JPH0332843B2 - - Google Patents
Info
- Publication number
- JPH0332843B2 JPH0332843B2 JP58071172A JP7117283A JPH0332843B2 JP H0332843 B2 JPH0332843 B2 JP H0332843B2 JP 58071172 A JP58071172 A JP 58071172A JP 7117283 A JP7117283 A JP 7117283A JP H0332843 B2 JPH0332843 B2 JP H0332843B2
- Authority
- JP
- Japan
- Prior art keywords
- peroxide
- copper
- oxide film
- wire
- stranded wire
- 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
Links
- 150000002978 peroxides Chemical class 0.000 claims description 20
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 16
- 229910052802 copper Inorganic materials 0.000 claims description 13
- 239000010949 copper Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 10
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 9
- 239000005751 Copper oxide Substances 0.000 claims description 9
- 229910000431 copper oxide Inorganic materials 0.000 claims description 9
- 239000004020 conductor Substances 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 2
- 238000009751 slip forming Methods 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical class O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- -1 dicumyl peroxide Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、酸化銅皮膜の素線絶縁体を施したケ
ーブル導体の製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method of manufacturing a cable conductor provided with a copper oxide film strand insulator.
[従来の技術]
銅素線を撚り合わせた導体を加湿雰囲気中
(150〜200℃、空気中または微量のイオウあるい
はイオウ化合物を加えた雰囲気中)に、保持し
て、酸化皮膜を形成する。[Prior Art] A conductor made of twisted copper wires is held in a humidified atmosphere (150 to 200°C, in air or in an atmosphere containing a trace amount of sulfur or a sulfur compound) to form an oxide film.
[発明が解決しようとする課題]
この方法では、実用化に必要な皮膜厚として、
0.5μm以上望ましくは1.0〜1.5μmの皮膜厚を形成
するのに、48〜100h/mの時間が必要であつた。[Problem to be solved by the invention] In this method, the film thickness required for practical use is as follows:
A time of 48 to 100 h/m was required to form a film thickness of 0.5 μm or more, preferably 1.0 to 1.5 μm.
また、最大厚/最小厚は2(μm)/0.5(μm)
で、皮膜厚の均一性が良くなかつた。 Also, maximum thickness / minimum thickness is 2 (μm) / 0.5 (μm)
However, the uniformity of the film thickness was not good.
[課題を解決するための手段]
(1) 走行する銅撚り線を液状過酸化物に浸した
後、
(2) 前記過酸化物のガス雰囲気中で、前記過酸化
物が熱分解を起こす温度以上に加熱する、
という方法をとる。[Means for solving the problem] (1) After immersing a running copper stranded wire in liquid peroxide, (2) In a gas atmosphere of the peroxide, the temperature at which the peroxide thermally decomposes is determined. The method is to heat it to a higher temperature.
なお、過酸化物としては、主に有機のものを用
いる。その中でも沸点が低くてガス化し易いもの
が良い。そのような有機の過酸化物の中には、過
酸化ジクミルなどのようにCVケーブルの架橋剤
に使われるものもあるが、そのようなものが特に
適している。 Note that as the peroxide, mainly organic ones are used. Among these, those that have a low boiling point and are easily gasified are preferred. Some such organic peroxides, such as dicumyl peroxide, which are used as crosslinking agents in CV cables, are particularly suitable.
[作用]
上記の液状過酸化物は加熱すると容易にガス化
して、酸素が遊離し、周囲雰囲気の酸素濃度が上
昇する。[Function] When the above liquid peroxide is heated, it easily gasifies, liberates oxygen, and increases the oxygen concentration in the surrounding atmosphere.
また加熱により酸素分子が活性化し、導線の表
面に容易に酸化銅皮膜が生成する。 In addition, oxygen molecules are activated by heating, and a copper oxide film is easily formed on the surface of the conductive wire.
