JPH0313295B2 - - Google Patents
Info
- Publication number
- JPH0313295B2 JPH0313295B2 JP56110496A JP11049681A JPH0313295B2 JP H0313295 B2 JPH0313295 B2 JP H0313295B2 JP 56110496 A JP56110496 A JP 56110496A JP 11049681 A JP11049681 A JP 11049681A JP H0313295 B2 JPH0313295 B2 JP H0313295B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- contact
- resistance
- carbides
- metals
- 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
Links
- 229910052751 metal Inorganic materials 0.000 claims description 20
- 239000002184 metal Substances 0.000 claims description 20
- 150000001247 metal acetylides Chemical class 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 10
- 150000004767 nitrides Chemical class 0.000 claims description 10
- -1 iron group metals Chemical class 0.000 claims description 9
- 229910052709 silver Inorganic materials 0.000 claims description 7
- 239000004332 silver Substances 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910002804 graphite Inorganic materials 0.000 claims description 4
- 239000010439 graphite Substances 0.000 claims description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 2
- 239000011651 chromium Substances 0.000 claims 2
- 239000011733 molybdenum Substances 0.000 claims 2
- 239000010955 niobium Substances 0.000 claims 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims 1
- 239000010937 tungsten Substances 0.000 claims 1
- 229910052720 vanadium Inorganic materials 0.000 claims 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims 1
- 229910045601 alloy Inorganic materials 0.000 description 20
- 239000000956 alloy Substances 0.000 description 20
- 238000003466 welding Methods 0.000 description 10
- 238000012360 testing method Methods 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000009413 insulation Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 230000001603 reducing effect Effects 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
Landscapes
- Manufacture Of Switches (AREA)
- Contacts (AREA)
- Conductive Materials (AREA)
Description
本発明は電流を通電開閉する機器に使用する電
気接点材料に関するものである。
又、特にAg−WC系合金の特性向上を目的と
したものである。Ag−WC系合金は従来その優
れた耐アーク性、耐溶着性のため気中しや断器、
開閉器等の機器の接点として広く使用されてい
る。
然るに最近、ノーヒユーズブレーカを始めとす
る気中しや断器や開閉器等の機器は小型、高性能
化のすう勢にあり、これに伴なつて接点材料への
負荷が厳しくなり、接点性能の向上が強く要請さ
れている。又、機器の小型化により接点寸法の小
型化、接触圧力の低下の傾向にあり、これによつ
て電流しや断時に生ずる消耗、飛散が増大し接点
の溶着や機器の絶縁劣化、更に定格電流開閉時に
温度上昇が起り易いといつた問題が生じている。
このような特性改善の要望に答えるものの一つ
としてAg−WC合金にグラフアイト(Gr)を添
加した接点が開発された。この接点は開閉時発生
したアーク熱でGrが還元ガスとなりWCの酸化を
防止して温度上昇を抑え、且つGrの潤滑性によ
り耐溶着性を高める効果がある。
しかしながら、Grの添加によつて逆に消耗、
絶縁特性が低下する欠点があつた。このため小型
高性能のしや断器や開閉器では可動接点にはAg
−WC接点、固定接点にはAg−WC−Gr接点とい
う組合せで使用せざるを得なかつた。しかし、可
動部と固定部で材質を変えて組合せることは部品
管理が極めて面倒なことである。更にこのような
組合せによる使用法でも最近の小型高性能の機器
では接触圧力が小さく、開閉時に発生するアーク
熱によつて異常な温度上昇、消耗、絶縁劣化、溶
着が多発し更に接点性能の改善が要望されてい
る。
本発明は以上の点に鑑みてなされたものであり
耐溶着性、耐消耗性、耐絶縁性を併せて具備し、
且つ温度上昇が低い実用性に優れた接点合金を提
供するものである。更に本発明合金は高価な銀量
を可成り少なくしても接点として使用可能な安価
な接点合金を提供するものである。
本発明による合金は、鉄族金属と銀に4A、
5A、6A族金属の炭化物、4A、5A、6A族金属の
窒化物及びグラフアイトを分散含有せしめ、且つ
鉄族金属中に一部若しくは全ての炭化物を固溶せ
しめたことを特徴とする電気接点材料である。
発明者等は先に銀に鉄族金属と各種炭化物を添
加した合金の検討を種々行なつた結果、該鉄族金
属中に炭化物の一部又は全部が固溶した合金が電
流の開閉時に発生するアーク熱での消耗、飛散が
極端に少なく機器の絶縁劣化や溶着の少ない効果
を示すことを見出した。鉄族金属や炭化物は耐酸
化性が悪く開閉時に発生するアーク熱によつて酸
化し、接触抵抗を増大させ機器の温度上昇が高く
なる欠点がある。このため鉄族金属や炭化物の酸
化防止として還元性に優れたGrを上記接点合金
に添加せしめると、Grは電気開閉時の熱で分解
して還元ガスを発生し鉄族金属や炭化物を酸化か
ら防止し接触抵抗を小さく抑え、機器の温度上昇
を低下せしめると共にGrの潤滑性により耐溶着
性を高めることが判つた。
即ち、銀中に、高温度での機械強度や結合強度
の優れた鉄族金属に炭化物を固溶せしめて耐消耗
性や耐溶着性を向上し、更に還元性と潤滑性の優
れたGrを添加することにより、従来のAg−WC
系やAg−WC−Gr系接点では期待できなかつた
高性能の耐溶着性、耐消耗性、耐絶縁性、温度上
昇特性を共に具備した合金を得ることが出来た。
本発明者等は、その後更に研究を進めた結果、
この系に更に4A、5A、6A族金属の窒化物を加え
ると、銀の融点以上の温度で焼結中にこれら窒化
物がFe族金属を介して炭化物と反応し、炭化物
が微細化され、高温下での変形が少なくなること
が判つた。更に、これら窒化物の添加により耐ア
ーク消耗性が大幅に改良されることが判つた。こ
れら特性は開閉時に発生するアーク熱で窒化物が
分散されたGrと反応し炭化物を形成し、この反
応が吸熱反応であること及びN2ガスを放出し消
