JP3254981B2 - Electrolyte for electrolytic capacitors - Google Patents

Electrolyte for electrolytic capacitors

Info

Publication number
JP3254981B2
JP3254981B2 JP25814995A JP25814995A JP3254981B2 JP 3254981 B2 JP3254981 B2 JP 3254981B2 JP 25814995 A JP25814995 A JP 25814995A JP 25814995 A JP25814995 A JP 25814995A JP 3254981 B2 JP3254981 B2 JP 3254981B2
Authority
JP
Japan
Prior art keywords
acid
ethenyl
electrolytic capacitor
electrolytic solution
electrolytic
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
JP25814995A
Other languages
Japanese (ja)
Other versions
JPH0982577A (en
Inventor
利幸 高野
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 JP25814995A priority Critical patent/JP3254981B2/en
Publication of JPH0982577A publication Critical patent/JPH0982577A/en
Application granted granted Critical
Publication of JP3254981B2 publication Critical patent/JP3254981B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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、通常、コンデンサ素子に電解液を含浸している。
この電解液は、特に中高圧用には、例えば、エチレング
リコール等の多価アルコール類を溶媒とし、これにアジ
ピン酸やスベリン酸、アゼライン酸、セバシン酸等の脂
肪族直鎖のジカルボン酸またはそれらの塩を溶質として
溶解した組成になっている。
2. Description of the Related Art An electrolytic capacitor such as an aluminum electrolytic capacitor generally has a capacitor element impregnated with an electrolytic solution.
This electrolytic solution is particularly used for medium and high pressures, for example, using a polyhydric alcohol such as ethylene glycol as a solvent, and adding adipic acid, suberic acid, azelaic acid, linear aliphatic dicarboxylic acid such as sebacic acid or the like. Has been dissolved as a solute.

【0003】ところで、近年、アルミ電解コンデンサの
損失を低下する要求が高まっている。アルミ電解コンデ
ンサの損失を低下するためには、電解液の比抵抗を下げ
ることが有効な手段の一つである。
[0003] In recent years, there has been an increasing demand for reducing the loss of aluminum electrolytic capacitors. One of the effective means for reducing the loss of the aluminum electrolytic capacitor is to lower the specific resistance of the electrolytic solution.

【0004】[0004]

【発明が解決しようとする課題】しかし、従来の多価ア
ルコールと脂肪族直鎖のジカルボン酸塩とを用いた電解
液では、高温度においてエステル反応を生じるため、比
抵抗が上昇し易い欠点がある。そのため、この電解液を
用いた電解コンデンサは、 tanδが上昇し、寿命を向上
し難い。
However, the conventional electrolytic solution using a polyhydric alcohol and an aliphatic straight-chain dicarboxylate causes an ester reaction at a high temperature, so that the specific resistance tends to increase. is there. Therefore, in an electrolytic capacitor using this electrolytic solution, tan δ increases, and it is difficult to improve the life.

【0005】本発明の目的は、以上の欠点を改良し、比
抵抗が低く、電解コンデンサのtanδ特性等を改善でき
寿命を向上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 disadvantages, has a low specific resistance, can improve the tan δ characteristics of the electrolytic capacitor, and can prolong the life.

【0006】[0006]

【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、多価アルコールを主な溶媒とする電解
コンデンサ用電解液において、2−エテニル−5−メチ
ルアジピン酸、2−エテニル−6−メチルピメリン酸、
2−エテニル−7−メチルスベリン酸、2−エテニル−
8−メチルアゼライン酸、2−エテニル−9−メチルセ
バシン酸、2−エテニル−9−エチルセバシン酸、2−
エチニル−9−エチルセバシン酸から選ばれたジカルボ
ン酸又はその塩を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 an electrolytic solution for an electrolytic capacitor containing a polyhydric alcohol as a main solvent, comprising 2-ethenyl-5-methylbenzene.
Luadipic acid, 2-ethenyl-6-methylpimelic acid,
2-ethenyl-7-methylsuberic acid, 2-ethenyl-
8-methylazelaic acid, 2-ethenyl-9-methylse
Basic acid, 2-ethenyl-9-ethylsebacic acid, 2-
It is intended to provide an electrolytic solution for an electrolytic capacitor, characterized by dissolving a dicarboxylic acid selected from ethynyl-9- ethylsebacic acid or a salt thereof.

