JPH02305422A - Metallized plastic film capacitor - Google Patents

Metallized plastic film capacitor

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Publication number
JPH02305422A
JPH02305422A JP12699789A JP12699789A JPH02305422A JP H02305422 A JPH02305422 A JP H02305422A JP 12699789 A JP12699789 A JP 12699789A JP 12699789 A JP12699789 A JP 12699789A JP H02305422 A JPH02305422 A JP H02305422A
Authority
JP
Japan
Prior art keywords
plastic film
organic peroxide
metallized plastic
sides
inorganic fine
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
Application number
JP12699789A
Other languages
Japanese (ja)
Inventor
Masashi Shimamoto
嶋本 昌司
Junji Kojima
小嶋 淳司
Mayumi Suzuki
真由美 鈴木
Yoshihiro Sakata
坂田 芳弘
Nobuyuki Kume
久米 信行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP12699789A priority Critical patent/JPH02305422A/en
Publication of JPH02305422A publication Critical patent/JPH02305422A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To manufacture the compound dielectric coated layers in high dielectric constant without deteriorating the electric characteristics etc., by a method wherein compound dielectric coated layers composed of polyphenylene oxide, inorganic fine powder and organic peroxide are provided. CONSTITUTION:Compound dielectric coated layers 4 composed of polypropylene oxide, inorganic fine powder and an organic peroxide are formed on both sides or one side of both side metallized plastic films 2 leaving electrode leading-out parts on both sides in the width direction and then laminated or wound around so as to form metallicon electrodes 5 on both sides. That is, the organic peroxide is contained in the compound dielectric composed of polyphenylene oxide and the inorganic powder in excellent electric characteristics and thermal resistance as the material for the dielectric coated layers 4 so that the organic peroxide may be decomposed by the Joule's heat in the shortcircuit current and reacted to an evaporated metal to form an insulator. Accordingly, the self-heating capacity can be increased as well as the compound dielectric coated layers 4 in high dielectric constant can be formed. Through these procedures, the title capacitor can be miniaturized without deteriorating both electric characteristics and coating workability.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、電子機器、情報機器等の電気回路に使用する
金属化プラスチックフィルム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 metallized plastic film capacitors used in electrical circuits of electronic equipment, information equipment, etc.

従来の技術 近年、電子機器等の軽薄短小化、高性能化が進む中で、
電子部品の小形化、高性能化への要望が高まってきてお
シ、金属化プラスチックフィルムコンデンサにおいても
これらへの取組が急務となりつつある。
Conventional technology In recent years, as electronic devices have become lighter, thinner, shorter, and more sophisticated,
As the demand for smaller size and higher performance of electronic components increases, it is becoming an urgent need to address these issues in metallized plastic film capacitors as well.

以下に従来の金属化プラスチックフィルムコンデンサに
ついて図面を用いて説明を行う。
A conventional metallized plastic film capacitor will be explained below using drawings.

第1図は従来の積層型金属化プラスチックフィルムコン
デンサの構造を示している。この図において、1はコン
デンサを構成する複合金属化フィルムであって、誘電体
フィルム2の両面に電極3をそれぞれ真空蒸着によって
形成すると共に、前記誘電体フィルム2の両面に、幅方
向両側に電極引出部を残して、その他の部分に誘電体塗
工層4を設けてなるものである。このように構成された
複合金属化フィルム1は必要枚数積層されると共に、こ
のフィルム積層体の幅方向両側端面部分にそれぞれメタ
リコン電極5を形成することにより、所期の金属化プラ
スチックフィルムコンデンサ素子が得られる。
FIG. 1 shows the structure of a conventional laminated metallized plastic film capacitor. In this figure, reference numeral 1 denotes a composite metallized film constituting a capacitor, in which electrodes 3 are formed on both sides of a dielectric film 2 by vacuum deposition, and electrodes 3 are formed on both sides of the dielectric film 2 in the width direction. A dielectric coating layer 4 is provided on the other parts except for the lead-out part. The required number of composite metallized films 1 thus constructed are laminated, and metallicon electrodes 5 are formed on both end faces in the width direction of this film laminate, thereby forming the desired metallized plastic film capacitor element. can get.

