JPH02225636A - Manufacture of electrical contact material - Google Patents
Manufacture of electrical contact materialInfo
- Publication number
- JPH02225636A JPH02225636A JP4477089A JP4477089A JPH02225636A JP H02225636 A JPH02225636 A JP H02225636A JP 4477089 A JP4477089 A JP 4477089A JP 4477089 A JP4477089 A JP 4477089A JP H02225636 A JPH02225636 A JP H02225636A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- electrical contact
- ag2o
- contact material
- moo3
- 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
Links
Landscapes
- Powder Metallurgy (AREA)
- Manufacture Of Switches (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は電気接点材料の製造方法、特に粉末冶金法によ
って製造されるAg系電気接点材料の製造方法に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for producing an electrical contact material, and particularly to a method for producing an Ag-based electrical contact material produced by a powder metallurgy method.
(従来技術とその問題点)
AgとAgに固溶しにくい金属(Mo、WlTi、Cr
、Coなど)の複合材料を電気接点として用いた場合の
一般的特徴として低接触抵抗特性や耐消耗特性には優れ
ているものの、耐溶着特性特に初期溶着を起こし易い。(Prior art and its problems) Ag and metals that are difficult to dissolve in Ag (Mo, WlTi, Cr)
, Co, etc.) are generally used as electrical contacts, although they are excellent in low contact resistance and wear resistance, they are susceptible to welding resistance, particularly initial welding.
たとえばワイブル分布パラメーターmで耐溶着性をみた
場合、mく1で初期溶着型に分類され、この欠点が致命
的欠点とされていた。また接点開閉時の消耗量は焼結密
度と関係があり、密度が不充分な場合、急激な消耗をも
らすものであった。For example, when looking at the welding resistance using the Weibull distribution parameter m, if m is less than 1, it is classified as an early welding type, and this defect was considered to be a fatal defect. Furthermore, the amount of wear during opening and closing of contacts is related to the sintered density, and if the density is insufficient, rapid wear occurs.
従来のAg+ (Agと固溶しにくい金属)材料の製造
方法はAg粉末とAgと固溶しにくい金属粉末を混合し
た後、圧縮、焼結、押出により所望形状のワイヤーに成
形していたが、このワイヤー中のAgと固溶しにくい金
属の粒子は10μm〜数10μmに凝集してしまってい
た。これは粉末の表面エネルギーが高いため、混合時に
同一金属粉が凝集してしまうからと考えられる。つまり
ワイヤー中のAgに固溶しにくい金属粒子の分散が均一
微細でないため初期溶着を起こすのである。The conventional manufacturing method for Ag+ (a metal that is difficult to form a solid solution with Ag) is to mix Ag powder and a metal powder that is difficult to form a solid solution with Ag, and then form it into a wire of the desired shape by compression, sintering, and extrusion. The metal particles in this wire, which are difficult to form a solid solution with Ag, had aggregated to a size of 10 μm to several tens of μm. This is thought to be because the powder has a high surface energy, so the same metal powders aggregate during mixing. In other words, the initial welding occurs because the metal particles, which are difficult to dissolve in Ag in the wire, are not uniformly and finely dispersed.
また粉末処理および焼結時にブリスターかのこり接点の
急激な消耗が問題となっていた。Also, rapid wear of the blisters and contacts during powder processing and sintering was a problem.
そこで本発明者等は鋭意攻究の結果、初期溶着を起こさ
ず、接点開閉時の急激な消耗の少ない電気接点材料の製
造方法を開発したものである。As a result of intensive research, the inventors of the present invention have developed a method for manufacturing electrical contact materials that does not cause initial welding and is less likely to be rapidly worn out when the contacts are opened and closed.
