JP3267311B2 - Solid electrolytic capacitor and method of manufacturing the same - Google Patents
Solid electrolytic capacitor and method of manufacturing the sameInfo
- Publication number
- JP3267311B2 JP3267311B2 JP17750591A JP17750591A JP3267311B2 JP 3267311 B2 JP3267311 B2 JP 3267311B2 JP 17750591 A JP17750591 A JP 17750591A JP 17750591 A JP17750591 A JP 17750591A JP 3267311 B2 JP3267311 B2 JP 3267311B2
- Authority
- JP
- Japan
- Prior art keywords
- solid electrolytic
- polymerization
- electrolytic capacitor
- manufacturing
- capacitor
- 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 - Lifetime
Links
- 239000003990 capacitor Substances 0.000 title claims description 45
- 239000007787 solid Substances 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 27
- 239000011888 foil Substances 0.000 claims description 21
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 229920001940 conductive polymer Polymers 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 6
- 239000007800 oxidant agent Substances 0.000 claims description 6
- -1 transition metal salt Chemical class 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- 239000011259 mixed solution Substances 0.000 claims description 2
- 229910052723 transition metal Inorganic materials 0.000 claims description 2
- 238000004804 winding Methods 0.000 claims description 2
- 238000002048 anodisation reaction Methods 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- PLNNMJRJPYQBBJ-UHFFFAOYSA-N [Fe+3].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 Chemical compound [Fe+3].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 PLNNMJRJPYQBBJ-UHFFFAOYSA-N 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- QKFFSWPNFCXGIQ-UHFFFAOYSA-M 4-methylbenzenesulfonate;tetraethylazanium Chemical compound CC[N+](CC)(CC)CC.CC1=CC=C(S([O-])(=O)=O)C=C1 QKFFSWPNFCXGIQ-UHFFFAOYSA-M 0.000 description 3
- 239000008151 electrolyte solution Substances 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000007784 solid electrolyte Substances 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 240000000907 Musa textilis Species 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
Landscapes
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、安価で製造工程が簡単
な固体電解コンデンサおよびその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solid electrolytic capacitor which is inexpensive and has a simple manufacturing process, and a method for manufacturing the same.
【0002】[0002]
【従来の技術】近年、電子機器のデジタル化に伴って、
高周波特性の良好なコンデンサへの要求が高まってい
る。しかし、一般の電解液を用いたアルミニウム電解コ
ンデンサの場合、イオン伝導によるため、高周波での容
量減少が極めて大きく、また比抵抗も極端に低くするこ
とはできないので、高周波でのインピーダンスが大きい
という欠点がある。一方固体電解コンデンサでは、前述
のような欠点はないが、固体電解質であるマンガンの比
抵抗があまり低くないため、高周波でのインピーダンス
はまだ不十分である。そこで、最近では有機半導体を用
いた固体電解コンデンサが広く研究されている。2. Description of the Related Art In recent years, with the digitization of electronic devices,
There is an increasing demand for capacitors having good high-frequency characteristics. However, in the case of an aluminum electrolytic capacitor using a general electrolytic solution, the capacitance at high frequencies is extremely reduced due to ionic conduction, and the specific resistance cannot be extremely reduced. There is. On the other hand, a solid electrolytic capacitor does not have the above-mentioned disadvantages, but the impedance at high frequencies is still insufficient because the specific resistance of manganese which is a solid electrolyte is not so low. Thus, recently, solid electrolytic capacitors using organic semiconductors have been widely studied.
【0003】[0003]
【発明が解決しようとする課題】有機半導体を固体電解
質として用いた固体電解コンデンサのうち、ピロール系
の導電性高分子を用いたものとしては、電極箔を板状と
した技術が種々開示されているが、体積効率が悪く、ま
た従来の電解液を用いた電解コンデンサとは製造工程が
全く異なるため、コストが高くなるという問題点があっ
た。Among the solid electrolytic capacitors using an organic semiconductor as a solid electrolyte, various techniques using a pyrrole-based conductive polymer as a plate-like electrode foil have been disclosed. However, there is a problem that the volume efficiency is poor and the cost is high because the manufacturing process is completely different from that of the conventional electrolytic capacitor using an electrolytic solution.
