JPH0449729B2 - - Google Patents

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Publication number
JPH0449729B2
JPH0449729B2 JP57068474A JP6847482A JPH0449729B2 JP H0449729 B2 JPH0449729 B2 JP H0449729B2 JP 57068474 A JP57068474 A JP 57068474A JP 6847482 A JP6847482 A JP 6847482A JP H0449729 B2 JPH0449729 B2 JP H0449729B2
Authority
JP
Japan
Prior art keywords
contact
silver
stacked body
copper
base metal
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
Application number
JP57068474A
Other languages
Japanese (ja)
Other versions
JPS58186115A (en
Inventor
Yukie Myagawa
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.)
Nidec Material Corp
Original Assignee
Higashifuji Mfg 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 Higashifuji Mfg Co Ltd filed Critical Higashifuji Mfg Co Ltd
Priority to JP6847482A priority Critical patent/JPS58186115A/en
Publication of JPS58186115A publication Critical patent/JPS58186115A/en
Publication of JPH0449729B2 publication Critical patent/JPH0449729B2/ja
Granted legal-status Critical Current

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  • Manufacture Of Switches (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔発明の詳細な説明〕 本願の発明は、接点材料と裏張り材、裏張り材
と台金とが安定した接合力をもち、かつ、安定し
た対溶着性を示す複合電気接点の製造方法に関す
るものである。 従来の銀−酸化物系複合電気接点の製造におい
ては、接点部分の素材として、Ag−Cd−Sn、
Ag−Sn−In−Cd、Ag−Sn−In等の合金の板材
を内部酸化処理したものをデイスク状に打ち抜い
て用いていたために、板厚の中心部に酸化物の希
薄層が存在し、出来上つた接点の使用中にその厚
さが減耗して行き接点表面が上記酸化物希薄層に
まで到達したときには、急激な消耗や溶着を多発
するという重大な問題があつた。 本願発明の目的の一つは、接点の素材として内
部酸化板材を使用することによつて生じる欠点を
除くことにあり、この目的達成のために、本願発
明では、内部酸化線材を素材として使用する。 上記の組成の合金線材を内部酸化処理すると、
同様に酸化物希薄層が生ずるが、これは、線材の
長手方向の中心線に沿うものである。この内部酸
化線材を輪切りにすると、その中心部に常に酸化
物希薄層が現れるが、それが線材の線断面全体に
占める割合はごく僅かである。この輪切りにした
線材を素材として使用すれば、上記の従来方法の
欠点が除去されることは明らかである。 本願発明のもう一つの目的は、線点材料の裏張
り材として、高価な銀合金に換え安価な銅又は銅
合金を用いることにある。これにより接点のコス
トは大幅に低減させることができる。 本願発明の更に他の目的は接点材料と裏張り
材、裏張り材と台金との接合を決定的に強固にす
ることである。この目的達成のために、抵抗溶接
による接合の際に、有機溶剤を接合面近傍に少量
注入して還元性ガスを発生させ、溶接時の大気雰
囲気を還元性ガスで置換するものである。これに
よつて、上記のように銀合金製の裏張り材に較べ
て接合力のやゝ劣る銅又は銅合金の裏張り材を用
いても、充分強固な接合を得ることができる。 この発明は、以上のような点に着目してなされ
たもので、内部酸化した銀−酸化物合金線を輪切
りにしたデイスクと銅又は銅合金線材を輪切りに
したデイスクとを重ね合せ、更にはその重ね合せ
体に台座をも組合せて、これらを抵抗溶接機を用
いて接合する際、通電して加熱接合する前に、接
合面近傍にアルコール等の有機溶剤を注入して、
各部の重ね合せ面の空気を有機溶剤が熱分解して
生ずる還元性ガスによつて置換し、還元性雰囲気
の中で接合が行われるようにし、このガスによつ
て接合面の清浄化および活性化をはかり、もつて
接合力の安定した銀−酸化物系複合接点の製造方
法を提供するものである。 すなわち第2図の如く、抵抗溶接機の上部電極
1と下部電極2の間に例えば内部酸化線材から得
たデイスクと銅又は銅合金線材から得たデイスク
とを組合せた複合接点材(可動用複合接点材3ま
たは固定用複合接点材4)をセツトしたのち、通
電して加熱接合を開始する前に、両極間の複合接
点材の重ね合せ面の近傍に有機溶剤を注入してま
わりの空気をまず置換し、通電加熱によつて有機
溶剤が分解しその還元雰囲気中で複合接点材の接
合を行うと従来法に比較して接合力の安定した接
点が得られる。第3図はリベツト型複合接点(6
または7)の場合を示したものである。また第4
図に示すごとく接点材の接合だけでなく接点材と
台金5との接合も同時に実施できる。尚、こゝで
いうデイスクは、円板のみならず多角形の板状小
片をも含むものである。なお両極間の接点材近傍
に注入または滴下すべき有機溶剤としては常温で
比較的高い蒸気圧を有し、かつ加熱に当つて容易
に還元性ガスとなるものであり、具体的にはメタ
ノール、エタノール等のアルコール類、アセトン
類等の有機溶剤が利用できる。 これらの有機溶剤を使用することによつて、ま
ず接点材近傍の酸素分圧が減少し、さらに通電加
熱により該接点材等が全く還元性雰囲気中で接合
されるため、複合接点における接合面及び台金と
のろう付け面において存在する酸化被覆が還元さ
れかつ接合面の活性化が行われ、しかるのち接合
されるので一層緊密な接合が行われるものと解釈
される。 実施例 1 本例は本発明による製造例を示すものである。 Ag−Sn−In−Cd系合金線を内部酸化して製造
したAg−SnO2−In2O3−CdO系(組成89%Ag−
11%酸化物)の合金線のφ2.9mmアニール線材と、
タフピツチ銅線のφ2.9mm線材とからそれぞれデイ
スクを切り出し、二種のデイスクを重ね合わせ、
これを複合ヘツダー機で加圧し、 可動用接点 6φ×3.0(1.2)mmテーパー12゜(接触
面20R付) 固定用接点 6.2φ×2.4(1.5)mmテーパー12゜(接
触面フラツト) の複合デイスクを作り、これを交流スポツト溶接
機(25KVA)で純Wを電極とし、極間の接合部
近傍にアルコールを注入したのち、成型条件を電
流7.800A、通電7HZ、加圧0.5Kg/cm2にしてメチ
ルアルコールの熱分解による還元雰囲気中で複合
デイスク型接点を成形し、これを抵抗ろう付けで
台金に銀ろう付けを行い後記の試験に供した。 実施例 2 本例も本発明による製造例を示すものである。 実施例1と同じ材料を用い、実施例1と同様な
操作で 可動用接点 6φ×1.5(0.8)〜3φ×1.5mmテーパ
ー12゜(接触面20R付) 固定用接点 6.2φ×1.5(0.8)〜3φ×1.5mmテー
パー12゜(接触面フラツト) の複合リベツトを作り、以下実施例1と同様にし
て、電極(この場合はAg20%W80%の合金を使
用)の間にセツトし、極間の接合部近傍にエチル
アルコールを注入したのち、通電成形して複合接
点を成形し、これを台金に銀ろう付けして後記の
