JPH06349321A - Conductive paste - Google Patents

Conductive paste

Info

Publication number
JPH06349321A
JPH06349321A JP13582693A JP13582693A JPH06349321A JP H06349321 A JPH06349321 A JP H06349321A JP 13582693 A JP13582693 A JP 13582693A JP 13582693 A JP13582693 A JP 13582693A JP H06349321 A JPH06349321 A JP H06349321A
Authority
JP
Japan
Prior art keywords
conductive paste
silver
holes
resistance
substantially spherical
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
JP13582693A
Other languages
Japanese (ja)
Inventor
秀次 ▲くわ▼島
Hideji Kuwashima
Shozo Yamana
章三 山名
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.)
Showa Denko Materials Co Ltd
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP13582693A priority Critical patent/JPH06349321A/en
Publication of JPH06349321A publication Critical patent/JPH06349321A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an excellent conductivity and a low cost, to reduce the insulating resistance between through holes, and to reduce the using amount of silver, by including a specific almost spherical form of minute particles, a copper powder, and a nitrophenyl hydrazine genus, to a conductive paste. CONSTITUTION:(A) 20 to 60wt% of almost a spherical form of minute particles whose particle size is less than 30mum, which consist of a plastic or an organic material, on whose surface a nickel plating with the thickness 1 to 3mum is applied, and a silver plating with the thickness 0.5 to 1mum is applied thereover, (B) a copper powder with the particle size less than 20mum, and (C) 0.05 to 2.0wt% of a nitrophenyl hydrazine genus of one sort or more selected from 3-nitrophenyl hydrazine and 3, 5-dinitrophenyl hydrazines, are mixed making the volume ratio of the A component and the B component 10:1 to 1:5.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は電気回路形成用の導電ペ
ーストに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a conductive paste for forming an electric circuit.

【0002】[0002]

【従来の技術】従来、プリント配線板、電子部品等の配
線導体を形成する方法として、導電性に優れた銀粉を含
有するペーストを塗布又は印刷して形成する方法が一般
的に知られている。
2. Description of the Related Art Conventionally, as a method for forming a wiring conductor of a printed wiring board, an electronic component or the like, a method of applying or printing a paste containing silver powder having excellent conductivity is generally known. .

【0003】[0003]

【発明が解決しようとする課題】銀粉を用いた導電ペー
ストは導電性が良好なことから印刷配線板、電子部品等
の配線導体や電極として使用されているが、これらは高
温多湿の雰囲気下で電界が印加されると、配線導体や電
極にマイグレーションと称する銀の電析が生じ電極間又
は配線間が短絡するという欠点が生じる。このマイグレ
ーションを防止するための方策はいくつか行われてお
り、導体の表面に防湿塗料を塗布するか又は導電ペース
トに窒素化合物などの腐食抑制剤を添加するなどの方策
が検討されているが十分な効果が得られるものではなか
った。
Since a conductive paste using silver powder has good conductivity, it is used as a wiring conductor or an electrode for printed wiring boards, electronic parts, etc., but these are used under a high temperature and high humidity atmosphere. When an electric field is applied, there is a drawback that a wiring conductor or an electrode is electro-deposited with silver called migration and a short circuit occurs between electrodes or between wirings. Several measures have been taken to prevent this migration, and measures such as applying a moisture-proof coating to the surface of the conductor or adding a corrosion inhibitor such as a nitrogen compound to the conductive paste have been studied, but it is sufficient. It was not possible to obtain such an effect.

【0004】また、導通抵抗の良好な導体を得るには銀
粉の配合量を多くしなければならず、銀粉が高価である
ことから導電ペーストも高価になるという欠点があっ
た。
Further, in order to obtain a conductor having good conduction resistance, it is necessary to increase the amount of silver powder blended, and the silver paste is expensive, so that the conductive paste is also expensive.

【0005】本発明はかかる欠点のない導電ペーストを
提供するものである。
The present invention provides a conductive paste that does not have such drawbacks.

