233 benzoic acid Nutrition 0.000 claims description 10
- 239000004327 boric acid Substances 0.000 claims description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 5
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 4
- CQXYINNETWHZTR-UHFFFAOYSA-N tritert-butyl phosphate Chemical compound CC(C)(C)OP(=O)(OC(C)(C)C)OC(C)(C)C CQXYINNETWHZTR-UHFFFAOYSA-N 0.000 claims description 4
- 239000012528 membrane Substances 0.000 abstract 1
- 239000002585 base Substances 0.000 description 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 22
- 229920001940 conductive polymer Polymers 0.000 description 22
- 238000009835 boiling Methods 0.000 description 16
- 239000004815 dispersion polymer Substances 0.000 description 16
- 150000001768 cations Chemical class 0.000 description 13
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 10
- 229910019142 PO4 Inorganic materials 0.000 description 10
- 239000010452 phosphate Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 6
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000002612 dispersion medium Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 4
- XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 4
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Natural products CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 3
- CPABJNKZWPNXQA-UHFFFAOYSA-N 5-ethyl-2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=C(CC)SC=C21 CPABJNKZWPNXQA-UHFFFAOYSA-N 0.000 description 3
- PIFHTLDQSLOKNG-UHFFFAOYSA-N 5-methyl-2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=C(C)SC=C21 PIFHTLDQSLOKNG-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 3
- 150000003577 thiophenes Chemical class 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- WVUYYXUATWMVIT-UHFFFAOYSA-N 1-bromo-4-ethoxybenzene Chemical compound CCOC1=CC=C(Br)C=C1 WVUYYXUATWMVIT-UHFFFAOYSA-N 0.000 description 2
- REACWASHYHDPSQ-UHFFFAOYSA-N 1-butylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1 REACWASHYHDPSQ-UHFFFAOYSA-N 0.000 description 2
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 2
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 2
- UDXXYUDJOHIIDZ-UHFFFAOYSA-N 2-phosphonooxyethyl prop-2-enoate Chemical compound OP(O)(=O)OCCOC(=O)C=C UDXXYUDJOHIIDZ-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 description 2
- PMDCZENCAXMSOU-UHFFFAOYSA-N N-ethylacetamide Chemical compound CCNC(C)=O PMDCZENCAXMSOU-UHFFFAOYSA-N 0.000 description 2
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- BTZVDPWKGXMQFW-UHFFFAOYSA-N Pentadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCC(O)=O BTZVDPWKGXMQFW-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N anhydrous trimethylamine Natural products CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Natural products CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- QVKQJEWZVQFGIY-UHFFFAOYSA-N dipropyl hydrogen phosphate Chemical compound CCCOP(O)(=O)OCCC QVKQJEWZVQFGIY-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
