US3785810A - Silver-metal oxide composite and method of manufacturing the same - Google Patents
Silver-metal oxide composite and method of manufacturing the same Download PDFInfo
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- US3785810A US3785810A US00211038A US3785810DA US3785810A US 3785810 A US3785810 A US 3785810A US 00211038 A US00211038 A US 00211038A US 3785810D A US3785810D A US 3785810DA US 3785810 A US3785810 A US 3785810A
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H1/00—Contacts
- H01H1/02—Contacts characterised by the material thereof
- H01H1/021—Composite material
- H01H1/023—Composite material having a noble metal as the basic material
- H01H1/0237—Composite material having a noble metal as the basic material and containing oxides
- H01H1/02372—Composite material having a noble metal as the basic material and containing oxides containing as major components one or more oxides of the following elements only: Cd, Sn, Zn, In, Bi, Sb or Te
- H01H1/02374—Composite material having a noble metal as the basic material and containing oxides containing as major components one or more oxides of the following elements only: Cd, Sn, Zn, In, Bi, Sb or Te containing as major component CdO
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/001—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
- C22C32/0015—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents
- C22C32/0021—Matrix based on noble metals, Cu or alloys thereof
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C5/00—Alloys based on noble metals
- C22C5/06—Alloys based on silver
- C22C5/10—Alloys based on silver with cadmium as the next major constituent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9265—Special properties
- Y10S428/929—Electrical contact feature
Definitions
- the invention relates to a silver-metal oxide composite, in particular silver-cadmium oxide, for use on contact pieces in low voltage switching apparatus, and to a method for its manufacture.
- Silver-metal oxide composites preferably silvercadmium oxide with 6 to 15% by weight CdO, have been used for quite some time as contact-surfacing material in low voltage switch apparatus.
- the advantage of these materials in relation to pure silver is a considerably lesser likelihood of welding during the switching operation, an arc-quenching effect which is essentially based on prevention of the resistance sparking of alternating current switch arcs and normally a longer service life in the switching arc.
- the contact materials produced in this way have a favorable welding behavior but inadequate resistance to ignition loss (see Metall 6, 1952, page 369). Even the addition of other oxides increased the service life only by a small amount (US. Pat. No. 2,796,346, British Patent Specification No. 683,343).
- the method of single pressing always produces highly porous brittle compound bodies with coarse oxide coatings and is therefore used in cases in which it is of more importance to ensure a high resistance to welding than a high resistance to ignition loss of the contacts, for example, in aviation switch units with low switch voltages.
- silver-cadmium oxide materials can be made by internal oxidation of melted homogenous silver-cadmium alloys (this method hereinafter being referred to as 01).
- this oxidation method represents a marked advance, at least as regards the ignition loss of the contacts (see US Pat. No. 2,673,167; Metall 10, 1956, page 628).
- the quality of the contact materials AgCdO with A CdO content of 6 to 15% by weight which are produced by internal oxidation, is mainly determined by the form in which the CdO is precipitated. It is generally considered that the best material was that in which the CdO was finely granulated and uniformly distributed throughout the volume. Thus one hoped to avoid in the case of interruption of the oxidation the formation of linear CdO precipitates and/or with CdO concentrations in the grain boundaries and heterogenous confining of Cd() agglomerates the tendency towards zones of low material strength and increased friction.
- grain-refining additives such as Ni, Co, Fe, Mo, Cr, Ti, Sn, Zn and V should be added in very small quantities (0.001 to 1 weight to the AgCd alloy (see German Patent Specification No. 1,153,178; British Patent Specifications Nos. 1,032,398 and 2,796,346) and/or that there should be an increase in the partial oxygen pressure during oxidation in order to ensure uniform precipitation and to make the brittle material deformable.
- the micrograph of a material which was produced in accordance with the method 01 shows homogenous distribution of the CdO particles (grain size D 5 microns).
- Such a structure was generally considered a prerequisite for optimal resistance to ignition loss since CdO concentration in the grain boundaries of the silver considerably weakens the matrix and leads in the switching operation to a destruction of the contact pieces along the grain boundaries.
