JPS60208013A - Method of producing strand insulated conductor - Google Patents

Method of producing strand insulated conductor

Info

Publication number
JPS60208013A
JPS60208013A JP6448584A JP6448584A JPS60208013A JP S60208013 A JPS60208013 A JP S60208013A JP 6448584 A JP6448584 A JP 6448584A JP 6448584 A JP6448584 A JP 6448584A JP S60208013 A JPS60208013 A JP S60208013A
Authority
JP
Japan
Prior art keywords
conductor
container
oxide film
copper
copper oxide
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.)
Granted
Application number
JP6448584A
Other languages
Japanese (ja)
Other versions
JPH0566689B2 (en
Inventor
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 JP6448584A priority Critical patent/JPS60208013A/en
Publication of JPS60208013A publication Critical patent/JPS60208013A/en
Publication of JPH0566689B2 publication Critical patent/JPH0566689B2/ja
Granted legal-status Critical Current

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  • Processes Specially Adapted For Manufacturing Cables (AREA)
  • Manufacturing Of Electric Cables (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Insulated Conductors (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】 木兄8A#′i表皮効果による交流抵抗を低減した素線
絶縁導体の製造方法の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a method for manufacturing a wire insulated conductor that reduces alternating current resistance due to the skin effect.

近時電力使用量の増大と発電所の大容量化に伴ない、電
力伝送線路の容量も大幅に増大しつつある。この大容量
化に伴って電力を伝送する寛カケーブルにおいても必然
的に容量増大のための性能改善が強く要求されている。
BACKGROUND OF THE INVENTION In recent years, with the increase in power consumption and the increase in the capacity of power plants, the capacity of power transmission lines is also increasing significantly. With this increase in capacity, there is a strong demand for performance improvements in the permissive cables that transmit power to increase the capacity.

電カケーブルの性能改善なしには線路建設費の増大を招
くばかシであるので、既設の線路に大答骨の九カケーブ
ルを布設することによりこの問題を解決しようとしてい
る。それには、電カケーブルの電流密度の増大が必要で
あるが、単に導体断面積を大きくしただけでは、所謂交
流の表皮効果による損失が急に増大する。これを解決す
るためには全素線を絶縁した緊線絶縁導体をJ−nいる
必要がある。
Without improving the performance of electric power cables, it would be foolish to increase the cost of line construction, so attempts are being made to solve this problem by laying nine major cables on the existing lines. To achieve this, it is necessary to increase the current density of the power cable, but simply increasing the conductor cross-sectional area will suddenly increase loss due to the so-called skin effect of alternating current. In order to solve this problem, it is necessary to use a ground wire insulated conductor in which all the wires are insulated.

従来、かかる素線絶縁導体を得る方法には種種の方法が
提案されているが、最も経済的な方法としては銅素線の
表面に酸化銅(CuO)の皮膜を形成せしめる方法であ
る。
Conventionally, various methods have been proposed for obtaining such a wire insulated conductor, but the most economical method is a method of forming a copper oxide (CuO) film on the surface of a copper wire.

酸化銅皮膜の形成法としては銅素線を撚合せた導体を気
密容器に収納し、アンモニア水又はアンモニアガスと酸
素を注入し、40〜100℃の温度範囲内の一定m度で
湿潤雰囲気下でルT定時間保持することにより各素線表
面に酸化銅皮膜を生成させる方法(特開昭57−21−
0517号)が提、案されている。
The method for forming a copper oxide film is to store a conductor made of twisted copper wires in an airtight container, inject ammonia water or ammonia gas and oxygen, and heat it in a humid atmosphere at a constant temperature within the temperature range of 40 to 100 degrees Celsius. A method of forming a copper oxide film on the surface of each strand by holding it for a certain period of time (Japanese Patent Laid-Open No. 57-21-
No. 0517) has been proposed and proposed.