【0004】また、陽極箔と陰極箔とを巻回したコンデ
ンサ素子を用いた技術もいくつか開示されている。たと
えば、特開昭64−24410号公報では、捲回型アル
ミニウム電解コンデンサ素子を導電性高分子化合物のモ
ノマー溶液に浸漬した後、有機酸またはその塩を共存さ
せた酸化剤溶液に浸漬して重合させる方法が開示されて
いる。しかしこの方法では、温度が高いと酸化反応によ
る重合が促進されるため素子の表面近くで優先的に導電
性高分子が形成され固化してしまい、素子内部まで均一
に重合させることが難しい。また、低温にすれば重合に
長時間を要するという問題点がある。Some techniques using a capacitor element in which an anode foil and a cathode foil are wound are also disclosed. For example, in JP-A-64-24410, a wound aluminum electrolytic capacitor element is immersed in a monomer solution of a conductive polymer compound and then immersed in an oxidizing agent solution coexisting with an organic acid or a salt thereof to polymerize. There is disclosed a method for causing this to occur. However, in this method, when the temperature is high, polymerization by an oxidation reaction is promoted, so that a conductive polymer is preferentially formed and solidified near the surface of the device, and it is difficult to uniformly polymerize the inside of the device. Further, when the temperature is lowered, there is a problem that a long time is required for polymerization.
【0005】特開平2−186616号公報では、陽極
箔と陰極箔との間に多孔質セパレータを介在させて巻回
した素子を用い、含浸用ピロール溶液に含浸し、酸化剤
溶液に浸漬してピロールの化学的重合を行った後、さら
に電解重合を行う方法が開示されている。しかし、この
方法は工程が繁雑であり、また電解重合の際にモノマー
が素子内部まで十分に供給され難いという問題点を有す
る。In Japanese Patent Application Laid-Open No. 2-186616, an element wound with a porous separator interposed between an anode foil and a cathode foil is used, impregnated with a pyrrole solution for impregnation, and immersed in an oxidant solution. A method is disclosed in which, after performing chemical polymerization of pyrrole, electrolytic polymerization is further performed. However, this method has a problem that the steps are complicated and that the monomer is not sufficiently supplied to the inside of the device during the electrolytic polymerization.
【0006】さらに特開平2−62028号公報には、
やはり捲回型コンデンサ素子を電解重合溶液中に浸漬し
て陰極箔を正極とし陽極箔を負極として電解重合する方
法が開示されている。しかし、電解重合の装置及び条件
が複雑であるばかりか、電解重合時に陽極箔が損傷する
恐れがあり、また導電性高分子は正極側から形成される
ので、負極の陽極箔のエッチング構造の内部まで均一に
形成することは難しい。Further, Japanese Patent Application Laid-Open No. 2-62028 discloses that
Also disclosed is a method of immersing a wound capacitor element in an electrolytic polymerization solution to perform electrolytic polymerization using a cathode foil as a positive electrode and an anode foil as a negative electrode. However, not only is the electrolytic polymerization apparatus and conditions complicated, but also the anode foil may be damaged during the electrolytic polymerization, and the conductive polymer is formed from the positive electrode side. It is difficult to form evenly.
【0007】本発明は上述の点に鑑みてなされたもので
あり、その目的とするところは、従来の電解コンデンサ
用の設備を利用して簡単な製造工程とし、安価で良好な
特性の固体電解コンデンサを提供することである。SUMMARY OF THE INVENTION The present invention has been made in view of the above points, and has as its object to provide a simple electrolytic process utilizing conventional electrolytic capacitor equipment, and to provide a solid electrolytic device having good characteristics at low cost. The purpose is to provide a capacitor.
【0008】[0008]
【課題を解決するための手段】上記目的による本発明で
は、陽極酸化により酸化皮膜を形成した陽極箔と、陰極
箔とをセパレータを介して巻回したコンデンサ素子を用
いた固体電解コンデンサの製造方法において、前記コン
デンサ素子への重合溶液の含浸を最終的に金属ケース内
で行った後、コンデンサ素子の陰極箔を正極、金属ケー
スを負極として電解重合を行い導電性高分子を形成させ
ることを特徴とする。前記重合溶液は、−30℃以下に
冷却された酸化剤と導電性高分子単量体とを含む混合溶
液を用いることが望ましい。そして、高分子単量体はピ
ロール又はその誘導体が酸化剤は有機スルホン酸、カル
ボン酸または有機硫酸化合物の遷移金属塩が利用でき
る。前記電解重合は、−20℃以上の温度下で行うこと
が好ましい。また、コンデンサ素子は金属ケースに挿入
する前にあらかじめ重合溶液を予備含浸しておくことも
できる。According to the present invention, there is provided a method for manufacturing a solid electrolytic capacitor using a capacitor element in which an anode foil having an oxide film formed by anodic oxidation and a cathode foil are wound via a separator. In the above, the capacitor element is finally impregnated with the polymerization solution in a metal case, and then a conductive polymer is formed by performing electrolytic polymerization using the cathode foil of the capacitor element as a positive electrode and the metal case as a negative electrode. And As the polymerization solution, it is desirable to use a mixed solution containing an oxidizing agent and a conductive polymer monomer cooled to −30 ° C. or lower. The polymer monomer may be pyrrole or a derivative thereof, and the oxidizing agent may be an organic sulfonic acid, a carboxylic acid, or a transition metal salt of an organic sulfate compound. The electrolytic polymerization is preferably performed at a temperature of -20 ° C or higher. The capacitor element may be pre-impregnated with a polymerization solution before being inserted into the metal case.
