US1675120A - Deposition of thorium from its vaporizable compounds - Google Patents

Deposition of thorium from its vaporizable compounds Download PDF

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US1675120A
US1675120A US605772A US60577222A US1675120A US 1675120 A US1675120 A US 1675120A US 605772 A US605772 A US 605772A US 60577222 A US60577222 A US 60577222A US 1675120 A US1675120 A US 1675120A
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thorium
filament
compound
deposition
compounds
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US605772A
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Marden John Wesley
Thomas Thomas Philip
Conley John Edward
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Westinghouse Lamp Co
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Westinghouse Lamp Co
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    • 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

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  • This invention relates to the deposition of thorium from compounds thereof in vaporous or gaseous form and more particularly to the coating of wire, electrodes or the like with metallic thorium, by heating the same in an atmosphere of the vapor of a compound of thorium.
  • An object of our invention is the formation of a coating of thorium from the-vapor of a volatile compound thereof.
  • Another object of our invention is the production of thorium metal plated upon filamentary material bya. convenient and continuous process, whereby the material is rendered more suitable for electron-emission or other purposes.
  • a further object of our invention is the activation or coating with metallic thorium, of comparatively great lengths of wire, consisting of tungsten or the like, by drawmg the same, while heated, through an atmosphere comprising the vapor of a thorium compound.
  • a still further object of our invention is the coating of filamentary material with thorium, either before or after introduction into an evacuated envelope for an electron device, by heating the filamentary material in an atmosphere comprising the vapor of a thorium compound.
  • One of these compounds is thorium acetyL acetonate, Th(C H,O )4.
  • Th(C H,O )4 This compound can be made very simply by adding acetyl acetone to a solution of thorium nitrate and after collecting and drying the precipitate crystallizing it from alcohol.
  • a little of this compound was placed in a radio tube with a non-thoriated tungsten filament and while the filament was heated to about 1600 C. the tube was also heated to about 350 C. to volatilize was determined by measuring the electronemission of the filament so activated, as compared with a similar filament which had not been activated.
  • thorium compounds which may be used for the same purpose, for example, thorium methyl, Th(CH )4 and thorium ethyl, Th(C H )4.
  • this activation may be accomplished by continuous processes by means of which long pieces of wire or filamentary material may be activated and afterwards introduced into electron devices.
  • a wire or filament 1 of tungsten, molybdenum or other similar refractory material, which it is desired to activate may be unwound from a spool 2, through a treating'chamber 3, upon a spool 4, driven from an suitable source of power (not shown).
  • T e treating chamber 3 is provided with an atmosphere of a vaporizable or volatile thorium compound, adapted to be decomposed by heat. This may be accomplished by heating an organic compound of thorium 5 in a retort or flask 6,as by means of a Bunsen burner or the like 7,
  • thorium compound which may be thorium acetyl acetonate, or other suitable thorium compound and cause it to pass through the tube or neck 8 of th retort into the treating chamber 3.
  • chamber 3 is preferably formed with a partition 11 and has two mercury contact cups 12 and '13, connected to a battery 14 or other suitable source of electricity through a switch 15 and rheostat 16, for the purpose of suitably heating the filament 1, preferably to. a temperature of about 1600 C., while passing between said mercury contact cups.
  • the filament may be wound up on the spool 4, or it may be coated with a protective var-' nish-like material prior to emerging from the treating chamber.
  • a protective var-' nish-like material prior to emerging from the treating chamber.
  • Such coating may be accomplished by providing a getter cup or other coating device 17, as indicated, with a pivoted pulley or wheel 18 partly submerged in a solution 19 of nitro-cellulose in amyl-acetate' or other suitable varnish-like material, whereby the filament, by passing over or around said pulley, 18, becomes coated with said material and is protected from oxidation before coming in contact with theatmosphere.
  • the coating of the filament as above described is desirable in some instances, as
  • the filament is to be kept a considerable length, ofetime before it is used in an electromemittin'g dcvice,-but is 'not essential to the practice of our invention.
  • the filament After pass ing from the coating device 17, the filament emerges from the treating chamber 3 through the aperture 9. and may be wound upon the spool 4. 1
  • a filament treated according to the afore described. process is activated so that, when used in an electron device, it shows an emissivity characteristic of metallic thorium.
  • the same result may be accomplished by activating the same after it is in place in an electron tube or the like, that is, a quantity of thorium acetyl acetonate, or other suitable ization thereof, so that the same may-be distilled into contact with the glowing filament.
  • the amount of thorium deposited on the hot filament de ends on the concentration of the vapor of t e thorium compound while the filament is glowed and the length of time the process is continued, as well as other factors, such as the degree of vacuum/
  • thorium acet l acetonate has been mentioned as the pre erred material, it is obvious that various other compounds of thorium, carbon and hydrogen may be used in the practice of our invention without departing from the spirit and scope thereof.
  • filamentary material or the like may be coated with pure thorium, unallo ed or mixed with other metal and in which it is not necessary to start with a material to be coated containing a thorium compound.
  • Filamentary material for electron emisthe spirit and Scope sion purposes comprising tungsten free from thorium compounds upon which has been thermally plated metallic thorium unmixed with other metallic material.
  • An electron device com rising an evacuated envelope containing a amentary cathode and a quantity of a vaporizable thorium compound, decomposable by heat tp deposit

