JP3347154B2 - Electrolyte for driving electrolytic capacitors - Google Patents
Electrolyte for driving electrolytic capacitorsInfo
- Publication number
- JP3347154B2 JP3347154B2 JP02610292A JP2610292A JP3347154B2 JP 3347154 B2 JP3347154 B2 JP 3347154B2 JP 02610292 A JP02610292 A JP 02610292A JP 2610292 A JP2610292 A JP 2610292A JP 3347154 B2 JP3347154 B2 JP 3347154B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- electrolyte
- electrolytic solution
- salt
- electrolytic capacitors
- 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 - Fee Related
Links
- 239000003990 capacitor Substances 0.000 title claims description 7
- 239000003792 electrolyte Substances 0.000 title description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 18
- 239000008151 electrolyte solution Substances 0.000 claims description 16
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 10
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 8
- 150000007524 organic acids Chemical class 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 5
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 5
- 235000010355 mannitol Nutrition 0.000 claims description 5
- WBJWXIQDBDZMAW-UHFFFAOYSA-N 2-hydroxynaphthalene-1-carbonyl chloride Chemical compound C1=CC=CC2=C(C(Cl)=O)C(O)=CC=C21 WBJWXIQDBDZMAW-UHFFFAOYSA-N 0.000 claims description 4
- PYHXGXCGESYPCW-UHFFFAOYSA-N alpha-phenylbenzeneacetic acid Natural products C=1C=CC=CC=1C(C(=O)O)C1=CC=CC=C1 PYHXGXCGESYPCW-UHFFFAOYSA-N 0.000 claims description 4
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 229930195725 Mannitol Natural products 0.000 claims description 2
- 239000000594 mannitol Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 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
- 238000013329 compounding Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、電解コンデンサの駆動
用電解液(以下電解液という)に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolytic solution for driving an electrolytic capacitor (hereinafter referred to as an electrolytic solution).
【0002】[0002]
【従来の技術】従来より低圧用電解液としては、エチレ
ングリコールを主溶媒とし、有機酸あるいはその塩を溶
解してなる電解液が用いられてきた。2. Description of the Related Art Conventionally, as an electrolyte for low pressure, an electrolyte obtained by dissolving an organic acid or a salt thereof with ethylene glycol as a main solvent has been used.
【0003】[0003]
【発明が解決しようとする課題】近年、電解コンデンサ
の低インピーダンス化、小型化、高信頼化に伴い、電解
液としては比抵抗が低く、広温度範囲で安定な電解液が
要求されているが、エチレングリコールを主溶媒とし、
有機酸あるいはその塩を溶解してなる電解液において
は、比抵抗を低くするために、電解液中の水分の配合比
を増大すると高温度雰囲気下における信頼性が著しく低
下するなどの問題を有するため、105℃品用電解液と
しては、γーブチロラクトンを主溶媒とし、フタル酸の
4級アンモニウム塩を溶解した電解液が一般に用いられ
ている。しかしながら、この電解液に使用するフタル酸
の4級アンモニウム塩は薬品コストが非常に高いため、
〔 エチレングリコール + 水 〕系電解液での10
5℃対応が望まれていた。In recent years, as the impedance of electrolytic capacitors has been reduced, downsized, and more reliable, an electrolytic solution having a low specific resistance and being stable over a wide temperature range has been required. , With ethylene glycol as the main solvent,
In an electrolytic solution obtained by dissolving an organic acid or a salt thereof, in order to lower the specific resistance, when the mixing ratio of water in the electrolytic solution is increased, there is a problem that reliability under a high-temperature atmosphere is significantly reduced. Therefore, as the electrolyte for 105 ° C. products, an electrolyte in which γ-butyrolactone is used as a main solvent and a quaternary ammonium salt of phthalic acid is dissolved is generally used. However, the quaternary ammonium salt of phthalic acid used in this electrolyte has a very high chemical cost,
[Ethylene glycol + water] based electrolyte solution
5 ° C. correspondence was desired.
