JPH03181114A - Electrolyte for driving electrolytic capacitor - Google Patents

Electrolyte for driving electrolytic capacitor

Info

Publication number
JPH03181114A
JPH03181114A JP32198889A JP32198889A JPH03181114A JP H03181114 A JPH03181114 A JP H03181114A JP 32198889 A JP32198889 A JP 32198889A JP 32198889 A JP32198889 A JP 32198889A JP H03181114 A JPH03181114 A JP H03181114A
Authority
JP
Japan
Prior art keywords
boric acid
butyrolactone
dissolved
gamma
solvent
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.)
Granted
Application number
JP32198889A
Other languages
Japanese (ja)
Other versions
JP2819475B2 (en
Inventor
Shuichi Tanno
丹野 修一
Hideyuki Takayama
高山 英行
Atsushi Takano
淳 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.)
Marcon Electronics Co Ltd
Original Assignee
Marcon Electronics Co Ltd
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 Marcon Electronics Co Ltd filed Critical Marcon Electronics Co Ltd
Priority to JP32198889A priority Critical patent/JP2819475B2/en
Publication of JPH03181114A publication Critical patent/JPH03181114A/en
Application granted granted Critical
Publication of JP2819475B2 publication Critical patent/JP2819475B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Electric Double-Layer Capacitors Or The Like (AREA)

Abstract

PURPOSE:To reduce the resistivity in the wide temperature range extending from low temperature to high temperature and besides to raise sparking voltage by using a solvent mainly composed of gamma-butyrolactone, and also adding boric acid dissolved in ethylene glycol. CONSTITUTION:First, tetramethyl ammonium salt of phthalic acid is dissolved as a solvent in the solvent mainly composed of gamma-butyrolactone, thus a low resistivity value is obtained though sparking voltage is low. Next, boric acid is added in such mixed liquid so as to elevate the sparking voltage without elevating the resistivity much. At this time the boric acid is hardly dissolved in the solvent mainly composed of gamma-butyrolactone, so boric acid is dissolved in a lactone solvent in such a means as to dissolve the boric acid once by the ester reaction with ethylglycol and add boric acid in the mixed liquid between gamma-butyrolactone and tetramethyl ammonium salt. As a result, sparking voltage rise can be made possible without elevating the resistivity value much.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、電解コンデンサ駆動用電解液に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to an electrolytic solution for driving an electrolytic capacitor.

[従来の技術] 従来、電解コンデンサ駆動用電解液としては、エチレン
グリリコールに、アジピン酸を初めとする有機カルボン
酸などを溶解した電解液が用いられている。しかしなが
ら、エチレングリコールは、低温域での粘度上昇が著し
い欠点があり、また、高温域における比抵抗の増大もし
くはそれに伴う損失の増大などの欠点がある。
[Prior Art] Conventionally, as an electrolytic solution for driving an electrolytic capacitor, an electrolytic solution in which an organic carboxylic acid such as adipic acid is dissolved in ethylene glycol has been used. However, ethylene glycol has drawbacks such as a significant increase in viscosity at low temperatures, and an increase in specific resistance or associated loss at high temperatures.

これに対し、低温における特性を改善する電解波として
、ジメチルホルムアミドやγ−ブチロラクトンを主溶媒
とし、マレイン酸やフタル酸の塩を溶質として用いた電
解コンデンサ駆動用電解液が存在している。
On the other hand, as an electrolytic wave that improves the characteristics at low temperatures, there is an electrolytic solution for driving an electrolytic capacitor that uses dimethylformamide or γ-butyrolactone as a main solvent and a salt of maleic acid or phthalic acid as a solute.

しかしながら、これらの電解コンデンサ駆動用電解液を
使用した場合、比抵抗は充分に低いものの、火花電圧が
低くなり、50V級以下の低電圧のコンデンサにしか使
用できないという欠点がある。
However, when these electrolytic capacitor driving electrolytes are used, although the specific resistance is sufficiently low, the spark voltage is low, and there is a drawback that they can only be used for low voltage capacitors of 50 V class or lower.