試験に供した。 実施例 3 本例も本発明による製造例を示すものである。 実施例1と同じ材料を用い、実施例1と同様な
操作で実施例2に示した複合リベツトを作り、こ
の複合リベツトと銅台金、銀ろうABG−1とを
電極(純Moを使用)の間にセツトし、極間の接
合部近傍にアセトンを注入したのち、実施例1と
同じ成型条件でもつて複合接点の成形および接点
と台金との銀ろう付けを同時に行い、後記の試験
に供した。 実施例 4 本例も本発明による製造例を示すものである。 内部酸化したAg−CdO−SnO2系(組成82.5%
Ag−16.5%Cd−1.0%α)合金線材を接点素材と
して用いた。すなわち、AgとNiを大気中で約
1500℃で溶解し、次の湯温度を1000℃に低下させ
てから50%Ag−50%CdのAg−Cd母合金、Snを
添加し、鋳造、加熱押出し後塑性加工により、
2.9mmφの線材とし、これを内部酸化炉中で750℃
3気圧の酸素雰囲気中で120時間保持して銀−酸
化物系線材とし、この線材を輪切りにして得たデ
イスクとタフピツチ銅線の2.9mmφ線材を輪切り
にして得たデイスクとを重ね合せ、これを複合ヘ
ツダー線で実施例2に示した複合リベツトと同じ
形の複合リベツトを作り、以下実施例1と同様に
して電極(この場合はW95%−残りNi−Cu合金
を使用)の間にセツトし、極間の接合部近傍にブ
タノールを注入したのち、通電成形して複合リベ
ツト接点を成形し、これを台金に銀ろう付けを行
い。後記の試験に供した。 比較例 1 本例は従来の接点材の製造例を示すものであ
る。 実施例1と同じ組成の合金を接点材として用い
加工後巾40mm厚さ10mmの接点素材とし、この一面
に約1mmの純銀板を熱圧着してろう付用銀層を形
成した。次にこの素材を加工して薄板にした後6
mmφと6.2mmφの接点形状に打抜き、これを内部
酸化炉中に700℃3気圧の酸素雰囲気中で48時間
保持して銀−酸化物系打抜デイスク型接点を下の
如く製作した。 可動用接点6φ×1.5mm(接触面20R付) 固定用接点6.2φ×1.2mm(接触面フラツト) これを抵抗ろう付けで台金に銀ろう付けを行
い、後記の試験に供した。 比較例 2 本例も従来の接点材の製造例を示すものであ
る。 実施例1〜3と同じ組成の合金を用いて、実施
例2〜3と同じ形状の複合リベツト型接点をヘツ
ダー成形の際に外周部にバリをほぼ全周に亘つて
ツバ状に生成せしめるに十分な強圧を加える製造
方法で制作し、バリ取り、熱処理して複合リベツ
ト型接点を製作した。これを抵抗ろう付けで台金
に銀ろう付けを行い、後記の試験に供した。 比較例 3 本例も従来の接点材の製造例を示すものであ
る。 実施例4と同じ組成の合金(Ag−CdO−SnO2
系)を用いて、比較例1と同じ操作を行つて銀−
酸化物系打抜デイスク型接点を下の如く製作し
た。 可動用接点6φ×1.5mm(接触面20R付) 固定用接点6.2φ×1.3mm(接触面フラツト) これを抵抗ろう付けで台金に銀ろう付けを行
い。後記の試験に供した。 比較例 4 本例も従来の接点材の製造例を示すものであ
る。 実施例4と同じ組成の合金を接点材として用
い、加工後巾40mm厚さ10mmの接点素材とし、この
面に約1mmの純銀板を熱圧着してろう付用銀層を
形成した。次に6mmφと6.2mmφの接点形状に打
抜き、これを内部酸化炉中に750℃3気圧の酸素
雰囲気中で48時間保持して銀−酸化物系打抜デイ
スク型接点をつくり、さらに6φ×0.8mmと6.2φ×
0.8mmの台金とろう付けを行い下の通りの張合せ
デイスク型接点とした。 可動用接点6.0φ×1.6(0.8)mm(接触面20R付) 固定用接点6.2φ×1.6(0.8mm)(接触面フラツト) これを抵抗ろう付けで台金に銀ろう付けを行い、
後記の試験に供した。 性能試験 1 本試験は接合強度と接点硬度を評価するもので
ある。 前記の製造例において製作した各接点材の常温
硬さおよび常温剪断強度を測定した。この結果を
第1表に示す。 本発明の方法に従つて製造した接点材に比較例
に掲げた接点材に比べて接合力が安定しているこ
とがわかる。 性能試験 2 本試験は消耗量、接触抵抗および溶着性を評価
するものである。すなわち、各接点の性能を確認
するために電圧AC220V、電流115A、力率、0.5
で三相5.5KW定格の電磁開閉器に組込み開閉テ
ストしたものであり、結果を第2表に示す。なお
試験前後の接触抵抗も併せて測定した。
[Detailed Description of the Invention] The present invention relates to a method for manufacturing a composite electrical contact in which the contact material and the backing material, the backing material and the base metal have stable bonding strength, and exhibit stable welding resistance. It is something. In the production of conventional silver-oxide composite electrical contacts, Ag-Cd-Sn, Ag-Cd-Sn,
Because plates of alloys such as Ag-Sn-In-Cd and Ag-Sn-In were punched out into disk shapes after being internally oxidized, a thin layer of oxide existed in the center of the plate thickness. When the thickness of the completed contact decreases during use and the contact surface reaches the thin oxide layer, there is a serious problem of rapid wear and frequent welding. One of the purposes of the present invention is to eliminate the drawbacks caused by using internally oxidized plate material as a material for contacts, and to achieve this purpose, the present invention uses internally oxidized wire material as a material. . When the alloy wire with the above composition is internally oxidized,
An oxide-poor layer also forms, but along the longitudinal centerline of the wire. When this internally oxidized wire is cut into rings, a dilute oxide layer always appears in the center, but this layer accounts for a very small percentage of the entire cross section of the wire. It is clear that the above-mentioned drawbacks of the conventional method can be eliminated by using this sliced wire as a raw material. Another object of the present invention is to use inexpensive copper or copper alloy instead of expensive silver alloy as the backing material for the dot material. This allows the cost of the contacts to be significantly reduced. Still another object of the present invention is to definitively strengthen the bond between the contact material and the backing material, and between the backing material and the base metal. To achieve this objective, when joining by resistance welding, a small amount of organic solvent is injected into the vicinity of the joint surface to generate a reducing gas, and the atmospheric atmosphere during welding is replaced with the reducing gas. As a result, even if a backing material made of copper or a copper alloy, which has a slightly inferior bonding strength as a backing material made of a silver alloy, is used as described above, a sufficiently strong bond can be obtained. This invention was made with attention to the above-mentioned points, and consists of superimposing a disc made of internally oxidized silver-oxide alloy wire cut into rings and a disc made of cut copper or copper alloy wire, and furthermore, When combining the stacked body with a pedestal and joining them using a resistance welder, before applying electricity and heating and joining, an organic solvent such as alcohol is injected into the vicinity of the joint surface.
The air on the overlapping surfaces of each part is replaced with a reducing gas produced by thermal decomposition of organic solvents, so that joining is performed in a reducing atmosphere, and this gas cleans and activates the joining surfaces. The object of the present invention is to provide a method for manufacturing a silver-oxide composite contact which has a stable bonding strength and a stable bonding force. In other words, as shown in Fig. 2, a composite contact material (composite for movable material), which is a combination of a disc made of internally oxidized wire and a disc made of copper or copper alloy wire, is placed between the upper electrode 1 and the lower electrode 2 of a resistance welding machine. After setting the contact material 3 or fixed composite contact material 4), before applying electricity and starting heating bonding, an organic solvent is injected near the overlapping surface of the composite contact material between the two electrodes to remove the surrounding air. First, the organic solvent is decomposed by heating with electricity, and the composite contact material is bonded in a reducing atmosphere to obtain a contact with a more stable bonding force than in the conventional method. Figure 3 shows a rivet type composite contact (6
Or 7) is shown. Also the fourth
As shown in the figure, not only the bonding of the contact material but also the bonding of the contact material and the base metal 5 can be performed simultaneously. Note that the term "disk" here includes not only a disc but also a polygonal plate-like piece. The organic solvent to be injected or dropped near the contact material between the two electrodes is one that has a relatively high vapor pressure at room temperature and easily becomes a reducing gas when heated; specifically, methanol, Alcohols such as ethanol and organic solvents such as acetone can be used. By using these organic solvents, the oxygen partial pressure in the vicinity of the contact material is first reduced, and then the contact materials are bonded in a completely reducing atmosphere through electrical heating, so that the bonding surface and It is understood that the oxidized coating present on the surface to be brazed with the base metal is reduced and the joint surfaces are activated and then joined, resulting in an even tighter joint. Example 1 This example shows a manufacturing example according to the present invention. Ag-SnO 2 -In 2 O 3 -CdO system (composition 89% Ag-
11% oxide) alloy wire φ2.9mm annealed wire,
Each disk was cut out from φ2.9mm Toughpitch copper wire, and the two types of disks were stacked together.
This is pressurized with a compound header machine, and a composite disk with a movable contact of 6φ x 3.0 (1.2) mm taper 12° (with a contact surface of 20R) and a fixed contact of 6.2φ x 2.4 (1.5) mm taper of 12° (flat contact surface) is created. was made using an AC spot welding machine (25KVA) using pure W as an electrode and injecting alcohol near the joint between the electrodes.Then, the molding conditions were set to 7.800A current, 7HZ current, and 0.5Kg/ cm2 pressure. A composite disk-type contact was formed in a reducing atmosphere due to thermal decomposition of methyl alcohol, silver-brazed to a base metal by resistance brazing, and subjected to the test described below. Example 2 This example also shows a manufacturing example according to the present invention. Using the same materials as in Example 1 and performing the same operations as in Example 1, Movable contact 6φ x 1.5 (0.8) to 3φ x 1.5mm taper 12° (with contact surface 20R) Fixed contact 6.2φ x 1.5 (0.8) A composite rivet with ~3φ x 1.5mm taper 12° (contact surface flat) was made and set between the electrodes (in this case, an alloy of 20% Ag and 80% W was used) in the same manner as in Example 1, and the gap between the electrodes was After injecting ethyl alcohol into the vicinity of the joint, a composite contact was formed by electroforming, which was silver-brazed to a base metal and subjected to the test described below. Example 3 This example also shows a manufacturing example according to the present invention. The composite rivet shown in Example 2 was made using the same materials as in Example 1 and in the same manner as in Example 1, and the composite rivet, copper base metal, and silver solder ABG-1 were used as an electrode (using pure Mo). After injecting acetone into the vicinity of the joint between the poles, molding of the composite contact and silver brazing between the contact and the base metal were performed at the same time under the same molding conditions as in Example 1. provided. Example 4 This example also shows a manufacturing example according to the present invention. Internally oxidized Ag-CdO-SnO 2 system (composition 82.5%
Ag-16.5%Cd-1.0%α) alloy wire was used as the contact material. In other words, Ag and Ni are approximately
Melt at 1500℃, then lower the temperature to 1000℃, add 50%Ag-50%Cd Ag-Cd master alloy, Sn, cast, heat extrusion, and then plastic working.
A wire rod of 2.9 mmφ was heated at 750℃ in an internal oxidation furnace.
A silver-oxide wire was obtained by holding it in an oxygen atmosphere of 3 atm for 120 hours, and a disc obtained by cutting this wire into rings and a disc obtained by cutting a 2.9 mmφ wire of Tuff Pitch copper wire into rings were stacked together. A composite rivet of the same shape as the composite rivet shown in Example 2 was made using a composite header wire, and then set between the electrodes (in this case, 95% W and the remaining Ni-Cu alloy) in the same manner as in Example 1. After injecting butanol near the joint between the poles, a composite rivet contact was formed by electroforming, and this was silver-brazed to the base metal. It was used for the test described below. Comparative Example 1 This example shows an example of manufacturing a conventional contact material. An alloy having the same composition as in Example 1 was used as a contact material to obtain a contact material having a width of 40 mm and a thickness of 10 mm after processing, and a pure silver plate of about 1 mm in thickness was thermocompression bonded to one side of the contact material to form a silver layer for brazing. Next, after processing this material and making it into a thin plate, 6
mmφ and 6.2 mmφ contacts, and held in an internal oxidation furnace at 700° C. in an oxygen atmosphere of 3 atm for 48 hours to produce a silver-oxide based punched disc type contact as shown below. Movable contact 6φ x 1.5mm (with contact surface 20R) Fixed contact 6.2φ x 1.2mm (contact surface flat) These were silver-brazed to the base metal using resistance brazing and used for the tests described below. Comparative Example 2 This example also shows an example of manufacturing a conventional contact material. Using an alloy with the same composition as in Examples 1 to 3, a composite rivet type contact having the same shape as in Examples 2 to 3 was formed with a burr-shaped burr on the outer periphery almost all the way around during header forming. It was manufactured using a manufacturing method that applies sufficient pressure, deburred, and heat treated to create a composite rivet type contact. This was silver-brazed to the base metal using resistance brazing, and was subjected to the test described below. Comparative Example 3 This example also shows an example of manufacturing a conventional contact material. Alloy with the same composition as Example 4 (Ag-CdO-SnO 2
The same operation as in Comparative Example 1 was carried out to obtain silver
An oxide-based stamped disk type contact was fabricated as shown below. Movable contact 6φ x 1.5mm (with 20R contact surface) Fixed contact 6.2φ x 1.3mm (flat contact surface) Resistance brazing these to the base metal using silver brazing. It was used for the test described below. Comparative Example 4 This example also shows an example of manufacturing a conventional contact material. An alloy having the same composition as in Example 4 was used as a contact material, and after processing, a contact material having a width of 40 mm and a thickness of 10 mm was obtained.A pure silver plate of approximately 1 mm was thermocompression bonded to this surface to form a silver layer for brazing. Next, contact shapes of 6 mmφ and 6.2 mmφ were punched, and these were kept in an internal oxidation furnace at 750°C in an oxygen atmosphere of 3 atm for 48 hours to create silver-oxide punched disk-type contacts, and further 6φ×0.8 mm and 6.2φ×
A 0.8mm base metal was brazed to create a laminated disk-type contact as shown below. Movable contact 6.0φ x 1.6 (0.8) mm (with contact surface 20R) Fixed contact 6.2φ x 1.6 (0.8 mm) (contact surface flat) Silver brazed to the base metal using resistance brazing.
It was used for the test described below. Performance test 1 This test evaluates the joint strength and contact hardness. The room temperature hardness and room temperature shear strength of each contact material produced in the above manufacturing example was measured. The results are shown in Table 1. It can be seen that the contact material manufactured according to the method of the present invention has a more stable bonding force than the contact material listed as a comparative example. Performance Test 2 This test evaluates the amount of wear, contact resistance, and weldability. That is, voltage AC220V, current 115A, power factor, 0.5 to check the performance of each contact.
It was assembled into a three-phase 5.5KW rated electromagnetic switch and tested for switching, and the results are shown in Table 2. The contact resistance before and after the test was also measured.

【表】【table】

【表】 ある。
[Table] Yes.

【表】 試験結果から明らかであるように、本発明の方
法によつて製造された複合電気接点は従来のAg
−SnO2−In2O3−CdO系打抜デイスク型接点より
も20〜50%省銀がはかられ、さらに寿命面で約2
倍の耐溶着耐消耗性が得られる。すなわち電極間
にセツトした接点材または接点材とろう付け台金
の近傍にアルコール等の有機溶剤を注入したのち
通電加熱して接合すれば、従来の方法で製造した
接点に比べてすぐれた接点性能が得られ、工業的
に大きな効果が期待される。
[Table] As is clear from the test results, the composite electrical contacts manufactured by the method of the present invention
−SnO 2 −In 2 O 3 −20% to 50% less silver than CdO-based punched disk type contacts, and approximately 2 times longer lifespan.
Double the welding and abrasion resistance. In other words, if an organic solvent such as alcohol is injected into the contact material set between the electrodes or in the vicinity of the contact material and the brazing base, and then electrically heated and bonded, superior contact performance can be achieved compared to contacts manufactured using conventional methods. is expected to have great industrial effects.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は複合接点材がセツトされる下部電極の
断面図、第2図および第3図はそれぞれデイスク
型複合接点、リベツト型複合接点の加熱成型工程
を、第4図は台金付のリベツト型複合接点の加熱
成型工程を示すものである。以上の図面において
いずれもaは可動用接点、bは固定用接点の場合
であつて、c,dは可動用、固定用各接点を台金
にセツトした状況を示す。 第1〜第4図において:1:上部電極、2:下
部電極、3:可動用デイスク型接点、4:固定用
デイスク型接点、5:台金、6:可動用リベツト
型接点、7:固定用リベツト型接点。 第5図は実施例1の接点の35万回開閉テスト後
の断面拡大写真、第6図は比較例1の接点の15万
回開閉テスト後の断面拡大写真を示す。
Figure 1 is a cross-sectional view of the lower electrode on which the composite contact material is set, Figures 2 and 3 illustrate the heat molding process for disk-type composite contacts and rivet-type composite contacts, respectively, and Figure 4 shows the rivet with base metal. This figure shows the heat molding process of a molded composite contact. In each of the above drawings, a indicates a movable contact, b indicates a fixed contact, and c and d indicate the state in which the movable and fixed contacts are set on the base metal. In Figures 1 to 4: 1: Upper electrode, 2: Lower electrode, 3: Movable disk-type contact, 4: Fixed disk-type contact, 5: Base metal, 6: Movable rivet-type contact, 7: Fixed Rivet type contacts. FIG. 5 shows an enlarged cross-sectional photograph of the contact of Example 1 after a 350,000-cycle opening/closing test, and FIG. 6 shows an enlarged cross-sectional photograph of the contact of Comparative Example 1 after a 150,000-cycle opening/closing test.