弧作用があるためと思われる。
図はこの反応の自由エネルギー変化を示すもの
であり、殆ど1500〓にてこの反応が進行すること
が判る。
鉄族金属はFe、Co、Niであり、5〜60重量%
であり好ましくは10〜50重量%が適当である。5
重量%以下では鉄族金属が銀中に分散し、炭化物
の固溶析出が起きず耐消耗性が向上しない。又60
重量%以上ではGrを添加しても接触抵抗が低下
せず温度上昇特性の向上効果がない。
炭化物としてはW、Mo、Ta、Nb、Ti、Cr等
の4A、5A、6A族の炭化物が効果があり、その量
としては5〜50重量%が好ましく、特に20〜50重
量%が特性が良い。炭化物が5重量%以下では
Ag中の炭化物量が少な過ぎて耐溶着性が不充分
であり、50重量%以上ではGrを添加しても接触
抵抗が低下せず温度上昇特性の向上が認められな
い。窒化物としてはTi、Zr、Nb、Cr、Mo、等
の4A、5A、6A族金属の窒化物が効果があり、そ
の量としては0.1〜30重量%が好ましく、特に0.5
〜20重量%が特性が良い。0.1重量%以下では耐
消耗性の効果が少なく、30重量%以上ではGrを
添加しても接触抵抗が上つて、温度上昇特性が逆
に低下するためである。
次にGrの有効範囲は1〜11重量%であり好ま
しくは3〜7重量%である。1重量%以下では鉄
族金属や炭化物が上記範囲内であつても温度上昇
特性の向上が認められず、又11重量%以上では合
金製造が困難であり実用性がない。
次に実施例によつて本発明による接点合金の特
徴を具体的に説明する。
実施例 1
第1表、第2表、第3表及び第4表に示した割
合で各粉末を配合し、混合後成型体を作り、該成
型体を水素雰囲気中で1100℃の温度で焼結した。
この焼結体を再加圧して気孔率が殆んど零の合金
を作製した。合金中第4表のものは比較材として
の従来の合金である。
TECHNICAL FIELD The present invention relates to electrical contact materials used in equipment that conducts current and switches on and off. In addition, it is particularly aimed at improving the properties of Ag-WC alloys. Conventionally, Ag-WC alloys have excellent arc resistance and welding resistance;
Widely used as contacts in equipment such as switches. However, in recent years, devices such as no-fuse breakers, disconnectors, switches, and other devices have become smaller and more sophisticated, and as a result, the load on contact materials has become severer, and contact performance has become worse. Improvement is strongly required. Additionally, due to the miniaturization of devices, there is a tendency for contact dimensions to become smaller and contact pressure to decrease, resulting in increased wear and tear that occurs when current is turned on or off, increased scattering, welding of contacts, deterioration of insulation of devices, and even lower rated current. Problems have arisen in that the temperature tends to rise when opening and closing. A contact made by adding graphite (Gr) to an Ag-WC alloy was developed as one way to meet the demand for improved characteristics. In this contact, Gr becomes a reducing gas due to the arc heat generated when opening and closing, preventing oxidation of WC, suppressing temperature rise, and increasing welding resistance due to the lubricity of Gr. However, the addition of Gr causes consumption and
The drawback was that the insulation properties deteriorated. For this reason, in small, high-performance circuit breakers and switches, the movable contacts contain Ag.
-The combination of Ag-WC-Gr contacts had to be used for WC contacts and fixed contacts. However, changing and combining materials for the movable part and the fixed part makes parts management extremely troublesome. Furthermore, even when using such a combination, the contact pressure is small in recent small, high-performance devices, and the arc heat generated during opening and closing often causes abnormal temperature rises, wear, insulation deterioration, and welding, and further improves contact performance. is requested. The present invention has been made in view of the above points, and has welding resistance, wear resistance, and insulation resistance.
In addition, the present invention provides a contact alloy with low temperature rise and excellent practicality. Furthermore, the alloy of the present invention provides an inexpensive contact alloy that can be used as a contact even if the amount of expensive silver is considerably reduced. The alloy according to the invention contains 4A in iron group metal and silver.