- P2 a more recent method of manufacture in which a mixture fillingof very finely distributed silver and cadmium oxide is sintered to blocksand then sealed by heat deformation using for example rollers or extrusion presses (see Metallisme 58, 1967, page 752; German Patent Publication P1,539,848,8).
- silver-metal oxide composites attain their highest degree of resistance to melting loss when the oxide particles were distributed as homogenously as possible in the silver matrix.
- the silver matrix is formed having in its structure concentrated metallic oxide grains at its grain boundaries, and the alloy comprises at least two of the following alloying metals: Ca, Sb, Mg, Be, Al, Sn, Mn, Bu and Zr.
- the oxide precipitation of the new contact material of the invention produces extremely finely granulated (D 0.1, micron) material, preferably in the grain boundaries of the silver matrix and in a considerably less extent in the Ag grain.
- This type of precipitation is obtained by an addition of at least two of the metals Ca, Li, Sb, Mg, Be, Al, Sn, Mn, Bi and Zr to the Ag/Cd base alloy.
- Ignition loss characteristics well above the average are shown by the following internally oxidized alloys (oxidation in oxygenated atmosphere at 600 to 850 C.):
- the materials produced are brittle and can be deformed only with great difficulty.
- the brittleness alone is, however, not an adequate criterion for a high resistance to ignition loss.
- An addition of for example 0.1 weight Mn alone to the AgCd alloy increases the hardness and the brittleness of the oxidized material considerably, but at the same time reduces the service life to about half that of a AgCdO material without additives which is easily deformable. Only the addition of a second element of the series listed above produces the unexpected effect.
- the material of the invention is suitable, in contrast to the known AgCdO materials as per Pl, P2and 01, for fast-switching low voltage switches.
- Method of manufacturing a brittle, homogeneous silver-cadmium oxide composite having grain boundaries and metal oxide grains enriched at said grain boundaries in a silver matrix which comprises: (1) mixing together to form an alloy silver, cadmium and at least two other alloy components selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, and (2) internally oxidizing said alloy in an oxidizing atmosphere at a temperature from about 600C to about 850C to precipitate extremely finely granulated oxide material in the grain boundaries of the silver matrix, the proportions by weight of components in said composite being from about 6% to about 15% of cadmium oxide, and from about 0.5% to about 6% of each oxide of said other alloy components.
- Met lfid according to claim 1 wherein the oxides of each of said other alloy components are present in amounts of from about 0.5% to about 2% by weight.
- Method of manufacturing contact pieces for low voltage switching which comprises (1) forming an alloy from silver, cadmium and at least two alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, (2) shaping said alloy into electrical contact pieces of desired size and shape, (3) internally oxidizing the contact pieces of said aloy in an oxidizing atmosphere at a temperature from about 600C to about 850C to precipitate extremely fine granulated oxide material in the grain boundaries of the silver, the proportions by weight of components in said oxidized alloy being from about 6% to about 15% of cadmium oxide, and from about 0.5% to about 6% of each oxide of said alloy metals, and (4) recovering the oxidized contact pieces suitable for long life low voltage switching operations.
- alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Composite Materials (AREA)
- Contacts (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Switches (AREA)
Abstract
The composite comprises a silver matrix having grain boundaries and metal oxide grains enriched at said grain boundaries of said silver matrix. An alloy is provided, which comprises silver, a second metallic component, and at least two alloying metals selected from the class consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium. Said second metallic component and said alloying metals are oxidized in said alloy to form said composite.
Description
United States Patent [191 Diirrwiichter et al.
