JPS6193505A - Conductive paste - Google Patents

Conductive paste

Info

Publication number
JPS6193505A
JPS6193505A JP21462684A JP21462684A JPS6193505A JP S6193505 A JPS6193505 A JP S6193505A JP 21462684 A JP21462684 A JP 21462684A JP 21462684 A JP21462684 A JP 21462684A JP S6193505 A JPS6193505 A JP S6193505A
Authority
JP
Japan
Prior art keywords
parts
conductive
weight
paste
conductive paste
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.)
Granted
Application number
JP21462684A
Other languages
Japanese (ja)
Other versions
JPH0311484B2 (en
Inventor
大嶽 崇雅子
堀場 保
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.)
Tokai Rika Co Ltd
Original Assignee
Tokai Rika 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 Tokai Rika Co Ltd filed Critical Tokai Rika Co Ltd
Priority to JP21462684A priority Critical patent/JPS6193505A/en
Publication of JPS6193505A publication Critical patent/JPS6193505A/en
Publication of JPH0311484B2 publication Critical patent/JPH0311484B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00Printed circuits
    • H05K1/02Details
    • H05K1/09Use of materials for the conductive, e.g. metallic pattern
    • H05K1/092Dispersed materials, e.g. conductive pastes or inks

Landscapes

  • Paints Or Removers (AREA)
  • Conductive Materials (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は導電性ペースト、特にフェールセーフ(安全故
障〕特性を有する導電性ペーストに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to electrically conductive pastes, particularly electrically conductive pastes with fail-safe properties.

従来の技術 3よび 従来の導電性ペースト、特にカーボンペーストを使用し
た各沖の部材、例えば電子電気機器のキーボードスイッ
チの接点やプリント板導体等においては、誤操作または
何らかの外部要因により高電圧や高温度が印加されると
、通電発熱と被着基体の樹脂部分の放電による絶縁破壊
が進行して炭化導電路が形成され、通電発熱燃焼に至り
、安全上問題となる危険性がある。
Conventional technology 3 and conventional conductive pastes, especially carbon paste, are used in various components such as keyboard switch contacts and printed circuit board conductors of electronic and electrical equipment, which may be subject to high voltage or high temperature due to incorrect operation or some external factor. When this voltage is applied, dielectric breakdown due to current heat generation and discharge of the resin portion of the adhered substrate progresses, and a carbonized conductive path is formed, leading to current heat generation combustion, which may pose a safety problem.

本発明は、従来の導電性ペーストの有する優れた導電性
と被着基体に対する良好な密着性を措うことなく、上記
問題点を解決する導電性ペーストを提供するためになさ
れたものである。
The present invention was made in order to provide a conductive paste that solves the above problems without sacrificing the excellent conductivity and good adhesion to an adherend substrate that conventional conductive pastes have.

即ち本発明は、バインダー樹脂100重量部あたり、導
電性粉末約10〜65重社部および高温で脱水して容量
変化を伴う無機フィラー(以下、無機フィラーという)
約40〜70重1部含有することを特徴とする導電性ペ
ーストに関する。
That is, the present invention uses about 10 to 65 parts of conductive powder per 100 parts by weight of the binder resin and an inorganic filler whose capacity changes when dehydrated at high temperatures (hereinafter referred to as inorganic filler).
The present invention relates to a conductive paste containing 1 part by weight of about 40 to 70 parts.

本発明に使用するバインダー樹脂は従来から導電性ペー
ストのバインダーとして使用されているものから適宜選
定すればよく、特に限定的ではないが、例えばポリビニ
ルブチラール樹脂とフェノールホルムアルデヒドやエポ
キシ樹脂との混合物又は共重合物やアクリル樹脂等が挙
げられる。
The binder resin used in the present invention may be appropriately selected from those conventionally used as binders for conductive pastes, and is not particularly limited. Examples include polymers and acrylic resins.

本発明に使用する導電性ペーストも特に限定的ではなく
、炭素粉末や金属粉末、例えばケッチェンブラックや銅
微粉末等、のいずれであってもよいが、高電圧印加等に
よってトラッキング破壊をある。
The conductive paste used in the present invention is not particularly limited, and may be carbon powder or metal powder, such as Ketjen black or fine copper powder, but tracking breakdown may occur due to high voltage application.

導電性粉末の配合”暑は上記バインダー樹脂100重層
部に対して約10〜65重1部、好ましくは約15〜3
0重着部で、xoM@部以下では十分な導電性が得られ
ず、また65重1部以上になると被着基体に対するペー
ストの密着性もしくは接着性が損なわれる。
The composition of the conductive powder is about 10 to 65 parts by weight, preferably about 15 to 3 parts by weight, per 100 parts by weight of the above binder resin.
If the amount of 0 parts is less than xoM@ part, sufficient conductivity cannot be obtained, and if the part of 65 parts is more than 1 part, the adhesion or adhesion of the paste to the substrate to be adhered will be impaired.

