JPS5852452A - Electrical contact material and manufacture - Google Patents

Electrical contact material and manufacture

Info

Publication number
JPS5852452A
JPS5852452A JP57152870A JP15287082A JPS5852452A JP S5852452 A JPS5852452 A JP S5852452A JP 57152870 A JP57152870 A JP 57152870A JP 15287082 A JP15287082 A JP 15287082A JP S5852452 A JPS5852452 A JP S5852452A
Authority
JP
Japan
Prior art keywords
oxide
frit
electrical contact
temperature
weight
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
Application number
JP57152870A
Other languages
Japanese (ja)
Inventor
ホルスト・ハイトジ−ク
ゲルノ−ト・イエツケル
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
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 Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Publication of JPS5852452A publication Critical patent/JPS5852452A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01HELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
    • H01H1/00Contacts
    • H01H1/02Contacts characterised by the material thereof
    • H01H1/021Composite material
    • H01H1/023Composite material having a noble metal as the basic material
    • H01H1/0237Composite material having a noble metal as the basic material and containing oxides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Composite Materials (AREA)
  • Materials Engineering (AREA)
  • Contacts (AREA)
  • Powder Metallurgy (AREA)
  • Manufacture Of Switches (AREA)
  • Coupling Device And Connection With Printed Circuit (AREA)
  • Conductive Materials (AREA)
  • Glass Compositions (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は貢雀属製′亀気接点、特に弱電流用接点の材料
及びその製法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a material for a contact made of Trigonium genus, particularly a contact for low current, and a method for manufacturing the same.

弱電流用の接点は、それぞれその使用条件に応じて、銀
−1金−、パラジウム−又は白金材料から製作される。
The contacts for low currents are made from silver-1-gold, palladium or platinum material, depending on the conditions of use.

材料の選択は、コストの他に開閉部の電圧、定格電流の
強さ、開閉頻度、開閉の確実性、機械負荷及び腐蝕性雰
囲気を顧慮して行うっ 接点材料には第一に、すぐれた耐摩耗性、良好な導電率
及び小さい接触抵抗が要求される。
In addition to cost, material selection takes into account switching voltage, rated current strength, switching frequency, switching reliability, mechanical load, and corrosive atmosphere. Abrasion resistance, good conductivity and low contact resistance are required.

更に接点材料は腐蝕してもならないし又錆を生じてもな
らない。それらの理由から、貴金属はそれ自体、理想的
な接点材料である。 唯、高価であること及び多くの適
用、にとっては硬度及び強度が低すき、従って耐摩耗性
が小さすぎることが欠点である。
Furthermore, the contact material must not corrode or rust. For these reasons, precious metals are ideal contact materials in their own right. The only disadvantages are that they are expensive and that their hardness and strength, and therefore their wear resistance, are too low for many applications.

従って強度性及び硬度を高めるために、殆どの場会純貴
金属と卑金属との合金を便用する。
Therefore, to increase strength and hardness, alloys of pure precious metals and base metals are often used.

その様な卑金属の例は銅及びニッケルである。Examples of such base metals are copper and nickel.

しかし接点材料としての貴金属合金は、導電率がより低
く、接触抵抗が高く又、卑金属量が多い場合には、酸化
−及び腐蝕の傾向が太きい。
However, noble metal alloys as contact materials have lower electrical conductivity, higher contact resistance, and are more prone to oxidation and corrosion if the base metal content is high.

従って本発明の課題は、高い耐摩耗性含有し、しかも導
電率が高く、耐酸化性及び耐腐蝕性で、貴金属含量が出
来るだけ少なす1、賃金属製電気接点用の材料並びにそ
の製法を見出すことであった。
It is therefore an object of the present invention to develop a material for metal electrical contacts that has high wear resistance, high electrical conductivity, oxidation and corrosion resistance, and has as low a precious metal content as possible, as well as a method for producing the same. It was to find out.

