JPH0760780B2 - Electrolytic solution for aluminum electrolytic capacitors - Google Patents

Electrolytic solution for aluminum electrolytic capacitors

Info

Publication number
JPH0760780B2
JPH0760780B2 JP61144588A JP14458886A JPH0760780B2 JP H0760780 B2 JPH0760780 B2 JP H0760780B2 JP 61144588 A JP61144588 A JP 61144588A JP 14458886 A JP14458886 A JP 14458886A JP H0760780 B2 JPH0760780 B2 JP H0760780B2
Authority
JP
Japan
Prior art keywords
electrolytic
electrolytic solution
boric acid
aluminum
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
Application number
JP61144588A
Other languages
Japanese (ja)
Other versions
JPS631021A (en
Inventor
彰一郎 森
誠 宇恵
和彦 井田
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Corp
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 Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to JP61144588A priority Critical patent/JPH0760780B2/en
Priority to US07/061,498 priority patent/US4786429A/en
Priority to EP87305396A priority patent/EP0251577B1/en
Priority to DE3789789T priority patent/DE3789789T2/en
Publication of JPS631021A publication Critical patent/JPS631021A/en
Publication of JPH0760780B2 publication Critical patent/JPH0760780B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Electric Double-Layer Capacitors Or The Like (AREA)
  • Networks Using Active Elements (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明によれば、電導度の高い優れたアルミ電解コンデ
ンサ用電解液(以下単に電解液と称することがある)が
得られる。
DETAILED DESCRIPTION OF THE INVENTION Industrial Field of the Invention According to the present invention, an excellent electrolytic solution for an aluminum electrolytic capacitor having high electrical conductivity (hereinafter sometimes simply referred to as electrolytic solution) can be obtained.

従来の技術 コンデンサの特性は種々の要因によつて決定されている
が、特にコンデンサ素子とともに外装ケースに収納され
る電解液の特性は、インピーダンスあるいは等価直列抵
抗(ESR)に大きな影響を及ぼすことが判明している。
2. Description of the Related Art Although the characteristics of capacitors are determined by various factors, the characteristics of the electrolytic solution that is housed in the outer case together with the capacitor element can greatly affect the impedance or equivalent series resistance (ESR). It's known.

たとえば、中高圧用電解コンデンサには、エチレングリ
コール溶媒に、硼酸もしくはそのアンモニウム塩を溶解
させた電解液が用いられているが、電導度が低く、コン
デンサの等価直列抵抗が高いという欠点を有している。
For example, an electrolytic solution in which boric acid or its ammonium salt is dissolved in an ethylene glycol solvent is used for medium- and high-voltage electrolytic capacitors, but it has the drawbacks of low electrical conductivity and high equivalent series resistance. ing.

発明が解決しようとする問題点 このため、近年多用されているスイツチングレギユレー
タの平滑用など、高周波領域にまで低等価直列抵抗が要
求されるものには使用することができない。
Therefore, it cannot be used for smoothing of a switching regulator which has been frequently used in recent years, such as one for which low equivalent series resistance is required even in a high frequency region.

また、この電解液は用いているエチレングリコール溶媒
の粘度が高く、凝固点が比較的高いことなどから、電解
液の電導度が低温で著しく減少し、電解コンデンサの低
温特性が悪く、さらに、エチレングリコールと硼酸との
エステル化反応で生ずる多量の水分のため100℃を越え
る電解コンデンサには使用できない等、使用温度範囲が
狭いという欠点がある。
In addition, since the viscosity of the ethylene glycol solvent used in this electrolyte is high and the freezing point is relatively high, the conductivity of the electrolyte is significantly reduced at low temperatures, and the low temperature characteristics of the electrolytic capacitor are poor. There is a drawback that the operating temperature range is narrow, such that it cannot be used in electrolytic capacitors exceeding 100 ° C due to the large amount of water generated by the esterification reaction between carboxylic acid and boric acid.

問題点を解決するための手段 本発明者は、上記硼酸系電解液の欠点を解決すべく鋭意
検討を行ない、従来の硼酸のアンモニウム塩が溶解しな
かつたγ−ブチロラクトンN,N−ジメチルホルムアミド
等の非プロトン性溶媒に硼酸の脂肪族四級アンモニウム
塩が溶解し、高い電導度を示すことを見い出し本発明を
完成した。
Means for Solving the Problems The present inventor has conducted diligent studies to solve the drawbacks of the boric acid-based electrolytic solution, and the conventional ammonium salt of boric acid was not dissolved γ-butyrolactone N, N-dimethylformamide, etc. It was found that the aliphatic quaternary ammonium salt of boric acid was dissolved in the aprotic solvent (1) and showed high conductivity, and the present invention was completed.

