JPS6219031B2 - - Google Patents
Info
- Publication number
- JPS6219031B2 JPS6219031B2 JP12878380A JP12878380A JPS6219031B2 JP S6219031 B2 JPS6219031 B2 JP S6219031B2 JP 12878380 A JP12878380 A JP 12878380A JP 12878380 A JP12878380 A JP 12878380A JP S6219031 B2 JPS6219031 B2 JP S6219031B2
- Authority
- JP
- Japan
- Prior art keywords
- hydrazine
- cable
- wires
- 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.)
- Expired
Links
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 46
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 25
- 239000005751 Copper oxide Substances 0.000 claims description 23
- 229910000431 copper oxide Inorganic materials 0.000 claims description 23
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 229910052802 copper Inorganic materials 0.000 claims description 12
- 239000010949 copper Substances 0.000 claims description 12
- 239000003495 polar organic solvent Substances 0.000 claims description 3
- 239000002131 composite material Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052987 metal hydride Inorganic materials 0.000 description 2
- 150000004681 metal hydrides Chemical class 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HFDWIMBEIXDNQS-UHFFFAOYSA-L copper;diformate Chemical compound [Cu+2].[O-]C=O.[O-]C=O HFDWIMBEIXDNQS-UHFFFAOYSA-L 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Manufacturing Of Electrical Connectors (AREA)
- Processing Of Terminals (AREA)
Description
本発明は銅素線の表面に銅酸化物皮膜を形成し
て素線相互間を絶縁した電力ケーブルの接続方法
に関するものである。
電力ケーブル、特に大電力用交流ケーブルは、
多数の銅素線を撚り合せて導体を形成し、これに
絶縁外層を設けたもので、中には撚り合せた導体
を断面扇状に圧縮成形し、これを数個撚り合せた
ものも用いられている。またこのような電力ケー
ブルのなかには中央部に冷却用絶縁油の流路を設
けたものも用いられている。このような構造の電
力ケーブルにおいては、電流が導体の外層部に集
中する所調表皮効果のため電力ロスが起り、特に
大電力用交流ケーブルでは電力ロスが一層顕著と
なる。これを防止するため、素線相互を絶縁する
ことにより電流の表皮集中を抑えている。
素線相互の絶縁方法としては、種々のものが知
られているが、素線表面を厚さ0.1〜3μの銅酸
化物で被覆する方法が性能及び生産性の点で最も
有力であり、エナメル皮膜を形成する方法はコス
ト的に不利である。
このような見地から最近銅酸化物を被覆して素
線相互間を絶縁した電力ケーブルが用いられてい
るが、このケーブルはその接続方法に離点があつ
た。例えばコネクターを用いる圧縮接続では、一
部の素線(最外層の素線)がコネクターと電気的
に接触したとしても、素線相互が絶縁されている
ため、全素線は電気的に接続されていない。同様
のことが他の接続方法、例えば溶接やロー付けな
どにおいても起る。このため信頼性の高いケーブ
ル接続を実現するため、ケーブルの接続に際し、
素線の絶縁被膜(銅酸化物)を除去することが要
求されている。
銅酸化物被膜を除去する方法としては、硫酸な
どの鉱酸溶液を用いて酸洗いする方法が知られて
いるが、腐食性物質を使用するため、ケーブル内
への残留を避けるため、処理作業と洗浄作業を撤
底させねばならず、更に銅を含有する酸性の毒性
液を排出するため、環境汚染にも充分な注意が必
要である。このため還元性溶液を用いて銅酸化物
を還元する方法が試みられているが、毒性液を使
用する欠点があつた。
本発明はこれに鑑み、種々検討の結果、毒性液
を用いることなく素線の銅酸化物被膜を能率よく
有効に除去することに成功し、高信頼性のある電
力ケーブルの接続方法を開発したもので、銅素線
の表面に銅酸化物被膜を形成して素線相互間を絶
縁した電力ケーブルの接続において、接続するケ
ーブル端末部より絶縁外層を除去して素線群を突
出せしめ、これにヒドラジン溶液を接触させて素
線表面の銅酸化物を化学的に還元した後ケーブル
の接続を行なうことを特徴とするものである。
即ち本発明は銅素線の表面に素線相互間の絶縁
のために銅酸化物被膜を形成した電力ケーブルを
接続するため、先ず接続するケーブルの端末部よ
り絶縁外層を皮剥等により除去して素線群を突出
せしめ、次に突出する素線群にヒドラジン溶液を
接触させて素線表面の銅酸化物を化学的に還元す
るものである。
ヒドラジン溶液としては、ヒドラジン、ヒドラ
ジンヒドラード(NH2・NH2・H2O)等を含有す
る水溶液や有機溶液で、ヒドラジン、ヒドラジン
ヒドラードは通常濃厚水溶液として市販されてお
り、これを水で希釈するか又は極性有機溶剤で希
釈する。
極性有機溶剤としてはメタノール、エタノー
ル、プロパノール等のアルコール類、アセトン、
メチルエチルケトン等のケトン類、ホルムアルデ
ヒド、アセトアルデヒド等のアルデヒド類を用い
る。ヒドラジン、ヒドラジンヒドラード等の濃度
は、還元力及び還元速度の主要な因子であり、1
%以上とすることが望ましい。また液温は重要な
加速要因であり、30℃以上として使用する方が工
業的に有利である。
ヒドラジンはアンモニヤや水化アミドを副生す
る反応もあり、単純ではないが、次式により銅酸
化物を還元する。
2CuO+NH2・NH2→2Cu+N2+2H2O
