JP4282385B2 - Electrolytic solution for electrolytic capacitor drive - Google Patents

Electrolytic solution for electrolytic capacitor drive Download PDF

Info

Publication number
JP4282385B2
JP4282385B2 JP2003183874A JP2003183874A JP4282385B2 JP 4282385 B2 JP4282385 B2 JP 4282385B2 JP 2003183874 A JP2003183874 A JP 2003183874A JP 2003183874 A JP2003183874 A JP 2003183874A JP 4282385 B2 JP4282385 B2 JP 4282385B2
Authority
JP
Japan
Prior art keywords
electrolytic
electrolytic solution
stearamide
oxyalkyl
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.)
Expired - Fee Related
Application number
JP2003183874A
Other languages
Japanese (ja)
Other versions
JP2005019774A (en
Inventor
昌大 鈴木
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.)
Nichicon Capacitor Ltd
Original Assignee
Nichicon Capacitor 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 Nichicon Capacitor Ltd filed Critical Nichicon Capacitor Ltd
Priority to JP2003183874A priority Critical patent/JP4282385B2/en
Publication of JP2005019774A publication Critical patent/JP2005019774A/en
Application granted granted Critical
Publication of JP4282385B2 publication Critical patent/JP4282385B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【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(以下、電解液と称す)の改良に関するものである。
【0002】
【従来の技術】
従来、電解コンデンサの電解液は、エチレングリコール等の多価アルコールを主溶媒とし、カルボン酸またはそのアンモニウム塩を溶解したものが用いられていた(例えば特許文献1、2参照)。
【0003】
【特許文献1】
特公平7−48460号公報(第2頁、表)
【特許文献2】
特公平7−63047号公報(第3頁、表1)
【0004】
【発明が解決しようとする課題】
しかしながら、上記の電解液にあっては、主溶媒であるエチレングリコールと有機カルボン酸とが反応してエステル化するときに生ずる水、または、電解コンデンサ素子中の電解紙に含有されている水が高温下でアルミニウム電極箔表面の酸化物と結合し、水和酸化物を生成し、この水和酸化物により、電解コンデンサの静電容量の減少、損失の増大等が起こり、信頼性が低下するという問題があった。
したがって、上記の水和酸化物の生成を抑えることができる組成の電解液が要求されていた。
【0005】
【課題を解決するための手段】
本発明は、上記課題を解決するため各種検討した結果、見出されたものであり、電解液に防水効果を持つN−オキシメチルステアロアミド等のN−オキシアルキルステアロアミンを溶解し、これにより電極箔表面を覆うことで、水和酸化物の生成を抑えようとするものである。
すなわち、本発明は、エチレングリコールを主体とする溶媒に、有機カルボン酸またはその塩と、ホウ酸またはそのアンモニウム塩と、以下の化学式で示されるN−オキシアルキルステアロアミドとを溶解し、N−オキシアルキルステアロアミドの溶解量が、電解液全体に対して0.1〜10.0wt%であることを特徴とする電解コンデンサの駆動用電解液である。
【0007】
さらに、上記N−オキシアルキルステアロアミドのオキシアルキル基としては、オキシメチル、オキシエチル、オキシプロピル、オキシ−iso−プロピルが好ましい。
【0008】
有機カルボン酸としては、アゼライン酸、セバシン酸、1,6−デカンジカルボン酸、5,6−デカンジカルボン酸、7−ビニルヘキサデセン−1,16−ジカルボン酸等を例示することができる。
【0009】
また、カルボン酸の塩としては、アンモニウム塩の他、メチルアミン、エチルアミン、t−ブチルアミン等の一級アミン塩、ジメチルアミン、エチルメチルアミン、ジエチルアミン等の二級アミン塩、トリメチルアミン、ジエチルメチルアミン、エチルジメチルアミン、トリエチルアミン等の三級アミン塩、テトラメチルアンモニウム、トリエチルメチルアンモニウム、テトラエチルアンモニウム等の四級アンモニウム塩等を例示することができる。
【0010】
【発明の実施の形態】
本発明の電解液に溶解したN−オキシメチルステアロアミドは、防水効果があり、その効果が持続するので、電極箔表面に吸着することにより、水がアルミニウム電極箔表面の酸化物と結合し、水和酸化物を作るのを抑えることができると考えられる。そのため、製品の初期特性を長時間持続できる。また、エチレングリコールに対し多量溶解するため、上記の効果はより確実なものとなる。
【0011】
【実施例】
以下、本発明の実施例を具体的に説明する。表1の組成で電解液を調合し、30℃における電解液の比抵抗と85℃における火花発生電圧(電解液の耐電圧)を測定し、表1の結果を得た。
【0012】
【表1】

