JPS63122112A - New electrolytic capacitor - Google Patents
New electrolytic capacitorInfo
- Publication number
- JPS63122112A JPS63122112A JP26670086A JP26670086A JPS63122112A JP S63122112 A JPS63122112 A JP S63122112A JP 26670086 A JP26670086 A JP 26670086A JP 26670086 A JP26670086 A JP 26670086A JP S63122112 A JPS63122112 A JP S63122112A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- electrolytic capacitor
- electrolyte
- specific resistance
- preferred
- 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.)
- Pending
Links
- 239000003990 capacitor Substances 0.000 title claims description 16
- 239000003792 electrolyte Substances 0.000 claims description 13
- -1 inorganic acid salt Chemical class 0.000 claims description 12
- 125000005497 tetraalkylphosphonium group Chemical group 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 239000008151 electrolyte solution Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-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
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-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
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 150000004714 phosphonium salts Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000003495 polar organic solvent Substances 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-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
- 239000005711 Benzoic acid Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 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
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019293 ammonium adipate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003985 ceramic capacitor Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- OSVXSBDYLRYLIG-UHFFFAOYSA-N chlorine dioxide Inorganic materials O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 1
- 125000002340 chlorooxy group Chemical class ClO[*] 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
- RBECNRCKEQGFRU-UHFFFAOYSA-N diethyl(dimethyl)phosphanium Chemical compound CC[P+](C)(C)CC RBECNRCKEQGFRU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- MBAKFIZHTUAVJN-UHFFFAOYSA-I hexafluoroantimony(1-);hydron Chemical compound F.F[Sb](F)(F)(F)F MBAKFIZHTUAVJN-UHFFFAOYSA-I 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical class O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 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 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 description 1
- SZWHXXNVLACKBV-UHFFFAOYSA-N tetraethylphosphanium Chemical compound CC[P+](CC)(CC)CC SZWHXXNVLACKBV-UHFFFAOYSA-N 0.000 description 1
- BXYHVFRRNNWPMB-UHFFFAOYSA-N tetramethylphosphanium Chemical compound C[P+](C)(C)C BXYHVFRRNNWPMB-UHFFFAOYSA-N 0.000 description 1
- XOGCTUKDUDAZKA-UHFFFAOYSA-N tetrapropylphosphanium Chemical compound CCC[P+](CCC)(CCC)CCC XOGCTUKDUDAZKA-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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- Inorganic Insulating Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、新規な駆動用電解液を使用した電解コンデン
サに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electrolytic capacitor using a novel driving electrolyte.
[従来の技術]
従来、電解コンデンサの駆動用電解液としては、エチレ
ングリコール等を主溶媒とし、これに電解質として有機
酸のアンモニウム塩のような金属からなる電極を侵食し
ない塩を溶解した電解液が一般に使用されている−
しかしながら、上記電解液は、一般に比抵抗が大きいた
めに低インピーダンス化することが困難であった。この
ため、電解コンデンサは、他の特性が優れているにもか
−わらず、高周波特性が、セラミツ°クコンデンサ等の
他のコンデンサに比べた劣っていた。[Prior Art] Conventionally, the driving electrolytic solution for an electrolytic capacitor is an electrolytic solution that uses ethylene glycol as the main solvent and dissolves therein as an electrolyte a salt that does not corrode metal electrodes, such as an ammonium salt of an organic acid. Generally used, however, it has been difficult to reduce the impedance of the electrolyte because it generally has a large specific resistance. For this reason, although electrolytic capacitors have excellent other characteristics, their high frequency characteristics are inferior to other capacitors such as ceramic capacitors.
従来、比較的小さい比抵抗の駆動用電解液として数種の
ものが知られている0例えば、アジピン酸アンモニウム
とエチレングリコールと水とからなる電解液で、水の含
有量が20重量%のものは、電導度として、約7mSを
有する。更に、比抵抗を下げるために、水の含有量を更
に高めることが考えられるが、電解液中の大きい水含有
量は、高温での電解液の蒸気圧の増大を招き、好ましく
ない。Conventionally, several types of driving electrolytes with relatively low resistivity have been known. For example, an electrolytic solution consisting of ammonium adipate, ethylene glycol, and water, with a water content of 20% by weight. has a conductivity of approximately 7 mS. Furthermore, in order to lower the specific resistance, it is conceivable to further increase the water content, but a large water content in the electrolytic solution is undesirable because it causes an increase in the vapor pressure of the electrolytic solution at high temperatures.
