JPS60112204A - Conductive composition for power cable - Google Patents
Conductive composition for power cableInfo
- Publication number
- JPS60112204A JPS60112204A JP21990983A JP21990983A JPS60112204A JP S60112204 A JPS60112204 A JP S60112204A JP 21990983 A JP21990983 A JP 21990983A JP 21990983 A JP21990983 A JP 21990983A JP S60112204 A JPS60112204 A JP S60112204A
- Authority
- JP
- Japan
- Prior art keywords
- conductive composition
- weight
- ethylene
- power cable
- parts
- 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.)
- Pending
Links
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- Conductive Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[発明の背景と目的]
本発明は、電カケーブルの内部導電層や外部導電層の形
成に用いられる導電性組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Background and Objects of the Invention] The present invention relates to a conductive composition used for forming an inner conductive layer or an outer conductive layer of an electric power cable.
従来、電カケーブルの内部導電層や外部導電層の形成に
用いられている導電性組成物は、一般にエチレン酢酸ビ
ニルコポリマ等のエチレン系ポリマに導電性付与剤とし
てアセチレンブラックを混合したものが多く使用されて
きている。Conventionally, conductive compositions used to form the internal conductive layer and external conductive layer of power cables are generally made by mixing ethylene-based polymers such as ethylene vinyl acetate copolymer with acetylene black as a conductivity imparting agent. It has been used.
しかしながら、十分な導電性を得ようとする場合、導電
性付与剤を多量に混和する必要があるため、組成物の粘
度が高くなり、例えば高速で押出するなどの厳しい加工
条件下では押出加工が難かしくなる。However, in order to obtain sufficient conductivity, it is necessary to mix a large amount of conductivity imparting agent, which increases the viscosity of the composition and makes extrusion difficult under severe processing conditions, such as extrusion at high speed. It becomes difficult.
この問題に対し、HAF、FEF、SRF等のファーネ
スブラックを用いることにより組成物の粘度を下げるこ
とができるが、反面、分散が十分てなく、導電層表面に
粗粒が発生して電気特性を大幅に低下させるという問題
がある。To solve this problem, the viscosity of the composition can be lowered by using a furnace black such as HAF, FEF, or SRF, but on the other hand, the dispersion is not sufficient and coarse particles are generated on the surface of the conductive layer, which deteriorates the electrical properties. The problem is that it significantly reduces the amount.
本発明は上記の状況に鑑みなされたもので、押出加工性
にすぐれると共に粗粒の発生が少なく、かつ十分な導電
性を付与できる導電性組成物の1に供を目的とするもの
である。The present invention was made in view of the above-mentioned circumstances, and an object of the present invention is to provide a conductive composition that has excellent extrusion processability, reduces generation of coarse particles, and can provide sufficient conductivity. .
[発明の概要]
本発明の導電性組成物は、エチレン系ポリマ100重量
部に対し、算術平均粒子径25〜40 mμ、よう素吸
着量40〜60mg/g、DBP吸油量(JISA法)
120〜150m1/100gのファーネスカーボンブ
ラックが単独あるいはアセチレンブラックとの併用で4
0重量部以上含有されていることを特徴とするものであ
る。[Summary of the invention] The conductive composition of the present invention has an arithmetic mean particle diameter of 25 to 40 mμ, an iodine adsorption amount of 40 to 60 mg/g, and a DBP oil absorption amount (JISA method) based on 100 parts by weight of the ethylene polymer.
120-150m1/100g of furnace carbon black alone or in combination with acetylene black
It is characterized by containing 0 parts by weight or more.
本発明において、エチレン系ポリマとは分子鎖中にエチ
レンを含むポリマ全体を指し、例えば、ポリエチレン、
エチレン酢酸ビニルコボマ、エチレンエチルアクリレー
トコポリマ、エチレンメチルアクリレートコポリマ、エ
チレンプロピレンコポリマ、エチレンブテンコポリマ、
エチレンペンテンコポリマ等である。更に、これらにス
チレンやアクリレート、アクリロニトリル等をグラフト
したものも含まれる。これらは単独あるいは2種以上併
用して使用可能である。In the present invention, the ethylene polymer refers to the entire polymer containing ethylene in the molecular chain, such as polyethylene,
Ethylene vinyl acetate copolymer, ethylene ethyl acrylate copolymer, ethylene methyl acrylate copolymer, ethylene propylene copolymer, ethylene butene copolymer,
Such as ethylene pentene copolymer. Furthermore, it also includes those grafted with styrene, acrylate, acrylonitrile, etc. These can be used alone or in combination of two or more.
