JPS586298B2 - Electrolyte for driving aluminum electrolytic capacitors - Google Patents
Electrolyte for driving aluminum electrolytic capacitorsInfo
- Publication number
- JPS586298B2 JPS586298B2 JP4889777A JP4889777A JPS586298B2 JP S586298 B2 JPS586298 B2 JP S586298B2 JP 4889777 A JP4889777 A JP 4889777A JP 4889777 A JP4889777 A JP 4889777A JP S586298 B2 JPS586298 B2 JP S586298B2
- Authority
- JP
- Japan
- Prior art keywords
- capacitor
- electrolyte
- electrolytic solution
- aluminum electrolytic
- electrolytic 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
Links
- 239000003990 capacitor Substances 0.000 title claims description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 7
- 229910052782 aluminium Inorganic materials 0.000 title claims description 7
- 239000003792 electrolyte Substances 0.000 title description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 26
- 239000008151 electrolyte solution Substances 0.000 claims description 14
- 229910052810 boron oxide Inorganic materials 0.000 claims description 10
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 10
- 150000003863 ammonium salts Chemical class 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 4
- 239000001361 adipic acid Substances 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- 230000000694 effects Effects 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 238000007789 sealing Methods 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- 230000002745 absorbent Effects 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- FLDCSPABIQBYKP-UHFFFAOYSA-N 5-chloro-1,2-dimethylbenzimidazole Chemical compound ClC1=CC=C2N(C)C(C)=NC2=C1 FLDCSPABIQBYKP-UHFFFAOYSA-N 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 239000001741 Ammonium adipate Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 235000019293 ammonium adipate Nutrition 0.000 description 2
- 238000005536 corrosion prevention Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
Description
【発明の詳細な説明】
本発明はアルミニウム電解コンデンサ駆動用電解液の改
良に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in electrolytes for driving aluminum electrolytic capacitors.
従来、この種電解液として、エチレングリコールを主溶
媒とし、これに有機カルボン酸のアンモニウム塩を溶解
したものが知られている。Conventionally, as this kind of electrolytic solution, one in which an ammonium salt of an organic carboxylic acid is dissolved in ethylene glycol as a main solvent is known.
斯る電解液は、コンデンサの低温特性などに於で秀れた
効果をもたらすが、半面、コンデンサの高温負荷試験中
に腐蝕が発生する欠点を有する。Such an electrolyte has excellent effects on the low-temperature characteristics of the capacitor, but on the other hand, it has the disadvantage of causing corrosion during high-temperature load tests of the capacitor.
即ち、この腐蝕を、図の典型的アルミニウム電解コンデ
ンサに於で説明すると、コンデンサは、巻回素子1、該
素子を収納するケース2、該ケースの開口を封ロし、合
成樹脂板4及びゴム板50合体からなる封口板3、外部
端子6、該外部端子とリード箔7とを接続する内部端子
8とから構成されるが、高温負荷試験中に、特にリード
箔7や内部端子8に腐蝕が見られる。That is, to explain this corrosion using the typical aluminum electrolytic capacitor shown in the figure, the capacitor consists of a wound element 1, a case 2 that houses the element, a sealed opening of the case, a synthetic resin plate 4, and a rubber plate. It is composed of a sealing plate 3 made up of a combination of plates 50, external terminals 6, and internal terminals 8 that connect the external terminals and lead foils 7. However, during the high temperature load test, the lead foils 7 and internal terminals 8 in particular were corroded. can be seen.
腐蝕は合成樹脂板4がフェノール樹脂製である場合に著
しく現われ、また充放電やリツプル電流を流すことによ
り加速され、ついにはリード箔7などが腐蝕切断される
に至る。Corrosion is noticeable when the synthetic resin plate 4 is made of phenolic resin, and is accelerated by charging and discharging or by passing a ripple current, and eventually the lead foil 7 and the like are corroded and cut.
従って本発明目的は、エチレングリコールと有機カルボ
ン酸のアンモニウム塩との組合せになる電解液に於で、
その秀れた特性を損うことなく、上記腐蝕の発生を防止
し得る改良されたアルミニウム電解コンデンサ駆動用電
解液を提供するにある。Therefore, the object of the present invention is to provide an electrolytic solution that is a combination of ethylene glycol and an ammonium salt of an organic carboxylic acid.
It is an object of the present invention to provide an improved electrolytic solution for driving an aluminum electrolytic capacitor that can prevent the above-mentioned corrosion without impairing its excellent properties.
即ち、本発明電解液は、主溶媒エチレングリコールにイ
オノーゲンとして有機カルボン酸のアンモニウム塩を溶
解した電解液に酸化ホウ素(B203)を2.0〜10
重量%添加したことを特徴とするものであり、これによ
り所期の目的が有効に達せられる。That is, the electrolytic solution of the present invention is prepared by dissolving an ammonium salt of an organic carboxylic acid as an ionogen in ethylene glycol as a main solvent, and adding 2.0 to 10% boron oxide (B203) to the electrolytic solution.
