US2586768A - Vacuum tube electrode element - Google Patents

Vacuum tube electrode element Download PDF

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Publication number
US2586768A
US2586768A US78233A US7823349A US2586768A US 2586768 A US2586768 A US 2586768A US 78233 A US78233 A US 78233A US 7823349 A US7823349 A US 7823349A US 2586768 A US2586768 A US 2586768A
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United States
Prior art keywords
nickel
vacuum tube
percent
electrode element
lanthanum
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Expired - Lifetime
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US78233A
Inventor
Francis E Bash
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Driver Harris Co
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Driver Harris Co
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Publication date
Application filed by Driver Harris Co filed Critical Driver Harris Co
Priority to US78233A priority Critical patent/US2586768A/en
Priority to GB3244/50A priority patent/GB713063A/en
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Publication of US2586768A publication Critical patent/US2586768A/en
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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J1/00Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
    • H01J1/02Main electrodes
    • H01J1/13Solid thermionic cathodes
    • H01J1/14Solid thermionic cathodes characterised by the material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J19/00Details of vacuum tubes of the types covered by group H01J21/00
    • H01J19/28Non-electron-emitting electrodes; Screens
    • H01J19/30Non-electron-emitting electrodes; Screens characterised by the material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2893/00Discharge tubes and lamps
    • H01J2893/0001Electrodes and electrode systems suitable for discharge tubes or lamps
    • H01J2893/0012Constructional arrangements
    • H01J2893/0019Chemical composition and manufacture
    • H01J2893/002Chemical composition and manufacture chemical
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/294Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
    • Y10T428/2958Metal or metal compound in coating

Definitions

  • sive coating generally an alkaline earth oxide on its surface.
  • the electrode elements such as a oath-- ode, are usually formed of a sleeve or wire of nickel coated with active oxides, such as barium or strontium oxide.
  • active oxides such as barium or strontium oxide.
  • the nickel used in the production of such cathodes will, of course, vary in composition.
  • the preparation of the nickel in the form in which it is to be used for the manufacture of cathode elements requires the melting of ingots and in this melting operation there is a tendency to form oxides.
  • the base nickel metal is substantially free of silicon, magnesium, titanium, aluminum and similar deoxidizers. These are the deoxidizers which are normally used in melting nickel to produce a malleable material which can be rolled to thin sheets of the order of .002 to .005" thick.
  • Inactive metals, such as iron and cobalt, are not considered harmful if not present in too large quantities.
  • slabs of electrolytically deposited nickel are melted in the usual manner, the normal procedure being followed up to the point where the metal is completely molten.
  • Misch metal In actual practice, I have employed one pound of Misch metal to a 1300 pound melt. This figure may, of course, vary. If the melting of the slabs is carried out in a manner that would normally result in the production of a minimum amount of nickel oxides, the quantity of Misch metal added may be less. Greater quantities of Misch metal up to as much as three pounds may be added.
  • the rare earth metals added to the melt reduce the nickel xides to nickel and the resulting rare earth oxides disappear from the molten bath.
  • the nickel so produced contains no more impurities than are present in the nickel slabs with the exception of the small amount of iron referred to. It is malleable, easily worked and annealed and therefore does not require the annealing treatments which are necessary with a nickel of high carbon content.
  • the desired quantities of rare earth metals such as cerium, lanthanum and didymium may be added directly.
  • the nickel produced would not contain the slight contamination of iron.
  • a vacuum tube having electrode elements at least one of which is composed of nickel and traces of rare earth metals.
  • a vacuum tube having electrode elements at least one of which is composed of nickel and traces of cerium and lanthanum.
  • a vacuum tube having electrode elements at least one of which is composed of nickel, a trace to 0.2 percent cerium and a trace to 0.2 percent lanthanum.
  • a cathode element for a vacuum tube consisting of nickel containing traces of rare earth metals, and an activating agent comprising an oxide coating thereon.
  • a cathode element for a vacuum tube consisting of nickel containing traces of cerium and lanthanum, and an activating agent comprising an oxide coating thereon.
  • a cathode element for a vacuum tube consisting of nickel containing a trace to 0.2 percent cerium and a trace to 0.2 percent lanthanum, and an activating agent comprising an oxide coating thereon.