Figure 0004282385
【0013】
表1の電解液で、直径10.0mm、長さ12.5mm、定格電圧350V、静電容量10μFのアルミニウム電解コンデンサを各10個作製した。これらの製品を105℃の恒温槽中で3000時間、定格電圧を印加し、静電容量とtanδを測定し、表2の結果を得た。
【0014】
【表2】
Figure 0004282385
【0015】
表2の結果より、N−オキシメチルステアロアミドを溶解した実施例は、従来例に比べて容量変化率、tanδの上昇が抑制されていることが分かる。表1、2の結果より、N−オキシメチルステアロアミドの電解液に対する溶解量は0.1〜10.0wt%の範囲が好ましい。0.1wt%未満では容量変化率、tanδの上昇の抑制効果が十分ではなく、10.0wt%を超えると電解液の比抵抗が上昇し、耐電圧が低下するため、不適当である。
【0016】
なお、実施例ではN−オキシアルキルステアロアミドとして、N−オキシメチルステアロアミドを用いたが、N−オキシエチルステアロアミド、N−オキシプロピルステアロアミド、N−オキシ−iso−プロピルステアロアミドでも実施例と同等の効果があった。N−オキシブチルステアロアミドは溶解に時間を要するため、上記N−オキシアルキルステアロアミドが好ましい。
【0017】
また、、本発明によるN−オキシアルキルステアロアミドの効果は、実施例に限定されるものではなく、先に例示した有機カルボン酸またはその塩を単独または複数溶解しても本実施例と同等の効果があった。
【0018】
【発明の効果】
上記のとおり、本発明による電解液は、N−オキシアルキルステアロアミドを溶解することで、アルミニウム電極箔表面に水和酸化物が生成することを抑えられ、電解コンデンサの静電容量変化率、tanδ上昇を抑制することができ、電解コンデンサの信頼性の向上を図ることができる。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to an improvement in an electrolytic solution for driving an electrolytic capacitor (hereinafter referred to as an electrolytic solution).
[0002]
[Prior art]
Conventionally, an electrolytic solution of an electrolytic capacitor in which a polyhydric alcohol such as ethylene glycol is used as a main solvent and a carboxylic acid or an ammonium salt thereof is dissolved (see, for example, Patent Documents 1 and 2).
[0003]
[Patent Document 1]
Japanese Patent Publication No. 7-48460 (2nd page, table)
[Patent Document 2]
Japanese Patent Publication No. 7-63047 (Page 3, Table 1)
[0004]
[Problems to be solved by the invention]
However, in the above electrolytic solution, water generated when the main solvent ethylene glycol and the organic carboxylic acid react and esterify, or water contained in the electrolytic paper in the electrolytic capacitor element Bonds with the oxide on the surface of the aluminum electrode foil at a high temperature to form a hydrated oxide. This hydrated oxide reduces the capacitance of the electrolytic capacitor, increases the loss, and decreases the reliability. There was a problem.
Therefore, an electrolytic solution having a composition capable of suppressing the formation of the hydrated oxide has been required.
[0005]
[Means for Solving the Problems]
The present invention has been found as a result of various studies to solve the above-mentioned problems, and has been found to dissolve an N-oxyalkyl stearamine such as N-oxymethyl stearamide having a waterproof effect in an electrolytic solution, By this, the production | generation of a hydrated oxide is going to be suppressed by covering the electrode foil surface.
That is, the present invention is a solvent composed mainly of ethylene glycol are dissolved with an organic carboxylic acid or a salt thereof, and boric acid or its ammonium salt, an N- oxyalkyl stearamide represented by the following formula, N -The electrolytic solution for driving an electrolytic capacitor , wherein the amount of oxyalkyl stearamide dissolved is 0.1 to 10.0 wt% with respect to the entire electrolytic solution.
[0007]
Furthermore, as the oxyalkyl group of the N-oxyalkyl stearamide, oxymethyl, oxyethyl, oxypropyl, and oxy-iso-propyl are preferable.
[0008]
Examples of the organic carboxylic acid include azelaic acid, sebacic acid, 1,6-decanedicarboxylic acid, 5,6-decanedicarboxylic acid, 7-vinylhexadecene-1,16-dicarboxylic acid and the like.
[0009]
In addition to ammonium salts, primary amine salts such as methylamine, ethylamine and t-butylamine, secondary amine salts such as dimethylamine, ethylmethylamine and diethylamine, trimethylamine, diethylmethylamine and ethyl Examples thereof include tertiary amine salts such as dimethylamine and triethylamine, and quaternary ammonium salts such as tetramethylammonium, triethylmethylammonium and tetraethylammonium.
[0010]
DETAILED DESCRIPTION OF THE INVENTION
N-oxymethyl stearamide dissolved in the electrolytic solution of the present invention has a waterproof effect, and the effect lasts. Therefore, when adsorbed on the electrode foil surface, water binds to the oxide on the aluminum electrode foil surface. It is thought that the production of hydrated oxide can be suppressed. Therefore, the initial characteristics of the product can be maintained for a long time. Moreover, since it melt | dissolves in large quantities with respect to ethylene glycol, said effect becomes more reliable.
[0011]
【Example】
Examples of the present invention will be specifically described below. An electrolytic solution was prepared with the composition shown in Table 1, and the specific resistance of the electrolytic solution at 30 ° C. and the spark generation voltage (withstand voltage of the electrolytic solution) at 85 ° C. were measured.
[0012]
[Table 1]
Figure 0004282385
[0013]
Ten aluminum electrolytic capacitors each having a diameter of 10.0 mm, a length of 12.5 mm, a rated voltage of 350 V, and a capacitance of 10 μF were produced from the electrolytic solution of Table 1. The rated voltage was applied to these products in a constant temperature bath at 105 ° C. for 3000 hours, the capacitance and tan δ were measured, and the results shown in Table 2 were obtained.
[0014]
[Table 2]
Figure 0004282385
[0015]
From the results of Table 2, it can be seen that the examples in which N-oxymethyl stearoamide was dissolved suppressed the increase in capacity change rate and tan δ as compared with the conventional example. From the results of Tables 1 and 2, the amount of N-oxymethyl stearoamide dissolved in the electrolyte solution is preferably in the range of 0.1 to 10.0 wt%. If it is less than 0.1 wt%, the effect of suppressing the increase in capacity change rate and tan δ is not sufficient, and if it exceeds 10.0 wt%, the specific resistance of the electrolytic solution increases and the withstand voltage decreases, which is inappropriate.
[0016]
In the examples, N-oxymethyl stearamide was used as the N-oxyalkyl stearamide, but N-oxyethyl stearamide, N-oxypropyl stearamide, N-oxy-iso-propyl stearamide was used. Roamide also had the same effect as the example. Since N-oxybutyl stearamide requires time for dissolution, the above N-oxyalkyl stearamide is preferable.
[0017]
In addition, the effect of the N-oxyalkyl stearamide according to the present invention is not limited to the examples, and even if the organic carboxylic acid or the salt thereof exemplified above is dissolved alone or plurally, it is equivalent to this example. There was an effect.
[0018]
【The invention's effect】
As described above, the electrolytic solution according to the present invention can suppress the formation of hydrated oxide on the aluminum electrode foil surface by dissolving N-oxyalkyl stearamide, and the capacitance change rate of the electrolytic capacitor, An increase in tan δ can be suppressed, and the reliability of the electrolytic capacitor can be improved.

