JPS6047011B2 - Manufacturing method of electrical contact material - Google Patents
Manufacturing method of electrical contact materialInfo
- Publication number
- JPS6047011B2 JPS6047011B2 JP4257280A JP4257280A JPS6047011B2 JP S6047011 B2 JPS6047011 B2 JP S6047011B2 JP 4257280 A JP4257280 A JP 4257280A JP 4257280 A JP4257280 A JP 4257280A JP S6047011 B2 JPS6047011 B2 JP S6047011B2
- Authority
- JP
- Japan
- Prior art keywords
- bismuth
- silver
- contact material
- electrical contact
- oxide
- 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 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 229910052797 bismuth Inorganic materials 0.000 claims description 18
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 18
- 238000005096 rolling process Methods 0.000 claims description 9
- 229910052709 silver Inorganic materials 0.000 claims description 9
- 239000004332 silver Substances 0.000 claims description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- 239000000956 alloy Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 238000005245 sintering Methods 0.000 claims description 4
- 238000005266 casting Methods 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 238000000034 method Methods 0.000 description 12
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- ASMQPJTXPYCZBL-UHFFFAOYSA-N [O-2].[Cd+2].[Ag+] Chemical compound [O-2].[Cd+2].[Ag+] ASMQPJTXPYCZBL-UHFFFAOYSA-N 0.000 description 6
- CJQSUEBYPDGXEY-UHFFFAOYSA-N bismuth;oxosilver Chemical compound [Bi].[Ag]=O CJQSUEBYPDGXEY-UHFFFAOYSA-N 0.000 description 6
- 229910001152 Bi alloy Inorganic materials 0.000 description 5
- 229910000416 bismuth oxide Inorganic materials 0.000 description 5
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- CCXYPVYRAOXCHB-UHFFFAOYSA-N bismuth silver Chemical compound [Ag].[Bi] CCXYPVYRAOXCHB-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000010953 base metal Substances 0.000 description 3
- 229910052793 cadmium Inorganic materials 0.000 description 3
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 2
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 238000000304 warm extrusion Methods 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910000925 Cd alloy Inorganic materials 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000001192 hot extrusion Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Extrusion Of Metal (AREA)
- Manufacture Of Switches (AREA)
Description
【発明の詳細な説明】
本発明は、電気接点材料、特に銀−酸化ビスマスを主
成分とする複合接点材料の製造方法に関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an electrical contact material, particularly a composite contact material containing silver-bismuth oxide as a main component.
従来より、放電を伴なう中電流用ないし大電流用の接
点としては、銀−酸化カドミウムが、電気接点に要求さ
れる耐溶着性、耐消耗性、接触抵抗 などの諸特性に優
れているために、広く用いられている。Conventionally, silver-cadmium oxide has been used as contacts for medium to high currents that involve discharge, and has excellent properties such as welding resistance, abrasion resistance, and contact resistance required for electrical contacts. Therefore, it is widely used.
しかしながら、この銀−酸化カドミウム材料には、その
製造上、溶解、熱間加工、洗浄等の処理工程において、
カドミウムが外部に排出されやすいという問題があつて
、公害防止対策上好ましくなく、また一般社会的にも、
適合しにくい材料になりつつある。そこで、カドミウム
による公害問題を解消し、しかも銀−酸化カドミウムに
匹敵する新しい接点材料の開発が強く要求される・に至
り、近年、にわかに各種の研究開発が行なわれている。
発明者らは、すでに銀−酸化ビスマス系の複合材料を
開発し、この材料によつて、銀−酸化カドミウムの代替
が可能であるとの見通しを得たが、その製造については
粉末焼結法に限られ、その結果、接点特性上においては
、消耗量が多いという問題が存在した。However, this silver-cadmium oxide material has certain problems during its manufacturing process, such as melting, hot processing, and cleaning.
There is a problem that cadmium is easily discharged to the outside, which is not desirable in terms of pollution prevention measures, and also from the viewpoint of general society.
It is becoming a material that is difficult to adapt. Therefore, there has been a strong demand for the development of a new contact material that solves the problem of cadmium pollution and is comparable to silver-cadmium oxide, and in recent years, various research and development efforts have been carried out.
