JPS5842651A - Electrically conductive paste - Google Patents

Electrically conductive paste

Info

Publication number
JPS5842651A
JPS5842651A JP13967581A JP13967581A JPS5842651A JP S5842651 A JPS5842651 A JP S5842651A JP 13967581 A JP13967581 A JP 13967581A JP 13967581 A JP13967581 A JP 13967581A JP S5842651 A JPS5842651 A JP S5842651A
Authority
JP
Japan
Prior art keywords
resin
prepolymer
solder
conductive
copper powder
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
JP13967581A
Other languages
Japanese (ja)
Inventor
Masayuki Saito
雅之 斉藤
Hiroshi Ohira
洋 大平
Teru Okunoyama
奥野山 輝
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.)
Toshiba Chemical Products Co Ltd
Toshiba Corp
Kyocera Chemical Corp
Original Assignee
Toshiba Chemical Products Co Ltd
Toshiba Corp
Toshiba Chemical Corp
Tokyo Shibaura Electric 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 Toshiba Chemical Products Co Ltd, Toshiba Corp, Toshiba Chemical Corp, Tokyo Shibaura Electric Co Ltd filed Critical Toshiba Chemical Products Co Ltd
Priority to JP13967581A priority Critical patent/JPS5842651A/en
Publication of JPS5842651A publication Critical patent/JPS5842651A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide paste which can form a cured surface having excellent printability and good solder wettability and solder adherability, and is useful for a conductor part of a printed circuit of electronic parts, a terminal part of electrodes etc., by closely filling a curable resin prepolymer having a specified MW with copper powder. CONSTITUTION:A solvent is added to a mixture consisting of 5-10wt% resin (A) composed mainly of a resin prepolymer having a number-average MW of 10,000 or above capable of reticulating after curing and 95-90wt% copper powder to obtain an electrically conductive paste. An insulating substrate is printed with this paste by means of screen printing. The resin component A is reticulated to form a cured surface which is then coated with molten solder to form an electrically conductive surface. Examples of said resin components A are a mixture of an OH group-contg. prepolymer such as a phenoxy resin and an amino resin etherified with a lower alochol, and a mixture of an ultraviolet curing resin prepolymer and a catalyst.

Description

【発明の詳細な説明】 この発明は、印刷性を良好にし且つ形成される硬化1i
ioFiんだ濡れ性を良好にする導電性は−ストに係り
、特に予定される硬化9面がはんだ付着及びその密着性
を良好にするよう改良された導電性イーストに関する。
DETAILED DESCRIPTION OF THE INVENTION This invention improves printability and cures 1i
The electrical conductivity that improves the wettability of ioFi relates to the conductive yeast, and particularly to the electrically conductive yeast whose intended hardening surface is improved to improve solder adhesion and its adhesion.

この導電性イーストは、特定された硬化性樹脂のプレポ
リマーに銅粉末を混合したもので、これ會所望基材に印
刷し硬化させた硬化面は、はんだを溶拳被嶺されて導電
面として供される。□この種の導電性ペーストで現在知
られているも(Daミツエノール脂、メランンm脂、キ
シレン樹脂、アルキッドm脂、エポキシ樹脂等数平均分
子量100〜2000@度の合成樹脂プレポリマーの#
M脂シワニス金属粉末を混合混練したものである3、用
いられる樹脂ワニスは塗膜の物理的、化学的安定性など
の使用目的に応じてこれ等の樹脂から選ばれた単独又は
組合わせに溶剤を加えたものでるる。
This conductive yeast is a mixture of copper powder and a prepolymer of a specified curable resin. After printing on the desired substrate and curing the hardened surface, solder is melted onto the hardened surface and used as a conductive surface. Served. □Currently known conductive pastes of this type (synthetic resin prepolymers with a number average molecular weight of 100 to 2000 degrees, such as Da mitsuenol fat, melane m fat, xylene resin, alkyd m fat, and epoxy resin)
3. The resin varnish used is selected from these resins alone or in combination, depending on the purpose of use, such as the physical and chemical stability of the coating film, and a solvent. Ruru is added.