[ Jan. 15, 1974 SILVER-METAL OXIDE COMPOSITE AND METHOD OF MANUFACTURING THE SAME Inventors: Eugen Emil Diirrwiichter,
Savosa/Ticino, Switzerland; Ulf Harmsen; Wilhelm Merl, both of Pforzheim, Germany Dr. Eugen Durrwachter DODUCO, Pforzheim, Germany Filed: Dec. 22, 1971 Appl. No.: 211,038
Assignee:
Foreign Application Priority Data Mar. 3, 1970 Germany 2011002 US. Cl 75/173 A Int. Cl. C226 5/00 Field of Search 75/173 R, 173 C References Cited UNITED STATES PATENTS 6/1957 Stumbock 75/173 R 4/1958 Gwyn 75/173 R X 3,472,654 10/1969 Comey et a1 75/173 R 3,515,542 6/1970 Larsen 75/173 R X 3,607,244 9/1971 Kabayama 75/173 R FOREIGN PATENTS OR APPLICATIONS 15,619 6/1970 Japan 75/173 R 1,139,281 11/1962 Germany 75/173 R 2,012,910 10/1970 Germany 75/173 R Primary Examiner-L. Dewayne Rutledge Assistant Examiner-E. L. Weise Attorney-John .l. McGlew et al.
[5 7 ABSTRACT 10 Claims, No Drawings SILVER-METAL OXIDE COMPOSITE AND METHOD OF MANUFACTURING THE SAME The invention relates to a silver-metal oxide composite, in particular silver-cadmium oxide, for use on contact pieces in low voltage switching apparatus, and to a method for its manufacture.
Silver-metal oxide composites, preferably silvercadmium oxide with 6 to 15% by weight CdO, have been used for quite some time as contact-surfacing material in low voltage switch apparatus. The advantage of these materials in relation to pure silver is a considerably lesser likelihood of welding during the switching operation, an arc-quenching effect which is essentially based on prevention of the resistance sparking of alternating current switch arcs and normally a longer service life in the switching arc.
In the manufacture of such materials, one known method is to mix mechanically powders of silver and cadmium oxide and to seal the powder mixture in a single pressing technique to the contact pieces which are then sintered below the melting point of silver. This method of manufacture is hereinafter referred to as P1.
The contact materials produced in this way have a favorable welding behavior but inadequate resistance to ignition loss (see Metall 6, 1952, page 369). Even the addition of other oxides increased the service life only by a small amount (US. Pat. No. 2,796,346, British Patent Specification No. 683,343). The method of single pressing always produces highly porous brittle compound bodies with coarse oxide coatings and is therefore used in cases in which it is of more importance to ensure a high resistance to welding than a high resistance to ignition loss of the contacts, for example, in aviation switch units with low switch voltages.
Significantly better silver-cadmium oxide materials can be made by internal oxidation of melted homogenous silver-cadmium alloys (this method hereinafter being referred to as 01). For the majority of low voltage switch units such as air-break contactors, motorprotective switches and cable protection switches, this oxidation method represents a marked advance, at least as regards the ignition loss of the contacts (see US Pat. No. 2,673,167; Metall 10, 1956, page 628).
The quality of the contact materials AgCdO with A CdO content of 6 to 15% by weight which are produced by internal oxidation, is mainly determined by the form in which the CdO is precipitated. It is generally considered that the best material was that in which the CdO was finely granulated and uniformly distributed throughout the volume. Thus one hoped to avoid in the case of interruption of the oxidation the formation of linear CdO precipitates and/or with CdO concentrations in the grain boundaries and heterogenous confining of Cd() agglomerates the tendency towards zones of low material strength and increased friction.
With a view to refinement of the grains it was therefore proposed, for example, that grain-refining additives such as Ni, Co, Fe, Mo, Cr, Ti, Sn, Zn and V should be added in very small quantities (0.001 to 1 weight to the AgCd alloy (see German Patent Specification No. 1,153,178; British Patent Specifications Nos. 1,032,398 and 2,796,346) and/or that there should be an increase in the partial oxygen pressure during oxidation in order to ensure uniform precipitation and to make the brittle material deformable.
Only in the applications mentioned above, in which the resistance to ignition loss is of less importance than the welding characteristics, were additives to cause embrittlement ever used, for example, Mg (US. Pat. No. 2,669,512).
The micrograph of a material which was produced in accordance with the method 01 shows homogenous distribution of the CdO particles (grain size D 5 microns). Such a structure was generally considered a prerequisite for optimal resistance to ignition loss since CdO concentration in the grain boundaries of the silver considerably weakens the matrix and leads in the switching operation to a destruction of the contact pieces along the grain boundaries.