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Description

June 26, 1928'. 1,675,120
' J. w. MARDEN ET AL I DEPOSITION 0F THORIUM FROM ITS VAPORIZABLE COMPOUNDS Filed Dec. 9. 22
INVENTORS JOHN w MARDEN THO/ms R THO/1H6 JOHN E. CONLEY BY ATTOR EY Patented June 26, 1928.
UNITED STATES PATENT OFF-ICE.
JOHN WESLEY MARDEN, OF EAST ORANGE, AND THOMASIPHILIP THOMAS AND JOHN EDWARD CONLEY, OF BLOOMFIELD, NEW JERSEY, ASSIGNORS TO WESTINGHOUSE LAMP COMPANY, A CORPORATION OF PENNSYLVANIA.
DEPOSITION OF THORIUM FROM ITS VAPORIZABLE COMPOUNDS.
Application filed December 9, 1922. Serial No. 605,772.
This invention relates to the deposition of thorium from compounds thereof in vaporous or gaseous form and more particularly to the coating of wire, electrodes or the like with metallic thorium, by heating the same in an atmosphere of the vapor of a compound of thorium.
An object of our invention is the formation of a coating of thorium from the-vapor of a volatile compound thereof.
Another object of our invention is the production of thorium metal plated upon filamentary material bya. convenient and continuous process, whereby the material is rendered more suitable for electron-emission or other purposes.
A further object of our invention is the activation or coating with metallic thorium, of comparatively great lengths of wire, consisting of tungsten or the like, by drawmg the same, while heated, through an atmosphere comprising the vapor of a thorium compound.
A still further object of our invention is the coating of filamentary material with thorium, either before or after introduction into an evacuated envelope for an electron device, by heating the filamentary material in an atmosphere comprising the vapor of a thorium compound.
Other objects and advantages of the invention will be apparent from the following detailed description.
Because of the fact that metallic thorium is such a good electron-emission material, various methods have been devised for developing the same on, or applying it to, wire or filamentary material for use as hot cathodes in electron devices. For example, in the copending application of Ralph E. Myers, Serial No. 57 8,47 0, filed July 29, 1922, Activation of thoriated filaments and assigned to the Westinghouse Lamp Company, is disclosed a method whereby a coating of thorium is developed on the surface of thoriated wire, composed of tungsten or the like, by heating the same in a hydrocarbon atmosphere. This result is accomplished by the reducing action of carbon on the thoria in the filament or wire.
In the copending application of Marden, Conley and Thomas, Serial No. 578,813, filed July 31, 1922, now Patent No. 1,487,174, of March 18, 1924, Electrolytic deposition of thorium and assigned to the \Vestinghouse Lamp Company, is disclosed a method of electroplating filamentary material wit-h inctallic thorium, simultaneously with another metal, such as lead or iron. It should be noted that, in the former application, it is necessary to use a filament containing thoriuln oxide, whereas, in the latter application, the coating of thorium is not pure but is mixed or alloyed with another metal.
According to our present invention, we have devised a means for applying a pure coating of thorium to tungsten, molybdenum or other similar material, by deposition from the vapor of a thorium compound. An attempt has been made to deposit thorium on a tungsten filament heated to a high degree in the vapor of thorium chloride. This experiment was not successful possibly because of the fact that the chloride was heated in glass and only a relatively low vapor pressure of the compound obtained. We have found that filamentary material -may be successfully coated with thorium by heating to a. high degree in the vapor of certain organic thorium compounds, that is, compounds of thorium, carbon and hydrogen. This method has been used successfully for activating, that is, causing an increase of electron emissivity in, tungsten wire.
Thorium forms certain organic compounds which are volatile or easily vaporized and may be distilled without decomposition. One of these compounds is thorium acetyL acetonate, Th(C H,O )4. This compound can be made very simply by adding acetyl acetone to a solution of thorium nitrate and after collecting and drying the precipitate crystallizing it from alcohol. In conducting our experiments, a little of this compound was placed in a radio tube with a non-thoriated tungsten filament and while the filament was heated to about 1600 C. the tube was also heated to about 350 C. to volatilize was determined by measuring the electronemission of the filament so activated, as compared with a similar filament which had not been activated. There are, undoubtedly,
many other organic thorium compounds" which may be used for the same purpose, for example, thorium methyl, Th(CH )4 and thorium ethyl, Th(C H )4.