但し粉末の分散性や印刷性を向上さぜるレベリング剤、
消泡剤等の添加剤を更に添加されたものもある。
However, leveling agents that improve powder dispersibility and printability,
Some also contain additives such as antifoaming agents.

このような導電性ペーストは、電子部品の電極或いは導
体部分の印刷回路等王として表面から電気伝導會増る用
途に使用されている。例えばプリント配置[板と厚膜抵
抗体とを組み合わせた混成集積回路基板で杜、導体部分
、抵抗体のit槓端子部分、更には可変抵抗器の導体部
分及び電極端子部分などが対象となる。これ等対象部材
は、近年高性能化、高Wi度化、小屋化、薄型化の傾向
を著しくし、導電性ペーストの@に対しても屯艮が望ま
れるに到っている。
Such conductive pastes are used in applications where electrical conductivity is increased from the surface, such as in printed circuits for electrodes or conductor parts of electronic components. For example, printed layout [a hybrid integrated circuit board that combines a plate and a thick film resistor], the conductor part, the IT terminal part of the resistor, and the conductor part and electrode terminal part of the variable resistor are targeted. In recent years, there has been a marked trend toward higher performance, higher Width, smaller dimensions, and thinner dimensions of these target members, and even conductive pastes have come to be desired.

現行のこれら導電性イーストは、プレポリマーとの混合
体を100重量−にするとき金属粉末の充填量が70〜
80重量%でしかない。ペーストとしての性状が維持さ
れなくなるためこの値以上に充填量音高めることが出来
ないのである。このため、このペーストを印桐後例えば
加熱して形成される硬化面のはんだ付着性に不満があり
、又硬化面に高電気導電性【必景とするような用途に対
して適しない欠点がある。
These current conductive yeasts have a metal powder loading of 70 to 70% when the mixture with prepolymer is 100% by weight.
It is only 80% by weight. Since the properties as a paste are no longer maintained, the filling volume cannot be increased beyond this value. For this reason, there is dissatisfaction with the solder adhesion of the cured surface formed by heating this paste after intaglio, and the cured surface has a drawback that it is not suitable for applications that require high electrical conductivity. be.

この発明は金属粉末、の混合割合を高めるように改良し
た導電性ペーストを提供するもので、即ち111数平均
分子量が10000以上て且つ硬化後に網状化される予
定の樹脂のプレポリ!−管主体とする樹脂分と、導電性
物資として粒径が101以下であシ且つ樹脂分tToわ
せた全量の90〜95重量−を占める銅粉末とを含む混
合体く溶剤tS加し良ものである導電性イースト、及び
(2)11脂脂分が、水酸基管架橋性官能基として備え
るプレポリ!−と、メタノール、エタノール、ブタノー
ルの何れか低級アルコールによりエーテル化されたア建
ノ樹脂とから成る前記11項に記載の導電性イーストに
ある。
The present invention provides a conductive paste improved to increase the mixing ratio of metal powder, that is, a pre-polymer paste of a resin having a 111 number average molecular weight of 10,000 or more and which is to be reticulated after curing. - A mixture containing resin, which is the main component of the tube, and copper powder, which is a conductive substance and has a particle size of 101 or less and accounts for 90 to 95% by weight of the total amount including the resin content tTo, with the addition of a solvent tS. conductive yeast, and (2) 11 fats and fats as a hydroxyl group crosslinkable functional group, prepoly! - and an adenyl resin etherified with a lower alcohol such as methanol, ethanol, or butanol.

この発明で樹脂分は、数平均分子量10000以上のプ
レポリマーのみから成ってよ〈又ア建ノ樹脂を併せて含
むものであってもよい、混合体は樹脂分と鋼看末O他例
えばレベリング剤、消泡剤勢添加剤を添加されたもので
あってもよろしい。
In this invention, the resin component consists only of a prepolymer having a number average molecular weight of 10,000 or more (it may also contain a building resin), and the mixture consists of a resin component and a steel powder, for example, a leveling resin. It is also possible to add antifoaming agents and antifoam additives.