【0009】[0009]
【作用】本発明によれば、コンデンサ素子までは従来の
電解液を用いた電解コンデンサと同じ製造工程でできる
ので、非常に安価に大量生産できる。また、酸化重合と
電解重合を組合せることにより、導電性高分子のコンデ
ンサ素子への充填率が上昇するので、周波数特性が向上
し、高周波における容量変化率とESRを低く抑えるこ
とができる。According to the present invention, up to the capacitor element can be manufactured in the same manufacturing process as the conventional electrolytic capacitor using the electrolytic solution, so that it can be mass-produced at very low cost. Further, by combining the oxidative polymerization and the electrolytic polymerization, the filling rate of the conductive polymer into the capacitor element is increased, so that the frequency characteristics are improved, and the capacitance change rate and the ESR at a high frequency can be suppressed low.
【0010】[0010]
【実施例】以下、実施例に基づいて本発明を詳細に説明
する。 実施例1 高純度アルミニウム箔を電気化学的に粗面化しその後陽
極酸化を行って誘電体皮膜を形成してなる陽極化成箔
と、粗面化しただけの陰極箔とを密度0.5g/cm3 の
マニラ麻を主体としたセパレータを介して巻回してアル
ミニウム乾式電解コンデンサ用の25V47μF(5φ
×11l)の巻回型コンデンサ素子を作製した(図示せ
ず)。次に、このコンデンサ素子をリン酸アンモニウム
水溶液等の化成液中に浸漬し、陽極箔裁断面や陽極リー
ド引出し部などを再化成処理した。続いてドデシルベン
ゼンスルホン酸鉄(III)25wt%と該ドデシルベンゼン
スルホン酸鉄(III)のモル数に対して3倍量のモル数の
ピロールを添加した−50℃のメタノール溶液0.15
mlをアルミニウムケース(5φ×11l)に注入してか
ら前記素子を挿入、含浸させた後25℃雰囲気中におい
てコンデンサ素子の陰極箔を正極、アルミニウムケース
を負極として5mAの定電流を印加し1時間の電解重合
を行った。その後、90℃10分の乾燥を行ってから樹
脂で封入しコンデンサとした(図示せず)。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail based on embodiments. Example 1 A high-purity aluminum foil was electrochemically roughened, followed by anodic oxidation to form a dielectric film, and a roughened cathode foil having a density of 0.5 g / cm. 3. Winding through a separator mainly composed of Manila hemp, 25V 47μF (5φ
× 11 l) was produced (not shown). Next, this capacitor element was immersed in a chemical conversion solution such as an ammonium phosphate aqueous solution, and the anode foil cut section, the anode lead lead-out portion, and the like were subjected to re-chemical treatment. Subsequently, 25 wt% of iron (III) dodecylbenzenesulfonate and pyrrole in an amount 3 times the number of moles of the iron (III) dodecylbenzenesulfonate were added.
After injecting the above element into an aluminum case (5φ × 11 l), impregnating and impregnating the element, a constant current of 5 mA was applied in a 25 ° C. atmosphere with the cathode foil of the capacitor element as the positive electrode and the aluminum case as the negative electrode for 1 hour. Was electrolytically polymerized. Thereafter, the capacitor was dried at 90 ° C. for 10 minutes, and sealed with a resin to form a capacitor (not shown).