It is characterized by the fact that it is added in an amount of % by weight, thereby effectively achieving the intended purpose.
本発明電解液に於で、酸化ホウ素の添加量が2.0重量
%より少ない場合には腐蝕抑制または防止効果が認めら
れない場合があり、一方10重量%を越えると腐蝕防止
効果は十分であるものべ副作用として電解液の粘度が高
くなり、電導度も低くなるため、コンデンサの低温特性
に於ける容量減少及び損失の増大を来たし好ましくない
。In the electrolytic solution of the present invention, if the amount of boron oxide added is less than 2.0% by weight, no corrosion suppression or prevention effect may be observed, whereas if it exceeds 10% by weight, the corrosion prevention effect may not be sufficient. As a side effect, the viscosity of the electrolytic solution increases and the conductivity decreases, which is undesirable because it causes a decrease in capacity and an increase in loss in the low-temperature characteristics of the capacitor.
従ってこれらの添加量範囲は本発明から除外される。Therefore, these addition amount ranges are excluded from the present invention.
又、本発明電解液に於で、有機カルボン酸のアンモニウ
ム塩としでは、アジピン酸、スベリン酸、セバチン酸な
どの各アンモニウム塩が好適である。In the electrolytic solution of the present invention, ammonium salts of organic carboxylic acids such as adipic acid, suberic acid, and sebacic acid are suitable.
更に、本発明電解液に於で、溶媒としてのエチレングリ
コールと溶質としての有機カルボン酸のアンモニウム塩
との含有割合は任意であり、通常斯る溶質は溶解量限度
内で使用される。Further, in the electrolytic solution of the present invention, the content ratio of ethylene glycol as a solvent and ammonium salt of an organic carboxylic acid as a solute is arbitrary, and the solute is usually used within the solubility limit.
以下本発明実施例を述べる。Examples of the present invention will be described below.
本発明実施例に於で、添加剤である酸化ホウ素は溶媒に
100℃前後で良く溶解し、従って通常の手法で溶媒、
溶質及び添加剤が混合されて電解液が作成され、次いで
その電解液を用いて既述の図示せる形態のコンデンサが
作成された。In the examples of the present invention, boron oxide, which is an additive, dissolves well in a solvent at around 100°C.
The solute and additives were mixed to form an electrolyte, which was then used to form a capacitor of the form described and illustrated.
以下の試験は斯るコンデンサによりなされたものである
。The following tests were conducted with such a capacitor.
尚コンデンサの定格は1 60V,680μFであり、
スリップル負荷試験は、温度85℃、リツプル電流6
0 Hz, 2 A,電流印加時間500時間の条件下
で行なわれた。The capacitor rating is 160V, 680μF,
The ripple load test was conducted at a temperature of 85°C and a ripple current of 6
The test was carried out under the conditions of 0 Hz, 2 A, and a current application time of 500 hours.
第1表に於て、Z/Zoは−25℃に於ける120Hz
でのインピーダンス(2と+20℃に於ける120Hz
でのインピーダンス(ZO)との比を表わし、この値が
小さいほど低温性が秀れている。In Table 1, Z/Zo is 120Hz at -25℃
impedance at (2 and 120Hz at +20°C)
The smaller this value is, the better the low-temperature properties are.
又第1表の試験に供されたコンデンサの封口板3を構成
する合成樹脂板4(図面参照)はフェノール樹脂からな
る。Furthermore, the synthetic resin plate 4 (see drawing) constituting the sealing plate 3 of the capacitor subjected to the tests shown in Table 1 is made of phenol resin.
第1表から明らかな如く、エチレングリコールト有機カ
ルボン酸のアンモニウム塩からなる基本電解液に酸化ホ
ウ素を添加した場合、基本電解液の秀れた低温特性をほ
とんど損うことなく有効な腐蝕防止をなすことができる
。As is clear from Table 1, when boron oxide is added to the basic electrolyte consisting of the ammonium salt of ethylene glycol organic carboxylic acid, effective corrosion prevention can be achieved without substantially impairing the excellent low-temperature properties of the basic electrolyte. It can be done.
斯る酸化ホウ素の添加効果はその添加量によって左右さ
れる。The effect of adding boron oxide depends on the amount added.
第2表に、基本電解液としてエチレングリコールとアジ
ピン酸アンモニウムを選んだ場合を典型例として添加量
効果を代表的に示す。Table 2 shows the additive amount effect as a typical example when ethylene glycol and ammonium adipate are selected as the basic electrolyte.
