US3498763A - Workable duplex structured ruthenium alloys - Google Patents
Workable duplex structured ruthenium alloys Download PDFInfo
- Publication number
- US3498763A US3498763A US806314A US3498763DA US3498763A US 3498763 A US3498763 A US 3498763A US 806314 A US806314 A US 806314A US 3498763D A US3498763D A US 3498763DA US 3498763 A US3498763 A US 3498763A
- Authority
- US
- United States
- Prior art keywords
- ruthenium
- alloy
- alloys
- matrix
- copper
- 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 - Lifetime
Links
- 229910000929 Ru alloy Inorganic materials 0.000 title description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 29
- 229910045601 alloy Inorganic materials 0.000 description 29
- 239000000956 alloy Substances 0.000 description 29
- 229910052707 ruthenium Inorganic materials 0.000 description 29
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 26
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 18
- 239000011159 matrix material Substances 0.000 description 17
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 13
- 229910052802 copper Inorganic materials 0.000 description 13
- 239000010949 copper Substances 0.000 description 13
- 229910052763 palladium Inorganic materials 0.000 description 13
- 229910052759 nickel Inorganic materials 0.000 description 9
- 238000005245 sintering Methods 0.000 description 7
- 235000019589 hardness Nutrition 0.000 description 5
- 230000008595 infiltration Effects 0.000 description 5
- 238000001764 infiltration Methods 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000010273 cold forging Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- BBKFSSMUWOMYPI-UHFFFAOYSA-N gold palladium Chemical compound [Pd].[Au] BBKFSSMUWOMYPI-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
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
-
- 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
-
- 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
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
- Y10T428/1216—Continuous interengaged phases of plural metals, or oriented fiber containing
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12458—All metal or with adjacent metals having composition, density, or hardness gradient
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12868—Group IB metal-base component alternative to platinum group metal-base component [e.g., precious metal, etc.]
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12875—Platinum group metal-base component
Definitions
- a cold-workable ruthenium alloy capable of being cold drawn to wire containing, by weight, about 60% to about 90% ruthenium, about 5% to about 40% copper, up to about 35 palladium and up to about nickel is produced by liquid-phase sintering, preferably by infiltration of copper or copper alloy into a ruthenium compact, at temperatures between 1083 C. and 1500 C.
- Such an alloy has the essential advantageous properties of pure ruthenium but can be worked.
- the more wear-resistant ruthenium grains stand out presenting, in effect, a substantially pure ruthenium surface. Deeper within the mass of the alloy the ruthenium grains are surrounded by and metallurgically bonded to the matrix metal.
- the matrix metal and the ruthenium co-operate to produce a workable alloy of substantial hardness and strength and appreciable ductility.
- an alloy composed of grains of ruthenium dispersed in a matrix contains by weight from 5% to copper, from 0 to 35% palladium and 0 to 10% nickel, the balance except for impurities being ruthenium and amounting to at least 60%.
- the impurities normally will not exceed 0.5%.
- the alloys according to the invention are made by powder-metallurgical methods which involve heating a powder compact to a sintering temperature at which the matrix melts but the ruthenium does not.
- This compact may initially consist of all the elements, or only of the ruthenium, the compact then being infiltrated with molten matrix at the sintering temperature, which may be from 1083 C. (the melting point of copper) to 1500 C. It is advantageous to subject a ruthenium compact to light sintering under vacuum before the infiltration.
- ruthenium enters the matrix, which indeed is believed to become substantially saturated in ruthenium, and the ruthenium grains, which are advantageously from 0.002 inch to 0.0002 inch in diameter, become metallurgically bonded to the matrix. It is found that in the process the grains of ruthenium tend to grow, and also to become rounded. Workability of the alloy depends to some extent upon this phenomenon, increasing as the spheroidicity of the ruthenium particles increases. Sagging or distortion occurs during sintering if the ruthe nium content is below 60% and the ductility of the alloy is low if the ruthenium is above 90%, the ruthenium con- 3,498,763 Patented Mar. 3, 1970 tent preferably not exceeding If the matrix amounts to less than 5% of the alloy, workability is lost.
- the matrix is binary, the alloy containing from 20% to 25% copper and either 1% to 5% nickel or 9% to 13% palladium.
