JPS5917135B2 - semiconductive composition - Google Patents

semiconductive composition

Info

Publication number
JPS5917135B2
JPS5917135B2 JP13837579A JP13837579A JPS5917135B2 JP S5917135 B2 JPS5917135 B2 JP S5917135B2 JP 13837579 A JP13837579 A JP 13837579A JP 13837579 A JP13837579 A JP 13837579A JP S5917135 B2 JPS5917135 B2 JP S5917135B2
Authority
JP
Japan
Prior art keywords
weight
parts
composition
vinyl acetate
polystyrene
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
JP13837579A
Other languages
Japanese (ja)
Other versions
JPS5661440A (en
Inventor
和憲 寺崎
興太郎 三尾
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
Original Assignee
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 Dainichi Nippon Cables Ltd filed Critical Dainichi Nippon Cables Ltd
Priority to JP13837579A priority Critical patent/JPS5917135B2/en
Publication of JPS5661440A publication Critical patent/JPS5661440A/en
Publication of JPS5917135B2 publication Critical patent/JPS5917135B2/en
Expired legal-status Critical Current

Links

Landscapes

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

Description

【発明の詳細な説明】 本発明は、架橋ポリエチレン絶縁電力ケーブル等のソリ
ッド型電力ケーブルの外部半導電層の構成材料として好
適の半導電性組成物番こ関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a semiconducting composition suitable as a constituent material of an outer semiconducting layer of a solid power cable such as a crosslinked polyethylene insulated power cable.

外部半導電層は、ケーブル運転時には絶縁層と密着して
空隙のないことがケーブルの電気的性能上必要であり、
一方、ケーブルの接続工事においては絶縁層と剥離容易
であることが要求される。剥離性の半導電組成物として
各種のものが従来から提案されているが、あるものは剥
離性は良好であつても、ペレットに加工することが困難
であつたり、粘性が高く押出加工が困難であつたりある
いは押出時の熱でスコーチを起しやすい欠点を有してい
たり、他のものは逆にペレット加工性等i には優れて
いても剥離性の面で欠点があるなどの理由から、必ずし
も満足のいく半導電性組成物が提案されているとはいい
難い。上記に鑑み、本発明はペレット加工性、耐スコー
チ性に優れ、而して押出加工が容易であつて、0 しか
も押出番こより、ポリエチレン、エチレン−プロピレン
系共重合体等の無極性乃至低極性有機ポリマーまたはそ
れらの架橋体からなる絶縁層に対して優れた密着性、易
剥離性の外部半導電層を形成し得る新規な半導電性組成
物を提案するもので5 ある。
For the electrical performance of the cable, it is necessary for the external semiconductive layer to be in close contact with the insulating layer without any gaps during cable operation.
On the other hand, in cable connection work, it is required that the insulation layer be easily peeled off. Various types of releasable semiconducting compositions have been proposed in the past, but some have good releasability but are difficult to process into pellets or have high viscosity and are difficult to extrude. This is because some materials have the disadvantage of being too hot or prone to scorching due to the heat during extrusion, while others have disadvantages in terms of peelability even though they are excellent in pellet processability. However, it cannot be said that a satisfactory semiconductive composition has been proposed. In view of the above, the present invention has excellent pellet processability and scorch resistance, and is easy to extrude. The present invention proposes a novel semiconductive composition that can form an external semiconductive layer with excellent adhesion and easy peelability to an insulating layer made of an organic polymer or a crosslinked product thereof.

本発明は酢酸ビニル含有量25重量、以上さらに好まし
くは35重量%以上のエチレン−酢酸ビニル共重合体(
以下EVA)100重量部と、メルトフローインデック
ス(以下MFI)5以上さi0らに好ましくは10以上
のポリスチレン20〜70重量部と、導電性カーボンブ
ラック及び有機過酸化物からなることを特徴とするもの
である。
The present invention provides an ethylene-vinyl acetate copolymer (
It is characterized by consisting of 100 parts by weight of EVA), 20 to 70 parts by weight of polystyrene having a melt flow index (hereinafter MFI) of 5 or more, more preferably 10 or more, conductive carbon black, and an organic peroxide. It is something.