【0004】[0004]
【課題を解決するための手段】本発明は上述の問題点を
解決するためのものである。すなわち、エチレングリコ
ールを主溶媒とし、5wt%以上のアジピン酸を主体と
した有機酸あるいはその塩および10wt%以上の水分
を溶解してなる溶液中に、ジフェニル酢酸,アゼライン
酸,セバシン酸から選ばれる少なくとも1種類以上の有
機酸あるいはその塩が0.5〜5wt%配合され、か
つ、マンニット,ソルビットの中から選ばれる少なくと
も1種類以上を0.5〜3wt%添加したことを特徴と
する電解液である。SUMMARY OF THE INVENTION The present invention is to solve the above-mentioned problems. That is, diphenylacetic acid, azelaic acid, and sebacic acid are selected from a solution prepared by dissolving an organic acid or a salt thereof containing 5% by weight or more of adipic acid and a water content of 10% by weight or more with ethylene glycol as a main solvent. Electrolysis characterized in that at least one kind of organic acid or a salt thereof is blended in an amount of 0.5 to 5 wt%, and at least one kind selected from mannite and sorbite is added in an amount of 0.5 to 3 wt%. Liquid.
【0005】[0005]
【作用】本発明に係わる電解液は、電解液の低比抵抗化
に伴う多量の水分配合においてもアルミニウム電極箔の
水和を防止し、高温雰囲気中においての信頼性を著しく
向上させる。The electrolytic solution according to the present invention prevents the hydration of the aluminum electrode foil even when a large amount of water is added to the electrolytic solution in order to lower the specific resistance of the electrolytic solution, and significantly improves the reliability in a high-temperature atmosphere.
【0006】[0006]
【実施例】以下、本発明の実施例について説明する。表
1は、本発明の電解液と従来の電解液の組成、比抵抗お
よび火花発生電圧についての比較例を示す。なお、表1
中電解液試料記号A,Bは従来例、C,D,E,F,
G,H,I,J,Kは本発明例である。Embodiments of the present invention will be described below. Table 1 shows a comparative example of the composition, specific resistance, and spark generation voltage of the electrolytic solution of the present invention and the conventional electrolytic solution. Table 1
Medium electrolyte sample symbols A and B are conventional examples, C, D, E, F,
G, H, I, J, and K are examples of the present invention.
【0007】[0007]
【表1】 [Table 1]
【0008】表1から明らかなように、本発明に係わる
試料記号C,D,E,F,G,H,I,J,Kの電解液
は従来の電解液に比べ、低比抵抗ながら高い耐電圧を有
する。表2は、表1に示す電解液を用いて試作した定格
25V 3300μFの電解コンデンサによる、10
5℃ 2000時間 高温負荷試験を行なった結果を示
す。As is clear from Table 1, the electrolytes of sample symbols C, D, E, F, G, H, I, J and K according to the present invention have a higher specific resistance than the conventional electrolytes. Withstand voltage. Table 2 shows the results obtained by using an electrolytic capacitor having a rated voltage of 25 V and a resistance of 3300 μF, which was manufactured using the electrolytic solution shown in Table 1.
The result of performing a high-temperature load test at 5 ° C. for 2,000 hours is shown.
【0009】[0009]
【表2】 [Table 2]
【0010】表2から明らかなように、本発明に係わる
試料記号C,D,E,F,G,H,I,J,Kの電解液
を用いた電解コンデンサは、従来の電解液を用いた電解
コンデンサに比べ、高温度雰囲気中における信頼性の低
下が改善されており、安価な〔 エチレングリコール
+ 水 〕系電解液での105℃対応が可能となった。
また、今回の実施例以外にも、キシロースなど各種多価
アルコールを試験したが、同様な結果が得られた。な
お、電解液の混合量に対してジフェニル酢酸,アゼライ
ン酸,セバシン酸およびマンニット,ソルビットの配合
量が0.5wt%未満の場合には上記の特性が得られ
ず、また、ジフェニル酢酸,アゼライン酸,セバシン酸
の配合量が5wt%を超える場合、あるいは、マンニッ
ト,ソルビットの配合量が3wt%を超える場合には、
電解液の析出が生じてしまう。As apparent from Table 2, the electrolytic capacitors using the electrolytes of the sample symbols C, D, E, F, G, H, I, J and K according to the present invention use a conventional electrolyte. Compared with electrolytic capacitors that have been improved in reliability at high temperatures,
+ Water] -based electrolyte solution at 105 ° C.
