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JPH04106B2 - - Google Patents

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Publication number
JPH04106B2
JPH04106B2 JP57177386A JP17738682A JPH04106B2 JP H04106 B2 JPH04106 B2 JP H04106B2 JP 57177386 A JP57177386 A JP 57177386A JP 17738682 A JP17738682 A JP 17738682A JP H04106 B2 JPH04106 B2 JP H04106B2
Authority
JP
Japan
Prior art keywords
weight
semiconductive
internal
layer
resin composition
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 - Lifetime
Application number
JP57177386A
Other languages
Japanese (ja)
Other versions
JPS5966436A (en
Inventor
Kunio Iwasaki
Kenji Uesugi
Hitoshi Kimura
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.)
Furukawa Electric Co Ltd
Original Assignee
Furukawa Electric 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 Furukawa Electric Co Ltd filed Critical Furukawa Electric Co Ltd
Priority to JP17738682A priority Critical patent/JPS5966436A/en
Publication of JPS5966436A publication Critical patent/JPS5966436A/en
Publication of JPH04106B2 publication Critical patent/JPH04106B2/ja
Granted 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】[Detailed description of the invention]

本発明は架橋ポリエチレン絶縁電力ケーブルの
内部半導電層を形成するに好適な半導電性樹脂組
成物に関するものである。 一般に架橋ポリエチレン絶縁電力ケーブルは導
体上に内部半導電層、絶縁層、必要に応じて外部
半導電層及びシースを押出し被覆により形成して
得ているものである。 これらの各層の内、特に内部半導電層の上面は
電界が最も高く、この界面にカーボンブラツクの
分散不良等による突起部が存在すると電界集中が
おこり、ケーブルの絶縁破壊強度を低下せしめる
ものであつた。従つて内部半導電層面は突起物の
ない極力平滑にすることが必要である。又内部半
導電層が絶縁層と同等以上の耐熱性を有すれば架
橋工程において高温度で架橋を行うことが出来る
ため架橋時間が短縮され生産性を向上せしめるこ
とができる。更に耐油性及び可撓性に良好な内部
半導電層をうることによりケーブルの特性を向上
せしめることができる。 而して従来の内部半導電層を構成する組成とし
てはエチレンアクリル酸エチル共重合体(A)又はエ
チレン酢酸ビニル共重合体(B)等のエチレン共重合
体に導電性カーボンブラツクを添加したものを使
用しているものであるが、ケーブルの絶縁材料と
して使用されるポリエチレンに比して(A)は耐油性
に劣り又(B)は耐熱性に劣るものであつた。従つて
ケーブルの特性は内部半導電層を構成する材料に
よつて著しく影響されるものであつた。 かゝる現況から内部半導電性材料としてポリエ
チレンを使用することが望ましいが、ポリエチレ
ン(高圧法低密度ポリエチレン)は多量のカーボ
ンブラツクを配合した場合、可撓性を喪失し且つ
内部半導電層の界面に突起部を発生せしめるとい
う問題を生ずるため使用することが出来ないもの
であつた。 本発明はかゝる現状に鑑み、耐熱性、耐油性を
改善し、しかも表面平滑な内部半導電層を形成し
得るための電力ケーブル用半導電性樹脂組成物を
見出したものである。即ち本発明は直鎖状低密度
ポリエチレン50〜95重量%とエチレン共重合体50
〜5重量%との混合物に所定量の導電性カーボン
ブラツクを配合したことを特徴とするものであ
る。 本発明において直鎖状低密度ポリエチレンと
は、エチレンと炭素数3以上のαオレフインとの
共重合体であり、長鎖分岐のないポリエチレンを
いうものである。その製法は気相法、液相法の何
れでもよく、密度は加工性を容易にするため
0.930g/cm3以下のものが望ましい。 又エチレン共重合体としては、例えばエチレン
アクリル酸エチル共重合体、エチレン酢酸ビニル
共重合体、エチレンプロピレンゴム等を使用する
ものである。 本発明においてエチレン共重合体の含有量を50
〜5重量%に限定した理由は、50重量%を超して
配合した場合には耐油性が低下するためであり、
又5重量%未満の場合には当該組成物を用いて形
成した半導電層の界面が荒れて突起を生成するた
めである。 なおエチレン共重合体の好ましい配合量範囲は
30〜50重量%である。又、導電性付与のためのカ
ーボンブラツクとしてはフアーネスブラツク、ア
セチレンブラツク、ケツチエンブラツク等何れを
使用してもよい。 次に本発明の実施例について説明する。 実施例1〜5及び比較例1〜4 第1表に示す組成によるベースポリマー100重
量部に対しアセチレンブラツク60重量部、酸化防
止剤0.3重量部、及びヂクミルパーオキサイド1.0
重量部を夫々添加し混練して本発明半導電性樹脂
組成物及び比較例半導電性樹脂組成物をえた。 斯くして得た半導電性樹脂組成物について性能
を試みるために180℃、10分間プレス架橋を行つ
た後JISK−6723に準じて耐油性試験(引張強度
残率%)を行つた、その結果は第1表に示す通り
である。 又上記の半導電性樹脂組成物を導体の外側に押
出被覆した内部半導電層を形成し、その外側にポ
リエチレンの絶縁層を設けて6.6KV250mm2のポリ
エチレン絶縁電力ケーブルを製造し、内部半導電
層の界面の状態並に電気的特性を試験した。その
結果は第1表に示す通りである。 なお第1表のベースポリマーの欄における数値
は何れも重量部である。
The present invention relates to a semiconductive resin composition suitable for forming an internal semiconductive layer of a crosslinked polyethylene insulated power cable. Generally, a crosslinked polyethylene insulated power cable is obtained by forming an inner semiconducting layer, an insulating layer, an outer semiconducting layer and a sheath as necessary on a conductor by extrusion coating. Among these layers, the electric field is highest especially on the upper surface of the internal semiconducting layer, and if there are protrusions at this interface due to poor dispersion of carbon black, etc., electric field concentration will occur, reducing the dielectric breakdown strength of the cable. Ta. Therefore, it is necessary to make the surface of the internal semiconducting layer as smooth as possible without any protrusions. Furthermore, if the internal semiconductive layer has heat resistance equal to or higher than that of the insulating layer, crosslinking can be carried out at high temperature in the crosslinking step, so crosslinking time can be shortened and productivity can be improved. Furthermore, by providing an internal semiconducting layer with good oil resistance and flexibility, the characteristics of the cable can be improved. The composition of the conventional internal semiconductive layer is one in which conductive carbon black is added to an ethylene copolymer such as ethylene ethyl acrylate copolymer (A) or ethylene vinyl acetate copolymer (B). However, compared to polyethylene, which is used as an insulating material for cables, (A) was inferior in oil resistance, and (B) was inferior in heat resistance. Therefore, the characteristics of the cable were significantly influenced by the material constituting the internal semiconducting layer. Under these circumstances, it is desirable to use polyethylene as the internal semiconductive material, but when polyethylene (high-pressure low-density polyethylene) is blended with a large amount of carbon black, it loses its flexibility and the internal semiconductive layer deteriorates. It could not be used because of the problem of generating protrusions at the interface. In view of the current situation, the present invention has been made to discover a semiconductive resin composition for power cables that has improved heat resistance and oil resistance and is capable of forming an internal semiconductive layer with a smooth surface. That is, the present invention uses 50 to 95% by weight of linear low density polyethylene and 50% by weight of ethylene copolymer.
5% by weight of conductive carbon black. In the present invention, linear low-density polyethylene is a copolymer of ethylene and α-olefin having 3 or more carbon atoms, and refers to polyethylene without long chain branches. The manufacturing method may be either a gas phase method or a liquid phase method, and the density is determined to facilitate workability.
It is desirable that the weight is 0.930g/cm 3 or less. Examples of the ethylene copolymer include ethylene ethyl acrylate copolymer, ethylene vinyl acetate copolymer, and ethylene propylene rubber. In the present invention, the content of ethylene copolymer is 50
The reason why it is limited to ~5% by weight is that oil resistance decreases when it is blended in excess of 50% by weight.
If the amount is less than 5% by weight, the interface of the semiconductive layer formed using the composition becomes rough and protrusions are formed. The preferred blending range of the ethylene copolymer is
It is 30-50% by weight. Further, as the carbon black for imparting conductivity, any of furnace black, acetylene black, butthorn black, etc. may be used. Next, examples of the present invention will be described. Examples 1 to 5 and Comparative Examples 1 to 4 60 parts by weight of acetylene black, 0.3 parts by weight of antioxidant, and 1.0 parts by weight of dicumyl peroxide per 100 parts by weight of the base polymer having the composition shown in Table 1.
Parts by weight of each were added and kneaded to obtain a semiconductive resin composition of the present invention and a comparative semiconductive resin composition. In order to test the performance of the semiconductive resin composition thus obtained, it was press-crosslinked at 180°C for 10 minutes and then subjected to an oil resistance test (tensile strength retention %) in accordance with JISK-6723.The results are as follows. is shown in Table 1. In addition, an internal semiconductive layer is formed by extruding the above semiconductive resin composition on the outside of the conductor, and a polyethylene insulating layer is provided on the outside to manufacture a 6.6 KV 250 mm 2 polyethylene insulated power cable. The electrical properties as well as the interfacial conditions of the layers were tested. The results are shown in Table 1. Note that all numerical values in the base polymer column of Table 1 are parts by weight.

【表】【table】

【表】 上表より明らかな如く本発明電力ケーブル用半
導電性組成物は耐油性、AC破壊電圧値が優れ且
つ導体上に押出成形した内部半導電層界面も突起
などは生成していない。これに対して比較例半導
電性組成物は内部半導電層の界面が良好な場合に
は耐油性が低下し、耐油性が良好であると内部半
導電層の界面が荒れて不良となるなど一長一短を
有するものであつた。 以上詳述した如く本発明の電力ケーブル用半導
電性樹脂組成物は耐油性、可撓性及び電気特性に
優れているため、この組成物により電力ケーブル
の内部半導電層を形成すれば優れた電気特性を有
する電力ケーブルが得られるなど極めて有用なも
のである。
[Table] As is clear from the above table, the semiconductive composition for power cables of the present invention has excellent oil resistance and AC breakdown voltage value, and no protrusions are formed at the interface of the internal semiconductive layer extruded onto the conductor. On the other hand, in the case of the comparative semiconductive composition, when the interface of the internal semiconductive layer is good, the oil resistance decreases, and when the oil resistance is good, the interface of the internal semiconductive layer becomes rough and becomes poor. It had its advantages and disadvantages. As detailed above, the semiconductive resin composition for power cables of the present invention has excellent oil resistance, flexibility, and electrical properties. The present invention is extremely useful as a power cable with electrical properties can be obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 直鎖状低密度ポリエチレン50〜95重量%とエ
チレン共重合体50〜5重量%との混和物に所定量
の導電性カーボンブラツクを配合してなることを
特徴とする電力ケーブル用半導電性樹脂組成物。
1. A semiconductive material for power cables, which is made by blending a predetermined amount of conductive carbon black into a mixture of 50 to 95% by weight of linear low-density polyethylene and 50 to 5% by weight of ethylene copolymer. Resin composition.
JP17738682A 1982-10-08 1982-10-08 Semiconductive resin composition Granted JPS5966436A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17738682A JPS5966436A (en) 1982-10-08 1982-10-08 Semiconductive resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17738682A JPS5966436A (en) 1982-10-08 1982-10-08 Semiconductive resin composition

Publications (2)

Publication Number Publication Date
JPS5966436A JPS5966436A (en) 1984-04-14
JPH04106B2 true JPH04106B2 (en) 1992-01-06

Family

ID=16030029

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17738682A Granted JPS5966436A (en) 1982-10-08 1982-10-08 Semiconductive resin composition

Country Status (1)

Country Link
JP (1) JPS5966436A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59215342A (en) * 1983-05-24 1984-12-05 Nippon Petrochem Co Ltd Resin composition for power cables
JPS60147456A (en) * 1984-01-11 1985-08-03 Hitachi Cable Ltd conductive composition
JPS60199041A (en) * 1984-03-22 1985-10-08 Fujikura Ltd Semiconductive composition
JPS60206855A (en) * 1984-03-30 1985-10-18 Fujikura Ltd Electrically semiconductive composition
JPS6112737A (en) * 1984-06-27 1986-01-21 Fujikura Ltd Mixture for semiconductive layer
JPS6112738A (en) * 1984-06-27 1986-01-21 Fujikura Ltd Mixture for semiconductive layer
JPH0680127B2 (en) * 1985-04-10 1994-10-12 古河電気工業株式会社 Semi-conductive resin composition
KR900002983B1 (en) * 1985-04-11 1990-05-03 Furukawa Electric Co Ltd Lead alloy foil for laminated tape
US8388868B2 (en) * 2010-02-01 2013-03-05 General Cable Technologies Corporation Vulcanizable copolymer semiconductive shield compositions

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5645933A (en) * 1979-09-25 1981-04-25 Mitsubishi Petrochem Co Ltd Electrically conductive resin composition
CA1195792A (en) * 1981-09-16 1985-10-22 William J. Michie, Jr. Drip irrigation tubing cross-linked by irradiation and extrudable tube forming composition
JPS58118839A (en) * 1982-01-08 1983-07-15 Hitachi Cable Ltd Semiconductive composition

Also Published As

Publication number Publication date
JPS5966436A (en) 1984-04-14

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