また過剰のヒドラジンは大気中の酸素と反応し
たり、接触的に分解し、次式に示すように窒素、
水素、アンモニヤに変わる。
2NH2・NH2→N2+2H2
3NH2・NH2→H2+4NH3
2NH2・NH2→N2+H2+2NH3
このようにヒドラジンは銅を腐食する性質が軽
微で、反応後には大部分がガス化してしまうた
め、厳密な洗浄を必要とせず、また残留物もケー
ブルや絶縁油を劣化することがない。このような
特徴は他の還元剤、例えば水素化ホウ素酸ナトリ
ウム(NaBH3)のような金属水素化物、ギ酸
(HCOOH)等では得られないものである。即ち
金属水素化物は強力な還元剤であるが、ナトリウ
ムやホウ酸などのイオン性の還元生成物を生じ、
またギ酸は酸であるためギ酸銅を生成するなど不
都合を起す。
本発明において、ヒドラジン溶液としては、水
溶液よりも極性有機溶液を使用する方が有利であ
る。例えばアルコール類の溶液を使用すれば同一
温度で2倍以上の還元速度を示し、作業を迅速化
する。また液の表面張力が小さいので、素線間に
速かに浸透し、より作業を迅速化する。更に素線
表面の銅酸化物を還元した後乾燥してから接続す
るものであるが、乾燥が容易である。これ等の特
徴はケーブルの接続作業に有効に作用する。
本発明により素線表面の銅酸化物を還元するた
めには、絶縁外層を皮剥ぎしてケーブル端末の素
線群を突出せしめ、これをヒドラジン溶液に浸漬
し、還元により銅の表面となつた所で引き上げ、
熱風等で乾燥するのが一般的である。またケーブ
ル端末より突出する素線群を70〜80℃に加熱して
おけば、溶液を加熱しなくても40〜50℃の温度で
迅速処理が可能となり、還元と乾燥とを5分以内
で完了することもできるようになる。素線間に毛
管力により溶液が浸透し、接続部以外にも拡がる
が、これに対しては浸透長を設定し、それ以上拡
がるのを適当な方法で防止すればよい。特に浸透
を避けなければならない場合には、浸漬部から離
れた素線群の外周面に内側に供気口又は排気口を
設けた還状体を密着させて取付け、供気口より圧
搾空気を圧送してエアーカーテンを形成するか、
又は排気口より真空ポンプ等で吸引することによ
り浸透液を遮断する。還状体は素線群の周囲に密
着するように取付けて外気と完全に遮断しておく
方が効果的であり、環状体の内周面に空隙を設け
て素線群全体に平均して作用させるなどの工夫を
すれば一層有効である。
電力ケーブルの接続工事は地下などの下方から
上方の受電部にジヨイントするケースが少なくな
い。このような場合突出する素線群を槽状に囲つ
て、該槽内にヒドラジン溶液を注入する方法が採
られるが、液もれと浸透防止のため、前記環状体
の取付け等の工夫が必要である。また簡単な方法
としては、ヒドラジン溶液を還元すべき素線群に
滴下したり、ハケを用いて塗布するのも有効であ
る。
このようにして還元処理した素線群は水又は溶
剤を用いて洗浄するか、又は洗浄することなく、
乾燥し、しかる後通常の接続作業を行なうもので
ある。
次に本発明の実施例について説明する。
実施例 1
厚さ約1.5μの酸化銅を被覆した直径2.3mmの銅
素線を88本撚合せた後圧縮成形したセグメント
(断面2000mm2)を6本合せ、その上に絶縁外層を
施した電力ケーブルの接続を行なつた。
先ずケーブル端末部の絶縁外層を約50cm皮剥し
て素線群を突出せしめた。次に素線群の先端から
15cmの位置に長さ10cmのゴム製筒状体を被せ、そ
の両端をテープでシールし、該筒状態の側面に設
けた孔よりコンプレツサーにより空気を圧入しな
がら素線群の先端から10cmまでを30℃のヒドラジ
ンヒドラード15%エタノール溶液に浸漬し、2分
後に引き上げ、続いてエタノールに15cmまで30秒
間浸漬した後ドライヤーにより3分間乾燥した。
このテーブルを解体し、素線群の還元処理した
内部を調べたところ酸化銅の黒色は全く目視でき
なかつた。また上記処理したケーブル2本を銅ス
リープを用いて圧縮接続した。この接続部の電気
抵抗を測定したところ8.5μΩであつた。尚比較
のため素線表面の酸化銅を除去することなく同様
に接続したものは100μΩ以上であつた。また素
線表面に酸化銅を被覆することなく撚合せた同様
のケーブルの接続部の電気抵抗は7.8μΩであつ
た。
実施例 2
実施例1において30℃のヒドラジンヒドラード
15%エタノール液に代えて第1表に示すヒドラジ
ンヒドラード溶液を用いて処理し、処理した内部
を調べると共に、同様にして接続した接続部の電
気抵抗を測定した。その結果を第1表に併記し
た。
The present invention relates to a method for connecting a power cable in which a copper oxide film is formed on the surface of copper wires to insulate the wires from each other. Power cables, especially high power AC cables,
A conductor is formed by twisting a large number of copper wires together, and an insulating outer layer is provided on this.Some conductors are compression-molded into a fan-shaped cross section, and several pieces of this are twisted together. ing. Also, some of these power cables are provided with a cooling insulating oil flow path in the center. In power cables having such a structure, power loss occurs due to the skin effect where current concentrates on the outer layer of the conductor, and power loss is particularly noticeable in high-power AC cables. To prevent this, the concentration of current on the skin is suppressed by insulating the wires from each other. Various methods are known for insulating wires from each other, but the most effective method in terms of performance and productivity is coating the wire surface with copper oxide with a thickness of 0.1 to 3 μm. The