第2表に於て、Z/ZQは第1表と同義であり、又、A
及びBは夫々、第2表の試験に供されたコンデンサの封
口板3を構成する合成樹脂板4がフェノール樹脂製であ
る場合及びポリプロピレン樹脂製である場合を示す。In Table 2, Z/ZQ has the same meaning as in Table 1, and A
and B indicate cases where the synthetic resin plate 4 constituting the sealing plate 3 of the capacitor subjected to the tests in Table 2 is made of phenol resin and polypropylene resin, respectively.
第2表から明らかな如く、酸化ホウ素の添加量が0.5
〜10重量%の範囲で有効であり、腐蝕作用の最も著し
いフェノール樹脂板を封口板に使つた場合でも2〜10
重量%の範囲で有効である。As is clear from Table 2, the amount of boron oxide added is 0.5
It is effective in the range of ~10% by weight, and even when the most corrosive phenolic resin board is used as the sealing board, it is effective in the range of 2 to 10% by weight.
Valid within a range of % by weight.
尚、本発明に於て、水素ガス発生によるコンデンサ内圧
上昇を防ぐための水素吸収剤を更に添加しても、斯る水
素吸収剤及び酸化ホウ素の夫々の効果は有効に生ずるこ
とが確認された。Furthermore, in the present invention, it has been confirmed that even if a hydrogen absorbent is further added to prevent an increase in the internal pressure of the capacitor due to the generation of hydrogen gas, the respective effects of the hydrogen absorbent and boron oxide are effectively produced. .
例えば、エチレンクリコール100cc、アジピン酸ア
ンモニウム5gからなる基本電解液に酸化ホウ素2重量
%及び水素吸収剤としてのジニトロフェノール0.5g
を添加した電解液を用いて第1表と同種の試験をなした
ところ、Z/ZQが、1.16、腐蝕発生がなく更にコ
ンデンサ内圧の上昇も認められなかった。For example, in a basic electrolyte solution consisting of 100 cc of ethylene glycol and 5 g of ammonium adipate, 2% by weight of boron oxide and 0.5 g of dinitrophenol as a hydrogen absorbent.
When the same type of test as shown in Table 1 was carried out using an electrolytic solution to which .
以上の説明より明らかな如く、本発明によれば、主溶媒
エチングリコールにイオノーゲンとして有機カルボン酸
のアンモニウム塩を溶解した電解液に酸化ホウ素を添加
することによりコンデンサ内での腐蝕が防止されて信頼
性の高いアルミニウム電解コンデンサを得ることができ
る。As is clear from the above description, according to the present invention, by adding boron oxide to an electrolytic solution in which an ammonium salt of an organic carboxylic acid as an ionogen is dissolved in ethyne glycol as a main solvent, corrosion inside a capacitor is prevented and reliability is achieved. It is possible to obtain an aluminum electrolytic capacitor with high performance.
図は典型的なアルミニウム電解コンデンサの断面図を示
し、1は巻回素子、2はケース、3は封目板である。The figure shows a cross-sectional view of a typical aluminum electrolytic capacitor, where 1 is a wound element, 2 is a case, and 3 is a sealing plate.
Claims (1)
ベリン酸、アジピン酸又はセバチン酸のアンモニウム塩
を溶解した電解液に酸化ホウ素を2,0〜10重量%添
加したことを特徴とするアルミニウム電解コンデンサ駆
動用電解液。1. An electrolytic solution for driving an aluminum electrolytic capacitor, characterized in that 2.0 to 10% by weight of boron oxide is added to an electrolytic solution prepared by dissolving an ammonium salt of suberic acid, adipic acid, or sebacic acid as an ionogen in ethylene glycol as a main solvent.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4889777A JPS586298B2 (en) | 1977-04-25 | 1977-04-25 | Electrolyte for driving aluminum electrolytic capacitors |
| DE19782816033 DE2816033A1 (en) | 1977-04-25 | 1978-04-13 | Electrolyte for aluminium capacitors - contg. carboxylic acid ammonium salt in ethylene glycol as main solvent contg. boric oxide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4889777A JPS586298B2 (en) | 1977-04-25 | 1977-04-25 | Electrolyte for driving aluminum electrolytic capacitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53132759A JPS53132759A (en) | 1978-11-18 |
| JPS586298B2 true JPS586298B2 (en) | 1983-02-03 |
Family
ID=12816049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4889777A Expired JPS586298B2 (en) | 1977-04-25 | 1977-04-25 | Electrolyte for driving aluminum electrolytic capacitors |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS586298B2 (en) |
| DE (1) | DE2816033A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3030800A1 (en) * | 1980-08-14 | 1982-02-25 | Siemens AG, 1000 Berlin und 8000 München | ELECTROLYTE CAPACITOR |
-
1977
- 1977-04-25 JP JP4889777A patent/JPS586298B2/en not_active Expired
-
1978
- 1978-04-13 DE DE19782816033 patent/DE2816033A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE2816033A1 (en) | 1978-11-02 |
| JPS53132759A (en) | 1978-11-18 |
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