These requirements are met by a more recent method of manufacture (hereinafter referred to as P2) in a powder metallurgical process in which a mixture fillingof very finely distributed silver and cadmium oxide is sintered to blocksand then sealed by heat deformation using for example rollers or extrusion presses (see Metallkunde 58, 1967, page 752; German Patent Publication P1,539,848,8).
It was therefore generally assumed that silver-metal oxide composites attain their highest degree of resistance to melting loss when the oxide particles were distributed as homogenously as possible in the silver matrix.
In contrast to this generally held opinion in the technology it has been shown, rather surprisingly, in the course of an extensive investigation of the contact behavior of internally oxidized silver-metal oxide composites that in some cases silver-cadmium oxide composites with very high grain boundary concentrations and striking brittleness of the contact pieces can result in an extraordinarily longservice life even under severe conditions. The behavior of this material contradicts all previous experience and cannot at the moment be scientifically explained.
Therefore, according to the present invention, in a method of manufacturing a material having a silver matrix from a silver-metal base alloy, in particular a silvermetal oxide composite for use in contact pieces, the silver matrix is formed having in its structure concentrated metallic oxide grains at its grain boundaries, and the alloy comprises at least two of the following alloying metals: Ca, Sb, Mg, Be, Al, Sn, Mn, Bu and Zr.
The oxide precipitation of the new contact material of the invention produces extremely finely granulated (D 0.1, micron) material, preferably in the grain boundaries of the silver matrix and in a considerably less extent in the Ag grain.
This type of precipitation is obtained by an addition of at least two of the metals Ca, Li, Sb, Mg, Be, Al, Sn, Mn, Bi and Zr to the Ag/Cd base alloy.
Ignition loss characteristics well above the average are shown by the following internally oxidized alloys (oxidation in oxygenated atmosphere at 600 to 850 C.):
Ag-Cd l0 Ca 0.7 Sn 0.6 Ni 0.2
Ag-Cd l1 Sn 1 Ca 0.3 Ni 0.3
Ag-Cd 12 Sb 0.5 Sn 0.5 Ca 0.3
Ag-Cd 12 Sn 0.5 Ca 0.3
Ag-Cd 12 Sb 0.5 Sn 0.5
Ag-Cd Be 0.3 Ca 0.3
The materials produced are brittle and can be deformed only with great difficulty.
The brittleness alone is, however, not an adequate criterion for a high resistance to ignition loss. An addition of for example 0.1 weight Mn alone to the AgCd alloy increases the hardness and the brittleness of the oxidized material considerably, but at the same time reduces the service life to about half that of a AgCdO material without additives which is easily deformable. Only the addition of a second element of the series listed above produces the unexpected effect.
EXAMPLE From 86.7% Ag, 12% Cd, 0.5% Sb, 0.5% Sn and 0.3% Ca (all by weight) an alloy is molten in an electrically heated furnace and cast in bar form. The soft bars are smoothed down and after repeated rolling and intermediate annealing at 650 C. in inert gas with a silver plate in accordance with known roller plating methods, so that they can subsequently be perfectly soldered to the contact supports. From the still soft plate the contact discs are now punched, for example, in dimensions of 16 X 16 X 2.1 mm. These contact discs are now internally oxidized for l 1 days at 700 C. under a pressure of 1 atmosphere above atmospheric pressure. The contact discs become brittle as a result. The structure of the silver matrix is fine-grained. On the grain boundaries the extremely small metallic oxide particles have collected together.
The service life of contact discs made from material produced in this manner is apparent from table 1 and it is there shown in comparison with AgCdO qualities which were produced in accordance with the powder metallurgical method P1 and P2or by internal oxidation of a known alloy 01.