即ち、本発明は硼酸の脂肪族四級アンモニウム塩を溶質
として使用することを特徴とするアルミ電解コンデンサ
用電解液を提供するものである。
That is, the present invention provides an electrolytic solution for an aluminum electrolytic capacitor, which uses an aliphatic quaternary ammonium salt of boric acid as a solute.

発明の具体的説明 本発明において溶質として用いられる硼酸の四級アンモ
ニウム塩における四級アンモニウム塩としては、テトラ
エチルアンモニウム、テトラプロピルアンモニウム、テ
トラブチルアンモニウム、メチルトリエチルアンモニウ
ム、メチルトリプロピルアンモニウム、メチルトリブチ
ルアンモニウム、ジメチルジエチルアンモニウム、ジメ
チルジプロピルアンモニウム、ジメチルジブチルアンモ
ニウム、エチルトリプロピルアンモニウム、エチルトリ
ブチルアンモニウム等の脂肪族四級アンモニウム塩、N,
N−ジメチルピロリジニウムを例示することができる。
Detailed Description of the Invention As the quaternary ammonium salt in the quaternary ammonium salt of boric acid used as a solute in the present invention, tetraethylammonium, tetrapropylammonium, tetrabutylammonium, methyltriethylammonium, methyltripropylammonium, methyltributylammonium, Aliphatic quaternary ammonium salts such as dimethyldiethylammonium, dimethyldipropylammonium, dimethyldibutylammonium, ethyltripropylammonium, ethyltributylammonium, N,
N-dimethylpyrrolidinium can be illustrated.

本発明の硼酸の四級アンモニウム塩を溶解させる溶媒と
しては、N−メチルホルムアミド、N−エチルホルムア
ミド、N,N−ジメチルホルムアミド、N,N−ジエチルホル
ムアミド、N−メチルアセトアミド、N−エチルアセト
アミド、N,N−ジメチルアセトアミド、N,N−ジエチルア
セトアミド、N−メチルピロリジノン等のアミド溶媒、
γ−ブチロラクトン、γ−バレロラクトン、δ−パレロ
ラクトン等のラクトン溶媒、エチレンカーボネート、プ
ロピレンカーボネート、ブチレンカーボネート等のカー
ボネート溶媒、エチレングリコール、グリセリン、メチ
ルセロソルブ等のアルコール溶媒、3−メトキシプロピ
オニトリル等のニトリル溶媒、およびトリメチルホスフ
エート等の燐酸エステル溶媒の単独あるいは混合溶媒を
例示することができる。
As a solvent for dissolving the quaternary ammonium salt of boric acid of the present invention, N-methylformamide, N-ethylformamide, N, N-dimethylformamide, N, N-diethylformamide, N-methylacetamide, N-ethylacetamide, N, N-dimethylacetamide, N, N-diethylacetamide, N-methylpyrrolidinone and other amide solvents,
lactone solvents such as γ-butyrolactone, γ-valerolactone and δ-parerolactone, carbonate solvents such as ethylene carbonate, propylene carbonate and butylene carbonate, alcohol solvents such as ethylene glycol, glycerin and methyl cellosolve, and 3-methoxypropionitrile. Examples thereof include nitrile solvents and phosphoric acid ester solvents such as trimethyl phosphate alone or in a mixed solvent.

上記溶媒に対する硼酸の四級アンモニウム塩の溶解量は
飽和濃度以下、好ましくは1〜40重量%である。
The amount of the quaternary ammonium salt of boric acid dissolved in the solvent is not more than the saturation concentration, preferably 1 to 40% by weight.

また、上記電解液中の溶解塩は中性塩でも酸性塩でも良
い。
The dissolved salt in the electrolytic solution may be a neutral salt or an acidic salt.

本発明の電解液は、本質的には、硼酸の四級アンモニウ
ム塩と溶媒よりなるが、電蝕防止、漏れ電流の低減等、
種々の目的で少量の助溶質を添加しても差し支えない。
The electrolytic solution of the present invention essentially consists of a quaternary ammonium salt of boric acid and a solvent, but prevents electrolytic corrosion, reduces leakage current, etc.
Small amounts of co-solutes can be added for various purposes.

発明の効果 本発明で溶質として使用する硼酸の四級アンモニウム塩
は溶媒に対する溶解性が良く、その電解液は高い電導度
を示し、凝固点〜沸点範囲の広い溶媒と伴に用いること
により、使用温度範囲の広いアルミ電解コンデンサ用電
解液となる。
EFFECT OF THE INVENTION The quaternary ammonium salt of boric acid used as a solute in the present invention has good solubility in a solvent, and its electrolytic solution exhibits a high electric conductivity, and is used in combination with a solvent having a wide range of freezing point to boiling point to obtain a working temperature. It is an electrolytic solution for a wide range of aluminum electrolytic capacitors.