[発明が解決しようとする課題] 上記のように、従来の電解コンデンサ駆動用電解波は、
低温域での粘度上昇や、高温域での比抵抗の増大もしく
はそれに伴う損失の増大などの欠点を有していた。また
、改善のためにジメチルホルムアミドやγ−ブチロラク
トンを主溶媒とし、マレイン酸やフタル酸の塩を溶質と
して用いた電解液には、このような欠点がない代りに、
火花電圧が低くなり、低電圧のコンデンサにしか対応で
きないという新たな欠点が存在していた。
[Problem to be solved by the invention] As mentioned above, the conventional electrolytic wave for driving an electrolytic capacitor is
It has disadvantages such as an increase in viscosity in a low temperature range, an increase in specific resistance in a high temperature range, and an accompanying increase in loss. In addition, for improvement, electrolytes using dimethylformamide or γ-butyrolactone as the main solvent and maleic acid or phthalic acid salts as solutes do not have these drawbacks.
A new drawback was that the spark voltage was lower, making it compatible only with low-voltage capacitors.

本発明は、このような従来技術の課題を解決するために
提案されたものであり、その目的は、低温から高温に渡
る広い範囲の温度領域において比抵抗を低減させ、且つ
、火花電圧を」1昇することにより、広い温度領域にお
いて、安定した高い特性を存する、長寿命で信頼性の高
い電解コンデンサの実現に貢献でき、しかも、より高い
電圧のコンデンサ、すなわち、具体的には100V級の
コンデンサへの使用が可能であるような、優れた電解コ
ンデンサ駆動用電解液を提供することである。
The present invention was proposed to solve the problems of the prior art, and its purpose is to reduce the specific resistance in a wide temperature range from low to high temperatures, and to reduce the spark voltage. 1. By increasing the voltage by 100 V, it is possible to contribute to the realization of long-life and highly reliable electrolytic capacitors that have stable and high characteristics over a wide temperature range. Moreover, it can be used for higher voltage capacitors, specifically 100V class capacitors. An object of the present invention is to provide an excellent electrolytic solution for driving an electrolytic capacitor, which can be used in capacitors.

[課題を解決するための手段] 本発明による電解コンデンサ駆動用電解液は、γ−ブチ
ロラクトンを主体とする溶媒に、フタル酸のテI・ラメ
チルアンモニウム塩を溶質として溶解し、さらに、エチ
レングリコールに溶解したホウ酸と、P−ニトロフェノ
ールまたはP−ニトロ安息香酸を添加、溶解したことを
特徴としている。
[Means for Solving the Problems] The electrolytic solution for driving an electrolytic capacitor according to the present invention is produced by dissolving teI-ramethylammonium salt of phthalic acid as a solute in a solvent mainly composed of γ-butyrolactone, and further dissolving teI-ramethylammonium salt of phthalic acid as a solute. It is characterized by adding and dissolving boric acid dissolved in , and P-nitrophenol or P-nitrobenzoic acid.

また、各材料の添加量は、エチレングリコールの濃度が
15〜20%、ホウ酸の濃度が0.5〜1%、P−ニト
ロフェノールまたはP−ニトロ安息香酸の濃度が0.5
〜1%であることが望ましい。この場合、エチレングリ
コールの濃度を15〜20%とするのは、15%を下回
る場合には、ホウ酸の溶解が円滑に進まず、20%を越
える量のエチレングリコールを添加した場合には、比抵
抗が増大してしまうからである。
The amounts of each material added are as follows: ethylene glycol concentration is 15-20%, boric acid concentration is 0.5-1%, and P-nitrophenol or P-nitrobenzoic acid concentration is 0.5%.
It is desirable that it be ~1%. In this case, the reason why the concentration of ethylene glycol is 15 to 20% is because if it is less than 15%, dissolution of boric acid will not proceed smoothly, and if ethylene glycol is added in an amount exceeding 20%, This is because the specific resistance increases.

[作用] 以−Lのような構成を有する本発明の電解コンデンサ駆
動用電解液の作用は次の通りである。
[Function] The action of the electrolytic solution for driving an electrolytic capacitor of the present invention having the configuration as shown below is as follows.

