JPS6046535B2 - Manufacturing method of electrolytic capacitor - Google Patents
Manufacturing method of electrolytic capacitorInfo
- Publication number
- JPS6046535B2 JPS6046535B2 JP8068380A JP8068380A JPS6046535B2 JP S6046535 B2 JPS6046535 B2 JP S6046535B2 JP 8068380 A JP8068380 A JP 8068380A JP 8068380 A JP8068380 A JP 8068380A JP S6046535 B2 JPS6046535 B2 JP S6046535B2
- Authority
- JP
- Japan
- Prior art keywords
- holder
- capacitor element
- oxide layer
- anode lead
- electrolytic 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
Links
- 239000003990 capacitor Substances 0.000 title claims description 38
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000000126 substance Substances 0.000 claims description 21
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 description 13
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- 229910052715 tantalum Inorganic materials 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229910052758 niobium Inorganic materials 0.000 description 3
- 239000010955 niobium Substances 0.000 description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000002048 anodisation reaction Methods 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000843 powder Substances 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
- 238000005245 sintering Methods 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Description
【発明の詳細な説明】
本発明は電解コンデンサの製造方法に関し、特に固体電
解コンデンサのコンデンサエレメントの化成方法の改良
に関するものてある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing an electrolytic capacitor, and particularly to an improvement in a method for forming a capacitor element of a solid electrolytic capacitor.
一般にこの種固体電解コンデンサは例えばタンタル、ニ
オブ、アルミニウムなどのように弁作用を有する金属粉
末を円柱状に加圧成形して焼結しなるコンデンサエレメ
ントに予め弁作用を有する金属線を陽極リードとして植
立し、この陽極り一 −ドの突出部分に第1の外部リー
ド部材を溶接すると共に、第2の外部リード部材をコン
デンサエレメントの周面に酸化層、半導体層を介して形
成された電極引出し層に半田付けし、然る後、コンデン
サエレメントの全周面を樹脂材にて被覆して構リ成され
ている。In general, this type of solid electrolytic capacitor is made by press-molding metal powder with a valve action, such as tantalum, niobium, or aluminum, into a cylindrical shape and sintering it.The capacitor element is made by using a metal wire with a valve action as an anode lead in advance. The first external lead member is welded to the protruding portion of the anode electrode, and the second external lead member is attached to the electrode formed on the circumferential surface of the capacitor element through an oxide layer and a semiconductor layer. The capacitor element is soldered to the lead-out layer, and then the entire circumferential surface of the capacitor element is covered with a resin material.
ところで、このコンデンサエレメントの表面(内表面も
含む)には誘電体としての酸化層か形成されているので
あるが、これの形成に当つては例えば第1図に示すよう
に、帯状の金属板よりなるホルダーAにコンデンサエレ
メントBを、それより導出された陽極リードCを一定の
ピッチ間隔にて固定することによつて吊設し、このコン
デンサエレメントB及び陽極リードCの一部が化成液に
浸漬される。By the way, an oxide layer is formed as a dielectric on the surface (including the inner surface) of this capacitor element, and when forming this, for example, as shown in Figure 1, a strip-shaped metal plate is used. A capacitor element B is suspended from a holder A made of a holder A, and an anode lead C led out from the holder A is fixed at a constant pitch, and a part of the capacitor element B and anode lead C is exposed to the chemical solution. immersed.
しカル乍ら、化成液の液温の管理が不充分になつたりす
ると、化成液の蒸気によつて化成液とホ・ルダーAの下
端部との間にバイパスが形成されてコンデンサエレメン
トBに流れる化成電流が減少してしまい、一定の化成時
間内において所望の酸化層を得ることができなくなる。However, if the temperature of the chemical liquid is insufficiently controlled, the vapor of the chemical liquid forms a bypass between the chemical liquid and the lower end of holder A, causing the condenser element B to The flowing anodization current decreases, making it impossible to obtain a desired oxide layer within a certain anodization time.