こ\で樹脂分の主体となるプレポリマーは数平均分子量
が10000以上である硬化性樹脂系Oものとした良め
、銅粉末の高密度充填!可能にしながら、イース)0印
刷性及び硬化面のはんだ付着性を倒れも良好にする。も
しもこれが10000未満であるときにはイースト状と
なる高密度充填は出来なくて、ペーストは粘性を失い、
スクリーン印ta等に不適轟となる。このプレポリマー
は主体が数平均分子量Vt10000以上とする例えば
フェノキシ樹脂、ポリブタジェンIf Ml s p−
ビニルフェノールポリマー、ポリエステル樹脂等熱硬化
性樹脂系であるものであって良い。但しこれ岬のプレポ
リ!−は、メタノール、エタノール、ブタノールの倒れ
かによりエーテル化された架橋剤のアさノ樹脂管混合し
又は反応させて樹脂分とされ、80℃〜260℃で硬化
される。又このプレポリマーを数平均分子量10000
以上の紫外線硬化mtm脂、例えば1.2ポリブタジエ
ン樹脂、エポキシ変性アクリル樹脂、インシフエノン等
としてもよい。この場金にはmyit分としてはプレポ
リ!−〇みでよく架橋剤を添加する1Fはないが触媒を
別に加えることになる。そして硬化面は紫外線照射によ
って得られることになる。
In this case, the prepolymer that is the main resin component is a curable resin type O with a number average molecular weight of 10,000 or more, and it is packed with high density copper powder! While making it possible to improve the ease of printing and the solder adhesion of the cured surface. If this value is less than 10,000, it will not be possible to form a yeast-like dense filling, and the paste will lose its viscosity.
It becomes inappropriate for screen markings, etc. This prepolymer mainly has a number average molecular weight Vt of 10,000 or more, such as phenoxy resin, polybutadiene If Ml sp-
It may be a thermosetting resin such as vinyl phenol polymer or polyester resin. However, this is a pre-poly of the cape! - is made into a resin by mixing or reacting an etherified crosslinking agent with methanol, ethanol, and butanol, and curing at 80°C to 260°C. Moreover, this prepolymer has a number average molecular weight of 10,000.
The above UV-curable MTM resins, such as 1.2 polybutadiene resin, epoxy-modified acrylic resin, insiphenone, etc., may also be used. In this case, the myit portion is pre-policed! - Although there is no 1F in which a crosslinking agent is often added, a catalyst must be added separately. A hardened surface is then obtained by irradiation with ultraviolet rays.

このような樹脂分に対し銅粉末は全体の90〜95重量
−を占めるように混合させることが出来る。
Copper powder can be mixed so as to account for 90 to 95% of the total weight of the resin.

この銅粉末混合量t90重量−未満にすると、硬化面の
社んだ付着性を良好にしない。又95重量−を超させる
時には、基材への密着性を不良にし、硬化後に脆弱にす
る。銅粉末形状は樹枝状、粒状。
If the amount of copper powder mixed is less than t90 by weight, the adhesion of the hardened surface to the cured surface will not be good. If the weight exceeds 95%, the adhesion to the substrate becomes poor and the resin becomes brittle after curing. The copper powder shape is dendritic and granular.

フレーク状等倒れであっても良く、又形状を単一にし、
或い社混合して用いてもよい。但し粒子の大きさ#i−
<−スト化【考慮して平均粒径lOμ以下とする。
It may be flattened like flakes, or it may have a single shape.
Alternatively, they may be used in combination. However, particle size #i-
<-Station [Considering the average particle diameter is set to be less than lOμ.

この導電性は−ス)l印刷又は塗布する相手基材は、フ
ェノール樹脂、エポキシ樹脂、ポリイミド檎脂、ポリエ
ステル樹脂、ポリエチレン11脂等掬脂から成るか、こ
れ等amとガラス繊維、紙。
The conductive material to be printed or coated is made of resin such as phenol resin, epoxy resin, polyimide resin, polyester resin, polyethylene 11 resin, etc., or is made of resin such as phenol resin, epoxy resin, polyimide resin, or resin, glass fiber, or paper.

