JPS62263625A - Electrolyte for driving electrolytic capacitor - Google Patents
Electrolyte for driving electrolytic capacitorInfo
- Publication number
- JPS62263625A JPS62263625A JP10715786A JP10715786A JPS62263625A JP S62263625 A JPS62263625 A JP S62263625A JP 10715786 A JP10715786 A JP 10715786A JP 10715786 A JP10715786 A JP 10715786A JP S62263625 A JPS62263625 A JP S62263625A
- Authority
- JP
- Japan
- Prior art keywords
- electrolyte
- electrolytic capacitor
- electrolytic solution
- electrolytic
- driving
- 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.)
- Pending
Links
- 239000003990 capacitor Substances 0.000 title claims description 18
- 239000003792 electrolyte Substances 0.000 title description 14
- 239000008151 electrolyte solution Substances 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000007513 acids Chemical class 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- OWCLRJQYKBAMOL-UHFFFAOYSA-N 2-butyloctanedioic acid Chemical compound CCCCC(C(O)=O)CCCCCC(O)=O OWCLRJQYKBAMOL-UHFFFAOYSA-N 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims 2
- 150000005846 sugar alcohols Polymers 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 239000004135 Bone phosphate Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- -1 boric acid ester Chemical class 0.000 description 1
- QUJSFPXBUIZZAC-UHFFFAOYSA-N boric acid;ethane-1,2-diol Chemical compound OCCO.OB(O)O QUJSFPXBUIZZAC-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- SPZBYSKKSSLUKN-UHFFFAOYSA-N diazanium;2-butyloctanedioate Chemical compound [NH4+].[NH4+].CCCCC(C([O-])=O)CCCCCC([O-])=O SPZBYSKKSSLUKN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Primary Cells (AREA)
- Control Of Indicators Other Than Cathode Ray Tubes (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
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もので、
同電解液の比抵抗を著しく低下させることによって電解
コンデンサの損失角の正接および高周波特性を改善し、
しかも静電容量の変化および漏れ電流の増加を抑えるこ
との可能な高温度で長寿命かつ信@竹の高い電解コンデ
ンサを提供するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an electrolytic solution for driving an electrolytic capacitor,
By significantly lowering the specific resistance of the electrolyte, the loss angle tangent and high frequency characteristics of electrolytic capacitors are improved.
Furthermore, the present invention provides an electrolytic capacitor that can be used at high temperatures, has a long life, and is highly reliable, capable of suppressing changes in capacitance and increases in leakage current.
[従来の技術と間刈点]
従来、特に中高圧用のアルミニウム電解コンデンサ駆動
用電解液としては、所謂エチレングリコール/硼酸エス
テル系の電解液が用いられでいる。この種の電解液は、
加熱によりエチレングリールと硼酸とのエステル化反応
が進み、この際に生成水が生じ、この水が電解コンデン
サ中のコンデンサ素Yの材料であるアルミニウム箔と反
応してこれを溶解し、かつ水素ガスを発生し゛Cコンデ
ンサの内圧ト昇をもたらすために、この′電解液を用い
た電解コンデンサはより高温1.fの1!的に対しては
使用できなかっ!6 、また、上述の問題を解決するた
めに、同系でニスデル化を促焦して生成へを除去した電
解液も提案されているか、水との反応は抑ルIされるも
のの、電解液の粘度か増大し、比抵抗がイしく高くなり
、この電解液を用いた電解コンデンサでは11尖114
の正接および高周波でのインピーダンスが著しく増大し
、高特性の要求には応えられないものであった。このよ
うな理由から、高温度用の電解コンデンサにはエチIノ
ングリコール/硼酸ニスデル系の電解液は用いられず、
比較的分子雀の大きい有機酸あるいはその塩を溶質とす
る有機酸系電解液が使用および検討されている。[Prior Art and Cutting Point] Conventionally, so-called ethylene glycol/boric acid ester-based electrolytes have been used as electrolytes for driving aluminum electrolytic capacitors, especially for medium and high voltages. This type of electrolyte is
Heating progresses the esterification reaction between ethylene glycol and boric acid, and water is produced at this time.This water reacts with the aluminum foil, which is the material of the capacitor element Y in the electrolytic capacitor, and dissolves it. Electrolytic capacitors using this 'electrolyte' operate at higher temperatures in order to generate gas and raise the internal pressure of the 'C' capacitor. 1 of f! Cannot be used against targets! 6. In addition, in order to solve the above-mentioned problem, an electrolytic solution in the same system that accelerates Nisderization and is removed from the formation has also been proposed, and although the reaction with water is suppressed, the electrolytic solution The viscosity increases, and the specific resistance becomes extremely high.