その上、化成液の蒸気によつてホルダーAが腐蝕され、
その腐蝕物が化成液に混入されると、高純度の酸化層を
形成することができなくなる。このために、漏洩電流特
性などが著しく損なわれる。従つて、従来においては陽
極リードCの長さを充分に長くすることによつて、仮に
化成液の液温管理が不充分になつて蒸気が多量に発生し
ても、ホルダーAと化成液との間にバイパスが形成され
ないように配置されているが、陽極リードCが例えばタ
ンタル、ニオブにて構成されている場合にはそれの価格
が極めて高いために、コンデンサの価格も高くなるとい
う欠点がある。Moreover, the holder A is corroded by the vapor of the chemical liquid,
If these corrosive substances are mixed into the chemical solution, it becomes impossible to form a highly pure oxide layer. For this reason, leakage current characteristics and the like are significantly impaired. Therefore, in the past, by making the length of the anode lead C sufficiently long, even if the liquid temperature control of the chemical liquid becomes insufficient and a large amount of steam is generated, the holder A and the chemical liquid can be connected to each other. However, if the anode lead C is made of tantalum or niobium, for example, it is extremely expensive, so the capacitor's price also increases. be.
本発明はこのような点に鑑み、ホルダーに対するコンデ
ンサエレメントの吊設長さを短くしても、化成液の蒸気
などによつて影響を受けることなく、確実に化成処理で
きる電解コンデンサの製造方法を提供するもので、以下
その一製造方法について説明する。In view of these points, the present invention provides a method for manufacturing an electrolytic capacitor that can be reliably chemically treated without being affected by the vapor of the chemical liquid even if the hanging length of the capacitor element relative to the holder is shortened. One of the manufacturing methods will be explained below.
まず、第2図に示すように、弁作用を有する帯状の金属
部材よりなるホルダー1の下端部分に例えは化成処理に
よつて酸化層2を形成する。First, as shown in FIG. 2, an oxide layer 2 is formed on the lower end portion of the holder 1, which is made of a band-shaped metal member having a valve function, by, for example, chemical conversion treatment.
次に、第3図に示すように、ホルダー1の酸化層形成部
分に弁作用を有する属部材にて構成されたコンデンサエ
レメント3を、それより導出された弁作用を有する金属
部材よりなる陽極リード4を溶接、圧着などによつて固
定することにより吊設する。尚、コンデンサエレメント
3のホルダー1に対する吊設長さLは従来の半分以下に
設定されている。そして、この状態のコンデンサエレメ
ント3及び陽極り,−ド4の一部を化成液に浸漬し、通
常の方法によつて、その表面に誘電体としての酸化層を
形成する。そして、さらに酸化層上に半導体層、電極引
出し層5を形成する。次に第4図に示すように、ホルダ
ー1より切離された陽極リード4の突出部分4aにL形
の第1の外部リード部材6を溶接すると共に、第2の外
部リード部材7を電極引出し層5に半田付けする。然る
後、コンデンサエレメント3の全周面を樹脂8にて被覆
することによつて固体電解コンデンサが得られる。この
ようにホルダー1の下端部分には化成処理に先立つて酸
化層2が形成されているので、コンデンサエレメント3
のホルダー1に対する吊設長さLが例えば5wL(従来
20TSfL)程度と極端に短くなつても、化成液の蒸
気によるホルダーと化成液間のバイパスの形成を防止で
きる。このために、コンデンサエレメント3に所定の化
成電流を流すことができるので、所望の酸化層を形成で
きる。しかも、化成液の蒸気がホルダー1の酸化層形成
部分に接触しても、ホルダー1の腐蝕は全く生じないの
で、腐蝕物の化成液への混入も全く生じ.ない。このた
めに、コンデンサエレメント3及び陽極リード4の表面
には高純度の酸化層を形成することができ、漏洩電流特
性を改善できる。又、コンデンサエレメント3のホルダ
ー1に対する吊設長さL即ち陽極リード4の長さは上述
のように大巾に短くすることができるので、例えば陽極
リード4としてタンタルを用いる場合にはそれ自身は勿
論のこと、製品の価格をも大巾に低減させることができ
るのみならず、資源の有効利用の観点からも好ましいも
のである。次に具体的実施例について説明する。Next, as shown in FIG. 3, a capacitor element 3 made of a metal member having a valve action is attached to the oxide layer forming portion of the holder 1, and an anode lead made of a metal member having a valve action is drawn out from the capacitor element 3. 