JPS62266818A - Solid electrolytic capacitor - Google Patents
Solid electrolytic capacitorInfo
- Publication number
- JPS62266818A JPS62266818A JP11106886A JP11106886A JPS62266818A JP S62266818 A JPS62266818 A JP S62266818A JP 11106886 A JP11106886 A JP 11106886A JP 11106886 A JP11106886 A JP 11106886A JP S62266818 A JPS62266818 A JP S62266818A
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic capacitor
- solid electrolytic
- oxide film
- organic metal
- electrode
- 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.)
- Granted
Links
- 239000003990 capacitor Substances 0.000 title claims description 14
- 239000007787 solid Substances 0.000 title claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 150000004703 alkoxides Chemical class 0.000 claims description 7
- 239000007784 solid electrolyte Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- 238000000151 deposition Methods 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 239000011572 manganese Substances 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000010407 anodic oxide Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
- Oscillators With Electromechanical Resonators (AREA)
- Glass Compositions (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
本発明は固体電解質の形成方法を改良した固体電解コン
デンサに関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a solid electrolytic capacitor with an improved method of forming a solid electrolyte.
従来の技術
従来固体電解質の形成方法としては、酸化皮膜を有する
弁金属電極を硝酸マンガン溶液に浸漬した後、加熱分解
処理を行い、二酸化マンガンとして電極に析出させてい
た。BACKGROUND OF THE INVENTION A conventional method for forming a solid electrolyte involves immersing a valve metal electrode having an oxide film in a manganese nitrate solution and then subjecting it to a thermal decomposition treatment to deposit manganese dioxide on the electrode.
発明が解決しようとする問題点
しかしながら、二酸化マンガン層を電極上に形成させる
際に、一般に硝酸マンガン溶液に浸漬した後、加熱分解
を行うため、硝酸により陽極酸化皮膜が損傷を受け、5
〜7回熱分解、再化成を行う必要があった。また、定格
電圧に対し、3〜4倍の電圧で化成する必要があった。Problems to be Solved by the Invention However, when a manganese dioxide layer is formed on an electrode, it is generally immersed in a manganese nitrate solution and then thermally decomposed, so the anodic oxide film is damaged by the nitric acid.
It was necessary to carry out thermal decomposition and reformation ~7 times. Further, it was necessary to perform chemical conversion at a voltage three to four times higher than the rated voltage.
問題点を解決するための手段
本発明は上述の問題を解決するため酸化皮膜に対し化学
作用の少ないアルコキシドなどの有機金属塩を使用して
固体電解質層を形成することを特徴とする固体電解コン
デンサである。Means for Solving the Problems In order to solve the above-mentioned problems, the present invention provides a solid electrolytic capacitor characterized in that a solid electrolyte layer is formed using an organic metal salt such as an alkoxide that has little chemical action on the oxide film. It is.
すなわち、弁金属電極の表面上に酸化皮膜層を形成し、
該酸化皮膜層上にアルコキシドなどの有機金属塩を付着
させ、加熱処理して固体電解質層を形成したことを特徴
とする固体電解コンデンサである。That is, an oxide film layer is formed on the surface of the valve metal electrode,
The solid electrolytic capacitor is characterized in that an organic metal salt such as an alkoxide is deposited on the oxide film layer and a solid electrolyte layer is formed by heat treatment.
作用
アルコキシドなどの有機金属塩をキシレンなどに溶解し
た溶液を化成処理を施したアルミニウム箔からなる弁金
属!掻の表面上に塗布し、乾燥後さらに加熱処理により
、焼成して有機゛金属を熱分解し、耐熱性に優れた固体
電解質層が形成できる。A valve metal made of aluminum foil that has been chemically treated with a solution of organic metal salts such as alkoxides dissolved in xylene, etc.! It is coated on the surface of the wafer, dried, and then heat-treated to sinter it to thermally decompose the organic metal, forming a solid electrolyte layer with excellent heat resistance.
塗布方法としては、ディッピング後引上げる方法が最も
良好であった。As for the coating method, the dipping and then pulling method was the most favorable.
焼成中のアルコキシドの熱分解反応の一般式は次式で示
される。The general formula for the thermal decomposition reaction of alkoxide during calcination is shown by the following formula.
M(OR)、 −一→ MO++/! ” RO
Rここに M:金属元素
R:アルキル基や他の有機物
このようにアルコキシドになる金属例えばマンガン、錫
などでその酸化物が半導体の性質を示すものを酸化アル
ミニウム面上に塗布し、熱分解法により析出させること
により酸化皮膜をほとんど損傷させることなく、耐熱性
に優れた固体電解質を生成することができる。M(OR), -1 → MO++/! ” R.O.
R here M: Metal element R: Alkyl group or other organic substance Metals that form alkoxides such as manganese, tin, etc., whose oxides exhibit semiconducting properties are coated on the aluminum oxide surface, and the thermal decomposition method is applied. A solid electrolyte with excellent heat resistance can be produced by precipitation with almost no damage to the oxide film.
実施例
陽極用電極として表面倍率を約100倍にエツチングし
たアルミニウム箔に14V化成を行い、細幅にスリフタ
−後、電解紙、陰極、電解紙の順に重ねて両極に引出し
リードを接続して巻回し、コンデンサ素子を作成した。Example As an electrode for the anode, an aluminum foil etched to a surface magnification of approximately 100 times was subjected to 14V chemical conversion, and after being slifted into a narrow width, electrolytic paper, cathode, and electrolytic paper were layered in this order, and lead leads were connected to both electrodes and wound. Then, a capacitor element was created.