【0007】多価アルコールは、エチレングリコールや
ジエチレングリコール、プロピレングリコール、1,4
−ブタンジオール、グリセリン等を用いる。
Polyhydric alcohols include ethylene glycol, diethylene glycol, propylene glycol, 1,4
Using butanediol, glycerin and the like;

【0008】なお、2−エテニル−5−メチルアジピン
酸、2−エテニル−6−メチルピメリン酸等のジカルボ
ン酸又はその塩の溶解量は1〜30wt%の範囲が良い。
すなわち、溶解量が1wt%未満では比抵抗を下げる効果
が低く、30wt%より多くなると飽和状態に近くなり電
解コンデンサの低温におけるtanδ 特性等が劣化し易
い。
[0008] 2-ethenyl-5-methyladipin
The dissolution amount of an acid, dicarboxylic acid such as 2-ethenyl-6-methylpimelic acid or a salt thereof is preferably in the range of 1 to 30% by weight.
That is, when the amount of dissolution is less than 1% by weight, the effect of lowering the specific resistance is low.

【0009】[0009]

【作用】2−エテニル−5−メチルアジピン酸、2−エ
テニル−6−メチルピメリン酸等のジカルボン酸等は、
主鎖のα炭素にメチル基などの脂肪族炭化水素基を有し
ているため、高温において多価アルコール類との間でエ
ステル化反応を生じにくい。従って、このジカルボン酸
を溶解した電解液を用いた電解コンデンサは、高温で長
時間使用しても、電解液の比抵抗が増大し難いため、ta
nδ が著しく上昇するのを防止できる。
Action 2-Ethenyl-5-methyladipate, 2-E
Dicarboxylic acids such as tenyl-6-methylpimelic acid ,
Since the α-carbon of the main chain has an aliphatic hydrocarbon group such as a methyl group, an esterification reaction with a polyhydric alcohol hardly occurs at a high temperature. Therefore, even if the electrolytic capacitor using the electrolytic solution in which the dicarboxylic acid is dissolved is used for a long time at a high temperature, the specific resistance of the electrolytic solution does not easily increase.
nδ can be prevented from significantly increasing.

【0010】また、2−エテニル−5−メチルアジピン
酸、2−エテニル−6−メチルピメリン酸等のジカルボ
ン酸等は、側鎖を有しているため、直鎖のジカルボン酸
であるアゼライン酸やセバシン酸等と比較して、多価ア
ルコール類に溶解し易く、低温特性に優れ、比抵抗を低
下できるとともに、火花発生電圧を高めることができ
る。
Also, 2-ethenyl-5-methyladipin
Acids and dicarboxylates such as 2-ethenyl-6-methylpimelic acid have side chains, so that they are more versatile than linear dicarboxylic acids such as azelaic acid and sebacic acid. It is easily soluble in polyhydric alcohols, has excellent low-temperature characteristics, can lower the specific resistance, and can increase the spark generation voltage.

【0011】さらに、2−エテニル−5−メチルアジピ
ン酸、2−エテニル−6−メチルピメリン酸等のジカル
ボン酸等は、その特異な分子構造のため、陽極箔と錯体
を形成し難い。そのため、電解コンデンサの容量減少も
改善できる。
Further, 2-ethenyl-5-methyladipi
Acids, dicarbonic acids such as 2-ethenyl-6-methylpimelic acid, and the like are difficult to form a complex with the anode foil because of their unique molecular structures. Therefore, the capacity of the electrolytic capacitor can be reduced.

【0012】[0012]

【実施例】以下、本発明を実施例に基づいて説明する。
多価アルコールはエチレングリコールを用い、これを溶
する。また、ジカルボン酸は、2−エテニル−5−
メチルアジピン酸、2−エテニル−6−メチルピメリン
酸、2−エテニル−7−メチルスベリン酸、2−エテニ
ル−8−メチルアゼライン酸、2−エテニル−9−メチ
ルセバシン酸、2−エテニル−9−エチルセバシン酸、
2−エチニル−9−エチルセバシン酸を用いる。そして
これらの溶液にアンモニア水を溶解し、ジカルボン酸を
アンモニウム塩とする。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below based on embodiments.
Polyhydric alcohol with ethylene glycol, which is referred to as solvent. The dicarboxylic acid is 2-ethenyl-5-
Methyl adipic acid, 2-ethenyl-6-methylpimelin
Acid, 2-ethenyl-7-methylsuberic acid, 2-ethenyl
Ru-8-methylazelaic acid, 2-ethenyl-9-methyl
Lucevanic acid, 2-ethenyl-9-ethylsebacic acid,
Use 2-ethynyl-9-ethylsebacic acid . Then, aqueous ammonia is dissolved in these solutions to convert the dicarboxylic acid into an ammonium salt.

