JPS5981366A - Electrically conductive adhesive - Google Patents

Electrically conductive adhesive

Info

Publication number
JPS5981366A
JPS5981366A JP19276082A JP19276082A JPS5981366A JP S5981366 A JPS5981366 A JP S5981366A JP 19276082 A JP19276082 A JP 19276082A JP 19276082 A JP19276082 A JP 19276082A JP S5981366 A JPS5981366 A JP S5981366A
Authority
JP
Japan
Prior art keywords
vinyl chloride
surface area
parts
vinyl acetate
conductive adhesive
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
JP19276082A
Other languages
Japanese (ja)
Other versions
JPS6144907B2 (en
Inventor
Masami Ishitobi
石飛 正已
Yasuo Ijiri
井尻 康夫
Hiroshi Oota
広 太田
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.)
Dainichi Nippon Cables Ltd
Tokyo Electric Power Co Holdings Inc
Original Assignee
Tokyo Electric Power Co Inc
Dainichi Nippon Cables 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 Tokyo Electric Power Co Inc, Dainichi Nippon Cables Ltd filed Critical Tokyo Electric Power Co Inc
Priority to JP19276082A priority Critical patent/JPS5981366A/en
Publication of JPS5981366A publication Critical patent/JPS5981366A/en
Publication of JPS6144907B2 publication Critical patent/JPS6144907B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Conductive Materials (AREA)

Abstract

PURPOSE:To provide an adhesive having excellent adhesion and flexibility as well as sufficient electrical conductivity, by blending carbon black having a high surface area with a vinyl chloride/vinyl acetate copolymer. CONSTITUTION:10-30pts.wt. carbon black having a high surface area [pref. having a specific surface area (BET method) of 500m<2>/g or above and a DBP oil absorption (JIS K-6221-1970) of 250ml/100g] and 20-100pts.wt. liquid plasticizer such as dibutyl phthalate are blended with 100pts.wt. vinyl chloride/vinyl acetate copolymer (pref. having a vinyl chloride content of 70-95wt%, a vinyl acetate content of 30-5wt%, and a degree of polymn. of 100-1,000). The resulting electrically conductive adhesive is suitable for use in bonding electrically conductive polyvinyl chlorides to each other or the electrically conductive polyvinyl chloride to metal, particularly lead.

Description

【発明の詳細な説明】 本発明は4電件の接着剤に関し、詳しくは、導電性のポ
リ塩化ビニル同士や導電性ポリ塩化ビニルと金属殊に鉛
との接着に好適の、塩化ビニル−酢酸ビニル系共電自体
と高表面積カーボンブラ・ツクとからなる導電性接着剤
を提案するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a four-electrode adhesive, in particular a vinyl chloride-acetic acid adhesive suitable for adhering conductive polyvinyl chloride to each other and conductive polyvinyl chloride to metals, especially lead. This paper proposes a conductive adhesive consisting of vinyl-based conductive material itself and high surface area carbon black.

導電性ポリ塩化ビニル層と導体とを電気的に襄触した状
態で接着するとき、接着剤々して導電性のものが要求さ
れる。ポリ塩化ビニル(以下、PVC)用の接着剤とし
ては多くのものが公知てあり、捷/ζ導電性イ」馬剤も
各種の金属粉”やカーポンプシックが知られているから
、それら公知の接着剤に導電性イ・1与剤を混合すわば
、一般に導電1−1接着剤が得られる。
When bonding a conductive polyvinyl chloride layer and a conductor in electrical contact, the adhesive is required to be conductive. There are many known adhesives for polyvinyl chloride (hereinafter referred to as PVC), and various types of conductive adhesives, various metal powders, and carponic adhesives are known. A conductive 1-1 adhesive is generally obtained by mixing a conductive 1-1 additive with the adhesive.

しかしながら充分な導電性を達成するために大量の導電
性伺Jう剤を混合する接着剤の接着性、柔軟性が大きく
阻害さノ1、逆に少量の混合の場合は充分な導電性のも
のが得られない。
However, in order to achieve sufficient conductivity, the adhesion and flexibility of adhesives that are mixed with a large amount of conductive thickening agent will be greatly impaired.On the other hand, if a small amount is mixed, the adhesive will have sufficient conductive properties. is not obtained.