導電性粉末の粒径は例えば炭素粉末の場合はmμのオー
ダーでこのような粒径の導電性炭素粉末が好ましい。
For example, in the case of carbon powder, the particle size of the conductive powder is on the order of mμ, and conductive carbon powder having such a particle size is preferable.

本発明に使用する無機フィラーは高温、例えば約200
°C〜600°Cで脱水して容量変化を伴う充填剤であ
って、前記のような異常発熱事故が発生した場合に、導
電性層に「亀裂」もしくは「脹」をもたらして異常発熱
部分を絶縁体に変えるフェールセーフ作用をする。
The inorganic filler used in the present invention can be used at high temperatures, e.g.
It is a filler that undergoes a change in capacity when dehydrated at a temperature of 600°C to 600°C, and if an abnormal heating accident occurs as described above, it will cause "cracks" or "swelling" in the conductive layer, causing abnormal heating parts. It has a fail-safe effect by converting it into an insulator.

このような無機フィラーとしては、金属水酸化物、例え
ば水酸化マグネシウム、水酸化アルミニウム、水酸化ニ
ッケル、水酸化カルシウム等または含水粘土鉱物、例え
ばバーミキュライト等が挙げられるが、脱水生成物が更
に高温で昇華してその結果亀裂を発生させる水酸化マグ
ネシウムおよび脹を発生させるバーミキュライトが好適
である。
Such inorganic fillers include metal hydroxides, such as magnesium hydroxide, aluminum hydroxide, nickel hydroxide, calcium hydroxide, etc., or hydrated clay minerals, such as vermiculite, but the dehydrated product may be heated to even higher temperatures. Magnesium hydroxide, which sublimes and results in cracking, and vermiculite, which causes swelling, are preferred.

無機フィラーの粒径は通常的0.1〜100μ、好まし
くは約0.1〜10μである。
The particle size of the inorganic filler is usually 0.1 to 100 microns, preferably about 0.1 to 10 microns.

無機フィラーの配合Iは前記バインダー樹脂100重量
部に対して         好ましくは約40〜70
重1部で、40重量部以下では本発明の所期の効果は確
実性に乏しく、70重性 層部以上になると導シペーストとしての接着性が低下す
る。
Blend I of the inorganic filler is preferably about 40 to 70 parts by weight based on 100 parts by weight of the binder resin.
If the amount is 1 part by weight or less than 40 parts by weight, the desired effect of the present invention will not be achieved reliably, and if it exceeds 70 parts by weight, the adhesiveness as a conductive paste will decrease.

本発明による導電性ペーストは所定口の前記のバインダ
ー樹脂、導電性粉末および無機フィラーを適宜の溶剤を
用いて常法によって混練することによって調製される。
The conductive paste according to the present invention is prepared by kneading predetermined amounts of the binder resin, conductive powder, and inorganic filler using a suitable solvent in a conventional manner.

溶剤の使用看は必要最小限にすべきであり、このような
溶剤としてはメチルエチルケトンとエチルアルコールと
の混合物等が例示されるが、メチルエチルケトンとエチ
ルアルコールとの混合?g 剤が一般的である。
The use of solvents should be kept to the minimum necessary. Examples of such solvents include a mixture of methyl ethyl ketone and ethyl alcohol, but a mixture of methyl ethyl ketone and ethyl alcohol? g agent is common.

導電性ペーストの希釈剤としては例えばブチルカルピト
ール等が使用される。
As a diluent for the conductive paste, for example, butyl calpitol or the like is used.

以上のようにして調製される導電性ペーストが適用され
る被着基体は特に限定的ではないが、各種の合成樹脂製
成形体、例えばポリエステルフィルム、セラミック基板
、フェノール樹脂積層板等が挙げられる。
The substrate to which the conductive paste prepared as described above is applied is not particularly limited, but includes various synthetic resin molded bodies, such as polyester films, ceramic substrates, phenolic resin laminates, and the like.

以下、本発明を実施例によって説明する。Hereinafter, the present invention will be explained by examples.