本発明において使用される導電性付与剤は、算術平均粒
子径、よう素吸着量、DBP吸油量が特定の範囲にある
ファーネスカーボンブラックであり、これは単独である
いはアセチレンブラックとの併用で使用される。The conductivity imparting agent used in the present invention is furnace carbon black whose arithmetic mean particle diameter, iodine adsorption amount, and DBP oil absorption amount are within a specific range, and this can be used alone or in combination with acetylene black. Ru.
算術平均粒子径は、25〜40mμの範囲にある必要が
あり、25mμ以下ではポリマと混練した時の粘度が大
きくなって加工性が悪くなり、40mμを越えると十分
な導電性を付与できない。また、篩にかけ149mμ以
上のものを除いた方がより効果的である。The arithmetic mean particle diameter must be in the range of 25 to 40 mμ; if it is less than 25 mμ, the viscosity will increase when kneaded with a polymer, resulting in poor processability; if it exceeds 40 mμ, sufficient conductivity cannot be imparted. Moreover, it is more effective to sieve to remove those of 149 mμ or more.
よう素吸着量は、40〜60mg/gの範囲にある必要
があり、4.0 m g / g以下では十分な導電性
を付与できなく、60mg/gを越えると粘度が大きく
なり加工性が悪化する。The amount of iodine adsorbed must be in the range of 40 to 60 mg/g; if it is less than 4.0 mg/g, sufficient conductivity cannot be imparted, and if it exceeds 60 mg/g, the viscosity will increase and processability will be impaired. Getting worse.
DBP吸油量(JISA法)は、120〜160m l
/ 100 gの範囲にある必要があり、120m1
/100g以下では十分な導電性を付与できず、150
m1/100gを越えるとポリマへの分散が悪化し、粗
粒が生じやすくなる。DBP oil absorption (JISA method) is 120-160ml
/ 100 g, 120 m1
/100g or less, sufficient conductivity cannot be imparted, and 150g
When m1/100g is exceeded, dispersion in the polymer deteriorates and coarse particles are likely to be formed.
かかる特定範囲のファーネスカーボンブラックを使用す
ることにより、ポリマへの分散が良好で加工性にすぐれ
、しかも十分な導電性を有する導電層の形成が可能とな
る。By using furnace carbon black in such a specific range, it is possible to form a conductive layer that has good dispersion in the polymer, excellent processability, and sufficient conductivity.
ファーネスカーボンブラックのエチレン系ポリマへの混
合量は、エチレン系ポリマ100重量部に対して40重
量部以上とする必要があり、これ以下では十分な導電性
を付与できない。その上限は目的とする導電性およびポ
リマの種類によフて異なるので特に限定しないが、加工
性を考慮すると120重量部である。The amount of furnace carbon black mixed into the ethylene polymer must be 40 parts by weight or more per 100 parts by weight of the ethylene polymer, and if it is less than this, sufficient conductivity cannot be imparted. The upper limit is not particularly limited since it varies depending on the desired conductivity and the type of polymer, but it is 120 parts by weight considering processability.
なお、アセチレンブラックとの併用の場合は、双方の合
計量が40重量部以上であればよいが、アセチレンブラ
ックの量はファーネスブラックと同量またはそれ以下と
するのが好ましい。When used in combination with acetylene black, the total amount of both may be 40 parts by weight or more, but it is preferable that the amount of acetylene black is the same as that of furnace black or less.
本発明の導電性組成物は、架橋性であっても非架橋性で
あってもよい。架橋性とする場合には、有機過酸化物と
して、ジクミルパーオキサイド、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・パーオキシ)ヘキ
シン−3に代表されるジアルキルパーオキサイド混合す
るのが適切である。The conductive composition of the present invention may be crosslinkable or non-crosslinkable. In the case of crosslinking, dicumyl peroxide, 1,3-bis(t-butyl peroxy isopropyl)benzene, 2,5-
It is appropriate to mix a dialkyl peroxide represented by dimethyl-2,5-di(t-butyl peroxy)hexyne-3.
本発明においては、上記成分以外に滑剤、酸化防止剤等
を従来組成物と同様に混合してもよい。In the present invention, in addition to the above-mentioned components, lubricants, antioxidants, etc. may be mixed in the same manner as in conventional compositions.
滑剤としては、ステアリン酸や金属酸及びエステル、ス
テアリン酸やオレイン酸とエチレンジアミンからなる脂
肪酸アミド、分子量1万以下の飽和炭化水素オリゴマの
1種または2種以上を併用して使用するのが好ましい。As the lubricant, it is preferable to use one or more of stearic acid, metal acids and esters, fatty acid amides made of stearic acid, oleic acid, and ethylenediamine, and saturated hydrocarbon oligomers with a molecular weight of 10,000 or less.
酸化防止剤としては、へ、4′−チオビス(3−メチル
−6−t−ブチルフェノール) 、N、N’−ジフェニ
ル−pフェニレンジアミン等ゴム用あるいはポリオレフ
ィン用として使用されているものを1種あるいは2種以
上併用して使用できる。As the antioxidant, one type or one of those used for rubber or polyolefins such as 4'-thiobis(3-methyl-6-t-butylphenol) and N,N'-diphenyl-p-phenylenediamine may be used. Two or more types can be used in combination.
[発明の実施例コ 第1表に示すような各種カーボンブラックを準備した。[Embodiments of the invention] Various carbon blacks as shown in Table 1 were prepared.
次いで、第2表に示す配命割合でもって各種成分をパン
バリ混練機でもって混合した。この混合物を65mm押
出機に投入し、断面積150mv/の銅導体周上に架橋
ポリエチレン絶縁体が厚さ6mmに被覆されているコア
外周に厚さ1mmでもって押出被覆した。押出機の温度
設定は供給部から計量化部に向かい、バレル帯域C1=
100℃、C2=110℃、C3=115℃、ダイス=
120℃であ)た。またスクリュウは、L/D=22、
回転数=2Orpmのものを用いた。Next, various ingredients were mixed using a panburi kneader at the proportions shown in Table 2. This mixture was put into a 65 mm extruder and extruded to a thickness of 1 mm to cover the outer periphery of a core coated with a cross-linked polyethylene insulator to a thickness of 6 mm on the circumference of a copper conductor having a cross-sectional area of 150 mv/. The temperature setting of the extruder goes from the feed section to the metering section, and the barrel zone C1=
100℃, C2=110℃, C3=115℃, Dice=
The temperature was 120°C. Also, the screw is L/D=22,
One with a rotation speed of 2 Orpm was used.
押出被覆後、250℃の窒素ガス雰囲気中で加熱架橋し
た。After extrusion coating, crosslinking was carried out by heating in a nitrogen gas atmosphere at 250°C.
導電性組成物および得られた電カケーブルについての評
価結果を第2表の下欄に示す。The evaluation results for the conductive composition and the obtained power cable are shown in the lower column of Table 2.
第 1 表
なお、第2表の評価において、ムーニー粘度は未架橋混
合物について測定し、1分子熱後の4分値が50ポイン
ト以下のものをO5これ以上のものをXとした。Table 1 In the evaluation shown in Table 2, the Mooney viscosity was measured for the uncrosslinked mixture, and those with a 4-minute value of 50 points or less after heating one molecule were designated as O5, and those with a higher value of 50 points or less were designated as X.
粗粒は押出表面で100μm以上の粗粒を目視により計
数し、10個/ 100 c rf以下のものを○、こ
れ以上のものを×とした。Coarse particles with a diameter of 100 μm or more were visually counted on the extrusion surface, and those with 10 pieces/100 crf or less were rated ○, and those with more than 10 pieces/100 crf were rated ×.
体積抵抗率は、90℃の恒温槽中て測定し、5゜0×1
0 Ω・Cm以下のものを○、これ以上のものを×とし
た。Volume resistivity was measured in a constant temperature bath at 90°C, and was measured at 5°0 x 1
Those below 0 Ω·Cm were marked ○, and those above this were marked ×.