この課題は本発明により、ガラスを1〜50容量係含有
する材料により解決されへ。有利にはガラスとして、4
00〜750℃の転移温度及び100℃よりも大きい軟
化範囲を有するフリット全使用する。
This problem is solved according to the invention by a material containing 1 to 50 volumes of glass. Advantageously as glass, 4
All frits with a transition temperature of 00-750°C and a softening range greater than 100°C are used.

転移温度は脆性状態から粘靭塑性状態へのフリットの転
移点であり、温度−物性カーブ中の角度により定められ
る。同測定はI) I N (ドイツ工業規格)523
24により、試料の膨張カーブに4腺’に引く方法で行
う。接線の交点に相当する温度を転移温度とする。通常
フリットは同温度において約10”Pa*secの粘度
を有する。
The transition temperature is the transition point of the frit from a brittle state to a viscoplastic state, and is determined by the angle in the temperature-physical property curve. The same measurement is I) I N (German Industrial Standard) 523
24, the expansion curve of the sample is drawn in four directions. Let the temperature corresponding to the intersection of the tangents be the transition temperature. Typically, the frit has a viscosity of about 10"Pa*sec at the same temperature.

軟化範囲はフリットの軟化開始点と半球温度との間の温
度範囲で、円筒形試料を加熱顕@鏡で観察して両限界値
を測定する。縁が丸みを帯びることで軟化開始点全定め
、更に円筒形試料が熔融して半球状になることで半球温
度を定める。軟化範囲は粘度の温度への依存性の尺度で
ある。
The softening range is the temperature range between the softening start point of the frit and the hemisphere temperature, and both limit values are measured by observing the cylindrical sample with a heated microscope. The rounded edge determines the softening starting point, and the hemispherical temperature is determined by the cylindrical sample melting into a hemispherical shape. Softening range is a measure of the dependence of viscosity on temperature.

イ1利には、酸化鉛及び/又は酸化亜鉛15〜75重量
%、二酸化珪素5〜65重量係重量化硼素0〜25重量
%及び酸化アルカ90〜20重針%を含有するフリット
を使用する。なお付加的に、酸化アルミニウム、二酸化
ジルコニウム、二酸化チタン及び/又は二酸化錫をそれ
ぞれ1(HHt%までフリットに添加することが出来る
For A1, a frit containing 15 to 75% by weight of lead oxide and/or zinc oxide, 5 to 65% by weight of silicon dioxide, 0 to 25% by weight of boron oxide, and 90 to 20% of alkali oxide by weight is used. . Additionally, aluminum oxide, zirconium dioxide, titanium dioxide and/or tin dioxide can be added to the frit up to 1 (HHt%) each.

低い転移温度及び広い軟化範囲を有するフリツ)f使用
することによって、貴金属ないしは?1金属会金の通常
の焼結温度よシも著しく低い温度でガラスがすでに軟化
し、液相焼結の過程によって材料の高い密度及び良好な
加工性を達成することが出来る。
By using frits with low transition temperature and wide softening range, noble metals or The glass is already softened at temperatures significantly lower than the usual sintering temperatures for single metal alloys, and high densities and good processability of the material can be achieved by the process of liquid phase sintering.

本発明による材料は、貴金属成分として有利に、・金、
銀及び/又はパラジウム、又はそれらの合金を含有する
The material according to the invention advantageously has as noble metal component: gold,
Contains silver and/or palladium, or alloys thereof.

1〜50容縫チ、特に1〜30容祉チのフリットケ貴金
属に硝加することによ!Ill、材料の貴金属含°量を
著しく減少することが出来、その場合相当する合金に比
較して導電率がそれ程低下することはなく、又耐腐蝕性
が低下することもない。更に同材料の耐摩耗性は相当す
る合金よりも高く、はんだ付は及び電気メツキ可能であ
り、良好な加工性をゼする。加工屑からの貴金属の回収
がより容易であることも利点である。
By adding nitrification to Fritke precious metals of 1 to 50 units, especially 1 to 30 units! Ill, the noble metal content of the material can be significantly reduced without significantly lowering the electrical conductivity or reducing the corrosion resistance compared to the corresponding alloy. Furthermore, the material has higher wear resistance than comparable alloys, is solderable and electroplatable, and has good processability. It is also an advantage that the recovery of precious metals from processing waste is easier.

図面は金−ガラス材料における導電率のガラス含量への
依存性を示す。通常の金合金の等電率は斜線音引いた領
域内にある。
The figure shows the dependence of electrical conductivity on glass content in gold-glass materials. The isoelectric constant of ordinary gold alloys is within the shaded area.

本発明の拐料は、貴金属粉末と1〜50容桁チ、有利に
は2〜30容jl(%のフリット微粉末との混合、プレ
ス、焼結及び熱同加工によって12造される。有利には
粒径〈250μ口]、特Vこ〈63 /4nの金属粉末
を1更用する。他方フリットはく50μIn、有利に(
・まく、tozzmの粒径が有利であることが立Mll
=された。更にフリット−及び金属粒子が球形又はほぼ
球形を有するのが有利である。粉末混付物全室温及び5
00〜5000バールの圧力においてプレスし、次いで
500〜950 ℃において焼結し、引続いて500〜
800℃及び100〜200パールの圧力において、特
に押出プレスにより、熱間力l工を行う。
The frit material of the present invention is prepared by mixing the noble metal powder with 1 to 50 volumes, preferably 2 to 30 volumes, of fine frit powder, pressing, sintering, and thermo-processing. A metal powder with a particle size of 250 μm and a special diameter of 63/4 nm is used.On the other hand, a frit with a particle size of 50 μm, preferably (
・It is clear that the particle size of tozzm is advantageous.
= was done. Furthermore, it is advantageous for the frit and the metal particles to have a spherical or approximately spherical shape. Powder admixture total room temperature and 5
Pressing at a pressure of 00-5000 bar, then sintering at 500-950 °C, followed by
Hot working is carried out, especially in an extrusion press, at 800 DEG C. and a pressure of 100 to 200 par.

1000〜3000パールのプレス圧及び550〜−8
00℃の焼結温度が有利である。加工の除のガラスの粘
度は109〜103Pa−3cc、有利には10511
 、 +I 3 e Cであるべきである。
Press pressure of 1000-3000 pars and 550--8
A sintering temperature of 0.000C is advantageous. The viscosity of the glass after processing is 109 to 103 Pa-3cc, preferably 10511
, +I3eC.

下。【シの実施例は不発明による材料及びその製法を詳
述するものである。
under. [Example 2] Detailed description of the material and method of making the same according to the invention.

例  1 平均粒径6374mの金粉末を、PbO10重hC%、
5i()+ 50 %、B2O315% s Al2O
35%、Z r 025係及び酸化アルカリ15係の組
成を有する、平均粒径〈10μInのフリット粉末12
容t %と、アセトン全添加して、混合する。フリット
の転移温度は430℃であシ、軟化範囲は170℃であ
る。同粉末混合物を室温及び1000パールにおいて、
理論密度値の約65壬の圧縮体密度tWするボルト形状
体にプレスし、引続いて900℃において1時間焼結す
る。その際に理論密度値の85係の密度になる。同″焼
結体全750℃に加熱し、次いで500℃及び150パ
ールのプレス圧で押出プレスする。引続いての薄板への
加工は、各対のリール間隙が0.5 mrnずつ減少す
る装置で、温度800℃において熱間圧延することによ
り行う。中間で焼な捷しく 550 ℃、10分1b1
)を行う常温圧延によって厚さ0.1+mnの薄゛板を
得る。
Example 1 Gold powder with an average particle size of 6374 m was mixed with PbO10% by weight and hC%.
5i() + 50%, B2O315% s Al2O
Frit powder 12 with an average particle size of <10 μIn, having a composition of 35%, Z r 025 and alkali oxide 15
Add all of the volume t% and acetone and mix. The transition temperature of the frit is 430°C and the softening range is 170°C. The same powder mixture at room temperature and 1000 pearls,
It is pressed into a bolt shape with a compressed body density tW of approximately 65 mm of the theoretical density value and subsequently sintered at 900° C. for 1 hour. At this time, the density becomes the 85th factor of the theoretical density value. The entire sintered body is heated to 750°C, and then extrusion pressed at 500°C and a press pressure of 150 pars.The subsequent processing into thin plates is performed using equipment that reduces the reel gap of each pair by 0.5 mrn. It is carried out by hot rolling at a temperature of 800°C.In the middle, it is rolled at 550°C for 10 minutes.
) A thin plate with a thickness of 0.1+mm is obtained by cold rolling.

IZ!+  2 平均粒径く63μm’に有する銀粉末を、例1に記載の
フリット粉末25y量係と混付し、室温及び1000パ
ールにおいて圧縮体にプレスし、750℃において1時
間焼結する。700℃及び150パールにおいて押出プ
レスを行って直i11.5mmの線材を得る。常温加工
(ピーニング、報引きンによって、線材の直径全0.4
 mmに減少すeことが出来る。
IZ! + 2 Silver powder having an average particle size of 63 μm' is mixed with a 25-y amount of frit powder described in Example 1, pressed into a compact at room temperature and 1000 pearls, and sintered at 750° C. for 1 hour. An extrusion press was performed at 700° C. and 150 pars to obtain a wire rod with a straight diameter of 11.5 mm. By normal temperature processing (peening and refining), the total diameter of the wire is 0.4
It can be reduced to mm.

【図面の簡単な説明】[Brief explanation of the drawing]

図1イ■は本発明による金−ガラス材料の導[L率とガ
ラス含量との関係を示す図である。
FIG. 1A is a diagram showing the relationship between the conductivity ratio and the glass content of the gold-glass material according to the present invention.

Claims (1)

【特許請求の範囲】 ■、 貴金属製電気接点の材料において、ガラスを1〜
50容量係含有すること全特徴とする、電気接点材料。 2、 貴金属として金、銀及び/又はノミラジウム又は
それらの合金を含有する特許請求の範囲第1項記載の材
料。 3、 ガラスとして、400〜750”Cの転移温度及
び100℃よりも大きい軟化範囲を有するフリットヲ含
有する特許請求の範囲第1項又は第2項記載の材料。 4 フリットが酸化鉛及び/又は酸化亜鉛15〜75重
量係、二酸化珪素5〜65重量%、酸化硼素0〜25重
量%、醸化アルカ’J O〜20重量係重量酸化アルミ
ニウム、酸化ジルコニウム、酸化チタン及び/又は酸化
錫それぞれO〜10重量係重量外る、特許請求の範囲第
1項〜第3項のいずれか1項に記載の材料。 5 フリットが粒径く10μmf有する、特許請求の範
囲第1項〜第4項のいずれか1項に記載の材料。 6 貴金属粉末とフリットとの混合、プレス。 焼結及び熱間力11工eこよって、ガラスを1〜50答
址係含有する賃金属製電気接点材料を製造するに当り、
プレスを室温及び5. IJ O〜5000ノζ−ルの
圧力において、引続いての焼結を500〜950℃の温
度において、最後の熱rbl加工全500〜800℃の
温度及びi o’o〜200パールの圧力において行う
こと全特徴とする、電気接点材料の製法。
[Claims] ■ In the material of the electrical contact made of precious metal, glass is
An electrical contact material characterized in that it contains a capacitance of 50%. 2. The material according to claim 1, which contains gold, silver and/or noradium or an alloy thereof as a noble metal. 3. The material according to claim 1 or 2, which contains, as glass, a frit having a transition temperature of 400 to 750"C and a softening range greater than 100"C. 4. The frit contains lead oxide and/or oxide. Zinc 15-75% by weight, silicon dioxide 5-65% by weight, boron oxide 0-25% by weight, brewed alkali'J O-20% by weight aluminum oxide, zirconium oxide, titanium oxide and/or tin oxide each O- 5. The material according to any one of claims 1 to 3, in which the frit has a particle size of 10 μmf. The material described in item 1. 6. Mixing and pressing of noble metal powder and frit. Sintering and hot pressing 11 steps to produce a metal electrical contact material containing 1 to 50 parts of glass. In this case,
Press at room temperature and 5. IJO at a pressure of ~5000 par, subsequent sintering at a temperature of 500-950 °C, final thermal RBL processing at a temperature of 500-800 °C and a pressure of i o'o ~200 °C. The manufacturing method of electrical contact materials, which is characterized by all of our activities.
JP57152870A 1981-09-04 1982-09-03 Electrical contact material and manufacture Pending JPS5852452A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE31350356 1981-09-04
DE19813135035 DE3135035A1 (en) 1981-09-04 1981-09-04 MATERIAL FOR ELECTRICAL CONTACTS AND METHOD FOR THE PRODUCTION THEREOF

Publications (1)

Publication Number Publication Date
JPS5852452A true JPS5852452A (en) 1983-03-28

Family

ID=6140863

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57152870A Pending JPS5852452A (en) 1981-09-04 1982-09-03 Electrical contact material and manufacture

Country Status (12)

Country Link
EP (1) EP0074507A3 (en)
JP (1) JPS5852452A (en)
AU (1) AU8710682A (en)
BR (1) BR8205135A (en)
DE (1) DE3135035A1 (en)
DK (1) DK303482A (en)
ES (1) ES8308445A1 (en)
NO (1) NO821899L (en)
PL (1) PL238134A1 (en)
PT (1) PT75233B (en)
YU (1) YU149282A (en)
ZA (1) ZA825763B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3312852C2 (en) * 1983-04-09 1985-06-05 Doduco KG Dr. Eugen Dürrwächter, 7530 Pforzheim Composite material that emits extinguishing gas when exposed to an arc
DE3402091C2 (en) * 1984-01-21 1994-01-13 Rau Gmbh G Composite material for electrical contact pieces
EP0369282B1 (en) * 1988-11-17 1995-06-14 Siemens Aktiengesellschaft Sintered contact material in low-tension switchgear, particularly for contactors
DE10038841C1 (en) 2000-08-04 2001-12-20 Heraeus Gmbh W C Silicon dioxide glass bulb used in a high power discharge lamp has a current duct made from a gas-tight composite material consisting of a precious metal and silicon dioxide

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4625848B1 (en) * 1966-04-15 1971-07-26
IT1032907B (en) * 1974-05-21 1979-06-20 Jenaer Glaswerk Schott & Gen COMPOSITE SINTERED MATERIAL OF GLASS AND METAL WITH COPPER CONTENT AND PROCEDURE FOR ITS MANUFACTURING
GB2085481B (en) * 1980-10-17 1985-01-09 Rca Corp Improved copper conductor inks

Also Published As

Publication number Publication date
AU8710682A (en) 1983-03-10
DE3135035A1 (en) 1983-03-24
DK303482A (en) 1983-03-05
ES513200A0 (en) 1983-08-16
PL238134A1 (en) 1983-05-09
EP0074507A2 (en) 1983-03-23
BR8205135A (en) 1983-08-09
ES8308445A1 (en) 1983-08-16
EP0074507A3 (en) 1983-04-20
NO821899L (en) 1983-03-07
YU149282A (en) 1985-03-20
ZA825763B (en) 1983-06-29
PT75233A (en) 1982-08-01
PT75233B (en) 1984-06-26

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