- composition of some alloys within the invention will now be given, the balance in each case being ruthenium. All the alloys were made by infiltration of a molten matrix into a ruthenium compact for two hours.
- the ruthenium powder had a particle size of about 4a (microns).
- the temperature of infiltration is given in each case, together with the extent to which the alloy could be reduced by cold forging Without intermediate anneals before edge cracks developed and the hardnesses of the primary phase (the ruthenium) and the secondary phase (the matrix).
- Cu Ni 0. percent mHV mHVr Alloys as described in the table are capable of being drawn to wire, with cold reductions in area of about 5% to 10% per pass being employed and with total cold reductions in area of 30% being realized without intermediate anneals. Wire having a diameter as small as 0.06 inch can be produced from these alloys.
- the alloys according to the invention are eminently suitable for electrical contacts since the alloys can be made into wire and upset or coldheaded to produce contact surfaces.
- the invention affords two additional advantages. One arises from the fact that the sintering of alloys of the kind in question is efiected in practice in a non-oxidizing atmosphere.
- the prior alloys containing palladium in the matrix are sintered in argon with or without partial vacuum because of the ease with which palladium picks up hydrogen.
- the present alloys that have a matrix of copper or copper and nickel can be sintered at substantially atmospheric pressure in hydrogen or a mixture of hydrogen and nitrogen, both of which are cheaper and more readily available than argon.
- the second additional advantage is that copper and nickel are less expensive than palladium and gold.
- a liquid-phase sintered alloy containing, by weight, about 5% to about 40% copper, up to about 35 palladium, up to about 10% nickel and the balance essentially ruthenium, with the ruthenium content being at having aduplex microstructureconsisting of rounded ru-- thenium grains in a matrix from the group consisting of copper and of copper alloyed with at least one metal from the group consisting of nickel and palladium and saturated with ruthenium.
- An alloy according to claim 1 containing not more than 80% palladium.
- An alloy according to claim 1 containing about 20% to about 25% copper and one metal from the group consisting of about 1% to about 5% nickel and 9% to about 13% palladium.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Composite Materials (AREA)
- Powder Metallurgy (AREA)
- Inert Electrodes (AREA)
Description
United States PatentO US. Cl. 29-1821 4 Claims ABSTRACT OF THE DISCLOSURE A cold-workable ruthenium alloy capable of being cold drawn to wire containing, by weight, about 60% to about 90% ruthenium, about 5% to about 40% copper, up to about 35 palladium and up to about nickel is produced by liquid-phase sintering, preferably by infiltration of copper or copper alloy into a ruthenium compact, at temperatures between 1083 C. and 1500 C.
In US. Patent No. 3,278,280, alloys composed of grains of ruthenium dispersed in a gold-palladium matrix and containing by weight from 5% to gold and 5% to 35% palladium, the balance except for impurities being ruthenium and amounting to at least 60%, are described.
Such an alloy has the essential advantageous properties of pure ruthenium but can be worked. At the surface of the alloy, the more wear-resistant ruthenium grains stand out presenting, in effect, a substantially pure ruthenium surface. Deeper within the mass of the alloy the ruthenium grains are surrounded by and metallurgically bonded to the matrix metal. By virtue of composition, the matrix metal and the ruthenium co-operate to produce a workable alloy of substantial hardness and strength and appreciable ductility. Although these previous alloys are workable, they cannot readily be drawn into wire.
We have now found that if the matrix of palladium and gold is replaced by a matrix of copper or an alloy of copper with nickel or palladium or both, the workability is improved such that the alloy can be readily drawn to wire.
Thus, according to the invention an alloy composed of grains of ruthenium dispersed in a matrix contains by weight from 5% to copper, from 0 to 35% palladium and 0 to 10% nickel, the balance except for impurities being ruthenium and amounting to at least 60%. The impurities normally will not exceed 0.5%.
The alloys according to the invention are made by powder-metallurgical methods which involve heating a powder compact to a sintering temperature at which the matrix melts but the ruthenium does not. This compact may initially consist of all the elements, or only of the ruthenium, the compact then being infiltrated with molten matrix at the sintering temperature, which may be from 1083 C. (the melting point of copper) to 1500 C. It is advantageous to subject a ruthenium compact to light sintering under vacuum before the infiltration.