従来の金属化プラスチックフィルムコンデンサにおいて
は、優れた電気特性を有しているポリエチレンテレフタ
レートが誘電体フィルムとして、ポリフェニレンオキサ
イドが誘電体塗工層として、主として用いられている。
In conventional metallized plastic film capacitors, polyethylene terephthalate, which has excellent electrical properties, is mainly used as the dielectric film, and polyphenylene oxide is mainly used as the dielectric coating layer.

これらの材料の比誘電率は高々3程度であシ、又フィル
ム、塗工膜共にすでに1μm程度まで薄膜化されている
The dielectric constant of these materials is about 3 at most, and both the film and the coating have already been made thin to about 1 μm.

発明が解決しようとする課題 ]ンデンサの静電容量は誘電体の誘電率と電極の面積に
比例し、電極間の距離に反比例することが知られている
。従って小形化、即ち単位体積当たりの静電容量を大き
くするためには、誘電体に高誘電率なものを用いるか、
又、は、誘電体の薄膜化を図ることが必要となる。
[Problems to be Solved by the Invention] It is known that the capacitance of a capacitor is proportional to the dielectric constant of the dielectric material and the area of the electrodes, and inversely proportional to the distance between the electrodes. Therefore, in order to downsize, that is, increase the capacitance per unit volume, it is necessary to use a dielectric with a high dielectric constant.
Also, it is necessary to make the dielectric thinner.

誘電体の高誘電率化の方法として有機高分子材料と、無
機微粉末の複合化が試みられている。
As a method of increasing the dielectric constant of dielectric materials, attempts have been made to combine organic polymer materials and inorganic fine powders.

金属化プラスチックフィルムコンデンサにおいても両面
金属化プラスチックフィルムの両面又は片面に、電気特
性や耐熱性の優れたポリフェニレンオキサイドと無機微
粉末とからなる複合誘電体を塗工し、コンデンサの小型
化を図ることが試みられている。しかしながら、金属化
プラスチックフィルムコンデンサ特有のセルフヒーリン
グ性がポリフェニレンオキサイドと無機微粉末とからな
る複合誘電体はポリフェニレンオキサイドのみからなる
誘電体に比較し悪く、特に外装を施した場合、酸素が供
給されず、セルフヒーリングの際の蒸着金属の酸化、つ
まシ金属酸化物化による絶縁性の確保が充分に行えず、
しばしば高温負荷試験において絶縁抵抗が低下するとい
う課題を有していた。
In the case of metallized plastic film capacitors, a composite dielectric consisting of polyphenylene oxide, which has excellent electrical properties and heat resistance, and inorganic fine powder is coated on both sides or one side of a double-sided metalized plastic film, thereby reducing the size of the capacitor. is being attempted. However, the self-healing property unique to metallized plastic film capacitors is poor in composite dielectrics made of polyphenylene oxide and inorganic fine powder compared to dielectrics made only of polyphenylene oxide, and especially when an exterior is applied, oxygen is not supplied. , oxidation of the deposited metal during self-healing, and insulating properties due to the formation of a metal oxide cannot be achieved sufficiently.
Often, there was a problem that insulation resistance decreased during high-temperature load tests.

又、誘電体の薄膜化については、上記のとおυ誘電体フ
ィルム及び塗工層ともにすでに1μm程度まで薄膜化さ
れており、これ以上の薄膜化は電気特性の劣化1作業性
の低下を招くため困難な状況にある。
Regarding the thinning of the dielectric, as mentioned above, both the dielectric film and the coating layer have already been thinned to about 1 μm, and making the film thinner than this will lead to deterioration of electrical properties and reduced workability. We are in a difficult situation.

本発明は、上記課題を解決するために、大幅な電気特性
の劣化及び塗工作業性の低下及び信頼性の低下を招くこ
となく塗工誘電体材料の高誘電率化を行うことにより、
コンデンサの小形化を図ることを目的とするものである
In order to solve the above-mentioned problems, the present invention aims to increase the dielectric constant of a coated dielectric material without significantly deteriorating electrical properties, reducing coating workability, or reducing reliability.
The purpose is to reduce the size of the capacitor.