【0013】次に、表1及び表2に示す組成の実施例の
電解液及び表3に示す従来の電解液について、初期と、
温度130℃の雰囲気中に2,000h放置後の各比抵
抗を測定した。測定時の温度は30℃とする。
Next, with respect to the electrolyte solutions of the examples having the compositions shown in Tables 1 and 2, and the conventional electrolyte solution shown in Table 3,
Each specific resistance was measured after being left for 2,000 hours in an atmosphere at a temperature of 130 ° C. The temperature during the measurement is 30 ° C.

【0014】[0014]

【表1】 [Table 1]

【0015】[0015]

【表2】 [Table 2]

【0016】[0016]

【表3】 [Table 3]

【0017】これらの表1〜表3に明らかな通り、実施
例1〜実施例は、初期値が296〜467Ω・cm、放
置後が569〜609Ω・cmとなる。これに対し、従来
例1〜従来例5は、初期値が330〜494Ω・cm、放
置後が834〜1,080Ω・cmとなる。すなわち、
2,000h放置後において、実施例1〜実施例は、
従来例1〜従来例5に比較して、約52.7〜73.0
%に低下する。
As is apparent from Tables 1 to 3, in Examples 1 to 7 , the initial value is 296 to 467 Ω · cm, and the value after standing is 569 to 609 Ω · cm. On the other hand, in Conventional Examples 1 to 5, the initial value is 330 to 494 Ω · cm, and the value after standing is 834 to 1,080 Ω · cm. That is,
After leaving for 2,000 hours, Examples 1 to 7
Approximately 52.7 to 73.0 compared to Conventional Examples 1 to 5.
%.

【0018】また、表1〜表3に示した組成からなる各
電解液を含浸した定格250V、330μFのアルミ電
解コンデンサについて、初期特性と高温負荷試験後の特
性を測定した。高温負荷試験は、定格電圧を連続印加
し、温度130℃の雰囲気中に2,000h放置して行
なう。試料数は各々20個づつとする。そして測定値は
平均値とし、表4に示した。
The initial characteristics and the characteristics after the high-temperature load test were measured for a rated 250 V, 330 μF aluminum electrolytic capacitor impregnated with each of the electrolytic solutions having the compositions shown in Tables 1 to 3. The high-temperature load test is performed by continuously applying a rated voltage and leaving it in an atmosphere at a temperature of 130 ° C for 2,000 hours. The number of samples is 20 each. The measured values were average values and are shown in Table 4.

【0019】[0019]

【表4】 [Table 4]

【0020】この表4から明らかな通り、初期特性につ
いては、実施例1〜実施例の場合が tanδ0.033
〜0.053、漏れ電流41〜52μAそして従来例1
〜従来例5の場合が tanδ0.036〜0.059、漏
れ電流60〜65μAとなる。すなわち、実施例1〜実
施例の場合の方が従来例1〜従来例5の場合に比較し
て、全体的に tanδが低く、漏れ電流が約63.1〜8
6.7%の大きさになっている。
As is clear from Table 4, the initial characteristics of Examples 1 to 7 were tan δ 0.033.
~0.053, leakage current 41 ~52Myuei and Conventional Example 1
Tan δ 0.036 to 0.059 and leakage current 60 to 65 μA in the case of Conventional Example 5. That is, in the case of Examples 1 to 7 , the tan δ is lower as a whole and the leakage current is about 63.1 to 8 compared to the cases of Conventional Examples 1 to 5.
It is 6.7% in size.

【0021】また、高温負荷試験後は、実施例1〜実施
の場合が、静電容量変化率−1.0〜−3.2%、
tanδ 0.064〜0.069、漏れ電流〜9μAと
なる。そして従来例1〜従来例5の場合が、静電容量変
化率−4.2〜−9.8%、tanδ 0.091〜0.1
30、漏れ電流16〜18μAとなる。すなわち、実施
例1〜実施例を用いた場合の方が、従来例1〜従来例
5の場合に比較して静電容量変化率が約10.2〜7
6.2%に押えられ、 tanδが約49.2〜75.8
%、漏れ電流が約44.4〜56.3%の大きさにな
る。
Further, after the high-temperature load test, the cases of Examples 1 to 7 show that the capacitance change rate is -1.0 to -3.2%,
tan δ 0.064 to 0.069 and leakage current 8 to 9 μA. In the case of Conventional example 1 to Conventional example 5, the capacitance change rate was -4.2 to -9.8%, tan δ 0.091 to 0.1.
30, a leakage current of 16 to 18 μA. That is, when the first to seventh embodiments are used, the capacitance change rate is about 10.2 to 7 as compared with the first to fifth examples.
6.2%, and tan δ is about 49.2 to 75.8
%, And the leakage current is about 44.4 to 56.3%.

