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JPS6045218B2 - conductive mixture - Google Patents
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JPS6045218B2 - conductive mixture - Google Patents

conductive mixture

Info

Publication number
JPS6045218B2
JPS6045218B2 JP553878A JP553878A JPS6045218B2 JP S6045218 B2 JPS6045218 B2 JP S6045218B2 JP 553878 A JP553878 A JP 553878A JP 553878 A JP553878 A JP 553878A JP S6045218 B2 JPS6045218 B2 JP S6045218B2
Authority
JP
Japan
Prior art keywords
present
mixture
rubber
parts
conductive mixture
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
Application number
JP553878A
Other languages
Japanese (ja)
Other versions
JPS5499154A (en
Inventor
義明 松賀
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.)
Hitachi Cable Ltd
Original Assignee
Hitachi Cable 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 Hitachi Cable Ltd filed Critical Hitachi Cable Ltd
Priority to JP553878A priority Critical patent/JPS6045218B2/en
Publication of JPS5499154A publication Critical patent/JPS5499154A/en
Publication of JPS6045218B2 publication Critical patent/JPS6045218B2/en
Expired legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Conductive Materials (AREA)

Description

【発明の詳細な説明】 本発明は電気絶縁材料との組合せあるいは単独で導電材
料として用いる作業性、導電性にすぐれた混和物に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a mixture that has excellent workability and conductivity when used in combination with an electrically insulating material or as a conductive material alone.

導電性混和物については従来から多くの研究が行われて
来た。
Many studies have been conducted on conductive mixtures.

このため多数の添加物、その添加方法が報告されている
が、相溶性、加工性、熱安定性、抵抗安定性などすべて
を満足するものは見出されていない。
For this reason, a large number of additives and methods of adding them have been reported, but none has been found that satisfies all of the requirements such as compatibility, processability, thermal stability, and resistance stability.

本発明は上記要望を満たしたものである。The present invention satisfies the above requirements.

すなわち、ポリオレフィンまたはゴムエラストマー10
榔に対して、炭素数が1〜4のアルキル基を1〜4個有
するアルキルフルオランセンあるいはアルキルピレンを
2〜m部含有し、さらにカーボンブラックを配合してな
る組成物は加工性にすぐれ、特に架橋反応の際の阻害性
、ブリードなどによる悪影響は認められず、体積抵抗率
を容易に低下させることを見出し、本発明に到達したも
のてある。
That is, polyolefin or rubber elastomer 10
A composition containing 2 to m parts of alkylfluoranthene or alkylpyrene having 1 to 4 alkyl groups having 1 to 4 carbon atoms and carbon black has excellent processability. In particular, we have found that the volume resistivity can be easily lowered without any adverse effects such as inhibition or bleeding during the crosslinking reaction, and have thus arrived at the present invention.

本発明の効果は、上記配合に基づき、加工時における作
業性の向上、混和物の特性向上等のすくれた点が示され
たことである。
The effects of the present invention are that, based on the above-mentioned formulation, excellent points such as improved workability during processing and improved properties of the mixture were demonstrated.

所期の体積抵抗率を得るためには、従来から使用されて
いるアセチレンブラックの113量、導電性フアーネス
ブラツク(XC−72)のIP量以下ですむ。上記すぐ
れた効果を示すアルキルフルオランセンあるいはアルキ
ルピレンは炭素数1〜4個のアルキル基、すなわちメチ
ル、エチル、プロピル、ブチル等の基が1〜4個の範囲
でフルオランセン核あるいはピレン核に結合せられたも
のである。
In order to obtain the desired volume resistivity, the amount of acetylene black used conventionally is less than 113, and the amount of IP of conductive furnace black (XC-72) is required. In the alkylfluoranthene or alkylpyrene that exhibits the above-mentioned excellent effects, an alkyl group having 1 to 4 carbon atoms, that is, 1 to 4 groups such as methyl, ethyl, propyl, butyl, etc., is bonded to the fluoranthene nucleus or pyrene nucleus. It was given to me.

これらのアルキル基は、これらの範囲で任意の位置に任
意の長さのものであつてよい。アルキル基を持たないも
のはポリオレフィンとの相溶性が不J良でブリードする
欠点がある。また、アルキル置換基の数が4個を超える
ものは合成にも難がある。
These alkyl groups may be of any length in any position within these ranges. Those without an alkyl group have poor compatibility with polyolefins and have the disadvantage of bleeding. Further, those having more than 4 alkyl substituents are difficult to synthesize.

本発明に使用されるアルキルフルオランセンおよびアル
キルピレンは次のようなものである。
The alkylfluoranthene and alkylpyrene used in the present invention are as follows.

X:1〜4の整数(但し、ここでアルキル基が2個以上
の場合、これらのアルキル基は同一又は異種であつても
よい。)その構造より考えて多数の異性体を有するもの
てあるが、本発明実施にあたつては純粋物質である必要
はなく、これらの異性体を含有しても差支えない。
X: An integer of 1 to 4 (However, if there are two or more alkyl groups, these alkyl groups may be the same or different types.) Considering the structure, there are many isomers. However, in carrying out the present invention, it is not necessary that the substance be a pure substance, and there is no problem even if it contains these isomers.

また本発明の範囲内であれば、各種アルキルフルオラン
センの混合物、アルキルピレンの混合物であつても何等
問題はない。本発明に使用されるアルキルフルオランセ
ン、アルキルピレン(以下多環芳香族油と略称する)の
使用量は、ポリマー(ポリオレフィンあるいはゴムエラ
ストマー)1(1)部に対して、2〜■部である。2部
以下では混和作業性向上効果、体積抵抗率低下効果がな
くなる。
Further, within the scope of the present invention, there is no problem even if a mixture of various alkylfluorancenes or a mixture of alkylpyrenes is used. The amount of alkylfluoranthene and alkylpyrene (hereinafter referred to as polycyclic aromatic oil) used in the present invention is 2 to 1 parts per 1 (1) part of the polymer (polyolefin or rubber elastomer). be. If the amount is less than 2 parts, the effect of improving mixing workability and reducing the volume resistivity will be lost.

また1娼を超えるとブリードの発生、作業性の低下(押
出機への食込みが悪くなる)などの欠点を生ずる恐れが
ある。本発明において多環芳香族油を添加するポリオレ
フィンとしては、ポリエチレン、ポリプロピレ゛ン、ポ
リブテン、エチレン〜プロピレン共重合体、エチレン〜
酢酸ビニル共重合体等であり、ゴムエラストマーとは、
ブチルゴム、ニトリルゴム、ポリクロロプレン、スチレ
ンブタジエンゴム、天然ゴム、シリコーンゴム等である
。多環芳香族油の添加による効果発現の要因は、先ず操
作油としての効果があるため、ポリマーにカーボンブラ
ックを練り込む際の加工性を向上させることは、ゴム工
業における操作油使用の場合と同様であり、また導電性
における操作油使用の場合と同様であり、また導電性に
ついては、多環芳香族の名の示す通り、構造的に電子が
流れ易い構造となつており、従つてカーボンブラック粒
子間を電子の流れ易い物質が満たすことになり、これが
体積抵抗率の低下となつて現われるものと考えられる。
Moreover, if it exceeds 1, there is a risk that defects such as occurrence of bleeding and reduction in workability (increased penetration into the extruder) may occur. In the present invention, polyolefins to which polycyclic aromatic oil is added include polyethylene, polypropylene, polybutene, ethylene-propylene copolymer, ethylene-
Rubber elastomers are vinyl acetate copolymers, etc.
These include butyl rubber, nitrile rubber, polychloroprene, styrene-butadiene rubber, natural rubber, silicone rubber, etc. The effect of adding polycyclic aromatic oil is primarily due to its effectiveness as an operating oil, so improving processability when incorporating carbon black into polymers is similar to when using operating oil in the rubber industry. It is similar to the case of using operating oil for conductivity, and as for conductivity, as the name of polycyclic aromatic compounds suggests, they have a structure that allows electrons to flow easily, so carbon It is thought that the space between the black particles is filled with a substance through which electrons can easily flow, and this appears as a decrease in volume resistivity.

以下、本発明の実施例について説明する。Examples of the present invention will be described below.

試料は、ロール練り混和物にDCP(ジキユミルパーオ
キサイド)2部(シリコーンゴムの場合はDCP2部の
他にトリアリルイソシアヌレート1部添加)添加し、1
65℃、100kg/Clt(ゲージ圧力)で1紛、厚
さ1朗に調整した。
The sample was prepared by adding 2 parts of DCP (dikymyl peroxide) to a roll-kneaded mixture (in the case of silicone rubber, 1 part of triallyl isocyanurate was added in addition to 2 parts of DCP), and
The powder was adjusted to 1 powder and 1 layer thick at 65° C. and 100 kg/Clt (gauge pressure).

この試料を幅10T$Lに裁断し、電極間距離8.5礪
をもつてホイートストンブリツジにより体積抵抗率を求
めた。この測定方法は、BS・2044(MethOd
−2)に準拠したものである。以上説明したところから
明らかな如く、本発明の導電性混和物は、導電性カーボ
ンブラックを含む混和物を調整するに際して、アルキル
フルオラセン、アルキルピレンの如き多環芳香族油を添
加することにより混和作業性を向上し、しかも体積低効
率が著しく低下するという相乗的効果が得られたもので
、電線・ケーブルを含む電気的用途、工業用、産業用途
に広く適用できる。
This sample was cut into a width of 10 T$L, and the volume resistivity was determined using a Wheatstone bridge with a distance between the electrodes of 8.5 cm. This measurement method is based on BS 2044 (MethOd
-2). As is clear from the above explanation, the conductive mixture of the present invention can be mixed by adding a polycyclic aromatic oil such as alkylfluoracene or alkylpyrene when preparing a mixture containing conductive carbon black. It has the synergistic effect of improving workability and significantly reducing volumetric efficiency, and can be widely applied to electrical applications, including electric wires and cables, industrial applications, and industrial applications.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリオレフィンまたはゴムエラストマー100部に
対して、炭素数が1〜4のアルキル基を1〜4個有する
アルキルフルオランセンあるいはアルキルピレンを2〜
10部含有し、さらにカーボンブラックが配合されてな
ることを特徴とする導電性混和物。
1 For 100 parts of polyolefin or rubber elastomer, add 2 to 4 alkylfluorancenes or alkylpyrenes having 1 to 4 alkyl groups having 1 to 4 carbon atoms.
A conductive mixture containing 10 parts of carbon black.
JP553878A 1978-01-20 1978-01-20 conductive mixture Expired JPS6045218B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP553878A JPS6045218B2 (en) 1978-01-20 1978-01-20 conductive mixture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP553878A JPS6045218B2 (en) 1978-01-20 1978-01-20 conductive mixture

Publications (2)

Publication Number Publication Date
JPS5499154A JPS5499154A (en) 1979-08-04
JPS6045218B2 true JPS6045218B2 (en) 1985-10-08

Family

ID=11613959

Family Applications (1)

Application Number Title Priority Date Filing Date
JP553878A Expired JPS6045218B2 (en) 1978-01-20 1978-01-20 conductive mixture

Country Status (1)

Country Link
JP (1) JPS6045218B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61293241A (en) * 1985-06-20 1986-12-24 Eiwa Kasei Kogyo Kk Electrically conductive elastomer composition containing vulcanized rubber powder
US8999200B2 (en) * 2002-07-23 2015-04-07 Sabic Global Technologies B.V. Conductive thermoplastic composites and methods of making

Also Published As

Publication number Publication date
JPS5499154A (en) 1979-08-04

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