Claims (1)

エチレングリコールを主溶媒とし、有機カルボン酸またはその塩と、ホウ酸またはそのアンモニウム塩と、N−オキシアルキルステアロアミドとを溶解し、N−オキシアルキルステアロアミドの溶解量が、電解液全体に対して0.1〜10.0wt%であることを特徴とする電解コンデンサの駆動用電解液。Using ethylene glycol as the main solvent, organic carboxylic acid or its salt, boric acid or its ammonium salt, and N-oxyalkyl stearamide are dissolved, and the amount of N-oxyalkyl stearamide dissolved in the entire electrolyte solution An electrolytic solution for driving an electrolytic capacitor, wherein the electrolytic solution is 0.1 to 10.0 wt% with respect to the electrolyte.
JP2003183874A 2003-06-27 2003-06-27 Electrolytic solution for electrolytic capacitor drive Expired - Fee Related JP4282385B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2003183874A JP4282385B2 (en) 2003-06-27 2003-06-27 Electrolytic solution for electrolytic capacitor drive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2003183874A JP4282385B2 (en) 2003-06-27 2003-06-27 Electrolytic solution for electrolytic capacitor drive

Publications (2)

Publication Number Publication Date
JP2005019774A JP2005019774A (en) 2005-01-20
JP4282385B2 true JP4282385B2 (en) 2009-06-17

Family

ID=34183800

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003183874A Expired - Fee Related JP4282385B2 (en) 2003-06-27 2003-06-27 Electrolytic solution for electrolytic capacitor drive

Country Status (1)

Country Link
JP (1) JP4282385B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4668766B2 (en) * 2005-10-31 2011-04-13 ニチコン株式会社 Electrolytic solution for electrolytic capacitor drive

Also Published As

Publication number Publication date
JP2005019774A (en) 2005-01-20

Similar Documents

Publication Publication Date Title
JP4282385B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4441393B2 (en) Electrolytic solution for driving aluminum electrolytic capacitors
JP4271528B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4214008B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4150254B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4063650B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4612241B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4039946B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4344564B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4555168B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4699652B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4637374B2 (en) Electrolytic solution for electrolytic capacitor drive
JP3963775B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4366170B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4520011B2 (en) Electrolytic solution for driving electrolytic capacitors
JP3976587B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4570789B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4570983B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4452174B2 (en) Electrolytic solution for driving aluminum electrolytic capacitors
JP4036695B2 (en) Electrolytic solution for driving electrolytic capacitors
JP4653355B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4699649B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4085009B2 (en) Electrolytic solution for electrolytic capacitor drive
JP4668766B2 (en) Electrolytic solution for electrolytic capacitor drive
JP3749913B2 (en) Electrolytic solution for electrolytic capacitor drive

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20051212

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20080620

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20080728

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20080926

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20090309

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20090317

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120327

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130327

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140327

Year of fee payment: 5

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees