JPS6365740B2 - - Google Patents

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Publication number
JPS6365740B2
JPS6365740B2 JP53117211A JP11721178A JPS6365740B2 JP S6365740 B2 JPS6365740 B2 JP S6365740B2 JP 53117211 A JP53117211 A JP 53117211A JP 11721178 A JP11721178 A JP 11721178A JP S6365740 B2 JPS6365740 B2 JP S6365740B2
Authority
JP
Japan
Prior art keywords
oxide
silver
composite oxide
dispersed
powder
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
JP53117211A
Other languages
Japanese (ja)
Other versions
JPS5543776A (en
Inventor
Jujiro Kodama
Yoshinari Amano
Tadashi Igarashi
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.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries 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 Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP11721178A priority Critical patent/JPS5543776A/en
Publication of JPS5543776A publication Critical patent/JPS5543776A/en
Publication of JPS6365740B2 publication Critical patent/JPS6365740B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は焼結銀−酸化物系電気接点材料に係
る。電気接点材料の要件としては衆知の如く、耐
溶着性、耐絶縁耐圧性、低接触抵抗性に富むこと
が望まれる。 従来、使用されている接点材料は、内部酸化法
によつて製造される銀−酸化物系合金が主流であ
つた。又1部において粉未冶金法によつて製造さ
れる銀−酸化物系合金も使用されている。内部酸
化法によつて製造される銀−酸化物系合金として
は、銀−酸化カドミウム系、銀−酸化亜鉛等、銀
−酸化錫系等が出るが、いずれも添加元素による
分散酸化物の形状のコントロール及び酸化物構造
変化によつて性能向上をはかつてきている。しか
しながら、内部酸化法の場合には、添加元素とし
て内部酸化が可能であることが前提となり、分散
する酸化物の構造及び量に制限があり、性能向上
に自ずと限界がある。又、分散する酸化物粒子の
大きさが表面と内部で異なり、内部に酸化物の希
薄部が生じて性能劣化する欠点がある。一方、粉
末冶金法による銀−酸化物系合金は、分散酸化物
の量、形状、種類及び分散度のコントロールが自
由であるという利点を持つているものの、性能的
にすぐれた材料が見出されていない。本発明者ら
は、内部酸化法による銀−酸化物系合金の性能が
向上する原因を種々検討することにより、分散酸
化物粒子の構造が性能に極めて大きく寄与するこ
とを見出し、本発明に到つたものである。 1例を上げるとAg−15cd−1Sn合金の内部酸
化接点は第1図に示す如く、内部酸化時に、
cd2SnO4を形成し、酸化物の熱的安定性が向上し
て耐溶着、耐消耗性がAg−15cdの内部酸化接点
より数倍向上する。 本発明は、あらかじめ生成された複合酸化物を
含む酸化物粒子と銀粉末とを混合、成型、焼結し
て内部酸化法によつて製造される合金と同一にす
ることを特徴としている。 さらに、本発明によれば複合酸化物の構造を多
く変化出来、且つその量も自由にコントロールで
きる特徴を有し、且つ内部酸化ではできない酸化
物の均一分散化が可能となり、性能向上を容易に
はかることが出来ることを見出した。 本発明による合金は、 (1) 粉末冶金法によつて製造される銀−酸化物系
合金であり、2種類の金属元素からなる複合酸
化物粒子を分散した電気接点材料であり、より
具体的には、 (2) 粉末冶金法によつて製造される銀−酸化物系
合金であり、カドミウム、錫、亜鉛、インジウ
ム、マンガン、アンチモンのうち2種からなる
複合酸化物粒子を分散した電気接点材料が提供
される。 本発明による複合酸化物は、2種の金属元素か
らなる結晶質(固溶体も含む)、無定形の酸化物
を包含する。構成する複合酸化物の組成は、その
主構成元素としてカドミウム、錫、亜鉛、インジ
ウム、マンガン、アンモチンが良い。これら複合
酸化物は電流開閉時に適度に分解、飛散していく
ために、温度上昇が比較的低く維持され、且つ、
耐熱性を十分に保持して耐溶着特性を向上せしめ
る働きがあるためである。 これら複合酸化物粒子は耐溶着性、耐絶縁性を
基本的に改善する作用がある。その組成範囲は、
1〜20wt%含有していることが必要である。 1wt%より少ないと分散強化作用が少なく接点
としての耐溶着性が著しく低下し、純銀の挙動に
等しくなるためであり、逆に20wt%をこすと耐
溶着性が向上するものの接点の固有抵抗が増大
し、温度上昇が著しく、電気接点としては不適当
になるためである。 尚、本発明においては複合酸化物が含有してい
ることが必須であるが、これ以外に通常の酸化物
が分散していてもかまわない。 次に本材料の製造方法について説明する。 複合酸化物粒子は、既知の方法、即ち酸化物
粉末を混合して熱処理する方法、硝酸塩、硫酸
塩、炭酸塩、塩化物塩の混合体を培焼する方法、
硝酸塩、硫酸塩、炭酸塩、塩化物塩の溶液を共
沈スプレーして後、培焼する方法、合金粉末の
酸化によつて製造される。 これらいずれかによつて製造された複合酸化物
をボールミル、アトライダーあるいは振動ミルに
よつて粉砕し、−325mesh、の粒度とする。この
粉末と銀粉末を所定割合に配合後、ボールミル、
アトライダーあるいは振動ミルによつて混合し、
この混合粉末を成型、焼結して後、押出あるいは
鍜造あるいは圧延加工によつて所望形成に加工す
ることによつて銀地中に複合酸化物が分散した本
発明材料を得ることが出来る。 次に実施例により本発明をより具体的に説明す
る。 実施例 1 第1表に示す割合で酸化物粉末および塩による
配合を行ない、ボールミル20時間混合後、第1表
中に示す条件にて熱処理し、混合粉末を得た。こ
れら粉末をボールミル20時間粉砕後、粉末に対し
てX線回析したところ、第1表に示す如く複合酸
化物が形成されていた。代表的なX線回析結果を
第2図、第3図に示す。 実施例 2 実施例1で得た粉末と、−325meshの電解粉末
を第2表に示す割合で配合后、20時間振動ミル混
合した。得られた混合粉末を2ton/cm2で成型して
後、700℃で空気中、20時間焼結した。この焼結
体を84に押出す。押出条件は700℃、押出速度20
mm/secである。この押出体についてX線回析し
た結果を第4図、第5図、第6図、第7図、第8
図に示す。この押出棒を伸線して2.4φにし、ヘツ
ダー加工により5φ×1.4×2.5φ×2.5×30Rのリベ
ツト接点を得た。 実施例 3 実施例2で得たリベツト接点を市販の安全ブレ
ーカーに組込み第3表に示す条件で、過負荷−耐
久試験后の温度上昇および過負荷−短絡試験を行
ない、絶縁耐圧および溶着にいたるまでの回数を
測定した。その結果を第4表に示す。 また、比較のため内部酸化法によるAg−10%
cdo、及び単純な酸化物粉末で実施例2と同一条
件にて作成した接点を加えた。尚、比較材の組成
は第2表に示すとおりである。 本結果により粉末冶金法によつて複合酸化物を
銀中に分散せしめた本発明の接点が単純に各々の
酸化物を分散させた接点、あるいは従来、主に使
用されている内部酸化によるAg−10%cdoに比べ
て耐溶着、耐絶縁、低接触抵抗特性をバランスよ
く具備していることが明らかである。 かように、本発明材料は、特に中電流用電気接
点材料として、優れた性能を示し、その工業的価
値は大である。
The present invention relates to a sintered silver-oxide electrical contact material. As is well known, electrical contact materials are desired to have excellent adhesion resistance, dielectric strength and low contact resistance. Conventionally, the main contact materials used have been silver-oxide alloys manufactured by internal oxidation. In some cases, silver-oxide alloys produced by non-powder metallurgy are also used. Silver-oxide based alloys produced by internal oxidation methods include silver-cadmium oxide, silver-zinc oxide, silver-tin oxide, etc., but all of these alloys have different shapes of dispersed oxides due to added elements. The performance has been improved by controlling the oxidation rate and changing the oxide structure. However, in the case of the internal oxidation method, it is assumed that internal oxidation is possible as an added element, and there are restrictions on the structure and amount of the oxide to be dispersed, which naturally limits performance improvement. Another disadvantage is that the size of the dispersed oxide particles differs between the surface and the inside, resulting in a thin oxide part inside, resulting in deterioration of performance. On the other hand, silver-oxide alloys produced by powder metallurgy have the advantage of being able to freely control the amount, shape, type, and degree of dispersion of dispersed oxides, but materials with superior performance have yet to be discovered. Not yet. The present inventors have investigated various reasons why the performance of silver-oxide alloys improved by the internal oxidation method, and have discovered that the structure of dispersed oxide particles greatly contributes to the performance, and have arrived at the present invention. It is ivy. To give an example, the internal oxidation contacts of Ag-15cd-1Sn alloy, as shown in Figure 1, undergo internal oxidation during internal oxidation.
CD 2 SnO 4 is formed, the thermal stability of the oxide is improved, and the welding resistance and abrasion resistance are several times better than that of Ag-15CD internal oxidation contacts. The present invention is characterized in that oxide particles containing a composite oxide produced in advance and silver powder are mixed, molded, and sintered to form the same alloy as produced by an internal oxidation method. Furthermore, according to the present invention, the structure of the composite oxide can be changed in many ways, and its amount can be controlled freely, and it is also possible to uniformly disperse the oxide, which cannot be done with internal oxidation, making it easy to improve performance. I discovered that it can be measured. The alloy according to the present invention is (1) a silver-oxide based alloy produced by a powder metallurgy method, and is an electrical contact material in which composite oxide particles made of two types of metal elements are dispersed; (2) An electrical contact, which is a silver-oxide alloy manufactured by powder metallurgy and has composite oxide particles made of two of cadmium, tin, zinc, indium, manganese, and antimony dispersed therein. Materials provided. The composite oxide according to the present invention includes crystalline (including solid solution) and amorphous oxides composed of two types of metal elements. The composition of the composite oxide is preferably such that its main constituent elements are cadmium, tin, zinc, indium, manganese, and ammothine. These composite oxides decompose and scatter appropriately when the current is switched on and off, so the temperature rise is kept relatively low, and
This is because it functions to maintain sufficient heat resistance and improve welding resistance. These composite oxide particles have the effect of fundamentally improving welding resistance and insulation resistance. Its composition range is
It is necessary to contain 1 to 20 wt%. This is because if it is less than 1wt%, the dispersion strengthening effect will be small and the welding resistance as a contact will be significantly reduced, and the behavior will be equivalent to that of pure silver.On the other hand, if it is less than 20wt%, the welding resistance will improve but the specific resistance of the contact will decrease. This is because the temperature rises significantly and becomes unsuitable as an electrical contact. In the present invention, it is essential that a composite oxide is contained, but a normal oxide may be dispersed in addition to this. Next, the manufacturing method of this material will be explained. Composite oxide particles can be produced by known methods, namely, a method of mixing oxide powders and heat treatment, a method of incubating a mixture of nitrates, sulfates, carbonates, and chlorides;
It is manufactured by spraying a solution of nitrates, sulfates, carbonates, and chlorides by coprecipitation and then calcination, or by oxidizing an alloy powder. The composite oxide produced by any of these methods is pulverized using a ball mill, an atrider, or a vibration mill to obtain a particle size of -325 mesh. After mixing this powder and silver powder in a predetermined ratio, ball mill,
Mixed by atrider or vibrating mill,
The material of the present invention in which the composite oxide is dispersed in the silver base can be obtained by molding and sintering this mixed powder and then processing it into a desired shape by extrusion, molding, or rolling. Next, the present invention will be explained in more detail with reference to Examples. Example 1 Oxide powder and salt were mixed in the proportions shown in Table 1, mixed in a ball mill for 20 hours, and then heat treated under the conditions shown in Table 1 to obtain a mixed powder. After pulverizing these powders in a ball mill for 20 hours, X-ray diffraction analysis of the powders revealed that a composite oxide was formed as shown in Table 1. Representative X-ray diffraction results are shown in FIGS. 2 and 3. Example 2 The powder obtained in Example 1 and -325mesh electrolytic powder were mixed in the proportions shown in Table 2, and then mixed in a vibrating mill for 20 hours. The obtained mixed powder was molded at 2 tons/cm 2 and then sintered at 700° C. in air for 20 hours. This sintered body is extruded into 84. Extrusion conditions are 700℃, extrusion speed 20
mm/sec. The results of X-ray diffraction of this extruded body are shown in Figures 4, 5, 6, 7, and 8.
As shown in the figure. This extruded rod was drawn to a diameter of 2.4φ, and a rivet contact of 5φ×1.4×2.5φ×2.5×30R was obtained by header processing. Example 3 The riveted contact obtained in Example 2 was assembled into a commercially available safety breaker, and under the conditions shown in Table 3, a temperature rise after overload-durability test and an overload-short circuit test were conducted to determine dielectric strength and welding. The number of times until The results are shown in Table 4. Also, for comparison, Ag-10% by internal oxidation method
Contacts made under the same conditions as Example 2 using cdo and simple oxide powder were added. The composition of the comparative material is as shown in Table 2. These results show that the contact of the present invention in which a composite oxide is dispersed in silver using a powder metallurgy method is different from the contact in which each oxide is simply dispersed, or the Ag- It is clear that it has a good balance of welding resistance, insulation resistance, and low contact resistance characteristics compared to 10% CDO. Thus, the material of the present invention exhibits excellent performance, especially as an electrical contact material for medium currents, and has great industrial value.

【表】 (注) 番号6は欠番である。
[Table] (Note) Number 6 is a missing number.

【表】 第 3 表 温度上昇 過負荷試験AC220V、150A、力率0.8 試 験 開閉回数 50回 耐久試験AC220V、20A、 開閉回数 5000回 上記試験後、温度上昇を測定 短絡試験 過負荷試験后、AC220V、1500A、力
率0.75で1極0→CO⇒2極0−CO⇒
2極COを溶着するまで繰返えす。
[Table] Table 3 Temperature rise Overload test AC220V, 150A, power factor 0.8 Test Opening and closing times 50 times Endurance test AC220V, 20A, opening and closing times 5000 times After the above test, measure the temperature rise Short circuit test After overload test, AC220V , 1500A, power factor 0.75, 1 pole 0 → CO ⇒ 2 poles 0 - CO ⇒
Repeat until the 2-electrode CO is welded.

【表】【table】 【図面の簡単な説明】[Brief explanation of drawings]

第1,2,3,4,5,6,7,8図は何れも
本願発明を説明するためのX線回折結果を示す図
表である。
Figures 1, 2, 3, 4, 5, 6, 7, and 8 are all charts showing X-ray diffraction results for explaining the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 銀基分散型合金において、2種類の金属元素
からなる複合酸化物粒子を1wt%以上20wt%以下
含有し、均一に分散し、かつ該複合酸化物粒子が
カドミウム、錫、亜鉛、インジウム、マンガン、
アンチモンのうちの2種からなる複合酸化物であ
ることを特徴とする焼結電気接点材料。
1 A silver-based dispersed alloy containing composite oxide particles of 1 wt% or more and 20 wt% or less consisting of two types of metal elements, uniformly dispersed, and containing cadmium, tin, zinc, indium, or manganese. ,
A sintered electrical contact material characterized by being a composite oxide consisting of two types of antimony.
JP11721178A 1978-09-21 1978-09-21 Sintered electric contact material Granted JPS5543776A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11721178A JPS5543776A (en) 1978-09-21 1978-09-21 Sintered electric contact material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11721178A JPS5543776A (en) 1978-09-21 1978-09-21 Sintered electric contact material

Publications (2)

Publication Number Publication Date
JPS5543776A JPS5543776A (en) 1980-03-27
JPS6365740B2 true JPS6365740B2 (en) 1988-12-16

Family

ID=14706133

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11721178A Granted JPS5543776A (en) 1978-09-21 1978-09-21 Sintered electric contact material

Country Status (1)

Country Link
JP (1) JPS5543776A (en)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4472211A (en) * 1982-05-20 1984-09-18 Chugai Denki Kogyo Kobushiki Kaisha Method of internally oxidizing Ag-Sn alloy contact material
JPS58218715A (en) * 1982-06-14 1983-12-20 田中貴金属工業株式会社 Electric contact material
JPS59185747A (en) * 1983-04-07 1984-10-22 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59185751A (en) * 1983-04-07 1984-10-22 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59185749A (en) * 1983-04-07 1984-10-22 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59185748A (en) * 1983-04-07 1984-10-22 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215443A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215444A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215441A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215438A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215436A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215437A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215435A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59215439A (en) * 1983-05-19 1984-12-05 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219436A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219442A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219441A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219434A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219439A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPS59219437A (en) * 1983-05-24 1984-12-10 Tanaka Kikinzoku Kogyo Kk Electrical contact material
JPH06104873B2 (en) * 1986-07-08 1994-12-21 富士電機株式会社 Silver-metal oxide contact material and manufacturing method thereof
US4817695A (en) * 1987-12-02 1989-04-04 Wingert Philip C Electrical contact material of Ag, SnO2, GeO2 and In2 O.sub.3

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6048578B2 (en) * 1977-11-18 1985-10-28 松下電器産業株式会社 electrical contact materials
JPS6018735B2 (en) * 1977-12-15 1985-05-11 松下電器産業株式会社 electrical contact materials
JPS6021215B2 (en) * 1978-02-22 1985-05-25 松下電器産業株式会社 electrical contact materials

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Publication number Publication date
JPS5543776A (en) 1980-03-27

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