JPS61235473A - Paint for resistor - Google Patents

Paint for resistor

Info

Publication number
JPS61235473A
JPS61235473A JP60077403A JP7740385A JPS61235473A JP S61235473 A JPS61235473 A JP S61235473A JP 60077403 A JP60077403 A JP 60077403A JP 7740385 A JP7740385 A JP 7740385A JP S61235473 A JPS61235473 A JP S61235473A
Authority
JP
Japan
Prior art keywords
powder
paint
resistance
carbon black
conductive 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.)
Granted
Application number
JP60077403A
Other languages
Japanese (ja)
Other versions
JPH0588484B2 (en
Inventor
Koji Tanabe
田辺 功二
Satoru Murakawa
村川 哲
Hiroshi Hasegawa
洋 長谷川
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 JP60077403A priority Critical patent/JPS61235473A/en
Publication of JPS61235473A publication Critical patent/JPS61235473A/en
Publication of JPH0588484B2 publication Critical patent/JPH0588484B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the title paint for resistors, which does not cause rise in resistance due to anodic oxidation, produces a less sliding noise and has good resistance to moisture and heat, by blending an electrically conductive powder composed of tungsten dioxide powder and carbon black and a synthetic resin. CONSTITUTION:In a paint for resistance obtd. by blending an electrically conductive powder and a synthetic resin, the paint is characterized in that part of the electrically conductive powder is tungsten dioxide (WO2) powder and the remainder thereof is carbon black in a weight ratio of the WO2 powder to the carbon black of pref. 95:5-10:90. The paint allows the quantity of the electrically conductive powder to be increased as compared with the case where carbon black alone is used. Accordingly, the paint has good workability, because it has proper thixotropic properties required of a paint in screen printing, etc.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は各種電子機器のプリント配線板、固定抵抗器、
可変抵抗器等の抵抗素子や電磁波シールド板、電波吸収
板、静電防止板等に使用する抵抗用塗料に関するもので
ある。
[Detailed Description of the Invention] Industrial Fields of Use The present invention is applicable to printed wiring boards of various electronic devices, fixed resistors,
The present invention relates to resistance paints used for resistance elements such as variable resistors, electromagnetic wave shielding plates, radio wave absorption plates, antistatic plates, etc.

従来の技術 従来、抵抗用塗料としては導電性粉末としてカーボンブ
ラック、例えばアセチレンブラックや黒鉛粉末をエポキ
シ樹脂やフェノール樹脂等の合成樹脂に分散させたもの
が知られている。又、印刷適性等の作業性や高負荷条件
等の環境安定性を向上させる目的でSin、粉末やTi
e2粉末等の絶縁性粉末をカーボンブラックとともに合
成樹脂中に分散させた抵抗用塗料が知られている。
BACKGROUND OF THE INVENTION Conventionally, as a resistive paint, one in which conductive powder such as carbon black such as acetylene black or graphite powder is dispersed in a synthetic resin such as an epoxy resin or a phenol resin is known. In addition, for the purpose of improving workability such as printability and environmental stability such as under high load conditions, we use Sin, powder, and Ti.
Resistance paints are known in which insulating powder such as e2 powder is dispersed together with carbon black in a synthetic resin.

発明が解決しようとする問題点 前記従来例の場合、高抵抗領域では抵抗組成中のカーボ
ンブラックの割合が極めて少ないため。
Problems to be Solved by the Invention In the case of the conventional example, the proportion of carbon black in the resistance composition is extremely small in the high resistance region.