更に、第四アンモニウム塩素と二基素性カルボン酸とを
、双極性溶媒と水との混合媒体中に溶解した高電導性の
電解液がある(特開昭58−78522号公報)。しか
し、この場合、電導度は実施例によれば、最高的9.4
mSであり、それほど大きいものではない。Furthermore, there is a highly conductive electrolytic solution in which quaternary ammonium chlorine and dibasic carboxylic acid are dissolved in a mixed medium of a dipolar solvent and water (Japanese Patent Application Laid-open No. 78522/1983). However, in this case, the electrical conductivity is the highest, according to the example, 9.4.
mS, which is not that large.
[発明の解決しようとする問題点]
本発明は、特に比抵抗が小さい即ち電導度が大きい駆動
用電解液を使用することにより、低インピーダン化し、
高周波特性の優れた電解コンデンサを提供することを目
的とする。[Problems to be Solved by the Invention] The present invention achieves low impedance by using a driving electrolyte having particularly low specific resistance, that is, high conductivity.
The purpose is to provide an electrolytic capacitor with excellent high frequency characteristics.
[問題点を解決するための手段]
本発明は、上記目的を良好に達成するものであり、本発
明は、少なくともテトラアルキルホスホニウム又はテト
ラアリールホスホニウムの有機酸塩又は無機酸塩を好ま
しくは1〜60重量%含む有機溶媒からなる駆動用電解
液を使用したことを特徴とする電解コンデンサにある。[Means for Solving the Problems] The present invention satisfactorily achieves the above object, and the present invention provides at least one organic or inorganic acid salt of tetraalkylphosphonium or tetraarylphosphonium, preferably one to one. An electrolytic capacitor characterized by using a driving electrolyte comprising an organic solvent containing 60% by weight.
上記テトラアルキルホスホニウムのアルキル基は、好ま
しくは炭素数1〜4のものが好ましく、例えばテトラメ
チルホスホニウム、テトラエチルホスホニウム、テトラ
プロピルホスホニウム、テトラブチルホスホニウム、ジ
メチルジエチルホスホニウムなどが溶解性入手性の点か
ら好ましい。The alkyl group of the above-mentioned tetraalkylphosphonium preferably has 1 to 4 carbon atoms, and for example, tetramethylphosphonium, tetraethylphosphonium, tetrapropylphosphonium, tetrabutylphosphonium, dimethyldiethylphosphonium, etc. are preferable from the viewpoint of solubility and availability. .
テトラアリールホスホニウムのアリール基は、ベンゼン
核が1〜2のものが好ましく、なかでもフェニル基であ
るのが好ましい、ベンゼン核には、適宜の置換基を有し
ていてもよい。The aryl group of the tetraarylphosphonium preferably has 1 to 2 benzene nuclei, and is particularly preferably a phenyl group. The benzene nucleus may have an appropriate substituent.
一方、無機酸塩としては、ホウ酸(BF4) 、六フッ
化リン酸(2丁−6)、過塩素酸(ClO2)、六フッ
化ヒ素酸(Ash)、六フッ化アンチモン酸(SbF6
)、四塩化アルミン酸(AICIn)の塩などが好まし
いが、なかでもClOs塩、BF4塩が特に好ましい。On the other hand, as inorganic acid salts, boric acid (BF4), hexafluorophosphoric acid (2-6), perchloric acid (ClO2), hexafluoroarsenic acid (Ash), hexafluoroantimonic acid (SbF6)
), salts of aluminic acid tetrachloride (AICIn), and the like are preferred, among which ClOs salts and BF4 salts are particularly preferred.
有機酸塩としては、鎖状ジカルボン醸(炭素数1−12
好ましくは2〜10)又は芳香族カルボン酸の塩が好ま
しく、なかでも、マレイン酸。As the organic acid salt, chain dicarbonate (carbon number 1-12
2 to 10) or salts of aromatic carboxylic acids are preferred, especially maleic acid.
コハク酸、グルタル酸、アジピン酸、安息香酸、フタル
酸、サリチル醸、ピロメリット酸。Succinic acid, glutaric acid, adipic acid, benzoic acid, phthalic acid, salicylic acid, pyromellitic acid.
ハロゲン化安息香酸などの塩が好ましい。また、 Rf
COO又はRfSO3で表わされる含フツ素有機酸塩も
好ましい、こへでRf基は、炭素数1〜8のフルオロア
ルキル基を示すが、なかでも炭素数1〜3のパーフルオ
ロアルキル基であるのが好ましい。Salts such as halogenated benzoic acids are preferred. Also, Rf
Fluorine-containing organic acid salts represented by COO or RfSO3 are also preferred, where the Rf group represents a fluoroalkyl group having 1 to 8 carbon atoms, especially a perfluoroalkyl group having 1 to 3 carbon atoms. is preferred.
