US2576129A - Nonemitting electron tube grid - Google Patents

Nonemitting electron tube grid Download PDF

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Publication number
US2576129A
US2576129A US569069A US56906944A US2576129A US 2576129 A US2576129 A US 2576129A US 569069 A US569069 A US 569069A US 56906944 A US56906944 A US 56906944A US 2576129 A US2576129 A US 2576129A
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grid
nonemitting
mossy
electron tube
tube
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US569069A
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Levin Irvin
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    • 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

Definitions

  • My invention relates to the coating of metals and, more particularly, to the coating of grid wires such as used in vacuum tubes.
  • a thermionic vacuum tube containing an electron source as a cathode, one or more grids of a bare metal, and a suitable anode
  • the hot grid or grids will thermionically emit electrons when material from the cathode evaporates onto it.
  • certain substances such as thoria, enhance the ability of an electron to escape to the outside of the heated cathode metal, such as tungsten. These substances will also enhance the electron escaping ability of the hot grid metal when deposited upon the grid so that the grid will emit.
  • Grid contamination means the molecular migration of thorium, barium, strontium or other materials which enhance the electron escaping ability of metallic surfaces from the vacuum tube cathode to the grid, causing said grid to primarily emit electrons.
  • the grid will, therefore, act as an electron-emitter and lose its controlling action. Previous methods of cleaning the grid to restore its controlling action called for an extra current source to electrically heat the grid wires when contamination effects were felt, thereby evaporating off the contaminating materials.
  • mossy layer of metal when a mossy layer of metal is placed over a grid wire, the heat emissivity of the wire becomes large.
  • This mossy layer may be a spongy state of the metal or even a properly sintered or fritted metallic structure. so long as the contaminating material from the cathode can be absorbed into the mossy surface and diffuse into the mossy sheath.
  • the large heat emissivity probably causes a large thermal gradient which, in turn, causes the contaminating material to diffuse toward the inner part of the sheath.
  • the thermal gradient is set up by the outer surface of the grid sheath being heated by radiation from the anode and the cathode.
  • the internal portion of the coating is cooled somewhat by the base metal underneath, thereby setting up a heat differential, or it may be a physicaamended April 30, 1928; 370 0. G. 757) 2 chemical combination between contaminating material and the mossy coating.
  • the actual mossy metallic grid coating is prepared from metals which do not melt or fuse at the maximum operating temperature of the grid. Common metals of this type are tantalum, zirconium, molybdenum and tungsten, although the six metals of the platinum family have been used.
  • the object of the invention is to provide a nonemitting electron tube grid.
  • the application of these coatings is: done by spraying or electro-phoretically depositing the powdered oxides or other compounds of tantalum, zirconium, molybdenum, tungsten and the six metals of the platinum family, which compounds are easily reduced to the metallic state in a vacuum at elevated temperatures.
  • Electrophoretic dep0siti0n.-2 grams of ignited tantalum pentoxide are dispersed in 100 c. c. of acetone.
  • the grid to be coated is rendered positive from 20 to 100 volts because the colloidal tantalum pentoxide micelle is negatively charged. No stirring is performed during electrophoresis.
  • the coated grid is then placed in a tantalum or molybdenum container under vacuum or reduced pressure and flash-heated by induction to 1600 C. for as short a time as possible. All traces of oxygen must be removed from the coating as well as the pumping system. The resulting grid is then mounted in the tube.
  • the mixture must be thoroughly homogeneous before spraying.
  • the coating is applied, allowed to dry, and then reduced in a vacuum at elevated temperatures.
  • An electron tube having a cathode coated with an evaporable material for increasing the electron emission therefrom, a control grid which becomes heated during the operation of said tube and which tends to become coated with said evaporable material during tube operation, and means for preventing said control grid, when so heated, from acting as an emitter of primary electrons due to the deposit of said evaporable material, said means comprising a mossy, continuous, metallic oxide-tree covering on said control grid of a metal selected from the refractory group comprising tantalum, zirconium, molybdenum, tungsten and the metals or the platinum group, whereby any evaporable material reaching said control grid is absorbed into said mossy covering and primary electron emission from said control grid is prevented.
  • An electron tube having a cathode coated with an evaporable material for increasing the electron emission therefrom, a control grid which becomes heated during the operation of said tube and which tends to become coated with said evaporable material during tube operation, and means for preventing said control grid, when so heated, from acting as an emitter of primary electrons due to the deposit of said evaporable material, said means comprising a mossy, continuous, metallic oxide-free covering on said control grid of a metal of the platinum group, whereby any evaporable material reaching said control grid is absorbed into said mossy covering and primary electron emission from said control grid is prevented.