上記に鑑み、本発明は接着性、柔軟性に優れ、しかも充
分な4電性を有する前記組成の接着剤を提案するもので
ある。
In view of the above, the present invention proposes an adhesive having the composition described above, which is excellent in adhesiveness and flexibility, and has sufficient tetraelectricity.

接着剤のベースとなる塩化ビニル−酢酸ビニル系共重合
体としては、塩イ乙ビニルと酢酸ビニルの二種のモノマ
ーが広い範囲の量比で共重合したもの、更には更に第三
のモノマーとして、マレイン酸、アクリル酸などの不飽
和カルボン酸を少量(好ましくは10重量係以下)含む
三元共重合体などが用いられる。重合度は100〜10
00程度が適当である。特に好丑しいものは、塩化ビニ
ル成分ニア0〜95%(重@飴、以下同様)、酢酸ビニ
ル成分、5〜30 % 、重゛合度100〜900、特
に300〜600の共重合体、塩化ビニル成分ニア9〜
92ol)、耐酸ヒ= ル成分: 7〜20%、マレイ
/酸: 0.1〜10係、重合度:100〜900の玉
元共取合体などである。
The vinyl chloride-vinyl acetate copolymer that serves as the base of the adhesive is a copolymer of two monomers, vinyl chloride and vinyl acetate, in a wide range of ratios, and also as a third monomer. A terpolymer containing a small amount (preferably 10% by weight or less) of an unsaturated carboxylic acid such as , maleic acid, or acrylic acid is used. The degree of polymerization is 100-10
Approximately 00 is appropriate. Particularly preferred are vinyl chloride components of 0 to 95% (heavy @ candy), vinyl acetate components of 5 to 30%, copolymers with a degree of polymerization of 100 to 900, especially 300 to 600, and chlorinated Vinyl component near 9~
92 ol), acid-resistant hydrogen component: 7 to 20%, male/acid ratio: 0.1 to 10, and degree of polymerization: 100 to 900.

塩化ビニル−酢酸ビニル系共重合体は二種以上を併用し
ても」、<、寸だ該共重合体100部(重量部、以下同
様)あたり50部以下、特に30部以下の少量であれは
接着性や柔軟性を改善する利オー1を混合使用してもよ
い。が\るイ′、A和1とし、では、アクリロニドl)
ル共重合体、塩化ゴム、ポリ鉛酸ビニル、ポリエステル
、ポリウレタ/、エポキシ樹脂、可塑剤などが例示でき
る。
Even if two or more types of vinyl chloride-vinyl acetate copolymers are used in combination, the amount may be as small as 50 parts or less, especially 30 parts or less per 100 parts (by weight, the same shall apply hereinafter) of the copolymer. may be used in combination with other additives that improve adhesion and flexibility. Assuming that \rui', A sum is 1, then acrylonide l)
Examples include rubber copolymers, chlorinated rubber, polyvinyl leadate, polyesters, polyurethanes, epoxy resins, and plasticizers.

このうち特に、好ましいものは結合アクリロニトリル量
:20〜50%、ムーニー粘度CM、L、、)40〜9
0のアクリロニh l)ル共重合体及び液状の可塑剤で
ある。
Among these, particularly preferred are: amount of bound acrylonitrile: 20-50%, Mooney viscosity CM, L, ) 40-9
0 acrylonitrile copolymer and a liquid plasticizer.

液状可塑剤として、たとえ(ばポリ塩化ビニルに通常用
いられるもの1例えば、ジブチルフタレート、ジオチル
フクレート、ジイソデシルフ1タレ−1・2等のフタル
酸エステル類、エポキシ化油、エボギシスファリン酸オ
クナル等のエポキン誘導体、ジオクチルアジペート、ジ
イソデンルアンベートなどのアジピン酸誘導体、オレイ
ン酸ブチル、ジオクチルセバケ−1・などの脂肪酸エス
テル類、トリオクチルトリメリテートなどのトリノリッ
ト酸誘導体、トリメタチルホスフx  ) 、h ’)
 クレジルホスフェ−ドナトノリン酸誘導体などが用い
られる。可塑剤の配合量は塩化ビニル−酢酸ビニル系共
重合体1.00部当り20〜100部が適当である。2
0部以下ては接着剤がもろくなり剥離強度が劣り、又、
100部を碧えると、接着剤が軟化して、接着剤自体の
強度が低くなるだめ剥離強度か劣る。
Examples of liquid plasticizers include those commonly used for polyvinyl chloride, such as phthalate esters such as dibutyl phthalate, diothyl fucrate, diisodecyl phthalate 1 and 2, epoxidized oils, and epoxysphalin. Epoquin derivatives such as acid ocnal; adipic acid derivatives such as dioctyl adipate and diisodenruambate; fatty acid esters such as butyl oleate and dioctyl sebaque-1; trinolitic acid derivatives such as trioctyl trimellitate; Methylphosph x), h')
Cresyl phosphate-donatonophosphoric acid derivatives and the like are used. The appropriate amount of the plasticizer is 20 to 100 parts per 1.00 parts of the vinyl chloride-vinyl acetate copolymer. 2
If it is less than 0 parts, the adhesive becomes brittle and has poor peel strength, and
If it exceeds 100 parts, the adhesive becomes soft and the strength of the adhesive itself decreases, resulting in poor peel strength.

高表面積ツアーポンプラックは、塩化ビニル−鞘酸ビニ
ル系共重合体に通常の方法で混練混合されたとき、その
高表面積の特徴にも七すき該共重合体中で良好な導電性
のネッ1−ワークを形成するので少量の使用で、而して
該共重合体の接着性、柔軟性に実質悪影響を及ぼすこと
なく・充分な導電性をイ」鳥する。高表面積カーボンブ
ラックの好ましいものはB TCT表面積が500+1
1. / S’以十てあり1.JIS K  622]
−1970によるDBP吸油量が250 ml/ 10
0 ’!以」−のものである。
The high surface area tour pump rack is also characterized by its high surface area when mixed with vinyl chloride-vinyl sheath copolymer in a conventional manner. - Since the copolymer is used to form a workpiece, a small amount of the copolymer is used, and sufficient conductivity can be achieved without substantially adversely affecting the adhesion and flexibility of the copolymer. The preferred high surface area carbon black is B TCT surface area of 500+1
1. / There are ten more than S' 1. JIS K 622]
- DBP oil absorption according to 1970 is 250 ml/10
0'! It is '-'.

1×10 Ωm以下程度の低い体積抵抗率を治する接着
剤は導■、性を治するものとして神々の有用な用途を有
する。所望の導電度によって、高表面積カーボンブラッ
クの配合量は変わるが一般的には樹り旨分に対して少な
くとも10%の配合で上記し/ξ導電度のものを得るこ
とができる。該カーボンブラックの配合量を多くすると
一層良導電性のものが得られるが、30係より多量に使
用したときは接着剤としての接着性、柔軟性に悪影響が
現われるので、30%以下とすることが好寸しい。該カ
ーボンブラ・ンクの特に好ましい配合量は、15〜2′
5%である。
Adhesives that cure volume resistivity as low as 1×10 Ωm or less have a divinely useful use as a cure for sex. The amount of high surface area carbon black blended varies depending on the desired electrical conductivity, but in general, the above-mentioned /ξ electrical conductivity can be obtained by blending the high surface area carbon black in an amount of at least 10% based on the wood content. If the amount of carbon black added is increased, a product with better conductivity can be obtained, but if it is used in an amount greater than 30%, the adhesion and flexibility of the adhesive will be adversely affected, so it should be kept at 30% or less. is in good shape. A particularly preferable blending amount of the carbon blank is 15 to 2'
It is 5%.

以下、実施例により本発明を一層詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例1〜4 塩化ビニ/L−酢酸ビニルニ元共重合体(塩化ビニル成
分、85%、酢酸ビニル成分°15%、31部均重合度
800)100部、ジオクチルフタレート40部と高表
面積カーボン ブラック(岡シンダ国、アクシー社、ケ
ッチェンブラッり、 B ■!;T表面積:1000m
/!  吸油量3407+1.t/ ] OO! )を
10都、15部、20部又は30部とをそれぞれ50’
Cに設定しプこ2本ロールにて均一に混合して実施例1
〜4の接着剤を得た。
Examples 1 to 4 100 parts of vinyl chloride/L-vinyl acetate di-copolymer (vinyl chloride component: 85%, vinyl acetate component: 15%, 31 parts homopolymerization degree: 800), 40 parts of dioctyl phthalate and high surface area carbon black (Okashinda country, Axie, Ketchenblatt, B ■!;T surface area: 1000m
/! Oil absorption amount 3407+1. t/ ] OO! ) for 10 copies, 15 copies, 20 copies or 30 copies for 50' each.
Example 1
-4 adhesive was obtained.

塩化ビニル−W[酸ビニルーマレイン酸三元共重合体(
塩化ビニル成分:86%、酢酸ビニル成分、13%、マ
レイノ酸成分:1%、平均重合度: 400 ) l 
O0部、及びジオクチルセバケーh :30部と実施例
1で使用の高表面積カーボノブラ・ツク10部、15部
、20部又は30部とを、それぞれ50°CiC設定し
た2本ロールにて均一に混合して冥施例5〜8の接着剤
を得実施例9〜10 塩化ビニル−酢酸ビニル二元共重合体(塩化ビニル成分
二80%、酢酸ビニル成分:20係Y均重合度+560
)100部、及び]・]リクレンルポスフエー1−60
部と高表面積カーボンブラック(ミラ油化社製、 B 
E i”表面積、900m2/!i’ +吸油量+ 3
50td/W )10部又は20部とを実施例]と同輩
表に均一混合して実施例9,10の接着剤を得た。
Vinyl chloride-W [acid vinyl-maleic acid terpolymer (
Vinyl chloride component: 86%, vinyl acetate component: 13%, maleino acid component: 1%, average degree of polymerization: 400) l
0 parts, and 30 parts of dioctyl sebaque h and 10 parts, 15 parts, 20 parts, or 30 parts of the high surface area carbonoblast used in Example 1 were uniformly mixed using two rolls each set at 50°CiC. Examples 9 to 10 Vinyl chloride-vinyl acetate binary copolymer (vinyl chloride component 280%, vinyl acetate component: 20 coefficient Y homopolymerization degree + 560
) 100 copies, and]・]Rekren Lupos Fae 1-60
and high surface area carbon black (manufactured by Mira Yuka Co., Ltd., B
E i” surface area, 900m2/!i’ + oil absorption + 3
Adhesives of Examples 9 and 10 were obtained by uniformly mixing 10 parts or 20 parts of 50 td/W) with Example] on the same scale.

実施例11〜12 実施例1で用いた二元共重合体100部、実施例9で用
いたカーボンブラック10部、又は20部、及び結合ア
クリロニトリル量:40%。
Examples 11-12 100 parts of the binary copolymer used in Example 1, 10 parts or 20 parts of the carbon black used in Example 9, and the amount of bound acrylonitrile: 40%.

l、−二−粘度(ML   ):80のアクリロニド1
+4 リル共重合体30部とを実施例】と同様にして均一に混
合して実施例11.]2の接着剤を得た。
l,-2-viscosity (ML): 80 acrylonide 1
Example 11. ] 2 adhesive was obtained.

実施例13〜14 塩化ビニル−酢酸ビニル−マレイン酸三元共重合体(塩
化ビニル成分ニア8%、酢酸ビニル)成分;17%、マ
レイン酸、5%、平均重合度:500)100部、実施
例1で用い/こ高表面積カーボンブラック10部、又は
20部とを実施例1と同様にして均一に混合し、実施例
13゜14の接着剤をイ47/こ。
Examples 13-14 Vinyl chloride-vinyl acetate-maleic acid terpolymer (vinyl chloride component: 8%, vinyl acetate component: 17%, maleic acid, 5%, average degree of polymerization: 500) 100 parts, carried out 10 parts or 20 parts of the high surface area carbon black used in Example 1 were mixed uniformly in the same manner as in Example 1, and the adhesives of Examples 13 and 14 were added.

実施1シ1]]で使用の二元共重合体100部と低表面
積カーボンブラック(、轡電件アセチレンブンツク、 
B E T表面積: 1.30711. / Y ) 
] O部又は30部とを実施例1と同様にして均一に混
合し比較例]、2の接着剤を得た。下表に各実施例、比
較例の20°Cにおける体積抵Jンし率と下記の方法で
測定した接着力をそれぞれ示す。同表から明らかな通り
、各実施例はいずれの評価項目についても優れたiti
性を示している。これに対して、比較例1d、接着性は
良好でを)つても体積抵抗率が過大であり、比較例2は
比較例1と反対の結果となっている。
100 parts of the binary copolymer used in Example 1]] and low surface area carbon black
BET surface area: 1.30711. /Y)
] O parts or 30 parts were uniformly mixed in the same manner as in Example 1 to obtain an adhesive of Comparative Example] and 2. The table below shows the volume resistivity at 20°C and the adhesive strength measured by the method below for each Example and Comparative Example. As is clear from the table, each example had excellent iti for all evaluation items.
It shows gender. On the other hand, although Comparative Example 1d had good adhesion, the volume resistivity was excessive, and Comparative Example 2 had a result opposite to Comparative Example 1.

接着剤の接着力−は、下記の方法で測定した。The adhesive strength of the adhesive was measured by the following method.

即ち、接着剤をトルニオチルエチルケト/の11部1混
合溶剤中へ溶かして30係溶液を作り、これを厚さ1.
 OOμの鉛箔又は導電(9−1) V C板へ塗布し
、80°Cで30分間乾燥し/ζ0乾燥後の上記鉛又は
導電P V CK tJ して、厚さ1(ンOIの導電
性ポリ塩化ビニルな乗ノロ、1.50 ’Cの熱プレス
によって、圧力(1,5K97 cm 、加圧時間4分
間プレスを行なって接着片を作成した。この接着)!l
を幅]、 Onun、長さ100 mmの短さく状とし
、2枚の被着体間のjsoq堝1 #if強度を引張速
度1.00 +rrm 7分で1lll+定し、試イ1
幅1. cm 、%りの剥離強度として9出(〜だ。
That is, the adhesive is dissolved in a mixed solvent of 11 parts and 1 part of torniothyl ethyl keto to make a 30% solution, and this is mixed to a thickness of 1.
OOμ lead foil or conductive (9-1) V C plate, dried at 80°C for 30 minutes / An adhesive piece was created by pressing polyvinyl chloride at a heating temperature of 1.50'C for 4 minutes at a pressure of 1.5K97 cm.
width], Onun, length 100 mm short strip shape, jsoq pot 1 #if strength between two adherends, tensile speed 1.00 + rrm 7 minutes, 1 lll + constant, trial 1
Width 1. The peel strength in cm and % is 9 (~).

Claims (1)

【特許請求の範囲】 1、 塩化ビニル−酢酸ビニル系共重合体と、該共重合
体100重量部あたり10〜30重量部の高表面積カー
ボンブラ・ツクとからなる導電性接着剤。 衆 2 塩化ビニル−酢酸ビニノ込共重合体]00重量部あ
たり20〜100重景部の液状可塑剤を含む特許請求の
範囲第1項の導電1」二接着剤。 3 塩化ビニル−酢酸ビニル系共重合体としで、塩化ビ
ニル成分ニア0〜95重M%、酢酸ビニル成分:5〜3
0重景カ、かつ重合度100〜900のものを用いる特
許請求の範囲第1項又は第2項の導電性接着剤。 4 塩化ビニル−酢酸ビニル系共重合体として、塩化ビ
ニル成分、79〜92重量φ、酢酸ビニル成分ニア〜2
0重量係、マレイン酸01〜10重量係、重合度:]0
0〜1900のものを用いる特許請求の範囲第1項又は
第2項の導電性接着剤。 5、 高表面積カーボンブラックとして、  BET表
面積が500フル/WJ2)、」二であり、JISK 
 6221−1970によるDBP吸油量が25 Q 
+++、 l / 1. OOS’以」−であるものを
用いる特許請求の範囲第」項〜第4功の導電性接着剤。
[Scope of Claims] 1. A conductive adhesive comprising a vinyl chloride-vinyl acetate copolymer and 10 to 30 parts by weight of high surface area carbon black per 100 parts by weight of the copolymer. 2. Vinyl chloride-vinino acetate copolymer] The conductive adhesive according to claim 1, which contains a liquid plasticizer in an amount of 20 to 100 parts by weight per 00 parts by weight. 3 Vinyl chloride-vinyl acetate copolymer, vinyl chloride component: 0-95% by weight, vinyl acetate component: 5-3
2. The conductive adhesive according to claim 1 or 2, wherein the conductive adhesive has a polymerization degree of 100 to 900. 4 As a vinyl chloride-vinyl acetate copolymer, vinyl chloride component, 79 to 92 weight φ, vinyl acetate component near to 2
0 weight ratio, maleic acid 01-10 weight ratio, degree of polymerization: ] 0
The conductive adhesive according to claim 1 or 2, wherein the conductive adhesive has a molecular weight of 0 to 1900. 5. As a high surface area carbon black, the BET surface area is 500 full/WJ2), and JISK
DBP oil absorption amount by 6221-1970 is 25Q
+++, l/1. The conductive adhesive according to claims 1 to 4, which uses an adhesive having OOS' or more.
JP19276082A 1982-11-02 1982-11-02 Electrically conductive adhesive Granted JPS5981366A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19276082A JPS5981366A (en) 1982-11-02 1982-11-02 Electrically conductive adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19276082A JPS5981366A (en) 1982-11-02 1982-11-02 Electrically conductive adhesive

