JPS59580B2 - Silver-oxide electrical contact materials - Google Patents

Silver-oxide electrical contact materials

Info

Publication number
JPS59580B2
JPS59580B2 JP52106522A JP10652277A JPS59580B2 JP S59580 B2 JPS59580 B2 JP S59580B2 JP 52106522 A JP52106522 A JP 52106522A JP 10652277 A JP10652277 A JP 10652277A JP S59580 B2 JPS59580 B2 JP S59580B2
Authority
JP
Japan
Prior art keywords
oxide
silver
electrical contact
weight
contact
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
Application number
JP52106522A
Other languages
Japanese (ja)
Other versions
JPS5383926A (en
Inventor
正雄 高橋
博信 山本
喬 奈良
憲博 井手
治 渡辺
勇三 山本
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.)
Tokuriki Honten Co Ltd
Original Assignee
Tokuriki Honten 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 Tokuriki Honten Co Ltd filed Critical Tokuriki Honten Co Ltd
Priority to JP52106522A priority Critical patent/JPS59580B2/en
Publication of JPS5383926A publication Critical patent/JPS5383926A/en
Publication of JPS59580B2 publication Critical patent/JPS59580B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Contacts (AREA)
  • Conductive Materials (AREA)

Description

【発明の詳細な説明】 本発明は新規な電気接点材料に関するもので特に従来よ
り比較的小電流のリレーからマグネットスイッチやブレ
ーカ−などの大電流域まで広汎に用いられてきた銀−酸
化カドミウム電気接点材料に代って、CdOを排し代替
酸化物を含有させるようにした銀合金接点材料に係るも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel electrical contact material, particularly silver-cadmium oxide electrical contact materials, which have been widely used in the past from relatively small current relays to large current ranges such as magnetic switches and breakers. This invention relates to a silver alloy contact material that excludes CdO and contains an alternative oxide instead of the contact material.

従来より電気接点材料としては種々のものが用いられて
いるが、特に銀−酸化カドミウム系接点は電気接点とし
て要求される耐溶着性、耐消耗性、低接触抵抗などの諸
電気特性にすぐれているため、その需要も年々上昇して
いるだけでなく、材料面の改良も重ねられており、また
これに関する学術的研究も多く、いわばこの系の材料、
製造技術の進歩は極限にまで達したといえよう。
Various materials have been used as electrical contact materials, but silver-cadmium oxide contacts in particular have excellent electrical properties such as welding resistance, abrasion resistance, and low contact resistance required for electrical contacts. Therefore, not only is the demand for this material increasing year by year, but the materials have also been improved over time, and there are many academic studies related to this.
It can be said that progress in manufacturing technology has reached its limit.

しかしながらこの銀−カドミウム系電気接点材料は既知
のようにその製造上、溶解、熱間加工、高温酸化、分析
及び回収などカドミウムを系外に排出し易い多数の工程
が含まれるので、当然その排出防止に努めなければなら
ず、このため殊に生産設備の拡大に伴って美大な公害防
止設備が必要となり、当該防止に多大なエネルギーが消
費されエネルギー資源問題にまで発展しようとしている
However, as is known, the production of this silver-cadmium electrical contact material involves many processes that easily discharge cadmium out of the system, such as melting, hot processing, high-temperature oxidation, analysis, and recovery. Efforts must be made to prevent pollution, and for this reason, especially with the expansion of production facilities, large-scale pollution prevention equipment is required, and a large amount of energy is consumed in the prevention, which is about to develop into an energy resource problem.

このため銀−酸化カドミウムによる当該製品を製造する
業者はこれに対し勿論充分な対策を構しているが、その
対策が十分であるからというだけでは、最早公害に対す
る社会情勢に対応していけず、このような接点だけを考
えていたのでは美大な設備投資により生産価格にまで重
大な影響を与えることになる。
For this reason, manufacturers of silver-cadmium oxide products have of course taken sufficient measures against this, but just because these measures are sufficient, it is no longer possible to respond to the social situation regarding pollution. If only such points of contact were considered, the huge capital investment would have a serious impact on production prices.