Description

Patented Nov. 27, 1951 NONEM'ITTING ELEGTRON TUBE GRID Irvin Levin, Asbury Park, N. .L, assignor to the United States of America as represented by the Secretary of War No Drawing. Application December 20, 1944, Serial No. 569,069
(Granted under the act of March 3, 1883, as
2 Claims.
The invention described herein may be manufactured and used by or for the Government for governmental purposes, without the payment to me of any royalty thereon.
My invention relates to the coating of metals and, more particularly, to the coating of grid wires such as used in vacuum tubes.
In a thermionic vacuum tube containing an electron source as a cathode, one or more grids of a bare metal, and a suitable anode, the hot grid or grids will thermionically emit electrons when material from the cathode evaporates onto it. The theoretical reasons for this may be summarized, as follows: certain substances, such as thoria, enhance the ability of an electron to escape to the outside of the heated cathode metal, such as tungsten. These substances will also enhance the electron escaping ability of the hot grid metal when deposited upon the grid so that the grid will emit. For this reason it has been found that a mossy or spongy refractory metallic coating on the grid surface will prevent thermionic emission because the contaminating material from the cathode probably can migrate below the top grid surface and thus be removed from the electric fields among the tube elements.
Grid contamination means the molecular migration of thorium, barium, strontium or other materials which enhance the electron escaping ability of metallic surfaces from the vacuum tube cathode to the grid, causing said grid to primarily emit electrons. The grid will, therefore, act as an electron-emitter and lose its controlling action. Previous methods of cleaning the grid to restore its controlling action called for an extra current source to electrically heat the grid wires when contamination effects were felt, thereby evaporating off the contaminating materials.
It has been found that when a mossy layer of metal is placed over a grid wire, the heat emissivity of the wire becomes large. This mossy layer may be a spongy state of the metal or even a properly sintered or fritted metallic structure. so long as the contaminating material from the cathode can be absorbed into the mossy surface and diffuse into the mossy sheath. The large heat emissivity probably causes a large thermal gradient which, in turn, causes the contaminating material to diffuse toward the inner part of the sheath. The thermal gradient is set up by the outer surface of the grid sheath being heated by radiation from the anode and the cathode. The internal portion of the coating is cooled somewhat by the base metal underneath, thereby setting up a heat differential, or it may be a physicaamended April 30, 1928; 370 0. G. 757) 2 chemical combination between contaminating material and the mossy coating.
The actual mossy metallic grid coating is prepared from metals which do not melt or fuse at the maximum operating temperature of the grid. Common metals of this type are tantalum, zirconium, molybdenum and tungsten, although the six metals of the platinum family have been used.
The object of the invention is to provide a nonemitting electron tube grid.
The application of these coatings is: done by spraying or electro-phoretically depositing the powdered oxides or other compounds of tantalum, zirconium, molybdenum, tungsten and the six metals of the platinum family, which compounds are easily reduced to the metallic state in a vacuum at elevated temperatures.
The following examples illustrate my invention:
(1) Electrophoretic dep0siti0n.-2 grams of ignited tantalum pentoxide are dispersed in 100 c. c. of acetone. The grid to be coated is rendered positive from 20 to 100 volts because the colloidal tantalum pentoxide micelle is negatively charged. No stirring is performed during electrophoresis. The coated grid is then placed in a tantalum or molybdenum container under vacuum or reduced pressure and flash-heated by induction to 1600 C. for as short a time as possible. All traces of oxygen must be removed from the coating as well as the pumping system. The resulting grid is then mounted in the tube.
(2) Spraying.The following spray mixture has been found adequate for depositing tantalum pentoxide onto grid wires:
Amyl acetate c.c. 800 Ethyl alcohol c. c. 200 Nitrocellulose (about dry) g. 20 Tantalum pentoxide g. .300
The mixture must be thoroughly homogeneous before spraying. The coating is applied, allowed to dry, and then reduced in a vacuum at elevated temperatures.
Having thus described my invention, I desire to secure by Letters Patent and claim:
1. An electron tube having a cathode coated with an evaporable material for increasing the electron emission therefrom, a control grid which becomes heated during the operation of said tube and which tends to become coated with said evaporable material during tube operation, and means for preventing said control grid, when so heated, from acting as an emitter of primary electrons due to the deposit of said evaporable material, said means comprising a mossy, continuous, metallic oxide-tree covering on said control grid of a metal selected from the refractory group comprising tantalum, zirconium, molybdenum, tungsten and the metals or the platinum group, whereby any evaporable material reaching said control grid is absorbed into said mossy covering and primary electron emission from said control grid is prevented.
2. An electron tube having a cathode coated with an evaporable material for increasing the electron emission therefrom, a control grid which becomes heated during the operation of said tube and which tends to become coated with said evaporable material during tube operation, and means for preventing said control grid, when so heated, from acting as an emitter of primary electrons due to the deposit of said evaporable material, said means comprising a mossy, continuous, metallic oxide-free covering on said control grid of a metal of the platinum group, whereby any evaporable material reaching said control grid is absorbed into said mossy covering and primary electron emission from said control grid is prevented.
IRVIN LEVIN.
REFERENCES crrEn The following references are of record in the fil of this patent:
UNITED STATES PATENTS Number Name Date 1,370,967 Hommel Mar. 8, 1921 1,639,698 Holbom Aug. 23, 1927 1,658,712 Fonda Feb. 7, 1928 1,794,315 Mullaney Feb. 24, 1931 1,880,937 Elsey Oct. 4, 1932 1,953,254 Parker Apr. 3, 1934 1,954,353 Ernst Apr. 10, 1934 2,263,164 Dailey Nov. 18, 1941 2,417,730 Becker Mar. 18, 1947 FOREIGN PATENTS Number Country Date 475,183 Great Britain Feb. 12, 1936
US569069A 1944-12-20 1944-12-20 Nonemitting electron tube grid Expired - Lifetime US2576129A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769112A (en) * 1953-06-11 1956-10-30 Westinghouse Electric Corp Discharge lamp, mount therefor, and method
US2885587A (en) * 1956-06-13 1959-05-05 Westinghouse Electric Corp Low pressure discharge lamp and method
US3037923A (en) * 1957-12-26 1962-06-05 Sylvania Electric Prod Process for electrophoretically coating a metal with particulate carbon material
US3041209A (en) * 1955-06-28 1962-06-26 Gen Electric Method of making a thermionic cathode
US3256458A (en) * 1962-11-22 1966-06-14 Csf Electrode structure
US3879276A (en) * 1974-04-10 1975-04-22 Int Standard Electric Corp Electrophoretic deposition of selenium

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1370967A (en) * 1918-05-16 1921-03-08 Hommel Oscar Ornamenting and protecting metal surfaces
US1639698A (en) * 1926-01-14 1927-08-23 Hazeltine Corp Electron-emitting cathode and process of preparing the same
US1658712A (en) * 1924-08-30 1928-02-07 Gen Electric Zirconium alloy
US1794315A (en) * 1924-10-09 1931-02-24 Gen Electric Electron-discharge apparatus
US1880937A (en) * 1928-02-04 1932-10-04 Westinghouse Electric & Mfg Co Process of carbonizing nickel or other metals
US1953254A (en) * 1931-11-12 1934-04-03 Rogers Radio Tubes Ltd Control electrode for electron discharge devices
US1954353A (en) * 1930-03-15 1934-04-10 Du Pont Material for decorating surfaces
GB475183A (en) * 1935-04-18 1937-11-12 Philips Nv Improvements in or relating to electric discharge tubes
US2263164A (en) * 1941-02-25 1941-11-18 Westinghouse Electric & Mfg Co Anode
US2417730A (en) * 1942-11-30 1947-03-18 Eitel Mccullough Inc Electron tube and method of making same

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1370967A (en) * 1918-05-16 1921-03-08 Hommel Oscar Ornamenting and protecting metal surfaces
US1658712A (en) * 1924-08-30 1928-02-07 Gen Electric Zirconium alloy
US1794315A (en) * 1924-10-09 1931-02-24 Gen Electric Electron-discharge apparatus
US1639698A (en) * 1926-01-14 1927-08-23 Hazeltine Corp Electron-emitting cathode and process of preparing the same
US1880937A (en) * 1928-02-04 1932-10-04 Westinghouse Electric & Mfg Co Process of carbonizing nickel or other metals
US1954353A (en) * 1930-03-15 1934-04-10 Du Pont Material for decorating surfaces
US1953254A (en) * 1931-11-12 1934-04-03 Rogers Radio Tubes Ltd Control electrode for electron discharge devices
GB475183A (en) * 1935-04-18 1937-11-12 Philips Nv Improvements in or relating to electric discharge tubes
US2263164A (en) * 1941-02-25 1941-11-18 Westinghouse Electric & Mfg Co Anode
US2417730A (en) * 1942-11-30 1947-03-18 Eitel Mccullough Inc Electron tube and method of making same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769112A (en) * 1953-06-11 1956-10-30 Westinghouse Electric Corp Discharge lamp, mount therefor, and method
US3041209A (en) * 1955-06-28 1962-06-26 Gen Electric Method of making a thermionic cathode
US2885587A (en) * 1956-06-13 1959-05-05 Westinghouse Electric Corp Low pressure discharge lamp and method
US3037923A (en) * 1957-12-26 1962-06-05 Sylvania Electric Prod Process for electrophoretically coating a metal with particulate carbon material
US3256458A (en) * 1962-11-22 1966-06-14 Csf Electrode structure
US3879276A (en) * 1974-04-10 1975-04-22 Int Standard Electric Corp Electrophoretic deposition of selenium

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