実験例 以下に実施例、比較例を挙げて本発明を更に具体的に説
明する。
Experimental Example The present invention will be described more specifically with reference to Examples and Comparative Examples below.

実施例1 γ−ブチロラクトン溶媒に10重量%の硼酸のテトラエチ
ルアンモニウム塩を溶解させて電解液を得た。この電解
液の25℃における電導度は4.9mS/cmであり、+,−−組
のアルミニウム平滑箔に4mA/cm2の定電流印加時の火花
発生電圧は330Vであつた。又、この電解液の電導度の温
度変化を第1図(ロ)に示した。
Example 1 An electrolyte solution was obtained by dissolving 10% by weight of tetraethylammonium salt of boric acid in a γ-butyrolactone solvent. The electroconductivity of this electrolyte at 25 ° C. was 4.9 mS / cm, and the spark generation voltage was 330 V when a constant current of 4 mA / cm 2 was applied to the + and −− sets of aluminum smooth foil. The temperature change of the electric conductivity of this electrolytic solution is shown in FIG.

実施例2〜4 実施例1においてγ−ブチロラクトン溶媒N,N−ジメチ
ルホルムアミド(実施例2)、プロピレンカーボネート
(実施例3)、エチレングリコール(実施例4)に代え
た時の電解液の電導度を第1表に示した。
Examples 2 to 4 Conductivity of an electrolytic solution when a γ-butyrolactone solvent N, N-dimethylformamide (Example 2), propylene carbonate (Example 3), and ethylene glycol (Example 4) in Example 1 were used. Is shown in Table 1.

比較例1〜4 実施例1〜4に使用した溶媒を用いて、溶質を従来の硼
酸アンモニウムに変えた時の結果を第1表に示した。
又、比較例4の電解液の電導度の温度変化を第1図
(■)に示した。
Comparative Examples 1 to 4 Table 1 shows the results when the solute was changed to conventional ammonium borate using the solvents used in Examples 1 to 4.
The temperature change of the electric conductivity of the electrolytic solution of Comparative Example 4 is shown in FIG. 1 (■).

なお、第1法では次の略号を使用した。The following abbreviations were used in the first method.

GBL:γ−ブチロラクトン DMF:N,N−ジメチルホルムアミド PC:プロピレンカーボネート EG:エチレングリコール GBL: γ-butyrolactone DMF: N, N-dimethylformamide PC: Propylene carbonate EG: Ethylene glycol

【図面の簡単な説明】[Brief description of drawings]

第1図は実施例1(□)及び比較例4(■)で得た電解
液の電導度の温度変化を示す図である。
FIG. 1 is a diagram showing the temperature change of the electric conductivity of the electrolytic solutions obtained in Example 1 (□) and Comparative Example 4 (■).

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】硼酸の四級アンモニウム塩を溶質として使
用することを特徴とするアルミ電解コンデンサ用電解
液。
1. An electrolytic solution for an aluminum electrolytic capacitor, characterized in that a quaternary ammonium salt of boric acid is used as a solute.
JP61144588A 1986-06-20 1986-06-20 Electrolytic solution for aluminum electrolytic capacitors Expired - Fee Related JPH0760780B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP61144588A JPH0760780B2 (en) 1986-06-20 1986-06-20 Electrolytic solution for aluminum electrolytic capacitors
US07/061,498 US4786429A (en) 1986-06-20 1987-06-15 Electrolyte for aluminum electrolytic capacitor
EP87305396A EP0251577B1 (en) 1986-06-20 1987-06-17 Ammonium salt solution as electrolyte for electrolytic capacitors
DE3789789T DE3789789T2 (en) 1986-06-20 1987-06-17 Ammonium salt solution as an electrolyte for electrolytic capacitors.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61144588A JPH0760780B2 (en) 1986-06-20 1986-06-20 Electrolytic solution for aluminum electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPS631021A JPS631021A (en) 1988-01-06
JPH0760780B2 true JPH0760780B2 (en) 1995-06-28

Family

ID=15365582

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61144588A Expired - Fee Related JPH0760780B2 (en) 1986-06-20 1986-06-20 Electrolytic solution for aluminum electrolytic capacitors

Country Status (1)

Country Link
JP (1) JPH0760780B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0381936B1 (en) * 1989-01-11 1995-11-29 Matsushita Electric Industrial Co., Ltd. An electrolyte for use in electrolytic capacitors
JP2939511B2 (en) * 1989-08-16 1999-08-25 岩崎通信機株式会社 Mobile phone system

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6132509A (en) * 1984-07-25 1986-02-15 昭和電工株式会社 Electrolyte for driving electrolytic condenser

Also Published As

Publication number Publication date
JPS631021A (en) 1988-01-06

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