Publications (2)

Publication Number Publication Date
JPS5981366A true JPS5981366A (en) 1984-05-11
JPS6144907B2 JPS6144907B2 (en) 1986-10-04

Family

ID=16296588

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19276082A Granted JPS5981366A (en) 1982-11-02 1982-11-02 Electrically conductive adhesive

Country Status (1)

Country Link
JP (1) JPS5981366A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0486307A2 (en) * 1990-11-13 1992-05-20 ASTER, Inc. Electrophoretic coatable sealant compositions
US5223106A (en) * 1990-11-13 1993-06-29 Aster, Inc. Method of using an electrophoretic coatable sealant composition in assembling automobile bodies
KR100429511B1 (en) * 2001-03-19 2004-05-04 주식회사 엠에스비케이 adhesive for shielding of electromagnetic wave and anti mildew and Manufacture Method
WO2010024094A1 (en) * 2008-08-25 2010-03-04 日本ゼオン株式会社 Thermally conductive pressure-sensitive adhesive composition, thermally conductive pressure-sensitive adhesive sheet, and electronic component

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0486307A2 (en) * 1990-11-13 1992-05-20 ASTER, Inc. Electrophoretic coatable sealant compositions
EP0486307A3 (en) * 1990-11-13 1993-04-21 Aster, Inc. Electrophoretic coatable sealant compositions
US5223106A (en) * 1990-11-13 1993-06-29 Aster, Inc. Method of using an electrophoretic coatable sealant composition in assembling automobile bodies
KR100429511B1 (en) * 2001-03-19 2004-05-04 주식회사 엠에스비케이 adhesive for shielding of electromagnetic wave and anti mildew and Manufacture Method
WO2010024094A1 (en) * 2008-08-25 2010-03-04 日本ゼオン株式会社 Thermally conductive pressure-sensitive adhesive composition, thermally conductive pressure-sensitive adhesive sheet, and electronic component

Also Published As

Publication number Publication date
JPS6144907B2 (en) 1986-10-04

Similar Documents

Publication Publication Date Title
TW442522B (en) Water based thick film conductive compositions
CN109929482B (en) Adhesive composition
US20050121657A1 (en) Thick film conductor compositions for use in membrane switch applications
GB1577583A (en) Plasticised vinyl chloride polymer containing adhesive agents
JPS5981366A (en) Electrically conductive adhesive
US3684755A (en) Coating composition of fluorocarbon polymeric material and insulated electrical conductors coated therewith
JPS60258902A (en) Method of producing polymer positive temperature coefficientresistor
EP0534847A1 (en) Plastisol compositions
JP2608195B2 (en) Thermoplastic urethane resin composition
EP0225067B1 (en) Chemically modified ethylene copolymer
JPS61118455A (en) Electrically conductive resin composition
JPH0753813A (en) Electrically conductive plastic composition
JPH0588857B2 (en)
JPH11181206A (en) Chlorinated vinyl chloride-based resin composition
JP3815840B2 (en) Adhesive composition
JPH03213336A (en) Multilayered laminate
JPS5810801B2 (en) Semiconductive resin composition with improved peelability
JPH0157138B2 (en)
JP2555534B2 (en) Veneer manufacturing method
JP2001131374A (en) Chlorinated vinyl chloride-based resin composition
JPH02273407A (en) Conductive grains and manufacture thereof
JPH07149935A (en) Fluororesin-coated molded article
JPS63113025A (en) Production of reel for carrier table
JP3366665B2 (en) Rigid polyvinyl chloride resin film for bonding
JPH09176426A (en) Fluororesin composition