During the sintering, ruthenium enters the matrix, which indeed is believed to become substantially saturated in ruthenium, and the ruthenium grains, which are advantageously from 0.002 inch to 0.0002 inch in diameter, become metallurgically bonded to the matrix. It is found that in the process the grains of ruthenium tend to grow, and also to become rounded. Workability of the alloy depends to some extent upon this phenomenon, increasing as the spheroidicity of the ruthenium particles increases. Sagging or distortion occurs during sintering if the ruthe nium content is below 60% and the ductility of the alloy is low if the ruthenium is above 90%, the ruthenium con- 3,498,763 Patented Mar. 3, 1970 tent preferably not exceeding If the matrix amounts to less than 5% of the alloy, workability is lost.
In the preferred alloys, the matrix is binary, the alloy containing from 20% to 25% copper and either 1% to 5% nickel or 9% to 13% palladium.
The composition of some alloys within the invention will now be given, the balance in each case being ruthenium. All the alloys were made by infiltration of a molten matrix into a ruthenium compact for two hours. The ruthenium powder had a particle size of about 4a (microns). The temperature of infiltration is given in each case, together with the extent to which the alloy could be reduced by cold forging Without intermediate anneals before edge cracks developed and the hardnesses of the primary phase (the ruthenium) and the secondary phase (the matrix).
TABLE I Micro- Micro- Composition, Reduction hardness hardness percent Temperature after coldprimary secondary of infiltration, forging, phase, phase,
Cu Ni 0. percent mHV mHVr Alloys as described in the table are capable of being drawn to wire, with cold reductions in area of about 5% to 10% per pass being employed and with total cold reductions in area of 30% being realized without intermediate anneals. Wire having a diameter as small as 0.06 inch can be produced from these alloys.
An element of considerable surprise is that with high hardness in the primary phase, that is to say above 550 mHV (as determined by means of the Vickers microhardness tester having a diamond indenter and using a 50 gram load), it is still possible to Work the alloys satisfactorily.
Because of their workability, the alloys according to the invention are eminently suitable for electrical contacts since the alloys can be made into wire and upset or coldheaded to produce contact surfaces.
The invention affords two additional advantages. One arises from the fact that the sintering of alloys of the kind in question is efiected in practice in a non-oxidizing atmosphere. The prior alloys containing palladium in the matrix are sintered in argon with or without partial vacuum because of the ease with which palladium picks up hydrogen. The present alloys that have a matrix of copper or copper and nickel can be sintered at substantially atmospheric pressure in hydrogen or a mixture of hydrogen and nitrogen, both of which are cheaper and more readily available than argon. The second additional advantage is that copper and nickel are less expensive than palladium and gold.
Although the present invention has been described in conjunction with preferred embodiments, it is to be understood that modifications and variations may be resorted to without departing from the spirit and scope of the invention as those skilled in the art will readily understand. Such modifications and variations are considered to be within the purview and scope of the inventionand appended claims.
I claim:
1. A liquid-phase sintered alloy containing, by weight, about 5% to about 40% copper, up to about 35 palladium, up to about 10% nickel and the balance essentially ruthenium, with the ruthenium content being at having aduplex microstructureconsisting of rounded ru-- thenium grains in a matrix from the group consisting of copper and of copper alloyed with at least one metal from the group consisting of nickel and palladium and saturated with ruthenium.
2. An alloy according to claim 1 containing not more than 80% palladium.
3. An alloy according to claim 1 containing about 20% to about 25% copper and one metal from the group consisting of about 1% to about 5% nickel and 9% to about 13% palladium.
