JP3254983B2 - Electrolyte for electrolytic capacitors - Google Patents

Electrolyte for electrolytic capacitors

Info

Publication number
JP3254983B2
JP3254983B2 JP26256095A JP26256095A JP3254983B2 JP 3254983 B2 JP3254983 B2 JP 3254983B2 JP 26256095 A JP26256095 A JP 26256095A JP 26256095 A JP26256095 A JP 26256095A JP 3254983 B2 JP3254983 B2 JP 3254983B2
Authority
JP
Japan
Prior art keywords
acid
specific resistance
ammonium
electrolyte
electrolytic capacitor
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 - Lifetime
Application number
JP26256095A
Other languages
Japanese (ja)
Other versions
JPH0982579A (en
Inventor
謙一 飯田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi AIC Inc
Original Assignee
Hitachi AIC Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi AIC Inc filed Critical Hitachi AIC Inc
Priority to JP26256095A priority Critical patent/JP3254983B2/en
Publication of JPH0982579A publication Critical patent/JPH0982579A/en
Application granted granted Critical
Publication of JP3254983B2 publication Critical patent/JP3254983B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は電解コンデンサ用電解液
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolytic solution for an electrolytic capacitor.

【0002】[0002]

【従来の技術】アルミ電解コンデンサ等の電解コンデン
サは、一般的に、コンデンサ素子に電解液を含浸した構
成になっている。この電解液は、例えば、エチレングリ
コールを溶媒とし、硼酸アンモニウムを溶質として溶解
した組成になっている。そしてこの組成のままでは、火
花発生電圧は高いが、比抵抗が大きく、電解コンデンサ
の損失が大きくなる。従って、火花発生電圧を下げるこ
となく、比抵抗を低下する目的で、特公昭62−800
4号に記載する通り、エチレングリコールにアジピン酸
またはその塩と、次亜リン酸アンモニウムとを溶解した
組成の電解液もある。
2. Description of the Related Art An electrolytic capacitor such as an aluminum electrolytic capacitor generally has a structure in which a capacitor element is impregnated with an electrolytic solution. This electrolytic solution has a composition in which, for example, ethylene glycol is used as a solvent and ammonium borate is used as a solute. With this composition, the spark generation voltage is high, but the specific resistance is large and the loss of the electrolytic capacitor is large. Accordingly, for the purpose of lowering the specific resistance without lowering the spark generation voltage, Japanese Patent Publication No. 62-800
As described in No. 4, there is also an electrolytic solution having a composition in which adipic acid or a salt thereof and ammonium hypophosphite are dissolved in ethylene glycol.

【0003】[0003]

【発明が解決しようとする課題】しかし、アジピン酸等
を溶解した電解液は、高温においてエステル化を生じ易
く、そのために比抵抗が増加する欠点がある。従って高
温において電解コンデンサの損失が増大してしまう。
However, an electrolytic solution in which adipic acid or the like is dissolved is liable to undergo esterification at a high temperature, and therefore has a drawback that the specific resistance increases. Therefore, the loss of the electrolytic capacitor increases at a high temperature.

【0004】本発明の目的は、以上の欠点を改良し、効
果的に比抵抗を低下でき、電解コンデンサの tanδ特性
等を改良できる電解コンデンサ用電解液を提供するもの
である。
An object of the present invention is to provide an electrolytic solution for an electrolytic capacitor which can improve the above-mentioned drawbacks, can effectively reduce the specific resistance, and can improve the tan δ characteristics and the like of the electrolytic capacitor.

【0005】[0005]

【課題を解決するための手段】本発明は、上記の目的を
達成するために、2,2,3−トリメチルグルタル酸、
2,2,4−トリメチルグルタル酸、2,3,4−トリ
メチルグルタル酸またはそれらの塩のうち一種類以上を
8%以上溶解することを特徴とする電解コンデンサ用電
解液を提供するものである。
SUMMARY OF THE INVENTION In order to achieve the above object, the present invention provides 2,2,3-trimethylglutaric acid,
2,2,4-trimethylglutaric acid, 2,3,4-tri
Methyl glutaric acid or one or more of their salts
Disclosed is an electrolytic solution for an electrolytic capacitor characterized by being dissolved by 8% or more .