4 is hung by fixing it by welding, crimping, etc. Note that the hanging length L of the capacitor element 3 with respect to the holder 1 is set to less than half of the conventional length. Then, the capacitor element 3 and part of the anode and electrode 4 in this state are immersed in a chemical solution, and an oxide layer as a dielectric is formed on the surface thereof by a conventional method. Then, a semiconductor layer and an electrode lead layer 5 are further formed on the oxide layer. Next, as shown in FIG. 4, an L-shaped first external lead member 6 is welded to the protruding portion 4a of the anode lead 4 separated from the holder 1, and the second external lead member 7 is pulled out from the electrode. Solder to layer 5. Thereafter, a solid electrolytic capacitor is obtained by covering the entire circumferential surface of the capacitor element 3 with a resin 8. As described above, since the oxide layer 2 is formed on the lower end portion of the holder 1 prior to the chemical conversion treatment, the capacitor element 3
Even if the hanging length L from the holder 1 becomes extremely short, for example, about 5 wL (conventionally 20 TSfL), formation of a bypass between the holder and the chemical liquid due to the vapor of the chemical liquid can be prevented. For this reason, a predetermined anodizing current can be passed through the capacitor element 3, so that a desired oxide layer can be formed. Moreover, even if the vapor of the chemical liquid comes into contact with the oxidized layer forming portion of the holder 1, no corrosion of the holder 1 occurs, so no corrosive substances are mixed into the chemical liquid. do not have. Therefore, a highly pure oxide layer can be formed on the surfaces of the capacitor element 3 and the anode lead 4, and leakage current characteristics can be improved. Furthermore, the hanging length L of the capacitor element 3 with respect to the holder 1, that is, the length of the anode lead 4, can be greatly shortened as described above, so for example, when tantalum is used as the anode lead 4, Needless to say, this method is preferable not only because it can greatly reduce the price of the product, but also from the viewpoint of effective use of resources. Next, specific examples will be described.
300×30×2tTI$Lのアルミニウム板よりなる
ホルダー1の下半分に、硼酸アンモニウムを化成液とし
て酸化層(Al。An oxide layer (Al) is applied to the lower half of the holder 1 made of an aluminum plate of 300 x 30 x 2 tTI$L using ammonium borate as a chemical solution.
O3)を形成する。そして、このホルダーの酸化層形成
部分にタンタル粉末を円柱状に加圧成形し焼結してなる
コンデンサエレメントを、それより導出されたタンタル
線よりなる陽極リードを一定のピッチ間隔にて圧着する
ことにより吊設する。尚、吊設長さは4Tr$Lに設定
されている。このコンデンサエレメント及び陽極リード
の一部を燐酸水溶液に浸漬し通常の方法により化成処理
し、それぞれの表面に酸化層を形成する。このようにし
て製作された固体電解コンデンサにおいて、漏洩電流の
不良発生率は従来のほぼ2〜3%にまで減少できた。O3) is formed. Then, a capacitor element made by press-molding tantalum powder into a cylindrical shape and sintering it is crimped onto the oxide layer forming part of this holder, and anode leads made of tantalum wire derived from the element are crimped at a constant pitch. It is suspended by. Note that the hanging length is set to 4Tr$L. This capacitor element and a portion of the anode lead are immersed in a phosphoric acid aqueous solution and subjected to chemical conversion treatment by a conventional method to form an oxide layer on their respective surfaces. In the solid electrolytic capacitor manufactured in this manner, the failure rate due to leakage current was reduced to about 2 to 3% compared to the conventional one.
又、価格面では陽極リードの短化によつて製品価格で2
0%ほどの低減を計ることができた。尚、本発明は何ら
上記実施例にのみ制約されることなく、例えばホルダー
はアルミニウムの他、タンタル、ニオブなどを用いるこ
ともできるし、それの酸化層の形成範囲も適宜に増減で
きる。Also, in terms of price, by shortening the anode lead, the product price can be reduced by 2.