まず、γ−ブチロラクトンを主体とする溶媒にフタル酸
のテトラメチルアンモニウム塩を溶質として溶解した場
合、火花電圧は低いながらも、低い比抵抗値を得ること
ができる。
First, when a tetramethylammonium salt of phthalic acid is dissolved as a solute in a solvent mainly composed of γ-butyrolactone, a low specific resistance value can be obtained although the spark voltage is low.

そして、このようなγ−ブチロラクトンとテトラメチル
アンモニウム塩との混合液にホウ酸を添加することによ
り、比抵抗値を余り上昇させることなしに、火花電圧を
」1昇することが可能となる。
By adding boric acid to such a mixed solution of γ-butyrolactone and tetramethylammonium salt, it is possible to increase the spark voltage by 1" without increasing the specific resistance value too much.

この場合、ホウ酸はγ−ブチロラクトンを主体とする溶
媒には溶解し難いため、本発明では、−旦エチレングリ
コールとのエステル化反応によりホウ酸を溶解し、この
状態で、γ−ブチロラクトンとテトラメチルアンモニウ
ム塩との混合液にホウ酸を添加するという画期的な手段
により、γブチロラクトン溶媒中にホウ酸を溶解させる
ことが可能となっており、この結果、前記のように、比
抵抗値を余り上昇させることなしに、火花電圧を上昇す
ることが可能となっている。
In this case, since boric acid is difficult to dissolve in a solvent mainly composed of γ-butyrolactone, in the present invention, boric acid is first dissolved by an esterification reaction with ethylene glycol, and in this state, γ-butyrolactone and tetra By the innovative means of adding boric acid to the mixture with methylammonium salt, it has become possible to dissolve boric acid in the γ-butyrolactone solvent, and as a result, as mentioned above, the specific resistance value has increased. This makes it possible to increase the spark voltage without increasing too much.

[実施例] 以下に、本発明による電解コンデンサ駆動用電解液の実
施例を説明する。
[Example] Examples of the electrolytic solution for driving an electrolytic capacitor according to the present invention will be described below.

まず、第1表に示すような組成比にて、従来技術による
3挿類の電解液(従来例1〜3)と、本発明による2挿
類の電解液(実施例1,2)とを生成し、それぞれの電
解液の火花電圧(V)および25℃における比抵抗を調
べたところ、第2表に示すような結果が得られた。
First, three types of electrolyte solutions according to the prior art (Conventional Examples 1 to 3) and two types of electrolyte solutions according to the present invention (Examples 1 and 2) were prepared at the composition ratios shown in Table 1. When the spark voltage (V) and specific resistance at 25° C. of each electrolytic solution were investigated, the results shown in Table 2 were obtained.

また、以上のような従来技術と本発明とによる5種類の
電解液を使用して、同定格63V−680μFのコンデ
ンサを試作し、恒温105℃にて定格電圧印加の高温負
荷試験を行ったところ、第3表および第4表に示すよう
な結果が得られた。
In addition, a capacitor with the same rating of 63V-680μF was prototyped using five types of electrolytes according to the conventional technology and the present invention as described above, and a high-temperature load test was conducted at a constant temperature of 105°C with the application of the rated voltage. , the results shown in Tables 3 and 4 were obtained.

第3表および第4表は、静電容量(μF)、損失角の正
接(tanδ)の各特性を示す表であり、6表とも、初
期特性と、1000時間後における特性、2000時間
後における特性を比較的に示している。(以下余白) 前記の第3表および第4表に示すように、従来例2,3
は、初期時点ですでに防爆弁が作動してしまい、63V
用として使用することは不可能であることがわかる。ま
た、従来例1は、初期の時点では、ある程度の特性を有
しているものの、それ以降の特性の劣化が著しく、10
00時間の高温11荷試験の後には、静電容量は7.3
%も減少し、また、損失角の正接も0.082と大きく
なっており、さらに、1500時間後には、防爆弁が作
動してしまう。
Tables 3 and 4 show the characteristics of capacitance (μF) and tangent of loss angle (tan δ), and Table 6 shows the initial characteristics, the characteristics after 1000 hours, and the characteristics after 2000 hours. Characteristics are shown comparatively. (The following is a blank space) As shown in Tables 3 and 4 above, Conventional Examples 2 and 3
In this case, the explosion-proof valve has already activated at the initial stage, and the 63V
It turns out that it is impossible to use it for personal purposes. In addition, although Conventional Example 1 has some characteristics at the initial stage, the characteristics deteriorate significantly after that, and 10
After 00 hours of high temperature 11 load test, the capacitance is 7.3
% decreased, and the tangent of the loss angle also increased to 0.082, and furthermore, the explosion-proof valve operated after 1500 hours.