課題を解決するための手段 上記目的を達成するために、本発明の金属化プラスチッ
クフィルムコンデンサは、両面金属化プラスチックフィ
ルムの両面又は片面に、電極引き出し部を幅方向の両側
に残して、ポリフェニレンオキサイドと、無機微粉末と
、有機過酸化物とからなる複合誘電体塗工層を形成し、
これを積層又は巻回して前記両側にメタリコン電極を形
成した構成を有している。
Means for Solving the Problems In order to achieve the above object, the metallized plastic film capacitor of the present invention has a polyphenylene oxide film on both sides or one side of the double-sided metallized plastic film, with electrode extension parts left on both sides in the width direction. , forming a composite dielectric coating layer consisting of inorganic fine powder and organic peroxide,
It has a structure in which metallicon electrodes are formed on both sides by laminating or winding these.

作  用 この構成により、誘電体塗工層の材料として、電気特性
や耐熱性の優れたポリフェニレンオキサイドと無機微粉
末とからなる複合誘電体へ有機過酸化物を含有させ、短
絡電流のジュール熱により有機過酸化物を分解し、蒸着
金属と反応させて絶縁体を形成するため、セルフヒーリ
ング性の改善が行えると共に、信頼性の高い複合誘電体
塗工層の形成を実現することができる。
Function: With this structure, an organic peroxide is incorporated into a composite dielectric made of polyphenylene oxide, which has excellent electrical properties and heat resistance, and an inorganic fine powder, as the material for the dielectric coating layer, and the Joule heat of short circuit current Since the organic peroxide is decomposed and reacted with the deposited metal to form an insulator, self-healing properties can be improved and a highly reliable composite dielectric coating layer can be formed.

尚、ここで有機過酸化物は、一般式R−00−R’(こ
の式で、RおよびR′は、水素またはアルキル基、シリ
ル基、アリル基、ベンゾイル基等の有機基)で表され、
最適な物としては、ジ−t−ブチルパーオキサイド、t
−ブチルパーオキサイド。
The organic peroxide here is represented by the general formula R-00-R' (in this formula, R and R' are hydrogen or an organic group such as an alkyl group, a silyl group, an allyl group, or a benzoyl group). ,
The most suitable one is di-t-butyl peroxide, t
-Butyl peroxide.

t−ブチルパーオキシトリフェニルシラン、クメンハイ
ドロパーオキサイド等があり、その他にベンゾイルパー
オキサイド、ラウロイルパーオキサイド、2,5−ジメ
チル2,5−ジ(t−ブチルパーオキシ)ヘキサン−3
,ジクミルパーオキサイド、t−ブナルバーオキシ2−
エチルへキサノート等がある。
There are t-butylperoxytriphenylsilane, cumene hydroperoxide, etc., as well as benzoyl peroxide, lauroyl peroxide, 2,5-dimethyl 2,5-di(t-butylperoxy)hexane-3
, dicumyl peroxide, t-bunalburoxy 2-
There are ethyl hexanautes, etc.

有機過酸化物の添加量についてはポリフェニレンオキサ
イドに対して0.1〜10.Owt %にて良好な結果
が得られる。添加量が0.1 wt %に満たない場合
は、十分な効果が得られず、10.0wt%を越えると
加湿時の容量変化が極度に増大する。
The amount of organic peroxide added is 0.1 to 10.0% relative to polyphenylene oxide. Good results are obtained at Owt%. If the amount added is less than 0.1 wt %, sufficient effects cannot be obtained, and if it exceeds 10.0 wt %, the volume change during humidification will be extremely increased.

無機微粉末の添加量については、20〜80 w tチ
にて良好な結果が得られる。含有量が20wtチに満た
ない場合は充分な高誘電率化が図れず、90wt%を越
えると加湿時の容量変化が極度に増大する。
Good results can be obtained when the amount of inorganic fine powder added is 20 to 80 wt. If the content is less than 20 wt %, a sufficiently high dielectric constant cannot be achieved, and if it exceeds 90 wt %, the capacitance change during humidification will be extremely increased.