この素子を電解液中で両極に13V印加し、15分間素
子エージングを行った。純水で洗浄後第1表に示す有機
金属塩溶液中にコンデンサ素子を浸漬し引上げ、120
℃で5分間乾燥したのち、350℃の雰囲気中で10分
間焼成した。この浸漬−乾燥−焼成を3回繰り返した後
、ケースに収納して樹脂封入し、エージングを行った。13V was applied to both electrodes of this device in an electrolytic solution, and the device was aged for 15 minutes. After washing with pure water, the capacitor element was immersed in the organic metal salt solution shown in Table 1 and pulled out.
After drying at ℃ for 5 minutes, it was fired for 10 minutes in an atmosphere of 350 ℃. After repeating this immersion-drying-baking process three times, it was placed in a case, sealed with resin, and aged.
なお、比較用試料として陽極用電極として化成電圧が1
4Vのものと60Vのものを上述と同様にコンデンサ素
子を作成し、硝酸マンガン溶液中に浸漬し、300℃で
焼成−再化成を実施した。この焼成−再化成を6回繰り
返した後、ケースに収納して樹脂封入し、エージングを
行った。その時の製品特性を第2表に示す。In addition, as a comparison sample, a chemical formation voltage of 1 was used as an anode electrode.
Capacitor elements of 4V and 60V were prepared in the same manner as described above, immersed in a manganese nitrate solution, and fired and reconstituted at 300°C. After repeating this firing-reforming process six times, it was placed in a case, sealed with resin, and aged. The product characteristics at that time are shown in Table 2.
コンデンサの定格は何れもlOV、33μFで第2表の
特性値は試料数10個の平均値を示す。The ratings of the capacitors are 1OV and 33 μF, and the characteristic values in Table 2 are the average values of 10 samples.
第1表
第2表
第2表に示したように、従来法の14V化成電圧のもの
は全数ショートし、60V化成電圧のものは漏れ電流が
高目であると共に、静電容量は本発明品の約20%どま
りであるのに対し、本発明品は実用性が充分であり、さ
らに熱的に安定であることから上述のコンデンサ素子に
直接トランスファモールド成型法により樹脂外装するこ
とが可能となり、アルミニウム電解コンデンサのチップ
化に有用である。As shown in Table 1 and Table 2, the conventional method with a 14V formation voltage short-circuited, and the 60V formation voltage had a high leakage current, and the capacitance was lower than that of the present invention. In contrast, the product of the present invention has sufficient practicality and is thermally stable, making it possible to directly cover the capacitor element with resin by transfer molding. Useful for making aluminum electrolytic capacitors into chips.
なお、上述の実施例は弁金属電極としてエツチングアル
ミニウム箔を用いた巻回型の固体電解コンデンサについ
て述べたが、弁金属電極が板状、焼結体などのアルミニ
ウム電極についても同様な効果がある。また有機金属塩
焼成の後に再化成を加えると、さらに漏れ電流が小さく
なる効果がある。In addition, although the above-mentioned embodiment described a wound type solid electrolytic capacitor using an etched aluminum foil as a valve metal electrode, the same effect can be obtained when the valve metal electrode is plate-shaped or an aluminum electrode such as a sintered body. . Furthermore, adding reconversion after firing the organic metal salt has the effect of further reducing leakage current.
発明の効果
以上のように本発明の電解コンデンサの特性は大幅に改
良されると共に、容易に量産化が可能であり、工業的な
らびに実用的価値の大なるものである。Effects of the Invention As described above, the characteristics of the electrolytic capacitor of the present invention are greatly improved, and it can be easily mass-produced, and has great industrial and practical value.
Claims (2)
皮膜層上にアルコキシドなどの有機金属塩を付着させ、
加熱処理して固体電解質層を形成したことを特徴とする
固体電解コンデンサ。(1) Forming an oxide film layer on the surface of the metal electrode, depositing an organic metal salt such as an alkoxide on the oxide film layer,
A solid electrolytic capacitor characterized by forming a solid electrolyte layer through heat treatment.
する有機金属塩であることを特徴とする特許請求の範囲
第1項記載の固体電解コンデンサ。(2) The solid electrolytic capacitor according to claim 1, wherein the alkoxide is an organic metal salt containing manganese or tin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11106886A JPH0719728B2 (en) | 1986-05-14 | 1986-05-14 | Method for manufacturing solid electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11106886A JPH0719728B2 (en) | 1986-05-14 | 1986-05-14 | Method for manufacturing solid electrolytic capacitor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62266818A true JPS62266818A (en) | 1987-11-19 |
JPH0719728B2 JPH0719728B2 (en) | 1995-03-06 |
Family
ID=14551572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11106886A Expired - Fee Related JPH0719728B2 (en) | 1986-05-14 | 1986-05-14 | Method for manufacturing solid electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0719728B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0247818A (en) * | 1988-08-10 | 1990-02-16 | Nichicon Corp | Manufacture of solid electrolytic capacitor |
JPH02251126A (en) * | 1989-03-24 | 1990-10-08 | Nichicon Corp | Manufacture of solid electrolytic capacitor |
-
1986
- 1986-05-14 JP JP11106886A patent/JPH0719728B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0247818A (en) * | 1988-08-10 | 1990-02-16 | Nichicon Corp | Manufacture of solid electrolytic capacitor |
JPH02251126A (en) * | 1989-03-24 | 1990-10-08 | Nichicon Corp | Manufacture of solid electrolytic capacitor |
Also Published As
Publication number | Publication date |
---|---|
JPH0719728B2 (en) | 1995-03-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |