JPS6147894B2 - - Google Patents
Info
- Publication number
- JPS6147894B2 JPS6147894B2 JP53017181A JP1718178A JPS6147894B2 JP S6147894 B2 JPS6147894 B2 JP S6147894B2 JP 53017181 A JP53017181 A JP 53017181A JP 1718178 A JP1718178 A JP 1718178A JP S6147894 B2 JPS6147894 B2 JP S6147894B2
- Authority
- JP
- Japan
- Prior art keywords
- oxide
- alloy
- electrical contact
- contact material
- alloys
- 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
- 229910045601 alloy Inorganic materials 0.000 claims description 23
- 239000000956 alloy Substances 0.000 claims description 23
- 229910017980 Ag—Sn Inorganic materials 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Description
【発明の詳細な説明】
本発明は、Ag−Sn酸化物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 The present invention relates to a method for producing an Ag-Sn oxide electrical contact material.
Agに酸化物を分散させた電気接点材料として
は、従来よりAg−CdO系合金が優れた電気接点
性能を有するので多方面にわたつて使用されてき
たが、Cdは人体に有害である為その使用は望ま
しくない。 Conventionally, Ag-CdO alloys have been used as electrical contact materials in a wide variety of fields because they have excellent electrical contact performance, but Cd is harmful to the human body, so it has not been used as an electrical contact material. Use is not recommended.
このようなことから近時Ag−CdO系合金に匹
適し得る電気接点性能を有する電気接点材料とし
て、AgにSn酸化物を分散させた合金が注目され
ているが、Ag中にSn酸化物を良好に分散させる
ことが困難であつた。即ちAg−Sn合金を内部酸
化すると、酸化条件によりAg中のSn酸化物の分
散状態は、Sn酸化物の堆積層を形成した不均一
な分散となるか、もしくは極めて微細なSn酸化
物の析出となる。この内特に後者の極めて微細な
Sn酸化物の析出は、Ag合金の塑性加工性を著し
く損い、Ag合金を極めて硬くすることになり、
その結果所定形状の電気接点を得ることが困難で
あつた。また前記の如くAg中にSn酸化物を適当
な大きさで均一に分散させることができない為
Ag−CdO系合金に比し電気接点性能が劣るもの
であつた。 For this reason, alloys in which Sn oxide is dispersed in Ag have recently been attracting attention as electrical contact materials with electrical contact performance comparable to Ag-CdO alloys. It was difficult to disperse it well. In other words, when an Ag-Sn alloy is internally oxidized, depending on the oxidation conditions, the dispersion state of Sn oxide in Ag may become non-uniform dispersion forming a deposited layer of Sn oxide, or extremely fine precipitation of Sn oxide may occur. becomes. Of these, especially the latter, extremely fine
Precipitation of Sn oxides significantly impairs the plastic workability of Ag alloys and makes them extremely hard.
As a result, it has been difficult to obtain electrical contacts with a predetermined shape. In addition, as mentioned above, it is not possible to uniformly disperse Sn oxide in Ag with an appropriate size.
The electrical contact performance was inferior to that of Ag-CdO alloys.
この為従来はAg粉と酸化Sn粉の混合、焼結に
よつてAg−Sn酸化物合金を作つていたが、この
粉体の混合、焼結方法によつてもAg中にSn酸化
物を良好に分散させることが困難で、Ag−CdO
系合金と同等の電気接点性能が得られなかつた。 For this reason, conventionally, Ag-Sn oxide alloy was made by mixing Ag powder and Sn oxide powder and sintering, but depending on the mixing and sintering method of this powder, Sn oxide in Ag It is difficult to disperse Ag−CdO well.
It was not possible to obtain electrical contact performance equivalent to that of the alloys.
本発明はかかる実状に鑑みてなされたものであ
り、Ag中にSn酸化物を適当な大きさで均一に分
散させ且つその合金の硬さを柔かくすることので
きるAg−Sn酸化物電気接点材料の製造方法を提
供せんとするものである。 The present invention was made in view of the above circumstances, and provides an Ag-Sn oxide electrical contact material that can uniformly disperse Sn oxide in Ag in an appropriate size and soften the hardness of the alloy. The purpose of this invention is to provide a method for manufacturing.
本発明のAg−Sn酸化物電気接点材料の製造方
法は、Ag中にSnを0.5〜12重量%含有せしめた合
金を、250〜600℃で内部酸化した後940〜960℃に
加熱することを特徴とするものである。 The method for producing the Ag-Sn oxide electrical contact material of the present invention involves internally oxidizing an alloy containing 0.5 to 12% Sn in Ag at 250 to 600°C and then heating it to 940 to 960°C. This is a characteristic feature.
つまり本発明の製造方法は、内部酸化法によつ
てAg中に極めて微細なSn酸化物を析出した合金
を、Agの融点近くの温度で熱処理を加えて、Ag
中のSn酸化物の分散状態を改善し且つ該合金の
硬さを柔かくするものである。 In other words, in the manufacturing method of the present invention, an alloy in which extremely fine Sn oxides are precipitated in Ag by an internal oxidation method is heat-treated at a temperature close to the melting point of Ag.
This improves the dispersion state of Sn oxide in the alloy and softens the hardness of the alloy.
本発明の製造方法に於いて、Ag中にSnを0.5〜
12重量%含有させる理由は、0.5重量%未満では
Agに対する酸化物の分散による効果が小さく、
12重量%を超えると内部酸化が著しく困難になる
からである。 In the production method of the present invention, Sn is added in Ag from 0.5 to
The reason for containing 12% by weight is that if it is less than 0.5% by weight,
The effect of oxide dispersion on Ag is small;
This is because if it exceeds 12% by weight, internal oxidation becomes extremely difficult.
またAg中にSnを0.5〜12重量%含有せしめた合
金を、250〜600℃で内部酸化する理由は、250℃
未満では内部酸化の進行の度合が遅く生産性が悪
く、600℃を超えると表面又は表面直下に酸化物
の緻密な層ができて酸素が侵入しにくくなつて、
内部酸化が困難となるからである。 Also, the reason why an alloy containing 0.5 to 12% by weight of Sn in Ag is internally oxidized at 250 to 600°C is that 250°C
If the temperature is below 600°C, the progress of internal oxidation will be slow and productivity will be poor; if it exceeds 600°C, a dense layer of oxide will form on the surface or just below the surface, making it difficult for oxygen to penetrate.
This is because internal oxidation becomes difficult.
さらに前記合金を内部酸化した後940〜960℃で
加熱する理由は、940℃未満ではAg中のSn酸化物
の分散状態を改善することができず、960℃を超
えるとAgとSn酸化物の分離が急速に起きてSn酸
化物の良好な分散状態を得ることができないから
である。 Furthermore, the reason why the alloy is heated at 940 to 960°C after internal oxidation is that below 940°C, the dispersion state of Sn oxide in Ag cannot be improved, and when it exceeds 960°C, the dispersion state of Sn oxide in Ag cannot be improved. This is because separation occurs rapidly and a good dispersion state of Sn oxide cannot be obtained.
次に本発明によるAg−Sn酸化物電気接点材料
の製造方法の効果を明瞭ならしめる為にその具体
的な実施例について説明する。 Next, in order to clarify the effects of the method for producing an Ag-Sn oxide electrical contact material according to the present invention, specific examples will be described.
実施例 1
Ag−Sn8重量%合金の1.0φmmの線材を、酸素
分圧9気圧中で450℃に加熱し200時間内部酸化し
てAg−Sn酸化物合金とした。この時の硬さは
Hv230で折り曲げることができなかつた。次に内
部酸化後のAg−Sn酸化物合金を大気中で945℃で
20分間加熱した。その時の硬さはHv110で、この
1.0φmmの線材を切断した後頭経2.0φmmのリベツ
ト形状になした。Example 1 A 1.0 φmm wire made of an 8% by weight Ag-Sn alloy was heated to 450° C. in an oxygen partial pressure of 9 atmospheres and internally oxidized for 200 hours to obtain an Ag-Sn oxide alloy. The hardness at this time is
I couldn't bend it with Hv230. Next, the Ag-Sn oxide alloy after internal oxidation was heated at 945℃ in the air.
Heat for 20 minutes. The hardness at that time was Hv110, and this
A rivet shape with an occipital diameter of 2.0φmm was made by cutting a 1.0φmm wire.
実施例 2
Ag−Sn8重量%合金を0.3φmm〜0.01φmmの粉
粒体になし酸素分圧9気圧中で450℃に加熱し120
時間内部酸化してAg−Sn酸化物合金の粉粒体を
作り、該粉粒体を950℃〜960℃で5分間加熱した
後、圧縮し押出加工にて線材となし、次いで伸線
により2.0φmmの線材となした。その時の硬さは
Hv90で、この2.0φmmの線材を切断した後頭経4.0
φmmのリベツト形状になした。Example 2 Ag-Sn 8% by weight alloy was made into powder of 0.3φmm to 0.01φmm and heated to 450°C in an oxygen partial pressure of 9 atm.
Ag-Sn oxide alloy powder is produced by internal oxidation for a period of time, heated at 950°C to 960°C for 5 minutes, compressed and extruded into a wire rod, and then wire-drawn to obtain a 2.0 It was made into a φmm wire rod. The hardness at that time
Occipital diameter 4.0 when cutting this 2.0φmm wire at Hv90
Made into a rivet shape of φmm.
以上で判るように本発明のAg−Sn酸化物電気
接点材料の製造方法は、Ag−Sn合金を内部酸化
しただけの硬さが硬く、極めて微細なSn酸化物
を析出したAg−Sn酸化物合金を、引き続き940〜
960℃で加熱することにより、硬さが柔かくなつ
て塑性加工性に優れ、またAg中のSn酸化物の分
散状態が改善されて、適度な大きさのSn酸化物
が均一に分散され、その分散状態はAg−CdO系
合金と略同等で、電気接点性能に優れたAg−Sn
酸化物電気接点材料を得ることができるという効
果がある。 As can be seen from the above, the method for producing the Ag-Sn oxide electrical contact material of the present invention is a method for producing an Ag-Sn oxide electrical contact material that is hard enough to be obtained by internally oxidizing the Ag-Sn alloy, and which has very fine Sn oxide precipitated. Alloy continues to be 940~
By heating at 960℃, the hardness becomes soft and has excellent plastic workability, and the dispersion state of Sn oxide in Ag is improved, and Sn oxides of appropriate size are uniformly dispersed. Ag-Sn has a dispersion state similar to that of Ag-CdO alloys and has excellent electrical contact performance.
This has the effect that an oxide electrical contact material can be obtained.
Claims (1)
を、250〜600℃で内部酸化した後、940〜960℃に
加熱することを特徴とするAg−Sn酸化物電気接
点材料の製造方法。1. A method for producing an Ag-Sn oxide electrical contact material, which comprises internally oxidizing an alloy containing 0.5 to 12% by weight of Sn in Ag at 250 to 600°C, and then heating it to 940 to 960°C. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1718178A JPS54110124A (en) | 1978-02-17 | 1978-02-17 | Production of electric contact material of aggsn oxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1718178A JPS54110124A (en) | 1978-02-17 | 1978-02-17 | Production of electric contact material of aggsn oxide |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54110124A JPS54110124A (en) | 1979-08-29 |
JPS6147894B2 true JPS6147894B2 (en) | 1986-10-21 |
Family
ID=11936768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1718178A Granted JPS54110124A (en) | 1978-02-17 | 1978-02-17 | Production of electric contact material of aggsn oxide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54110124A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4412971A (en) * | 1982-02-11 | 1983-11-01 | Chugai Denki Kogyo K.K. | Electrical contact materials of internally oxidized Ag-Sn-Bi alloy |
JPS63286541A (en) * | 1987-05-18 | 1988-11-24 | Tanaka Kikinzoku Kogyo Kk | Ag oxide electrical contact material |
JP2849663B2 (en) * | 1988-12-26 | 1999-01-20 | 田中貴金属工業株式会社 | Electrical contact material and manufacturing method thereof |
JP5567395B2 (en) * | 2010-05-29 | 2014-08-06 | 日本電産サンキョーシーエムアイ株式会社 | Silver-oxide based electrical contact materials |
-
1978
- 1978-02-17 JP JP1718178A patent/JPS54110124A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS54110124A (en) | 1979-08-29 |
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