Description

Patented Feb. 26, 1 952 VACUUM TUBE ELECTRODEaELEMF- NT Francis E. Bash, Morristown, N, J., assignpr t Driver-Harris Company, Harrison, N. .1., a; cornotation of New Jersey No prawing. Application February 24, 1949, w Serial No. 78,233
sive coating, generally an alkaline earth oxide on its surface.
With the highamplification factors in vacuum tubes employed today electron emission from the grids and anodes of the tubes must be reduced to a minimum as this emission causes considerable background noises and a reduction of efiiciency. The electrode elements, such as a oath-- ode, are usually formed of a sleeve or wire of nickel coated with active oxides, such as barium or strontium oxide. The nickel used in the production of such cathodes will, of course, vary in composition. The preparation of the nickel in the form in which it is to be used for the manufacture of cathode elements requires the melting of ingots and in this melting operation there is a tendency to form oxides. Heretofore it has been the usual practice to add various deoxidizing agents, such as magnesium, silicon, calcium or the like to the melt to keep the formation of nickel oxides at a minimum. However, to effectively deoxidize the nickel, it has been found necessary to use an excess of such deoxidizers with the result that small amounts of these deoxidizers remain in the melt. It has been established that emissions of electrons from the oxide coated cathode are increased by the presence of such deoxidizing elements in the nickel from which the oathode is made.
Sub-Committee VIII on Metallic Materials for Radio Tubes and Incandescent Lamps, of Committee 3-4 on Electrical Heating, Resistance, and Related Alloys, of The American Society for Testing Materials, has classified cathode materials into passive, normal and active. In the passive type the base nickel metal is substantially free of silicon, magnesium, titanium, aluminum and similar deoxidizers. These are the deoxidizers which are normally used in melting nickel to produce a malleable material which can be rolled to thin sheets of the order of .002 to .005" thick. Inactive metals, such as iron and cobalt, are not considered harmful if not present in too large quantities.
The necessity of deoxidizing any nickel oxides formed during the melt and at the same time of producing a final nickel product from which the usual deoxidizing elements are absent, has resulted in the practice of manufacturing the passive type electrodes from electrolytically de- 6 c s. (01. era-s46) positednickel. The slabs of electrolytic nickel are melted with carbon additions, thecarbo'n being added to reduc'the oxides'in the molten bath to produce the nickel m'ardrnwmch canlb'e hotan d cold rolled to produce thin sheets. I-Ie're again, the deoxidize'r m'ustbe used in' an excess so that at the end of the melt the nickel contains from .20 to .50 percent carbon; It-is then necessary to later remove the carbonfrom the nickel by heating it in the presence 'of' wet hydrogen. This operation is along and expensive onland again has a tendency to oxidizethelnickel sheet after the carbon has been removed.
I have found that slabs of electrolytically deposited nickel can be melted to produce a malleable metal which can be hot and cold worked without adding either the usual deoxidizers, the presence of which in the final nickel product is objectionable, or without adding carbon in excess. I accomplish this by the addition of rare earth metals, such as are found in the alloy known as Misch metal. While the composition of Misch metal varies, generally speaking, it consists essentially of 40 percent cerium, 30 percent lanthanum, and 30 percent didymium, balance ytterbium and iron. The lanthanum and didymium proportions of the Misch metal may contain small quantities of the other rare earth metals.
In carrying out the invention, slabs of electrolytically deposited nickel are melted in the usual manner, the normal procedure being followed up to the point where the metal is completely molten. At that point I add a small quantity of Misch metal to the bath. In actual practice, I have employed one pound of Misch metal to a 1300 pound melt. This figure may, of course, vary. If the melting of the slabs is carried out in a manner that would normally result in the production of a minimum amount of nickel oxides, the quantity of Misch metal added may be less. Greater quantities of Misch metal up to as much as three pounds may be added. The rare earth metals added to the melt reduce the nickel xides to nickel and the resulting rare earth oxides disappear from the molten bath. Spectrographic analyses of the cast and processed metal show traces of cerium and lanthanum. The amounts of cerium and lanthanum present do not exceed .2 percent. Likewise, if iron is present in the Misch metal, it is retained in the nickel forming about .12 to a maximum of .20 percent of the final product. The presence of such a effect and the nickel so produced is entirely satisfactory for the manufacture of passive cathode elements.
The nickel so produced contains no more impurities than are present in the nickel slabs with the exception of the small amount of iron referred to. It is malleable, easily worked and annealed and therefore does not require the annealing treatments which are necessary with a nickel of high carbon content.
Instead of adding the rare earth metals in the form of Misch metal, the desired quantities of rare earth metals, such as cerium, lanthanum and didymium may be added directly. In such case the nickel produced would not contain the slight contamination of iron.
I claim:
1. A vacuum tube having electrode elements at least one of which is composed of nickel and traces of rare earth metals.
2. A vacuum tube having electrode elements at least one of which is composed of nickel and traces of cerium and lanthanum.
3. A vacuum tube having electrode elements at least one of which is composed of nickel, a trace to 0.2 percent cerium and a trace to 0.2 percent lanthanum.
4. A cathode element for a vacuum tube consisting of nickel containing traces of rare earth metals, and an activating agent comprising an oxide coating thereon.
5. A cathode element for a vacuum tube consisting of nickel containing traces of cerium and lanthanum, and an activating agent comprising an oxide coating thereon.
6. A cathode element for a vacuum tube consisting of nickel containing a trace to 0.2 percent cerium and a trace to 0.2 percent lanthanum, and an activating agent comprising an oxide coating thereon.
FRANCIS E. BASH.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS

Claims (1)

1. A VACUUM TUBE HAVING ELECTRODE ELEMENTS AT LEAST ONE OF WHICH IS COMPOSED OF NICKEL AND TRACES OF RATE EARTH METALS.
US78233A 1949-02-24 1949-02-24 Vacuum tube electrode element Expired - Lifetime US2586768A (en)

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US78233A US2586768A (en) 1949-02-24 1949-02-24 Vacuum tube electrode element
GB3244/50A GB713063A (en) 1949-02-24 1950-02-08 Improvements in electrode elements

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2911376A (en) * 1951-11-01 1959-11-03 Patent Treuhand Ges Fuer Elektrische Gluehlampen Mbh Activating material for electrodes in electric discharge devices
US2924737A (en) * 1957-05-20 1960-02-09 Philips Corp Glow discharge tube
US2983602A (en) * 1957-09-24 1961-05-09 Armour Res Found Cobalt alloys
US3312856A (en) * 1963-03-26 1967-04-04 Gen Electric Rhenium supported metallic boride cathode emitters
FR2401230A1 (en) * 1977-08-27 1979-03-23 Ngk Spark Plug Co NICKEL-BASED ALLOY SUITABLE PARTICULARLY FOR THE HEATING ELEMENT OF AN INCANDESCENT CANDLE
US4612164A (en) * 1984-11-01 1986-09-16 Inco Alloys International, Inc. Nickel copper alloys with enhanced malleability and improved sulfide distribution

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1689338A (en) * 1921-11-19 1928-10-30 Western Electric Co Electron-discharge device
US1753298A (en) * 1927-01-03 1930-04-08 New Process Metals Corp Purifying rare gases
US1916410A (en) * 1928-08-22 1933-07-04 Westinghouse Electric & Mfg Co Alloy
US2075718A (en) * 1935-03-07 1937-03-30 Firm Heraeus Vacuumachmetze Ag Heat-resisting implement
US2204391A (en) * 1939-04-29 1940-06-11 Rca Corp Cathode for electron discharge devices
US2246162A (en) * 1938-08-17 1941-06-17 Gen Electric Thermionic cathode treatment
US2304353A (en) * 1935-05-09 1942-12-08 Int Nickel Co Heat resistant alloy
US2456370A (en) * 1945-02-19 1948-12-14 Int Nickel Co Process for producing electrodeposited nickel strip containing boron

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1689338A (en) * 1921-11-19 1928-10-30 Western Electric Co Electron-discharge device
US1753298A (en) * 1927-01-03 1930-04-08 New Process Metals Corp Purifying rare gases
US1916410A (en) * 1928-08-22 1933-07-04 Westinghouse Electric & Mfg Co Alloy
US2075718A (en) * 1935-03-07 1937-03-30 Firm Heraeus Vacuumachmetze Ag Heat-resisting implement
US2304353A (en) * 1935-05-09 1942-12-08 Int Nickel Co Heat resistant alloy
US2246162A (en) * 1938-08-17 1941-06-17 Gen Electric Thermionic cathode treatment
US2204391A (en) * 1939-04-29 1940-06-11 Rca Corp Cathode for electron discharge devices
US2456370A (en) * 1945-02-19 1948-12-14 Int Nickel Co Process for producing electrodeposited nickel strip containing boron

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2911376A (en) * 1951-11-01 1959-11-03 Patent Treuhand Ges Fuer Elektrische Gluehlampen Mbh Activating material for electrodes in electric discharge devices
US2924737A (en) * 1957-05-20 1960-02-09 Philips Corp Glow discharge tube
US2983602A (en) * 1957-09-24 1961-05-09 Armour Res Found Cobalt alloys
US3312856A (en) * 1963-03-26 1967-04-04 Gen Electric Rhenium supported metallic boride cathode emitters
FR2401230A1 (en) * 1977-08-27 1979-03-23 Ngk Spark Plug Co NICKEL-BASED ALLOY SUITABLE PARTICULARLY FOR THE HEATING ELEMENT OF AN INCANDESCENT CANDLE
US4612164A (en) * 1984-11-01 1986-09-16 Inco Alloys International, Inc. Nickel copper alloys with enhanced malleability and improved sulfide distribution

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Publication number Publication date
GB713063A (en) 1954-08-04

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