高湿度雰囲気中で電流を流すと陽極酸化が発生し、カー
ボンブラックが炭酸ガスとして気化する結果、抵抗値が
加速度的に上昇し、無限大(絶縁物)にまでなる欠点を
有していた。更にS10□粉末やTie、粉末等の絶縁
性粉末を含有させた抵抗用塗料においては1例えば可変
抵抗器用抵抗素子等摺動接点として用いる場合、摺動雑
音が高くなる欠点を有していた。又、電流導通パスはカ
ーボンブラック及びその相互の接触によるものであるた
め、カーボンブラックの割合の少ない高抵抗領域では湿
度や温度の変動時の抵抗値変化が大きい欠点を有してい
た。
When a current is passed in a high humidity atmosphere, anodic oxidation occurs, and the carbon black vaporizes as carbon dioxide gas, which causes the resistance value to increase at an accelerated rate, reaching infinity (insulating material). Furthermore, resistance paints containing insulating powders such as S10□ powder, Tie powder, etc. have the disadvantage of high sliding noise when used as sliding contacts, such as resistance elements for variable resistors. Furthermore, since the current conduction path is due to carbon black and their mutual contact, there is a drawback that in a high resistance region where the proportion of carbon black is small, the resistance value changes greatly when humidity or temperature fluctuates.

本発明はこのような問題点を解決するもので、従来のよ
うな陽極酸化による抵抗値上昇がなく。
The present invention solves these problems and eliminates the increase in resistance caused by anodic oxidation as in the conventional method.

摺動接点として用いた場合、摺動雑音が低く、しかも耐
湿、耐熱特性が良好な抵抗用塗料を提供することを目的
とするものである。
The object of the present invention is to provide a resistance coating material that has low sliding noise and good moisture resistance and heat resistance properties when used as a sliding contact.

問題点を解決するための手段 この問題点を解決するために本発明は、少なくとも導電
性粉末と合成樹脂よりなる抵抗用塗料において、前記導
電性粉末の一部が二酸化タングステン(WO,)の粉末
であり、他の部分がカーボンブラックであるものである
Means for Solving the Problem In order to solve this problem, the present invention provides a resistive paint made of at least conductive powder and a synthetic resin, in which part of the conductive powder is tungsten dioxide (WO) powder. The other part is carbon black.

作用 この構成により、高湿度雰囲気中で電流を流しても陽極
酸化による抵抗値上昇もなく、耐湿、耐熱特性も良好で
、摺動接点として用いた場合、摺動雑音も低くなる。
Function: With this structure, there is no increase in resistance due to anodization even when current is passed in a high humidity atmosphere, the moisture resistance and heat resistance are good, and when used as a sliding contact, the sliding noise is low.

実施例 以下、本発明の実施例について、図面に基づいて説明す
る。
Embodiments Hereinafter, embodiments of the present invention will be described based on the drawings.

即ち、本発明は少なくとも導電性粉末と合成樹脂よりな
る抵抗用塗料において、前記導電性粉末の一部が二酸化
タングステン(WO2)の粉末であり、他の部分がカー
ボンブラックで構成され。
That is, the present invention provides a resistive paint comprising at least conductive powder and synthetic resin, in which a portion of the conductive powder is tungsten dioxide (WO2) powder and the other portion is carbon black.

WO2粉末とカーボンブラックの重量比率を95=5〜
10:90としたものである。
The weight ratio of WO2 powder and carbon black is 95 = 5 ~
The time was set at 10:90.