The tangent and impedance at high frequencies increased significantly, making it impossible to meet the demands for high characteristics. For these reasons, ethyl non-glycol/Nisder borate electrolytes are not used in high-temperature electrolytic capacitors.
Organic acid-based electrolytes containing organic acids or their salts with relatively large molecular weights as solutes have been used and studied.
中高圧用の有機酸系電解液の溶質としては特公昭60−
13293号f 、Q解コンデンサ駆動用電解液jが公
知であるが、このような三塩基性酸(l 6−デカンジ
カルボン酸)を含む電解液は従宋からのエチレングリコ
ール−硼酸系の電解液に比較して抵抗が低く、優れた電
気特性のコンデンサを得ることができる。しかし、火花
電圧が4゜Ov付近てあり、定格電圧400Vの製品へ
の適用は困難であった。As a solute in organic acid-based electrolytes for medium and high pressures,
No. 13293 f, an electrolytic solution j for driving a Q solution capacitor is known, but such an electrolytic solution containing a tribasic acid (l 6-decanedicarboxylic acid) is an ethylene glycol-boric acid based electrolytic solution from the Congregation Song Dynasty. It is possible to obtain a capacitor with lower resistance and superior electrical characteristics compared to the conventional capacitor. However, the spark voltage was around 4°Ov, making it difficult to apply it to products with a rated voltage of 400V.
[発明の改良点と概要]
しかるに5本発明は上述のような欠点を除去し得るもの
で、具体的には総炭素数が12乃至34で側鎖にビニル
基またはカルホキシル基をh゛する三塩基性酸あるいは
その塩の中の1袖または2H以上を用いることによって
定格電圧400Vで使用することが可能な電解コンデン
サ駆動用電解液を提fルするものである。[Improvements and Summary of the Invention] However, the present invention can eliminate the above-mentioned drawbacks. Specifically, the present invention can eliminate the above-mentioned drawbacks. The present invention provides an electrolytic solution for driving an electrolytic capacitor that can be used at a rated voltage of 400 V by using one or more of basic acids or salts thereof.
[実施例]
先ず、総炭素数が12〜34の側鎖にビニル基またはカ
ルボキシル基を有する三塩基性酸の具体例を示す。[Example] First, specific examples of tribasic acids having a total number of carbon atoms of 12 to 34 and having a vinyl group or a carboxyl group in the side chain will be shown.
本発明において、溶媒としてはエチレングリコール等の
)価アルコール類の中の1種または2種以上からなるも
のが使用される。In the present invention, the solvent used is one or more of alcohols (such as ethylene glycol).
次に、1.6−デカンジカルボン酸あるいはその塩、↓
5よび化合物1〜5である三塩基性酸あるいはその塩の
混合物を溶媒に溶解した本発明に係る電解液の実り八個
を従来例と共に?1fi1表に示す。Next, 1,6-decanedicarboxylic acid or its salt, ↓
5 and Compounds 1 to 5, a mixture of tribasic acids or salts thereof, dissolved in a solvent. It is shown in the 1fi1 table.
電解液組成はwt%、比1氏抗(Ω・cm)は液温が2
0”Cの6のである。また、火花電圧は85℃の乙ので
ある。The electrolyte composition is wt%, and the ratio of resistance (Ω・cm) is 2 when the liquid temperature is 2.
The spark voltage is 6°C at 0"C. Also, the spark voltage is 85°C.
第1kに示した電解液のうち、従求例1,2および実施
例3の電解液を使用した電解コノ>2ンサ(定格4 Q
OV −10μF ) 0)各20 % M ツい−
Cの温度105°C3定格電圧印加100t)時間の高
温負荷試験の結果を第2表に示す。Among the electrolytes shown in No. 1k, electrolytic converters using the electrolytes of Comparative Examples 1 and 2 and Example 3 (rating 4 Q
OV -10μF) 0) Each 20% M
Table 2 shows the results of a high-temperature load test at a temperature of 105° C. and a rated voltage applied for 100 t) hours.