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- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
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- 235000002906 tartaric acid Nutrition 0.000 description 1
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Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
Description
電解コンデンサの製造方法を以下に詳細に説明する。
導電性高分子分散液を前記コンデンサ素子に接触させた後、乾燥させることで、導電性高分子を付着させることができる。次に、導電性高分子を付着させたコンデンサ素子を、電解液と共に金属ケースに収納することで電解コンデンサを作製することができる。
該接触させる方法は、任意の方法でよいが、浸漬させる方法が好ましく挙げられる。
上述した導電性高分子分散液は、ドーパント成分をドープしたポリチオフェン誘導体と、分散媒と、を少なくとも含有することを特徴とする導電性高分子分散液である。
これらの中でも、ポリスチレンスルホン酸が特に好ましく挙げられる。
バインダ樹脂としては、熱硬化性樹脂又は熱可塑性樹脂が好ましく挙げられる。具体的には、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリエチレンナフタレート等のポリエステル、ポリイミド、ポリアミドイミド等のポリイミド、ポリフッ化ビニリデン、ポリフッ化ビニル、ポリテトラフルオロエチレン等のフッ素樹脂、ポリビニルアルコール、ポリビニルエーテル、ポリビニルブチラール、ポリ酢酸ビニル、ポリ塩化ビニル等のビニル樹脂、エポキシ樹脂、キシレン樹脂、ポリウレタン、フェノール系樹脂、ポリエーテル、アクリル系樹脂及びこれらの共重合体等が挙げられる。
本発明に用いる電解液について説明する。本発明に用いる電解液は、有機溶媒と電解質塩とを少なくとも含有するものである。
これらの中でも、リン酸トリn−ブチル、リン酸トリi−ブチル、リン酸トリt−ブチルから選ばれる一種がより好ましく、リン酸トリn−ブチルが特に好ましく挙げられる。
上述したように酸成分を混合して用いることで、電解液中のアミンの遊離を抑制する効果があるので、よりESRにおける耐熱性に優れた電解コンデンサを得ることができる。
酸成分と塩基成分とのモル比が、200:1〜2:1であることが好ましく、100:1〜5:1であることがより好ましく挙げられ、20:1〜5:1であることが特に好ましく挙げられる。該モル比にすることで、初期のESRが小さく、かつ、より優れたESRにおける耐熱性を有する電解コンデンサを得ることができる。
1.0質量%未満の場合、十分な電気特性が得られない欠点があり、60質量%超の場合、比抵抗が上昇する欠点がある。
<電解液の製造>
77.1gのサリチル酸(酸成分)と、22.9gの1−メチルイミダゾール(塩基成分)をγ−ブチルラクトン1000mlに加え、80℃で溶解し減圧濃縮し水を留去して、電解液を得た。
14.2gの3,4−エチレンジオキシチオフェンと、42.6gのポリスチレンスルホン酸(質量平均分子量:75,000)を2000mlのイオン交換水に溶かした溶液とを20℃で混合して混合溶液を得た。
得られた混合溶液を20℃に保ち、撹拌しながら、200mlのイオン交換水に溶かした29.6gの過硫酸アンモニウムと8.0gの硫酸第二鉄の酸化触媒溶液とを添加し、3時間撹拌して反応させた。
陽極に用いる弁作用金属として、表面をエッチングし、粗面化処理を施したエッチドアルミニウム箔(縦2mm×横300mm)を用い、該アルミニウム箔に、アジピン酸アンモニウム水溶液中、電圧90Vで化成処理を行って誘電体層を形成した陽極にリード端子を取り付け、また、アルミニウム箔からなる陰極にリード端子を取り付け、それらのリード端子付き陽極と陰極とをセパレータを介して対向させることにより、コンデンサ素子を作製した。
該コンデンサ素子を上記電解液に含浸させた。この電解液を含浸したコンデンサ素子を、筒状のアルミニウムよりなる外装ケースに収納し、外装ケースの開口端部にリード線を導出する貫通孔を有するブチルゴムの封口体を挿入し、さらに外装ケースの端部を加締めることにより電解コンデンサの封口を行い、定格電圧35V、静電容量150μFの電解コンデンサを作製した。
電解コンデンサの等価直列抵抗(ESR)は周波数100kHzで測定した。初期状態及び125℃で500時間負荷試験を行ない、電解コンデンサのESRを評価した。
表1に対応するように、酸成分・塩基成分の量を調整した以外は、実施例1と同様にして電解コンデンサを作製し、ESRの評価を行った。実施例1〜8、比較例1〜3の測定結果を表1に示す。
比較例1〜3よりも実施例1〜8の方が、初期のESRが23mΩ以下と小さく、かつ、ESRにおける優れた耐熱性を有していることがわかる。特に実施例2〜6の二次電池は、変化率が8.5%以下であり、ESRにおける耐熱性に優れていることがわかる。
塩基成分と酸成分とのモル比は1:10に統一し、2種類の酸成分を用いた場合は、酸成分中におけるそれぞれの酸成分のモル数を変えて評価した。なお、電解液に用いた塩基成分は、1−メチルイミダゾールであり、0.068mol/Lである。実施例1と同様にして電解コンデンサのESRの評価を行った。結果を表2に示す。
Claims (5)
- 誘電体酸化皮膜を有する弁作用金属と対向陰極箔とがセパレータを介して巻回させたコンデンサ素子と、電解液と共に前記コンデンサ素子を収納した金属ケースからなる電解コンデンサにおいて、
該コンデンサ素子に、ドーパント成分をドープしたポリチオフェン誘導体が付着しており、
電解液が、酸成分と塩基成分とを含む電解質塩と、有機溶媒と、を含有し、
酸成分と塩基成分とのモル比が、200:1〜2:1であることを特徴とする電解コンデンサ。 - 酸成分が、フタル酸、マレイン酸、サリチル酸、安息香酸、ジメチロールプロパン酸、ジメチロールブタン酸、ジメチロールペンタン酸、パラトルエンスルホン酸、ナフタレンスルホン酸からなる群より選ばれる少なくとも一種であることを特徴とする請求項1に記載の電解コンデンサ。
- 酸成分が、フタル酸、マレイン酸、サリチル酸、グリコール酸、安息香酸からなる群より選ばれる少なくとも一種と、
ジメチロールプロパン酸、ジメチロールブタン酸、ジメチロールペンタン酸からなる群より選ばれる少なくとも一種と、
からなる混合物であることを特徴とする請求項1に記載の電解コンデンサ。 - 酸成分が、フタル酸、マレイン酸、サリチル酸、安息香酸、ジメチロールプロパン酸、ジメチロールブタン酸、ジメチロールペンタン酸、パラトルエンスルホン酸、ナフタレンスルホン酸からなる群より選ばれる少なくとも一種と、
リン酸化合物又はホウ酸化合物と、