これらの従来例1〜3に比べ、本発明による実施例1.
2は、1000時間の高温負荷試験の後にも、静電容量
の減少は、2.0%〜2.1%程度に止どめられ、また
、損失角の正接についても、微小の増加しか見られない
。さらに、2000時間後においても、静電容量は、初
期に比べて4゜3%〜4.5%程度減少するに止どめら
れ、また、損失角の正接も、0.042〜0.045と
、充分に低い値に押えられている。これらのことから、
本発明による電解コンデンサ駆動用電解液(実施例1.
2)を使mした場合には、高温度中での経時変化が極め
て小さく、安定した高い特性を維持でき、長寿命を有す
るような電解コンデンサを実現でき、特に、50Vを越
える高電圧のコンデンサにも使用可能であることがわか
る。さらに、本発明による前記の各電解液(実施IJi
l、2)は、100V級までのコンデンサの使用に耐え
られることが確認されている。
In comparison with these conventional examples 1 to 3, Example 1 according to the present invention.
2, even after a 1000-hour high-temperature load test, the decrease in capacitance remained at about 2.0% to 2.1%, and only a slight increase was observed in the tangent of the loss angle. I can't do it. Furthermore, even after 2000 hours, the capacitance decreased by only 4.3% to 4.5% compared to the initial value, and the loss angle tangent also decreased by 0.042 to 0.045. The value has been kept to a sufficiently low level. from these things,
Electrolytic solution for driving an electrolytic capacitor according to the present invention (Example 1.
When using 2), it is possible to realize an electrolytic capacitor that has very little change over time at high temperatures, maintains stable and high characteristics, and has a long life, especially for high voltage capacitors exceeding 50V. It turns out that it can also be used. Furthermore, each of the above-mentioned electrolytes according to the present invention (implementation IJi
1, 2) has been confirmed to be able to withstand the use of capacitors up to 100V class.

[発明の効果] 以上説明したように、本発明の電解コンデンサ駆動用電
解液は、特にγ−ブチロラクトンを主体とする溶媒を使
用すると共に、エチレングリコールに溶解したホウ酸を
添加することにより、従来の電解液に比べて、低温から
高温に渡る広い範囲の温度領域における比抵抗が低減し
ており、且つ、火花電圧が上昇している。
[Effects of the Invention] As explained above, the electrolytic solution for driving an electrolytic capacitor of the present invention uses a solvent mainly composed of γ-butyrolactone and adds boric acid dissolved in ethylene glycol. Compared to the electrolytic solution shown in Figure 1, the specific resistance is reduced over a wide temperature range from low to high temperatures, and the spark voltage is increased.

従って、このような本発明の電解コンデンサ駆動用電解
液を使用すれば、従来に比べて、広い温度領域において
、安定した高い特性を有する、長寿命で信頼性の高い電
解コンデンサの実現に貢献でき、しかも、100V級の
コンデンサへの使用が可能であるような、優れた電解コ
ンデンサ駆動用電解液を提供でき、工業的実用性の面で
多大な効果を得られる。
Therefore, by using the electrolytic solution for driving electrolytic capacitors of the present invention, it is possible to contribute to the realization of long-life, highly reliable electrolytic capacitors that have stable and high characteristics over a wide temperature range compared to conventional capacitors. Moreover, it is possible to provide an excellent electrolytic solution for driving an electrolytic capacitor that can be used in a 100V class capacitor, and a great effect can be obtained in terms of industrial practicality.

Claims (2)

【特許請求の範囲】[Claims] (1)γ−ブチロラクトンを主体とする溶媒に、フタル
酸のテトラメチルアンモニウム塩を溶質として溶解し、
さらに、エチレングリコールに溶解したホウ酸と、P−
ニトロフェノールまたはP−ニトロ安息香酸を添加、溶
解したことを特徴とする電解コンデンサ駆動用電解液。
(1) Dissolving tetramethylammonium salt of phthalic acid as a solute in a solvent mainly composed of γ-butyrolactone,
Furthermore, boric acid dissolved in ethylene glycol and P-
An electrolytic solution for driving an electrolytic capacitor, characterized in that nitrophenol or P-nitrobenzoic acid is added and dissolved therein.
(2)エチレングリコールの濃度が15〜20%、ホウ
酸の濃度が0.5〜1%、P−ニトロフェノールまたは
P−ニトロ安息香酸の濃度が0.5〜1%であることを
特徴とする請求項1に記載の電解コンデンサ駆動用電解
液。
(2) The concentration of ethylene glycol is 15-20%, the concentration of boric acid is 0.5-1%, and the concentration of P-nitrophenol or P-nitrobenzoic acid is 0.5-1%. The electrolytic solution for driving an electrolytic capacitor according to claim 1.
JP32198889A 1989-12-11 1989-12-11 Electrolyte for driving electrolytic capacitors Expired - Lifetime JP2819475B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32198889A JP2819475B2 (en) 1989-12-11 1989-12-11 Electrolyte for driving electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32198889A JP2819475B2 (en) 1989-12-11 1989-12-11 Electrolyte for driving electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH03181114A true JPH03181114A (en) 1991-08-07
JP2819475B2 JP2819475B2 (en) 1998-10-30

Family

ID=18138669

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32198889A Expired - Lifetime JP2819475B2 (en) 1989-12-11 1989-12-11 Electrolyte for driving electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP2819475B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008085240A (en) * 2006-09-29 2008-04-10 Nichicon Corp Electrolytic solution for driving electrolytic capacitor, and electrolytic capacitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008085240A (en) * 2006-09-29 2008-04-10 Nichicon Corp Electrolytic solution for driving electrolytic capacitor, and electrolytic capacitor

Also Published As

Publication number Publication date
JP2819475B2 (en) 1998-10-30

Similar Documents

Publication Publication Date Title
JPH03181114A (en) Electrolyte for driving electrolytic capacitor
JP2625464B2 (en) Electrolyte for driving electrolytic capacitors
JPS63261820A (en) Electrolyte for driving electrolytic capacitor
JP2812689B2 (en) Electrolyte for driving electrolytic capacitors
JP2731250B2 (en) Electrolyte for driving electrolytic capacitors
JPH01103820A (en) Electrolyte for driving electrolytic capacitor
JPH05315195A (en) Electrolyte for driving electrolytic capacitor
JP3612671B2 (en) Electrolytic solution for electrolytic capacitor drive
JP3376749B2 (en) Electrolyte for driving electrolytic capacitors
JPH0412512A (en) Driving electrolyte of aluminum electrolytic capacitor
JP3212322B2 (en) Electrolyte for driving electrolytic capacitors
JPH01114017A (en) Electrolyte for driving electrolytic capacitors
JP3311768B2 (en) Electrolyte for driving electrolytic capacitors
JPH01227420A (en) Electrolyte for driving electrolytic capacitor
JP3240066B2 (en) Electrolyte for driving electrolytic capacitors
JPH031819B2 (en)
JPH03187210A (en) Electrolytis solution for driving electrolytic capacitor
JPH01209712A (en) Driving electrolyte of electrolytic capacitor
JPH04330708A (en) Electrolytic solution for driving electrolytic capacitor
JPH03153012A (en) Electrolyte for actuating electrolytic capacitor
JPH04263412A (en) Electrolyte for driving of electrolyte capacitor
JPH03241811A (en) Electrolytic capacitor driving electrolyte
JPS63301514A (en) Electrolyte for driving aluminum electrolytic capacitor
JPH0837132A (en) Electrolyte for driving electrolytic capacitor
JPH07120616B2 (en) Electrolytic solution for driving electrolytic capacitors