しかしながら、この方法では導体サイズが比較的小さい
場合すなわち導体を構成する素線数が少ない場合には、
導体の内外層のどの素線も一様に酸化銅皮膜が形成され
るが、導体サイズが大きくなると、導体の内外層の銅素
線に形成される酸化銅皮膜の厚さが均一になシ難いとい
う欠点があった。
However, with this method, when the conductor size is relatively small, that is, when the number of strands constituting the conductor is small,
A copper oxide film is uniformly formed on all the wires in the inner and outer layers of the conductor, but as the conductor size increases, the thickness of the copper oxide film formed on the copper wires in the inner and outer layers of the conductor becomes less uniform. The drawback was that it was difficult.

すなわち、アンモニア水又はアンモニアガス及び酸素等
の存在する湿潤雰囲気下での酸化銅皮膜の生成機構はア
ンモニアを含む水蒸気が銅の表面に接触凝縮することに
よシ、酸素による銅の酸化反応が急速に進むというもの
であるが、極めて多くの銅素線を撚合せた導体でしかも
これを圧縮成形して占積率を85〜95%まで高めた大
サイズ導体の場合には、これら反応性ガスと接触するチ
ャンスの多い導体の最外層の素線から酸化皮膜の生成が
生じ、順次内部へ進行するため、導体の内層部及び外層
部ともに一様に酸化皮膜が形成されるためには極めて長
時間を要するという欠点があった。
In other words, the formation mechanism of a copper oxide film in a humid atmosphere containing ammonia water or ammonia gas and oxygen is due to water vapor containing ammonia contacting and condensing on the copper surface, resulting in a rapid oxidation reaction of copper by oxygen. However, in the case of large-sized conductors that are made by twisting an extremely large number of copper wires, and which are compression-molded to increase the space factor to 85-95%, these reactive gases are An oxide film is formed from the outermost wire of the conductor, which has a high chance of coming into contact with the conductor, and progresses to the inside of the conductor. The drawback was that it was time consuming.

本発明は、大サイズ導体であっても比較的短時間に導体
の内外層のどの緊線も均一な厚さの酸化銅皮膜を形成す
る方法を提供することを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a method for forming a copper oxide film of uniform thickness on all the wires in the inner and outer layers of a conductor in a relatively short period of time even in the case of a large-sized conductor.

すなわち、本発明は、銅素線を撚合せた導体を気密容器
内で、アンモニアガス0.5容器1%JL上と酸素10
容量−以上の存在する、相対湿度80%以上の雰囲気で
かつ大気圧よシO〜50■Hg低い圧力下で40〜10
0℃の温度に保持することKより銅素線表面に酸化銅皮
膜を生成することを特徴とする素線絶縁導体の製造方法
である。
That is, in the present invention, a conductor made of twisted copper wires is placed in an airtight container with ammonia gas 0.5 container 1% JL and oxygen 10
In an atmosphere with a relative humidity of 80% or more, and at a pressure lower than atmospheric pressure by 0 to 50 μHg, the capacity is 40 to 10
This is a method for producing an insulated wire conductor characterized by forming a copper oxide film on the surface of the copper wire by holding the wire at a temperature of 0°C.

気密容器内を大気圧よ#)0〜50mHg低い圧力下す
なわち0〜−50 mHgの負圧に保持することKよシ
、導体の内層部及び外層部に位置するどの銅素線の表面
にもほぼ一様に酸化銅皮81急が形成されるが、その理
由は明らかでない。
The inside of the airtight container must be maintained at a pressure 0 to 50 mHg lower than atmospheric pressure, that is, a negative pressure of 0 to -50 mHg. Copper oxide skin 81 is formed almost uniformly, but the reason is not clear.