さらに、撚り線の内部に侵入していた液状過酸
化物も、その場所(撚り線内部)で加熱によりガ
ス化するので、撚り線内外における酸素濃度が余
り違わなくなり、酸化銅皮膜の生成も撚り線内外
で大差が無くなる。すなわち、酸化銅皮膜生成の
均一性が良くなる。 Furthermore, the liquid peroxide that has entered the inside of the stranded wire is gasified by heating at that location (inside the stranded wire), so the oxygen concentration inside and outside the stranded wire is no longer much different, and the formation of a copper oxide film is also reduced. There will be no big difference between inside and outside the line. That is, the uniformity of copper oxide film formation is improved.
[実施例]
第1図において、10は銅撚り線である。これ
はチヤンバ12内において、液状過酸化物14
(たとえば過酸化ジクミル)内に浸され、それか
ら酸化チヤンバ16内にはいる。[Example] In FIG. 1, 10 is a copper stranded wire. This is carried out in the chamber 12 by liquid peroxide 14.
(e.g. dicumyl peroxide) and then enters the oxidation chamber 16.
酸化チヤンバ16内には高温(150℃程度)の
ガス状過酸化物18(たとえば過酸化ジクミルガ
ス)が入つていて、そのような雰囲気の中で銅撚
り線10は高周波誘導コイル20によつて150℃
程度(液状過酸化物が熱分解を起こす温度以上)
に加熱される。 The oxidation chamber 16 contains a gaseous peroxide 18 (for example, dicumyl peroxide gas) at a high temperature (approximately 150°C), and the stranded copper wire 10 is heated by the high-frequency induction coil 20 in this atmosphere. 150℃
Degree (above the temperature at which liquid peroxide thermally decomposes)
heated to.
すると、銅撚り線10に付着していた液状過酸
化物が分解して、銅撚り線10の周囲だけでなく
内部にも、活性化した酸素ガスが、高濃度で、か
つほぼ均一に存在するようになる。 Then, the liquid peroxide adhering to the copper strands 10 is decomposed, and activated oxygen gas is present not only around the copper strands 10 but also inside the copper strands 10 at a high concentration and almost uniformly. It becomes like this.
そのため、銅撚り線10の各素線の表面に酸化
銅皮膜が、早くかつほぼ均一に生成する。 Therefore, a copper oxide film is quickly and almost uniformly formed on the surface of each strand of the copper stranded wire 10.
なお、実用化に必要な皮膜厚として0.5μm以上
望ましくは1.0〜1.5μmの皮膜厚を形成するのに、
12〜30h/mの時間で済み(従来は48〜100h/
m)、また、生成された酸化銅皮膜の最大厚/最
小厚は1.2(μm)/0.5(μm)であつた(従来は
2(μm)/0.5(μm))。 In addition, to form a film thickness of 0.5 μm or more, preferably 1.0 to 1.5 μm, which is necessary for practical use,
It only takes 12-30h/m (previously it took 48-100h/m)
m), and the maximum/minimum thickness of the produced copper oxide film was 1.2 (μm)/0.5 (μm) (conventionally 2 (μm)/0.5 (μm)).
過酸化物に架橋剤を使用するときは、以上のよ
うにして素線絶縁した銅撚り線10をそのまま押
出し機22のところに導いてゴムまたはプラスチ
ツク絶縁体を被覆し、かつ架橋筒24内において
架橋を行うことができる。 When a crosslinking agent is used in the peroxide, the stranded copper wire 10 insulated as described above is directly guided to the extruder 22, coated with a rubber or plastic insulator, and placed in the crosslinking tube 24. Crosslinking can be carried out.
その訳は、銅撚り線10内にガス状過酸化物が
残つていても、それはもともと架橋剤として使わ
れるものであるから絶縁体に悪い影響を与えない
ためである。 The reason for this is that even if gaseous peroxide remains in the copper strands 10, it will not have a negative effect on the insulator since it is originally used as a crosslinking agent.