The inventors have already developed a silver-bismuth oxide-based composite material and have obtained the prospect that this material can replace silver-cadmium oxide, but the powder sintering method is not yet suitable for its production. As a result, there was a problem in terms of contact characteristics, such as a large amount of wear.
すなわち、通常、銀−酸化物系複合材料の製造法とし
ては、銀一酸化カドミウムを例にとるならば、銀−カド
ミウム合金のインゴットを作り、これを加工して最終接
点形状に近いものとし、酸化雰囲気中にて加熱して、カ
ドミウムを選択的に内部酸化させ、次にこれを素材とし
て、所望の接点形状に仕上げるいわゆる内部酸化法と、
銀粉末と酸化カドミウム粉末を均質に混合し、その後、
これを金型に装填してプレス成型し、加熱焼結するいわ
ゆる焼結法に大別される。In other words, the usual method for manufacturing silver-oxide composite materials, taking silver cadmium monoxide as an example, is to create an ingot of silver-cadmium alloy, process this to make it close to the final contact shape, A so-called internal oxidation method in which cadmium is selectively internally oxidized by heating in an oxidizing atmosphere, and then this is used as a material to form a desired contact shape.
Mix silver powder and cadmium oxide powder homogeneously, then
This is broadly classified into the so-called sintering method, in which the material is loaded into a mold, press-molded, and then heated and sintered.
近年、接点特性上の耐消耗性などの点から、小型の接点
製造においては、ほとんど内部酸化法が利用され、大型
の形状で内部酸化にきわめて長時間を要する場合のみ焼
結法が用いられるというのが実情である。しかるに、上
述したような銀一酸化ビスマス複合材料は、銀−ビスマ
ス合金がビスマスの固溶限界内すなわち5.1重量%以
下(600℃)であつても、冷間加工が極めて困難な材
料である。その加工が可能な方法は熱間鍛造、熱間押出
しのような加熱状態における加工法である。そのために
、最終的に内部酸化できるような形状まで加工すること
は、製造条件、製造設備にかなりの配慮が必要であつて
、これらの方法によつても困難なものである。ビスマス
合金が難加工材であるのは、ビスマスが脆い金属であり
、そして銀−ビスマス系の合金においては、結晶粒界ビ
スマスが偏析しやすく、したがつて、より難加工性材料
になつているためである。In recent years, the internal oxidation method is mostly used to manufacture small contacts due to wear resistance and other characteristics of contacts, and the sintering method is used only when large-sized contacts require an extremely long time for internal oxidation. That is the reality. However, the silver-bismuth monoxide composite material described above is a material that is extremely difficult to cold-work even if the silver-bismuth alloy is within the solid solubility limit of bismuth, that is, 5.1% by weight or less (600°C). be. Methods that allow this processing include processing methods in a heated state such as hot forging and hot extrusion. Therefore, processing to a shape that can ultimately be internally oxidized requires considerable consideration in manufacturing conditions and manufacturing equipment, and is difficult even with these methods. Bismuth alloys are difficult to process because bismuth is a brittle metal, and in silver-bismuth alloys, bismuth tends to segregate at grain boundaries, making them even more difficult to process. It's for a reason.
銀−ビスマス合金接点材料は、これまでにもいくつかそ
の例が見受けられる。それらのほとんどは、ビスマス含
有量が1重量%以下のものであつて、いずれもビスマス
濃度が上昇すると、加工が困難になることを指摘してい
る。また、上記材料では、ビスマスが粒界に析出する現
象を利用して、ビスマスを酸素のキャリアとして使用し
、酸化の遅い他の合金添加元素を酸化させて、所望の内
部酸化を達成するという方法がとられている。しかるに
、本発明の対象とする材料は、酸化ビスマスが主要成分
で、かつ、銀マトリクス中に均質に分散することが望ま
れ、上述のようなビスマスが結晶粒界に析出されるなら
ば、接点特性上において、所望の特性が得られなくなる
のは明白である。Several examples of silver-bismuth alloy contact materials have been seen so far. Most of them have a bismuth content of 1% by weight or less, and all of them point out that processing becomes difficult as the bismuth concentration increases. In addition, in the above materials, the desired internal oxidation is achieved by utilizing the phenomenon that bismuth precipitates at grain boundaries and using bismuth as an oxygen carrier to oxidize other alloy additive elements that oxidize slowly. is taken. However, the material targeted by the present invention has bismuth oxide as its main component, and it is desired that it be homogeneously dispersed in the silver matrix. It is clear that desired characteristics cannot be obtained.
本発明は、ビスマスを1重量%以上含む銀一酸化ビスマ
ス系接点材料の加工上における難点を解決し、内部酸化
法によつて得られる接点特性を享受し得る製造法を提供
するものである。The present invention solves the difficulties in processing silver-bismuth monoxide-based contact materials containing 1% by weight or more of bismuth, and provides a manufacturing method that can enjoy the contact characteristics obtained by internal oxidation.
本発明の対象となるビスマス酸化物は、各種の接点用添
加一物として利用される金属酸化物の中では、下記のよ
うに比較的硬度の低い酸化物と考えてよい。酸化カドミ
ウム・・・・・・3.0(鉱物スケール)酸化銅
・・・4.0酸化ビスマス ・・・・・4.5
酸化亜鉛 ・・・・4.5
酸化錫 ・・・・・6.5
酸化インジウム・・・・・・7.0
酸化アルミニウム・・・9.0
(サムソノフ監修、日ソ通信社、1酸化物便覧ョより)
したがつて、酸化ビスマスを銀マトリクスに均質に分散
すれば、比較的、加工性のよい材料が得・られるものと
予測される。Bismuth oxide, which is the object of the present invention, can be considered to be an oxide with relatively low hardness as described below among metal oxides used as additives for various contacts. Cadmium oxide...3.0 (mineral scale) copper oxide
...4.0 Bismuth oxide ...4.5 Zinc oxide ...4.5 Tin oxide ...6.5 Indium oxide ...7.0 Aluminum oxide ...・9.0 (Supervised by Samsonov, Nippon-Soviet Press, Monooxide Handbook)
Therefore, it is expected that if bismuth oxide is homogeneously dispersed in a silver matrix, a material with relatively good processability will be obtained.
発明者らは、この点について、種々実験研究した結果、
下記のような手法によれ、銀マトリクス中に、酸化ビス
マスを均質に分散させることが可能であることを見い出
した。まず、所望の組成比の銀−ビスマス合金を溶解し
てから、これを鋳造する。As a result of various experimental studies on this point, the inventors found that
We have discovered that it is possible to homogeneously disperse bismuth oxide in a silver matrix by the method described below. First, a silver-bismuth alloy having a desired composition ratio is melted and then cast.
鋳型は、水冷が望ましく、また水冷によらない場合には
、鋳込み量の10〜2@の重量を有する鉄製の鋳型が好
ましい。これは、溶湯を急冷鋳込みすることによつて、
ビ″スマスが偏析することを防止するためである。これ
により作製されるインゴットは、ただちに、圧延ロール
機によつて、荒粉砕し、合金粒とする。合粒の形状とし
ては、厚さが0.7〜2TG1好ましくは1.0〜1.
5TfrIn(7)鱗片状が好ましい。鱗片状とするに
は、圧延ロール機を用いて行なうが、合金の加工能が低
いため、圧延によりインゴットにクラックが入り、随時
適当な鱗片状粒子に転化される。次に、鱗片状の合金粒
に内部酸化処理を施し、合金中に含まれるビスマスを酸
化物とし、さらにその他の卑金属が含有されておれば、
それらをも含めて酸化物として銀地中に析出させる。内
部酸化処理は、酸化雰囲気中において600〜800℃
の加熱処理によつて行なわれる。次に、この内部酸化粒
を、再度圧延ロール機によつて厚さ0.7TIr1n以
下て先の荒粉砕時の粒子厚さの好ましくは50%以下と
する。このときに、上記酸化処理によつて銀マトリクス
中に分散した酸化物粒子は、粉砕され微細化されて、最
終線材としたときの機械加工性付与に大きな影響を及ぼ
す。0.7Tn!n以下の厚さに圧延された粉粒チップ
は、洗浄されたのち、円筒型に装填され、成型され、次
いで焼結される。The mold is preferably water-cooled, and if water-cooling is not used, an iron mold having a weight of 10 to 2@2 of the casting amount is preferred. This is achieved by rapidly cooling and casting the molten metal.
This is to prevent segregation of bismuth. The ingot thus produced is immediately coarsely crushed using a rolling mill to form alloy grains. 0.7-2TG1 preferably 1.0-1.
5TfrIn(7) is preferably scaly. A rolling mill is used to make the ingot into flakes, but since the processing ability of the alloy is low, the ingot cracks during rolling and is converted into appropriate flake-like particles at any time. Next, the flaky alloy grains are subjected to internal oxidation treatment to convert the bismuth contained in the alloy into an oxide, and if other base metals are also contained,
These are also deposited as oxides in the silver base. Internal oxidation treatment is performed at 600-800℃ in an oxidizing atmosphere.
This is done by heat treatment. Next, the internally oxidized grains are again milled to a thickness of 0.7 TIr1n or less, preferably 50% or less of the particle thickness during the previous rough crushing. At this time, the oxide particles dispersed in the silver matrix by the above-mentioned oxidation treatment are crushed and made into fine particles, which greatly affects the machinability imparted to the final wire rod. 0.7Tn! The powder chips rolled to a thickness of n or less are washed, loaded into a cylindrical shape, molded, and then sintered.
このようにして、作られた焼結円筒ビルツトは、温間押
出しによつて、素線材に加工される。このようにして作
製された素線材は、通常銀マトリクス中に10〜15重
量%の酸化物を含む状態において10〜20%の伸び率
を示し、接点鋲を作製するためのヘッダー加工などに十
分供し得る接点素材となる。前述の本発明の製法をより
明確にするために、次にその実施例をあげて説明する。The sintered cylinder built in this way is processed into a wire material by warm extrusion. The wire material produced in this way usually exhibits an elongation rate of 10 to 20% in a state containing 10 to 15% by weight of oxide in the silver matrix, which is sufficient for processing headers to make contact studs. It becomes a contact material that can be used. In order to make the above-mentioned manufacturing method of the present invention more clear, the following examples will be given and explained.
主要成分である銀,ビスマス,さらには必要に応じて、
他の添加金属を加えて総重量200gとし、それを溶解
した。The main ingredients are silver and bismuth, and if necessary,
Other additive metals were added to give a total weight of 200 g, which was dissolved.
溶解は、アルミナるつぼを使用し、アルゴン雰囲気にて
、高周波炉を用いて行なわれた。溶湯は、15×30×
70w1m3の寸法の製鉄鋳型に鋳込まれた。鋳型重量
は4k9程であり、インゴットが急冷され、ビスマスの
偏析が生じないように配慮した。このようにして作製し
たインゴットを、ただちに圧延機を用いて厚さ2〜0.
7?の小片に荒粉砕した。ビスマスを1重量%以上含む
銀合金は、冷間加工性がほとんどないため、厚さ15T
$Lのインゴットを圧延すると、おのずとクラックが入
り、鱗片状のチップに粉砕された。これを650′Cの
空気中にて、6C$111間加熱し、ビスマスおよびそ
の他に添加されている卑金属成分を選択的に酸化した。
この実施例においては、表に示すように、ビスマス以外
の卑金属元素として、錫,亜鉛,インジウムなどを使用
した。次に、これを再度圧延ロール機によつて、厚さを
前記小片の50%以下となるように粉砕圧延した。これ
を、溶剤にて洗浄した後、2077!77!径の円筒型
に装填し、8トン/C!lの圧力で成型し。次いで、こ
の成型体を800℃の温度で、空気中にて2時間加熱焼
結した。さらに、この焼結体を径20.577!77!
の温間加熱型に装填して、400℃、8トン/Aiの圧
力で成型し、再度800′Cの温度で空気中において4
時間焼結した。その後、この焼結体は、550℃の温間
押出しにより、3T$t径の線材に加工された。この線
材は、引き続いて2w0n径まで冷間伸線され、機械強
度、すなわち、引張り強さ、伸びを測定した。参考まで
に、この種の線材において、加工性の優れている銀一酸
化カドミウム(1鍾量%)の値を示す。この表の結果に
示されるように、本発明の製造法によれば、銀一酸化ビ
スマス系接点素線材においても、十分な加工性を有する
材料が得られるものであり、銀一酸化ビスマス系接点の
実用価値を5大巾に高めることができる。Melting was carried out using an alumina crucible in an argon atmosphere using a high frequency furnace. The molten metal is 15×30×
It was cast into a steel mold with dimensions of 70w1m3. The weight of the mold was approximately 4k9, and care was taken to ensure that the ingot was cooled rapidly and segregation of bismuth did not occur. The ingot thus produced was immediately rolled using a rolling mill to a thickness of 2 to 0.
7? coarsely ground into small pieces. Silver alloys containing 1% by weight or more of bismuth have almost no cold workability, so the thickness is 15T.
When the $L ingot was rolled, it naturally cracked and was crushed into scaly chips. This was heated in air at 650'C for 6C$111 to selectively oxidize bismuth and other base metal components added.
In this example, as shown in the table, tin, zinc, indium, etc. were used as base metal elements other than bismuth. Next, this was crushed and rolled again using a rolling mill so that the thickness was 50% or less of the above-mentioned small pieces. After washing this with a solvent, 2077!77! Loaded into a cylindrical shape with a diameter of 8 tons/C! Molded at a pressure of 1. Next, this molded body was heated and sintered in air at a temperature of 800° C. for 2 hours. Furthermore, this sintered body has a diameter of 20.577!77!
It was charged into a warm heating mold of
Sintered for hours. Thereafter, this sintered body was processed into a wire rod with a diameter of 3T$t by warm extrusion at 550°C. This wire was subsequently cold drawn to a diameter of 2w0n, and its mechanical strength, ie, tensile strength and elongation, were measured. For reference, the value of silver cadmium monoxide (1 weight %), which has excellent workability in this type of wire, is shown. As shown in the results in this table, according to the manufacturing method of the present invention, a material with sufficient workability can be obtained even for silver-bismuth monoxide-based contact wires, and silver-bismuth monoxide-based contacts The practical value of can be increased by 50%.
Claims (1)
し、それを冷却してインゴットとし、このインゴットを
、圧延ロール機で荒粉砕して小片とし、これを内部酸化
し、さらに、鱗片状の薄片に再度圧延してから、成型焼
結してビレツトを作り、これを押出して、接点の素材を
得ることを特徴とする電気接点素材の製造方法。 2 銀およびビスマスを主成分とする合金がビスマスを
少なくとも1重量%以上含むことを特徴とする特許請求
の範囲第1項記載の電気接点素材の製造方法。 3 圧延ロール機にて荒粉砕された小片の厚さが0.7
〜2mmの厚さであることを特徴とする特許請求の範囲
第1項記載の電気接点素材の製造方法。 4 圧延ロール機にて再粉砕された鱗片状チップの厚さ
が、荒粉砕された小片の厚さの50%以下であることを
特徴とする特許請求の範囲第1項記載の電気接点素材の
製造方法。[Claims] 1. Casting a molten metal of an alloy containing silver and bismuth as main components, cooling it to form an ingot, coarsely crushing the ingot into small pieces using a rolling mill, and internally oxidizing the ingot. A method for producing an electrical contact material, further comprising rolling the material into a scale-like thin piece again, forming and sintering it to form a billet, and extruding the billet to obtain a contact material. 2. The method for producing an electrical contact material according to claim 1, wherein the alloy containing silver and bismuth as main components contains at least 1% by weight of bismuth. 3 The thickness of the small pieces roughly crushed by the rolling mill is 0.7
2. The method of manufacturing an electrical contact material according to claim 1, wherein the material has a thickness of 2 mm. 4. The electrical contact material according to claim 1, characterized in that the thickness of the scale-like chips re-pulverized with a rolling mill is 50% or less of the thickness of the coarsely-pulverized small pieces. Production method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4257280A JPS6047011B2 (en) | 1980-03-31 | 1980-03-31 | Manufacturing method of electrical contact material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4257280A JPS6047011B2 (en) | 1980-03-31 | 1980-03-31 | Manufacturing method of electrical contact material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56139220A JPS56139220A (en) | 1981-10-30 |
| JPS6047011B2 true JPS6047011B2 (en) | 1985-10-19 |
Family
ID=12639774
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4257280A Expired JPS6047011B2 (en) | 1980-03-31 | 1980-03-31 | Manufacturing method of electrical contact material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6047011B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW517095B (en) | 1999-04-23 | 2003-01-11 | Tanaka Precious Metal Ind Co L | Method for producing Ag-ZnO electric contact material and electric contact material produced thereby |
-
1980
- 1980-03-31 JP JP4257280A patent/JPS6047011B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56139220A (en) | 1981-10-30 |
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