実施例 以下、本発明の実施例を比較例を参照しながら説明する
。なお、この実施例の金属化プラスチックフィルムコン
デンサは基本的には、第1図に示した一般的な構造と同
様であるため、共通する部分については、その説明を省
略する。本発明の実施例では、誘電体塗工層4として、
塗工時の無機微粉末の含有量が20〜80wt%、有機
過酸化物の含有量がポリフェニレンオキサイドに対して
0.1〜10.0 w t%であることを特徴とした複
合誘電体塗工層を用いる。
EXAMPLES Hereinafter, examples of the present invention will be described with reference to comparative examples. The metallized plastic film capacitor of this embodiment basically has the same general structure as shown in FIG. 1, so the explanation of the common parts will be omitted. In the embodiment of the present invention, as the dielectric coating layer 4,
A composite dielectric coating characterized in that the content of inorganic fine powder during coating is 20 to 80 wt%, and the content of organic peroxide is 0.1 to 10.0 wt% based on polyphenylene oxide. Use layers.

第1表に本発明の実施例1〜6および比較例1〜5に複
合誘電体塗工層に含有するTiO2量、pp○に対する
2、5−ジメチル2,5−ジ(を−ブチルパーオキシ)
ヘキサン−3の添加量を示す。
Table 1 shows the amount of TiO2 contained in the composite dielectric coating layer for Examples 1 to 6 of the present invention and Comparative Examples 1 to 5, 2,5-dimethyl 2,5-di(to-butylperoxy )
The amount of hexane-3 added is shown.

塗工液はポリフェニレンオキサイドの粉末ト2.5−ジ
メチル2,6−ジ(t−ブチルパーオキシ)ヘキサン−
3をトリクレンに均一に溶解した後、平均−欠粒径0.
2μmのT 102を添加、撹拌混合し、更に、ボール
ミルによって48Hr処理し、TiO2を均一に分散さ
せることにより得た。
The coating liquid is polyphenylene oxide powder and 2,5-dimethyl 2,6-di(t-butylperoxy)hexane.
After uniformly dissolving 3 in trichlene, the average defective particle size was 0.
2 μm of T 102 was added, stirred and mixed, and further treated with a ball mill for 48 hours to uniformly disperse TiO2.

なお、比較例1については、ポリフェニレンオキサイド
の粉末をトリクレンに均一に溶解させることにより得た
Note that Comparative Example 1 was obtained by uniformly dissolving polyphenylene oxide powder in trichlene.

これらの塗工液をグラビアコータを用いて膜厚2μmの
アルミニウム蒸着両面金属化ポリエチレンテレフタレー
トフィルム上に、電極引出部を幅方向の両側に残して塗
工し、風乾燥後、更に120’C,I Hr乾燥させる
ことによシ、膜厚1μmの複合誘電体塗工層4を得た。
These coating solutions were applied using a gravure coater onto a 2-μm-thick aluminum vapor-deposited double-sided metalized polyethylene terephthalate film, leaving electrode lead-out portions on both sides in the width direction, and after air drying, the coating was further heated at 120'C. By drying for 1 hour, a composite dielectric coating layer 4 having a thickness of 1 μm was obtained.

これによって得られた複合金属化フィルム1を500層
積層し、130℃、2Ky/ctdで2Hr加熱プレス
を行b、両側の電極引出部へ亜鉛を金属溶射し、メタリ
コン電極5を形成して前掲の図面に示したものと同構造
で、4.Om X 4.6 g X 2.1閾の寸法を
有するコンデンサを得た。
500 layers of the composite metallized film 1 obtained in this manner were laminated, heat-pressed at 130° C. and 2 Ky/ctd for 2 hours b, and zinc was metal sprayed onto the electrode lead-out portions on both sides to form the metallicon electrodes 5 described above. It has the same structure as shown in the drawing of 4. A capacitor with dimensions of Om x 4.6 g x 2.1 threshold was obtained.