本発明の範囲にある実施例1〜8ではいずれの特性の良
好である。しかしながら、ファーネスカーボン含有量が
規定値以下の比較例1ては満足する導電性が得られず、
アセチレンブラック単独使用の比較例2はムーニー粘度
が大きく押出加工性が悪い。また、比較例3〜8では粗
粒による外観と体積抵抗重大による導電性の双方または
一方の特性が不十分である。Examples 1 to 8, which fall within the scope of the present invention, were good in all properties. However, in Comparative Example 1 where the furnace carbon content was below the specified value, satisfactory conductivity could not be obtained.
Comparative Example 2 in which acetylene black was used alone had a large Mooney viscosity and poor extrusion processability. Further, in Comparative Examples 3 to 8, both or one of the characteristics of appearance due to coarse particles and conductivity due to significant volume resistance are insufficient.
[発明の効果]
以上説明してきた通り、本発明は特殊ファーネスブラッ
クを導電性付与剤とした導電性組成物を提供するもので
あり、押出加工性にすぐれ、粗粒による外観不良を防止
でき、しかもすぐれた導電性を有する導電層を形成する
ことが可能となる。[Effects of the Invention] As explained above, the present invention provides a conductive composition using special furnace black as a conductivity imparting agent, which has excellent extrusion processability, can prevent poor appearance due to coarse particles, Moreover, it becomes possible to form a conductive layer having excellent conductivity.
Claims (1)
粒子径25〜40mμ、よう素吸着量40〜60mg/
g、DBP吸油11(JISA法)120〜150m1
/100gのファーネスカーボンブラックが単独あるい
はアセチレンブラックとの併用で40重量部以上含有さ
れていることを特徴とする電カケーブル用導電性組成物
。(1) Arithmetic mean particle diameter 25-40 mμ, iodine adsorption amount 40-60 mg/100 parts by weight of ethylene polymer
g, DBP oil absorption 11 (JISA method) 120-150ml
1. An electrically conductive composition for power cables, comprising 40 parts by weight or more of /100 g of furnace carbon black alone or in combination with acetylene black.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21990983A JPS60112204A (en) | 1983-11-22 | 1983-11-22 | Conductive composition for power cable |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21990983A JPS60112204A (en) | 1983-11-22 | 1983-11-22 | Conductive composition for power cable |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60112204A true JPS60112204A (en) | 1985-06-18 |
Family
ID=16742921
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21990983A Pending JPS60112204A (en) | 1983-11-22 | 1983-11-22 | Conductive composition for power cable |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60112204A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61171003A (en) * | 1985-01-23 | 1986-08-01 | 住友電気工業株式会社 | Power cable |
JPS63168905A (en) * | 1986-12-30 | 1988-07-12 | 株式会社フジクラ | Power cable |
US6086792A (en) * | 1999-06-30 | 2000-07-11 | Union Carbide Chemicals & Plastics Technology Corporation | Cable semiconducting shields |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5782904A (en) * | 1980-11-11 | 1982-05-24 | Furukawa Electric Co Ltd | External semiconductive layer forming composition for power cable |
JPS5846517A (en) * | 1981-09-12 | 1983-03-18 | 日立電線株式会社 | Crosslinked polyolefin insulated power cable |
-
1983
- 1983-11-22 JP JP21990983A patent/JPS60112204A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5782904A (en) * | 1980-11-11 | 1982-05-24 | Furukawa Electric Co Ltd | External semiconductive layer forming composition for power cable |
JPS5846517A (en) * | 1981-09-12 | 1983-03-18 | 日立電線株式会社 | Crosslinked polyolefin insulated power cable |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61171003A (en) * | 1985-01-23 | 1986-08-01 | 住友電気工業株式会社 | Power cable |
JPH0426163B2 (en) * | 1985-01-23 | 1992-05-06 | Sumitomo Electric Industries | |
JPS63168905A (en) * | 1986-12-30 | 1988-07-12 | 株式会社フジクラ | Power cable |
US6086792A (en) * | 1999-06-30 | 2000-07-11 | Union Carbide Chemicals & Plastics Technology Corporation | Cable semiconducting shields |
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