JPH09320904A - Driving electrolyte for electrolytic capacitor - Google Patents
Driving electrolyte for electrolytic capacitorInfo
- Publication number
- JPH09320904A JPH09320904A JP13624396A JP13624396A JPH09320904A JP H09320904 A JPH09320904 A JP H09320904A JP 13624396 A JP13624396 A JP 13624396A JP 13624396 A JP13624396 A JP 13624396A JP H09320904 A JPH09320904 A JP H09320904A
- Authority
- JP
- Japan
- Prior art keywords
- salt
- organic acid
- electrolytic capacitor
- electrolyte
- dissolved
- 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 abstract description 17
- 239000003792 electrolyte Substances 0.000 title abstract description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 15
- 150000007524 organic acids Chemical class 0.000 claims abstract description 14
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 239000008151 electrolyte solution Substances 0.000 claims description 21
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 abstract description 10
- 238000001179 sorption measurement Methods 0.000 abstract description 5
- 230000007423 decrease Effects 0.000 abstract description 4
- 238000013329 compounding Methods 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000009918 complex formation Effects 0.000 description 3
- 239000010407 anodic oxide Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電解コンデンサの
駆動用電解液に関するものである。TECHNICAL FIELD The present invention relates to an electrolytic solution for driving an electrolytic capacitor.
【0002】[0002]
【従来の技術】従来、中高圧用のアルミニウム電解コン
デンサの駆動用電解液(以下、単に電解液と称する。)
には、エチレングリコールを主体とした溶媒に有機酸ま
たはその塩を溶解した電解液が用いられている。これら
の電解液は、アルミニウムに対する高電圧化成能力を有
することが必要であり、そのため多種多様の有機酸種が
検討されてきた。2. Description of the Related Art Conventionally, an electrolytic solution for driving an aluminum electrolytic capacitor for medium and high voltage (hereinafter, simply referred to as an electrolytic solution).
For this, an electrolytic solution in which an organic acid or a salt thereof is dissolved in a solvent mainly composed of ethylene glycol is used. These electrolytes are required to have a high-voltage conversion capacity for aluminum, and therefore various organic acid species have been investigated.
【0003】[0003]
【発明が解決しようとする課題】これまでに高電圧化成
能力を有するものとして見い出された有機酸またはその
塩を配合した電解液は、高い電圧領域で使用可能な電解
コンデンサを実現できるようにしてきたが、これらのア
ルミニウム電解コンデンサは、高温中での長期信頼性試
験において、静電容量減少、tanδ増大等の信頼性の
低下をもたらすという欠点を有するものでもあった。An electrolytic solution containing an organic acid or a salt thereof, which has been found to have a high-voltage conversion ability, has been used to realize an electrolytic capacitor which can be used in a high voltage range. However, these aluminum electrolytic capacitors also have the drawback of causing a decrease in reliability such as a decrease in capacitance and an increase in tan δ in a long-term reliability test at high temperature.
【0004】[0004]
【課題を解決するための手段】本発明者は上述した問題
について種々検討した結果、その主たる原因は、電解液
中の有機酸あるいはその塩が電極表面上で錯体形成反応
し、その錯体形成物が電解液中に溶出することによるも
のであって、その錯体形成反応を防ぐには、電解液にプ
ロパルギルアルコ−ルを添加すれば効果があることを見
い出した。As a result of various studies on the above-mentioned problems, the present inventor has found that the main cause is that an organic acid or a salt thereof in an electrolytic solution undergoes a complex-forming reaction on the electrode surface to form a complex-forming product. It has been found that the addition of propargyl alcohol to the electrolytic solution is effective for preventing the complex formation reaction.
【0005】即ち、エチレングリコ−ルを主溶媒とし、
有機酸またはその塩を溶解し、プロパルギルアルコ−ル
を0.5〜5重量%配合することを特徴とする電解コン
デンサの電解液である。That is, using ethylene glycol as the main solvent,
An electrolytic solution for an electrolytic capacitor, which comprises dissolving an organic acid or a salt thereof, and adding 0.5 to 5% by weight of propargyl alcohol.
