JPH0311486B2 - - Google Patents
Info
- Publication number
- JPH0311486B2 JPH0311486B2 JP21462584A JP21462584A JPH0311486B2 JP H0311486 B2 JPH0311486 B2 JP H0311486B2 JP 21462584 A JP21462584 A JP 21462584A JP 21462584 A JP21462584 A JP 21462584A JP H0311486 B2 JPH0311486 B2 JP H0311486B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- carbon
- resin
- carbon 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.)
- Expired
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 33
- 229910052799 carbon Inorganic materials 0.000 claims description 21
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000011256 inorganic filler Substances 0.000 claims description 8
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 8
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052622 kaolinite Inorganic materials 0.000 claims description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 4
- 229920001568 phenolic resin Polymers 0.000 claims description 4
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 4
- 229910052900 illite Inorganic materials 0.000 claims description 3
- VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 claims description 3
- 229920003987 resole Polymers 0.000 claims description 2
- -1 detsuite Chemical compound 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000000758 substrate Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 5
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000011134 resol-type phenolic resin Substances 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Conductive Materials (AREA)
Description
産業上の利用分野
本発明は、プラスチツクやセラミツク等の基体
に対する優れた密着性と高い導電性を有するカー
ボンペーストに関する。
従来の技術および発明が解決しようとする問題点
従来から電子電気工業分野において、例えばフ
レキシブル配線板の導板、抵抗体、接点等に使用
されているカーボンペーストは導電性炭素粉末に
バインダー、例えばポリビニルブチラール樹脂と
フエノール樹脂又はエポキシ樹脂との混合体又は
共重合体等、および溶剤、例えびメチルエチルケ
トン、エタノール、ブチルカルビトール等を適宜
配合することによつて調製されているが、基体、
特にポリエステルやセラミツク等の耐熱性の優れ
た基体に対する優れた密着性と高い導電性を兼備
したカーボンペーストは得られていない。
本発明は、基本に対する優れた密着性と高い導
電性を兼有して広範囲に利用可能なカーボンペー
ストを提供するためになされたものである。
問題点を解決するための手段
即ち本発明は、ポリビニルブチラール樹脂およ
びレゾール型フエノールホルムアルデヒド樹脂か
らなるバインダー樹脂100重量部あたり、炭素粉
末10〜65重量部およびカオリナイト、デツカイト
およびイライトから成る群から選択される1種ま
たは2種以上の無機フイラー8〜30重量部を含有
することを特徴とするカーボンペーストに関す
る。
本発明に使用するバインダー樹脂はポリビニル
ブチラール樹脂およびレゾール型フエノールホル
ムアルデヒド樹脂からなるものである。
炭素粉末は従来からカーボンペーストに常用さ
れているもの、例えばケツチエンブラツクECや
アセチレンブラツク等の高導電性のものを使用す
ればよく、その配合量は、上記のバインダー樹脂
100重量部に応じて約10〜65重量部である。炭素
粉末の配合量が約65重量部以上になると導電性は
増すが、密着性もしくは接着性が低下し、また約
10重量部以下になると高い導電性は得られない。
炭素粉末の粒径は通常約10mμ〜100mμであ
るが、通常これらの粒子の集合体である二次粒子
径やこれらの連鎖体が重要である。
本発明に使用する無機フイラーとしてはカオリ
ナイト、デツカイトおよびイライトが挙げられ、
これらは所望により2種以上併用してもよい。こ
れらの無機フイラーは、系の粘度を増加させない
で比較的多量に配合でき、また、導電性と接着性
の向上にも寄与できる。
無機フイラーの配合量は前記のバインダー樹脂
100重量部に対して約8〜30重量部で、約8重量
部以下では本発明の所期の効果は得難く、約30重
量部以上になると系の粘土が増加すると共に導電
性も向上しなくなるし接着性も低下する。
無機フイラーの粘径は通常好ましくは約0.1〜
10μである。
本発明によるカーボンペーストは所定量の前記
のバインダー樹脂、炭素粉末および無機フイラー
を適宜の溶剤を用いて混練することによつて調製
される。
溶剤の使用量は必要最少限にすべきであり、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。
カーボンペーストの希釈剤としてはブチルカル
ビトール等が使用される。
以上のようにして調製されるカーボンペースト
は通常約30〜80%の揮発成分を含有しているの
で、所定の被着基体、例えばポリエステルフイル
ム、セラミツクタイル、アルミナプレート等の上
に所望の膜厚の約1.3〜3倍の厚さに塗布もしく
は印刷した後、熱処理に付される。熱処理の条件
はカーボンペーストの性状、使用目的、被着基体
の種類等に応じて適宜選定すればよく、通常は約
120〜190℃で約0.5〜5時間処理する。例えば被
着基体がセラミツク焼結体の場合には、150で0.5
〜1時間熱処理した後、400℃で1時間熱処理す
ると導電性が向上する。
以下、本発明を実施例によつて説明する。
実施例 1
ポリブチラール樹脂60重量部およびレゾール系
フエノール樹脂40重量部を、CH3COC2H5と
C2H5OH混合溶媒〔CH3COC2H5:C2H5OH=
70:30(重量比)〕120重量部にほぼ室温で滴下し
て飴状の粘着性混合物とし、これに導電性炭素粉
末(ケツチエンブラツクEC)30重量部を添加し、
さらにブチルカルビトール100重量部を加え、こ
の混合物を乳鉢で押し潰しながら混練し、この混
練物にさらにカオリナイト(粒径:5μ)30重量
部配合して本発明によるカーボンペーストを調製
した。
得られたカーボンペーストをポリエスチルフイ
ルム(厚さ:50μ)上に印刷し(印刷面積:16mm
×10mm;被覆厚:0.1mm)、150℃で1時間の熱処
理に付して、硬化した導電性カーボン膜(厚さ:
約30μ)を形成させた。
この導電性カーボン膜の密着強度および電気抵
抗を測定し、結果を表−1に示す。
実施例 2〜4
実施例1の手順に準拠して、表−1の条件によ
つて形成させた導電性カーボン膜の密着性および
電気抵抗を測定し、結果を表−1に示す。
比較例 1〜6
実施例1の手順に準拠して、表−1の条件によ
つて形成させた導電性カーボン膜の密着性および
電気抵抗を測定し、結果を表−1に示す。
INDUSTRIAL APPLICATION FIELD The present invention relates to a carbon paste having excellent adhesion to substrates such as plastics and ceramics and high electrical conductivity. Prior Art and Problems to be Solved by the Invention Conventionally, in the electronic and electrical industry, carbon paste, which has been used for conductive plates, resistors, contacts, etc. of flexible wiring boards, is a combination of conductive carbon powder and a binder, such as polyvinyl. It is prepared by appropriately blending a mixture or copolymer of butyral resin and phenol resin or epoxy resin, and a solvent such as methyl ethyl ketone, ethanol, butyl carbitol, etc.
In particular, a carbon paste that has both excellent adhesion to substrates with excellent heat resistance such as polyester and ceramics and high conductivity has not been obtained. The present invention was made in order to provide a carbon paste that has both excellent adhesion to base materials and high conductivity and can be used in a wide range of applications. Means for Solving the Problems According to the present invention, per 100 parts by weight of a binder resin consisting of a polyvinyl butyral resin and a resol-type phenol formaldehyde resin, 10 to 65 parts by weight of carbon powder and a carbon powder selected from the group consisting of kaolinite, detsuite and illite are used. The present invention relates to a carbon paste containing 8 to 30 parts by weight of one or more inorganic fillers. The binder resin used in the present invention is composed of polyvinyl butyral resin and resol type phenol formaldehyde resin. The carbon powder can be one that has been commonly used in carbon pastes, such as highly conductive ones such as Kettchen Black EC or Acetylene Black, and the amount of carbon powder to be blended is the same as that of the binder resin mentioned above.
Approximately 10-65 parts by weight, depending on 100 parts by weight. When the amount of carbon powder blended exceeds about 65 parts by weight, conductivity increases, but adhesion or adhesion decreases, and
If the amount is less than 10 parts by weight, high conductivity cannot be obtained. The particle size of carbon powder is usually about 10 mμ to 100 mμ, but the secondary particle size, which is usually an aggregate of these particles, and the chain of these particles are important. Inorganic fillers used in the present invention include kaolinite, detsuite and illite;
Two or more of these may be used in combination if desired. These inorganic fillers can be added in relatively large amounts without increasing the viscosity of the system, and can also contribute to improving conductivity and adhesiveness. The amount of inorganic filler is the same as the binder resin described above.
The amount is about 8 to 30 parts by weight per 100 parts by weight, and if it is less than about 8 parts by weight, it is difficult to obtain the desired effect of the present invention, and if it is more than about 30 parts by weight, the clay content of the system increases and the conductivity also improves. It will disappear and the adhesion will also decrease. The viscosity diameter of the inorganic filler is usually preferably about 0.1~
It is 10μ. The carbon paste according to the present invention is prepared by kneading predetermined amounts of the binder resin, carbon powder, and inorganic filler using an appropriate solvent. The amount of solvent used should be kept to the minimum necessary, and examples of such solvents include a mixture of methyl ethyl ketone and ethyl alcohol. Butyl carbitol or the like is used as a diluent for carbon paste. Since the carbon paste prepared as described above usually contains about 30 to 80% volatile components, it can be applied to a desired substrate such as polyester film, ceramic tile, alumina plate, etc. to a desired thickness. After coating or printing to a thickness of about 1.3 to 3 times the thickness of the film, it is subjected to heat treatment. Heat treatment conditions may be selected appropriately depending on the properties of the carbon paste, purpose of use, type of substrate, etc., and are usually approximately
Process at 120-190°C for about 0.5-5 hours. For example, if the adherend substrate is a ceramic sintered body, 150 is 0.5
After heat treatment for ~1 hour, conductivity is improved by heat treatment at 400°C for 1 hour. Hereinafter, the present invention will be explained with reference to Examples. Example 1 60 parts by weight of polybutyral resin and 40 parts by weight of resol type phenolic resin were mixed with CH 3 COC 2 H 5.
C 2 H 5 OH mixed solvent [CH 3 COC 2 H 5 :C 2 H 5 OH=
70:30 (weight ratio)] was added dropwise to 120 parts by weight at approximately room temperature to form a candy-like sticky mixture, and to this, 30 parts by weight of conductive carbon powder (Ketschen Black EC) was added.
Furthermore, 100 parts by weight of butyl carbitol was added, the mixture was kneaded while being crushed in a mortar, and 30 parts by weight of kaolinite (particle size: 5 μm) was further added to the kneaded mixture to prepare a carbon paste according to the present invention. The obtained carbon paste was printed on a polyester film (thickness: 50μ) (printing area: 16mm).
x 10mm; coating thickness: 0.1mm), heat treated at 150℃ for 1 hour to harden the conductive carbon film (thickness:
approximately 30μ) was formed. The adhesion strength and electrical resistance of this conductive carbon film were measured, and the results are shown in Table 1. Examples 2 to 4 According to the procedure of Example 1, the adhesion and electrical resistance of conductive carbon films formed under the conditions shown in Table 1 were measured, and the results are shown in Table 1. Comparative Examples 1 to 6 According to the procedure of Example 1, the adhesion and electrical resistance of conductive carbon films formed under the conditions shown in Table 1 were measured, and the results are shown in Table 1.
【表】
比較例 7
炭素粉末、フエノール系樹脂バインダーおよび
メチルエチルケトン・エタノール・ブチルカルビ
トール混合溶剤を含有する市販品カーボンペース
ト(成分の配合割合は不明で、カオリナイト等の
無機フイラーは含有せず)について実施例1と同
様の操作および測定をおこなつたところ、密着強
度の評価はBで、電気抵抗は170KΩであつた。
発明の効果
本発明によるカーボンペーストは従来のカーボ
ンペーストに比べて数倍の導電率を有すると共
に、種々の被着基体、特に、耐熱性、耐屈曲性お
よび耐候性に極めて優れたポリエスエテルフイル
ムに対する密着性がよいため、例えばフレキシブ
ル配線板の導体、抵抗体、および接点(例えば特
開昭58−189919号に記載されたようなキーボード
スイツチの固定側および可動側の接点)等の材料
として利用できるばかりでなく、フレキシブルフ
イルム状発熱体として水道管等の凍結防止にも利
用でき、また熱線吸収体としても利用でき(例え
ばポリエステル容器にカーボンペーストを塗布
し、これを赤外線で硬化させれば直射日光の吸収
能の高い温水器として利用できる)、更にアルミ
ナ基板やタイル板等のセラミツク焼結体製の発熱
体や抵抗体材料としても利用できる。[Table] Comparative Example 7 Commercially available carbon paste containing carbon powder, phenolic resin binder, and mixed solvent of methyl ethyl ketone, ethanol, and butyl carbitol (composition ratio of ingredients is unknown, does not contain inorganic filler such as kaolinite) When the same operations and measurements as in Example 1 were carried out, the adhesion strength was evaluated as B, and the electrical resistance was 170KΩ. Effects of the Invention The carbon paste according to the present invention has electrical conductivity several times higher than that of conventional carbon pastes, and is effective for various adherent substrates, especially polyester films that have extremely excellent heat resistance, bending resistance, and weather resistance. Due to its good adhesion, it can be used as a material for, for example, conductors of flexible wiring boards, resistors, and contacts (for example, contacts on the fixed side and movable side of keyboard switches as described in JP-A-58-189919). In addition, it can be used as a flexible film heating element to prevent water pipes from freezing, and it can also be used as a heat ray absorber (for example, by applying carbon paste to a polyester container and curing it with infrared rays, it can be used in direct sunlight). It can be used as a water heater with high absorption capacity), and can also be used as a material for heating elements and resistors made of ceramic sintered bodies such as alumina substrates and tile plates.
Claims (1)
フエノールホルムアルデヒド樹脂からなるバイン
ダー樹脂100重量部あたり、炭素粉末10〜65重量
部およびカオリナイト、デツカイトおよびイライ
トから成る群から選択される1種または2種以上
の無機フイラー8〜30重量部を含有することを特
徴とするカーボンペースト。1. 10 to 65 parts by weight of carbon powder and one or more inorganic fillers selected from the group consisting of kaolinite, detsuite, and illite per 100 parts by weight of binder resin consisting of polyvinyl butyral resin and resol type phenol formaldehyde resin 8 A carbon paste characterized by containing ~30 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21462584A JPS6193506A (en) | 1984-10-12 | 1984-10-12 | Carbon paste |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21462584A JPS6193506A (en) | 1984-10-12 | 1984-10-12 | Carbon paste |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6193506A JPS6193506A (en) | 1986-05-12 |
JPH0311486B2 true JPH0311486B2 (en) | 1991-02-18 |
Family
ID=16658828
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21462584A Granted JPS6193506A (en) | 1984-10-12 | 1984-10-12 | Carbon paste |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6193506A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2308127A (en) * | 1995-12-15 | 1997-06-18 | Ams Polymers | Radiation absorbing materials |
-
1984
- 1984-10-12 JP JP21462584A patent/JPS6193506A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6193506A (en) | 1986-05-12 |
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