[発明の効果]
走行する銅撚り線を液状過酸化物に浸した後、
加熱するので、銅撚り線に付着していた液状過酸
化物が分解して、銅撚り線の外側だけでなく内側
においても、素線の周りに活性化したガス状の酸
素が、連続的に、高濃度で、かつほぼ均一に存在
するようになる。[Effect of the invention] After soaking the running copper stranded wire in liquid peroxide,
As it is heated, the liquid peroxide adhering to the copper strands decomposes, and activated gaseous oxygen is continuously generated around the strands, not only on the outside of the copper strands but also on the inside. , will be present at high concentration and almost uniformly.
そのため、酸化銅皮膜の生成が、撚り線の外側
の素線においても内側の素線においても、ほぼ同
様に早く行われ、かつ生成する酸化銅皮膜の厚さ
もほぼ同程度になり、均一性が良くなる。 Therefore, the copper oxide film is formed almost equally quickly on both the outer and inner strands of the stranded wire, and the thickness of the copper oxide film that is formed is also approximately the same, resulting in improved uniformity. Get better.
第1図は本発明の説明図。
10:銅撚り線、14:液状過酸化物、16:
酸化チヤンバ、18:ガス状過酸化物、20:高
周波誘導加熱コイル、22:押出し機、24:架
橋筒。
FIG. 1 is an explanatory diagram of the present invention. 10: Copper stranded wire, 14: Liquid peroxide, 16:
Oxidation chamber, 18: gaseous peroxide, 20: high frequency induction heating coil, 22: extruder, 24: crosslinking tube.
Claims (1)
後、前記過酸化物のガス雰囲気中で、前記過酸化
物が熱分解を起こす温度以上に加熱することによ
り、前記銅線の表面に連続して酸化銅皮膜を生成
するようにしたことを特徴とする、素線絶縁ケー
ブル導体の製造方法。 2 過酸化物がゴム・プラスチツク電力ケーブル
用の架橋剤であることを特徴とする、特許請求の
範囲第1項に記載の素線絶縁ケーブル導体の製造
方法。[Scope of Claims] 1. The running copper stranded wire is immersed in liquid peroxide, and then heated in a peroxide gas atmosphere to a temperature higher than the temperature at which the peroxide thermally decomposes. A method for manufacturing a bare wire insulated cable conductor, characterized in that a copper oxide film is continuously formed on the surface of a copper wire. 2. The method for manufacturing a bare wire insulated cable conductor according to claim 1, characterized in that the peroxide is a crosslinking agent for rubber-plastic power cables.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7117283A JPS59196513A (en) | 1983-04-22 | 1983-04-22 | Method of producing strand insulated cable conductor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7117283A JPS59196513A (en) | 1983-04-22 | 1983-04-22 | Method of producing strand insulated cable conductor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59196513A JPS59196513A (en) | 1984-11-07 |
JPH0332843B2 true JPH0332843B2 (en) | 1991-05-15 |
Family
ID=13452969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7117283A Granted JPS59196513A (en) | 1983-04-22 | 1983-04-22 | Method of producing strand insulated cable conductor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59196513A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55117817A (en) * | 1979-03-01 | 1980-09-10 | Fujikura Ltd | Method of forming strand insulating film |
JPS566324A (en) * | 1979-06-26 | 1981-01-22 | Fujikura Ltd | Method of forming insulating film on copper wire |
-
1983
- 1983-04-22 JP JP7117283A patent/JPS59196513A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55117817A (en) * | 1979-03-01 | 1980-09-10 | Fujikura Ltd | Method of forming strand insulating film |
JPS566324A (en) * | 1979-06-26 | 1981-01-22 | Fujikura Ltd | Method of forming insulating film on copper wire |
Also Published As
Publication number | Publication date |
---|---|
JPS59196513A (en) | 1984-11-07 |
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