EVAの酢酸ビニル含有量を25重量部以上とする理由
は酢酸ビニル含有量が25重量%未満でj5はこの組成
物にて形成された半導電層は、絶縁層との接着強度が大
きくなり著しく接続作業性が悪いからである。また、ポ
リスチレンについて、JISK6870に従つて測定し
たが、MFI5未満のものでは得ら10れた組成物の溶
融粘度が高く押出加工性が劣るからである。
The reason why the vinyl acetate content of EVA is set to 25 parts by weight or more is that when the vinyl acetate content is less than 25% by weight, the semiconductive layer formed with this composition has a significantly increased adhesive strength with the insulating layer. This is because the connection workability is poor. Further, polystyrene was measured according to JIS K6870, and if the MFI was less than 5, the resulting composition would have a high melt viscosity and poor extrusion processability.

EVAIOO重量部、ポリスチレン20〜70重量部と
する理由は、ポリスチレンの配合量が20重量部未満の
組成物ではペレット加工性が不十分35であり、また7
0重量部より多くなるとその組成物では、絶縁層上に実
用上十分な接着強度をもつ半導電層が得られず、かつ組
成物の溶融粘度が著ハ【−しく高く押出加工が困難とな
るからである。
The reason why parts by weight of EVAIOO and polystyrene are 20 to 70 parts by weight is that pellet processability is insufficient in a composition containing less than 20 parts by weight of polystyrene;
If the amount exceeds 0 parts by weight, the composition will not be able to form a semiconducting layer with practically sufficient adhesive strength on the insulating layer, and the melt viscosity of the composition will be extremely high, making extrusion processing difficult. It is from.

結局本発明に供される樹脂素材としては、上記特定のE
VAとポリスチレンとが前記の限定配合範囲内において
調整された場合においてのみ、ペレツト加工性、押出加
工性に優れかつ絶縁層に対して優れた密着性、易剥離性
の外部半導電層を形成し得る組成物が得られるのである
。この様な樹脂素材に半導電層として必要な導電性を与
えるための導電性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
EClなど周知の導電性カーボンブラツクが電力ケーブ
ル用半導電性組成物として要求される導電性を付与する
に必要な量で用いられる。
In the end, the resin material used in the present invention is the above-mentioned specific E
Only when VA and polystyrene are adjusted within the above-mentioned limited blending range, an external semiconductive layer with excellent pellet processability and extrusion processability, excellent adhesion to the insulating layer, and easy peelability can be formed. The resulting composition is obtained. As conductive carbon blacks for imparting conductivity necessary for a semiconductive layer to such resin materials, well-known conductive carbon blacks such as furnace black, acetylene black, and ketten black ECl are used as semiconducting materials for power cables. It is used in an amount necessary to impart the electrical conductivity required for the composition.

たとえば、フアーネスブラツク、チヤンネルブラツク、
アセチレンブラツク等の低乃至中表面積の導電性カーボ
ンブラツクの場合、樹脂素材(即ちEVAとポリスチレ
ン)合計量100重量部あたり40〜70重量部程度で
あり、一方、ケツチエンブラツク(アクゾ一社製)等の
高表面積を有する導電性カーボンブラツクの場合では樹
脂累材の合計量100重量部あたり10〜30重量部程
度である。
For example, Furness Black, Channel Black,
In the case of conductive carbon black with a low to medium surface area such as acetylene black, the amount is about 40 to 70 parts by weight per 100 parts by weight of the total amount of resin material (that is, EVA and polystyrene), while Kettien Black (manufactured by Akzo Corporation) In the case of conductive carbon black having a high surface area, the amount is about 10 to 30 parts by weight per 100 parts by weight of the total amount of resin composite.

本発明組成物には必要に応じて老化防止剤、安定剤等を
加えることができる。
Anti-aging agents, stabilizers, etc. can be added to the composition of the present invention, if necessary.

