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JPS5919612B2 - Method for manufacturing strand insulated cable conductor - Google Patents
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JPS5919612B2 - Method for manufacturing strand insulated cable conductor - Google Patents

Method for manufacturing strand insulated cable conductor

Info

Publication number
JPS5919612B2
JPS5919612B2 JP1269481A JP1269481A JPS5919612B2 JP S5919612 B2 JPS5919612 B2 JP S5919612B2 JP 1269481 A JP1269481 A JP 1269481A JP 1269481 A JP1269481 A JP 1269481A JP S5919612 B2 JPS5919612 B2 JP S5919612B2
Authority
JP
Japan
Prior art keywords
conductor
copper
insulated cable
wires
cable conductor
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
JP1269481A
Other languages
Japanese (ja)
Other versions
JPS57128410A (en
Inventor
章二 志賀
晃 松田
雅雄 星野
忠之 植松
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 JP1269481A priority Critical patent/JPS5919612B2/en
Publication of JPS57128410A publication Critical patent/JPS57128410A/en
Publication of JPS5919612B2 publication Critical patent/JPS5919612B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は電力ケーブル導体特に大容量送電に使用される
表皮効果を低減した素線絶縁ケーブル導体の製造方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a power cable conductor, particularly a bare wire insulated cable conductor with reduced skin effect used for large capacity power transmission.

電力ケーブル導体には直径2〜31の銅線を撚り合せた
撚線が使用される。
A stranded wire made by twisting copper wires with a diameter of 2 to 31 mm is used for the power cable conductor.

撚り合せ後ロール等で圧縮成形して各素線間の空隙をな
くしコンパクトにすることも広く行われている。さらに
、大容量導体では分割導体と称して素線を撚り合せた後
断面形状を扇形に圧縮成形したセグメントを所望数用い
て断面円形に組合せて使用されている。かかる分割導体
においては各セグメント間は紙やプラスチックテープを
巻いて絶縁されている場合が多い。例えば導体断面積2
00麗12の6分割導体では各セグメントは直径2.3
nの銅素線を88本撚り合せた後体積充填率85〜90
%に圧縮されかつ扇形に成形される。交流送電の大容量
化とともに導体サイズが巨大化されつつあるが導体サイ
ズが巨大化すると急に表皮効果及び近接効果に起因する
送電損失が顕著化している。
It is also widely practiced to compact the wires by compression-molding them using rolls or the like after twisting to eliminate gaps between the wires. Furthermore, in the case of large capacity conductors, a desired number of segments, called split conductors, which are obtained by compression molding the strands of strands into a fan-shaped cross section, are used in combination to form a circular cross section. In such divided conductors, each segment is often insulated by wrapping paper or plastic tape. For example, conductor cross-sectional area 2
In the 00 Rei 12 6-segment conductor, each segment has a diameter of 2.3
After twisting 88 copper wires of n, the volume filling rate is 85 to 90.
% and shaped into a fan shape. As the capacity of AC power transmission increases, the size of conductors is becoming larger, and as the size of conductors becomes larger, transmission losses due to skin effect and proximity effect suddenly become more noticeable.

特に表皮効果損は重大であり、導体を多分割化し各セグ
メント間を絶縁するとともに各素線をも絶縁して導体外
表面への電流集中を防止することが本質的な対策とされ
ている。従来素線を絶縁する方法としてエナメル被覆し
た銅素線を使用する例がある。
Skin effect loss is particularly important, and the essential countermeasure is to divide the conductor into multiple segments and insulate each segment, as well as insulate each strand to prevent current concentration on the outer surface of the conductor. Conventionally, there is an example of using an enamel-coated copper wire as a method of insulating wire.

素線の撚り合せと圧縮成形の加工工程に耐え得るには2
0〜30μ以上の膜厚のエナメル被覆を必要とし極めて
コスト高となつてしまう。このためより安価な絶縁物・
として酸化銅を表面に形成した銅線を利用する試みが
ある。酸化銅は銅線を大気中で高温(例えば300℃以
上)で酸化されることによつて容易にその表面に生成で
きるが脆弱で密着性に乏しく実用的でない。これに代つ
てアルカリ性の水溶液中で亜塩素酸などの酸化剤の助け
をかりて化学的に酸化処理する方法が採用される。この
ように湿式的に生成した酸化銅は微結晶体からなり、比
較的加工性及び密着性に富む特性を有する。撚り合せや
圧縮成形の加工に耐え得るには2〜3μ以上の膜厚が必
要であるが、湿式的にこのような厚膜を形成するには多
大の化学薬品と長時間を要するのでやはりコスト高とな
ることは不可避である。これを改善するために撚り合せ
や圧縮成形等の加工を行つた後に湿式的に酸化銅を形成
する試み、すなわち撚線又はセグメントを化成処理する
試みがある。しかしこの方法では撚線やセグメントの内
部の素線、特に撚り合せや圧縮成形による素線同志の線
接触部分を完全に絶縁するには、超音波の作用などによ
り線間への処理液の浸入を促進するなどの工夫をしても
1μ以上の平均膜厚を形成しなければならない欠点があ
つた。本発明はかかる実情に鑑みて鋭意研究した結果な
されたものであり、素線絶縁効果の大きい高性能のケー
ブル導体を経済的でかつ高生産性で製造する方法を提供
するものである。
To withstand the process of twisting strands and compression molding 2
This requires an enamel coating with a thickness of 0 to 30 μm or more, resulting in extremely high costs. For this reason, cheaper insulators and
There is an attempt to use copper wire with copper oxide formed on its surface. Copper oxide can be easily produced on the surface of a copper wire by oxidizing it in the atmosphere at high temperatures (eg, 300° C. or higher), but it is brittle and has poor adhesion, making it impractical. Instead, a method of chemical oxidation treatment using an oxidizing agent such as chlorous acid in an alkaline aqueous solution is adopted. Copper oxide wet-produced in this way is composed of microcrystals and has relatively good processability and adhesion. A film thickness of 2 to 3 μm or more is required to withstand the processing of twisting and compression molding, but forming such a thick film using a wet process requires a large amount of chemicals and a long time, which is costly. It is inevitable that the price will rise. In order to improve this problem, there has been an attempt to wet-form copper oxide after processing such as twisting or compression molding, that is, an attempt has been made to chemically treat the stranded wires or segments. However, with this method, in order to completely insulate the wires inside the twisted wires and segments, especially the contact parts of the wires that are formed by twisting or compression molding, it is difficult to completely insulate the wires inside the twisted wires or segments, especially when the treatment liquid enters between the wires due to the action of ultrasonic waves. Even if efforts were made to promote this, there was a drawback that an average film thickness of 1 μm or more had to be formed. The present invention was made as a result of intensive research in view of the above circumstances, and provides an economical and highly productive method for manufacturing a high-performance cable conductor with a large wire insulation effect.

すなわち、本発明は銅素線を撚り合せた導体を加湿雰囲
気中に保持して各銅線表面に平均0.1μ以上の腐食生
成物を形成することを特徴とする素線絶縁ケーブル導体
の製造方法である。
That is, the present invention relates to the production of a strand insulated cable conductor, which is characterized in that a conductor made of stranded copper strands is held in a humidified atmosphere to form corrosion products with an average size of 0.1μ or more on the surface of each copper wire. It's a method.

本発明は、軟質金属である銅線が撚り合せやさらに圧縮
成形加工で互に深く食込んだ素線相互の接触部の微細な
深い間隙にまで迅速に素線表面に腐食生成物の.′被膜
を形成する方法である。つまり本発明では、液体よりも
一段と拡散性のよい気体状態で水分を侵入させ、そこで
液体の水に変換することにより、酸素などによる銅の腐
食反応が急速に行なわれるものである。要するに撚線素
線の細部への腐食反5応物質の供給は拡散性のよい気体
状態で行い、そこでの反応は反応性が極度に高い液体状
態でなすようにしたものである。したがつて、本発明で
は銅素線を撚り合せた導体を加湿雰囲気中に保持するだ
けで、素線間細部4に空気中の酸素と水分が共に気体状
態で容易に侵入し、そこで水分は液体状態となり、酸素
は液体の水に溶解して溶存酸素となり銅と急速に反応し
て腐食生成物の被膜を形成する。
The present invention eliminates corrosion products on the surface of copper wires, which are soft metals, and can quickly be deposited on the surface of the wires even in the minute and deep gaps where the wires are in contact with each other, where the copper wires are twisted or compressed into each other. 'This is a method of forming a film. In other words, in the present invention, the corrosion reaction of copper by oxygen and the like occurs rapidly by allowing moisture to enter in a gaseous state, which has better diffusivity than liquid, and converting it to liquid water. In short, the corrosion reacting substance is supplied to the details of the stranded wire in a gaseous state with good diffusivity, and the reaction therein is carried out in a liquid state with extremely high reactivity. Therefore, in the present invention, by simply holding a conductor made of twisted copper wires in a humidified atmosphere, oxygen and moisture in the air can easily enter the inter-wire details 4 in a gaseous state. In the liquid state, the oxygen dissolves in the liquid water to form dissolved oxygen, which rapidly reacts with the copper to form a film of corrosion products.

かくして形成される被膜の厚さは平均0.1μ以上あれ
ば素線絶縁ケーブル導体としての機能を果すことができ
る。本発明において加湿雰囲気の湿度は相対湿度で約8
0%以上、好ましくは90%以上あればよい。このとき
の温度は室温でもよいが、加温した方がより急速に反応
が進むので約40℃以上が好ましい。反応に要する時間
は、湿度、温度、雰囲気などによつて著しく異なるが、
単に空気を加湿しただけの雰囲気では通常1〜7日間で
ある。
If the thickness of the coating thus formed is on average 0.1 .mu. or more, it can function as a stranded insulated cable conductor. In the present invention, the humidity of the humidified atmosphere is approximately 8 in terms of relative humidity.
It is sufficient if it is 0% or more, preferably 90% or more. The temperature at this time may be room temperature, but the reaction proceeds more rapidly when heated, so it is preferably about 40° C. or higher. The time required for the reaction varies significantly depending on humidity, temperature, atmosphere, etc.
In an atmosphere where the air is simply humidified, it usually takes 1 to 7 days.

処理方法としても特に限定されるものではなく、例えば
銅素線を撚り合せた導体をコイル状に巻いた状態で加湿
加温したチヤンバ一中に放置するだけでよく、これによ
り、酸化銅を主体とする黒色の被膜が素線表面に形成さ
れる。
The treatment method is not particularly limited; for example, a conductor made of twisted copper wires may be wound into a coil and left in a humidified and heated chamber. A black coating is formed on the surface of the wire.

なおチヤンバ一内の条件は一定に保持するよりは、湿度
又は温度を上下にサイクル的に変化させることにより反
応が一層促進され有益である。さらに、本発明では、加
湿雰囲気中にイオウ又はイオウ化合物を微量共存させる
ことにより、反応に要する時間を著しく短縮できる。
Note that, rather than keeping the conditions within the chamber constant, it is advantageous to cyclically change the humidity or temperature up and down to further promote the reaction. Furthermore, in the present invention, by allowing a trace amount of sulfur or a sulfur compound to coexist in the humidified atmosphere, the time required for the reaction can be significantly shortened.

これは、イオウ化合物やイオウが反応を触媒的に促進す
るためと考えられる。用いられるイオウ化合物又はイオ
ウとしては例えば硫化水素、亜硫酸ガス、三酸化イオウ
又はイオウ単体などがあり、中でも硫化水素の作用は最
も顕著である。硫化水素は加湿雰囲気中0.1〜1−の
極微量で約100倍以上、また亜硫酸ガスは50〜10
0卿の微量で約10倍の反応促進効果をそれぞれ発揮す
る。したがつて、本発明では、微量のイオウ化合物やイ
オウを加湿雰囲気中に共存させることにより、反応所要
時間を数時間から約1日位に短縮できる。
This is thought to be because sulfur compounds and sulfur catalytically promote the reaction. Examples of the sulfur compound or sulfur that can be used include hydrogen sulfide, sulfur dioxide gas, sulfur trioxide, and simple sulfur, among which hydrogen sulfide has the most remarkable effect. Hydrogen sulfide has a trace amount of 0.1 to 1-1 in a humidified atmosphere, about 100 times more, and sulfur dioxide gas has a 50 to 10
Even a small amount of 0% each exhibits about 10 times the reaction promotion effect. Therefore, in the present invention, by allowing a small amount of sulfur compound or sulfur to coexist in the humidified atmosphere, the time required for the reaction can be shortened from several hours to about one day.

イオウ又はイオウ化合物のかかる触媒的促進作用は加温
下において始めて起きる。かくして得られた腐食生成物
被膜中には硫化銅も極少量含まれるが問題はない。しか
し過剰のイオウ化合物を加湿雰囲気中に共存させた場合
には硫化銅を主体とした脆弱な被膜となるので多量のイ
オウ化合物の共存は避けなければならない。なお、加湿
雰囲気中に共存させたイオウ化合物は微量であるから処
理終了後のチヤンバ一内のガスを脱硫処理することによ
り容易に除毒できる。本発明において銅素線を撚り合せ
た導体とは所望本数の銅素線を単に撚り合せただけの導
体またはさらにこの導体に圧縮成形を施してなる導体な
どであり、その導体形状については何ら限定されない。
Such a catalytic promoting effect of sulfur or sulfur compounds only occurs under heating. The corrosion product film thus obtained also contains a very small amount of copper sulfide, but this is not a problem. However, if an excessive amount of sulfur compounds are allowed to coexist in a humidified atmosphere, a brittle coating consisting mainly of copper sulfide will result, so the coexistence of large amounts of sulfur compounds must be avoided. Note that since the amount of sulfur compounds coexisting in the humidified atmosphere is small, it can be easily detoxified by desulfurizing the gas in the chamber after the treatment is completed. In the present invention, a conductor made by twisting copper wires is a conductor made by simply twisting a desired number of copper wires together, or a conductor obtained by compression molding this conductor, and there are no restrictions on the shape of the conductor. Not done.

分割導体については各セグメントを本発明によつて処理
した後でセグメントを分割導体に成形するのが一般であ
るが、セグメントを腐食生成物形成処理せず分割導体に
成形した後で本発明による処理を行つてもよい。以上の
如く、本発明では、湿式腐食反応に必要な水分を先ず気
体状態で供給するので撚線導体の内部素線間の微小な間
隙にまで迅速かつ一様に水分が供給され、そこで凝縮し
て液体状の水となり、その結果内部の素線間にも撚線導
体表面の素線と大差なくほぼ等しい厚さの絶縁被膜が形
成されることになる。
For segmented conductors, it is common to treat each segment according to the present invention and then form the segments into segmented conductors. You may do so. As described above, in the present invention, since the moisture necessary for the wet corrosion reaction is first supplied in a gaseous state, the moisture is quickly and uniformly supplied to the minute gaps between the internal strands of the stranded conductor, where it condenses. As a result, an insulating coating is formed between the internal wires with a thickness that is almost the same as that of the wires on the surface of the stranded wire conductor.

したがつて、導体内外の素線に形成される絶縁被膜の厚
さに大差が見られた従来の湿式酸化処理法では、導体の
表面に位置する素線に形成される絶縁被膜が著しく厚く
なるまで処理しないと内部素線に電気絶縁に必要なだけ
の厚さの被膜が生成されないので全体として平均肉厚が
2〜3μと厚くなつていたのに対して、本発明では、上
記の如く内外素線ともほぼ等しい厚さの皮膜が均一に生
成されるので、平均肉厚が少なくとも0.1μでその電
気的機能を果すものである。
Therefore, in the conventional wet oxidation treatment method, where there was a large difference in the thickness of the insulation coating formed on the strands inside and outside the conductor, the insulation coating formed on the strands located on the surface of the conductor was significantly thicker. However, in the present invention, as described above, the inner and outer wires are thicker than the average thickness of 2 to 3μ because the internal wires cannot be coated with the thickness necessary for electrical insulation. Since a film of approximately the same thickness as the wire is uniformly produced, the electrical function can be achieved with an average thickness of at least 0.1 μm.

しかも本発明では被膜生成反応自体は、湿式的に行われ
るので、従来の乾式酸化処理法とは異なり、緻密で密着
性に富みかつ比較的加工性の良い絶縁被膜が容易に得ら
れる。
Moreover, in the present invention, the film formation reaction itself is carried out wetly, so unlike conventional dry oxidation treatment methods, an insulating film that is dense, highly adhesive, and relatively processable can be easily obtained.

次に本発明を実施例及び比較例で説明する。Next, the present invention will be explained using Examples and Comparative Examples.

実施例 1直径2.37!Lm軟銅線88本を撚り合せ
、これを断面扇形に圧縮成形してセグメントを得た。
Example 1 Diameter 2.37! Eighty-eight Lm annealed copper wires were twisted together and compression molded into a fan-shaped cross section to obtain segments.

このセグメント約120mをコイル状に巻き、これを6
個、相対湿度95%、温度60℃のチヤンバ一内に7日
間放置した。かくして処理したセグメントの一部を切断
し、カソード還元法(電解液0.1N−KCIl電解電
流密度0.5mA/d)により平均酸化被膜厚を測定し
たところ、0.15μであつた。
This segment is wound approximately 120m into a coil, and this is
The sample was left in a chamber at a relative humidity of 95% and a temperature of 60° C. for 7 days. A part of the thus treated segment was cut and the average oxide film thickness was measured by cathodic reduction method (electrolyte solution 0.1N-KCl, electrolytic current density 0.5 mA/d) and found to be 0.15μ.

次にかくして得たセグメントを6本撚り合せて導体断面
積2000m1の6分割導体とした。
Next, six segments thus obtained were twisted together to form a six-divided conductor with a conductor cross-sectional area of 2000 m1.

この6分割導体について直流抵抗値(RD)と50Hz
交流抵抗値(RA)とを夫々測定し、表皮効果係数RA
γ=一一1を求めたところγ=0.08であつた。
DC resistance value (RD) and 50Hz for this 6-divided conductor
AC resistance value (RA) and skin effect coefficient RA are measured respectively.
When γ=111 was calculated, γ=0.08.

R1 ・比較例
1セグメントの腐食生成処理を全く行わずに実施例1
と同様にして6分割導体を得て、これについて表皮効果
係数γ及び自然生成の酸化膜厚を実施例1と同様にして
求めたところγ=0.14、被膜厚平均0.018μで
あつた。
R1 ・Comparative example Example 1 without performing any corrosion generation treatment on one segment
A 6-segmented conductor was obtained in the same manner as above, and the skin effect coefficient γ and naturally formed oxide film thickness were determined in the same manner as in Example 1. γ = 0.14, and the average film thickness was 0.018μ. .

実施例 2 直径2.3mm軟銅線88本を撚り合せ、これを断面扇
形に圧縮成形してセグメントを得た。
Example 2 Eighty-eight annealed copper wires each having a diameter of 2.3 mm were twisted together and compressed into a fan-shaped cross section to obtain segments.

次に、このセグメントを6本撚り合せて導体断面積20
00關2の6分割導体とした後、この導体50mを相対
湿度98%、温度50℃のチヤンバ一内に15日間放置
して腐食生成処理をした。かくして得た導体について、
実施例1と同様にして平均酸化皮膜厚と表皮効果係数を
それぞれ求めたところ、皮膜厚は0.4μ、表皮効果係
数γは0.03であつた。
Next, six of these segments are twisted together to create a conductor with a cross-sectional area of 20
After forming a 6-segmented conductor of 0.00 m2, 50 m of this conductor was left in a chamber at a relative humidity of 98% and a temperature of 50° C. for 15 days to undergo corrosion formation treatment. Regarding the conductor thus obtained,
When the average oxide film thickness and skin effect coefficient were determined in the same manner as in Example 1, the film thickness was 0.4 μm and the skin effect coefficient γ was 0.03.

比較例 2 導体の腐食生成処理を1日間行つた以外は、実施例2と
同様にして得た導体について平均酸化皮膜厚と表皮効果
係数とを求めたところ、皮膜厚は0.07μであり、表
皮効果係数γは0.12であつた。
Comparative Example 2 The average oxide film thickness and skin effect coefficient were determined for a conductor obtained in the same manner as in Example 2, except that the conductor was subjected to corrosion generation treatment for one day, and the film thickness was 0.07μ. The skin effect coefficient γ was 0.12.

実施例 3 実施例2において、相対湿度98%、温度50℃のチヤ
ンバ一内での15日間放置に代えて、相対湿度9001
)、温度80℃のチヤンバ一内での5日間放置にした他
はすべて実施例2と同様にして導体を処理した。
Example 3 In Example 2, instead of leaving the sample in a chamber at a relative humidity of 98% and a temperature of 50° C. for 15 days, a relative humidity of 9001
), the conductor was treated in the same manner as in Example 2, except that it was left in a chamber at a temperature of 80° C. for 5 days.

かくして得た導体について実施例1と同様にして求めた
平均酸化皮膜厚と表皮効果係数γはそれぞれ、0.7μ
と0.03であつた。
The average oxide film thickness and skin effect coefficient γ of the thus obtained conductor, which were determined in the same manner as in Example 1, were each 0.7μ.
and 0.03.

実施例 4 実施例2において、相対湿度98%、温度50℃のチヤ
ンバ一内での15日間放置に代えて、相対温度800I
)、SO2ガス50―添加、温度50℃のチヤンバ一内
での3日間放置にした他はすべてa実施例2と同様にし
て導体を処理した。
Example 4 In Example 2, instead of leaving the sample in a chamber at a relative humidity of 98% and a temperature of 50°C for 15 days, a relative temperature of 800I was used.
), SO2 gas was added at 50°C, and the conductor was treated in the same manner as in Example 2, except that it was left in a chamber at a temperature of 50°C for 3 days.

かくして得た導体について実施例1と同様にして求めた
平均皮膜厚と表皮効果係数γはそれぞれ0.4μと0.
05であつた。
The average film thickness and skin effect coefficient γ of the thus obtained conductor were determined in the same manner as in Example 1, and were 0.4μ and 0.4μ, respectively.
It was 05.

実施例 5 実施例2において相対湿度98%、温度50℃のチヤン
バ一内での15日間放置に代えて、相対湿度90q6、
H,Sガス0.5P!l添加、温度50℃のチヤンバ一
内での2日間放置にした他はすべて実施例2と同様にし
て導体を処理した。
Example 5 Instead of leaving it in a chamber at a relative humidity of 98% and a temperature of 50°C for 15 days in Example 2, a relative humidity of 90q6,
H, S gas 0.5P! The conductor was treated in the same manner as in Example 2, except that 1 was added and the conductor was left in a chamber at a temperature of 50° C. for 2 days.

かくして得た導体について実施例1と同様にして求めた
平均皮膜厚と表皮効果係数γとはそれぞれ065μと0
.03であつた。
The average film thickness and skin effect coefficient γ of the thus obtained conductor were determined in the same manner as in Example 1, and were 065μ and 0, respectively.
.. It was 03.

実施例 6 実施例1において相対湿度95%、温度60℃のチヤン
バ一内での7日間放置に代えて、相対湿度95%、H2
Sガス1―添加、温度60℃のチヤンバ一内での12時
間放置にした他はすべて実施例1と同様にして導体を得
た。
Example 6 Instead of leaving the sample in a chamber at a relative humidity of 95% and a temperature of 60° C. for 7 days in Example 1, a temperature of 95% relative humidity and H2
A conductor was obtained in the same manner as in Example 1, except that S gas 1 was added and the sample was left in a chamber at a temperature of 60° C. for 12 hours.

かくして得た導体について実施例1と同様にして求めた
平均皮膜厚と表皮効果係数γとはそれぞれ0.6μと0
.03であつた。
The average film thickness and skin effect coefficient γ of the thus obtained conductor were determined in the same manner as in Example 1, and were 0.6 μ and 0, respectively.
.. It was 03.