【0011】 実施例2 実施例1と同じ巻回型コンデンサ素子を用い、再化成処
理を施した後、ドデシルベンゼンスルホン酸鉄(III)2
5wt%と該ドデシルベンゼンスルホン酸鉄(III)のモル
数の6倍量のモル数のピロールを添加した−50℃のメ
タノール溶液中に浸漬して予備含浸した。次に前記メタ
ノール溶液0.15mlをアルミニウムケースに入れそこ
へ前記コンデンサ素子を挿入して含浸させた後、25℃
でそのまま20分放置し化学酸化重合を行いさらに実施
例1と同様にして、電解重合を行った。その後、90℃
10分の乾燥を行ってから樹脂で封入しコンデンサとし
た(図示せず)。Example 2 The same wound type capacitor element as in Example 1 was subjected to re-chemical treatment, and then iron (III) dodecylbenzenesulfonate 2
It was pre-impregnated by immersion in a methanol solution at -50 ° C to which 5% by weight and 6 moles of pyrrole of the iron (III) dodecylbenzenesulfonate were added. Next, 0.15 ml of the methanol solution was placed in an aluminum case, and the capacitor element was inserted thereinto for impregnation.
, And then allowed to stand for 20 minutes to perform chemical oxidative polymerization. Further, electrolytic polymerization was performed in the same manner as in Example 1. Then 90 ° C
After drying for 10 minutes, it was sealed with resin to obtain a capacitor (not shown).
【0012】比較例1 実施例1と同じ巻回型コンデンサ素子を用い、再化成し
てから、ピロール4:パラトルエンスルホン酸テトラエ
チルアンモニウム6:メタノール2の溶液を含浸させた
後、過硫酸アンモニウム20wt%、パラトルエンスルホ
ン酸テトラエチルアンモニウム10wt%を含む水溶液に
1時間浸漬して重合した。重合終了後、90℃10分の
乾燥を行ってから金属ケースに封入しコンデンサとし
た。Comparative Example 1 The same wound type capacitor element as used in Example 1 was used for re-chemical formation, and then impregnated with a solution of pyrrole 4: tetraethylammonium paratoluenesulfonate 6: methanol 2, and 20% by weight of ammonium persulfate. The polymer was immersed in an aqueous solution containing 10% by weight of tetraethylammonium paratoluenesulfonate for 1 hour to carry out polymerization. After completion of the polymerization, the mixture was dried at 90 ° C. for 10 minutes, and then sealed in a metal case to obtain a capacitor.
【0013】比較例2 実施例1と同じ巻回型コンデンサ素子を用い、再化成し
てから、ピロール4:パラトルエンスルホン酸テトラエ
チルアンモニウム6:メタノール2の溶液を含浸させた
後、陰極リードと陽極リード間に陰極リードが正となる
ように5Vの電圧を印加し、1時間の電解重合を行っ
た。重合終了後、90℃10分の乾燥を行ってから金属
ケースに封入しコンデンサとした。Comparative Example 2 The same wound type capacitor element as used in Example 1 was used for re-chemical formation, and then impregnated with a solution of pyrrole 4: tetraethylammonium paratoluenesulfonate 6: methanol 2, followed by a cathode lead and an anode. A voltage of 5 V was applied between the leads so that the cathode lead was positive, and electrolytic polymerization was performed for 1 hour. After completion of the polymerization, the mixture was dried at 90 ° C. for 10 minutes, and then sealed in a metal case to obtain a capacitor.
【0014】以上のようにして作製したコンデンサを8
5℃雰囲気中で10V印加し3時間のエージングを行っ
た後、定格電圧を10Vとして諸特性を測定した。その
結果を表1に示す。The capacitor manufactured as described above is
After applying 10 V in a 5 ° C. atmosphere and performing aging for 3 hours, various characteristics were measured at a rated voltage of 10 V. Table 1 shows the results.
【0015】[0015]
【表1】 [Table 1]
【0016】表1から明らかなように、本発明による実
施例は陽極箔のエッチングピット内部まで効果的に導電
性高分子が充填できるため容量出現率が極めて高い。ま
た、高周波におけるESRも低い値を実現できる。As is clear from Table 1, in the embodiment according to the present invention, since the conductive polymer can be effectively filled into the etching pits of the anode foil, the capacity appearance ratio is extremely high. Also, a low value of the ESR at a high frequency can be realized.
【0017】以上本発明につき好適な実施例をあげて種
々説明したが、本発明はこの実施例に限定されるもので
はない。たとえば、陽極箔は実施例では交流エッチング
による海綿状エッチング構造のものを用いたが、直流エ
ッチングによるトンネル型構造のものも利用できる。陰
極箔としては固体電解コンデンサとしては陰極容量が必
要ないのでエッチングしてなくても良い。セパレータで
は、天然繊維ばかりか合成繊維を利用することもでき
る。Although the present invention has been described in various embodiments with reference to preferred embodiments, the present invention is not limited to these embodiments. For example, the anode foil has a spongy etching structure by AC etching in the embodiment, but a tunnel type structure by DC etching can also be used. The cathode foil does not need to be etched because a solid electrolytic capacitor does not require a cathode capacity. In the separator, not only natural fibers but also synthetic fibers can be used.
