JPS5867838A - Electric contact material - Google Patents

Electric contact material

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Publication number
JPS5867838A
JPS5867838A JP56166855A JP16685581A JPS5867838A JP S5867838 A JPS5867838 A JP S5867838A JP 56166855 A JP56166855 A JP 56166855A JP 16685581 A JP16685581 A JP 16685581A JP S5867838 A JPS5867838 A JP S5867838A
Authority
JP
Japan
Prior art keywords
oxide
weight
alloy
oxides
contact material
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.)
Pending
Application number
JP56166855A
Other languages
Japanese (ja)
Inventor
Sankichi Shinoda
三吉 信太
Yasuhiro Ogawa
泰弘 小川
Akiyoshi Takeshima
竹島 明美
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP56166855A priority Critical patent/JPS5867838A/en
Publication of JPS5867838A publication Critical patent/JPS5867838A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To make it possible to magnify the switch load of a slide switch to an arc generating region, by dispersing oxides of Bi and Sn in an Ag alloy comprising a specific amount of Ag and In in a specific amount. CONSTITUTION:In an Ag alloy consisting of, on the basis of wt%, 3-20 In and the remainder Ag, oxides of Bi and Sn are dispersed. These oxides are dispersed as Bi2O3 and SnO2 but the amounts thereof are adjusted to, on the basis of wt%, 0.5-3 Bi and 0.5-4 Sn as metals. Other than these oxides, in order to reduce consumption due to arc, 0.5-2 In oxide expressed in terms of metal be arbitrarily added and dispersed.

Description

【発明の詳細な説明】 本発明はムダマトリクスに金属酸化物を分散させた電気
接点材料に関するもので、突入電流が0〜30ム、定常
電流が0〜3ム程度までの交流(ムC)負荷を開閉する
スライドスイッチに用いて好適な電気接点材料を提供す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrical contact material in which metal oxides are dispersed in a waste matrix. The present invention provides an electrical contact material suitable for use in slide switches that open and close loads.

金属酸化物を利用した複合接点材料としては、ムg−C
(50接点材料が広く利用され、近時においては五g−
8nO2系材料なども利用されるようになって来た。
Mug-C is a composite contact material using metal oxides.
(50 contact materials are widely used, and recently 5g-
8nO2-based materials have also come into use.

しかるに、近年、電子機器用の各種スイッチにおいては
、安全上の規制に伴なう接触信頼性の改善、あるいは使
い易さの面から、軽操作性、小型化などが要求され、ス
ライドスイッチ形式により数ム程度までの負荷を開閉す
る傾向が見られるようになって来た。その結果、スライ
ドスイッチ用接点材料として多用されて来たばね材1例
えばりん青銅(Sn7〜9重量%、 P 0.03〜0
.35重量%、残部On )にムgを2〜1oμの厚さ
で張り合わせた材料においては、アークによる消耗によ
り十分な寿命特性が得られない状況を呈している。一方
、アーク消耗に対しては、前述のムy−3 。
However, in recent years, various switches for electronic devices have been required to be easier to operate and more compact in order to improve contact reliability in accordance with safety regulations and to improve ease of use. There is a growing tendency to open and close loads up to several micrometers. As a result, spring materials 1, such as phosphor bronze (Sn 7-9% by weight, P 0.03-0), have been widely used as contact materials for slide switches.
.. In the case of a material in which Mug is laminated to a thickness of 2 to 1 μm to 35% by weight (the balance is On), sufficient life characteristics cannot be obtained due to wear due to arcing. On the other hand, for arc consumption, the above-mentioned Mu-y-3.

CdO,ム(1−8n02系の材料が望ましいのである
が、機械的な摺、動特性に問題があり、かつまた、スラ
イドスイッチ用材料として用いる場合、ばね材に張り合
わせ、これを圧延加工等により所望の厚さに加工するが
、この点に難点が認められた。
CdO, Mu (1-8n02 material) is desirable, but it has problems with mechanical sliding and dynamic properties, and when used as a material for slide switches, it is pasted onto a spring material and then rolled. Although it was processed to the desired thickness, a difficulty was recognized in this point.

本発明は上記した点に鑑みて成されたものであり、基本
的には、ムfl −I n 合金より成るマトリクスに
BizO3を主要成分とする酸化物を分散した材料を提
供し、スライドスイッチの特性を改良しようとするもの
である。
The present invention has been made in view of the above-mentioned points, and basically provides a material in which an oxide containing BizO3 as a main component is dispersed in a matrix made of a fl -I n alloy, and is used to create a slide switch. This is an attempt to improve the characteristics.