更に、このコンデンサの電極引出部に設けた亜鉛に、0
.5 Ql11径の半田鍍金鉄線を溶接し、エポキシ樹
脂を0.4〜0.6.の厚さで外装することでコンデン
サ素子を得た。
Furthermore, the zinc provided at the electrode lead-out part of this capacitor was
.. 5 Weld a solder-plated iron wire with a diameter of Ql11, and apply epoxy resin of 0.4 to 0.6. A capacitor element was obtained by packaging with a thickness of .

このコンデンサ素子について20°C、I KHzにお
ける静電容量と誘電正接、およびDC50Vにおける初
期絶縁抵抗と、高温負荷試験(100°C1D Ce 
3 V 、 1000Hr)後の絶縁抵抗不良率と、耐
湿放置試験(60°C、90〜9 s% RH,500
Hr )前後の容量変化率をそれぞれ測定した。その結
果を第1表に示す。絶縁抵抗不良率は、試料数50にお
いて、DC50Vにおける絶縁抵抗が1×10 Ω以下
の割合を百分率にて示した。その他の特性値は試料数2
0における平均値を示した。
Regarding this capacitor element, the capacitance and dielectric loss tangent at 20°C and I KHz, the initial insulation resistance at 50V DC, and the high temperature load test (100°C, 1D Ce
Insulation resistance defect rate after 3 V, 1000 Hr) and humidity resistance test (60°C, 90-9 s% RH, 500
The rate of change in capacity before and after Hr ) was measured. The results are shown in Table 1. The insulation resistance failure rate is expressed as a percentage of the insulation resistance at 50 VDC of 1×10 Ω or less in 50 samples. Other characteristic values are sample number 2
The average value at 0 is shown.

T 102の添加量が、20wt%に満たない場合は高
誘電率化が図れていない。80wt%を越えると高誘電
率化は図れるが、加湿時の容量変化が極度に増大した。
If the amount of T 102 added is less than 20 wt%, a high dielectric constant cannot be achieved. If it exceeds 80 wt%, a high dielectric constant can be achieved, but the capacitance change during humidification increases extremely.

2.6−ジメチル2.6−ジ(t−ブチルパーオキシ)
ヘキサン−3の添加量が、ポリフェニレンオキサイドに
対して0.1wt%に満たない場合はT z O2を添
加したものにおいて高温負荷後の絶縁抵抗がDCsoV
において、1X109Q以下のものがあった。10.0
wt%を越えると加湿時の容量変化が極度に増大した。
2,6-dimethyl 2,6-di(t-butylperoxy)
If the amount of hexane-3 added is less than 0.1 wt% with respect to polyphenylene oxide, the insulation resistance after high temperature load will be DCsoV in the product with TzO2 added.
Among them, there were some with 1X109Q or less. 10.0
When the amount exceeded wt%, the change in capacity during humidification was extremely increased.

なお、本実施例では、有機過酸化物として、2.6−ジ
メチル2.5−ジ(t−ブチルパーオキシ)ヘキサン−
3を用いたが、有機過酸化物であれば、他の材料におい
ても同様の効果を得ることができる。また、本実施例で
は無機微粉末として、Ti○ を配合分散したが、その
他、B a T i O3゜S r T 1O3T P
 b T iO3等の無機微粉末を単独あるいは2種以
上を混合したものでも同様の効果を得ることができる。
In this example, 2,6-dimethyl 2,5-di(t-butylperoxy)hexane was used as the organic peroxide.
3 was used, but similar effects can be obtained with other materials as long as they are organic peroxides. Furthermore, in this example, Ti○ was blended and dispersed as the inorganic fine powder, but in addition, B a T i O3゜S r T 1O3T P
Similar effects can be obtained using inorganic fine powders such as b TiO3 alone or in combination of two or more.