method of forming a film is disadvantageous in terms of cost. From this point of view, power cables coated with copper oxide to insulate the strands from each other have recently been used, but these cables have discrete points in their connection method. For example, in a compression connection using a connector, even if some of the strands (the outermost layer of strands) come into electrical contact with the connector, all the strands are electrically connected because the strands are insulated from each other. Not yet. The same thing happens with other connection methods, such as welding and brazing. Therefore, in order to achieve a highly reliable cable connection, when connecting the cable,
It is required to remove the insulation coating (copper oxide) from the wire. A known method for removing copper oxide coatings is pickling with a mineral acid solution such as sulfuric acid, but since it uses a corrosive substance, treatment work must be carried out to avoid it remaining inside the cable. Cleaning operations must be abolished, and since acidic and toxic liquid containing copper is discharged, sufficient attention must be paid to environmental pollution. For this reason, attempts have been made to reduce copper oxide using a reducing solution, but this method has the drawback of using a toxic solution. In view of this, as a result of various studies, the present invention has succeeded in efficiently and effectively removing the copper oxide coating on bare wires without using toxic liquids, and has developed a highly reliable power cable connection method. In the connection of power cables in which a copper oxide film is formed on the surface of copper wires to insulate the wires from each other, the outer insulation layer is removed from the terminals of the cables to be connected to make the wires protrude. The cable is connected after the copper oxide on the surface of the wire is chemically reduced by bringing the wire into contact with a hydrazine solution. That is, in the present invention, in order to connect a power cable in which a copper oxide film is formed on the surface of a copper wire to insulate the wires from each other, the outer insulating layer is first removed from the terminal end of the cable to be connected by stripping or the like. A group of wires is made to protrude, and then a hydrazine solution is brought into contact with the protruding group of wires to chemically reduce the copper oxide on the surface of the wires. Hydrazine solutions are aqueous or organic solutions containing hydrazine, hydrazine hydrade (NH 2 NH 2・H 2 O), etc. Hydrazine and hydrazine hydrade are usually commercially available as concentrated aqueous solutions, which can be mixed with water. Dilute or dilute with polar organic solvents. Examples of polar organic solvents include alcohols such as methanol, ethanol, and propanol, acetone,
Ketones such as methyl ethyl ketone and aldehydes such as formaldehyde and acetaldehyde are used. The concentration of hydrazine, hydrazine hydrade, etc. is the main factor of reducing power and reduction rate.
% or more is desirable. In addition, the liquid temperature is an important acceleration factor, and it is industrially advantageous to use the liquid at a temperature of 30°C or higher. Hydrazine has reactions that produce ammonia and hydrated amide as by-products, and although it is not simple, copper oxide is reduced by the following formula. 2CuO+NH 2・NH 2 →2Cu+N 2 +2H 2 O Excess hydrazine reacts with oxygen in the atmosphere or decomposes catalytically, producing nitrogen,
Hydrogen changes to ammonia. 2NH 2・NH 2 →N 2 +2H 2 3NH 2・NH 2 →H 2 +4NH 3 2NH 2・NH 2 →N 2 +H 2 +2NH 3In this way, hydrazine has a slight tendency to corrode copper, but after the reaction it corrodes to a large extent. Since the parts are gasified, there is no need for rigorous cleaning, and the residue does not deteriorate the cable or insulating oil. These characteristics are not available with other reducing agents, such as metal hydrides such as sodium borohydride (NaBH 3 ), formic acid (HCOOH), and the like. That is, metal hydrides are strong reducing agents, but they produce ionic reduction products such as sodium and boric acid,
Furthermore, since formic acid is an acid, it causes disadvantages such as producing copper formate. In the present invention, it is more advantageous to use a polar organic solution as the hydrazine solution than an aqueous solution. For example, if an alcohol solution is used, the reduction rate will be more than twice as high at the same temperature, speeding up the work. Also, since the surface tension of the liquid is low, it quickly penetrates between the strands of wire, making the work even faster. Furthermore, the copper oxide on the surface of the strands is reduced and then dried before connection, and drying is easy. These features work effectively for cable connection work. In order to reduce the copper oxide on the surface of the wire according to the present invention, the outer insulating layer is peeled off to make the wire group at the end of the cable protrude, and this is immersed in a hydrazine solution to reduce the copper surface. I pulled it up at a place,
It is common to dry with hot air. In addition, if the group of wires protruding from the cable end is heated to 70-80℃, rapid processing can be performed at a temperature of 40-50℃ without heating the solution, and reduction and drying can be done within 5 minutes. You will also be able to complete it. The solution penetrates between the strands due to capillary force and spreads beyond the connection part, but to prevent this, a penetration length can be set and further spread can be prevented by an appropriate method. In particular, when penetration must be avoided, a circular body with an air supply port or exhaust port on the inside is attached tightly to the outer peripheral surface of the wire group away from the immersed part, and compressed air is supplied from the air supply port. Pressure feed to form an air curtain, or
Alternatively, the permeate can be shut off by suctioning from the exhaust port with a vacuum pump or the like. It is more effective to attach the annular body tightly around the wire group to completely isolate it from the outside air. It will be even more effective if you try to make it work. When connecting power cables, there are many cases in which the cables are jointed from below, such as underground, to the power receiving section above. In such cases, a method is adopted in which the protruding strands are surrounded by a tank and the hydrazine solution is injected into the tank, but in order to prevent liquid leakage and penetration, it is necessary to devise measures such as attaching the annular body. It is. Furthermore, as a simple method, it is effective to drop a hydrazine solution onto the group of wires to be reduced or to apply it using a brush. The strands of wire that have been reduced in this way can be cleaned with water or a solvent, or without cleaning.
After drying, normal connection work can be performed. Next, examples of the present invention will be described. Example 1 88 copper wires with a diameter of 2.3 mm coated with copper oxide with a thickness of about 1.5 μ were twisted together and then compression-molded into 6 segments (cross section 2000 mm 2 ), which were then combined with an insulating outer layer. Connected the power cable. First, about 50 cm of the outer insulating layer at the end of the cable was peeled off to expose the wires. Next, from the tip of the wire group
A 10cm long rubber cylinder is placed over the 15cm position, both ends of which are sealed with tape, and air is injected using a compressor through the hole provided on the side of the cylinder, extending up to 10cm from the tip of the wire group. It was immersed in a 15% ethanol solution of hydrazine hydrade at 30°C, pulled out after 2 minutes, then immersed in ethanol to a depth of 15 cm for 30 seconds, and then dried with a dryer for 3 minutes. When this table was dismantled and the inside of the reduced wire group was examined, the black color of copper oxide was not visible at all. Further, the two cables treated above were compressed and connected using a copper sleeve. When the electrical resistance of this connection was measured, it was 8.5 μΩ. For comparison, a wire connected in the same manner without removing the copper oxide on the surface of the wire had a resistance of 100 μΩ or more. Furthermore, the electrical resistance of the connection part of a similar cable twisted without coating the surface of the wires with copper oxide was 7.8 μΩ. Example 2 Hydrazine hydrade at 30°C in Example 1
The hydrazine hydrade solution shown in Table 1 was used in place of the 15% ethanol solution, and the treated interior was examined and the electrical resistance of the connected joints was measured in the same manner. The results are also listed in Table 1.