実施例1 ポリブチラール樹脂60%メチエルエチルケトン溶液1
00gおよびフェノール[l1u50%エタノール溶液
75yを混合し、この中に導電性炭素粉末(ケッチェン
ブラックEC)30gを押し潰しながら充分に混練した
後、水酸化マグネシウム601を配合し、さらに希釈剤
としてブチルカルピトール200gを加えてカーボンペ
ーストを調製した。
Example 1 Polybutyral resin 60% methyl ethyl ketone solution 1
00g and phenol [l1u50% ethanol solution 75y were mixed, and 30g of conductive carbon powder (Ketjenblack EC) was thoroughly kneaded while being crushed. Then, magnesium hydroxide 601 was blended, and butyl was added as a diluent. A carbon paste was prepared by adding 200 g of calpitol.

得られたカーボンペーストを、41gM間隔て電極を設
置した絶縁体(ナイロン系樹脂成型品)の凹部(4羽×
10絹×1.0羽)に入れ、150 ”Cで1時間の熱
処理に付してカーボンペースト埋込み抵抗体を作成した
。電極をトラッキング試験機の出口端子に接続し、印加
電圧を高めてゆき、微少放電の発生し始めたところで、
通電流が0.4Aになるまで電圧を急激に上げ、以後は
電圧を一定に保って抵抗体の発熱燃焼状況を観察してフ
ェールセーフ特性を評価した。結果を表−1に示す。
The obtained carbon paste was applied to the recesses (4 blades ×
A carbon paste embedded resistor was created by heat-treating at 150''C for 1 hour.The electrode was connected to the outlet terminal of a tracking tester, and the applied voltage was increased. , when a minute discharge begins to occur,
The voltage was rapidly increased until the current was 0.4 A, and thereafter the voltage was kept constant to observe the state of heat generation and combustion of the resistor to evaluate fail-safe characteristics. The results are shown in Table-1.

上記カーボンペーストを絶縁体上に塗布しく塗布厚:1
00μ〕、150°Cで1時間の熱処理に付して硬化カ
ーボン膜(膜厚:約30μ)を形成させて密着性を評価
した。結果を表−1に示す。
Apply the above carbon paste onto the insulator. Application thickness: 1
00 μ] and 150° C. for 1 hour to form a cured carbon film (thickness: approximately 30 μ), and the adhesion was evaluated. The results are shown in Table-1.

また、テトロンフィルム上に上記カーボンペーストを塗
布しく塗布厚:100μ;塗布面積:16XIQ、ff
肩)、150°Cで1時間の熱処理に付して硬化カーボ
ン膜(膜厚:30μ)を形成させ、端部に3ffNXI
QiWNの黄銅板(厚さ:l、Qm+w)を置き、30
0gで加圧し、黄銅板間の電気抵抗値を測定した。結果
を表−1に示す。
Also, apply the above carbon paste on the Tetron film. Application thickness: 100μ; Application area: 16XIQ, ff
shoulder), heat treated at 150°C for 1 hour to form a hardened carbon film (thickness: 30μ), and 3ffNXI on the edge.
Place a QiWN brass plate (thickness: l, Qm+w) and
A pressure of 0 g was applied, and the electrical resistance value between the brass plates was measured. The results are shown in Table-1.

実施例2 水酸化マグネシウムの代りにバーミキュライト粉末(粒
径二5μ)を60ダ使用する以外は実施例1と同様にし
て調製した硬化カーボン膜のフェールセーフ特性、密着
性および電気抵抗を実施例1と同様にして調べた。結果
を表−1に示す。
Example 2 The fail-safe properties, adhesion, and electrical resistance of a cured carbon film prepared in the same manner as in Example 1 except that 60 Da of vermiculite powder (particle size 25 μm) was used instead of magnesium hydroxide were evaluated in Example 1. I investigated in the same way. The results are shown in Table-1.

参考例 市販のフェノール樹脂系バインダー含有カーボンペース
ト(他の配合成分および成分配合割合は不明)4009
に水酸化マグネシウム60gを配合したペーストを使用
して実施例1と同様にして、硬化カーボン膜のフェール
セーフ特性、密着性gよび電気抵抗値を調べた。結果を
表−1に示す〇比1咬例1 水酸化マグネシウムを配合しない以外は実施例1と同様
にして調製した硬化カーボン膜のフェールセーフ特性、
密着性および電気抵抗値を実施例1と同様にして調べ、
結果を表−1に示す。
Reference example: Commercially available carbon paste containing phenolic resin binder (other components and component ratios are unknown) 4009
In the same manner as in Example 1, using a paste containing 60 g of magnesium hydroxide, the fail-safe characteristics, adhesion g, and electrical resistance of the cured carbon film were investigated. The results are shown in Table 1. 〇 Ratio 1 Bite Example 1 Fail-safe characteristics of the cured carbon film prepared in the same manner as in Example 1 except that magnesium hydroxide was not added.
Adhesion and electrical resistance values were examined in the same manner as in Example 1,
The results are shown in Table-1.