In addition, various polyhydric alcohols such as xylose were tested in addition to the examples, and similar results were obtained. If the amount of diphenylacetic acid, azelaic acid, sebacic acid, mannite, and sorbite is less than 0.5 wt% with respect to the amount of the electrolytic solution, the above characteristics cannot be obtained. When the compounding amount of acid and sebacic acid exceeds 5 wt%, or when the compounding amount of mannitol and sorbite exceeds 3 wt%,
Electrolyte deposition occurs.
【0011】[0011]
【発明の効果】以上の結果から明らかなように、エチレ
ングリコールを主溶媒とし、5wt%以上のアジピン酸
を主体とした有機酸あるいはその塩および10wt%以
上の水分を溶解してなる電解液中に、ジフェニル酢酸,
アゼライン酸,セバシン酸から選ばれる少なくとも1種
類以上の有機酸あるいはその塩が0.5〜5wt%配合
され、かつ、マンニット,ソルビットの中から選ばれる
少なくとも1種類以上を0.5〜3wt%添加したこと
を特徴とする電解液は、アルミニウム電極箔の水和反応
を防止し、広温度範囲において優れた特性を示し、か
つ、4級アンモニウム塩を用いた電解液に比べ非常に安
価であるため、工業的ならびに実用的価値の大なるもの
である。As is evident from the above results, an electrolytic solution obtained by dissolving an organic acid or a salt thereof containing 5% by weight or more of adipic acid and 10% by weight or more of water with ethylene glycol as a main solvent. And diphenylacetic acid,
At least one kind of organic acid selected from azelaic acid and sebacic acid or a salt thereof is blended in an amount of 0.5 to 5 wt%, and at least one kind selected from mannite and sorbite is contained in an amount of 0.5 to 3 wt%. The added electrolyte prevents the hydration reaction of the aluminum electrode foil, exhibits excellent characteristics in a wide temperature range, and is very inexpensive compared to the electrolyte using a quaternary ammonium salt. Therefore, it is of great industrial and practical value.
フロントページの続き (56)参考文献 特開 昭63−96906(JP,A) 特開 平3−125417(JP,A) 特開 平3−235318(JP,A) (58)調査した分野(Int.Cl.7,DB名) H01G 9/035 Continuation of the front page (56) References JP-A-63-96906 (JP, A) JP-A-3-125417 (JP, A) JP-A-3-235318 (JP, A) (58) Fields investigated (Int) .Cl. 7 , DB name) H01G 9/035
Claims (1)
t%以上のアジピン酸を主体とした有機酸あるいはその
塩および10wt%以上の水分を溶解してなる溶液中
に、ジフェニル酢酸,アゼライン酸,セバシン酸から選
ばれる少なくとも1種類以上の有機酸あるいはその塩が
0.5〜5wt%配合され、かつ、マンニット,ソルビ
ットの中から選ばれる少なくとも1種類以上を0.5〜
3wt%添加したことを特徴とする電解コンデンサの駆
動用電解液。An ethylene glycol as a main solvent and 5 w
At least one or more organic acids selected from diphenylacetic acid, azelaic acid, and sebacic acid or a solution thereof in which at least t% or more of an adipic acid-based organic acid or a salt thereof and at least 10 wt% of water are dissolved. 0.5 to 5 wt% of a salt is blended, and at least one selected from mannitol and sorbite is used in an amount of 0.5 to 5 wt%.
An electrolytic solution for driving an electrolytic capacitor, wherein 3 wt% is added.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP02610292A JP3347154B2 (en) | 1992-01-16 | 1992-01-16 | Electrolyte for driving electrolytic capacitors |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP02610292A JP3347154B2 (en) | 1992-01-16 | 1992-01-16 | Electrolyte for driving electrolytic capacitors |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05190392A JPH05190392A (en) | 1993-07-30 |
JP3347154B2 true JP3347154B2 (en) | 2002-11-20 |
Family
ID=12184236
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP02610292A Expired - Fee Related JP3347154B2 (en) | 1992-01-16 | 1992-01-16 | Electrolyte for driving electrolytic capacitors |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3347154B2 (en) |
-
1992
- 1992-01-16 JP JP02610292A patent/JP3347154B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH05190392A (en) | 1993-07-30 |
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