We were able to measure a reduction of approximately 0%. It should be noted that the present invention is not limited to the above-described embodiments; for example, the holder may be made of tantalum, niobium, etc. in addition to aluminum, and the range in which the oxide layer is formed can be increased or decreased as appropriate.
又、コンデンサエレメントは金属粉末を加圧成形するこ
とによつて構成する他、線材、板材などによつて構成す
ることもできる。さらにはコンデンサは湿式の電解コン
デンサに適用することもできる。以上のように本発明に
よれば、ホルダーの所望部分に酸化層を形成することに
よつて、コンデンサエレメントのホルダーに対する吊設
長さを短くしても、化成液ないしその蒸気からの影響を
受けることなく、確実に化成処理できる上、特性、価格
で大巾な改善が期待てきる。Further, the capacitor element may be formed by press-molding metal powder, or may also be formed from a wire rod, a plate material, or the like. Furthermore, the capacitor can also be applied to a wet electrolytic capacitor. As described above, according to the present invention, by forming an oxide layer on a desired portion of the holder, even if the hanging length of the capacitor element from the holder is shortened, it is not affected by the chemical liquid or its vapor. In addition to being able to reliably perform chemical conversion treatment without any problems, drastic improvements in properties and price are expected.
第1図は従来のホルダー部材の側面図、第2図〜第4図
は本発明方法を説明するための図であつて、第2図はホ
ルダーに酸化層を形成した状態を示す側面図、第3図は
ホルダーにコンデンサエレメントを吊設した状態を示す
側断面図、第4図は完成状態の固体電解コンデンサを示
す側断面図である。
図中、1はホルダー、2は酸化層、3はコンデンサエレ
メント、4は陽極リードである。FIG. 1 is a side view of a conventional holder member, FIGS. 2 to 4 are diagrams for explaining the method of the present invention, and FIG. 2 is a side view showing a state in which an oxide layer is formed on the holder. FIG. 3 is a side sectional view showing a capacitor element suspended from a holder, and FIG. 4 is a side sectional view showing a completed solid electrolytic capacitor. In the figure, 1 is a holder, 2 is an oxide layer, 3 is a capacitor element, and 4 is an anode lead.
Claims (1)
下端部分に酸化層を形成する工程と、ホルダーの酸化層
形成部分に弁作用を有する金属部材にて構成されたコン
デンサエレメントを、それより導出された弁作用を有す
る金属部材よりなる陽極リードを固定することによつて
吊設する工程と、ホルダーに吊設されたコンデンサエレ
メント及び陽極リードの表面に化成処理によつて酸化層
を形成する工程とを含むことを特徴とする電解コンデン
サの製造方法。1. A step of forming an oxide layer on the lower end portion of a holder made of a band-shaped metal member having a valve action, and a step of forming a capacitor element made of a metal member having a valve action on the oxide layer forming portion of the holder. a step of suspending the anode lead by fixing it to the anode lead made of a metal member having a valve action, and a step of forming an oxide layer by chemical conversion treatment on the surfaces of the capacitor element and the anode lead suspended in the holder. A method for manufacturing an electrolytic capacitor, comprising:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8068380A JPS6046535B2 (en) | 1980-06-13 | 1980-06-13 | Manufacturing method of electrolytic capacitor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8068380A JPS6046535B2 (en) | 1980-06-13 | 1980-06-13 | Manufacturing method of electrolytic capacitor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS577113A JPS577113A (en) | 1982-01-14 |
| JPS6046535B2 true JPS6046535B2 (en) | 1985-10-16 |
Family
ID=13725138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8068380A Expired JPS6046535B2 (en) | 1980-06-13 | 1980-06-13 | Manufacturing method of electrolytic capacitor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6046535B2 (en) |
-
1980
- 1980-06-13 JP JP8068380A patent/JPS6046535B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS577113A (en) | 1982-01-14 |
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