4. An electrical contact made of the alloy of claim 1 and having a contact surface produced thereon by cold work.
References Cited UNITED STATES PATENTS BENJAMIN R. PADGETT, Primary Examiner A. I. STEINER, Assistant Examiner US. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB04237/68A GB1188773A (en) | 1968-03-25 | 1968-03-25 | Ruthenium Alloys. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3498763A true US3498763A (en) | 1970-03-03 |
Family
ID=10037521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US806314A Expired - Lifetime US3498763A (en) | 1968-03-25 | 1969-03-11 | Workable duplex structured ruthenium alloys |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3498763A (en) |
| BE (1) | BE730408A (en) |
| DE (1) | DE1914631C3 (en) |
| FR (1) | FR2004686A6 (en) |
| GB (1) | GB1188773A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4324588A (en) * | 1979-08-17 | 1982-04-13 | Engelhard Corporation | Arc erosion resistant composite materials and processes for their manufacture |
| US9004969B2 (en) | 2011-10-24 | 2015-04-14 | Federal-Mogul Ignition Company | Spark plug electrode and spark plug manufacturing method |
| US9130358B2 (en) | 2013-03-13 | 2015-09-08 | Federal-Mogul Ignition Company | Method of manufacturing spark plug electrode material |
| US9337624B2 (en) | 2012-10-12 | 2016-05-10 | Federal-Mogul Ignition Company | Electrode material for a spark plug and method of making the same |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0188444B1 (en) * | 1984-06-27 | 1989-03-15 | AT&T Corp. | Electrical contacts comprising palladium alloy and connectors made therefrom |
| DE4206420C2 (en) * | 1992-02-29 | 1994-10-06 | Epe Eppensteiner Gmbh & Co | filter |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2470034A (en) * | 1945-11-27 | 1949-05-10 | Mallory & Co Inc P R | Electric contact formed of a ruthenium composition |
| US2983996A (en) * | 1958-07-30 | 1961-05-16 | Mallory & Co Inc P R | Copper-tungsten-molybdenum contact materials |
| US3301641A (en) * | 1964-01-27 | 1967-01-31 | Mallory & Co Inc P R | Tungsten-ruthenium alloy and powdermetallurgical method of making |
| US3320056A (en) * | 1965-05-14 | 1967-05-16 | Robert F Stoops | Liquid phase extrusion for forming refractory materials |
| US3362799A (en) * | 1964-05-13 | 1968-01-09 | Int Nickel Co | Ductile ruthenium alloy and process for producing the same |
| US3441409A (en) * | 1967-01-26 | 1969-04-29 | Chase Brass & Copper Co | Method of producing a corrosion resistant alloy of cu-ni by liquid phase sintering |
-
1968
- 1968-03-25 GB GB04237/68A patent/GB1188773A/en not_active Expired
-
1969
- 1969-03-11 US US806314A patent/US3498763A/en not_active Expired - Lifetime
- 1969-03-22 DE DE1914631A patent/DE1914631C3/en not_active Expired
- 1969-03-25 FR FR6908731A patent/FR2004686A6/fr not_active Expired
- 1969-03-25 BE BE730408D patent/BE730408A/xx unknown
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2470034A (en) * | 1945-11-27 | 1949-05-10 | Mallory & Co Inc P R | Electric contact formed of a ruthenium composition |
| US2983996A (en) * | 1958-07-30 | 1961-05-16 | Mallory & Co Inc P R | Copper-tungsten-molybdenum contact materials |
| US3301641A (en) * | 1964-01-27 | 1967-01-31 | Mallory & Co Inc P R | Tungsten-ruthenium alloy and powdermetallurgical method of making |
| US3362799A (en) * | 1964-05-13 | 1968-01-09 | Int Nickel Co | Ductile ruthenium alloy and process for producing the same |
| US3320056A (en) * | 1965-05-14 | 1967-05-16 | Robert F Stoops | Liquid phase extrusion for forming refractory materials |
| US3441409A (en) * | 1967-01-26 | 1969-04-29 | Chase Brass & Copper Co | Method of producing a corrosion resistant alloy of cu-ni by liquid phase sintering |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4324588A (en) * | 1979-08-17 | 1982-04-13 | Engelhard Corporation | Arc erosion resistant composite materials and processes for their manufacture |
| US9004969B2 (en) | 2011-10-24 | 2015-04-14 | Federal-Mogul Ignition Company | Spark plug electrode and spark plug manufacturing method |
| US9337624B2 (en) | 2012-10-12 | 2016-05-10 | Federal-Mogul Ignition Company | Electrode material for a spark plug and method of making the same |
| US9130358B2 (en) | 2013-03-13 | 2015-09-08 | Federal-Mogul Ignition Company | Method of manufacturing spark plug electrode material |
Also Published As
| Publication number | Publication date |
|---|---|
| BE730408A (en) | 1969-09-25 |
| DE1914631B2 (en) | 1973-05-30 |
| DE1914631A1 (en) | 1969-10-09 |
| DE1914631C3 (en) | 1973-12-13 |
| GB1188773A (en) | 1970-04-22 |
| FR2004686A6 (en) | 1969-11-28 |
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