TABLE 1 Maximum number of switching operations: 60,000-l20,000 210,000-280,000 300,000-450,000
Material produced as per process:
AgCdO l2 as per Pl AgCdO 12 as per l AgCdO 12 as per P2 Material according to the invention 500,000-750,000
Apart from the considerably longer service life, the appearance of the contact parts after this extreme load is noteworthy. The surface of the contact pieces made from the new material is in spite of the appearance of many microscopic cracks very uniformly eroded and in comparison with the surface of contact pieces made from AgCdO which have been produced by the known methods, it shows no silver concentration nor droplets of welded material at the edge.
For these reasons, namely (1) low ignition loss (2) uniform ignition loss and (3) no formation of droplets of welded material, the material of the invention is suitable, in contrast to the known AgCdO materials as per Pl, P2and 01, for fast-switching low voltage switches.
What is claimed is:
1. Method of manufacturing a brittle, homogeneous silver-cadmium oxide composite having grain boundaries and metal oxide grains enriched at said grain boundaries in a silver matrix, which comprises: (1) mixing together to form an alloy silver, cadmium and at least two other alloy components selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, and (2) internally oxidizing said alloy in an oxidizing atmosphere at a temperature from about 600C to about 850C to precipitate extremely finely granulated oxide material in the grain boundaries of the silver matrix, the proportions by weight of components in said composite being from about 6% to about 15% of cadmium oxide, and from about 0.5% to about 6% of each oxide of said other alloy components.
2. Met lfid according to claim 1, wherein the oxides of each of said other alloy components are present in amounts of from about 0.5% to about 2% by weight.
3. Method according to claim 1, wherein said alloy is formed from 86.7% silver, 12% cadmium, 0.5% antimony, 0.5% tin, and 0.3% calcium, all of said percents being by weight.
4. Method according to claim 1, wherein said alloy is formed from 88.5% silver, 10% cadmium, 0.7% calcium, 0.6% tin, and 0.2% nickel, all of said percents being by weight.
w 6. Method according to claim 1, wherein said alloy is formed from 86.7% silver, 12% cadmium, 0.5% antimony, 0.5% tin, 0.3% calcium, all of said percents being by weight.
7. Method according to claim 1, wherein said alloy is formed from 87.2% silver, 12% cadmium, 0.5% tin, 0.3% calcium, all of said percents being by weight.
8. Method according to claim 1, wherein said alloy is formed from 87% silver, 12% cadmium, 0.5% antimony and 0.5% tin, all of said percents being by weight.
9. Method of manufacturing contact pieces for low voltage switching which comprises (1) forming an alloy from silver, cadmium and at least two alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, (2) shaping said alloy into electrical contact pieces of desired size and shape, (3) internally oxidizing the contact pieces of said aloy in an oxidizing atmosphere at a temperature from about 600C to about 850C to precipitate extremely fine granulated oxide material in the grain boundaries of the silver, the proportions by weight of components in said oxidized alloy being from about 6% to about 15% of cadmium oxide, and from about 0.5% to about 6% of each oxide of said alloy metals, and (4) recovering the oxidized contact pieces suitable for long life low voltage switching operations.
10. Composite of silver-cadmium oxide with at least two oxides of alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, said composite consisting essentially of a silver matrix, fine grains of oxide less than 0.1 micron diameter in the grain boundaries of the silver matrix and in considerably less extent in the silver grain, the amounts by weight of components other than silver in said composite being from about 6% to about 15% cadmium oxide, and from about 0.5% to about 6% of each of said oxides of alloy metals.
Claims (9)
- 2. Method according to claim 1, wherein the oxides of each of said other alloy components are present in amounts of from about 0.5% to about 2% by weight.
- 3. Method according to claim 1, wherein said alloy is formed from 86.7% silver, 12% cadmium, 0.5% antimony, 0.5% tin, and 0.3% calcium, all of said percents being by weight.
- 4. Method according to claim 1, wherein said alloy is formed from 88.5% silver, 10% cadmium, 0.7% calcium, 0.6% tin, and 0.2% nickel, all of said percents being by weight.
- 5. Method according to claim 1, wherein said alloy is formed from 87.4% silver, 11% cadmium, 1% tin, 0.3% calcium, 0.3% nickel, all of said percents being by weight.