不織布、布勢會組舎わせた絶縁性材から成るか。Is it made of non-woven fabric or fabric-assembled insulating material?

金属例えばアル4ニウム、鉄、ステンレス、銅轡板又は
フィルム上に1例えばアクリル樹脂、エポキシ樹脂、ポ
リエチレンllI4m1岬を被侵した被覆材から成るか
、又はシリカ、アル建す、アル(ノシリケート勢無機絶
縁性材から成るものであって良い。これ等基材面にこの
導電性は−ス)tEI−ルコータ、スクリーン印刷尋に
よシ印刷又はディッピング其の他によ多塗布する。
It consists of coating materials such as acrylic resins, epoxy resins, polyethylene llI4m1 capes on metals such as aluminum, iron, stainless steel, copper cladding or films, or silica, aluminum-based, al(nosilicate-based) coatings. The conductive material may be made of an inorganic insulating material.The conductive material is coated on the surface of the substrate by a method such as an EL coater, screen printing, dipping or dipping.

導電性イーストの硬化は樹脂分の主体が熱硬化性樹脂で
あるとき80〜250 UK、空気或いは窒素の如き不
活性ガス雰囲気中で昇温させる。この導電性イーストの
樹脂分が、例えば架硫剤としてエーテル化されたアミノ
樹脂を含み、ポリシタリエンM 4111 、?−ビニ
ルフェノール樹脂又はポリエステル樹脂等の何れか主体
樹脂とから成るものであるとき、加熱により架橋剤と主
体樹脂の水酸基とが縮合反応を起こして、三次元網状構
造を形成する。この過程で銅粉は相互に接触して連結さ
れる1、そして導電性を充分にするためKii!!化面
にはんだt溶aさせて被覆する。この硬化面ははんだ−
れ性【良好にし且つはんだ付着性を良好にする。
When the resin component is mainly a thermosetting resin, the conductive yeast is cured by raising the temperature to 80 to 250 UK in an inert gas atmosphere such as air or nitrogen. The resin component of this conductive yeast contains, for example, an etherified amino resin as a cross-sulfurizing agent, and polycitaryene M 4111, ? - When the resin is composed of a main resin such as a vinylphenol resin or a polyester resin, heating causes a condensation reaction between the crosslinking agent and the hydroxyl groups of the main resin to form a three-dimensional network structure. In this process, the copper powders are brought into contact with each other and connected 1, and in order to ensure sufficient electrical conductivity, Kii! ! The exposed surface is coated with solder. This hardened surface is solder-
Good solderability and good solder adhesion.

仁01m由は明らかでないが、架橋剤としての7ミノ樹
脂とはんだとの相互作用が、はんだtaじく性賓を凌駕
丁ゐものと思われる。このため良好な導電面が得られ、
例えば各種実装品【結合させた印刷回路とすることが出
来る。
The reason for this is not clear, but it is thought that the interaction between the 7-mino resin as a cross-linking agent and the solder is what surpasses the soldering properties of the guests. Therefore, a good conductive surface is obtained,
For example, various mounted products [combined printed circuits] can be used.

この導電性イーストの硬化面にはんだeiwai被覆す
るKは溶融はんだ浴Kil触させるとよい。或いははん
だ又ははんだクリームt−硬化面上において加熱溶融し
てもよろしい。はんだは錫、鉛はんだ組成の@、これに
更に銀、銅尋を配合した組成のもの、錫単独組成のもの
勢であって嵐い。又硬化1fK#fんだ管被覆する際は
んだフラックス管適用することもさし支えない。
The hardened surface of the conductive yeast is preferably coated with solder in a molten solder bath. Alternatively, solder or solder cream may be heated and melted on the hardened surface. The solder is composed of tin and lead solder, those containing silver and copper fat, and those containing only tin. It is also possible to apply a solder flux tube when coating the cured 1fK#f solder tube.