【0006】[0006]

【課題を解決するための手段】本発明は表面にニッケル
メッキが施され、さらにその上面に銀メッキが施された
粒径が30μm以下の略球形の微粒子、銅粉及びニトロ
フェニルヒドラジン類を含む導電ペーストに関する。
The present invention includes substantially spherical fine particles having a particle diameter of 30 μm or less, copper particles and nitrophenylhydrazines, the surfaces of which are nickel-plated and the upper surfaces of which are silver-plated. Regarding conductive paste.

【0007】本発明における略球形の微粒子とはプラス
チック又は無機材料からなるもので、その形状は大略球
形であり少なくともその長径が30μm以下であればよ
く、導電性であればより好ましい。なお粒径が30μm
を越える略球形の微粒子を用いると印刷時にスクリーン
が目詰りしたり、ペーストの伸びが悪くなり印刷性が劣
るなどの欠点が生じる。略球形の微粒子の表面に施すニ
ッケルメッキの厚さは特に制限はないが1〜2μmであ
ればよく、またニッケルメッキの上面に施す銀メッキは
厚さが厚いほど導電性を高め易いが、コストが高くなる
ので0.5〜1μmの厚さで十分である。なおニッケル
メッキ及び銀メッキの処理方法については公知の方法が
採用され特に制限はない。
The substantially spherical fine particles in the present invention are made of a plastic or an inorganic material, and the shape thereof is a substantially spherical shape, and the major axis thereof may be at least 30 μm or less, and it is more preferable if it is conductive. The particle size is 30 μm
The use of substantially spherical fine particles exceeding the range causes drawbacks such as clogging of the screen during printing, poor elongation of the paste and poor printability. The thickness of the nickel plating applied to the surface of the substantially spherical fine particles is not particularly limited, but may be 1 to 2 μm, and the thicker the silver plating applied to the upper surface of the nickel plating, the easier it is to increase the conductivity, but the cost is low. The thickness is 0.5 to 1 μm, which is sufficient. The nickel plating and silver plating treatment methods are well known and are not particularly limited.

【0008】銅粉はその粒径が小さいほど好ましく、例
えば20μm以下であることが好ましく、10μm以下
であれば略球形の微粒子の粒間に均一に分散されやすい
のでさらに好ましい。略球形の微粒子と銅粉の比率は導
体の抵抗とマイグレーションの防止の点から体積比で1
0:1〜1:5(略球形の微粒子:銅粉)であることが
好ましい。ニトロフェニルヒドラジン類としては、3−
ニトロフェニルヒドラジン及び3,5−ジニトロフェニ
ルヒドラジンの一種又はこれらの混合物を用いることが
好ましい。ニトロフェニルヒドラジン類の含有量は導電
ペーストの固形分に対してマイグレーションの防止と経
済性から0.05〜2.0重量%であることが好まし
い。
The smaller the particle size of the copper powder is, the more preferable it is, for example, 20 μm or less is preferable, and the particle size of 10 μm or less is more preferable because it is likely to be uniformly dispersed among the particles of the substantially spherical fine particles. The ratio of the substantially spherical fine particles to the copper powder is 1 by volume in terms of resistance of the conductor and prevention of migration.
It is preferably from 0: 1 to 1: 5 (substantially spherical fine particles: copper powder). As nitrophenylhydrazines, 3-
It is preferable to use one or a mixture of nitrophenylhydrazine and 3,5-dinitrophenylhydrazine. The content of the nitrophenylhydrazines is preferably 0.05 to 2.0% by weight with respect to the solid content of the conductive paste from the viewpoint of preventing migration and economy.

【0009】導電ペーストは上記の材料以外に液状のエ
ポキシ樹脂、フェノール樹脂、不飽和ポリエステル樹脂
等の有機質の接着剤成分及び必要に応じてテルピネオー
ル、エチルカルビトール、カルビトールアセテート等の
溶媒、微小黒鉛粉末、ベンゾチアゾール、ベンズイミダ
ゾール等の腐食抑制剤などを含有する。略球形の微粒子
の含有量は導電ペーストの固形分に対して導体の抵抗と
経済性から20〜60重量%であることが好ましく、3
0〜60重量%であればさらに好ましい。
In addition to the above materials, the conductive paste is an organic adhesive component such as liquid epoxy resin, phenol resin and unsaturated polyester resin, and if necessary, a solvent such as terpineol, ethyl carbitol and carbitol acetate, and fine graphite. It contains powders, corrosion inhibitors such as benzothiazole and benzimidazole. The content of the substantially spherical fine particles is preferably 20 to 60% by weight in terms of the resistance of the conductor and the economical efficiency with respect to the solid content of the conductive paste.
More preferably, it is 0 to 60% by weight.