WO3は従来より公知であるが、Wo、粉末単独でフェ
ノール樹脂等の合成樹脂中に分散せしめて抵抗用塗料と
した場合、第1図に示す如く高湿度や高温度の雰囲気中
では抵抗値の変動が極めて大きい、WO,粉末とカーボ
ンブラックとを組み合わせることによって、第2図に抵
抗用塗料の塗膜構造を示すように、高湿度や高温度雰囲
気中で抵抗値の変動が極度に少なくなるのは、WO2粉
末1とカーボンブラック2の構造に原因するものと推察
できる。即ち、WO8粉末1は粒状であるのに対し、カ
ーボンブラック2はストラフチャーと呼ばれる連鎖状の
1.構造を有している0粒状構造や連鎖構造単独の導電
粉体を使用した場合には粉末粒子を相互に結着している
合成樹脂の吸脱湿や熱による膨張・収縮のため粉末粒子
の相互の接触状態は雰囲気の状態によって密になる場合
と粗になる場合ができる。一方、抵抗値は導電性粉体自
体の抵抗と粉体相互の接触抵抗の総和として表わされる
ものであるから前記粒状粉末や連鎖状粉末単独の場合、
温湿度雰囲気の変動における抵抗値の変動が大きくなる
ものと考えられる。第2図に示すようにWoi粉末1と
カーボンブラック2を混合して合成樹脂3中に分散させ
た場合、雰囲気の変動による合成樹脂の吸脱湿や熱での
膨張・収縮が発生しても第3図の概念図で示すように導
電バス4が得られ易いために抵抗値変化が少ないものと
推察される。更に、カーボンブラックもWO2も良好な
導電材料であるため、摺動接点として使用した場合、摺
動雑音のレベルはカーボンブラック単独の場合に比較し
ても低くなる。又、高抵抗領域においても、WO2は温
湿度に対して安定なことや従来に比較して抵抗皮膜中の
合成樹脂比率を低下させ得るため、吸湿を少なくできる
ことから陽極酸化も実質的に防止できる。又、本発明に
よる抵抗用塗料は塗料中の導電性粉末量が従来のカーボ
ン単独の場合に比較して多くできるため、適度なチクソ
トロピックな性質を有しており、スクリーン印刷等の作
業性も良いものである。
WO3 has been known for a long time, but when it is dispersed as a powder alone in a synthetic resin such as phenol resin and used as a resistance paint, the resistance value decreases in an atmosphere of high humidity and temperature, as shown in Figure 1. By combining WO powder, which has extremely large fluctuations, and carbon black, the fluctuations in resistance value can be extremely reduced in high humidity and high temperature environments, as shown in Figure 2, which shows the film structure of the resistance paint. It can be inferred that this is caused by the structure of WO2 powder 1 and carbon black 2. That is, while the WO8 powder 1 is granular, the carbon black 2 is a chain-like 1. When using a conductive powder with a zero-grain structure or a chain structure alone, the powder particles may absorb moisture and expand/contract due to heat and the synthetic resin that binds the powder particles together. The state of mutual contact can be either dense or rough depending on the state of the atmosphere. On the other hand, since the resistance value is expressed as the sum of the resistance of the conductive powder itself and the contact resistance between the powders, in the case of the granular powder or chain powder alone,
It is thought that the resistance value fluctuates greatly due to fluctuations in temperature and humidity atmosphere. As shown in Figure 2, when Woi powder 1 and carbon black 2 are mixed and dispersed in synthetic resin 3, even if the synthetic resin absorbs and desorbs moisture due to changes in the atmosphere and expands and contracts due to heat. As shown in the conceptual diagram of FIG. 3, it is presumed that the change in resistance value is small because the conductive bus 4 is easily obtained. Furthermore, since both carbon black and WO2 are good conductive materials, when used as sliding contacts, the level of sliding noise is lower than when using carbon black alone. Furthermore, even in the high resistance range, WO2 is stable with respect to temperature and humidity and can lower the synthetic resin ratio in the resistance film compared to conventional ones, so moisture absorption can be reduced and anodic oxidation can be virtually prevented. . Furthermore, since the resistive paint according to the present invention can contain a larger amount of conductive powder than conventional carbon alone, it has appropriate thixotropic properties and is easy to work with, such as screen printing. It's good.

次に具体実施例について説明する。Next, specific examples will be described.

具体実施例1 平均粒径0.2μ閣のWO8粉末255 g 、アセチ
レンブラック40g1人造黒鉛5gを秤量混合してエポ
キシ樹脂(油化シェル、品名:エビコート815)20
0g中に三本ロールで分散させた0次にイミダゾール系
硬化剤20gを加え、エチルカルピトールアセテートを
添加して塗料粘度100ボイズに調整し、抵抗用塗料を
得た。
Specific Example 1 255 g of WO8 powder with an average particle size of 0.2 μm, 40 g of acetylene black, and 5 g of artificial graphite were weighed and mixed to make 20 epoxy resin (Yuka Shell, product name: Ebicoat 815).
20 g of a 0-order imidazole curing agent dispersed in 0 g using a triple roll was added, and ethyl carpitol acetate was added to adjust the paint viscosity to 100 voids to obtain a resistance paint.