Claims (1)

【特許請求の範囲】 1 接点材料と裏張り材とを組み合わせた複合電
気接点の製造方法であつて、内部酸化してなる銀
−酸化物系合金線材を輪切りにして得たデイスク
と銅または銅合金線材を輪切りにして得たデイス
クとを重ね合わせ、この重ね合わせ体を抵抗溶接
機の電極間に装入し、少なくとも重ね合わせ体の
重ね合わせ面の空気を置換するに足る量の分解ガ
スを生成する有機溶剤を重ね合わせ体の周囲に注
入し、ついで直ちに重ね合わせ体を加圧通電する
ことを特徴とする接点材料と裏張り材との接合力
の安定した銀−酸化物系複合電気接点の製造方
法。 2 接点材、裏張り材および台金を組み合わせた
複合電気接点の製造方法であつて、内部酸化して
なる銀−酸化物系合金線材を輪切りにして得たデ
イスク、銅または銅合金線材を輪切りにして得た
デイスク、および台金材をこの順序に重ね合わ
せ、この重ね合わせ体を抵抗溶接機の電極間に装
入し、少なくとも重ね合わせ体の各重ね合わせ面
の空気を置換するに足るに量の分解ガスを生成す
る有機溶剤を重ね合わせ体の周囲に注入し、つい
で直ちに重ね合わせ体を加圧通電することを特徴
とする接点材料と裏張り材および裏張り材と台金
材の接合力の安定した銀−酸化物系複合電気接点
の製造方法。
[Claims] 1. A method for manufacturing a composite electrical contact combining a contact material and a lining material, which comprises discs obtained by slicing internally oxidized silver-oxide alloy wire and copper or copper. The disks obtained by cutting the alloy wire into rings are stacked together, and the stacked body is inserted between the electrodes of a resistance welding machine, and at least enough decomposition gas to displace the air on the overlapped surfaces of the stacked body is applied. A silver-oxide composite electrical contact with stable bonding strength between a contact material and a backing material, which is characterized by injecting the generated organic solvent around the laminated body and then immediately applying pressure and current to the laminated body. manufacturing method. 2. A method for manufacturing a composite electrical contact combining a contact material, a backing material, and a base metal, in which a disk obtained by slicing internally oxidized silver-oxide alloy wire material, and a disk obtained by slicing copper or copper alloy wire material into rings. Layer the disk obtained by above and the base metal material in this order, insert this stacked body between the electrodes of a resistance welding machine, and remove at least enough air to displace the air on each overlapping surface of the stacked body. Bonding of a contact material and a backing material, and of a backing material and a base metal material, characterized by injecting an organic solvent that generates a large amount of decomposed gas around the stacked body, and then immediately applying pressure and electricity to the stacked body. A method for producing a silver-oxide composite electrical contact with stable force.
JP6847482A 1982-04-23 1982-04-23 Method of producing silver-oxide series electric contact Granted JPS58186115A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6847482A JPS58186115A (en) 1982-04-23 1982-04-23 Method of producing silver-oxide series electric contact

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6847482A JPS58186115A (en) 1982-04-23 1982-04-23 Method of producing silver-oxide series electric contact

Publications (2)

Publication Number Publication Date
JPS58186115A JPS58186115A (en) 1983-10-31
JPH0449729B2 true JPH0449729B2 (en) 1992-08-12

Family

ID=13374715

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6847482A Granted JPS58186115A (en) 1982-04-23 1982-04-23 Method of producing silver-oxide series electric contact

Country Status (1)

Country Link
JP (1) JPS58186115A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20110138532A (en) * 2010-06-21 2011-12-28 현대모비스 주식회사 Electric booster brake system and pressure vibration control method

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5287866B2 (en) 2008-02-08 2013-09-11 富士電機機器制御株式会社 Electric contact manufacturing method and electric contact manufacturing apparatus

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5588216A (en) * 1978-12-25 1980-07-03 Mitsubishi Electric Corp Method of welding electric contact
JPS5880220A (en) * 1981-11-05 1983-05-14 三菱電機株式会社 How to join electrical contacts

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20110138532A (en) * 2010-06-21 2011-12-28 현대모비스 주식회사 Electric booster brake system and pressure vibration control method

Also Published As

Publication number Publication date
JPS58186115A (en) 1983-10-31

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