発明の詳細 な説明したように本発明の金属化プラスチックフィルム
コンデンサは誘電体塗工層として、ポリフェニレンオキ
サイドと、無機微粉末と、有機過酸化物とからなる複合
誘電体塗工層を設けたことにより、大幅な電気特性の劣
化及び塗工作業性の低下及び信頼性の低下を招くことな
く塗工誘電体材料の高誘電率化を実現した複合誘電体塗
工層が得られる。
As described in detail of the invention, the metallized plastic film capacitor of the present invention has a composite dielectric coating layer composed of polyphenylene oxide, inorganic fine powder, and organic peroxide as a dielectric coating layer. As a result, a composite dielectric coating layer can be obtained in which the dielectric constant of the coated dielectric material is increased without causing significant deterioration of electrical properties, reduction in coating workability, or reduction in reliability.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は一般的な積層型金属化プラスチックフィルムコ
ンデンサの構造を示す要部断面図である。 1・・・・・・複合金属化フィルム、2・・・・・・誘
電体フィルム、3・・・・・・蒸着電極、4・・・・・
・誘電体塗工層、6・・・・・・メタリコン電極。 代理人の氏名 弁理士 粟 野 重 孝 ほか1名ノ 
−−− ネ檗1属メ已フィルム ? −−−が■j体フィルム 3−−一蒸着電麺 弓2−−−m呵8N唾冒ζイj鉢J塗−ズ=ン1囮「5
−m−メタリコン電極 第1図
FIG. 1 is a sectional view of essential parts showing the structure of a general laminated metallized plastic film capacitor. 1... Composite metallized film, 2... Dielectric film, 3... Vapor deposited electrode, 4...
・Dielectric coating layer, 6...Metallicon electrode. Name of agent: Patent attorney Shigetaka Awano and one other person
−−− Neboku 1 genus Mei 已 film? --- is■j body film 3--1 vapor-deposited denmen bow 2--m 8N spitting
-m- Metallicon electrode Figure 1

Claims (3)

【特許請求の範囲】[Claims] (1)両面金属化プラスチックフィルムの両面又は片面
に、電極引き出し部を幅方向の画側に残して、ポリフェ
ニレンオキサイドと、無機微粉末と、有機過酸化物とか
らなる複合誘電体塗工層を形成し、これを積層又は巻回
して前記両側にメタリコン電極を形成したことを特徴と
する金属化プラスチックフィルムコンデンサ。
(1) A composite dielectric coating layer consisting of polyphenylene oxide, inorganic fine powder, and organic peroxide is applied to both sides or one side of a double-sided metallized plastic film, leaving the electrode extension part on the image side in the width direction. 1. A metallized plastic film capacitor characterized in that metallicon electrodes are formed on both sides by laminating or winding the metallized plastic film capacitor.
(2)複合誘電体塗工層の塗工時の無機微粉末の含有量
が20〜80wt%,有機過酸化物の含有量がポリフェ
ニレンオキサイドに対して0.1〜10.0wt%であ
ることを特徴とする請求項1記載の金属化プラスチック
フィルムコンデンサ。
(2) The content of inorganic fine powder during coating of the composite dielectric coating layer is 20 to 80 wt%, and the content of organic peroxide is 0.1 to 10.0 wt% relative to polyphenylene oxide. The metallized plastic film capacitor of claim 1, characterized in that:
(3)無機微粉末が、TiO_2,BaTiO_3,S
rTiO_3,PbTiO_3の単独、あるいは2種以
上を混合したものであることを特徴とする請求項1記載
の金属化プラスチックフィルムコンデンサ。
(3) The inorganic fine powder is TiO_2, BaTiO_3, S
The metallized plastic film capacitor according to claim 1, characterized in that it is composed of rTiO_3 and PbTiO_3 alone or in combination of two or more thereof.
JP12699789A 1989-05-19 1989-05-19 Metallized plastic film capacitor Pending JPH02305422A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12699789A JPH02305422A (en) 1989-05-19 1989-05-19 Metallized plastic film capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12699789A JPH02305422A (en) 1989-05-19 1989-05-19 Metallized plastic film capacitor

Publications (1)

Publication Number Publication Date
JPH02305422A true JPH02305422A (en) 1990-12-19

Family

ID=14949114

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12699789A Pending JPH02305422A (en) 1989-05-19 1989-05-19 Metallized plastic film capacitor

Country Status (1)

Country Link
JP (1) JPH02305422A (en)

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