容器内のアンモニアガス濃度は0.5容器%以上、酸素
濃度は10容量チ以上で、さらに相対湿度は80チ以上
にする必要がある。いずれもこれ以下では、本発明の目
的とする迅速な酸化銅皮膜の形成は期待できないからで
ある。アンモニアガス濃度、酸素濃度及び相対湿度はい
ずれも高い程、迅速に酸化銅皮膜が生成する。
The ammonia gas concentration in the container must be 0.5% or more, the oxygen concentration must be 10% by volume or more, and the relative humidity must be 80% or more. This is because if the amount is less than this, rapid formation of a copper oxide film, which is the object of the present invention, cannot be expected. The higher the ammonia gas concentration, oxygen concentration, and relative humidity, the faster the copper oxide film is formed.

1だ、容器内の圧力をO〜−50mugの負圧に保持す
る方法としては、導体を気密容器内に収納後、真空引き
して減圧後アンモニア水又はアンモニアガス及び酸素を
入れてもよく、あるいはアンモニア水又はアンモニアガ
ス及び酸素を入れた後減圧してもよい。
1. As a method of maintaining the pressure inside the container at a negative pressure of O to -50 mg, the conductor may be housed in an airtight container, the container may be evacuated, and after the pressure is reduced, ammonia water or ammonia gas and oxygen may be added. Alternatively, the pressure may be reduced after adding ammonia water or ammonia gas and oxygen.

容器内の圧力を一50■進よシさらに減圧した雰囲気で
は良好な緻密な黒化皮膜(CuO皮膜)が形成されない
。容器内の圧力が大気圧よシ高い正圧では導体の内層部
と外層部の素線表面に厚さの一様な酸化銅皮膜を得るK
は極めて長時間を要し実用性がない。
A good dense blackened film (CuO film) cannot be formed in an atmosphere in which the pressure inside the container is increased by 150 μm and further reduced. When the pressure inside the container is higher than atmospheric pressure and is positive, a copper oxide film with a uniform thickness can be obtained on the wire surface of the inner and outer layers of the conductor.
takes an extremely long time and is not practical.

次に本発明を実施例で説明する。Next, the present invention will be explained with examples.

実施例1 直径2.3 tmの軟銅線88本を撚合せ、これを断面
扇形に圧縮成形した占積率93%のセグメントヲ鉄製気
密容器に入れ真空ポンプで容器内の圧力を−20mHH
に減圧した後、20%礎度のアンモニア水を入れ、容器
内の温度を約60℃とし、容器内の酸素濃度を15〜2
0容量チに、また相対湿度を95〜100チに保持して
、容器内の圧力を真空ポンプで一20mHgの負圧に保
ったまま10時間経過後、セグメントを取シ出した。
Example 1 88 annealed copper wires with a diameter of 2.3 tm were twisted together, and a segment with a space factor of 93%, which was compression-molded into a fan-shaped cross section, was placed in an airtight steel container and the pressure inside the container was raised to -20 mHH using a vacuum pump.
After reducing the pressure to
After 10 hours, the segment was taken out while maintaining the volume at 0 and the relative humidity at 95 to 100 degrees, and keeping the pressure inside the container at a negative pressure of -20 mHg using a vacuum pump.

実施例2 実施例1で用いたのと同じ未処理セグメントをステンレ
ス製気容器度に入れ、容器内を一10mHgに真空引き
した後、湿ったアンモニアガス、酸素ガスを注入し、ア
ンモニアガス&[ヲ1゜〜15容量チ、酸素濃度を20
〜25答量チに、相対湿度を90〜95チに保持して温
度約65℃で容器内の圧力を一10■Hgの負圧に保っ
たまま10時間経過後セグメントを取り川した。
Example 2 The same untreated segment used in Example 1 was placed in a stainless steel air container, the inside of the container was evacuated to -10 mHg, and moist ammonia gas and oxygen gas were injected, and ammonia gas & [ヲ1゜~15capacity, oxygen concentration 20
After 10 hours, the segment was removed while keeping the relative humidity at 90 to 95 degrees, the temperature at about 65 DEG C., and the pressure inside the container at a negative pressure of 110 inches Hg.

実施例3 実施例1で用いたのと同じ未処理セグメントをステンレ
ス製気密容器に入れ、中に水をはった後、容器内のアン
モニアガス娘度5〜10’J埜チ、酸素濃度10〜15
容量チ、相対湿度80〜90チとし、容器内を絶えず一
30mHgに真空引きして減圧状態とし、容器内温度約
70℃で10時間経過後にセグメントを取り出した。
Example 3 The same untreated segment used in Example 1 was placed in a stainless steel airtight container, and water was poured into the container. ~15
The capacity was set at 100 °C and the relative humidity was set at 80-90 °C, the inside of the container was constantly evacuated to -30 mHg to create a reduced pressure state, and the segment was taken out after 10 hours at a temperature inside the container of about 70°C.

比較例1 実施例1において容器を真空?ン!で減圧せずに、絶え
ず大気圧よp 0.2 kg/cm高い正圧になるよう
にした以外は、実施例1と全く同じ条件で実験を行った
Comparative Example 1 Is the container vacuumed in Example 1? hmm! The experiment was conducted under exactly the same conditions as in Example 1, except that the pressure was not reduced and the positive pressure was constantly maintained at a value p 0.2 kg/cm higher than atmospheric pressure.

比較例2 実施例3において容器を真空引きせずに、絶えず大気圧
よF) 0.5 ky/cm2高い正圧になるようにし
た以外は実施例3と全く同じ条件で実験を行った。
Comparative Example 2 An experiment was conducted under exactly the same conditions as in Example 3, except that in Example 3, the container was not evacuated and the positive pressure was constantly maintained at 0.5 ky/cm2 higher than atmospheric pressure.

比較例3 実施例2において、アンモニアガスallO91容偏・
チにした以外は実施例2と全く同じ条件で実験を行った
Comparative Example 3 In Example 2, the ammonia gas allO91 volume biased
The experiment was conducted under exactly the same conditions as in Example 2, except that the temperature was changed to 1.

比較例4 実施例2において、酸素濃度を5容貴チにした以外は実
施例2と全く同じ条件で実験を行った。
Comparative Example 4 In Example 2, an experiment was conducted under exactly the same conditions as in Example 2, except that the oxygen concentration was changed to 5 volumes.

比較例5 実施例2において、相対湿度を60%とした以外は実施
例2と全く同じ条件で実験を行った。
Comparative Example 5 In Example 2, an experiment was conducted under exactly the same conditions as in Example 2, except that the relative humidity was 60%.

次に上記各実施例及び各比較例で得たセグメントの酸化
銅皮膜厚をカソード還元法(電解液Q、 l N −K
Ct 、電流密度0.5 mA/an ) Icより測
定した。尚、酸化皮膜厚測定はセグメントを構成してい
る各層毎の素線について行った。セグメントを構成する
中心素線を第1層とし、順次外側に向って第2層、第3
層、第4層、第51装(最外層)とした。かくして測定
した結果を次表に示す。
Next, the copper oxide film thickness of the segments obtained in each of the above examples and comparative examples was measured by cathodic reduction method (electrolyte Q, lN-K
Ct was measured at a current density of 0.5 mA/an) Ic. Incidentally, the oxide film thickness measurement was performed on the strands of each layer constituting the segment. The central strand constituting the segment is the first layer, and the second and third layers are sequentially placed outward.
The fourth layer was the 51st layer (outermost layer). The results thus measured are shown in the table below.

以上、実施例から明らかな如く、本発明によれば、セグ
メントを構成している各層の素線ともほぼ一様な酸化銅
皮膜厚が得られる。これに対して比較例では、いずれも
最外層の素線には若干の酸化銅皮膜が形成されているも
のの内層部の素線にはほとんど酸化銅皮膜が形成されて
いない。
As is clear from the examples above, according to the present invention, a substantially uniform copper oxide coating thickness can be obtained for the wires of each layer constituting the segment. On the other hand, in the comparative examples, although some copper oxide films were formed on the outermost layer wires, almost no copper oxide film was formed on the inner layer wires.