【0010】[0010]

【実施例】以下本発明の実施例を説明する。 実施例1 平均粒径が20μmで最大径が28μmのポリスチレン
製の略球形の微粒子(日立化成工業製)100gを、無
水クロム酸を400g/リットル及び硫酸を350g/
リットル含む65℃の混酸中で10分間表面処理した。
次にこの略球形の微粒子を水洗、乾燥後、塩化第一スズ
を10g/リットル及び塩酸を5mリットル/リットル
含む23℃の水溶液に3分間浸漬したのちイオン交換水
で洗浄し、さらに塩化パラジウムを0.2g/リットル
及び塩酸を2mリットル/リットル含む30℃の水溶液
に3分間浸漬したのちイオン交換水で洗浄し、次いで8
0℃に加熱したニッケルメッキ浴(日本カニゼン製、商
品名S680)に15分間浸漬して厚さが1.5μmの
ニッケルメッキを施した。この後ニッケルメッキを施し
た略球形の微粒子を水洗、乾燥後、アンモニア水溶液を
添加して透明化させた硝酸銀を50g/リットル含む1
リットルの水溶液中に撹拌して分散化させながら該水溶
液をガスバーナーで弱く加熱し、ニッケルメッキの上面
に厚さが0.6μmの銀メッキを施したニッケルメッキ
−銀メッキ付着略球形の微粒子を得た。
EXAMPLES Examples of the present invention will be described below. Example 1 100 g of polystyrene substantially spherical fine particles (made by Hitachi Chemical Co., Ltd.) having an average particle diameter of 20 μm and a maximum diameter of 28 μm, 400 g / liter of chromic anhydride and 350 g / liter of sulfuric acid.
The surface treatment was carried out for 10 minutes in a mixed acid containing 65 liters at 65 ° C.
Next, the substantially spherical fine particles are washed with water, dried, immersed in an aqueous solution of stannous chloride of 10 g / liter and hydrochloric acid of 5 ml / liter at 23 ° C. for 3 minutes and then washed with ion-exchanged water, and further palladium chloride is added. Immersion in an aqueous solution containing 0.2 g / liter and 2 ml / liter of hydrochloric acid at 30 ° C. for 3 minutes, followed by washing with ion-exchanged water, then 8
It was immersed in a nickel plating bath (manufactured by Nippon Kanigen, trade name S680) heated to 0 ° C. for 15 minutes to apply a nickel plating having a thickness of 1.5 μm. After this, the nickel-plated substantially spherical fine particles are washed with water, dried, and then added with an aqueous ammonia solution to make the silver nitrate transparent and contain 50 g / liter of silver nitrate.
While stirring and dispersing in an aqueous solution of 1 liter, the aqueous solution is heated weakly with a gas burner, and nickel-plated silver-plated substantially spherical fine particles having silver plating of 0.6 μm thick on the upper surface of nickel plating are formed. Obtained.