以下II!論例につ−て述べる。Below is II! Let's talk about examples.

11)平均粒1110jIの電解銅粉[−94重量部と
、樹脂分として数平均分子量1400Gのフェノ中シ樹
脂5重量部及びメチルエーテル化メランン樹脂1重量部
と、溶剤としてフェノキシ樹脂に併せられたブチルカル
ピトールアセテ−)15重量部とを七う建ツク羨三本ロ
ールによ)混線して実施例導電性イーストとする。
11) Electrolytic copper powder with an average particle size of 1110JI [-94 parts by weight, 5 parts by weight of phenolic resin with a number average molecular weight of 1400 G as resin component and 1 part by weight of methyl etherified melane resin, combined with phenoxy resin as a solvent] Example conductive yeast was prepared by mixing 15 parts by weight of butyl carpitol acetate (15 parts by weight) using a three-roll roll.

とのば−ストを用い、 180メツシエシトロンスクリ
ーンのスクリーン印刷機によ〉東芝ケ建カル1MKL−
4のエポキシ樹脂から威る基材面に巾1sw全長20a
11のパターンを印刷する。次に雰囲気温度IJiG℃
で1時間加熱反応させる。室1mK冷却後厚さ20sの
イースト硬化面が得られる。
Toshiba Kencal 1MKL-
Width 1sw total length 20a on the base material surface made of 4 epoxy resin
Print 11 patterns. Next, the ambient temperature IJiG℃
Heat and react for 1 hour. After cooling to 1 mK in the chamber, a yeast hardened surface with a thickness of 20 seconds is obtained.

(2]  樹脂分中生体のプレポリ−r −1r数平均
分子量20000のイソフタル酸ポリエステルにかえ、
その他の項については前記例と全く同様にして導電性イ
ース)l形成する。
(2) In the resin component, the biological prepoly-r-1r is replaced with isophthalic acid polyester having a number average molecular weight of 20,000,
Regarding the other terms, the conductive ester is formed in exactly the same manner as in the previous example.

この例についても前記例と同様に4−スト硬化面【作る
In this example as well, a 4-stroke hardened surface is created in the same manner as in the previous example.

両例によ)形成された硬化面全体にはんだフッククス管
塗布後、錫63嚢、銅0.5優のはんだを240℃で溶
融し付着させる。次表にイーストの状態、印刷性、はん
だ付着性にっiてのl[IIJ結釆管示す。
After applying a Fuchs tube of solder to the entire hardened surface formed in both examples, solder containing 63 tin and 0.5 copper is melted at 240° C. and adhered. The following table shows the condition of yeast, printability, and solder adhesion.

この表で比較例として併記されている導電性イースト(
3〕は、実施例+1) K f用したとjitUilの
電解銅粉を94重量−に対し、*脂分として数平均分子
量3800のエポキシ樹脂5,5重量部及びイミダゾー
ル架橋剤0,5重量−と、溶剤としてエポキシ樹脂に用
いられたブチルカルピトールアセテート少量とを混練し
たものである。又同じく導電性2−スト(43if実論
例11)K使用したとfill援の電解銅粉を80重量
IsK対し、樹脂分として実施例(27と同様のプレポ
リマーを適用した例である。
Conductive yeast (
3] is Example + 1) Kf was used and jitUil's electrolytic copper powder was 94% by weight, *5.5 parts by weight of epoxy resin with a number average molecular weight of 3800 as fat and 0.5 parts by weight of imidazole crosslinking agent. and a small amount of butylcarpitol acetate used as a solvent for epoxy resin. This is an example in which the same prepolymer as in Example (27) was applied as the resin component to 80 weight IsK of electrolytic copper powder filled with conductive 2-stroke (43if Practical Example 11) K.