Instead of activating the filament in an electron tube after the same is in place therein as the cathode thereof, this activation may be accomplished by continuous processes by means of which long pieces of wire or filamentary material may be activated and afterwards introduced into electron devices.
The invention will better be understood by referring to the accompanying drawing which illustrates, partly in longitudinal section and partly diagrammatically, apparatus for practicing our invention.
In the drawing, a wire or filament 1 of tungsten, molybdenum or other similar refractory material, which it is desired to activate, may be unwound from a spool 2, through a treating'chamber 3, upon a spool 4, driven from an suitable source of power (not shown). T e treating chamber 3 is provided with an atmosphere of a vaporizable or volatile thorium compound, adapted to be decomposed by heat. This may be accomplished by heating an organic compound of thorium 5 in a retort or flask 6,as by means of a Bunsen burner or the like 7,
to vaporize or distill the thorium compound, which may be thorium acetyl acetonate, or other suitable thorium compound and cause it to pass through the tube or neck 8 of th retort into the treating chamber 3.
The vapor will then flow to the other end of the treating chamber 3 and emerge therefrom at aperture 9. As shown, chamber 3 is preferably formed with a partition 11 and has two mercury contact cups 12 and '13, connected to a battery 14 or other suitable source of electricity through a switch 15 and rheostat 16, for the purpose of suitably heating the filament 1, preferably to. a temperature of about 1600 C., while passing between said mercury contact cups.
As the filament emerges from the treating chamber 3, it may be wound up on the spool 4, or it may be coated with a protective var-' nish-like material prior to emerging from the treating chamber. Such coating may be accomplished by providing a getter cup or other coating device 17, as indicated, with a pivoted pulley or wheel 18 partly submerged in a solution 19 of nitro-cellulose in amyl-acetate' or other suitable varnish-like material, whereby the filament, by passing over or around said pulley, 18, becomes coated with said material and is protected from oxidation before coming in contact with theatmosphere.
The coating of the filament as above described is desirable in some instances, as
where the filament is to be kept a considerable length, ofetime before it is used in an electromemittin'g dcvice,-but is 'not essential to the practice of our invention. After pass ing from the coating device 17, the filament emerges from the treating chamber 3 through the aperture 9. and may be wound upon the spool 4. 1
The reaction which takes place when the filament is heated to a high degree in an atmosphere of the vapor of thorium acetyl acetonate is not definitelyfknown, but it is believed that said thorium compound decomposes to. deposit thorium on the filament, with the formation of carbon monoxide, one or more hydrocarbons and perhaps hydrogen.
However, a filament treated according to the afore described. process is activated so that, when used in an electron device, it shows an emissivity characteristic of metallic thorium.
Instead of activating such a filament before introduction into an electron device, the same result may be accomplished by activating the same after it is in place in an electron tube or the like, that is, a quantity of thorium acetyl acetonate, or other suitable ization thereof, so that the same may-be distilled into contact with the glowing filament.
The amount of thorium deposited on the hot filament de ends on the concentration of the vapor of t e thorium compound while the filament is glowed and the length of time the process is continued, as well as other factors, such as the degree of vacuum/ Although thorium acet l acetonate has been mentioned as the pre erred material, it is obvious that various other compounds of thorium, carbon and hydrogen may be used in the practice of our invention without departing from the spirit and scope thereof.
ccording to our invention, we have devised a means whereby filamentary material or the like may be coated with pure thorium, unallo ed or mixed with other metal and in which it is not necessary to start with a material to be coated containing a thorium compound.
Although we have described what we now consider to be preferred embodiments of our invention, it is to be understood thatthe same are merely illustrative and that modifications will suggest themselves to those skilled in the art, within of the appended claims.
What is claimed is:
1. Filamentary material for electron emisthe spirit and Scope sion purposes comprising tungsten free from thorium compounds upon which has been thermally plated metallic thorium unmixed with other metallic material.
2. An electron device com rising an evacuated envelope containing a amentary cathode and a quantity of a vaporizable thorium compound, decomposable by heat tp deposit
US605772A 1922-12-09 1922-12-09 Deposition of thorium from its vaporizable compounds Expired - Lifetime US1675120A (en)

