JPS60155635A - Electrical contact material - Google Patents
Electrical contact materialInfo
- Publication number
- JPS60155635A JPS60155635A JP1376284A JP1376284A JPS60155635A JP S60155635 A JPS60155635 A JP S60155635A JP 1376284 A JP1376284 A JP 1376284A JP 1376284 A JP1376284 A JP 1376284A JP S60155635 A JPS60155635 A JP S60155635A
- Authority
- JP
- Japan
- Prior art keywords
- electrical contact
- contact material
- weight
- oxide
- 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.)
- Granted
Links
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- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Conductive Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
この発明は電気接点材料具体的には銀と他の金属酸化物
を含む複合合金から成る電気接点材料に関したとえば電
磁接触機、リレーブレーカ等種々の電気機器に組み込ま
れる電気接点に供されるものである。[Detailed Description of the Invention] [Technical Field] This invention relates to an electrical contact material, specifically an electrical contact material made of a composite alloy containing silver and other metal oxides, and is used for various electrical devices such as electromagnetic contactors and relay breakers. It is used for electrical contacts built into.
電気接点材料は一般に消耗が少く、溶着しにくく、かつ
接触抵抗の低い特性が要求される。回路の入力、出力の
働きをするリレーでは特に入出力の際に流れる突入電流
に耐え得る溶着性が特に要求される。Electrical contact materials are generally required to have characteristics such as low wear, resistance to welding, and low contact resistance. Relays that function as input and output of a circuit are especially required to have weldability that can withstand the rush current that flows during input and output.
従来は銀−酸化カドミウム、銀−ニッケル、銀酸化スズ
系の電気接点材料が広く知られている。Conventionally, electrical contact materials based on silver-cadmium oxide, silver-nickel, and silver-tin oxide are widely known.
銀−酸化カドミュムは耐溶着性に優れ、銀−酸化スズ系
は耐消耗性に優れ、又銀−ニッケルは接触抵抗特性に優
れている。Silver-cadmium oxide has excellent adhesion resistance, silver-tin oxide has excellent wear resistance, and silver-nickel has excellent contact resistance characteristics.
最近、耐溶着性に優れた電気接点材料として銀−酸化ビ
スマス系が注目され、たとえば特開昭52−1496号
公報にはビスマス0.1〜3重量%、リチウム、カルシ
ウムのいずれか1種又は2種を合計で0.05〜3重量
%含ませたのが開示されている。Recently, the silver-bismuth oxide system has attracted attention as an electrical contact material with excellent welding resistance. It is disclosed that the two types are contained in a total amount of 0.05 to 3% by weight.
いずれにし・τも耐溶着性、接触抵抗特性、耐消耗性各
々の性能は接点の開閉動作における信頼性を左右し、信
頼性に欠けると機器の誤動作?誘発する。In any case, the performance of τ as well as welding resistance, contact resistance characteristics, and abrasion resistance influences the reliability of the contact opening/closing operation, and if reliability is lacking, the equipment will malfunction. provoke.
この発明は銀−酸化ビスマス系電気接点材料の耐溶着性
と耐消耗性を高めた中電流用として有用な電気接点材料
全提供するものである。The present invention provides all electrical contact materials useful for medium current applications, which have improved welding resistance and abrasion resistance of silver-bismuth oxide electrical contact materials.
すなわちこの発明は銀と他の金属酸化物を含む複合合金
から成る電気接点材料に2いて他の金属酸化物としてビ
スマスを金属基準で3重ji%を越えて6重量%、リチ
ウム全金属基準で0.05乃至3重量%含むことを特徴
とする電気接点材料を提供するものである。In other words, the present invention provides an electrical contact material consisting of a composite alloy containing silver and other metal oxides, in which bismuth is added as the other metal oxide to more than 6% by weight on a metal basis, and lithium is added in an amount exceeding 6% by weight on a total metal basis. The present invention provides an electrical contact material characterized by containing 0.05 to 3% by weight.
以下、この発明の詳細な説明する。The present invention will be described in detail below.
この発明は銀−酸化ビスマス系で酸化リチウ°ムを含ま
せた従来公知のものを基準におくと酸化ビスマス濃度が
高濃度である点に特徴がある。すなわち酸化ビスマスが
0.1重量%レベルで高特性を示し、3重量幅までは濃
度が高くなるにつれて劣化する傾向にあっ、tにもかか
わらず、確認の結果酸化ビスマスが3重量91越えて耐
溶着性と耐消耗性が改善される事実を確保した。The present invention is characterized in that the concentration of bismuth oxide is higher than that of conventional silver-bismuth oxide containing lithium oxide. In other words, bismuth oxide exhibits high properties at the 0.1% by weight level, and tends to deteriorate as the concentration increases up to 3% by weight. It was ensured that the weldability and wear resistance were improved.