また、本発明組成物で用いる架橋剤(加硫剤)としては
、たとえば、ジクミルバーオキサイド、1,3−ビス(
t−ブチルパーオキシイソプロピル)ベンゼン、2,5
−ジメチル−2,5−ジ(t−ブチルバーオキシ)ヘキ
シン一3等の有機過酸化物架橋剤が好適に用いられる。
第1表及び第2表に本発明組成物の実施例の組成(重量
部)及び各種特性を比較例のそれとともに示す。
Further, examples of the crosslinking agent (vulcanizing agent) used in the composition of the present invention include dicumyl peroxide, 1,3-bis(
t-butylperoxyisopropyl)benzene, 2,5
An organic peroxide crosslinking agent such as -dimethyl-2,5-di(t-butylbaroxy)hexyne-3 is preferably used.
Tables 1 and 2 show the compositions (parts by weight) and various properties of Examples of the compositions of the present invention, as well as those of Comparative Examples.

各特性はそれぞれ次に示す方法で評価した。Each characteristic was evaluated by the method shown below.

剥離性,各半導電組成物をオープンロールにて混合調整
し、架橋剤の分解温度以下で1mm厚にプレス成形する
Peelability: Each semiconducting composition is mixed and adjusted using an open roll, and press-molded to a thickness of 1 mm at a temperature below the decomposition temperature of the crosslinking agent.

一方、ポリエチレン(Ml;1)100重量部、ジクミ
ルバーオキサイド2,0重量部及び4,45−チオビス
−(6−t−ブチル−3−メチルフエノール)0.3重
量部とからなる組成物を上記同様の方法で混合調整し、
架橋剤の分解温度以下で1mr厚にプレス成形する。こ
の両シートを重ねて180℃、30分間、50k9/礪
2の条件でプレス加硫して架橋した貼合せ試料(大きさ
約10?角)シートを作成する。次いで半導電組成物層
にのみ匙インチの巾でポリエチレン層にまで達するきり
こみを行い、この?インチ巾のきりこまれた部分をAE
IC規格に準じてポリエチレン層に対して垂直に剥離し
、その剥離に要する力(Kg)の平均値を求める。ペレ
ツト加工性; 1m71L厚の未架橋シート2枚を重ね、上下両側から
ガラス板で挟んだ状態で40℃、3時間加熱したあと、
2枚のシート間の粘着の有無を調べ、全く粘着しなかつ
たもの◎、粘着したものを×、多少粘着したが粘着の程
度が極く軽度のものを01比較的よく粘着したものを△
で示した。
On the other hand, a composition comprising 100 parts by weight of polyethylene (Ml; 1), 2.0 parts by weight of dicumyl peroxide, and 0.3 parts by weight of 4,45-thiobis-(6-t-butyl-3-methylphenol). Mix and adjust in the same manner as above,
Press molding to a thickness of 1 ml at a temperature below the decomposition temperature of the crosslinking agent. These two sheets were stacked and press vulcanized at 180° C. for 30 minutes at a pressure of 50 k9/cm2 to create a crosslinked bonded sample sheet (about 10 square meters in size). Next, an inch-wide cut is made only in the semiconductive composition layer, reaching all the way to the polyethylene layer. AE the inch-wide cut-out part
The polyethylene layer is peeled off perpendicularly to the polyethylene layer in accordance with the IC standard, and the average value of the force (Kg) required for the peeling is determined. Pellet processability: Two uncrosslinked sheets of 1m71L thickness were stacked and sandwiched between glass plates from both the top and bottom sides and heated at 40°C for 3 hours.
The presence or absence of adhesion between the two sheets was examined, and those with no adhesion at all were ◎, those with adhesion were rated as ×, those with some adhesion but the degree of adhesion were extremely light were 01, and those with relatively good adhesion were △.
It was shown in

シート間の粘着性が少い程、ペレツトとした場合、ペレ
ツト同志の粘着がなく、而して押出機のホツパ一に供給
したときホツバ一内でペレツト同志のブ油ツキングが生
じ難く、また、ペレツト状態での保管、輸送等が容易で
ある〇耐スコーチリ ブラベンダプラスチケータを用いチヤンバ一温度110
℃、25RPMの条件下でのトルク上昇開始時間を測定
した。
The lower the adhesiveness between the sheets, the less the pellets will stick to each other when made into pellets, and when fed to the hopper of an extruder, the pellets will be less likely to stick together in the hopper. Easy to store, transport, etc. in pellet form 〇Using scorch-resistant rubber bender plasticator, the chamber temperature is 110℃.
The torque increase start time was measured under the conditions of ℃ and 25 RPM.