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2427592A (en) * 1943-07-31 1947-09-16 Rca Corp Thorium compound protective coatings for reflecting surfaces
US2430520A (en) * 1945-03-06 1947-11-11 Glass Science Inc Deposition of metal on glass from metal formates
US2630780A (en) * 1946-12-21 1953-03-10 Falck Hakan Fredrik Device for depositing thin metallic layers
US2704728A (en) * 1951-10-08 1955-03-22 Ohio Commw Eng Co Gas plating metal objects with copper acetylacetonate
US2880115A (en) * 1955-07-13 1959-03-31 Ohio Commw Eng Co Method of gas plating light metals
US2958899A (en) * 1953-10-09 1960-11-08 Int Resistance Co Apparatus for deposition of solids from vapors
US3092511A (en) * 1958-11-19 1963-06-04 Sperry Rand Corp Magnetic devices and preparation thereof
US3092510A (en) * 1959-03-02 1963-06-04 Sperry Rand Corp Magnetic devices and preparation thereof
US3268362A (en) * 1961-05-26 1966-08-23 Rca Corp Deposition of crystalline niobium stannide

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2427592A (en) * 1943-07-31 1947-09-16 Rca Corp Thorium compound protective coatings for reflecting surfaces
US2430520A (en) * 1945-03-06 1947-11-11 Glass Science Inc Deposition of metal on glass from metal formates
US2630780A (en) * 1946-12-21 1953-03-10 Falck Hakan Fredrik Device for depositing thin metallic layers
US2704728A (en) * 1951-10-08 1955-03-22 Ohio Commw Eng Co Gas plating metal objects with copper acetylacetonate
US2958899A (en) * 1953-10-09 1960-11-08 Int Resistance Co Apparatus for deposition of solids from vapors
US2880115A (en) * 1955-07-13 1959-03-31 Ohio Commw Eng Co Method of gas plating light metals
US3092511A (en) * 1958-11-19 1963-06-04 Sperry Rand Corp Magnetic devices and preparation thereof
US3092510A (en) * 1959-03-02 1963-06-04 Sperry Rand Corp Magnetic devices and preparation thereof
US3268362A (en) * 1961-05-26 1966-08-23 Rca Corp Deposition of crystalline niobium stannide

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