比較例 アセチレンブラック60g、人造黒鉛7gをエポキシ樹
脂(油化シェル、品名:エビコート815) 200g
中に分散させ、イミダゾール系硬化剤20gを加え、エ
チルカルピトールアセテートを添加して塗料粘度100
ボイズに調整し、抵抗用塗料を得た。
Comparative Example 60g of acetylene black, 7g of artificial graphite and 200g of epoxy resin (Yuka Shell, product name: Ebicoat 815)
20g of imidazole curing agent was added, and ethyl carpitol acetate was added to make the paint viscosity 100.
Adjustments were made to the voids and a resistance paint was obtained.

比較試験例 前記具体実施例1及び比較例の抵抗用塗料を夫々フェノ
ール積層板にスクリーン印刷法にてパターン印刷し、1
60℃30分間でエポキシ樹脂を硬化させた。前記具体
実施例1及び比較例による夫々の抵抗素子について下記
の比較試験を行なった。
Comparative Test Example The resistive paints of Specific Example 1 and Comparative Example were each pattern-printed on a phenol laminate using a screen printing method.
The epoxy resin was cured at 60°C for 30 minutes. The following comparative tests were conducted on the respective resistance elements according to the specific example 1 and comparative example.

試験1;70℃の恒温槽に放置し1000時間後迄の抵
抗値変化率を測定、試験2:60℃90〜95%相対湿
度槽に放置し1000時間後迄の抵抗値変化率を測定、
試験3;60℃90〜95%相対湿度槽中で抵抗素子の
両端に直流電圧24Vを印加し、1000時間後迄の抵
抗値変化率を測定、試験4; 抵抗塗膜上を銀メツキベ
リリウム銅の金属刷子を加圧20 g 、 15mm/
秒の速度で摺動させたときの摺動雑音を測定(抵抗素子
両端に直流電圧24V印加)、 これら試験1〜3の結
果を第4図(a)〜(Q)に夫々示す、尚第4図(a)
〜(Q)において(A)は具体実施例1の抵抗変化特性
、(B)は比較例の抵抗変化特性である。又、試験4の
結果を次表に示す。
Test 1: Leave in a constant temperature bath at 70°C and measure the rate of change in resistance value after 1000 hours. Test 2: Leave in a 60°C 90-95% relative humidity bath and measure the rate of change in resistance value after 1000 hours.
Test 3: Apply a DC voltage of 24 V to both ends of the resistance element in a 60°C 90-95% relative humidity chamber, and measure the rate of change in resistance value after 1000 hours. Test 4: Silver-metsuki beryllium copper on the resistive coating. Press a metal brush of 20 g, 15 mm/
The sliding noise was measured when sliding at a speed of 1.2 seconds (DC voltage 24 V applied across the resistance element). The results of these tests 1 to 3 are shown in Figures 4 (a) to (Q), respectively. Figure 4 (a)
In ~(Q), (A) is the resistance change characteristic of the specific example 1, and (B) is the resistance change characteristic of the comparative example. In addition, the results of Test 4 are shown in the following table.

具体実施例2 具体実施例1と同一の各材料を使用し、カーボンブラッ
クとWO3粉末の比率を変化させたときの抵抗用塗料に
ついて比較試験例と同様の方法で1000時間後の耐湿
及び耐熱抵抗変化率を調べた。
Specific Example 2 Using the same materials as in Specific Example 1 and varying the ratio of carbon black and WO3 powder, the moisture resistance and heat resistance after 1000 hours were measured in the same manner as in the comparative test example. We investigated the rate of change.

その結果を第1図に示す。The results are shown in FIG.