(問題点を解決するだめの手段)
本発明の製造方法は粉末冶金法により電気接点材料を製
造する方法においてAg粉末とAgに固溶しにくい金属
粉末両方を金属酸化物粉末として混合した後、その金属
酸化物粉末を還元することを特徴とするものである。す
なわち金属粉末を酸化物粉末として混合することによっ
て凝集を防ぐと同時に金属酸化物の脆性を生かし混合時
に金属酸化物粉末をくだき、粒子を微細にすることをね
らったものである。したがってAgと固溶しにくい金属
以外の金属を添加剤として添加してもこれらの効果は阻
害されない。(Means for Solving the Problems) The manufacturing method of the present invention is a method for manufacturing electrical contact materials by powder metallurgy, in which both Ag powder and metal powder that is difficult to dissolve in Ag are mixed as metal oxide powder, and then It is characterized by reducing the metal oxide powder. That is, the aim is to prevent agglomeration by mixing metal powder as oxide powder, and at the same time to take advantage of the brittleness of metal oxide and break up the metal oxide powder during mixing to make the particles finer. Therefore, these effects are not inhibited even if metals other than metals that are difficult to form a solid solution with Ag are added as additives.
なお混合装置としてはV型混合機、ボールミル、粉砕機
などがあり、これらを併用してもよい。また金属酸化物
粉末の還元はH20生成発熱による急激な焼結収縮をさ
けるため段階的に行なう事が好ましく、まず300〜5
00℃で酸化銀を加熱分解した後、500〜950℃で
酸化モリブデン又は酸化タングステンを還元することに
より、ブリスターの少ない焼結体を得る事ができる。こ
の為密度の上昇が不充分なためにおこる接点開閉時の急
激な消耗量の増加をおさえることに成功した。The mixing device includes a V-type mixer, a ball mill, a pulverizer, and the like, and these may be used in combination. In addition, it is preferable to reduce the metal oxide powder in stages to avoid rapid sintering shrinkage due to heat generated by H20.
By thermally decomposing silver oxide at 00°C and then reducing molybdenum oxide or tungsten oxide at 500 to 950°C, a sintered body with fewer blisters can be obtained. As a result, we succeeded in suppressing the rapid increase in consumption when opening and closing contacts, which occurs due to insufficient increase in density.
(比較例1)
A g −M o 10wt%合金となるように調整し
たAg粉末とM003粉末をV型混合機により3時間予
備混合後、内径50φ報のルツボに充填して温度800
℃H2雰囲気で還元処理した。次に圧縮、焼結を繰返し
、熱間で押出し、引抜加工して2.5φ叩及び2φ順の
線材とした。この線材の断面を金属顕微鏡で観察したと
ころ、Mo粒子は全て5μm以下であった。(Comparative Example 1) Ag powder and M003 powder adjusted to form an A g -Mo 10 wt% alloy were premixed for 3 hours using a V-type mixer, and then filled into a crucible with an inner diameter of 50φ and heated to a temperature of 800.
Reduction treatment was carried out in a H2 atmosphere. Next, compression and sintering were repeated, followed by hot extrusion and drawing to produce wire rods in the order of 2.5φ and 2φ. When the cross section of this wire was observed with a metallurgical microscope, all Mo particles were 5 μm or less in size.
(比較例2)
Ag−W10wt%合金となるように調整したAg粉末
とWO1粉末をV型混合機により3時間予備混合後、内
径50φmmのルツボに充填して温度800’c H2
雰囲気で還元処理した。次に圧縮、焼結を繰返し、熱間
で押出し、引抜加工して2.5φ止及び2φ■の線材と
した。この線材の断面を金属顕微鏡で観察したところW
粒子は全て5μm以下であった。(Comparative Example 2) Ag powder and WO1 powder adjusted to form an Ag-W10wt% alloy were premixed for 3 hours using a V-type mixer, then filled into a crucible with an inner diameter of 50φmm and heated to a temperature of 800'C H2.
Reduction treatment was carried out in the atmosphere. Next, compression and sintering were repeated, followed by hot extrusion and drawing to obtain wire rods of 2.5φ and 2φ. When the cross section of this wire was observed with a metallurgical microscope, W
All particles were 5 μm or less.
(従来例)
Ag粉末450 gとW粉末50gをV型混合機にて3
時間混合後、内径50a*の金型に充填して、温度80
0℃真空中で1時間熱処理を行った。次に圧縮、焼結を
繰返し、熱間押出し、引抜加工して2.5φ閤及び2φ
■の線材となした。この線材の断面を金属顕微鏡で観察
したところ、W粒子は15μm〜60μmの範囲であっ
た。(Conventional example) 450 g of Ag powder and 50 g of W powder were mixed in a V-type mixer.
After mixing for a while, it is filled into a mold with an inner diameter of 50a*, and the temperature is 80℃.
Heat treatment was performed in a vacuum at 0° C. for 1 hour. Next, compression and sintering were repeated, hot extrusion, and drawing were performed to form 2.5φ and 2φ
■It was made into a wire rod. When the cross section of this wire was observed with a metallurgical microscope, the W particles were in the range of 15 μm to 60 μm.
上記実施例1,2及び従来例で得た線材をヘッダー加工
して頭径4間、膨径2絽、全長2.7mmで5μm以下
であった。The wire rods obtained in Examples 1 and 2 and the conventional example were subjected to header processing and had a head diameter of 4 mm, an expanded diameter of 2 电, a total length of 2.7 mm, and 5 μm or less.
(実施例1)
A g −M o 10wt%合金となるように調整し
たAg2O粉末とM o O*粉末をV型混合機により
3時間予備混合後、内径50φ市のルツボに充填して4
00t: N 2雰囲気中でA、 g 20を熱分解し
た後、H2ガス雰囲気に置換した後、800℃まで昇温
し還元処理した。次いで圧縮、焼結を縫返し、熱間で押
出し、引抜加工して2.5φr!1111及び2φ市の
線材とした。この線材の断面を金属顕微鏡で観察したと
ころW粒子は全て5μm以下であった。(Example 1) After pre-mixing Ag2O powder and MoO* powder, which were adjusted to form an A g -Mo 10 wt% alloy, using a V-type mixer for 3 hours, they were filled into a crucible with an inner diameter of 50 φ.
00t: After thermally decomposing A, g20 in a N 2 atmosphere, the atmosphere was replaced with an H 2 gas atmosphere, and then the temperature was raised to 800° C. for reduction treatment. Next, compression, sintering, sewing, hot extrusion, and drawing process are performed to 2.5φr! 1111 and 2φ city wire rods were used. When the cross section of this wire was observed using a metallurgical microscope, all of the W particles were 5 μm or less in size.
(実施例2)
A g −W lht%合金となるように調整したAg
zO粉末とWO,粉末をV型混合機により3時間予備混
合後、内径50φm111のルツボに充填して400℃
N2雰囲気中でAgzOを熱分解した後、H2ガス雰囲
気に置換した後、800℃まで昇温し還元処理した。次
に圧縮、焼結を繰返し、熱間で押出し、引抜加工して2
.5φ止及び2φmmの線材とした。(Example 2) Ag adjusted to form an A g -W lht% alloy
After pre-mixing the zO powder, WO, and powder for 3 hours using a V-type mixer, they were filled into a crucible with an inner diameter of 50φm111 and heated to 400°C.
After thermally decomposing AgzO in a N2 atmosphere, the atmosphere was replaced with a H2 gas atmosphere, and then the temperature was raised to 800°C for reduction treatment. Next, compression and sintering are repeated, hot extrusion, and drawing process.
.. The wire rod had a diameter of 5φ and a diameter of 2φmm.
この線材の断面を金属M微鏡で観察したところW粒子は
全て5μm以下であった。When the cross section of this wire was observed with a metal M microscope, all of the W particles were 5 μm or less in size.
(以下余白)
上記の表で明らかなように、実施例1.2の接点は従来
例のものに比し、Agに固溶しにくい金属粒子がワイヤ
ーに均一微細に分布しているため、特性寿命も2倍以上
に伸び、ワイブル分布パラメーターmも1以上で初期溶
着の発生がなかったことがわかる。(Leaving space below) As is clear from the table above, the contact of Example 1.2 has a uniform and fine distribution of metal particles that are difficult to dissolve in Ag compared to the conventional example, so the characteristics It can be seen that the life span was more than doubled, and the Weibull distribution parameter m was 1 or more, indicating that no initial welding occurred.
(発明の効果)
以上詳述した通り、本発明の電気接点の製造方法によれ
ば、Ag−Agに固溶しにくい金属系電気接点材料の初
期溶着を防止できるという優れた効果がある。(Effects of the Invention) As detailed above, the method for manufacturing an electrical contact of the present invention has the excellent effect of preventing the initial welding of metallic electrical contact materials that are difficult to dissolve in Ag-Ag.
出願人 田中貴金属工業株式会社Applicant: Tanaka Kikinzoku Kogyo Co., Ltd.
Claims (1)
を分散した電気接点材料の粉末冶金法による製造方法に
おいて、酸化銀粉末及び酸化モリブデン又は酸化タング
ステンを混合した後、この混合粉末を容器に充填後、3
00℃〜500℃で酸化銀を加熱分解し、次いで500
℃〜950℃で酸化モリブデン又は酸化タングステンを
還元して予備ビレットとなし、次いで圧縮、焼結を繰返
すことにより押出用ビレットとなすことを特徴とする電
気接点材料の製造方法。1. In the powder metallurgical manufacturing method of an electrical contact material in which molybdenum or tungsten metal particles are dispersed in an Ag base, after mixing silver oxide powder and molybdenum oxide or tungsten oxide, and filling this mixed powder into a container, 3
Silver oxide is thermally decomposed at 00°C to 500°C, then 500°C
1. A method for producing an electrical contact material, which comprises reducing molybdenum oxide or tungsten oxide at a temperature of .degree. C. to 950.degree. C. to obtain a preliminary billet, followed by repeated compression and sintering to obtain a billet for extrusion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4477089A JPH02225636A (en) | 1989-02-23 | 1989-02-23 | Manufacture of electrical contact material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4477089A JPH02225636A (en) | 1989-02-23 | 1989-02-23 | Manufacture of electrical contact material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02225636A true JPH02225636A (en) | 1990-09-07 |
Family
ID=12700652
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4477089A Pending JPH02225636A (en) | 1989-02-23 | 1989-02-23 | Manufacture of electrical contact material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02225636A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102151830A (en) * | 2011-03-08 | 2011-08-17 | 郴州雄风稀贵金属材料股份有限公司 | Preparation method of silver-rare earth refractory metal oxide electrical contact material |
| JPWO2014136617A1 (en) * | 2013-03-05 | 2017-02-09 | 株式会社アライドマテリアル | Electrical contact materials and breakers |
| CN111028978A (en) * | 2019-12-26 | 2020-04-17 | 攀枝花学院 | (Ti,Mo)C/TiB2Al/Cu electric contact material and preparation method and application thereof |
-
1989
- 1989-02-23 JP JP4477089A patent/JPH02225636A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102151830A (en) * | 2011-03-08 | 2011-08-17 | 郴州雄风稀贵金属材料股份有限公司 | Preparation method of silver-rare earth refractory metal oxide electrical contact material |
| JPWO2014136617A1 (en) * | 2013-03-05 | 2017-02-09 | 株式会社アライドマテリアル | Electrical contact materials and breakers |
| CN111028978A (en) * | 2019-12-26 | 2020-04-17 | 攀枝花学院 | (Ti,Mo)C/TiB2Al/Cu electric contact material and preparation method and application thereof |
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