【0018】[0018]
【発明の効果】本発明によれば、アルミニウム乾式電解
コンデンサ用の素子を用いることができるので、製造工
程が簡略となり、安価かつ良好な特性の固体電解コンデ
ンサを提供することができる。According to the present invention, since a device for an aluminum dry electrolytic capacitor can be used, the manufacturing process is simplified, and a solid electrolytic capacitor having good characteristics at low cost can be provided.
フロントページの続き (58)調査した分野(Int.Cl.7,DB名) H01G 9/028 H01G 9/00 Continuation of front page (58) Field surveyed (Int.Cl. 7 , DB name) H01G 9/028 H01G 9/00
Claims (6)
箔と、陰極箔とをセパレータを介して巻回したコンデン
サ素子を用いた固体電解コンデンサの製造方法におい
て、前記コンデンサ素子への重合溶液の含浸を最終的に
金属ケース内で行った後、コンデンサ素子の陰極箔を正
極、金属ケースを負極として電解重合を行い導電性高分
子を形成させることを特徴とする固体電解コンデンサの
製造方法。1. A method for manufacturing a solid electrolytic capacitor using a capacitor element obtained by winding an anode foil having an oxide film formed by anodization and a cathode foil through a separator, wherein the capacitor element is impregnated with a polymerization solution. Is performed in a metal case, and then a conductive polymer is formed by performing electrolytic polymerization using the cathode foil of the capacitor element as the positive electrode and the metal case as the negative electrode to form a conductive polymer.
た酸化剤と導電性高分子単量体とを含む混合溶液である
ことを特徴とする請求項1記載の固体電解コンデンサの
製造方法。2. The method for manufacturing a solid electrolytic capacitor according to claim 1, wherein said polymerization solution is a mixed solution containing an oxidizing agent cooled to -30 ° C. or lower and a conductive polymer monomer. .
おいて行うことを特徴とする請求項1または2記載の固
体電解コンデンサの製造方法。3. The method according to claim 1, wherein the electrolytic polymerization is performed at a temperature of −20 ° C. or higher.
する前に、あらかじめ前記重合溶液を予備含浸しておく
ことを特徴とする請求項1、2または3記載の固体電解
コンデンサの製造方法。4. The method for producing a solid electrolytic capacitor according to claim 1, wherein said polymerization solution is pre-impregnated before inserting said capacitor element into a metal case.
導体であり、酸化剤が有機スルホン酸、カルボン酸また
は有機硫酸化合物の遷移金属塩であることを特徴とする
請求項1、2、3または4記載の固体電解コンデンサの
製造方法。5. The method according to claim 1, wherein the polymer monomer is pyrrole or a derivative thereof, and the oxidizing agent is a transition metal salt of an organic sulfonic acid, a carboxylic acid or an organic sulfate compound. Or a method for manufacturing a solid electrolytic capacitor according to item 4.
造方法により製造したことを特徴とする固体電解コンデ
ンサ。6. A solid electrolytic capacitor manufactured by the manufacturing method according to claim 1, 2, 3, 4, or 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17750591A JP3267311B2 (en) | 1991-06-22 | 1991-06-22 | Solid electrolytic capacitor and method of manufacturing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17750591A JP3267311B2 (en) | 1991-06-22 | 1991-06-22 | Solid electrolytic capacitor and method of manufacturing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04373116A JPH04373116A (en) | 1992-12-25 |
JP3267311B2 true JP3267311B2 (en) | 2002-03-18 |
Family
ID=16032084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17750591A Expired - Lifetime JP3267311B2 (en) | 1991-06-22 | 1991-06-22 | Solid electrolytic capacitor and method of manufacturing the same |
Country Status (1)
Country | Link |
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JP (1) | JP3267311B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0536575A (en) * | 1991-07-31 | 1993-02-12 | Sanyo Electric Co Ltd | Solid electrolytic capacitor and its manufacture |
JP4776567B2 (en) * | 2007-02-28 | 2011-09-21 | 三洋電機株式会社 | Manufacturing method of solid electrolytic capacitor |
-
1991
- 1991-06-22 JP JP17750591A patent/JP3267311B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH04373116A (en) | 1992-12-25 |
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