発明の効果 以上のように本発明によれば、高湿度雰囲気中で電流を
流しても陽極酸化による抵抗値上昇がなく、耐湿、耐熱
特性も良好で、摺動接点として用いた場合摺動雑音も低
く、且つカーボンブラック単独の場合に比較して導電性
粉末量を多くできるため、スクリーン印刷等の際に塗料
特性として要求される適度なチクソトロビックな性質を
有しているため作業性も良いものである。又、使用する
各材料については何れも安価であることから、産業上極
めて有用なものである。
Effects of the Invention As described above, according to the present invention, there is no increase in resistance due to anodization even when current is passed in a high humidity atmosphere, the moisture resistance and heat resistance are good, and there is no sliding noise when used as a sliding contact. It also has a lower amount of conductive powder compared to the case of carbon black alone, so it has the appropriate thixotropic properties required as paint properties for screen printing, etc., and is easy to work with. It's good. In addition, since the materials used are all inexpensive, they are extremely useful industrially.

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

図面は本発明の実施例を示すもので、第1図はカーボン
ブラックとWO2粉末との比率と抵抗変化特性との関係
を示すグラフ、第2図は本発明による抵抗用塗料の塗膜
構造図、第3図は塗膜中の導電バスの概念図、第4図(
a)〜(c)は本発明及び比較例による比較試験例を示
すグラフである。 1・・・WO2粉末、2・・・カーボンブラック、3・
・・合成樹脂、4・・・導電パス 代理人   森  本  義  弘 第1図
The drawings show examples of the present invention. Figure 1 is a graph showing the relationship between the ratio of carbon black and WO2 powder and resistance change characteristics, and Figure 2 is a diagram of the coating film structure of the resistance paint according to the present invention. , Figure 3 is a conceptual diagram of the conductive bus in the coating film, Figure 4 (
a) to (c) are graphs showing comparative test examples according to the present invention and comparative examples. 1...WO2 powder, 2...carbon black, 3.
... Synthetic resin, 4... Conductive path agent Yoshihiro Morimoto Figure 1

Claims (1)

【特許請求の範囲】 1、少なくとも導電性粉末と合成樹脂よりなる抵抗用塗
料において、前記導電性粉末の一部が二酸化タングステ
ン(WO_2)の粉末であり、他の部分がカーボンブラ
ックである抵抗用塗料。 2、二酸化タングステン(WO_2)粉末とカーボンブ
ラックの重量比率が95:5〜10:90である特許請
求の範囲第1項記載の抵抗用塗料。
[Scope of Claims] 1. A resistive paint made of at least a conductive powder and a synthetic resin, wherein a part of the conductive powder is tungsten dioxide (WO_2) powder and the other part is carbon black. paint. 2. The resistance paint according to claim 1, wherein the weight ratio of tungsten dioxide (WO_2) powder and carbon black is 95:5 to 10:90.
JP60077403A 1985-04-11 1985-04-11 Paint for resistor Granted JPS61235473A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60077403A JPS61235473A (en) 1985-04-11 1985-04-11 Paint for resistor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60077403A JPS61235473A (en) 1985-04-11 1985-04-11 Paint for resistor

Publications (2)

Publication Number Publication Date
JPS61235473A true JPS61235473A (en) 1986-10-20
JPH0588484B2 JPH0588484B2 (en) 1993-12-22

Family

ID=13632937

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60077403A Granted JPS61235473A (en) 1985-04-11 1985-04-11 Paint for resistor

Country Status (1)

Country Link
JP (1) JPS61235473A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02165505A (en) * 1988-12-20 1990-06-26 Showa Denko Kk Conductive paste
JP2007250207A (en) * 2006-03-13 2007-09-27 Kyocera Chemical Corp Conductive wax, conductive molding material, and conductive molded product
JP2008291157A (en) * 2007-05-28 2008-12-04 Sumitomo Metal Mining Co Ltd Blue particulate-dispersed body, and article using the same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02165505A (en) * 1988-12-20 1990-06-26 Showa Denko Kk Conductive paste
JP2007250207A (en) * 2006-03-13 2007-09-27 Kyocera Chemical Corp Conductive wax, conductive molding material, and conductive molded product
JP2008291157A (en) * 2007-05-28 2008-12-04 Sumitomo Metal Mining Co Ltd Blue particulate-dispersed body, and article using the same

Also Published As

Publication number Publication date
JPH0588484B2 (en) 1993-12-22

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