An electrical contact characterized by containing carbides of group 5A and 6A metals, nitrides and graphite of group 4A, 5A and 6A metals dispersed therein, and in which some or all of the carbides are dissolved in the iron group metal. It is the material. The inventors previously conducted various studies on alloys in which iron group metals and various carbides were added to silver, and as a result, they found that alloys in which some or all of the carbides were solidly dissolved in the iron group metals were generated when the current was switched on and off. It has been found that there is extremely little wear and tear due to arc heat, and the effect of reducing insulation deterioration and welding of equipment. Iron group metals and carbides have poor oxidation resistance and are oxidized by arc heat generated during opening and closing, increasing contact resistance and increasing the temperature of the equipment. Therefore, when Gr, which has excellent reducing properties, is added to the above contact alloy to prevent the oxidation of iron group metals and carbides, Gr decomposes with the heat of electrical switching and generates reducing gas, preventing the oxidation of iron group metals and carbides. It was found that the lubricity of Gr increases welding resistance, reduces contact resistance, reduces equipment temperature rise, and improves welding resistance due to the lubricity of Gr. In other words, carbide is solid-dissolved in iron group metals, which have excellent mechanical strength and bonding strength at high temperatures, to improve wear resistance and welding resistance. By adding conventional Ag-WC
We were able to obtain an alloy with high performance welding resistance, abrasion resistance, insulation resistance, and temperature rise characteristics that could not be expected from the Ag-WC-Gr type or Ag-WC-Gr type contacts. As a result of further research, the inventors found that
When nitrides of group 4A, 5A, and 6A metals are further added to this system, these nitrides react with carbides via Fe group metals during sintering at temperatures above the melting point of silver, and the carbides become fine. It was found that deformation at high temperatures was reduced. Furthermore, it has been found that the addition of these nitrides significantly improves arc wear resistance. These characteristics are thought to be due to the fact that the nitrides react with the dispersed Gr due to the arc heat generated during opening and closing to form carbides, and this reaction is an endothermic reaction and releases N2 gas, which has an arc-extinguishing effect. The figure shows the free energy change of this reaction, and it can be seen that this reaction proceeds almost at 1500㎜. Iron group metals are Fe, Co, Ni, 5-60% by weight
and preferably 10 to 50% by weight. 5
If it is less than % by weight, the iron group metal will be dispersed in the silver, and solid solution precipitation of carbides will not occur, resulting in no improvement in wear resistance. Also 60
If it exceeds the weight percentage, even if Gr is added, the contact resistance will not decrease and there will be no effect of improving the temperature rise characteristics. As carbides, 4A, 5A, and 6A group carbides such as W, Mo, Ta, Nb, Ti, and Cr are effective, and the amount thereof is preferably 5 to 50% by weight, particularly 20 to 50% by weight, which improves the properties. good. If the carbide content is less than 5% by weight,
The amount of carbide in Ag is too small, resulting in insufficient adhesion resistance, and even if Gr is added in an amount of 50% by weight or more, the contact resistance does not decrease and no improvement in temperature rise characteristics is observed. As the nitride, nitrides of group 4A, 5A, and 6A metals such as Ti, Zr, Nb, Cr, and Mo are effective, and the amount thereof is preferably 0.1 to 30% by weight, particularly 0.5% by weight.
~20% by weight has good properties. This is because if it is less than 0.1% by weight, the effect on wear resistance is small, and if it is more than 30% by weight, even if Gr is added, the contact resistance increases and the temperature increase property is adversely reduced. Next, the effective range of Gr is 1 to 11% by weight, preferably 3 to 7% by weight. If it is less than 1% by weight, no improvement in temperature rise characteristics will be observed even if the iron group metal or carbide is within the above range, and if it is more than 11% by weight, it will be difficult to manufacture the alloy and it will not be practical. Next, the characteristics of the contact alloy according to the present invention will be specifically explained with reference to Examples. Example 1 Each powder was blended in the proportions shown in Table 1, Table 2, Table 3, and Table 4. After mixing, a molded body was made, and the molded body was sintered at a temperature of 1100°C in a hydrogen atmosphere. concluded.
This sintered body was pressurized again to produce an alloy with almost zero porosity. Among the alloys, those in Table 4 are conventional alloys as comparative materials.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
上述のようにして作成した合金について
ASTM試験機により通電特性と消耗特性の評価
を行つた。条件としては、AC100V、50A、
pf1.0、接触圧力200gr、開離力200gr、接点形状
5×5×1.5tmmとし、2万回の開閉を行なつた。
2万回開閉での電圧のバラツキ幅と消耗量の結果
を第5表に示す。[Table] About the alloys made as described above
The current carrying characteristics and wear characteristics were evaluated using an ASTM testing machine. The conditions are AC100V, 50A,
pf1.0, contact pressure 200gr, opening force 200gr, contact shape 5x5x1.5tmm, and opened and closed 20,000 times.
Table 5 shows the results of voltage variation and amount of wear after 20,000 openings and closings.
【表】【table】
【表】
実施例 2
実施例1で作成した合金、A1、B2、C2及び比
較材D1、D2、D3、D4の合金から可動接点4×
7×2mmの寸法に、固定接点8×8×2mmの寸法
に切削加工したのち台金に抵抗ろう付けで接合せ
しめ、これを50A定格の配線用しや断器に組込み
下記に示す試験条件にて接点性能評価をした結
果、第6表を得た。
試験条件:
過負荷試験:AC220V、200Apf 50回
耐久試験:AC220V、50Apf 54回
温度上昇試験:AC220V、50A 2H
短絡試験:AC220V、7.5KA pf0.5、1PO−CO、
2PO−CO[Table] Example 2 Movable contacts 4× were made from the alloys prepared in Example 1, A1, B2, C2, and comparative materials D1, D2, D3, D4.
After cutting the fixed contact to a size of 8 x 8 x 2 mm to a size of 7 x 2 mm, it was bonded to the base metal by resistance brazing, and this was assembled into a 50A rated wiring cutter and tested under the test conditions shown below. As a result of contact performance evaluation, Table 6 was obtained. Test conditions: Overload test: AC220V, 200Apf 50 times Endurance test: AC220V, 50Apf 54 times Temperature rise test: AC220V, 50A 2H Short circuit test: AC220V, 7.5KA pf0.5, 1PO-CO,
2PO−CO
【表】【table】
【表】
第6表で示すように本発明合金は消耗量が少な
く温度上昇が低く、絶縁耐圧も高く高性能の接点
特性を有していることが判る。
本発明合金は上述の通り接点性能が優れている
のみでなく、鉄族金属、炭化物を多量に含有して
おり高価な銀量を大幅に節減できるので工業的価
値の高いものである。[Table] As shown in Table 6, it can be seen that the alloy of the present invention has low wear, low temperature rise, high dielectric strength and high performance contact characteristics. The alloy of the present invention not only has excellent contact performance as described above, but also contains a large amount of iron group metals and carbides, and the amount of expensive silver can be significantly reduced, so it is of high industrial value.
図は窒化物とグラフアイトから炭化物を生成す
る際の自由エネルギー変化を示す図である。
The figure shows the change in free energy when carbide is produced from nitride and graphite.
Claims (1)
が5〜50重量%、グラフアイト1〜11重量%、鉄
族金属5〜60重量%、4A、5A、6A族金属の窒化
物が0.1〜30重量%残部銀の焼結材からなること
を特徴とする電気接点材料。 2 炭化物がタングステン、モリブデン、タンタ
ル、ニオブ、チタン、クロムのうち少なくとも1
種の炭化物であることを特徴とする特許請求の範
囲1項記載の電気接点材料。 3 窒化物がチタン、ジルコニウム、ニオブ、ク
ロム、モリブデン、バナジウム、タンタルのうち
少なくとも1種の窒化物であることを特徴とする
特許請求の範囲1項記載の電気接点材料。[Claims] 1. 5 to 50% by weight of carbides of metals from groups 4A, 5A, and 6A of the periodic table of elements, 1 to 11% by weight of graphite, 5 to 60% by weight of iron group metals, 4A, 5A, and 6A. An electrical contact material comprising a sintered material containing 0.1 to 30% by weight of group metal nitride and the balance being silver. 2 The carbide is at least one of tungsten, molybdenum, tantalum, niobium, titanium, and chromium.
The electrical contact material according to claim 1, characterized in that it is a carbide of seeds. 3. The electrical contact material according to claim 1, wherein the nitride is at least one of titanium, zirconium, niobium, chromium, molybdenum, vanadium, and tantalum.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56110496A JPS5811753A (en) | 1981-07-15 | 1981-07-15 | electrical contact materials |
| DE19823213265 DE3213265A1 (en) | 1981-04-10 | 1982-04-08 | ELECTRICAL CONTACT MATERIAL |
| FR8206295A FR2503926B1 (en) | 1981-04-10 | 1982-04-09 | ELECTRIC CONTACT MATERIALS |
| US06/367,603 US4457780A (en) | 1981-04-10 | 1982-04-12 | Electric contact materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56110496A JPS5811753A (en) | 1981-07-15 | 1981-07-15 | electrical contact materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5811753A JPS5811753A (en) | 1983-01-22 |
| JPH0313295B2 true JPH0313295B2 (en) | 1991-02-22 |
Family
ID=14537224
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56110496A Granted JPS5811753A (en) | 1981-04-10 | 1981-07-15 | electrical contact materials |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5811753A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000510581A (en) * | 1996-03-29 | 2000-08-15 | ユニバーシティー オブ ブリティッシュ コロンビア | Platelet count assay using platelet granule protein |
| WO2011162107A1 (en) | 2010-06-22 | 2011-12-29 | 株式会社アライドマテリアル | Electrical contact material |
| JP4898977B2 (en) | 2010-06-22 | 2012-03-21 | 株式会社アライドマテリアル | Electrical contact material |
| JP5134166B2 (en) | 2010-09-21 | 2013-01-30 | 株式会社アライドマテリアル | Electrical contact material |
-
1981
- 1981-07-15 JP JP56110496A patent/JPS5811753A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5811753A (en) | 1983-01-22 |
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