伺れについてもイーストの状態、印刷性、はんだ付着性
を実施例に係ると同様KI!察表示しである。
The state of the yeast, printability, and solder adhesion were also evaluated in the same manner as in the examples. It shows the observation.

table

Claims (1)

【特許請求の範囲】 11+  数平均分子量が10000以上で且つ硬化頓
に網状化される予定の樹脂プレポリマーを主体とする樹
脂分と、導電性物置として粒径が10μ以下でToり且
り樹脂分管あわせた全量Q90〜95重量慢會占める銅
粉末と【含む混合体に溶剤を添加したものであるととt
−特徴とする導電性ペースト (2)  41脂分が、水酸基を架橋性官能基として備
えるプレポリ!−と、メタノール、エタノール。 ブタノールの倒れか低級アルコールによりエーテル化さ
れたアミノ樹脂とから成ることを特徴とする特許請求の
範囲第1項に記載の導電性ペースト
[Claims] 11+ A resin component mainly consisting of a resin prepolymer having a number average molecular weight of 10,000 or more and which is to be reticulated upon curing, and a resin with a particle size of 10 μ or less as a conductive container. If a solvent is added to a mixture containing copper powder and a total weight of Q90 to 95 including the divided tubes,
-Characteristic conductive paste (2) 41 Prepoly whose fat content has hydroxyl groups as crosslinkable functional groups! -, methanol, and ethanol. The conductive paste according to claim 1, characterized in that it is made of butanol or an amino resin etherified with a lower alcohol.
JP13967581A 1981-09-07 1981-09-07 Electrically conductive paste Pending JPS5842651A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13967581A JPS5842651A (en) 1981-09-07 1981-09-07 Electrically conductive paste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13967581A JPS5842651A (en) 1981-09-07 1981-09-07 Electrically conductive paste

Publications (1)

Publication Number Publication Date
JPS5842651A true JPS5842651A (en) 1983-03-12

Family

ID=15250796

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13967581A Pending JPS5842651A (en) 1981-09-07 1981-09-07 Electrically conductive paste

Country Status (1)

Country Link
JP (1) JPS5842651A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60260663A (en) * 1984-06-06 1985-12-23 Toshiba Chem Corp Electrically conductive paste
JPS61243844A (en) * 1985-04-23 1986-10-30 Hitachi Ltd Thermosetting resin composition, laminated sheet and production thereof
JPS6254357U (en) * 1985-09-25 1987-04-04
US5376403A (en) * 1990-02-09 1994-12-27 Capote; Miguel A. Electrically conductive compositions and methods for the preparation and use thereof
US5853622A (en) * 1990-02-09 1998-12-29 Ormet Corporation Transient liquid phase sintering conductive adhesives
JP2015168825A (en) * 2014-03-04 2015-09-28 ヘレウス プレシャス メタルズ ノース アメリカ コンショホーケン エルエルシー solderable conductive polymer thick film composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60260663A (en) * 1984-06-06 1985-12-23 Toshiba Chem Corp Electrically conductive paste
JPH0149390B2 (en) * 1984-06-06 1989-10-24 Toshiba Chem Prod
JPS61243844A (en) * 1985-04-23 1986-10-30 Hitachi Ltd Thermosetting resin composition, laminated sheet and production thereof
JPH0513184B2 (en) * 1985-04-23 1993-02-19 Hitachi Seisakusho Kk
JPS6254357U (en) * 1985-09-25 1987-04-04
JPH0519236Y2 (en) * 1985-09-25 1993-05-20
US5376403A (en) * 1990-02-09 1994-12-27 Capote; Miguel A. Electrically conductive compositions and methods for the preparation and use thereof
US5830389A (en) * 1990-02-09 1998-11-03 Toranaga Technologies, Inc. Electrically conductive compositions and methods for the preparation and use thereof
US5853622A (en) * 1990-02-09 1998-12-29 Ormet Corporation Transient liquid phase sintering conductive adhesives
JP2015168825A (en) * 2014-03-04 2015-09-28 ヘレウス プレシャス メタルズ ノース アメリカ コンショホーケン エルエルシー solderable conductive polymer thick film composition

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