以上の如く、本発明方法によれば、導体素線上に形成さ
れる腐食生成物皮膜は、導体内部の素線間にも均一に生
成されるので、膜厚が薄くても各素線間の電気絶縁作用
を有効に発揮できるばかりでなく、密着かつ緻密である
のでケーブル使用中に導体が受ける機械的及び熱的変形
にも充分耐え得ることができる。
As described above, according to the method of the present invention, the corrosion product film formed on the conductor strands is evenly formed between the strands inside the conductor, so even if the film thickness is thin, Not only can it effectively exert an electrical insulation effect, but since it is tightly adhered and dense, it can sufficiently withstand the mechanical and thermal deformation that the conductor undergoes while the cable is in use.

また本発明による処理は、コイル状に巻いた導体を収納
できるチヤンバ一と、温度、湿度などを発生制御する簡
単安価な装置とからなり、小スペースしか必要としない
設備で行うことができる。
Furthermore, the treatment according to the present invention can be carried out with equipment that requires only a small space, as it consists of a chamber that can accommodate a coiled conductor and a simple and inexpensive device that generates and controls temperature, humidity, etc.

その作業としても所定時間放置した後チヤンバ一から取
り出し、そのまま導体として使用できるという単純なも
のである。したがつて、多量の有毒薬剤や用水を使用し
、かつその廃水処理を不可欠とする従来の湿式処理法に
比べて生産性、経済性共に著しくすぐれている。
The process is as simple as leaving it for a predetermined period of time, then taking it out of the chamber and using it as a conductor. Therefore, it is significantly superior in both productivity and economy compared to conventional wet treatment methods that use large amounts of toxic chemicals and water and require wastewater treatment.

Claims (1)

【特許請求の範囲】 1 銅素線を撚り合せた導体を加湿雰囲気中に保持して
各銅素線の表面に水分を気体状態にて侵入させた後、液
体の水に変換せしめ酸素等と反応して平均0.1μ以上
の腐食生成物を形成することを特徴とする素線絶縁ケー
ブル導体の製造方法。 2 上記加湿雰囲気中に微量のイオウ又はイオウ化合物
を共存させることを特徴とする特許請求の範囲第1項記
載の素線絶縁ケーブル導体の製造方法。 3 銅素線を撚り合せた上記導体が分割導体であること
を特徴とする特許請求の範囲第1項又は第2項記載の素
線絶縁ケーブル導体の製造方法。 4 銅素線を撚り合せた上記導体が銅素線を撚り合せた
後、圧縮成形された導体であることを特徴とする特許請
求の範囲第1項又は第2項記載の素線絶縁ケーブル導体
の製造方法。
[Claims] 1. A conductor made of stranded copper wires is held in a humidified atmosphere to allow moisture to enter the surface of each copper wire in a gaseous state, and then to be converted to liquid water and mixed with oxygen, etc. 1. A method for producing a stranded insulated cable conductor, which comprises reacting to form corrosion products with an average size of 0.1 μ or more. 2. The method for manufacturing a stranded insulated cable conductor according to claim 1, characterized in that a trace amount of sulfur or a sulfur compound is allowed to coexist in the humidified atmosphere. 3. The method for manufacturing a strand insulated cable conductor according to claim 1 or 2, wherein the conductor made of copper strands twisted together is a divided conductor. 4. The strand insulated cable conductor according to claim 1 or 2, wherein the conductor made of copper strands is a conductor that is compression-molded after stranding the copper strands. manufacturing method.
JP1269481A 1981-01-30 1981-01-30 Method for manufacturing strand insulated cable conductor Expired JPS5919612B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1269481A JPS5919612B2 (en) 1981-01-30 1981-01-30 Method for manufacturing strand insulated cable conductor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1269481A JPS5919612B2 (en) 1981-01-30 1981-01-30 Method for manufacturing strand insulated cable conductor

Publications (2)

Publication Number Publication Date
JPS57128410A JPS57128410A (en) 1982-08-10
JPS5919612B2 true JPS5919612B2 (en) 1984-05-08

Family

ID=11812479

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1269481A Expired JPS5919612B2 (en) 1981-01-30 1981-01-30 Method for manufacturing strand insulated cable conductor

Country Status (1)

Country Link
JP (1) JPS5919612B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63104417U (en) * 1986-12-25 1988-07-06

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63104417U (en) * 1986-12-25 1988-07-06

Also Published As

Publication number Publication date
JPS57128410A (en) 1982-08-10

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