JPS627255B2 - - Google Patents
Info
- Publication number
- JPS627255B2 JPS627255B2 JP6272785A JP6272785A JPS627255B2 JP S627255 B2 JPS627255 B2 JP S627255B2 JP 6272785 A JP6272785 A JP 6272785A JP 6272785 A JP6272785 A JP 6272785A JP S627255 B2 JPS627255 B2 JP S627255B2
- Authority
- JP
- Japan
- Prior art keywords
- oxide
- arc
- weight
- lithium
- silver
- 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
- 239000000463 material Substances 0.000 claims description 22
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 229910052709 silver Inorganic materials 0.000 claims description 16
- 239000004332 silver Substances 0.000 claims description 16
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims description 9
- 229910001947 lithium oxide Inorganic materials 0.000 claims description 9
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 8
- 229910052744 lithium Inorganic materials 0.000 claims description 8
- 229910003437 indium oxide Inorganic materials 0.000 claims description 6
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 6
- 229910001887 tin oxide Inorganic materials 0.000 claims description 6
- 229910044991 metal oxide Inorganic materials 0.000 claims description 5
- 150000004706 metal oxides Chemical class 0.000 claims description 5
- 239000011787 zinc oxide Substances 0.000 claims description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 229910001882 dioxygen Inorganic materials 0.000 claims description 4
- 229910052738 indium Inorganic materials 0.000 claims description 4
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims 1
- 238000003466 welding Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- -1 iron group metals Chemical class 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- MOFOBJHOKRNACT-UHFFFAOYSA-N nickel silver Chemical compound [Ni].[Ag] MOFOBJHOKRNACT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910018068 Li 2 O Inorganic materials 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- QTJOIXXDCCFVFV-UHFFFAOYSA-N [Li].[O] Chemical compound [Li].[O] QTJOIXXDCCFVFV-UHFFFAOYSA-N 0.000 description 1
- ASMQPJTXPYCZBL-UHFFFAOYSA-N [O-2].[Cd+2].[Ag+] Chemical compound [O-2].[Cd+2].[Ag+] ASMQPJTXPYCZBL-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- IVQODXYTQYNJFI-UHFFFAOYSA-N oxotin;silver Chemical compound [Ag].[Sn]=O IVQODXYTQYNJFI-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
Landscapes
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Manufacture Of Switches (AREA)
Description
[技術分野]
この発明は電気接点に使用する材料の製造技術
の分野に属する。
[背景技術]
従来から電磁接触機、リレー等の電気機器に銀
−酸化カドミユウム系、銀−酸化スズ系、銀−ニ
ツケル系の接点材料が使用されていた。これらの
接点は溶着、消耗共に少ない接点として知られ、
一方銀−ニツケル接点は消耗が少なく、加工性が
優れた接点として知られている。しかし、これら
の接点材料はいずれれも電磁駆動力によりアーク
を走らせて限流するタイプのノーヒユーズブレー
カ用の接点として使用した際に、短絡時に流れる
大電流によりアークが生じ、このアークの「切
れ」が不充分なため短絡遮断性能が劣るという欠
点があり、この性能の改良が望まれていた。
本発明者らは、アークの「切れ」を改良するた
めに種々研究を重ねた結果、銀素地に酸化リチユ
ウムを配合した接点材料を開発し、すでに特許出