更に又鎖中に酸化カドミウムを分散させることは、接点
表面の清浄作用、溶着力の低減などの電気的緒特性を改
善するものとして確かに効果的であるが、このような効
果を充分に果してきたのは特に交流回路においてであり
、極性の変化しない直流回路において当該接点材料を使
用したときは、比較的耐溶着性に乏しく接点の開閉によ
る接触抵抗の増加にも著しい難点があるのであって、そ
の原因は当該接点のアノード側からカソード側に向って
アノード成分が転移し、カソードの接続部に接点母材と
異なる一種の変質層を形成するためと提唱されており、
この欠点はCdOを用いる限り解消できぬ宿命ともいえ
よう。
Furthermore, dispersing cadmium oxide in the chain is certainly effective in improving electrical characteristics such as cleaning the contact surface and reducing welding force, but it is not possible to fully achieve these effects. This is especially true in AC circuits, and when this contact material is used in DC circuits where the polarity does not change, it has relatively poor welding resistance and has a significant drawback in increasing contact resistance when the contacts open and close. It has been proposed that the cause of this is that the anode component transfers from the anode side to the cathode side of the contact, forming a type of altered layer at the cathode connection that is different from the contact base material.
This drawback can be said to be a fate that cannot be overcome as long as CdO is used.

そこで上記の如きカドミウムによる公害問題を解消し、
しかもAg−Cd0系の電気接点材料に匹敵する新しい
材質の開発が注目されるに至り、近時にわかに各種の研
究がなされはじめ、鎖中にLaの酸化物を分散させた電
気接点材料(日本金属学会誌第36巻8号765頁(1
972))なども発表されているわけである。
Therefore, we solved the pollution problem caused by cadmium as mentioned above,
Moreover, the development of new materials comparable to Ag-Cd0-based electrical contact materials has attracted attention, and recently various researches have begun to be conducted. Academic Journal Vol. 36, No. 8, p. 765 (1)
972)) have also been announced.

しかしこのような開発の理論的根拠の一端はAgに分散
すべき酸化物の揮発し易さを尺度として、一般にはCd
Oよりも蒸気圧の低い酸化物の方が効果的であり、しか
も蒸気圧の低い酸化物を用いる方が電気接点としての開
閉時に生ずるアークにより接点表層から逸散した成分を
、拡散により接点内部から補う割合が少くなるので、八
gに対する酸化物の添加量が少くても効果的であるとも
提唱され、実際にそのような酸化物をCdOの代りに用
いることが提案されているのである。
However, part of the theoretical basis for such development is that Cd is generally used as a measure of the volatilization of oxides to be dispersed in Ag.
An oxide with a lower vapor pressure is more effective than O, and the use of an oxide with a lower vapor pressure allows the components dissipated from the surface layer of the contact due to the arc that occurs when opening and closing the electrical contact to be diffused into the inside of the contact. It has been proposed that it is effective even if the amount of oxide added to 8g is small because the supplementation ratio is small, and it has actually been proposed to use such an oxide in place of CdO.

本発明は斜上の諸点に鑑み、Cd成分を含まない酸化物
の接点特性に寄与する役割について再検討を行い、この
結果上記の如き既成観念を排し考想を新たにして研究を
重ねたもので、その思考基盤は電気接点の表面の清浄化
作用やアークに対する諸現象、例えば消弧作用などが、
添加する酸化物の特性、特にその蒸気圧の温度特性に最
も関係が深いとする考え方に基づいている。
In view of the above points, the present invention reconsidered the role of oxides that do not contain Cd components in contributing to the contact characteristics, and as a result, we rejected the preconceived notions mentioned above, renewed our thinking, and conducted repeated research. The basis of this idea is that the cleaning effect on the surface of electrical contacts and various phenomena related to arcs, such as arc extinguishing effects, are
It is based on the idea that it is most closely related to the characteristics of the oxide to be added, especially its vapor pressure and temperature characteristics.

そこで本発明の目的は当該蒸気圧に関し、約500〜1
500℃の温度範囲でCdOの蒸気圧より高い酸化物に
着目し、この中で毒性の少ないsb酸化物をAg中に含
有させることにより、Ag−Cd0系のものと同等以上
の接点表向清浄化作用を発揮させるようにするだけでな
く、さらにsbの酸化物だけでなく、Agに固溶し難い
Be、Ca、CoXFeXNi、5iXTh、TiXZ
rの酸化物一種を分散することにより、合金製造工程中
における中乃至高温処理によって、当該合金の結晶粒が
粗大化する欠点を防止し、以て結晶粒を一層微細化しよ
うとするにある。
Therefore, the object of the present invention is to reduce the vapor pressure to approximately 500 to 1
Focusing on oxides with a higher vapor pressure than CdO in the temperature range of 500°C, by incorporating sb oxide, which is less toxic, into Ag, surface cleaning of the contact is equivalent to or higher than that of Ag-CdO type. In addition to oxidation of sb, Be, Ca, CoXFeXNi, 5iXTh, and TiXZ, which are difficult to dissolve in Ag, are
By dispersing one type of oxide of r, it is possible to prevent the crystal grains of the alloy from becoming coarse due to medium to high temperature treatment during the alloy manufacturing process, and thereby to further refine the crystal grains.

上記目的を有する本発明の特徴は銀を主成分とし、これ
に金属成分が0.1〜6.2重量%となるsbの酸化物
と、金属成分が0,01〜1.5重量%となるB e
XCa 、COXF e XN iXS I XT h
%Ti、Zrの酸化物一種とが分散されていることに
ある。
The feature of the present invention having the above object is that silver is the main component, and sb oxide with a metal component of 0.1 to 6.2% by weight and a metal component of 0.01 to 1.5% by weight are added. Naru Be
XCa, COXF e XN iXS I XT h
%Ti and one kind of oxide of Zr are dispersed.

このような電気接点材料を製造するには既知のように焼
結法(粉末冶金法)によっても内部酸化法(溶製法)に
よってもよいが、生産コスト上から後者が多用されるこ
と5なる。
Although such electrical contact materials can be manufactured by the known sintering method (powder metallurgy method) or internal oxidation method (melting method), the latter method is often used due to production costs5.

そして溶製法の場合には、sbと上記BeXCa。In the case of the melting method, sb and the above BeXCa.

Co等を固溶させた銀合金につき、これを酸化雰囲気中
で高温に保持させることにより、その表面より酸素を侵
入させながら、長時間当該酸化を続けることにより素材
中に、全面的にSbc!:Be、Ca、Co等の酸化物
を分散させること\なり、一方焼結の場合にはAg微粉
とSb1そしてBe。
By holding a silver alloy containing Co, etc. as a solid solution at a high temperature in an oxidizing atmosphere and continuing the oxidation for a long time while allowing oxygen to penetrate from the surface, Sbc! : Dispersing oxides such as Be, Ca, Co, etc. On the other hand, in the case of sintering, Ag fine powder, Sb1 and Be are used.

Ca、 Co等の粉末を混合し、加圧成形後に焼結した
ものを酸化してから焼結したり、あるいはよく混合させ
た酸化アンチモン粉と酸化べjJ IJウム粉、酸化カ
ルシウム粉、酸化コバルト粉等を加圧焼成することによ
って当該酸化物が鎖中に分散せる銀−酸化物系の電気接
点材料を製することもできるのである。
Mix powders of Ca, Co, etc., sinter after pressure forming, oxidize and sinter, or mix well with antimony oxide powder, benzium oxide powder, calcium oxide powder, cobalt oxide powder. It is also possible to produce a silver-oxide electrical contact material in which the oxide is dispersed in the chain by pressurizing the powder or the like.

しかしこの際どのような製法によるにせよ、sbの酸化
物はその金属成分であるsbが0.1〜6.2重量%で
なくてはならず、こ5でAgへのsb添加量の上限を6
.2重量%に限定しなければならない理由は、Ag−S
b合金のα個溶体におけるsbの最大固溶限が、300
°Cで6,2重量%であり、この添加量を超過するsb
を添加した場合には著しく加工性が阻害されること\な
り電気接点材料の量産が不能となるからである。
However, no matter what manufacturing method is used at this time, the sb oxide must contain 0.1 to 6.2% by weight of sb, which is the metal component, and this 5 sets the upper limit for the amount of sb added to Ag. 6
.. The reason why it must be limited to 2% by weight is that Ag-S
The maximum solid solubility limit of sb in α individual solution of b alloy is 300
6,2% by weight at °C and exceeding this addition amount sb
This is because, if added, the processability will be significantly inhibited, making it impossible to mass produce the electrical contact material.

また前記焼結法により製造した場合にあっても、粒子間
の結合力が弱いためアーク消耗量が多く接点材料として
望ましい特性が得られなくなる。
Furthermore, even when manufactured by the sintering method, the bonding force between the particles is weak, so arc consumption is large and desirable properties as a contact material cannot be obtained.

一方0.1重量%未満の添加量であると、後述するよう
な添加効果が得られず、その目的を達成し得ないこと5
なる。
On the other hand, if the amount added is less than 0.1% by weight, the addition effect described below cannot be obtained and the purpose cannot be achieved5.
Become.

さらに本発明では前記の如<Be、CaXCo、Fe、
NiX5iXThXTi、Zrの酸化物を金属成分が0
.05〜55〜5重量%範囲で分散させる必要がある。
Furthermore, in the present invention, as described above, <Be, CaXCo, Fe,
NiX5iXThXTi, Zr oxide with 0 metal components
.. It is necessary to disperse in the range of 0.05 to 55 to 5% by weight.

こ\で上記の如き添加元素は、何れもsbがAgに対し
て可溶性であり、再結晶組織における結晶粒の微細化に
寄与するものでないのに反し、Agに対して難溶性であ
るため、当該添加により結晶粒の成長を積極的に抑制し
、内部酸化などの高温処理においても、微細な結晶を維
持でき、また酸化物の粒子を極く微細なものとして、耐
アーク消耗性や耐溶性などの接点特性を向上させる効果
がある。
In this case, the above-mentioned additive elements are poorly soluble in Ag, whereas sb is soluble in Ag and does not contribute to the refinement of crystal grains in the recrystallized structure. This addition actively suppresses the growth of crystal grains, maintaining fine crystals even during high-temperature treatments such as internal oxidation, and makes the oxide particles extremely fine, improving arc wear resistance and melting resistance. It has the effect of improving contact characteristics such as.

しかしこれら添加元奏の添加量は、その添加方法につき
工夫をこらしても2重量係以上は技術的に困難であると
いうだけでなく、1.5重量係を越えた添加は粒界、粒
内に偏在して材料の均質化が得られず、接点特性に悪影
響を及ぼすこと\なり、また0、01重量係満たない添
加では、結晶粒や酸化物粒子の抑制効果が期待できない
However, it is not only technically difficult to add more than 2 weight ratios even if we try to improve the addition method; If the amount is less than 0.01% by weight, no effect of suppressing crystal grains or oxide particles can be expected.

こ5で本発明の一実施例を示せば99.5重量係以上の
純度を有するAgXSbそしてBeXCa、Co等の原
料を用い、これを大気中にてガス溶解することにより、
AgにSb3重量重量Ti0.3重量係が含有された鋳
塊を製造し、この鋳塊の表層を面側後、その一面に薄い
純銀板を熱圧着して、ろう付は用の銀層を形成する。
Here, one embodiment of the present invention is shown by using raw materials such as AgXSb, BeXCa, and Co having a purity of 99.5 weight coefficient or higher, and by dissolving them in gas in the atmosphere.
An ingot containing 0.3% by weight of Sb3 and 0.3% by weight of Ti is produced in Ag, and after the surface layer of this ingot is face-sided, a thin pure silver plate is thermocompression bonded to one side, and a silver layer for brazing is applied. Form.

次に当該素材を冷間圧延して厚さ2關の板にした後、プ
レス機により直径5mmの円盤状に打抜き、これを内部
酸化炉に入れ、大気を炉内に導入しな**から650℃
で180時間加熱し、5bXTiを酸化して本発明合金
を製造した。
Next, the material is cold-rolled into a plate with a thickness of 2 mm, then punched into a disc shape with a diameter of 5 mm using a press machine, and placed in an internal oxidation furnace, without introducing atmospheric air into the furnace. 650℃
The alloy of the present invention was produced by heating for 180 hours to oxidize 5bXTi.

さらに上記方法と全く同一の工程により、(イ)Ag
−3%Sb 0.3 %Fe(ロ)A、g−3%5
b−0,3%N’i(ハ)Ag −3%Sb −0,3
%C。
Furthermore, by the same process as the above method, (a) Ag
-3%Sb 0.3%Fe(b)A, g-3%5
b-0,3%N'i (c)Ag -3%Sb -0,3
%C.

に)Ag −3%Sb −0,3%Be (ホ)Ag −3%Sb 0.3 %Ca(へ)A
g −3係5b−0,3係S1 (ト) Ag −3%Sb O,
3つbTh(ffi Ag −3%Sb −0,3%
Zrの本発明合金を得た。
)Ag -3%Sb -0.3%Be (E)Ag -3%Sb 0.3%Ca (He)A
g -3rd unit 5b-0, 3rd unit S1 (g) Ag -3%Sb O,
3bTh(ffi Ag -3%Sb -0,3%
A Zr alloy according to the invention was obtained.

そして接点試験用として上記各種合金の裏側に形成され
た銀層と接点保持用の台座とを銀ろう付けして試料とし
、接点試験にはASTM接点試験機(AC100V、3
0A)、アーク消耗試験機(AC200V、10A)を
用い、従来多く利用されている代表的な電気接点材料と
比較しながら下表にあげた各項ごとに試験条件を選定し
、各接点材とも同一条件下で試験を行った。
For contact testing, the silver layer formed on the back side of the above various alloys and the pedestal for holding contacts were soldered with silver to prepare a sample.
Using an arc wear tester (AC200V, 10A), we selected test conditions for each item listed in the table below while comparing with typical electrical contact materials that have been widely used in the past. Tests were conducted under the same conditions.

以上のように本発明によれば、上表の如<Ag−Ca2
系合金と略同程度の特性をもち、その消費量ではむしろ
稍低減でき、しかも溶着回数も可成り低下させることが
できたのであり、勿論Cdの不使用により公害の心配を
も解消することができた。
As described above, according to the present invention, <Ag-Ca2
It has almost the same properties as the other alloys, and the amount consumed can be reduced considerably, and the number of welds can also be significantly reduced.Of course, the non-use of Cd also eliminates concerns about pollution. did it.

Claims (1)

【特許請求の範囲】[Claims] 1 銀を主成分とし、これに金属成分が0.1〜6.2
重量%となるsbの酸化物と、金属成分が0.01〜1
.5重量%となるBe、CalCoXFelNiXSl
% Th、TiXZrの酸化物一種とが分散されている
ことを特徴とする銀−酸化物系の電気接点材料。
1 The main component is silver, and the metal component is 0.1 to 6.2
sb oxide and metal component are 0.01 to 1% by weight
.. 5% by weight of Be, CalCoXFelNiXSl
% Th, a type of oxide of TiXZr is dispersed therein.A silver-oxide-based electrical contact material.
JP52106522A 1977-09-05 1977-09-05 Silver-oxide electrical contact materials Expired JPS59580B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52106522A JPS59580B2 (en) 1977-09-05 1977-09-05 Silver-oxide electrical contact materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52106522A JPS59580B2 (en) 1977-09-05 1977-09-05 Silver-oxide electrical contact materials

Publications (2)

Publication Number Publication Date
JPS5383926A JPS5383926A (en) 1978-07-24
JPS59580B2 true JPS59580B2 (en) 1984-01-07

Family

ID=14435725

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52106522A Expired JPS59580B2 (en) 1977-09-05 1977-09-05 Silver-oxide electrical contact materials

Country Status (1)

Country Link
JP (1) JPS59580B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58107447A (en) * 1981-12-18 1983-06-27 Tanaka Kikinzoku Kogyo Kk Material for sliding contact

Also Published As

Publication number Publication date
JPS5383926A (en) 1978-07-24

Similar Documents

Publication Publication Date Title
KR100194504B1 (en) Manufacturing Method of Silver-Metal Oxide Composite
US5236523A (en) Silver- or silver-copper alloy-metal oxide composite material
US4672008A (en) Internal oxidized Ag-Sn-In system alloy electrical contact composite
JPH0135914B2 (en)
Pandey et al. Comparison of properties of silver-tin oxide electrical contact materials through different processing routes
JPS59580B2 (en) Silver-oxide electrical contact materials
JP4947850B2 (en) Method for producing Ag-oxide based electrical contact material
US3508320A (en) Electrical contact materials and method of making same
JPS6128733B2 (en)
JPS5925018B2 (en) Silver monoxide-based electrical contact materials
JPH0120216B2 (en)
JPS5925017B2 (en) Silver monoxide-based electrical contact materials
JPH04289139A (en) Silver-oxide type electrical contact material
JPH04235234A (en) Electrical contact material of silver-oxide series
JPH04289140A (en) Silver-oxide type electrical contact material
JPH04235239A (en) Electrical contact material of silver-oxide series
JPH04235235A (en) Electrical contact material of silver-oxide series
JPH04235237A (en) Electrical contact material of silver-oxide series
JPH04235238A (en) Electrical contact material of silver-oxide series
JPH04235236A (en) Electrical contact material of silver-oxide series
JPH04289141A (en) Silver-oxide type electrical contact material
JPS6367536B2 (en)
JPH0463137B2 (en)
JPS6367537B2 (en)
TWI307102B (en)