JPH0341371Y2 - - Google Patents
Info
- Publication number
- JPH0341371Y2 JPH0341371Y2 JP4034782U JP4034782U JPH0341371Y2 JP H0341371 Y2 JPH0341371 Y2 JP H0341371Y2 JP 4034782 U JP4034782 U JP 4034782U JP 4034782 U JP4034782 U JP 4034782U JP H0341371 Y2 JPH0341371 Y2 JP H0341371Y2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- thin film
- properties
- conductive
- 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
- 239000010408 film Substances 0.000 claims description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 13
- 229910052802 copper Inorganic materials 0.000 claims description 13
- 239000010949 copper Substances 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 239000010409 thin film Substances 0.000 claims description 9
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 150000002978 peroxides Chemical class 0.000 claims description 5
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- -1 sialyl peroxide Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000009975 flexible effect Effects 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
Landscapes
- Non-Insulated Conductors (AREA)
Description
この考案は、耐薬品性、耐水性、可撓性などの
諸特性に優れた導電性薄葉体に関するものであ
る。
近年電力ケーブルの各種特性に対する要求には
非常に厳しいものがあり、このような電力ケーブ
ルに用いられる半導電層形成用導電性薄葉体に対
し当然、その防水性、防湿性、耐薬品性、可撓性
及び接着性等に非常に高度の特性が要求される。
しかし一般に、
(i) 熱可撓性樹脂に導電性カーボンを配合して導
電性組成物を得る場合に、100〜104Ω−cmと云
つた導電度を得るにはカーボン配合量を樹脂
100重量部に対して40〜150重量部と大量に配合
しなければならず、かかる大量のカーボンが混
入された樹脂組性物はこれをフイルム又はシー
ト状にすることが非常にむづかしく、たとえ加
工し得たとしてもその引張強度、低温脆性、可
撓性などの機械的特性が著しく低下してしまう
こと、
(ii) 熱可撓性樹脂は本来遮水性、耐薬品性などに
は優れているが、特殊な薬品に接するなど苛酷
な使用条件下では長期間にその機能が著しく低
下してしまう、
(iii) 上記の点に鑑み、金属シートに前記の半導電
性樹脂シートを積層した積層体も多数あるが、
両材料は本来物理的、化学的性質が異ることか
らその間の接着力が微弱であり、充分な機能を
発揮し得る積層体を得ることはむづかしい。そ
して両者を適切な接着剤を用いて接着積層し得
たとしても該接着剤が絶縁体であることから得
られる薄葉体の厚さ方向の導電性を得ることは
因難である、
などの種々の理由から上記の諸特性に関して前
述した高度の要求を満足する導電性薄葉体を得る
ことは非常に因難なのが実情である。
ここに考案者等はかかる問題点を解決すべく鋭
意検討を重ねた結果、銅フイルムに対して特に選
択された半導電性組成物を用いることにより上述
の相互の接着力が少なくとも2Kg/15mm幅と著し
く向上し上記の問題が解決されることを見出しこ
の考案を完成するに至つたものである。
即ちこの考案は、銅フイルムの少なくとも一面
に、エチレンプロピレンゴム100重量部(以下の
部は重量部)に対して導電性カーボン20〜100部、
及び過酸化物0.5〜5部を配合した組成物からな
る半導電性樹脂層を設けてなる導電性薄葉体であ
る。
この考案による導電性薄葉体が上記の諸特性を
著しく向上させる理由は以下の如く考えられる。
即ち銅フイルムが本来の耐薬品性、耐水性などに
優れて居り、又エチレンプロピレンゴム組成物に
より可撓性の著しい向上が認められ、そして該組
成物中の特に過酸化物が何等かの原因にて前記銅
フイルム表面に多孔質な数10Åの酸化皮膜層を生
成させ、これにゴム樹脂分が充填されて両材料即
ち銅/導電性組成物間の接着力を飛躍的に増大さ
せこれらの相剰作用で上記特性の全体を向上させ
ることができたものである。
この考案における導電性カーボンブラツクとし
ては、商品名ケツチエンブラツクEC(オランダ、
アクゾ社製)、アセチレンブラツク、フアーネス
ブラツクなどが用いられ、これらは上述の導電性
具体的には100〜105Ω−cmを考慮してエチレンプ
ロピレンゴム100部に対して20〜100部が混合され
る。
次にこの考案で用いられる過酸化物としては、
ハイドロパーオキサイド、シアルキルパーオ
キサイド、シアシルパーオキサイド、ケトン
パーオキサイド、アルキルパーエステル、パ
ーオキシジカーボネート、過酸化水素などがあ
り、これらはエチレンプロピレンゴム100部に対
して0.5〜5部の使用割合である。
過酸化物が、この下限以下では、銅の表面に多
孔質な酸化皮膜層を形成させる能力がなく、その
ため、銅とエチレンプロピレンゴム間で良好な接
着強度が得られない。
又上限を超えるとエチレンプロピレンゴムその
ものの物理特性が低下するためで好ましくない。
この考案において銅フイルムに対して上述の半
導電性組成物層を接着させる際の温度は130〜160
℃、圧力は5Kg/cm2以上にすることが肝要であ
る。これらの温度又は圧力の範囲外では上述した
特性、特に通常必要な接着力約2Kg/15mmが得ら
れず好ましくない。
本考案にて用いる銅フイルムの厚さは10μ〜
2000μまた半導電性樹脂層の厚さは20μ〜5000μで
ある。
第1図にはこの考案の好ましい実施例を示した
が図において1は銅フイルム、2は半導電性樹脂
層である。
この考案は以上の説明及び後記実施例から明ら
かな如く、銅フイルムに対して特定の選択された
半導電性樹脂層を設けたことにより、特に両者の
接着力を向上させそれにより上記諸特性を著しく
改善させ得たものでありその工業的効果は非常に
大である。
以下実施例によりこの考案を具体的に説明す
る。
実施例1〜2、比較例1〜4
次表の金属フイルム及び導電性樹脂を同表条件
下にプレスして貼り合せ導電性薄葉体を得、該薄
体の接着力を調べ結果を同表に示した。
This invention relates to a conductive thin film that has excellent properties such as chemical resistance, water resistance, and flexibility. In recent years, there have been very strict requirements for various properties of power cables, and it is natural that the conductive thin film used for forming semiconductive layers in such power cables must have waterproof, moisture-proof, chemical-resistant, and flexible properties. Extremely high characteristics such as flexibility and adhesiveness are required. However, in general, (i) when blending conductive carbon into a thermoflexible resin to obtain a conductive composition, in order to obtain a conductivity of 10 0 to 10 4 Ω-cm, the carbon content must be increased by increasing the amount of carbon in the resin.
A large amount of carbon must be blended, 40 to 150 parts by weight per 100 parts by weight, and it is very difficult to make a resin composition into a film or sheet with such a large amount of carbon mixed in. Even if it could be processed, its mechanical properties such as tensile strength, low-temperature brittleness, and flexibility would be significantly reduced. (ii) Thermoflex resins inherently have excellent water-blocking properties and chemical resistance. However, under harsh usage conditions such as contact with special chemicals, its functionality deteriorates significantly over a long period of time. There are many laminates,
Since the two materials originally have different physical and chemical properties, the adhesive force between them is weak, and it is difficult to obtain a laminate that can exhibit sufficient functionality. Even if the two could be bonded and laminated using a suitable adhesive, it would be difficult to obtain conductivity in the thickness direction of the thin film because the adhesive is an insulator. For these reasons, the reality is that it is very difficult to obtain a conductive thin film that satisfies the above-mentioned high requirements regarding the above-mentioned properties. As a result of intensive studies to solve these problems, the inventors have found that by using a semiconductive composition specially selected for the copper film, the above-mentioned mutual adhesion force can be increased to at least 2 kg/15 mm width. They found that the above problem was solved by significantly improving the results, and completed this invention. That is, in this invention, 20 to 100 parts of conductive carbon is added to 100 parts by weight of ethylene propylene rubber (the following parts are parts by weight) on at least one side of the copper film.
This is a conductive thin film body provided with a semiconductive resin layer made of a composition containing 0.5 to 5 parts of peroxide. The reason why the conductive thin film material according to this invention significantly improves the above-mentioned properties is considered as follows.