願をしている。すなわち銀素地に酸素リチユウム
(Li2O)を配合することによりアークの「切れ」
が改良されるのである。しかも接点材料として重
要な耐溶着性も改良されるのである。そしてこの
接点材料は充分実用的なものであつた。しかし、
さらに高度な実用的価値を得るためには、耐消耗
性に関して、さらに改良を図る必要があることが
分かつた。そこで、さらに研究を続けた結果、以
下に説明する本願発明に到達したのである。
[発明の目的]
この発明は、アークの「切れ」、耐溶着性、耐
消耗性の改良された接点材料を提供するための、
より優れた製造方法を提供することを目的として
なされた。
[発明の開示]
この発明は、銀を素地とし、これに酸化亜鉛
(ZnO)、酸化スズ(SnO2)、酸化インジユウム
(In2O3)からなる群から選ばれた1種または2種
以上の金属酸化物を金属換算で0.02〜1.0重量
%、および酸化リチユウム(Li2O)をリチユウ
ム換算で0.1〜3.0重量%含有させ、さらに鉄族金
属を0.1〜1.0重量%含有させた接点材料の製法で
あつて、前記の銀素地に予め亜鉛または/および
スズまたは/およびインジユウムを、さらにリチ
ユウムおよび鉄族金属を溶融混合させた後、酸素
ガス雰囲気中で加熱処理することを特徴とする接
点材料の製法を提供するものである。以下、この
発明を詳しく説明する。
この発明において銀素地に含有させる酸化リチ
ユウムはアークの「切れ」および耐溶着性を改良
するのに役立つ。銀素地に酸化リチユウムを含有
させることによりアークの「切れ」が改良される
理由は明確ではないが、酸化リチユウムが銀素地
の中に分散するとアークが出やすくなり、従つて
アークが分散する結果、アークが動き易くなり、
結局アークの「切れ」が良くなるものと考えられ
る。そして、この酸化リチユウムの配合量はリチ
ユウム換算で0.1〜3.0重量%(以下%と略す)含
有させるのが望ましい。3.0%を超えた含有量で
は接点として要求される電気伝導度が低くなり、
耐溶着性、耐消耗性が十分でなく、一方0.1%未
満ではアークの「切れ」が十分でなくなる。な
お、0.8〜1.5%の範囲が一層好ましい結果を与え
る。
つぎに、銀素地に含有せしめる酸化亜鉛、酸化
スズおよび酸化インジユウムについて説明する。
この金属酸化物の含有量は、金属換算で0.02〜
1.0%が好ましく、さらには0.2〜0.6%の範囲が一
層好ましい。これらの範囲の上限を超えた含有量
であると電気伝導度の低下を招き、耐溶着性をあ
まり改良しない。一方、下限を外れると耐消耗性
に関して改良の効果が少なくなる。
ここでさらに鉄族に属する金属である鉄、ニツ
ケル、コバルトを、前記亜鉛、スズ、インジユウ
ム、リチユウムなどの金属と共に銀素地に予め含
有させ、つぎに内部酸化の処理をするようにする
と、耐消耗性、耐溶着性を一層向上させる効果が
あることが判つた。前記鉄族金属の添加により耐
溶着性、耐消耗性が改良される理由は明らかでは
ないが、銀の結晶粒を微細化させるためであろう
と推定される。含有量は、接点材料全体の中に
0.1〜1.0%の範囲で含有させるのが望ましい。下
限より少ないと結晶粒の微細化効果がなく、一方
上限を超えると鉄族金属の分布が偏析する結果、
溶着、消耗共に改良の効果が不充分となる。
なお、内部酸化法については、通常の手段が採
用され、その具体的内容については実施例におい
て説明される。
以下、実施例、比較例に基づき説明する。
実施例
銀を素地金属として使用し、これに酸化リチユ
ウム、そしてさらに酸化亜鉛、酸化スズ、酸化イ
ンジユウム、鉄族金属等を配合した接点材料を調
製した。その具体的配合は第1表に示した。
なお、接点材料の製造条件を詳しく開示すると
以下の通りである。
まず、銀の中に前記亜鉛、スズおよびインジユ
ウムのいずれか1種と、リチユウムと鉄族金属を
所定量添加し、アルゴンガス雰囲気中で溶解させ
た。溶解の後に金型を使用して棒状に鋳造し、つ
ぎに650℃で8時間窒素ガス雰囲気中で焼鈍し
た。これに銀板を圧着した後、圧延し、1mmの板
材とした。その後、750℃、酸素ガス雰囲気中で
100時間加熱し、内部酸化した。これを打ち抜き
加工した後、ろう付けし、ASTM試験および短
絡試験用試料とした。
(アーク特性の判定法)
前記の試料をノーヒユーズブレーカに組み込ん
でASTM法により耐短絡試験を行い、アーク膠
着時間の測定を行つた。ここでアーク膠着時間と
は接点間でアークが発生した時に、アークが動か
ずに停まつている時間である。すなわち、アーク
発生と同時に電磁力が生じ、最終的に、この電磁
力によりアークが移動するが、膠着時間とはアー
クが発生してから移動するまでの時間である。ア
ーク遮断性能は、膠着時間が短い程よい。なお、
短絡電流は5.2KAであつた。
(耐消耗性、耐溶着性の判定法)
ASTMによる接点試験を行つた。条件は以下
の通りであつた。
負荷:交流単層、100V、40A
接触力:200g
解離力:340g
接点形状:可動接点は5Φ、12Rの球状固定接点
は5Φでフラツト状
最終開閉回数:10万回
なお、消耗量は3個のデータの平均値で、溶着
性能は3個のデータの合計溶着回数で評価した。
[Technical Field] This invention belongs to the field of manufacturing technology for materials used in electrical contacts. [Background Art] Conventionally, silver-cadmium oxide-based, silver-tin oxide-based, and silver-nickel-based contact materials have been used in electrical equipment such as electromagnetic contactors and relays. These contacts are known for their low welding and wear and tear.
On the other hand, silver-nickel contacts are known for their low wear and tear and excellent workability. However, when these contact materials are used as contacts for no-fuse breakers, which limit the current by running an arc using electromagnetic driving force, the large current that flows during a short circuit generates an arc, causing the arc to break. '' is insufficient, resulting in poor short-circuit breaking performance, and improvements in this performance have been desired. The inventors of the present invention have conducted various studies to improve the "breakage" of the arc, and as a result have developed a contact material containing lithium oxide in a silver base material, and have already filed a patent application for the contact material. In other words, by adding lithium oxygen (Li 2 O) to the silver base, the arc can be cut.
is improved. Furthermore, the welding resistance, which is important as a contact material, is also improved. This contact material was sufficiently practical. but,
In order to obtain even higher practical value, it was found that it was necessary to further improve the wear resistance. Therefore, as a result of further research, the present invention described below was achieved. [Object of the Invention] This invention provides a contact material with improved arc "breakage", welding resistance, and wear resistance.
The aim was to provide a better manufacturing method. [Disclosure of the Invention] This invention is based on silver, and one or more selected from the group consisting of zinc oxide (ZnO), tin oxide (SnO 2 ), and indium oxide (In 2 O 3 ). A contact material containing 0.02 to 1.0% by weight of metal oxides, 0.1 to 3.0% by weight of lithium oxide (Li 2 O) in terms of lithium, and 0.1 to 1.0% by weight of iron group metals. A contact material that is manufactured by melting and mixing zinc and/or tin and/or indium, and further lithium and iron group metals in advance on the above-mentioned silver base material, and then heat-treating the mixture in an oxygen gas atmosphere. It provides a manufacturing method. This invention will be explained in detail below. In this invention, the lithium oxide contained in the silver matrix is useful for improving arc "breakage" and welding resistance. It is not clear why the inclusion of lithium oxide in the silver base improves arc cutting, but when lithium oxide is dispersed in the silver base, it becomes easier to generate an arc, and as a result of the dispersion of the arc, The arc becomes easier to move,
It is thought that the "cutting" of the arc will improve after all. The amount of lithium oxide blended is preferably 0.1 to 3.0% by weight (hereinafter abbreviated as %) in terms of lithium. If the content exceeds 3.0%, the electrical conductivity required for the contact will be low.
Welding resistance and abrasion resistance are insufficient, and on the other hand, if it is less than 0.1%, the "cutting" of the arc will not be sufficient. Note that a range of 0.8 to 1.5% gives more preferable results. Next, zinc oxide, tin oxide, and indium oxide contained in the silver base will be explained.
The content of this metal oxide is 0.02~ in terms of metal.
It is preferably 1.0%, and more preferably in the range of 0.2 to 0.6%. If the content exceeds the upper limit of these ranges, the electrical conductivity will decrease and the welding resistance will not be improved much. On the other hand, if the lower limit is exceeded, the effect of improving wear resistance will be reduced. Furthermore, if iron, nickel, and cobalt, which are metals belonging to the iron group, are added to the silver base in advance along with metals such as zinc, tin, indium, and lithium, and then subjected to internal oxidation treatment, wear resistance is improved. It was found that this method has the effect of further improving the properties and welding resistance. The reason why the welding resistance and abrasion resistance are improved by the addition of the iron group metal is not clear, but it is presumed that it is because the silver crystal grains are made finer. The content is in the whole contact material.
It is desirable to contain it in the range of 0.1 to 1.0%. If it is less than the lower limit, there will be no grain refining effect, while if it exceeds the upper limit, the distribution of iron group metals will become segregated.
The improvement effect becomes insufficient for both welding and wear. Note that for the internal oxidation method, a usual method is employed, and the specific details thereof will be explained in the examples. The following is a description based on Examples and Comparative Examples. Example A contact material was prepared by using silver as a base metal and adding lithium oxide, zinc oxide, tin oxide, indium oxide, iron group metal, etc. to the base metal. The specific formulation is shown in Table 1. The detailed manufacturing conditions for the contact material are as follows. First, a predetermined amount of any one of zinc, tin, and indium, lithium, and an iron group metal were added to silver and dissolved in an argon gas atmosphere. After melting, it was cast into a bar using a mold, and then annealed at 650°C for 8 hours in a nitrogen gas atmosphere. After a silver plate was crimped onto this, it was rolled to obtain a 1 mm plate material. Then, at 750℃ in an oxygen gas atmosphere.
Heated for 100 hours for internal oxidation. After punching this, it was brazed and used as a sample for ASTM tests and short circuit tests. (Method for Determining Arc Characteristics) The above sample was assembled into a no-fuse breaker, and a short circuit resistance test was conducted using the ASTM method, and the arc sticking time was measured. Here, the arc stagnation time is the time during which the arc remains motionless when it occurs between the contacts. That is, an electromagnetic force is generated at the same time as the arc is generated, and ultimately the arc moves due to this electromagnetic force, but the sticking time is the time from when the arc is generated until it moves. The shorter the sticking time, the better the arc interrupting performance. In addition,
The short circuit current was 5.2KA. (Method for determining wear resistance and welding resistance) A contact test was conducted using ASTM. The conditions were as follows. Load: AC single layer, 100V, 40A Contact force: 200g Dissociation force: 340g Contact shape: Movable contact is 5Φ, 12R spherical fixed contact is 5Φ and flat Final number of openings and closings: 100,000 times The wear amount is 3 The welding performance was evaluated based on the average value of the data, and the total number of weldings for the three pieces of data.
【表】
上記材料につき接点としての特性を試験した結
果を第2表に示した。[Table] Table 2 shows the results of testing the properties of the above materials as contacts.
【表】
なお、実施例No.3.4.5における鉄族金属添加の
効果として結晶粒の大きさを顕微鏡で測定したと
ころ実施例No.3にあつては47μ、実施例No.4にお
いては50μ、実施例No.5においては45μであつ
た。
これに対し、後に述べる比較例No.6については
結晶粒の大きさは122μであつた。
比較例
第3表の配合により、そして比較例No.1〜5ま
では焼結法により、比較例No.6は内部酸化法によ
り比較のための実験を行つた。その他の条件は実
施例と同様にして実験を行つた。性能試験の結果
は第4表に示した。[Table] Furthermore, as an effect of the addition of iron group metals in Example No. 3.4.5, the size of crystal grains was measured using a microscope and found to be 47 μ in Example No. 3 and 50 μ in Example No. 4. , in Example No. 5, it was 45μ. On the other hand, in Comparative Example No. 6, which will be described later, the crystal grain size was 122μ. Comparative Example Comparative experiments were conducted using the formulations shown in Table 3, using the sintering method for Comparative Examples Nos. 1 to 5, and using the internal oxidation method for Comparative Example No. 6. The experiment was conducted under the same conditions as in the example. The results of the performance test are shown in Table 4.
【表】【table】
【表】
[発明の効果]
この発明は、銀を素地とし、これに酸化亜鉛、
酸化スズ、酸化インジユウムからなる群から選ば
れた1種以上の金属酸化物を金属換算で0.02〜
1.0%、および酸化リチユウムをリチユウム換算
で0.1〜3.0%含有させ、さらに鉄族金属を0.1〜
1.0%含有させた接点材料の製法であつて、前記
の銀素地に予め酸化亜鉛または/および酸化スズ
または/および酸化インジユウムを、および酸化
リチユウムおよび鉄族金属を溶融混合させた後、
酸素ガス雰囲気中で加熱処理することを特徴とす
るので、アークの「切れ」、耐溶着性、耐消耗性
が改良された接点材料を提供することができる効
果がある。[Table] [Effects of the invention] This invention uses silver as a base material, and zinc oxide,
One or more metal oxides selected from the group consisting of tin oxide and indium oxide with a metal equivalent of 0.02~
1.0%, and 0.1 to 3.0% of lithium oxide in terms of lithium, and 0.1 to 3.0% of iron group metals.
A method for producing a contact material containing 1.0%, in which zinc oxide and/or tin oxide and/or indium oxide and lithium oxide and iron group metal are melt-mixed in advance into the above-mentioned silver base, and then
Since the method is characterized by heat treatment in an oxygen gas atmosphere, it is effective in providing a contact material with improved arc "breakage", welding resistance, and wear resistance.
Claims (1)
酸化インジユウムからなる群から選ばれた1種ま
たは2種以上の金属酸化物を金属換算で0.02重量
%以上1.0重量%未満、および酸化リチユウムを
リチユウム換算で0.1重量%以上3.0重量%以下の
範囲で含有させ、さらに鉄族金属を0.1重量%以
上1.0重量%以下の範囲で含有させた接点材料の
製法であつて、前記の銀素地に予め亜鉛または/
およびスズまたは/およびインジユウムを、さら
にリチユウムおよび鉄族金属を溶融混合させて鋳
造した後、酸素ガス雰囲気中で加熱処理すること
を特徴とする接点材料の製法。1 Silver is the base material, and zinc oxide, tin oxide,
One or more metal oxides selected from the group consisting of indium oxide in a range of 0.02% by weight or more and less than 1.0% by weight in terms of metal, and lithium oxide in a range of 0.1% by weight or more and less than 3.0% by weight in terms of lithium. A method for manufacturing a contact material containing an iron group metal in a range of 0.1% by weight or more and 1.0% by weight or less, wherein the above-mentioned silver substrate is preliminarily coated with zinc or/or iron group metal.
and tin and/or indium, further lithium and an iron group metal are melt-mixed, cast, and then heat-treated in an oxygen gas atmosphere.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6272785A JPS60234932A (en) | 1985-03-25 | 1985-03-25 | Manufacture of contact material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6272785A JPS60234932A (en) | 1985-03-25 | 1985-03-25 | Manufacture of contact material |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56212324A Division JPS58117843A (en) | 1981-12-29 | 1981-12-29 | Contact material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60234932A JPS60234932A (en) | 1985-11-21 |
| JPS627255B2 true JPS627255B2 (en) | 1987-02-16 |
Family
ID=13208682
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6272785A Granted JPS60234932A (en) | 1985-03-25 | 1985-03-25 | Manufacture of contact material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60234932A (en) |
-
1985
- 1985-03-25 JP JP6272785A patent/JPS60234932A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60234932A (en) | 1985-11-21 |
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