すでに、本願出願人は、ムIマl−IJクス中にBi2
O3の池に5n02 、In2O3などの酸化物を分散
した材料を提案して米だ。これらの材料は、ムg−cd
The applicant has already developed Bi2 during the multi-IJ class.
We proposed a material in which oxides such as 5n02 and In2O3 are dispersed in an O3 pond. These materials are
.

などと同様に耐溶着性およびアーク消耗に対しては優れ
た特性を示すが、摺動特性には必ずしも満足の得られる
傾向を示すものではない。さらにまだ、ばね材に容易に
張り合わせることが可能な材料でもない。しかし他面に
おいては、CdOに比較して蒸気圧の低い酸化物から構
成されていることから、張り合わせ時の接合層の欠陥発
生が少ないこと、あるいは酸化物としては硬度が低いB
12O3を含むものであるところから、比較的良好な加
工・性が得られ、延展がある程度可能である等の長所が
ある。
Although it shows excellent properties in terms of welding resistance and arc wear similar to the above, it does not necessarily show a tendency to be satisfactory in terms of sliding properties. Furthermore, it is not yet a material that can be easily attached to spring materials. However, on the other hand, since it is composed of an oxide with a lower vapor pressure than CdO, there are fewer defects in the bonding layer during bonding, or B has a low hardness compared to CdO.
Since it contains 12O3, it has advantages such as relatively good processability and ability to be spread to a certain extent.

本発明者らは、かかる特質を有する材料について、摺動
特性の改良方策、ばね材に対する張り合わせ方策、およ
びスライドスイッチ用材料として必要十分なアーク特性
の保持について検討した結果、ムgマトリクスにInを
添加してム9−In合金マトリクスとし、これにBi2
O3およびSnO□を分散するか、あるいはさらにIn
2O3を加えて分赦しだ材料によって所期の目的を達成
し得ることを見い出した。
The present inventors investigated methods for improving the sliding properties of materials with such characteristics, methods for laminating them with spring materials, and maintaining arc properties necessary and sufficient as materials for slide switches. As a result, the inventors added In to the mug matrix. Bi2 is added to form a Mu9-In alloy matrix, and Bi2
Disperse O3 and SnO□ or further In
It has been found that the intended purpose can be achieved by adding 2O3 to the material.

次に、本発明に係る上記材料について詳述する。Next, the above-mentioned material according to the present invention will be explained in detail.

本発明の電気接点材料は、ムg−In合金マトリクス中
に81とanの酸化物を含有する。これらの酸化物は複
合化しBi28n20.、0形となっている。そして、
BiとSnの組成比率によってsnの酸化物SnO2あ
るいはBiの酸化物Bi2O3を含有する。そして、特
にアークによる消耗を少なくするだめには、上記酸化物
の他にInの酸化物が添加される。
The electrical contact material of the present invention contains oxides of 81 and an in a Mug-In alloy matrix. These oxides are composited into Bi28n20. , it is 0 type. and,
Depending on the composition ratio of Bi and Sn, it contains an oxide of sn, SnO2, or an oxide of Bi, Bi2O3. In addition to the above-mentioned oxides, an oxide of In is added especially in order to reduce wear due to arcing.

本発明の電気接点材料は上述の如き構成のものであるが
、これら構成素材の含有量は、材料の金属元素全体の重
量比で、ムfl −In合金マトリクスのInが3〜2
0重量%、各酸化物が、金属換算値でBio、5〜3重
量%、 sn O,5〜4重量%。
The electrical contact material of the present invention has the above-mentioned structure, and the content of these constituent materials is such that the In of the fl-In alloy matrix is 3 to 2 in terms of the weight ratio of all metal elements in the material.
0% by weight, each oxide is 5 to 3% by weight in terms of metal, and snO is 5 to 4% by weight.

そしてムgが残部である。Inの酸化物を加える場合は
、上記に金属換算値で0.6〜2重量%の量が添加され
る。
And Mug is the remainder. When adding In oxide, it is added in an amount of 0.6 to 2% by weight in terms of metal.

本発明の電気接点材料において、ムI合金マトリクスを
構成するムg−In合金は、先にも記したように、スラ
イドスイッチ用として摺動特性を向上させ、機械的摩耗
の減少、凝着の防止、摩擦力の低減などに効果を示す。
In the electrical contact material of the present invention, the Mug-In alloy constituting the Mug-In alloy matrix improves sliding properties for slide switches, reduces mechanical wear, and prevents adhesion. It is effective in preventing friction and reducing frictional force.

加えてばね材に張り合わせる場合、通常熱圧着法が取ら
れるが、酸化物含有材料は圧着力が弱く、その後の圧延
工程などにおいて接着層が剥離することが見られるが、
Inを添加した場合、ばね材がCu系合金である時には
、ム9−cu−Inの共晶溶融による液相接合が見られ
、接合層の接着欠陥が少なくなる。Ag合金マトリクス
中のIn添加量の下限は、上述の効果を引き出すための
最少量によって決められる。
In addition, when bonding to spring materials, thermocompression bonding is usually used, but oxide-containing materials have weak bonding force, and the adhesive layer may peel off during the subsequent rolling process.
In the case where In is added and the spring material is a Cu-based alloy, liquid phase bonding due to eutectic melting of Mu9-cu-In is observed, reducing adhesion defects in the bonding layer. The lower limit of the amount of In added in the Ag alloy matrix is determined by the minimum amount to bring out the above-mentioned effects.

他方、その上限は機械的加工能によって、あるい汀接触
抵抗特性によって制限を受ける。
On the other hand, its upper limit is limited by mechanical processability or by the surface contact resistance characteristics.

次に、本発明の電気接点材料に含まれる酸化物について
説明する。主たる酸化物として含まれるB1とSnの酸
化物(Bi2Sn207)は、Biミノ化物(Bi20
3 )とaHの酸化物(SnOz)をモル比で1:2の
割合にてγoo’c〜900°Cの範囲で加熱すること
により、黄縁石構造を持つ酸化物として生成する。その
融点は12oo0C以上にあり、昇華性を示しム、9I
n合金マトリクス中に分散させることにより、アークに
よる消耗の改善効果が大きい。ム9−In合金マトリク
ス中に、上記B1−5nの酸化物、あるいけさらに加え
てInの酸化物を分散させる手法としては、ムgにBi
Next, the oxide contained in the electrical contact material of the present invention will be explained. The oxide of B1 and Sn (Bi2Sn207) contained as the main oxide is Bi minide (Bi20
By heating an oxide (SnOz) of 3) and aH at a molar ratio of 1:2 in the range of γoo'c to 900°C, an oxide having a yellow curb structure is produced. Its melting point is above 12oo0C and shows sublimation, 9I
By dispersing it in the n-alloy matrix, the effect of reducing wear due to arc is significant. As a method for dispersing the above-mentioned B1-5n oxide, or even an In oxide in the Mug9-In alloy matrix,
.

Sn  、さらにはInを添加した合金粉を作り、これ
を酸化雰囲気中にて加熱して、Bi 、 Sn、Inを
選択的に酸化させる。いわゆる内部酸化法を取リ、内部
酸化合金粉とし、これに別途作製したム9−In粉を加
えて均質に混合し、さらに焼結し、五g−in合金マト
リクス中に、酸化物を分散する方法を取る。この方法に
おいて前記B1−5nの酸化物は、最初にムyをマトリ
クスとした合金粉中に生成させるが、B1−8nの酸化
物を複合酸化物Bi25n207の状態で生成させるだ
めには、前記モル比より換算し、Sn重量をx 、 S
n重量をyとしだ時、’7’z −0,67の関係にあ
る必要がある。
An alloy powder to which Sn and further In are added is prepared and heated in an oxidizing atmosphere to selectively oxidize Bi, Sn, and In. The so-called internal oxidation method was used to obtain internal oxidation alloy powder, and separately prepared Mu9-In powder was added to it, mixed homogeneously, and further sintered to disperse the oxide in the 5g-in alloy matrix. take the method. In this method, the B1-5n oxide is first produced in an alloy powder containing Muy as a matrix, but in order to produce the B1-8n oxide in the form of a composite oxide Bi25n207, the molarity Converting from the ratio, the Sn weight is x, S
When n weight is y, it is necessary to have a relationship of '7'z -0,67.

しかしながら、Bllj合金中において偏析しやすいた
めに、内部酸化処理において確実にBi25n2Q7の
状態に転化させることは困難であり、Biの酸化物(B
 1203) 、 S nの酸化物(SnOz)が若干
量単独で存在することもある。また、当然のことながら
上記y//xの値が0.67より大きくなれば、Bi酸
化物が単独で存在する機会が少なくなり、Snの酸(ヒ
物含有量が増加して来る。y4の値が0.67より小さ
くなれば、この逆の傾向になることは明らかである。し
かして、本発明の電気接点−材料の用途である負荷電流
のやや大きいスライドスイッチ接点の場合は、上記への
値がo、67よより大きく、Snの酸化物がB1−5n
酸化物と共存している状態で消耗量が少ない。しかし、
Sn酸化物が増加すると加工性が悪化しやすく、特によ
り消耗量を少なくするために、Inの酸化物を加えた場
合は、その傾向が著しい。したがって、Sn量は弘=2
程度までに抑えることが総合的にメリットをもたらすと
言える。先に記した酸化物に転化させる金属成分の組成
比は、上述の如き条件下で求められたもので、Bi 、
Sn  、Inの各最少量は、本発明に係る電気接点材
料の目的とした用途に対して添加効果の認められる下限
であり、各最多量に、ばね材に対する張り合わせの可能
性、あるいは圧延やスライドスイッチ接点としての曲げ
、打抜きなどの加工性などの面より制限を受ける量であ
る。
However, it is difficult to reliably convert Bi into the Bi25n2Q7 state during internal oxidation treatment because it tends to segregate in the Bllj alloy, and Bi oxide (B
1203), an oxide of Sn (SnOz) may be present alone in a small amount. Also, as a matter of course, if the value of y//x becomes larger than 0.67, there will be fewer chances for Bi oxide to exist alone, and the Sn acid (arsenic content) will increase.y4 It is clear that the opposite trend will occur if the value of is smaller than 0.67.However, in the case of a slide switch contact with a rather large load current, which is the application of the electrical contact material of the present invention, the above-mentioned value is larger than o, 67, and the Sn oxide is B1-5n
Low consumption as it coexists with oxides. but,
As the amount of Sn oxide increases, workability tends to deteriorate, and this tendency is particularly noticeable when In oxide is added to reduce the amount of wear. Therefore, the amount of Sn is Hiroshi = 2
It can be said that keeping it to a certain level brings overall benefits. The composition ratios of the metal components to be converted into the oxides described above were determined under the conditions described above, and include Bi,
The minimum amounts of Sn and In are the lower limits at which the addition effect is recognized for the intended use of the electrical contact material according to the present invention, and the maximum amounts of each include the possibility of bonding to spring materials, rolling or sliding. This amount is limited by the workability of bending and punching as a switch contact.

以上説明した本発明の電気接点材料について、より具体
的に実施例にもとづいて説明する。
The electrical contact material of the present invention described above will be described in more detail based on Examples.

本発明の組成に従って、ムg、 Bi、 Sn、 In
を含量600g秤量する。Inは、酸化物として含有さ
せる場合、マトリクスに含有させる分と別に秤量する。
According to the composition of the invention, Mug, Bi, Sn, In
Weigh out 600g of When In is included as an oxide, it is weighed separately from the amount to be included in the matrix.

ムgはBi、Snおよび酸化物として含有させるだめの
Inのいずれもが固溶し得る量と、残部マトリクス用I
nとの合金用に分ける。例えば、次表に示す試料No、
7の可動接点用材料の場合。
Mug has an amount that can dissolve any of Bi, Sn, and In to be contained as an oxide, and the remaining I for the matrix.
Separate for alloys with n. For example, sample No. shown in the following table,
In the case of material for movable contacts in item 7.

マトリクスは10重量%のInを含むムg−In合金で
、この中に金属換算として、3重量%のBl。
The matrix is a Mug-In alloy containing 10% by weight of In, in which 3% by weight of Bl is added in terms of metal.

2重量%のSn 、1重量%のInを含むものであルカ
ラ、夫々)秤量値1dBi 15g、 sn 10g。
Lucara contains 2% by weight of Sn and 1% by weight of In, respectively) weighing value 1dBi 15g, sn 10g.

酸化物用として工nsy、マトリクス用としてIn50
,9.五g420gの計500gとする。ここで、ムg
420gのうち3oogを分離して。
Insy for oxide, In50 for matrix
,9. 5g and 420g for a total of 500g. Here, mug
Separate 3oog out of 420g.

これにBiltsg、Sn 1og、In 5gを加え
溶解し、内部酸化合金用粉体を作製するために、加圧窒
素ガスによる溶湯噴霧装置にて粉化し60〜326メソ
シ一程度の合金粉体とする。この粉体は、700°Cの
温度で50時間大気中にて加熱処理されて、ムgマトリ
クス中にBi、SH,Inなどが選択的に酸化された内
部酸化合金粉となる。
Add and melt Biltsg, Sn 1og, and In 5g to this, and in order to create powder for internal oxidation alloy, powder it in a molten metal spraying device using pressurized nitrogen gas to obtain an alloy powder of about 60 to 326 mesosi. . This powder is heat-treated in the air at a temperature of 700° C. for 50 hours to become an internally oxidized alloy powder in which Bi, SH, In, etc. are selectively oxidized in the mug matrix.

他方、ムgの残部120gとマトリクス用rneogは
、同様に溶解後、溶湯噴霧装置によってム(1−In 
 合金粉とされる。以上はNo、7の試料を例として述
べたが、他の試料についても大略同様に行われる。これ
らの粉体は均質に混合されたのち30m/m径の円筒型
に装填され、4トン/ctfrの加圧力で成型される。
On the other hand, the remaining 120 g of Mug and Rneog for matrix were melted in the same manner, and then mixed with Mug (1-In) using a molten metal spraying device.
It is considered to be an alloy powder. The above description has been made using sample No. 7 as an example, but the process is roughly the same for other samples as well. These powders were homogeneously mixed, then loaded into a cylindrical mold with a diameter of 30 m/m, and molded under a pressure of 4 tons/ctfr.

成型されたビレットは、窒素ガス雰囲気にて700’C
〜860°Cで焼結される。
The molded billet was heated at 700'C in a nitrogen gas atmosphere.
Sintered at ~860°C.

なおこの場合、マl−1クス部分の流出が生ずるので温
度上昇勾配に配慮し、内部酸化処理) IJクス中にI
nの拡散が行なわれるようにする。このように焼結され
たビレットは、次に、460°G8トン/Caの条件に
て再度成型されたのち、前回と同様の条件にて焼結熱処
理される。そしてこの焼結体H,550〜e o oo
cの湿間押出しによって、3om7m径から、巾20 
m7m厚さ3 m7m ノ板状に加工される。さらに、
冷間圧延によって1m7゜の厚さまで圧延したのち、表
面をスコッチプライトにより研磨清浄にする。他方、ば
ね材の素材として厚さ9′m/rrL、巾30−の8重
量%Sn りん青銅板を準備し、その表面を同じくスコ
ソチブラめっきを10〜20μの厚さで施す。そして、
先に加工した1TL/rrL厚の酸化物−人9合金板を
Inめっき面に重ね合わせ、耐熱治具により密着させた
のち、窒素ガス雰囲気中650C〜760Gにて1時間
熱処理し圧着する。この時、Inめっきは液相拡散する
がムt/−In  マトリクス中のInお相乗作用を示
し、欠陥の少ない接合状態が得られる。最後に、この接
合材を焼鈍さ圧延を繰返すことにより厚さ70μまで加
工ける。
In this case, since the IJ part will flow out, the temperature rise gradient should be taken into account and the internal oxidation treatment (internal oxidation treatment)
n diffusion is performed. The billet thus sintered is then molded again under the conditions of 460°G and 8 tons/Ca, and then subjected to sintering heat treatment under the same conditions as before. And this sintered body H, 550~e o oo
By wet extrusion of c.
Processed into a plate shape with a thickness of 3 m and 7 m. moreover,
After cold rolling to a thickness of 1 m7°, the surface is polished and cleaned using Scotch prite. On the other hand, an 8 wt % Sn phosphor bronze plate having a thickness of 9'm/rrL and a width of 30 mm is prepared as a material for the spring material, and its surface is similarly plated with Scosotibra to a thickness of 10 to 20 microns. and,
The previously processed 1TL/rrL thick oxide-Jin9 alloy plate is superimposed on the In-plated surface and brought into close contact with a heat-resistant jig, and then heat treated at 650C to 760G in a nitrogen gas atmosphere for 1 hour and pressure bonded. At this time, the In plating undergoes liquid phase diffusion, but exhibits a synergistic effect with the In in the Mut/-In matrix, resulting in a bonded state with fewer defects. Finally, this bonding material can be processed to a thickness of 70 μm by repeating annealing and rolling.

上述の如くにして得られた素材は、スライドスイッチの
可動側接点として成形加工され、特性評価に供された。
The material obtained as described above was molded into a movable contact of a slide switch and subjected to characteristic evaluation.

なお、試験用スライドスイッチの固定側接点としては、
厚さ0.6%の黄銅板に2μ厚さのムyめっきを施した
材料を用い、捷た、通常スライドスイッチに使用される
合成油による接点潤滑剤をム9めっき面に塗布した。特
性の比較試料として、可動接点に厚さ7μのム夕を張り
合わせた総厚7oμによるりん青銅接点、固定側接点に
上述と同一の材料、潤滑剤を用いたスライスイッチの評
価はコンデンサ負荷とし、ムC3oV 、定常3ム、イ
ンランシー30ムの負荷回路を2万回開閉し、その後の
接触抵抗、接点の消耗状態を観察することにより行った
。その結果を次表に示す。
In addition, the fixed side contact of the test slide switch is as follows:
A brass plate with a thickness of 0.6% was coated with a 2μ thick muy plating, and a contact lubricant made of synthetic oil, which was scraped and normally used for slide switches, was applied to the mu9 plating surface. As a comparison sample of characteristics, a phosphor bronze contact with a total thickness of 7μ with a 7μ thick layer pasted on the movable contact, and a slice switch using the same material and lubricant as above for the fixed contact were evaluated with a capacitor load. The test was carried out by opening and closing a load circuit of 3oV, 3oV steady, and 30mu in run-time 20,000 times, and then observing the contact resistance and wear and tear of the contacts. The results are shown in the table below.

(以下余白)  3 気接点材料は、動作試験後においても実用上十分な特性
を示している。また、材料の消耗、摩耗が少ないことは
スイッチ接点間の絶縁性の向トに結びつき、安全上にお
いても好ましい傾向を示す。
(Left below) 3. The gas contact material shows sufficient characteristics for practical use even after the operation test. In addition, less consumption and wear of the material leads to better insulation between the switch contacts, which is also favorable in terms of safety.

他方、現在広く利用されているby単独材の場合に、試
料NO68に示すようにアーク消耗によりばね材である
りん青銅面が露出し、一部のものについてはりん青銅面
に孔が発生したものもある。
On the other hand, in the case of single material by, which is currently widely used, the phosphor bronze surface of the spring material is exposed due to arc consumption, as shown in sample No. 68, and in some cases, holes are formed on the phosphor bronze surface. There is also.

以上説明したように、本発明の電気接点材料は。As explained above, the electrical contact material of the present invention.

スライドスイッチの開閉負荷をアーク発生領域まで拡大
することを可能とするものであり、その実用的価値t/
′i極めて高いものである。
It is possible to expand the switching load of the slide switch to the arc generation area, and its practical value is
'i is extremely high.

Claims (2)

【特許請求の範囲】[Claims] (1)  Ag合金マl−IJクスに金属酸化物を分散
させた電気接点材料であって、前記金属酸化物か金属換
算値にして、Biを0.6〜3重量%、Snを0.5〜
4重量%含み、さらに前記ムg合金マトリクス成分が、
Inを3〜20重量%含み、残部がムgより成ることを
特徴とする電気接点材料。
(1) An electrical contact material in which a metal oxide is dispersed in an Ag alloy matrix (IJ), in which the metal oxide contains 0.6 to 3% by weight of Bi and 0.6% to 3% by weight of Sn and 0.6% to 3% by weight of Sn. 5~
4% by weight, and further the above-mentioned mug alloy matrix component,
An electrical contact material comprising 3 to 20% by weight of In, with the remainder being mug.
(2)  ムI合金マ) I+クスに金属酸化物を分散
させた電気接点材料であって、前記金属酸化物か金属換
算値にして、B1を0.5〜3重量%、Snを0.6〜
4重量%、工nf:0.6〜2重量%含み、さらに前記
ムy合金マトリクス成分が% Inを3〜20重量%含
み、残部が五gより成ることを特徴とする電気接点材料
(2) An electrical contact material in which a metal oxide is dispersed in an I+ alloy, and the metal oxide contains 0.5 to 3% by weight of B1 and 0.5% by weight of Sn. 6~
An electrical contact material characterized in that the alloy matrix component contains 3 to 20% by weight of In and the balance is 5 g.
JP56166855A 1981-10-19 1981-10-19 Electric contact material Pending JPS5867838A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56166855A JPS5867838A (en) 1981-10-19 1981-10-19 Electric contact material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56166855A JPS5867838A (en) 1981-10-19 1981-10-19 Electric contact material

Publications (1)

Publication Number Publication Date
JPS5867838A true JPS5867838A (en) 1983-04-22

Family

ID=15838891

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56166855A Pending JPS5867838A (en) 1981-10-19 1981-10-19 Electric contact material

Country Status (1)

Country Link
JP (1) JPS5867838A (en)

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