【0006】2,2,3−トリメチルグルタル酸や2,
2,4−トリメチルグルタル酸、2,3,4−トリメチ
ルグルタル酸の構造式は、各々化1〜化の通りであ
る。
[0006] 2,2,3-trimethylglutaric acid and 2,2
2,4-trimethylglutaric acid, 2,3,4-trimethyl
The structural formulas of luglutaric acid are as shown in Chemical formulas 1 to 3 , respectively.

【0007】[0007]

【化1】 Embedded image

【0008】[0008]

【化2】 Embedded image

【0009】[0009]

【化3】 Embedded image

【0010】[0010]

【作用】2,2,3−トリメチルグルタル酸、2,2,
4−トリメチルグルタル酸、2,3,4−トリメチルグ
ルタル酸やそれらの塩は、側鎖を有するジカルボン酸で
あり、直鎖のジカルボン酸であるアジピン酸に比較し
て、化成性と溶解性に優れている。そのため、電解液の
火花発生電圧を高くでき、比抵抗を低下できる。また、
このトリメチルグルタル酸等は、主鎖のα位にメチル基
を有していて、この立体障害によるエチレングリコール
等のグリコール類とエステル化反応を生じ難くなってい
る。そのため、電解液は高温度でも安定した比抵抗を示
す。そして電解コンデンサの寿命を長くできる。
[Action] 2,2,3-trimethylglutaric acid, 2,2,2
4-trimethylglutaric acid, 2,3,4-trimethylg
Rutaric acid and salts thereof are dicarboxylic acids having a side chain, and are more excellent in chemical conversion and solubility than adipic acid which is a linear dicarboxylic acid. Therefore, the spark generation voltage of the electrolyte can be increased, and the specific resistance can be reduced. Also,
This trimethylglutaric acid or the like has a methyl group at the α-position of the main chain, and is less likely to cause an esterification reaction with glycols such as ethylene glycol due to the steric hindrance. Therefore, the electrolyte exhibits a stable specific resistance even at a high temperature. And the life of the electrolytic capacitor can be extended.

【0011】[0011]

【実施例】以下、本発明を実施例に基づいて説明する。
グリコール類はエチレングリコールを用いる。そしてこ
のエチレングリコールだけを、あるいはγ−ブチロラク
トンを混合して溶媒とする。また、この溶媒に、2,
2,3−トリメチルグルタル酸アンモニウムや2,2,
4−トリメチルグルタル酸アンモニウム、2,3,4−
トリメチルグルタル酸アンモニウムを溶解する。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below based on embodiments.
Glycols use ethylene glycol. Then, this ethylene glycol alone or γ-butyrolactone is mixed to form a solvent. Also, in this solvent,
Ammonium 2,3-trimethylglutarate and 2,2
Ammonium 4-trimethylglutarate, 2,3,4-
Dissolve ammonium trimethylglutarate .

【0012】なお、2,2,3−トリメチルグルタル酸
アンモニウム、2,2,4−トリメチルグルタル酸アン
モニウム、2,3,3−トリメチルグルタル酸アンモニ
ウム、2,3,4−トリメチルグルタル酸アンモニウ
ム、アジピン酸アンモニウムのエチレングリコールに対
する各溶解度を表1に示した。
Incidentally, ammonium 2,2,3-trimethylglutarate, ammonium 2,2,4-trimethylglutarate, ammonium 2,3,3-trimethylglutarate, ammonium 2,3,4-trimethylglutarate, adipine Table 1 shows the solubility of ammonium acid in ethylene glycol.