これは銀マトリックスに分散し叱ビスマス単体とリチウ
ム単体はX線回折の結果内部酸化でα及びβB+20s
とLiBiO2を生成していることが判明し、これに起
目するものである。この様に耐消耗性と耐溶着性に寄与
する酸化ビスマス並びにリチウムとビスマスの複合酸化
物の生成は金属基準で3重ist越え6重量%まででか
っ、金属基準でリチウムt−0,05重量%乃至3重量
%の範囲に制限される。すなわちビスマスが金属基準で
3重量%未満では耐溶着性、耐消耗性ともその改善効果
が少く、6重量%を越えると閤析を生じ、その結果均一
な組織が得られない。リチウムが金属基準で0.055
重量%満では添加効果がなく、3重量%を越えると内部
酸化処理で酸化物が著るしく結晶粒界に凝集するからで
ある。This is dispersed in a silver matrix, and as a result of X-ray diffraction, bismuth alone and lithium alone are internally oxidized to α and βB + 20s.
It has been found that LiBiO2 is generated, and this is a cause for concern. In this way, the production of bismuth oxide and composite oxides of lithium and bismuth, which contribute to wear resistance and welding resistance, exceeds triple ist on a metal basis and reaches up to 6% by weight, and lithium t-0.05 weight% on a metal basis. % to 3% by weight. That is, if bismuth is less than 3% by weight based on the metal, the effect of improving both welding resistance and abrasion resistance will be small, and if it exceeds 6% by weight, precipitation will occur, and as a result, a uniform structure will not be obtained. Lithium is 0.055 based on metal standards
This is because if the amount is less than 3% by weight, there is no effect of addition, and if it exceeds 3% by weight, the oxide will significantly aggregate at grain boundaries due to internal oxidation treatment.
さらに効果的なのは鉄族元素、鉄、コバルト、又はニッ
ケルを加えることである。これはビスマス酸化物、リチ
ウムとビスマスの複合酸化物の性状が球状であるので分
散が良好である反面肥大化の傾向を示すのでこの肥大化
を抑制する点で効果がある。この効果は鉄族元素が結晶
粒微細化の作用に起因するものであって0.01乃至0
.5重量%の範囲が適当である。すなわち0.01重i
s未満では微細化の作用がな(,0,5重量%を越える
と偏析を生じるため接点性能を阻害することになる。More effective is the addition of iron group elements, iron, cobalt, or nickel. Since bismuth oxide, a composite oxide of lithium and bismuth, has a spherical shape, it is well dispersed, but on the other hand, it tends to become enlarged, so it is effective in suppressing this enlargement. This effect is due to the effect of iron group elements on refining crystal grains, which ranges from 0.01 to 0.
.. A range of 5% by weight is suitable. That is, 0.01 weight i
If it is less than s, there is no effect of refining (and if it exceeds 0.5% by weight, segregation will occur and the contact performance will be impaired.
さらに積極的に肥大化を阻止するためにはリチウムより
も酸化物生成自由エネルギーの小さい金属元素を添加す
ると良い。これらの金属元素を添加したのを内部酸化す
ると、酸化の過程はこれらの金属元素が先ず酸化されて
核として析出し、この核のまわりにビスマス、リチウム
の酸化物及びこれらの複合酸化物が析出し、鎖中に微細
な金属酸化物が分散した電気接点材料を構成することが
できるからである。−これら生成自由エネルギーの小さ
い金属元素としてはマグネシウム、アルミニウム、ケイ
素、カルシュム等でいずれか11!i以上を選択して添
加され、内部酸化に供さnるのである。添加量について
は0.01乃至1重量%が適当である。すなわち0.0
1重量−未満では効果が認められず1重量%’を越える
と接点への加工性が著るしく阻害されるからである。In order to more actively prevent enlargement, it is recommended to add a metal element that has a lower free energy of oxide formation than lithium. When these metal elements are added and internally oxidized, the oxidation process is such that these metal elements are first oxidized and precipitated as a nucleus, and bismuth, lithium oxides, and their composite oxides are precipitated around this nucleus. This is because it is possible to construct an electrical contact material in which fine metal oxides are dispersed in the chains. -These metal elements with low free energy of formation include magnesium, aluminum, silicon, calcium, etc. Any 11! More than i is selectively added and subjected to internal oxidation. The appropriate amount to add is 0.01 to 1% by weight. i.e. 0.0
If the amount is less than 1% by weight, no effect will be observed, and if it exceeds 1% by weight, the processability into contacts will be significantly inhibited.
以上の様に球状のビスマス酸化物、ビスマスとリチウム
の酸化物が所定量分散した内部酸化型の電気接点材料は
耐溶着性、耐消耗性に優れており上記の酸化物を微細に
析出させるとさらにこれらの性能の改善かできる。As mentioned above, the internal oxidation type electrical contact material in which spherical bismuth oxide or bismuth and lithium oxide is dispersed in a predetermined amount has excellent welding resistance and wear resistance. Further improvements in these performances are possible.
以下、実施例を挙げる。Examples are given below.