比較例2 炭素粉末の配合量を15gとする以外は比較例1と同様
である。測定結果を表−1に示す。
Comparative Example 2 Comparative Example 2 was the same as Comparative Example 1 except that the amount of carbon powder was 15 g. The measurement results are shown in Table-1.

比較例3 水酸化マグネシウムを配合しない以外は前記参考例と同
様である。測定結果を表−1に示す。
Comparative Example 3 Same as the above reference example except that magnesium hydroxide was not blended. The measurement results are shown in Table-1.

表−1 1)放電によって過電流が発生すると同時に硬化カーボ
ン膜に亀裂または脹が生じ、電流計の読みがゼロとなっ
て発熱がとまる。
Table 1 1) At the same time as overcurrent occurs due to discharge, cracks or swelling occur in the cured carbon film, the ammeter reading becomes zero, and heat generation stops.

2〕放電開始後、電圧を下げて電流を0.4Aに設定す
ると放電−を継続するか、完熟燃焼する。
2] After the start of discharge, lower the voltage and set the current to 0.4A to continue the discharge or complete combustion.

3)供試体をナイフで削った場合、カケ、ハガレ等がな
く、かんな屑の様に削れまた、被着体に加熱硬化させた
カーボンペースト膜上に1朋間隔で縦横各11本の直交
する切り目を入れ10(L個の桝目を作りその上にセロ
ハンテープを圧着後急激に引剥しても何の変化もみられ
ない。
3) When the specimen was scraped with a knife, there was no chipping or peeling, and it was scraped like planer shavings.Also, 11 pieces were perpendicular to each other vertically and horizontally at 1-square intervals on the carbon paste film that had been heated and hardened on the adherend. Even if 10 (L) squares were made and cellophane tape was crimped on top of the squares and then rapidly peeled off, no change was observed.

発明の効果 本発明による導電性ペーストは導電性および密着性の点
で従来の導電性ペーストと比べて全く遜色がなく、過熱
や異常発熱に起因する安全りの問題を効果的に解消する
。従って本発明による導電性ペーストは特に電気電子工
業の分野にぢいて利用されている従来の導電性ペースト
と問題なく代替し得る。
Effects of the Invention The conductive paste according to the present invention is completely comparable to conventional conductive pastes in terms of conductivity and adhesion, and effectively eliminates safety problems caused by overheating and abnormal heat generation. The electrically conductive paste according to the invention can therefore easily replace the conventional electrically conductive pastes used in particular in the electrical and electronic industry.

Claims (1)

【特許請求の範囲】 1、バインダー樹脂100重量部あたり、導電性粉末約
10〜65重量部および高温で脱水して容量変化を伴う
無機フィラー約40〜70重量部含有することを特徴と
する導電性ペースト。 2、無機フィラーが水酸化マグネシウムまたはバーミキ
ュライトである第1項記載の導電性ペースト。
[Claims] 1. A conductive material containing, per 100 parts by weight of binder resin, about 10 to 65 parts by weight of a conductive powder and about 40 to 70 parts by weight of an inorganic filler whose capacity changes when dehydrated at high temperatures. sex paste. 2. The conductive paste according to item 1, wherein the inorganic filler is magnesium hydroxide or vermiculite.
JP21462684A 1984-10-12 1984-10-12 Conductive paste Granted JPS6193505A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21462684A JPS6193505A (en) 1984-10-12 1984-10-12 Conductive paste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21462684A JPS6193505A (en) 1984-10-12 1984-10-12 Conductive paste

Publications (2)

Publication Number Publication Date
JPS6193505A true JPS6193505A (en) 1986-05-12
JPH0311484B2 JPH0311484B2 (en) 1991-02-18

Family

ID=16658845

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21462684A Granted JPS6193505A (en) 1984-10-12 1984-10-12 Conductive paste

Country Status (1)

Country Link
JP (1) JPS6193505A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007046214A1 (en) * 2005-10-20 2007-04-26 Toyo Aluminium Kabushiki Kaisha Paste composition and solar battery element using the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007046214A1 (en) * 2005-10-20 2007-04-26 Toyo Aluminium Kabushiki Kaisha Paste composition and solar battery element using the same
JP4949263B2 (en) * 2005-10-20 2012-06-06 東洋アルミニウム株式会社 Paste composition and solar cell element using the same
US8877100B2 (en) 2005-10-20 2014-11-04 Toyo Aluminium Kabushiki Kaisha Paste composition and solar cell element using the same
NO339124B1 (en) * 2005-10-20 2016-11-14 Toyo Aluminium Kk Pasta material and solar cell element where used

Also Published As

Publication number Publication date
JPH0311484B2 (en) 1991-02-18

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