JPS62271411A - Electrolytic capacitor - Google Patents
Electrolytic capacitorInfo
- Publication number
- JPS62271411A JPS62271411A JP11348586A JP11348586A JPS62271411A JP S62271411 A JPS62271411 A JP S62271411A JP 11348586 A JP11348586 A JP 11348586A JP 11348586 A JP11348586 A JP 11348586A JP S62271411 A JPS62271411 A JP S62271411A
- Authority
- JP
- Japan
- Prior art keywords
- salt
- electrolytic capacitor
- tetrahydrophthalic
- anhydride
- electrolytic
- 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 20
- 239000003792 electrolyte Substances 0.000 claims description 12
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 claims description 10
- -1 amine salt Chemical class 0.000 claims description 8
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 claims description 5
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 239000002798 polar solvent Substances 0.000 claims description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000008151 electrolyte solution Substances 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 150000008064 anhydrides Chemical class 0.000 description 5
- 239000011888 foil Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000003495 polar organic solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KMOUUZVZFBCRAM-UHFFFAOYSA-N 1,2,3,6-tetrahydrophthalic anhydride Chemical compound C1C=CCC2C(=O)OC(=O)C21 KMOUUZVZFBCRAM-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- ILUAAIDVFMVTAU-UHFFFAOYSA-N cyclohex-4-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CC=CCC1C(O)=O ILUAAIDVFMVTAU-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- WSGYTJNNHPZFKR-UHFFFAOYSA-N 3-hydroxypropanenitrile Chemical compound OCCC#N WSGYTJNNHPZFKR-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- FOWDZVNRQHPXDO-UHFFFAOYSA-N propyl hydrogen carbonate Chemical compound CCCOC(O)=O FOWDZVNRQHPXDO-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Oscillators With Electromechanical Resonators (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】
3、発明の詳細な説明
[産業上の利用分野]
本発明は、新規な駆動用電解液を使用した電解コンデン
サに関する。Detailed Description of the Invention 3. Detailed Description of the Invention [Field of Industrial Application] The present invention relates to an electrolytic capacitor using a novel driving electrolyte.
[従来の技術]
アルミニウム等の弁作用金属の箔をセパレータとともに
巻回してコンデンサ素子とした電解コンデンサは、一般
にコンデンサ素子に駆動用電解液を含浸し、アルミニウ
ム等の金属ケースや合成樹脂製のケースにコンデンサ素
子が収納され密閉した構造を有する。[Prior Art] Electrolytic capacitors are made by winding a foil of a valve metal such as aluminum together with a separator to form a capacitor element.Generally, the capacitor element is impregnated with a driving electrolyte, and the capacitor element is impregnated with a driving electrolyte, and a metal case such as aluminum or a case made of synthetic resin is used. It has a sealed structure in which the capacitor element is housed.
従来、かかる電解コンデンサの駆動用電解液としては、
エチレングリコール等を主溶媒とし、これに電解質とし
て飽和有機酸のアンモニウム塩のように金属からなる電
極を侵食しない塩を溶解した電解液が一般に使用されて
いる。Conventionally, the driving electrolyte for such electrolytic capacitors is
Generally used is an electrolytic solution in which ethylene glycol or the like is used as the main solvent, and a salt that does not corrode metal electrodes, such as an ammonium salt of a saturated organic acid, is dissolved therein as an electrolyte.
(特公昭5g−13019号公報等参照)しかしながら
、上記電解液は、陰極箔の腐食や解離したアンモニア(
NH3)の蒸散のため高温での特性劣化が大きいという
欠点があった。なかでも、高温無負荷で放置した後の漏
洩電流の増大が著しい。(Refer to Japanese Patent Publication No. 5g-13019, etc.) However, the above electrolyte solution does not cause corrosion of the cathode foil or dissociated ammonia (
There was a drawback that characteristics deteriorated significantly at high temperatures due to evaporation of NH3). Among these, the leakage current increases significantly after being left unloaded at high temperatures.
[発明の解決しようとする問題点]
本発明は、前述の欠点を解消し、高温安定性の優れ、特
に高温無負荷で放置後も漏洩電流の増加が小さい電解コ
ンデンサを提供することを目的とする。[Problems to be Solved by the Invention] An object of the present invention is to eliminate the above-mentioned drawbacks and to provide an electrolytic capacitor that has excellent high-temperature stability and in particular exhibits a small increase in leakage current even after being left unloaded at high temperatures. do.
[問題点を解決するための手段]
本発明は、上記目的を良好に達成するものであり、本発
明は、テトラヒドロフタル酸、無水テトラヒドロフタル
酸又はそれらの塩が溶解された有機極性溶媒からなる駆
動用電解液が使用されたことを特徴とする電解コンデン
サを提供するものである。[Means for Solving the Problems] The present invention satisfactorily achieves the above objects. The present invention provides an electrolytic capacitor characterized in that a driving electrolyte is used.
駆動用電解液を構成するテトラヒドロフタル酸又は無水
テトラヒドロフタル酸としては。Tetrahydrophthalic acid or tetrahydrophthalic anhydride constituting the driving electrolyte.
Δl〜Δ4−テトラヒドロフタル酸、即ち、それぞれシ
クロヘキセン−1,2−ジカルボン酸、シクロヘキセン
−1,8−ジカルボン酸、シクロヘキセン−3,4−ジ
カルボン酸及びシクロヘキセン−4,5−ジカルボン酸
又はその無水物の全てが包含される。なかでも、Δ4−
テトラヒドロフタル(IJ、即ち、シクロヘキセン−4
,5−ジカルボン酸無水又はその無水物が、低い電導性
を有するので好ましい、テトラヒドロフタル酸又はその
無水物は本発明の目的を阻害しない程度において、適宜
の置換基を有していてもよい。Δl to Δ4-tetrahydrophthalic acid, i.e. cyclohexene-1,2-dicarboxylic acid, cyclohexene-1,8-dicarboxylic acid, cyclohexene-3,4-dicarboxylic acid and cyclohexene-4,5-dicarboxylic acid or anhydride thereof, respectively All are included. Among them, Δ4−
Tetrahydrophthal (IJ, i.e. cyclohexene-4
, 5-dicarboxylic acid anhydride or its anhydride is preferred because it has low conductivity, and tetrahydrophthalic acid or its anhydride may have an appropriate substituent to the extent that the object of the present invention is not impaired.
テトラヒドロフタル酸又は無水テトラヒドロフタル酸の
塩としては、アンモニウム塩、アミン塩、第四アンモニ
ウム塩又はアルカル金属堪が包含される。アミン塩とし
ては、好ましくは炭素数1〜4を有する第1級〜第3級
アルキルアミン塩、なかでもトリメチルアミン塩、トリ
エチルアミン塩が使用される。Salts of tetrahydrophthalic acid or tetrahydrophthalic anhydride include ammonium salts, amine salts, quaternary ammonium salts, or alkali metal salts. As the amine salt, preferably used are primary to tertiary alkylamine salts having 1 to 4 carbon atoms, especially trimethylamine salt and triethylamine salt.
第四アンモニウム塩としては、好ましくは一般式R4N
’で示されるが、この場合Rは、芳香族置換基を有する
ことある炭素数1〜10、特には1〜3のアルキル基で
ある。またアルカリ金属塩としては、カリウム又はナト
リウム塩の使用が好ましい。The quaternary ammonium salt preferably has the general formula R4N
', in which case R is an alkyl group having 1 to 10 carbon atoms, particularly 1 to 3 carbon atoms, which may have an aromatic substituent. Further, as the alkali metal salt, it is preferable to use potassium or sodium salt.
上記極性有機溶媒としては、電解コンデンサに通常使用
される極性有機溶媒であればいずれも使用できる。好ま
しい溶媒としては、アミド類、ラクトン類、グリコール
類、硫黄化合物類及び/又は炭酸塩類が使用できる。好
ましい具体例としては、炭酸プロピル、ジメチルホルム
アミド、N−メチルホルムアミド、ブチロラクトン、N
−メチルピロリドン、ジメチルスルホキシド、エチレン
シアノヒドリン、エチレングリコール、エチレングリコ
ールモノ又はジアルキルエーテル等が挙げられるである
。As the polar organic solvent, any polar organic solvent commonly used in electrolytic capacitors can be used. As preferred solvents, amides, lactones, glycols, sulfur compounds and/or carbonates can be used. Preferred specific examples include propyl carbonate, dimethylformamide, N-methylformamide, butyrolactone, N
- Methylpyrrolidone, dimethyl sulfoxide, ethylene cyanohydrin, ethylene glycol, ethylene glycol mono- or dialkyl ethers, and the like.
カルボン酸第四アンモニウム塩の極性有機溶媒中におけ
る含有量は、種々に選ぶことができるが、飽和溶液の状
態が最も比抵抗が小さい。Although the content of the carboxylic acid quaternary ammonium salt in the polar organic solvent can be selected variously, the resistivity is the lowest in the state of a saturated solution.
かくして芳香族カルボン酸第四アンモニウム塩の含有量
(濃度)は、電解液中好ましくは1〜50重量%、特に
は5〜40重量%が適切である。Thus, the content (concentration) of the aromatic carboxylic acid quaternary ammonium salt in the electrolytic solution is preferably 1 to 50% by weight, particularly 5 to 40% by weight.
本発明で、テトラヒドロフタル酸、その無水物又はその
塩を含む駆動用電解液を得る場合、これらの物質を有機
極性溶媒に添加することもできるが、溶媒中でこれらの
物質を形成する前駆物質を別個に溶媒に加えて、溶媒中
で形成することもできる。In the present invention, when obtaining a driving electrolyte containing tetrahydrophthalic acid, its anhydride, or its salt, these substances can be added to an organic polar solvent, but precursors that form these substances in the solvent It can also be formed in a solvent by adding it separately to the solvent.
本発明において、電解液中の水の含有は必ずしも必須で
はないが、水が含有された場合は、更に比抵抗を小さく
できるため好ましい。しかし、水の含有量を過度に多く
した場合には、ケースの膨れ、電極箔の腐食を増大させ
るので、水の含有量は、電解液中好ましくは0.1〜2
0重量%、特には0.5〜15重量%が好ましい。また
、電解液のpHは必要に応じて適宜のpH調整剤を添加
することにより、好ましくは4〜8特には5〜7に制御
される。In the present invention, water is not necessarily contained in the electrolytic solution, but it is preferable if water is contained because the specific resistance can be further reduced. However, if the water content is excessively increased, it increases the swelling of the case and the corrosion of the electrode foil, so the water content in the electrolyte is preferably 0.1 to 2.
0% by weight, especially 0.5-15% by weight is preferred. Further, the pH of the electrolytic solution is preferably controlled to 4 to 8, particularly 5 to 7, by adding an appropriate pH adjuster as necessary.
本発明の電解コンデンサには、種々の態様のコンデンサ
が包含される。典型的態様としては、紙等の適宜のセパ
レータで分離したアルミニウム箔陽極とアルミニウム箔
陰極とを使用し、これらを円筒状に巻いたものをコンデ
ンサ素子とし、この素子に駆動用電解液を含浸させる。The electrolytic capacitor of the present invention includes various types of capacitors. In a typical embodiment, an aluminum foil anode and an aluminum foil cathode separated by a suitable separator such as paper are used, these are wound into a cylindrical shape to form a capacitor element, and this element is impregnated with a driving electrolyte. .
電解液の含浸量としてはセパレータに対して、好ましく
は50〜300重量%とされる。電解液が含浸された素
子は、耐食性を有する金属や合成樹脂等のケースに収納
し、密封した構造にされる。The amount of electrolytic solution impregnated is preferably 50 to 300% by weight based on the separator. The element impregnated with the electrolytic solution is housed in a case made of corrosion-resistant metal, synthetic resin, or the like, and has a sealed structure.
以下、本発明の実施例について説明する。Examples of the present invention will be described below.
[実施例コ
各実施例は、表−1に示されるテトラヒドロフタル酸、
その無水物又はその塩を溶質として極性有機溶媒に溶解
させ、必要ならば、カルボン酸を加えることでpHを調
整し、電解液とした。[Example Each example contains tetrahydrophthalic acid shown in Table 1,
The anhydride or its salt was dissolved as a solute in a polar organic solvent, and if necessary, the pH was adjusted by adding a carboxylic acid to prepare an electrolytic solution.
種々調製した電解液を使用してアルミニウムを電極とす
る電解コンデンサ(100V、47μF)を製作し、高
温無負荷試験(125°C)における漏れ電流の変化を
測定した。その結果を比較例とともに表1に示す0表中
()内は重量%を示す。Electrolytic capacitors (100V, 47μF) with aluminum electrodes were manufactured using variously prepared electrolytes, and changes in leakage current were measured in a high temperature no-load test (125°C). The results are shown in Table 1 together with comparative examples. In Table 0, the numbers in parentheses indicate weight %.
表 1
[発明の効果]
本発明の電解コンデンサは、高温無負荷試験(125°
C)での漏れ電流の変化が小さい高温安定性の優れた電
解コンデンサが得られる。Table 1 [Effects of the invention] The electrolytic capacitor of the invention was tested in a high temperature no-load test (125°
An electrolytic capacitor with excellent high temperature stability and small change in leakage current in C) can be obtained.
Claims (3)
酸又はそれらの塩が溶解された有機極性溶媒からなる駆
動用電解液が使用されたことを特徴とする電解コンデン
サ。(1) An electrolytic capacitor characterized in that a driving electrolyte comprising an organic polar solvent in which tetrahydrophthalic acid, tetrahydrophthalic anhydride, or a salt thereof is dissolved is used.
酸の塩が、アンモニウム塩、アミン塩又は第四アンモニ
ウム塩である特許請求の範囲(1)の電解コンデンサ。(2) The electrolytic capacitor according to claim (1), wherein the salt of tetrahydrophthalic acid or tetrahydrophthalic anhydride is an ammonium salt, an amine salt, or a quaternary ammonium salt.
酸又はそれらの塩が、有機極性溶媒中1〜50重量%溶
解された特許請求の範囲(1)又は(2)の電解コンデ
ンサ。(3) The electrolytic capacitor according to claim (1) or (2), wherein 1 to 50% by weight of tetrahydrophthalic acid, tetrahydrophthalic anhydride, or a salt thereof is dissolved in an organic polar solvent.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11348586A JPS62271411A (en) | 1986-05-20 | 1986-05-20 | Electrolytic capacitor |
US07/049,297 US4734821A (en) | 1986-05-13 | 1987-05-13 | Electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11348586A JPS62271411A (en) | 1986-05-20 | 1986-05-20 | Electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62271411A true JPS62271411A (en) | 1987-11-25 |
Family
ID=14613480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11348586A Pending JPS62271411A (en) | 1986-05-13 | 1986-05-20 | Electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62271411A (en) |
-
1986
- 1986-05-20 JP JP11348586A patent/JPS62271411A/en active Pending
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