【表】
実施例 3
厚さ0.3μの酸化銅を被覆した直径2.3mmの銅素
線18本を撚合せ、その上にポリエチレン絶縁層を
設けた電力ケーブルの接続を行なつた。
先ずケーブル端末部の絶縁層を15cm皮剥して素
線群を突出せしめ、先端から10cmの部分に温風を
吹き付けながらヒドラジンヒドラード50%のメタ
ノール溶液を筆で塗布した。2.5分間に1回の割
合で塗布し、5分間処理した。続いて5分間乾燥
した。これを銅スリープを用いて圧縮接続し、接
続部の電気抵抗を測定したところ5.9μΩであつ
た。尚無処理の接続部の電気抵抗は100μΩ以上
であり、酸化銅を被覆しない同種ケーブルの接続
部の電気抵抗は5.5μΩであつた。
このように本発明によれば有害な副作用や廃出
物を生ずることなく、迅速かつ効果的に銅素線表
面の銅酸化物を除去することができるもので、従
来法に比べ微少間隙にまで除去処理が短時間で出
来るばかりか、撚り合せた素線群からも銅酸化物
を完全に除去することができる等、素線絶縁ケー
ブルの接続上の緒問題を解決することができる顕
著な効果を奏するものである。[Table] Example 3 Eighteen copper wires each having a diameter of 2.3 mm and coated with copper oxide having a thickness of 0.3 μm were twisted together, and a power cable having a polyethylene insulating layer provided thereon was connected. First, 15 cm of the insulation layer at the end of the cable was peeled off to expose the strands of wire, and a 50% methanol solution of hydrazine hydride was applied with a brush to a 10 cm area from the tip while blowing hot air. It was applied once every 2.5 minutes and treated for 5 minutes. Subsequently, it was dried for 5 minutes. This was compressed and connected using a copper sleeve, and the electrical resistance of the connection was measured and found to be 5.9 μΩ. The electrical resistance of the untreated connection was 100 μΩ or more, and the electrical resistance of the same type of cable without copper oxide coating was 5.5 μΩ. As described above, according to the present invention, it is possible to quickly and effectively remove copper oxides from the surface of copper wire without producing harmful side effects or waste products, and it is possible to remove copper oxides from the surface of copper wires even in minute gaps compared to conventional methods. Not only can the removal process be done in a short time, but copper oxide can also be completely removed from twisted strands, which is a remarkable effect in solving the connection problems of stranded insulated cables. It is something that plays.
Claims (1)
相互間を絶縁した電力ケーブルの接続において、
接続するケーブル端末部より絶縁外層を除去して
素線群を突出せしめ、これにヒドラジン溶液を接
触させて素線表面の銅酸化物を化学的に還元した
後、ケーブルの接続を行なうことを特徴とする電
力ケーブルの接続方法。 2 ヒドラジンを溶解し得る極性有機溶剤に、ヒ
ドラジンを溶解したヒドラジン溶液を用いる特許
請求の範囲第1項記載の電力ケーブルの接続方
法。[Claims] 1. In the connection of a power cable in which a copper oxide composite film is formed on the surface of copper wires to insulate the wires from each other,
The cable is connected after removing the insulating outer layer from the end of the cable to be connected to make the strands protrude and contacting them with a hydrazine solution to chemically reduce the copper oxide on the surface of the strands. How to connect the power cable. 2. The method for connecting power cables according to claim 1, which uses a hydrazine solution in which hydrazine is dissolved in a polar organic solvent capable of dissolving hydrazine.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12878380A JPS5753082A (en) | 1980-09-17 | 1980-09-17 | Method of connecting power cable |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12878380A JPS5753082A (en) | 1980-09-17 | 1980-09-17 | Method of connecting power cable |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5753082A JPS5753082A (en) | 1982-03-29 |
| JPS6219031B2 true JPS6219031B2 (en) | 1987-04-25 |
Family
ID=14993342
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12878380A Granted JPS5753082A (en) | 1980-09-17 | 1980-09-17 | Method of connecting power cable |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5753082A (en) |
-
1980
- 1980-09-17 JP JP12878380A patent/JPS5753082A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5753082A (en) | 1982-03-29 |
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