上記極性有機溶媒体としては、電解コンデンサに通常使
用される極性有機溶媒であればいずれも使用できる。好
ましい溶媒としては、ホルムアミド類、ラクトン類、グ
リコール類、硫黄化合物又は炭酸塩類が使用できる。好
ましい具体例としては、スルホラン炭酸プロピル、ジメ
チルホルムアミド、N−メチルホルムアミド、ブチロラ
クトン、N−メチルピロリドン、ジメチルスルホキッド
、エチレン、シアンヒドリン、エチレングリコール、エ
チレングリコールのモノアルキルエーテル等が使用でき
る。As the polar organic solvent, any polar organic solvent commonly used in electrolytic capacitors can be used. As preferred solvents, formamides, lactones, glycols, sulfur compounds or carbonates can be used. Preferred specific examples include propyl sulfolane carbonate, dimethylformamide, N-methylformamide, butyrolactone, N-methylpyrrolidone, dimethylsulfokide, ethylene, cyanohydrin, ethylene glycol, monoalkyl ether of ethylene glycol, and the like.
テトラアルキルホスホニウム塩、あるいは、テトラアリ
ールホスホニウム塩の含有量が少ないときには、比抵抗
が十分に小さくならないために好ましくなく、逆にあま
り大きくしても、ある程度以上比抵抗は低下しないので
意味がない、ホスホニウム塩の電解液中の濃度としては
、 1〜BO重量%が好ましく、さらには、3〜40f
f1量%が特に好ましい。When the content of the tetraalkylphosphonium salt or the tetraarylphosphonium salt is small, it is not preferable because the specific resistance will not become sufficiently small, and conversely, even if the content is too large, the specific resistance will not decrease beyond a certain level, so there is no point. The concentration of the phosphonium salt in the electrolytic solution is preferably 1 to BO% by weight, more preferably 3 to 40f.
Particularly preferred is f1 amount%.
電解液中に20重量%以下の水を加えても良い、水を加
えることにより、比抵抗を若干小さくすることができる
。ただし、20重量%を超えて加えることは、高温にお
けるコンデンサの内圧を増大させるので好まルくない。20% by weight or less of water may be added to the electrolytic solution. By adding water, the specific resistance can be made slightly smaller. However, adding more than 20% by weight is not preferable because it increases the internal pressure of the capacitor at high temperatures.
本発明の電解コンデンサには種々の好ましくはアルミニ
ウムコンデンサが包含される。典型的態様としては、紙
等の適宜のスペーサで分離したアルミニウム箔陽極とア
ルミニウム箔陰極とを使用し、これらを円筒状に巻いた
ものをコンデンサ素子とし、この素子に駆動用電解液を
含浸させる。電解液の含浸量としては、好ましくは、5
0〜300重量%とされる。電解液が含浸された素子は
、耐食性を有する金属や合成樹脂等のケースに収納し、
密封した構造にされる。Electrolytic capacitors of the present invention include a variety of preferably aluminum capacitors. In a typical embodiment, an aluminum foil anode and an aluminum foil cathode separated by a suitable spacer such as paper are used, these are wound into a cylindrical shape to form a capacitor element, and this element is impregnated with a driving electrolyte. . The amount of electrolyte impregnated is preferably 5
The content is 0 to 300% by weight. The element impregnated with the electrolyte is housed in a case made of corrosion-resistant metal or synthetic resin.
It is made into a sealed structure.
以下に、本発明の好ましい態様を示した具体例により、
更に説明する。Below, specific examples showing preferred embodiments of the present invention,
I will explain further.
なお、本発明は、上記の証明及び実施例により、制限的
に解釈されるべきでなく、本発明の範囲内で種々の変更
が可能である0例えば、本発明に使用される駆動用電解
液には、必要により、本発明の目的を阻害しない範囲で
他の物質、例えば、有機カルボン酸、ホウ酸、リン酸、
多価アルコール、アンモニア、アミンなどを添加するこ
ともできることはもちろんである。Note that the present invention should not be construed as being limited by the above proofs and examples, and various modifications can be made within the scope of the present invention.For example, the driving electrolyte used in the present invention If necessary, other substances such as organic carboxylic acids, boric acid, phosphoric acid,
Of course, polyhydric alcohols, ammonia, amines, etc. can also be added.
