US3229147A - Thermionic emitter and method of making same - Google Patents
Thermionic emitter and method of making same Download PDFInfo
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- US3229147A US3229147A US135547A US13554761A US3229147A US 3229147 A US3229147 A US 3229147A US 135547 A US135547 A US 135547A US 13554761 A US13554761 A US 13554761A US 3229147 A US3229147 A US 3229147A
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- barium
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- reducing agent
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- activator compound
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- 238000004519 manufacturing process Methods 0.000 title description 16
- 239000012190 activator Substances 0.000 claims description 41
- 150000001875 compounds Chemical class 0.000 claims description 33
- 229910052788 barium Inorganic materials 0.000 claims description 31
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 24
- 239000011159 matrix material Substances 0.000 claims description 21
- FZTPSPNAZCIDGO-UHFFFAOYSA-N barium(2+);silicate Chemical compound [Ba+2].[Ba+2].[O-][Si]([O-])([O-])[O-] FZTPSPNAZCIDGO-UHFFFAOYSA-N 0.000 claims description 11
- 239000003638 chemical reducing agent Substances 0.000 description 32
- 230000008020 evaporation Effects 0.000 description 16
- 238000001704 evaporation Methods 0.000 description 16
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 13
- 229910052750 molybdenum Inorganic materials 0.000 description 13
- 239000011733 molybdenum Substances 0.000 description 13
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 13
- 229910052721 tungsten Inorganic materials 0.000 description 13
- 239000010937 tungsten Substances 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 229910052715 tantalum Inorganic materials 0.000 description 11
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 11
- 239000000470 constituent Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000013508 migration Methods 0.000 description 8
- 230000005012 migration Effects 0.000 description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
- 239000003870 refractory metal Substances 0.000 description 7
- 239000010936 titanium Substances 0.000 description 7
- 229910052719 titanium Inorganic materials 0.000 description 7
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 5
- 239000011876 fused mixture Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 150000001247 metal acetylides Chemical class 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000011819 refractory material Substances 0.000 description 5
- 229910021332 silicide Inorganic materials 0.000 description 5
- 229910052726 zirconium Inorganic materials 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- 230000001427 coherent effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000001553 barium compounds Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details 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
- H01J1/02—Main electrodes
- H01J1/13—Solid thermionic cathodes
- H01J1/20—Cathodes heated indirectly by an electric current; Cathodes heated by electron or ion bombardment
- H01J1/28—Dispenser-type cathodes, e.g. L-cathode
Definitions
- Dispenser-type emitters usually comprise a porous refractory metal matrix impregnated with an activator compound adapted upon thermal dissociation of the compound to provide an elemental alkaline earth metal which migrates to the surface of the matrix and thus is available as an emissive film.
- an activator compound adapted upon thermal dissociation of the compound to provide an elemental alkaline earth metal which migrates to the surface of the matrix and thus is available as an emissive film.
- Much of the effort devoted to the development of dispenser-type emitters heretofore has been for the provision of systems characterized by low effective work functions and, thus, adapted for high density electron emission within a given operating temperature range.
- Much development effort has also been directed toward the provision of emitters characterized by low evaporation rates of the activator material in the mentioned operating range, thereby to provide for prolonged operating life.
- thermionic emitters and a method of manufacturing same which are adapted for providing dispenser type emitters characterized by low effective work functions and reduced evaporation rates.
- My present invent-ion contemplates improved emitters and a method of manufacturing same effective for affording a dispenser type emitter characterized by a low eifective work function and further reduced evaporation rates.
- a primary object of my invention is to provide a new and improved thermionic emitter of the dispenser type.
- Another object of my invention is to provide new and improved dispenser-type emitters characterized by low effective work functions and low evaporation rates of the activator materials during operation of the devices incorporating the emitters.
- Another object of my invention is to provide new and improved dispenser-type emitters involving a new and improved system of constituents effective for thermally controlling the rate of production of an activator material in the matrix and thereby controlling the rate of evaporation of the activator.
- Another object of my invention is to provide new and improved thermionic emitters of the dispenser type which are adapted for prolonged high density emission operation.
- Another object of my invention is to provide new and improved thermionic emitters of the dispenser type which can be easily manufactured and which are not subject to the evolution of undesirable gases during manufacture or subsequent use.
- Still another object of my invention is to provide a new and improved method of manufacturing a dispensertype thermionic emitter.
- my invention contemplates a new and improved emitter of the dispenser type comprising a compressed Patented Jan. 11, 1966 ice fused body of powdered constituents consisting essentially of (l) a refractory matrix material selected prefera'bly from the group consisting of tungsten, tantalum and molybdenum and the silicides, carbides and borides of these materials and combinations thereof; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitan'ate; and (3) a reducing agent selected from the group consisting of aluminum, zirconium and titanium and combinations thereof.