- 6. Method according to claim 1, wherein said alloy is formed from 86.7% silver, 12% cadmium, 0.5% antimony, 0.5% tin, 0.3% calcium, all of said percents being by weight.
- 7. Method according to claim 1, wherein said alloy is formed from 87.2% silver, 12% cadmium, 0.5% tin, 0.3% calcium, all of said percents being by weight.
- 8. Method according to claim 1, wherein said alloy is formed from 87% silver, 12% cadmium, 0.5% antimony and 0.5% tin, all of said percents being by weight.
- 9. Method of manufacturing contact pieces for low voltage switching which comprises (1) forming an alloy from silver, cadmium and at least two alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, (2) shaping said alloy into electrical contact pieces of desired size and shape, (3) internally oxidizing the contact pieces of said alloy in an oxidizing atmosphere at a temperature from about 600*C to about 850*C to precipitate extremely fine granulated oxide material in the grain boundaries of the silver, the proportions by weight of components in said oxidized alloy being from about 6% to about 15% of cadmium oxide, and from about 0.5% to about 6% of each oxide of said alloy metals, and (4) recovering the oxidized contact pieces suitable for long life low voltage switching operations.
- 10. Composite of silver-cadmium oxide with at least two oxides of alloy metals selected from the group consisting of calcium, antimony, magnesium, beryllium, aluminum, tin, manganese, and zirconium, said composite consisting essentially of a silver matrix, fine grains of oxide less than 0.1 micron diameter in the grain boundaries of the silver matrix and in considerably less extent in the silver grain, the amounts by weight of components other than silver in said composite being from about 6% to about 15% cadmium oxide, and from about 0.5% to about 6% of each of said oxides of alloy metals.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2011002A DE2011002C3 (en) | 1970-03-09 | 1970-03-09 | Internally oxidized contact material on the basis of silver-cadmium oxide produced by melt metallurgy |
Publications (1)
Publication Number | Publication Date |
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US3785810A true US3785810A (en) | 1974-01-15 |
Family
ID=5764522
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00211038A Expired - Lifetime US3785810A (en) | 1970-03-09 | 1971-12-22 | Silver-metal oxide composite and method of manufacturing the same |
Country Status (6)
Country | Link |
---|---|
US (1) | US3785810A (en) |
CH (1) | CH549864A (en) |
DE (1) | DE2011002C3 (en) |
ES (1) | ES388906A1 (en) |
FR (1) | FR2084338A5 (en) |
GB (1) | GB1336461A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4050930A (en) * | 1975-06-24 | 1977-09-27 | Sumitomo Electric Industries, Ltd. | Electrical contact material |
US4396420A (en) * | 1979-07-21 | 1983-08-02 | Dornier System Gmbh | Process for making Ag powder with oxides |
US4452651A (en) * | 1982-07-08 | 1984-06-05 | Chugai Denki Kogyo K.K. | Electrical contact materials and their production method |
US4452652A (en) * | 1982-07-08 | 1984-06-05 | Akira Shibata | Electrical contact materials and their production method |
DE3335274A1 (en) * | 1983-09-29 | 1985-04-18 | G. Rau GmbH & Co, 7530 Pforzheim | METHOD FOR PRODUCING A CONTACT MOLDING PIECE AND CONTACT MOLDING PRODUCED BY THIS |
US4904317A (en) * | 1988-05-16 | 1990-02-27 | Technitrol, Inc. | Erosion resistant Ag-SnO2 electrical contact material |
EP0465128A2 (en) * | 1990-06-28 | 1992-01-08 | Sumitomo Metal Mining Company Limited | Silver- or silver-copper alloy-metal oxide composite material and process of producing the same |