【0022】[0022]

【発明の効果】本発明によれば、2−エテニル−5−メ
チルアジピン酸、2−エテニル−6−メチルピメリン
酸、2−エテニル−7−メチルスベリン酸、2−エテニ
ル−8−メチルアゼライン酸、2−エテニル−9−メチ
ルセバシン酸、2−エテニル−9−エチルセバシン酸、
2−エチニル−9−エチルセバシン酸から選ばれたジカ
ルボン酸又はその塩を溶解しているため、比抵抗が低
く、高温に対して安定していて、電解コンデンサの tan
δ特性や漏れ電流特性、高温特性を改善でき寿命を向上
できる電解コンデンサ用電解液が得られる。
According to the present invention, 2-ethenyl-5-meth
Tildipic acid, 2-ethenyl-6-methylpimelin
Acid, 2-ethenyl-7-methylsuberic acid, 2-ethenyl
Ru-8-methylazelaic acid, 2-ethenyl-9-methyl
Lucevanic acid, 2-ethenyl-9-ethylsebacic acid,
Since dicarbonic acid or a salt thereof selected from 2-ethynyl-9-ethylsebacic acid is dissolved, the specific resistance is low, the temperature is stable to high temperatures, and the tan of the electrolytic capacitor is low.
An electrolytic solution for an electrolytic capacitor that can improve δ characteristics, leakage current characteristics, and high-temperature characteristics and can prolong its life can be obtained.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 多価アルコールを主な溶媒とする電解コ
ンデンサ用電解液において、2−エテニル−5−メチル
アジピン酸、2−エテニル−6−メチルピメリン酸、2
−エテニル−7−メチルスベリン酸、2−エテニル−8
−メチルアゼライン酸、2−エテニル−9−メチルセバ
シン酸、2−エテニル−9−エチルセバシン酸、2−エ
チニル−9−エチルセバシン酸から選ばれたジカルボン
酸又はその塩を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 a polyhydric alcohol as a main solvent, comprising: 2-ethenyl-5-methyl
Adipic acid, 2-ethenyl-6-methylpimelic acid, 2
-Ethenyl-7-methylsuberic acid, 2-ethenyl-8
-Methylazelaic acid, 2-ethenyl-9-methylseba
Synic acid, 2-ethenyl-9-ethylsebacic acid, 2-E
An electrolytic solution for an electrolytic capacitor, wherein a dicarboxylic acid selected from tinyl-9-ethylsebacic acid or a salt thereof is dissolved.
JP25814995A 1995-09-11 1995-09-11 Electrolyte for electrolytic capacitors Expired - Lifetime JP3254981B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25814995A JP3254981B2 (en) 1995-09-11 1995-09-11 Electrolyte for electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25814995A JP3254981B2 (en) 1995-09-11 1995-09-11 Electrolyte for electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH0982577A JPH0982577A (en) 1997-03-28
JP3254981B2 true JP3254981B2 (en) 2002-02-12

Family

ID=17316211

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25814995A Expired - Lifetime JP3254981B2 (en) 1995-09-11 1995-09-11 Electrolyte for electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP3254981B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6452620B1 (en) 1999-04-08 2002-09-17 Gerber Scientific Products, Inc. Methods and apparatus for improved thermal printing

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4529258B2 (en) * 2000-09-01 2010-08-25 日油株式会社 Electrolytic solution for electrolytic capacitor driving and electrolytic capacitor
HU228776B1 (en) * 2001-12-11 2013-05-28 Okamura Oil Mill Ltd Composition for electrolytic solution and process for producing the same
JP2005093448A (en) * 2002-08-22 2005-04-07 Sanyo Chem Ind Ltd Electrolyte
TW200634127A (en) * 2004-12-15 2006-10-01 Tamurakaken Corp An electrically conductive adhesive, electrical part and electrical part module were made of it
CN101521117B (en) * 2009-03-27 2011-06-29 深圳新宙邦科技股份有限公司 preparation method of alpha- dicarboxylic acids for electrolyte for aluminium electrolytic capacitor
JP6131136B2 (en) * 2013-07-12 2017-05-17 国立大学法人三重大学 Electrolytic capacitor driving electrolyte and electrolytic capacitor using the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6452620B1 (en) 1999-04-08 2002-09-17 Gerber Scientific Products, Inc. Methods and apparatus for improved thermal printing
US6680743B2 (en) 1999-04-08 2004-01-20 Gerber Scientific Products, Inc. Methods and apparatus for improved thermal printing

Also Published As

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