【0011】一方ビスフェノールA型エポキシ樹脂(油
化シェルエポキシ製、商品名エピコート834)60重
量部及びビスフェノールA型エポキシ樹脂(油化シェル
エポキシ製、商品名エピコート828)40重量部を予
め加温溶解させ、次いで室温に冷却した後2エチル4メ
チルイミダゾール(四国化成製)5重量部、3−ニトロ
フェニルヒドラジン(和光純薬製、試薬)1重量部、エ
チルカルビトール(和光純薬製、試薬)20重量部及び
ブチルセロソルブ(和光純薬製、試薬)20重量部を加
えて均一に混合して樹脂組成物とし、この樹脂組成物1
46gに上記で得たニッケルメッキ−銀メッキ付着略球
形の微粒子を500g及び銅粉(福田金属箔粉製、商品
名SPC−4)を200g加えて撹拌らいかい機及び3
本ロールで均一に分散して導電ペーストを得た。
On the other hand, 60 parts by weight of bisphenol A type epoxy resin (made by oiled shell epoxy, trade name Epicoat 834) and 40 parts by weight of bisphenol A type epoxy resin (made by oiled shell epoxy, trade name Epicoat 828) are heated and dissolved in advance. Then, after cooling to room temperature, 5 parts by weight of 2 ethyl 4-methyl imidazole (manufactured by Shikoku Kasei), 1 part by weight of 3-nitrophenylhydrazine (manufactured by Wako Pure Chemical Industries, reagent), ethyl carbitol (manufactured by Wako Pure Chemical Industries, reagent) This resin composition 1 was prepared by adding 20 parts by weight and 20 parts by weight of butyl cellosolve (manufactured by Wako Pure Chemical Industries, reagent) and mixing them uniformly to obtain a resin composition.
To 46 g, 500 g of the nickel-plated-silver-plated substantially spherical fine particles obtained above and 200 g of copper powder (Fukuda Metal Foil Powder, trade name SPC-4) were added, and a stirring mixer and 3
This roll was uniformly dispersed to obtain a conductive paste.

【0012】次に上記で得た導電ペーストを厚さが1.
6mmで直径が0.8mm(φ)のスルーホールを形成
した紙フェノール銅張積層板(日立化成工業製、商品名
MCL−437F)に図1に示すテストパターンを印刷
すると共にこれをスルーホール1に充てんしたものを大
気中で60℃30分さらに160℃30分の条件で加熱
処理して配線板を得た。なお図1において2は紙フェノ
ール銅張積層板である。次に得られた配線板の抵抗を測
定した。その結果銅箔の抵抗を除いたスルーホール1の
抵抗は40mΩ/穴であり、隣り合うスルーホール間の
絶縁抵抗は108Ω以上であった。該配線板の冷熱衝撃
試験を実施した結果、スルーホール1の抵抗は62mΩ
/穴であった。また該配線板の湿中負荷試験を実施した
結果、スルーホール間の絶縁抵抗は108Ω以上であっ
た。なお、冷熱試験条件は125℃30分〜−65℃3
0分を100サイクル行い、湿中負荷試験は40℃90
%RH中、隣り合うライン間に50Vの電圧を印加して
1000時間保持した。
Next, the conductive paste obtained above has a thickness of 1.
The test pattern shown in FIG. 1 is printed on a paper phenol copper clad laminate (Hitachi Chemical Co., Ltd., trade name MCL-437F) in which a through hole having a diameter of 6 mm and a diameter of 0.8 mm (φ) is formed. The wiring board was obtained by heat-treating the material filled in the above in the atmosphere under the conditions of 60 ° C. for 30 minutes and 160 ° C. for 30 minutes. In FIG. 1, 2 is a paper phenol copper clad laminate. Next, the resistance of the obtained wiring board was measured. As a result, the resistance of the through hole 1 excluding the resistance of the copper foil was 40 mΩ / hole, and the insulation resistance between adjacent through holes was 10 8 Ω or more. As a result of the thermal shock test of the wiring board, the resistance of the through hole 1 is 62 mΩ.
/ It was a hole. Moreover, as a result of performing a wet and medium load test on the wiring board, the insulation resistance between the through holes was 10 8 Ω or more. The cold heat test conditions are 125 ° C. 30 minutes to −65 ° C. 3
100 cycles of 0 minutes, 90 ° C for humidity and medium load test
In% RH, a voltage of 50 V was applied between adjacent lines and held for 1000 hours.

【0013】実施例2 3−ニトロフェニルヒドラジンに代えて3,5−ジニト
ロフェニルヒドラジン(和光純薬製、試薬)を用いた以
外は実施例1と同様の工程を経て得た樹脂組成物146
gに実施例1で用いたニッケルメッキ−銀メッキ付着略
球形の微粒子を450g及び銅粉を350g加えて実施
例1と同様の方法で均一に混合分散して導電ペーストを
得た。以下実施例1と同様の工程を経て配線板を作製し
てその特性を評価した。その結果、スルーホールの抵抗
は33mΩ/穴であり、スルーホール間の絶縁抵抗は1
8Ω以上であった。また該配線板の冷熱衝撃試験を実
施した結果、スルーホールの抵抗は47mΩ/穴であ
り、湿中負荷試験の結果では、スルーホール間の絶縁抵
抗は108Ω以上であった。
Example 2 A resin composition 146 obtained through the same steps as in Example 1 except that 3,5-dinitrophenylhydrazine (a reagent manufactured by Wako Pure Chemical Industries, Ltd.) was used in place of 3-nitrophenylhydrazine.
To g, 450 g of nickel-plated silver-plated substantially spherical fine particles and 350 g of copper powder used in Example 1 were added and uniformly mixed and dispersed in the same manner as in Example 1 to obtain a conductive paste. A wiring board was manufactured through the same steps as in Example 1 and the characteristics thereof were evaluated. As a result, the resistance of the through holes is 33 mΩ / hole, and the insulation resistance between the through holes is 1
Was 0 8 Ω or more. As a result of the thermal shock test of the wiring board, the resistance of the through holes was 47 mΩ / hole, and the result of the wet and medium load test showed that the insulation resistance between the through holes was 10 8 Ω or more.

【0014】実施例3 実施例1で得た樹脂組成物146gに実施例1で用いた
ニッケルメッキ−銀メッキ付着略球形の微粒子を320
g及び銅粉を200g加えて実施例1と同様の方法で均
一に混合分散して導電ペーストを得た。以下実施例1と
同様の工程を経て配線板を作製してその特性を評価し
た。その結果、スルーホールの抵抗は48mΩ/穴であ
り、スルーホール間の絶縁抵抗は108Ω以上であっ
た。また該配線板の冷熱衝撃試験を実施した結果、スル
ーホールの抵抗は70mΩ/穴であり、湿中負荷試験の
結果では、スルーホール間の絶縁抵抗は108Ω以上で
あった。
Example 3 To 146 g of the resin composition obtained in Example 1, 320 particles of substantially spherical particles attached to nickel plating-silver plating used in Example 1 were added.
g and 200 g of copper powder were added and uniformly mixed and dispersed in the same manner as in Example 1 to obtain a conductive paste. A wiring board was manufactured through the same steps as in Example 1 and the characteristics thereof were evaluated. As a result, the resistance of the through holes was 48 mΩ / hole, and the insulation resistance between the through holes was 10 8 Ω or more. As a result of the thermal shock test of the wiring board, the resistance of the through holes was 70 mΩ / hole, and the result of the wet and medium load test showed that the insulation resistance between the through holes was 10 8 Ω or more.

【0015】比較例1 3−ニトロフェニルヒドラジンを添加しない以外は実施
例1と同様の方法で得た樹脂組成物145gにフレーク
状銀粉(徳力化学研究所製、商品名TCG−1)を25
0g加えて実施例1と同様の方法で均一に混合分散して
導電ペーストを得た。以下実施例1と同様の工程を経て
配線板を作製してその特性を評価した。その結果、スル
ーホールの抵抗は48mΩ/穴であり、スルーホール間
の絶縁抵抗は108Ω以上であった。また該配線板の冷
熱衝撃試験を実施した結果、スルーホールの抵抗は67
mΩ/穴であり、湿中負荷試験の結果では、スルーホー
ル間の絶縁抵抗は配線板5枚のうち1枚107Ω台に低
下しているものがあった。
Comparative Example 1 To 145 g of a resin composition obtained by the same method as in Example 1 except that 3-nitrophenylhydrazine was not added, 25 flakes of silver powder (TCG-1 manufactured by Tokuriki Kagaku Kenkyusho) were used.
0 g was added and uniformly mixed and dispersed in the same manner as in Example 1 to obtain a conductive paste. A wiring board was manufactured through the same steps as in Example 1 and the characteristics thereof were evaluated. As a result, the resistance of the through holes was 48 mΩ / hole, and the insulation resistance between the through holes was 10 8 Ω or more. Further, as a result of the thermal shock test of the wiring board, the resistance of the through hole was 67.
It was mΩ / hole, and as a result of the wet and medium load test, in some cases, the insulation resistance between the through holes was reduced to the order of 10 7 Ω per 5 wiring boards.