からなる混合物であることを特徴とする請求項1に記載の電解コンデンサ。 - リン酸化合物が、リン酸トリn−ブチル、リン酸トリi−ブチル、リン酸トリt−ブチルからなる群より選ばれる一種であることを特徴とする請求項4に記載の電解コンデンサ。
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019065951A1 (ja) * | 2017-09-29 | 2019-04-04 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
WO2019131478A1 (ja) * | 2017-12-28 | 2019-07-04 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
WO2023054502A1 (ja) * | 2021-09-30 | 2023-04-06 | 日本ケミコン株式会社 | 固体電解コンデンサ |
WO2023054504A1 (ja) * | 2021-09-30 | 2023-04-06 | 日本ケミコン株式会社 | 固体電解コンデンサ及び製造方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01103821A (ja) * | 1987-07-10 | 1989-04-20 | Matsushita Electric Ind Co Ltd | 電解コンデンサ駆動用電解液 |
JPH07240350A (ja) * | 1994-02-28 | 1995-09-12 | Hitachi Aic Inc | 電解コンデンサ用電解液 |
JPH09171943A (ja) * | 1995-12-19 | 1997-06-30 | Matsushita Electric Ind Co Ltd | 電解液およびそれを用いた電気化学素子 |
JP2012109635A (ja) * | 2012-03-13 | 2012-06-07 | Panasonic Corp | 電解コンデンサ |
JP2013191897A (ja) * | 2013-07-04 | 2013-09-26 | Panasonic Corp | 電解コンデンサ |
WO2017017947A1 (ja) * | 2015-07-29 | 2017-02-02 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
-
2016
- 2016-05-31 JP JP2016108190A patent/JP6687309B2/ja active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01103821A (ja) * | 1987-07-10 | 1989-04-20 | Matsushita Electric Ind Co Ltd | 電解コンデンサ駆動用電解液 |
JPH07240350A (ja) * | 1994-02-28 | 1995-09-12 | Hitachi Aic Inc | 電解コンデンサ用電解液 |
JPH09171943A (ja) * | 1995-12-19 | 1997-06-30 | Matsushita Electric Ind Co Ltd | 電解液およびそれを用いた電気化学素子 |
JP2012109635A (ja) * | 2012-03-13 | 2012-06-07 | Panasonic Corp | 電解コンデンサ |
JP2013191897A (ja) * | 2013-07-04 | 2013-09-26 | Panasonic Corp | 電解コンデンサ |
WO2017017947A1 (ja) * | 2015-07-29 | 2017-02-02 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11195664B2 (en) | 2017-09-29 | 2021-12-07 | Panasonic Intellectual Property Management Co., Ltd. | Electrolytic capacitor |
JP7336686B2 (ja) | 2017-09-29 | 2023-09-01 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
CN111149183A (zh) * | 2017-09-29 | 2020-05-12 | 松下知识产权经营株式会社 | 电解电容器 |
WO2019065951A1 (ja) * | 2017-09-29 | 2019-04-04 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
JPWO2019065951A1 (ja) * | 2017-09-29 | 2020-11-05 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
US11715605B2 (en) | 2017-09-29 | 2023-08-01 | Panasonic Intellectual Property Management Co., Ltd. | Electrolytic capacitor |
CN111615735A (zh) * | 2017-12-28 | 2020-09-01 | 松下知识产权经营株式会社 | 电解电容器 |
US11244792B2 (en) | 2017-12-28 | 2022-02-08 | Panasonic Intellectual Property Management Co., Ltd. | Electrolytic capacitor |
CN111615735B (zh) * | 2017-12-28 | 2022-06-17 | 松下知识产权经营株式会社 | 电解电容器 |
JPWO2019131478A1 (ja) * | 2017-12-28 | 2020-12-17 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
WO2019131478A1 (ja) * | 2017-12-28 | 2019-07-04 | パナソニックIpマネジメント株式会社 | 電解コンデンサ |
WO2023054502A1 (ja) * | 2021-09-30 | 2023-04-06 | 日本ケミコン株式会社 | 固体電解コンデンサ |
WO2023054504A1 (ja) * | 2021-09-30 | 2023-04-06 | 日本ケミコン株式会社 | 固体電解コンデンサ及び製造方法 |
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