(実施例)
まず、主要元素の銀、リチウム、ビスマスの他に添加元
素の鉄、コバルト、アルミニウム、マグネシウム、ケイ
素、カルシウムを選択して組合わせtものをアルゴン雰
囲気中で高周波炉を用いて廖解し折面18X12111
1の角型金型に鋳込み、所望組成の合金インゴットを得
た。このインゴットを窒素雰囲気中で700℃、10時
間の加熱灯鈍會行なった。次にこれは加工性が悪く圧延
かできないため、このインゴットをカッターにて厚さl
■に切断して板材としてこれを抜き工程、成型工程で処
理して固定接点45、可動接点φ5×12Rの形状とし
、酸素中で700℃20時間加熱継続し内部酸化した。(Example) First, in addition to the main elements silver, lithium, and bismuth, additional elements iron, cobalt, aluminum, magnesium, silicon, and calcium were selected and combined in a high-frequency furnace in an argon atmosphere. Unraveling surface 18X12111
The mixture was cast into a square mold (No. 1) to obtain an alloy ingot having a desired composition. This ingot was subjected to heating lamp annealing at 700° C. for 10 hours in a nitrogen atmosphere. Next, since this ingot has poor workability and cannot be rolled, a cutter is used to cut this ingot to a thickness of l.
It was cut into pieces (2) and processed as a plate material through a punching step and a molding step to form a fixed contact 45 and a movable contact φ5×12R, and was heated continuously in oxygen at 700° C. for 20 hours to undergo internal oxidation.
この内部酸化して得た接点の1+fr面を金属顕微鏡で
蜆察し々ところ球状の酸化物が内部まで分散している組
織を確認して内部:12化が終fしていることを認めた
。When the 1+fr surface of the contact obtained by internal oxidation was observed under a metallurgical microscope, a structure in which spherical oxides were dispersed deep inside was confirmed, and it was confirmed that the internal oxidation had been completed.
次にこの様にしで得た接点をASTM型摺点試1検・幾
を用いて開閉試験を行った。その条件は次のとおりであ
る。Next, the contacts thus obtained were subjected to an opening/closing test using an ASTM type sliding point tester. The conditions are as follows.
成 圧 交流100v
鑞 流 突入電流118A、定常20A接触力 100
I
開離力 150.9
開閉回数 lX104回
接点数 3対
この試験結果を下記に示すと表のとおりである。Forming pressure AC 100V Soldering current Rush current 118A, Steady 20A Contact force 100
I Opening force 150.9 Number of opening/closing times 1 x 104 times Number of contacts 3 pairs The test results are shown in the table below.
なお、溶着回数及び消耗量とも1対当りの子均値で示し
fc0又比較例については実施例と同一条件で作ったも
のである。In addition, both the number of welding times and the amount of wear are expressed as the average value per pair, fc0, and the comparative example was made under the same conditions as the example.
この発明は上記の実施例で種々の組成で示す如く、ビス
マスの増磁によって溶着回数、消耗量が減少し、優れた
電気接点材料を与えるものである。As shown in the various compositions in the above embodiments, this invention provides an excellent electrical contact material in which the number of times of welding and the amount of wear are reduced by increasing the magnetization of bismuth.
Claims (4)
接点材料において他の金属酸化物としてビスマスを金属
基準で3重量%を越えて6重量%、リチウムを金属基準
で0.05乃至3重f%含むことを特徴とする電気接点
材料。(1) In an electrical contact material made of a composite alloy containing silver and other metal oxides, the other metal oxides include bismuth of more than 3% by weight and 6% by weight on a metal basis, and lithium of 0.05 to 6% on a metal basis. An electrical contact material characterized by containing triple f%.
官むことを特徴とする特許請求の範囲第1項記載の電気
接点材料。(2) The electrical contact material according to claim 1, which contains an iron group element of 0.01 to 0.5 weight percent on a metal basis.
金属酸化物を金属基準で0.01乃至1重量%含むこと
を特徴とする特許請求の範囲第1項又は第2項記載の電
気接点材料、3(3) The electrical contact material according to claim 1 or 2, characterized in that it contains 0.01 to 1% by weight of a metal oxide smaller than the free energy of formation of lithium oxide, 3
て、金属酸化物がマグネシウム、アルミニウム、ケイ素
、カルシウムの群から選ばれた1種又は2種以上を含む
もの。(4) The electrical contact material according to claim 3, in which the metal oxide contains one or more selected from the group consisting of magnesium, aluminum, silicon, and calcium.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1376284A JPS60155635A (en) | 1984-01-25 | 1984-01-25 | Electrical contact material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1376284A JPS60155635A (en) | 1984-01-25 | 1984-01-25 | Electrical contact material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60155635A true JPS60155635A (en) | 1985-08-15 |
JPS633011B2 JPS633011B2 (en) | 1988-01-21 |
Family
ID=11842262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1376284A Granted JPS60155635A (en) | 1984-01-25 | 1984-01-25 | Electrical contact material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60155635A (en) |
-
1984
- 1984-01-25 JP JP1376284A patent/JPS60155635A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS633011B2 (en) | 1988-01-21 |
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