US20050089439A1 (en) * | 2002-12-10 | 2005-04-28 | Hiroyuki Keduka | Silver alloy for reflective film of optical recording medium |
CN105220003A (en) * | 2015-10-25 | 2016-01-06 | 无棣向上机械设计服务有限公司 | A kind of high temperature resistant silver alloy and preparation method thereof |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4883392A (en) * | 1972-02-15 | 1973-11-07 | ||
US3933485A (en) * | 1973-07-20 | 1976-01-20 | Chugai Denki Kogyo Kabushiki-Kaisha | Electrical contact material |
US3933486A (en) * | 1974-02-12 | 1976-01-20 | Chugai Denki Kogyo Kabushiki-Kaisha | Silver-metal oxide composite and method of manufacturing the same |
US4150982A (en) * | 1978-03-13 | 1979-04-24 | Chugai Denki Kogyo Kabushiki-Kaisha | AG-Metal oxides electrical contact materials containing internally oxidized indium oxides and/or tin oxides |
FR2499760B1 (en) * | 1981-02-12 | 1990-08-10 | Chugai Electric Ind Co Ltd | MATERIAL FOR MAKING ELECTRICAL CONTACTS |
JPS6355822A (en) * | 1986-08-26 | 1988-03-10 | 松下電工株式会社 | Contact material |
JPH03215635A (en) * | 1990-01-19 | 1991-09-20 | Chugai Electric Ind Co Ltd | Internal oxidation of electrical contact material and electrical contact material |
-
1970
- 1970-03-09 DE DE2011002A patent/DE2011002C3/en not_active Expired
-
1971
- 1971-01-28 CH CH124571A patent/CH549864A/en not_active IP Right Cessation
- 1971-03-04 ES ES388906A patent/ES388906A1/en not_active Expired
- 1971-03-09 FR FR7108023A patent/FR2084338A5/fr not_active Expired
- 1971-04-19 GB GB2161071A patent/GB1336461A/en not_active Expired
- 1971-12-22 US US00211038A patent/US3785810A/en not_active Expired - Lifetime
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4050930A (en) * | 1975-06-24 | 1977-09-27 | Sumitomo Electric Industries, Ltd. | Electrical contact material |
US4396420A (en) * | 1979-07-21 | 1983-08-02 | Dornier System Gmbh | Process for making Ag powder with oxides |
US4452651A (en) * | 1982-07-08 | 1984-06-05 | Chugai Denki Kogyo K.K. | Electrical contact materials and their production method |
US4452652A (en) * | 1982-07-08 | 1984-06-05 | Akira Shibata | Electrical contact materials and their production method |
DE3335274A1 (en) * | 1983-09-29 | 1985-04-18 | G. Rau GmbH & Co, 7530 Pforzheim | METHOD FOR PRODUCING A CONTACT MOLDING PIECE AND CONTACT MOLDING PRODUCED BY THIS |
US4574014A (en) * | 1983-09-29 | 1986-03-04 | G. Rau Gmbh & Co. | Process for manufacturing a formed contact part |
US4904317A (en) * | 1988-05-16 | 1990-02-27 | Technitrol, Inc. | Erosion resistant Ag-SnO2 electrical contact material |
EP0465128A2 (en) * | 1990-06-28 | 1992-01-08 | Sumitomo Metal Mining Company Limited | Silver- or silver-copper alloy-metal oxide composite material and process of producing the same |
EP0465128A3 (en) * | 1990-06-28 | 1992-09-23 | Sumitomo Metal Mining Company Limited | Silver- or silver-copper alloy-metal oxide composite material and process of producing the same |
US5236523A (en) * | 1990-06-28 | 1993-08-17 | Akira Shibata | Silver- or silver-copper alloy-metal oxide composite material |
US20050089439A1 (en) * | 2002-12-10 | 2005-04-28 | Hiroyuki Keduka | Silver alloy for reflective film of optical recording medium |
CN105220003A (en) * | 2015-10-25 | 2016-01-06 | 无棣向上机械设计服务有限公司 | A kind of high temperature resistant silver alloy and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
ES388906A1 (en) | 1973-05-16 |
DE2011002B2 (en) | 1973-01-04 |
DE2011002A1 (en) | 1971-09-30 |
CH549864A (en) | 1974-05-31 |
DE2011002C3 (en) | 1978-10-05 |
GB1336461A (en) | 1973-11-07 |
FR2084338A5 (en) | 1971-12-17 |
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