【0016】比較例2 3−ニトロフェニルヒドラジンを添加しない以外は実施
例1と同様の方法で得た樹脂組成物145gに実施例1
で用いたニッケルメッキ−銀メッキ付着略球形の微粒子
を170g加えて実施例1と同様の方法で均一に混合分
散して導電ペーストを得た。以下実施例1と同様の工程
を経て配線板を作製してその特性を評価した。その結
果、スルーホールの抵抗は180mΩ/穴であり、スル
ーホール間の絶縁抵抗は108Ω以上であった。また該
配線板の冷熱衝撃試験を実施した結果、スルーホールの
抵抗は450mΩ/穴となり、冷熱衝撃試験前に比較し
て2.5倍の増加となった。また湿中負荷試験の結果で
は、スルーホール間の絶縁抵抗は108Ω以上であっ
た。
Comparative Example 2 145 g of a resin composition obtained in the same manner as in Example 1 except that 3-nitrophenylhydrazine was not added.
In the same manner as in Example 1, 170 g of the nickel-plated-silver-plated substantially spherical fine particles used in Example 1 were added and uniformly dispersed to obtain a conductive paste. A wiring board was manufactured through the same steps as in Example 1 and the characteristics thereof were evaluated. As a result, the resistance of the through holes was 180 mΩ / hole, and the insulation resistance between the through holes was 10 8 Ω or more. As a result of a thermal shock test of the wiring board, the resistance of the through hole was 450 mΩ / hole, which was 2.5 times as much as that before the thermal shock test. In addition, as a result of the humidity and medium load test, the insulation resistance between the through holes was 10 8 Ω or more.

【0017】[0017]

【発明の効果】本発明になる導電ペーストは配線板にお
けるスルーホールの抵抗が実用レベルの導電ペーストで
あり、また湿中負荷試験後におけるスルーホール間の絶
縁抵抗の低下が小さく、さらにニッケルメッキ−銀メッ
キ付着略球形の微粒子を使用することにより銀の使用量
を少なくできるなど経済的にも優れた導電ペーストであ
る。
INDUSTRIAL APPLICABILITY The conductive paste according to the present invention is a conductive paste in which the resistance of the through holes in the wiring board is at a practical level, the insulation resistance between the through holes after the wet and medium load test is small, and the nickel plating is It is a conductive paste that is economically excellent in that the amount of silver used can be reduced by using silver-plated substantially spherical fine particles.

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

【図1】紙フェノール銅張積層板に導電ペーストを印刷
すると共にスルーホールに充てんした状態を示す平面図
である。
FIG. 1 is a plan view showing a state in which a conductive paste is printed on a paper phenol copper clad laminate and the through holes are filled.

【符号の説明】[Explanation of symbols]

1 スルーホール 2 紙フェノール銅張積層板 1 Through hole 2 Paper phenol copper clad laminate

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 表面にニッケルメッキが施され、さらに
その上面に銀メッキが施された粒径が30μm以下の略
球形の微粒子、銅粉及びニトロフェニルヒドラジン類を
含む導電ペースト。
1. A conductive paste containing nickel particles on the surface and silver particles on the upper surface, and substantially spherical fine particles having a particle diameter of 30 μm or less, copper powder, and nitrophenylhydrazines.
【請求項2】 ニトロフェニルヒドラジン類が3−ニト
ロフェニルヒドラジン及び3,5−ジニトロフェニルヒ
ドラジンの一種又はこれらの混合物である請求項1記載
の導電ペースト。
2. The conductive paste according to claim 1, wherein the nitrophenylhydrazine is one of 3-nitrophenylhydrazine and 3,5-dinitrophenylhydrazine or a mixture thereof.
JP13582693A 1993-06-07 1993-06-07 Conductive paste Pending JPH06349321A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13582693A JPH06349321A (en) 1993-06-07 1993-06-07 Conductive paste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13582693A JPH06349321A (en) 1993-06-07 1993-06-07 Conductive paste

Publications (1)

Publication Number Publication Date
JPH06349321A true JPH06349321A (en) 1994-12-22

Family

ID=15160699

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13582693A Pending JPH06349321A (en) 1993-06-07 1993-06-07 Conductive paste

Country Status (1)

Country Link
JP (1) JPH06349321A (en)

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