第2表 (400V ・10,4zF)[発明の効果]
第2表から分かるように従来例1では、K1失角の正接
が実施例1に対して約3倍にもなっている。また、従来
例2では電解液の火花電圧不足により製品化することが
できなかった。Table 2 (400V/10.4zF) [Effects of the Invention] As can be seen from Table 2, in Conventional Example 1, the tangent of the K1 loss angle is about three times that of Example 1. Furthermore, in Conventional Example 2, it could not be commercialized due to insufficient spark voltage of the electrolyte.
この実施例から明らかなように本発明の電解液は従来の
1.6−デカンジカルボン酸を用いた電解液に比べて、
比抵抗は若干上昇する乙のの火花電圧については20〜
40V上昇し、従来通用することのできなかった定格電
圧400vの電解コンデンサについて通用できるもので
ある。As is clear from this example, the electrolytic solution of the present invention has a
The specific resistance will rise slightly, but the spark voltage will be 20~20.
The capacitor increases by 40V and can be used with electrolytic capacitors with a rated voltage of 400V, which was previously not possible.
[発明の実用化の範囲]
なお、本発明に係る電解液の成分中、総炭素数が12〜
34の側鎖にビニル基またはカルボキシル基を有する三
塩基性酸あるいはその塩の混合量は1〜10wt%の範
囲が好ましい。総炭素数が12〜34の側鎖にビニル基
またはカルボキシル基を有する三塩基性酸あるいはその
塩の混合Mの増加に伴って電解液の火花電圧は」二がる
が、10wt%以Fでは火花電圧は向上しない。例えば
、1.6−デカンジカルボン酸アンモニウム塩を5wt
%含む電解液に化合物1 (n=5)を添加したときの
濃度と火花電圧の変化を第1図に示す。[Scope of practical application of the invention] In addition, in the components of the electrolytic solution according to the present invention, the total number of carbon atoms is 12 to 12.
The mixing amount of the tribasic acid having a vinyl group or carboxyl group in the side chain of 34 or its salt is preferably in the range of 1 to 10 wt%. The spark voltage of the electrolyte decreases as the mixture M of tribasic acid or its salt having a vinyl group or carboxyl group in the side chain with a total carbon number of 12 to 34 increases, but at 10 wt% or more F Spark voltage does not improve. For example, 5wt of 1,6-decanedicarboxylic acid ammonium salt
Figure 1 shows the changes in concentration and spark voltage when Compound 1 (n = 5) was added to an electrolytic solution containing %.
第1図は1.6−デカンジカルボン酸アンモニウム塩に
対する化合物1 (n=5)の添加濃度と電解液の火花
電圧との関係を示す特性図である。FIG. 1 is a characteristic diagram showing the relationship between the concentration of Compound 1 (n=5) added to 1.6-decanedicarboxylic acid ammonium salt and the spark voltage of the electrolytic solution.
Claims (2)
よび総炭素数が12乃至34で側鎖にビニル基またはカ
ルボキシル基を有する二塩基性酸あるいはその塩の中の
1種または2種以上からなる溶質と、有機極性溶媒とか
らなることを特徴とする電解コンデンサ駆動用電解液。(1) 1,6-decanedicarboxylic acid or a salt thereof, and one or more dibasic acids having a total number of carbon atoms of 12 to 34 and having a vinyl group or a carboxyl group in the side chain, or a salt thereof. An electrolytic solution for driving an electrolytic capacitor characterized by comprising a solute and an organic polar solvent.
多価アルコール類の中の1種または2種以上からなるこ
とを特徴とする電解コンデンサ駆動用電解液。(2) The electrolytic solution for driving an electrolytic capacitor according to claim (1), wherein the organic polar solvent is composed of one or more types of polyhydric alcohols.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10715786A JPS62263625A (en) | 1986-05-09 | 1986-05-09 | Electrolyte for driving electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10715786A JPS62263625A (en) | 1986-05-09 | 1986-05-09 | Electrolyte for driving electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62263625A true JPS62263625A (en) | 1987-11-16 |
Family
ID=14451943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10715786A Pending JPS62263625A (en) | 1986-05-09 | 1986-05-09 | Electrolyte for driving electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62263625A (en) |
-
1986
- 1986-05-09 JP JP10715786A patent/JPS62263625A/en active Pending
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