【0006】[0006]
【発明の実施の形態】上記の高電圧化成能力を有する有
機酸あるいはその塩は、高温下で長期間放置すると、電
解コンデンサの陽極化成皮膜表面に吸着し、錯体形成反
応を起こし、その反応物が電解液中に溶出する。BEST MODE FOR CARRYING OUT THE INVENTION The above-mentioned organic acid or salt thereof having a high-voltage conversion ability is adsorbed on the surface of an anodized film of an electrolytic capacitor when left at high temperature for a long period of time to cause a complex formation reaction, and its reaction product Elutes in the electrolyte.
【0007】錯体形成物が溶解し始めると、陽極箔特性
が著しく低下し、アルミニウム電解コンデンサの長期高
温信頼性の低下を招くことになる。When the complex-forming product begins to dissolve, the characteristics of the anode foil are remarkably deteriorated and the long-term high temperature reliability of the aluminum electrolytic capacitor is deteriorated.
【0008】特に、高温負荷の場合、電解コンデンサ中
の陽極化成皮膜の溶解が大であり、tanδの増大を生
じさせる。一方、無負荷においては錯体形成反応物の吸
着量が大となり、漏れ電流を増加させることとなる。In particular, under a high temperature load, the anodized film in the electrolytic capacitor is largely dissolved, which causes an increase in tan δ. On the other hand, when no load is applied, the amount of the complex-forming reactant adsorbed becomes large, which increases the leakage current.
【0009】プロパルギルアルコ−ルは、分子内中に三
重結合を有し、アルミニウム電解コンデンサの陽極酸化
皮膜と強力に結合することによって、電解液に溶解する
ことのない安定した吸着皮膜を生成する。この吸着皮膜
は、有機酸またはその塩が陽極酸化皮膜表面に吸着する
よりも速く、上記酸化皮膜表面全体にわたって形成され
るので、これにより電解液中の有機酸またはその塩によ
る皮膜への吸着、錯体形成、さらには電解液への溶出を
防ぐことができ、長期にわたって安定した陽極酸化皮膜
を得ることができる。Propargyl alcohol has a triple bond in the molecule and strongly binds to the anodic oxide film of the aluminum electrolytic capacitor to form a stable adsorption film that is not dissolved in the electrolytic solution. This adsorption film is formed over the entire surface of the oxide film faster than the organic acid or its salt adsorbs on the surface of the anodic oxide film, so that the adsorption of the organic acid or its salt in the electrolytic solution on the film, Complex formation and further elution into the electrolytic solution can be prevented, and a stable anodized film can be obtained for a long period of time.
【0010】[0010]
【実施例】以下、本発明の具体的実施例について説明す
る。表1〜表4に実施例として本発明に係る電解液(試
料記号A−1〜A−3、B−1〜B−3、C−1〜C−
3、D−1〜D−3)および比較のための従来の電解液
(試料記号A−0、B−0、C−0、D−0)の組成、
30℃における比抵抗、および85℃における耐電圧を
示す。EXAMPLES Specific examples of the present invention will be described below. The electrolytic solutions according to the present invention (sample symbols A-1 to A-3, B-1 to B-3, C-1 to C- as examples are shown in Tables 1 to 4).
3, D-1 to D-3) and compositions of conventional electrolytic solutions (sample symbols A-0, B-0, C-0, D-0) for comparison,
The specific resistance at 30 ° C. and the withstand voltage at 85 ° C. are shown.
【0011】[0011]
【表1】 [Table 1]
【0012】[0012]
【表2】 [Table 2]
【0013】[0013]
【表3】 [Table 3]
【0014】[0014]
【表4】 [Table 4]
【0015】表1〜表4から明らかなように、本発明に
係る試料記号A−1〜A−3、B−1〜B−3、C−1
〜C−3、D−1〜D−3の電解液は、従来の電解液
(試料記号A−0、B−0、C−0、D−0)と同等の
比抵抗と耐電圧を有する。As is clear from Tables 1 to 4, sample symbols A-1 to A-3, B-1 to B-3, C-1 according to the present invention.
To C-3 and D-1 to D-3 have the same specific resistance and withstand voltage as conventional electrolytic solutions (sample symbols A-0, B-0, C-0, D-0). .
【0016】上記電解液を用いて定格450V−330
μFのアルミニウム電解コンデンサを製作し、105℃
中で定格電圧印加試験および無負荷試験を行った結果を
それぞれ表5、表6に示す。印加試験においては400
0時間、高温無負荷試験においては2000時間での特
性値である。Using the above electrolytic solution, a rating of 450 V-330
Made an aluminum electrolytic capacitor of μF, 105 ℃
The results of the rated voltage application test and the no-load test are shown in Table 5 and Table 6, respectively. 400 in the applied test
It is a characteristic value at 0 hours and at 2000 hours in a high temperature no-load test.