[実施例と比較例]
表1に、ホスホニウム塩を用いた例を、比較例と共に示
す。比較例に比べて、比抵抗を半分以下にできることが
わかった。また、表2に、表1の電解液を用いて製作し
た、35V、220JLFのコンデンサの特性を示す。[Examples and Comparative Examples] Table 1 shows examples using phosphonium salts along with comparative examples. It was found that the specific resistance could be reduced to less than half that of the comparative example. Furthermore, Table 2 shows the characteristics of a 35V, 220JLF capacitor manufactured using the electrolyte shown in Table 1.
表3には、他のカルボン酸と組合わせて使用した例を示
す0表より、第4級アンモニウム塩を加えることで、火
花電圧を低下させることなく、比抵抗を低減できること
がわかる。Table 3 shows examples of use in combination with other carboxylic acids, which shows that by adding a quaternary ammonium salt, the specific resistance can be reduced without reducing the spark voltage.
表1
表 2
表3
[発明の効果]
本発明の電解コンデンサは、比抵抗が著しく低い、即ち
、電導性が大きい駆動用電解液を使用することにより、
低インピーダンス化可能となり、高周波特性が優れる。Table 1 Table 2 Table 3 [Effects of the Invention] The electrolytic capacitor of the present invention has extremely low specific resistance, that is, by using a driving electrolyte having high conductivity,
It enables low impedance and has excellent high frequency characteristics.
更に、火花電圧、低温〜高温での特性も従来と同様に優
れた性能を有する。Furthermore, the spark voltage and low-temperature to high-temperature characteristics are as excellent as those of the prior art.
手続ネi17正(↓F 昭和62年/ρ月/q日Procedure Nei17 Positive (↓F 1986/ρ month/q day
Claims (2)
ホスホニウムの有機酸塩又は無機酸塩を有機溶媒中に溶
解させた駆動用電解液を使用したことを特徴とする電解
コンデンサ。(1) An electrolytic capacitor characterized by using a driving electrolyte in which an organic or inorganic acid salt of tetraalkylphosphonium or tetraarylphosphonium is dissolved in an organic solvent.
である特許請求の範囲第1項記載の電解コンデンサ。(2) Concentration of organic acid salt or inorganic acid salt is 1 to 60% by weight
An electrolytic capacitor according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26670086A JPS63122112A (en) | 1986-11-11 | 1986-11-11 | New electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26670086A JPS63122112A (en) | 1986-11-11 | 1986-11-11 | New electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63122112A true JPS63122112A (en) | 1988-05-26 |
Family
ID=17434467
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26670086A Pending JPS63122112A (en) | 1986-11-11 | 1986-11-11 | New electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63122112A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11219866A (en) * | 1998-02-03 | 1999-08-10 | Nippon Chemicon Corp | Electrolytic capacitor electrolyte and electrolytic capacitor provided therewith |
JPH11243037A (en) * | 1997-12-25 | 1999-09-07 | Nippon Chemicon Corp | Electrolyte solution for electrolytic capacitor and electrolytic capacitor using the electrolyte solution |
US7460357B2 (en) | 2001-05-11 | 2008-12-02 | Mitsubishi Chemical Corporation | Electrolyte for electrolytic capacitor and electrolytic capacitor using the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62272512A (en) * | 1986-05-20 | 1987-11-26 | 三菱化学株式会社 | Electrolyte for electrolytic capacitor |
JPS6314417A (en) * | 1986-07-07 | 1988-01-21 | 三菱油化株式会社 | Electrolyte for capacitor |
-
1986
- 1986-11-11 JP JP26670086A patent/JPS63122112A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62272512A (en) * | 1986-05-20 | 1987-11-26 | 三菱化学株式会社 | Electrolyte for electrolytic capacitor |
JPS6314417A (en) * | 1986-07-07 | 1988-01-21 | 三菱油化株式会社 | Electrolyte for capacitor |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11243037A (en) * | 1997-12-25 | 1999-09-07 | Nippon Chemicon Corp | Electrolyte solution for electrolytic capacitor and electrolytic capacitor using the electrolyte solution |
JPH11219866A (en) * | 1998-02-03 | 1999-08-10 | Nippon Chemicon Corp | Electrolytic capacitor electrolyte and electrolytic capacitor provided therewith |
US7460357B2 (en) | 2001-05-11 | 2008-12-02 | Mitsubishi Chemical Corporation | Electrolyte for electrolytic capacitor and electrolytic capacitor using the same |
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