次に、各実施例及び各比較例で得たセグメントについて
、それぞれ6本撚合せて分割導体を得、これら分割導体
のAC抵抗(RAc)とDC抵抗(RD、 )とを測定
したところ、両抵抗の比(RAC/ RDC)は、本発
明による上記実施例の分割導体では1.05〜1.10
でアシ、これに対して、上記比較例の分割導体では1.
2〜14でしかもその比のバラツキが極めて大きかった
Next, for the segments obtained in each example and each comparative example, six divided conductors were obtained by twisting each segment, and the AC resistance (RAc) and DC resistance (RD, ) of these divided conductors were measured. The ratio of resistance (RAC/RDC) is 1.05 to 1.10 for the divided conductor of the above embodiment according to the present invention.
In contrast, the divided conductor of the above comparative example had 1.
2 to 14, and the variation in the ratio was extremely large.

尚、酸化銅皮膜を形成していない銅素紗からなる分割導
体では1.3〜1.4であった。したがって本発明によ
る素線絶縁導体は表皮効果による交流損失が著しく低減
されていることが明らかである。
Incidentally, in the case of a divided conductor made of copper gauze without a copper oxide film formed thereon, it was 1.3 to 1.4. Therefore, it is clear that the strand insulated conductor according to the present invention has significantly reduced AC loss due to the skin effect.

以上の如く、本発明によれば、導体を(メジ族している
どの層の銅素線表面にも厚さのほぼ一様な酸化銅皮膜を
形成することができ、その結果、表皮効果による交流損
失を著しく低減し7だ素線絶縁導体が得られるものであ
る。
As described above, according to the present invention, it is possible to form a copper oxide film with a substantially uniform thickness on the surface of copper wire in any layer of the conductor. A seven-wire insulated conductor with significantly reduced AC loss can be obtained.

Claims (1)

【特許請求の範囲】[Claims] (1) 銅素線を撚合せた導体を気密容器内で、アンモ
ニアガス0.5容量チ以上と酸素lO容容量板以上存在
する、相対湿度80%以上の雰囲気でかつ大気圧よりO
〜50+a+Hg低い圧力下で40〜100℃の温度に
保持することにより銅素線表面に酸化銅皮膜を生成する
ことを特徴とする緊線絶縁導体の製造方法。
(1) A conductor made of stranded copper wires is heated in an airtight container in an atmosphere with a relative humidity of 80% or more and an atmosphere with a relative humidity of 80% or more and an atmosphere containing 0.5 or more volumes of ammonia gas and 100% or more oxygen.
~50+a+Hg A method for manufacturing a wire insulated conductor, characterized by forming a copper oxide film on the surface of a copper wire by maintaining the temperature at a temperature of 40 to 100° C. under a low pressure.
JP6448584A 1984-03-31 1984-03-31 Method of producing strand insulated conductor Granted JPS60208013A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6448584A JPS60208013A (en) 1984-03-31 1984-03-31 Method of producing strand insulated conductor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6448584A JPS60208013A (en) 1984-03-31 1984-03-31 Method of producing strand insulated conductor

Publications (2)

Publication Number Publication Date
JPS60208013A true JPS60208013A (en) 1985-10-19
JPH0566689B2 JPH0566689B2 (en) 1993-09-22

Family

ID=13259562

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6448584A Granted JPS60208013A (en) 1984-03-31 1984-03-31 Method of producing strand insulated conductor

Country Status (1)

Country Link
JP (1) JPS60208013A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19643609B4 (en) * 1996-10-14 2007-07-19 Pirelli Cavi E Sistemi S.P.A. Manufacturing device for applying an oxide layer on the individual wires of a stranded copper conductor

Also Published As

Publication number Publication date
JPH0566689B2 (en) 1993-09-22

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