- a refractory matrix material selected prefera'bly from the group consisting of tungsten, tantalum and molybdenum and the silicides, carbides and borides of these materials and combinations thereof
- an activator compound selected from the group consisting of barium orthosilicate and barium orthotitan'ate
- a reducing agent selected from the group consisting of aluminum, zir
- the emitter is preferably manufactured by admixing uniformly the powdered constituents and then compressing the mixture with a predetermined pressure effective for fusing the powdered constituents into a compressed coherent body having a consistency and internal structure whereby the body is adapted for uniform migration to the surface thereof of elemental activator upon chemical reduction of the activator compound.
- the reducing agent and operating temperature control the rate of activator production in the body and thus control the rate of evaporation of the activator.
- FIGURE 1 is a sectional view of a dispenser type emitter constructed according to an embodiment of my invention
- FIGURE 2 is a fragmentary somewhat schematic illustration of apparatus and the method employable in manufacturing my improved emitter
- FIGURE 3 is a fragmentary sectional view illustrating another modified form of my invention.
- FIGURE 4 is a fragmentary sectionalized view illustrating still another modified form of my invention.
- FIGURE 1 a thermionic emitter of the dispenser type generally designated 10 and constructed according to an embodiment of my invention.
- the emitter 10 is supported in a flared end of a cathode holder 11 which can be formed of a refractory metal such as tungsten, tantalum or molybdenum. It is to be understood that the cathode holder 11 need not be flared and can comprise a straightw-alled cylindrical or tubular member of any desired cross-sectional configuration.
- a heating element 12 is contained in the holder 11 and is adapted when energized to heat the emitter 10, thereby to effect a desired reaction between an activator compound and a reducing agent contained in the emitter 1t) and for thereby effecting reduction of the activator compound and production of elemental barium for migration thereof to an active surface of the emitter designated 13.
- the emitter 10 comprises a compressed fused body of powdered constituents of approximately 325 mesh and consisting essentially of (1) a refractory matrix material preferably selected from the group consisting of tungsten, tantalum and molybdenum, the silicides, carbides and borides of tungsten, tantalum and molybdenum and combinations thereof; (2) an activator compound selected from the group consisting of barium orthosilicate (Ba SiOQ and barium orthotitanate (Ba TiO.,) and combinations thereof, and (3) a reducing agent selected from the group consisting of aluminum, zirconium and titanium.
- a refractory matrix material preferably selected from the group consisting of tungsten, tantalum and molybdenum, the silicides, carbides and borides of tungsten, tantalum and molybdenum and combinations thereof
- an activator compound selected from the group consisting of barium orthosilicate (Ba SiOQ and barium orthotitanate (B
- the emitter 10 is preferably formed of a uniform, compressed fused mixture of powders of one of the mentioned refractory materials, one of the mentioned activator compounds and one of the reducing agents.
- combinations of the refractory materials as well as combinations of the active compounds can be employed .in practicing my invention.
- aluminum, zirconium and titanium can be effectively employed as the reducing agent in practicing my invention, aluminum is preferred.
- the use of titanium as a reducing agent should be avoided.
- the above-discussed mixture is compressed at approximately 70 to 80 tons per square inch to a desired shape and whereby the particles constituting the powdered constituents are fused together to provide a coherent unitary body.
- fused is used to mean that the particles constituting the body are blended together or joined as the result of pressure applied to the mixture in much the same way that metal members can be joined or fused by the application of pressure in the manner generally referred to in the art as cold welding.
- FIGURE 2 Illustrated in FIGURE 2 is apparatus whereby the device of FIGURE 1 can be constructed.
- This apparatus comprises a female die 14 adapted for holding the cathode holder 11 firmly in an inverted position against a smooth surface die 15 while a quantity of the mixture of the above-discussed metal powders designated 16 is compressed by activation of a ramrod 17.
- the rod 17 is actuated with a force effective for compressing the mixture at the mentioned 70 to 80 tons per square inch.
- the desired plug-like form of the emitter illustrated in FIGURE 1 is obtained and the emitter is formed as a compressed fused body having a desired consistency and porosity which contributes .to the effectiveness of the emitter in providing a desired low effective work function and insuring uniform coverage of the active surface 13 with elemental barium during energization of a heater 12.
- the reducing agent in the emitter Upon heating of the emitter in a vacuum, as by incorporation of the emitter in a vacuum discharge device and energization of the heater 12, the reducing agent in the emitter is effective for chemically reducing the activator compound and thereby producing elemental barium for diffusion through the body and migration uniformly to the active surface 13.
- the reducing agent be rendered effective for chemically reducing the barium compound and thus producing elemental barium.
- the amount of barium appearing at the active surface 13 is controlled and, thus, is not subject to rapid evaporation.
- the reducing agent is effective when heated for continuously causing the production of barium from the activator compound and, thus, the device is adapted for continuous replenishment of the active surface with barium to maintain the active surface for high density emission operation and a substantially reduced effective work function. Included below are the reactions obtained in the present device when tungsten is the refractory metal and aluminum is utilized as the reducing agent and whereby the production of barium results:
- any one of the above-mentioned matrix materials can be substituted therefor.
- aluminum (Al) is indicated as the reducing agent employed, any one of the above-noted reducing agents may be alternatively employed except, however, in the case of barium orthotitanate where the use of titanium as a reducing agent should be avoided.