【0017】[0017]
【表5】 [Table 5]
【0018】[0018]
【表6】 [Table 6]
【0019】表5から明らかなように本発明に係る試料
記号A−1〜A−3、B−1〜B−3、C−1〜C−
3、D−1〜D−3の電解液を用いた電解コンデンサ
は、105℃定格電圧印加試験において、従来の電解液
(試料記号A−0、B−0、C−0、D−0)に比して
tanδ増加が著しく抑えられており、また、静電容量
変化および漏れ電流変化についても改善されている。ま
た、105℃無負荷試験においても表6から明らかなよ
うに、実施例では従来例より漏れ電流の増加が小さく、
静電容量変化およびtanδ変化も小さく、安定してい
る。ここで、プロパルギルアルコールの配合量は、0.
5〜5重量%配合した場合に効果があり、0.5重量%
未満では効果がなく、5重量%を超えると電解液の高電
圧化成能力が低下する。As is clear from Table 5, sample symbols A-1 to A-3, B-1 to B-3, C-1 to C- according to the present invention.
The electrolytic capacitors using the electrolytic solutions of Nos. 3, D-1 to D-3 are the conventional electrolytic solutions (sample symbols A-0, B-0, C-0, D-0) in the 105 ° C rated voltage application test. The increase in tan δ is significantly suppressed, and the change in capacitance and the change in leakage current are also improved. Also, as is clear from Table 6 in the 105 ° C. no-load test, the increase in the leakage current in the example is smaller than that in the conventional example,
The change in capacitance and the change in tan δ are small and stable. Here, the blending amount of propargyl alcohol is 0.
Effective when combined with 5 to 5% by weight, 0.5% by weight
If it is less than 5% by weight, there is no effect, and if it exceeds 5% by weight, the high-voltage conversion ability of the electrolytic solution decreases.
【0020】[0020]
【発明の効果】以上のように、本発明に係るアルミニウ
ム電解コンデンサの電解液は、従来の電解液に比べ、高
温下で信頼性の高いアルミニウム電解コンデンサを提供
することができ、工業的ならびに実用的価値の大なるも
のである。INDUSTRIAL APPLICABILITY As described above, the electrolytic solution of the aluminum electrolytic capacitor according to the present invention can provide a highly reliable aluminum electrolytic capacitor at high temperature as compared with the conventional electrolytic solution, and can be industrially and practically used. Is of great value.
Claims (1)
酸またはその塩を溶解し、プロパルギルアルコ−ルを
0.5〜5重量%配合することを特徴とする電解コンデ
ンサの駆動用電解液。1. An electrolytic solution for driving an electrolytic capacitor, which comprises ethylene glycol as a main solvent, an organic acid or a salt thereof dissolved therein, and 0.5 to 5% by weight of propargyl alcohol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13624396A JPH09320904A (en) | 1996-05-30 | 1996-05-30 | Driving electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13624396A JPH09320904A (en) | 1996-05-30 | 1996-05-30 | Driving electrolyte for electrolytic capacitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09320904A true JPH09320904A (en) | 1997-12-12 |
Family
ID=15170639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13624396A Pending JPH09320904A (en) | 1996-05-30 | 1996-05-30 | Driving electrolyte for electrolytic capacitor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09320904A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006156706A (en) * | 2004-11-30 | 2006-06-15 | Nichicon Corp | Driving electrolyte of electrolytic capacitor |
| JP2006351913A (en) * | 2005-06-17 | 2006-12-28 | Nichicon Corp | Electrolyte for driving electrolytic capacitor |
-
1996
- 1996-05-30 JP JP13624396A patent/JPH09320904A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006156706A (en) * | 2004-11-30 | 2006-06-15 | Nichicon Corp | Driving electrolyte of electrolytic capacitor |
| JP2006351913A (en) * | 2005-06-17 | 2006-12-28 | Nichicon Corp | Electrolyte for driving electrolytic capacitor |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
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Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20050422 |
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| A131 | Notification of reasons for refusal |
Effective date: 20050801 Free format text: JAPANESE INTERMEDIATE CODE: A131 |
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