Claims (1)

【特許請求の範囲】 1 酢酸ビニル含有量25重量%以上のエチレン−酢酸
ビニル共重合体100重量部と、メルトフローインデッ
クスが5以上のポリスチレン20〜70重量部と導電性
カーボンブラック及び有機過酸化物からなる半導電性組
成物。 2 エチレン−酢酸ビニル共重合体の酢酸ビニル含有量
が35重量%以上である特許請求の範囲第1の半導電性
組成物。 3 ポリスチレンのメルトフローインデックスが10以
上である特許請求の範囲第1項又は第2項の半導電性組
成物。
[Claims] 1. 100 parts by weight of an ethylene-vinyl acetate copolymer having a vinyl acetate content of 25% by weight or more, 20 to 70 parts by weight of polystyrene having a melt flow index of 5 or more, conductive carbon black, and organic peroxide. A semiconducting composition consisting of 2. The first semiconductive composition of claim 1, wherein the vinyl acetate content of the ethylene-vinyl acetate copolymer is 35% by weight or more. 3. The semiconductive composition according to claim 1 or 2, wherein the polystyrene has a melt flow index of 10 or more.
JP13837579A 1979-10-25 1979-10-25 semiconductive composition Expired JPS5917135B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13837579A JPS5917135B2 (en) 1979-10-25 1979-10-25 semiconductive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13837579A JPS5917135B2 (en) 1979-10-25 1979-10-25 semiconductive composition

Publications (2)

Publication Number Publication Date
JPS5661440A JPS5661440A (en) 1981-05-26
JPS5917135B2 true JPS5917135B2 (en) 1984-04-19

Family

ID=15220457

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13837579A Expired JPS5917135B2 (en) 1979-10-25 1979-10-25 semiconductive composition

Country Status (1)

Country Link
JP (1) JPS5917135B2 (en)

Also Published As

Publication number Publication date
JPS5661440A (en) 1981-05-26

Similar Documents

Publication Publication Date Title
US4169816A (en) Electrically conductive polyolefin compositions
TW402623B (en) Carbon black treated with polyethylene glycol, a process for preparing the same and a polymeric composition comprising the treated carbon black
JPS62501201A (en) Insulated cable and its manufacturing method
FR2528616A1 (en) HOT DEFORMATION RESISTANT THERMOPLASTIC SEMICONDUCTOR COMPOSITION, AND ISOLATED ELECTRICAL CONDUCTOR COMPRISING THE SAME
EP1342247B1 (en) Power cable
US4400580A (en) Process for producing crosslinked polyethylene insulated cable
JPS6164739A (en) Semiconductive resin composition having both bondability and strippability
JPS5917135B2 (en) semiconductive composition
JPS6215962B2 (en)
JP2001115791A (en) Waterproof sheet for tunnel
JPS5810801B2 (en) Semiconductive resin composition with improved peelability
TW416060B (en) Cable semiconductor shield compositions
EP0210425A2 (en) Compositions based on mixtures of ethylene-ethyl, acrylate copolymers and ethylene-vinyl acetate-vinyl chloride terpolymers
JPS5929921B2 (en) Hands-on-the-scenes construction
JPS5846517A (en) Crosslinked polyolefin insulated power cable
JPS6215963B2 (en)
JPS5835220B2 (en) How to use the handshake method
JPS59176341A (en) Thermally conductive material
JPS6259723B2 (en)
JPH031144B2 (en)
JPS5962656A (en) Semiconducting composition
JPH04363808A (en) Semiconductive composition material and power cable
JPS627938B2 (en)
CN115181372A (en) Preparation method of insulated cable material with high volume resistivity
JPS5840707A (en) Crosslinked polyethylene insulated power cable