【0013】[0013]

【表1】 [Table 1]

【0014】この表1から明らかな通り、2,2,3−
トリメチルグルタル酸アンモニウム等のトリメチルグル
タル酸塩の溶解度が47〜54%であるのに対し、アジ
ピン酸アンモニウムが14.5%となっている。すなわ
ち、前者の方が後者の3倍以上、エチレングリコールに
溶解する。
As apparent from Table 1, 2,2,3-
The solubility of trimethylglutarate such as ammonium trimethylglutarate is 47-54%, while that of ammonium adipate is 14.5%. That is, the former dissolves in ethylene glycol at least three times the latter.

【0015】次に、表2に示した組成の実施例、比較例
および従来の電解液について、温度30℃のときの比抵
抗と温度85℃のときの火花発生電圧とを測定した。
Next, specific resistance at a temperature of 30 ° C. and spark generation voltage at a temperature of 85 ° C. were measured for Examples , Comparative Examples and conventional electrolytes having the compositions shown in Table 2. did.

【0016】[0016]

【表2】 [Table 2]

【0017】この表2から明らかな通り、実施例1〜実
施例は、比抵抗が262〜283Ω・cm、火花発生電
圧が430〜440Vとなる。また、従来例1及び従来
例2は、比抵抗が350〜370Ω・cm、火花発生電圧
が400〜430Vとなる。すなわち、実施例1〜実施
は、従来例1〜従来例2に比較して、比抵抗が約
0.8〜80.1%に低下し、火花発生電圧が最大1.
倍高くなっている。
As apparent from Table 2, in Examples 1 to 3 , the specific resistance is 262 to 283 Ω · cm, and the spark generation voltage is 430 to 440 V. Further, in Conventional Examples 1 and 2, the specific resistance is 350 to 370 Ω · cm, and the spark generation voltage is 400 to 430 V. That is, the first to third examples have a specific resistance of about 7 compared to the first and second examples.
0.8 to 80.1 %, and the spark generation voltage is up to 1.
It is one time higher.

【0018】また、実施例1〜実施例3、比較例及び従
来例1の各電解液について、これらを耐熱ビンに入れ、
温度110℃の雰囲気中に放置して、比抵抗及びエステ
ル化率を測定した。比抵抗の測定温度は30℃とする。
測定結果は表3に示した。
Further, each of the electrolytes of Examples 1 to 3, Comparative Example and Conventional Example 1 was placed in a heat-resistant bottle,
The sample was left in an atmosphere at a temperature of 110 ° C., and the specific resistance and the esterification ratio were measured. The measurement temperature of the specific resistance is 30 ° C.
Table 3 shows the measurement results.

【0019】[0019]

【表3】 [Table 3]

【0020】この表3から明らかな通り、1,000h 放置
後において、実施例1〜実施例は、比抵抗が478〜
544Ω・cm、エステル化率が36〜64%となる。ま
た、従来例1は、比抵抗が 1,855Ω・cm、エステル化率
が98%となる。すなわち、実施例1〜実施例は、従
来例1に比較して、比抵抗が約29.3%以下にそして
エステル化率が約65.3%以下に低下している。
As is clear from Table 3, after leaving for 1,000 hours, Examples 1 to 3 showed a specific resistance of 478 to
544 Ω · cm, and the esterification ratio is 36 to 64 %. Further, in Conventional Example 1, the specific resistance is 1,855 Ω · cm, and the esterification ratio is 98%. That is, in Examples 1 to 3 , the specific resistance is reduced to about 29.3 % or less and the esterification rate is reduced to about 65.3% or less, as compared with Conventional Example 1.