That is, the copper film has excellent inherent chemical resistance and water resistance, and the ethylene propylene rubber composition has been found to significantly improve flexibility. A porous oxide film layer of several tens of angstroms is formed on the surface of the copper film, and this is filled with rubber resin to dramatically increase the adhesive force between the two materials, that is, the copper/conductive composition. All of the above characteristics could be improved through a mutual effect. The conductive carbon black used in this invention was manufactured under the trade name Ketschen Black EC (made in the Netherlands).
Akzo Corporation), acetylene black, furnace black, etc. are used, and these are used in an amount of 20 to 100 parts per 100 parts of ethylene propylene rubber, taking into account the above-mentioned conductivity of 10 0 to 10 5 Ω-cm. are mixed. Next, the peroxides used in this idea are:
Hydroperoxide, sialkyl peroxide, sialyl peroxide, ketone peroxide, alkyl perester, peroxydicarbonate, hydrogen peroxide, etc. are used in a proportion of 0.5 to 5 parts per 100 parts of ethylene propylene rubber. It is. If the peroxide is below this lower limit, there is no ability to form a porous oxide film layer on the surface of copper, and therefore good adhesive strength cannot be obtained between copper and ethylene propylene rubber. Moreover, exceeding the upper limit is not preferable because the physical properties of the ethylene propylene rubber itself deteriorate. In this invention, the temperature when adhering the above-mentioned semiconductive composition layer to the copper film is 130 to 160.
It is important that the temperature and pressure be at least 5 kg/cm 2 . If the temperature or pressure is outside these ranges, the above-mentioned properties, especially the normally required adhesion strength of about 2 kg/15 mm, cannot be obtained, which is not preferable. The thickness of the copper film used in this invention is 10μ ~
2000μ, and the thickness of the semiconductive resin layer is 20μ to 5000μ. A preferred embodiment of this invention is shown in FIG. 1, where 1 is a copper film and 2 is a semiconductive resin layer. As is clear from the above description and the examples below, this invention provides the copper film with a specifically selected semiconductive resin layer to improve the adhesive strength between the two, thereby achieving the above-mentioned properties. This was a significant improvement, and its industrial effects are very large. This invention will be specifically explained below with reference to Examples. Examples 1 to 2, Comparative Examples 1 to 4 The metal films and conductive resin shown in the following table were pressed under the conditions in the table to obtain a conductive thin film body, and the adhesive strength of the thin body was examined and the results are shown in the table below. It was shown to.
【表】【table】
【表】
上表の結果によれば本考案の特性向上は比較例
に比べて著しいことが明らかである。[Table] According to the results in the above table, it is clear that the characteristics of the present invention are significantly improved compared to the comparative example.
図面はこの考案の導電性薄葉体の断面図であ
る。
1……銅フイルム、2……半導電性樹脂層。
The drawing is a cross-sectional view of the conductive thin film body of this invention. 1... Copper film, 2... Semiconductive resin layer.
Claims (1)
ピレンゴム100重量部に対して導電性カーボン20
〜100重量部及び過酸化物0.5〜5重量部を配合し
た組成物からなる半導電性樹脂層を設けたことを
特徴とする導電性薄葉体。 At least one side of the copper film is coated with 20 parts by weight of conductive carbon per 100 parts by weight of ethylene propylene rubber.
1. A conductive thin film comprising a semiconductive resin layer comprising a composition containing ~100 parts by weight and 0.5 to 5 parts by weight of peroxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4034782U JPS58144712U (en) | 1982-03-24 | 1982-03-24 | conductive thin film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4034782U JPS58144712U (en) | 1982-03-24 | 1982-03-24 | conductive thin film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58144712U JPS58144712U (en) | 1983-09-29 |
JPH0341371Y2 true JPH0341371Y2 (en) | 1991-08-30 |
Family
ID=30051573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4034782U Granted JPS58144712U (en) | 1982-03-24 | 1982-03-24 | conductive thin film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58144712U (en) |
-
1982
- 1982-03-24 JP JP4034782U patent/JPS58144712U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS58144712U (en) | 1983-09-29 |
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