【0021】さらに、表2に示した組成の電解液を含浸
した定各250V、1,000μF のアルミ電解コンデンサ
について、初期特性及び高温負荷試験後の特性を測定し
た。高温負荷試験は、定格電圧250Vを連続印加し、
温度110℃の雰囲気中に1,000h〜2,000h放置して行
った。試料数は各々20個とする。測定値は平均値とし
て表4に示した。
Further, the initial characteristics and the characteristics after the high-temperature load test were measured for a constant 250 V, 1,000 μF aluminum electrolytic capacitor impregnated with an electrolyte having the composition shown in Table 2. In the high temperature load test, a rated voltage of 250 V is continuously applied,
The test was carried out in an atmosphere at a temperature of 110 ° C. for 1,000 to 2,000 hours. The number of samples is 20 each. The measured values are shown in Table 4 as average values.

【0022】[0022]

【表4】 [Table 4]

【0023】この表4から明らかな通り、2,000h 放置
後において、実施例1〜実施例は、tanδが4.0〜
4.3%、漏れ電流が5μAとなる。そして従来例1
は、tanδが13.8%、漏れ電流が9μAとなる。す
なわち、実施例1〜実施例は、従来例1に比較して、
tanδ が約32.1%以下にそして漏れ電流が5/9の
大きさになっている。
As is clear from Table 4, after leaving for 2,000 hours, Examples 1 to 3 showed tan δ of 4.0 to 4.0.
4.3 % and a leakage current of 5 μA. And Conventional Example 1
Has a tan δ of 13.8% and a leakage current of 9 μA. That is, Example 1 to Example 3 were compared with Conventional Example 1
The tan δ is less than about 32.1 % and the leakage current is 5/9.

【0024】[0024]

【発明の効果】以上の通り、本発明によれば、2,2,
3−トリメチルグルタル酸、2,2,4−トリメチルグ
ルタル酸、2,3,4−トリメチルグルタル酸やそれら
の塩を8%以上溶解しているため、溶解性等に優れてい
て比抵抗を低下でき、高温度でも安定した比抵抗を有
し、電解コンデンサの tanδ特性等を向上でき、その寿
命を改善できる電解コンデンサ用電解液が得られる。
As described above, according to the present invention ,
3-trimethylglutaric acid, 2,2,4-trimethylg
Rutaric acid, 2,3,4-trimethylglutaric acid and the like
Dissolves 8% or more of its salt, it is excellent in solubility, etc., it can lower the specific resistance, has stable specific resistance even at high temperature, can improve the tan δ characteristics of electrolytic capacitors, etc., and improves its life The resulting electrolytic solution for an electrolytic capacitor is obtained.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 電解コンデンサ用電解液において、2,
2,3−トリメチルグルタル酸、2,2,4−トリメチ
ルグルタル酸、2,3,4−トリメチルグルタル酸また
はそれらの塩のうち一種類以上を8%以上溶解すること
を特徴とする電解コンデンサ用電解液。
1. An electrolytic solution for an electrolytic capacitor , comprising:
2,3-trimethylglutaric acid, 2,2,4-trimethyl
Luglutaric acid, 2,3,4-trimethylglutaric acid or
Is an electrolytic solution for electrolytic capacitors, characterized in that at least one of these salts is dissolved in 8% or more .
JP26256095A 1995-09-14 1995-09-14 Electrolyte for electrolytic capacitors Expired - Lifetime JP3254983B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26256095A JP3254983B2 (en) 1995-09-14 1995-09-14 Electrolyte for electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26256095A JP3254983B2 (en) 1995-09-14 1995-09-14 Electrolyte for electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH0982579A JPH0982579A (en) 1997-03-28
JP3254983B2 true JP3254983B2 (en) 2002-02-12

Family

ID=17377511

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26256095A Expired - Lifetime JP3254983B2 (en) 1995-09-14 1995-09-14 Electrolyte for electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP3254983B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4019230B2 (en) * 1997-05-19 2007-12-12 日本ケミコン株式会社 Electrolytic solution for electrolytic capacitors
JP4529258B2 (en) * 2000-09-01 2010-08-25 日油株式会社 Electrolytic solution for electrolytic capacitor driving and electrolytic capacitor

Also Published As

Publication number Publication date
JPH0982579A (en) 1997-03-28

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