- the activator compound was in each case in the systems included in the above chart 9.5% and the reducing agent was 0.5% of the composition of the system under test, it is to be understood that the percentage compositions of the systems can vary and still be characterized by desirably low effective work function and evaporation rates, although the indicated percentage composition in the chart has been found highly satisfactory.
- the temperature 1250 K. was arbitrarily selected for test purposes, and the effective work functions and the activator evaporation rates indicated are those calculated for this temperature.
- the effective work functions and evaporation rates will vary, of course, with different temperatures and can be determined by use of calculations well-known to those skilled in the art.
- FIGURE 3 Illustrated in FIGURE 3 is a modified form of my Invention in which the emitter is generally designated 20.
- a base member 21 is provided which is preferably formed of a refractory metal such as tungsten, stantalum or molybdenum.
- the base member 21 carries as a coating thereon a body of the compressed fused mixture employed in forming the emitter 10 in FIGURE 1.
- the coating 22 is fused to the base member 21 and the formation of the coating 22 and the fusion thereof to the base member can be effected by the use of die means similar in function to that illustrated in FIGURE 2.
- a heating element 23 Provided for cooperating with the emitter 20 is a heating element 23.
- the base 21 and the coating 22 are heated, whereby the reducing agent in the coating 22 is efiective for reducing chemically the barium orthosilicate or barium orthotitanate in the mixture for producing barium for migration to the outer surface of the coating 22.
- the amount of barium produced is controllable, whereby the device is adapted for relatively low evaporation of the activator.
- the emitter can be in a tubular form instead of the planar form illustrated.
- FIGURE 4 Illustrated in FIGURE 4 is another modified form of my invention.
- an emitter generally designated 25 is tubular in form and comprises a unitary compressed fused and self-sustaining cylinder of the mixture employed in manufacturing the plug-like emitter 10 in FIGURE 1 and the emissive coating 22 in FIGURE 3.
- the member 26 contains a heating element 27 adapted when energ zed for heating the member 26 thereby to provide the desired reaction between the reducing agent and the activator compound in the member 26 for producing elemental barium to enable diffusion thereof through the member 26 and migration to the outer surface thereof.
- the evaporation rate of the barium is controlled by the amount of reaction occurring between the activator compound and the reducing agent contained in the matrix and, thus, the amount of barium produced and which can be vaporized is controllable.
- a thermionic emitter comprising a porous refractory matrix and a mixture consisting of an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate and a discrete reducing agent for said activator compound dispersed in said matrix.
- a thermionic emitter comprising a densely packed fused mixture of powders consisting of a refractory matrix material, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate, and a reducing agent for said activator compound and which is in addition to and not a constituent of said matrix material.
- a thermionic emitter according to claim 2, wherein said mixture is positioned in one end of a tubular refractory metal support member and said support member contains heating means adapted when energized to effect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
- a thermionic emitter according to claim 2, wherein said mixture comprises a coating fused to a refractory metal base member associated with heating means adapted when energized to effect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
- a thermionic emitter according to claim 2, wherein said mixture is in an integral self-sustaining form and contains heating means adapted when energized to elfect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
- a thermionic emitter comprising a body of compressed fused powdered constituents consisting essentially of: (1) a refractory matrix material selected from the group consisting of tungsten, tantalum and molybdenum, and the silicides, borides and carbides of tungstens, tantalum and molybdenum; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and (3) a discrete reducing agent selected from the group consisting of aluminum, zirconium and titanium.
- a thermionic emitter comprising the steps of providing a powdered mixture consisting essentially of a refractory material, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate and a discrete reducing agent, and compressing said mixture at a pressure of between about tons to tons per square inch into a densely packed coherent body until the particles of the constituents are fused together, thereby to provide a .porous matrix formed of said refractory material and having said activator compound and reducing agent dispersed in the pores of said matrix.
- the method of manufacturing a thermionic emitter comprising the steps of providing a powdered mixture consisting essentially of (l) a refractory matrix material selected from the group consisting of tungsten, tantalum and molybdenum, and the silicides, borides and carbides of tungsten, tantalum and molybdenum; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and (3) a discrete reducing agent selected from the group consisting of aluminum, Zirconium and titanium and combinations thereof, and compressing said mixture at a pressure of between approximately 70 and 80 tons per square inch for effecting a densely packed body wherein the particles of the constituents are fused, thereby to provide a porous matrix formed of said refractory material and having said reducing agent dispersed in the pores of said matrix.
- a thermionic emitter comprising a densely packed fused mixture of powders consisting of a refractory metal selected from the group consisting of tungsten, tantalum and molybdenum, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate, and aluminum.
- a thermionic emitter comprising a densely packed fused mixture of powders consisting of materials selected from the group consisting of tantalum, tungsten and molybdenum; an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and aluminum, and said activator compound and aluminum comprising approximately 9.5% and approximately 0.5%, respectively, by weight of said mixture.
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- Solid Thermionic Cathode (AREA)
Description
Jan. 11, 1966 J. H. AFFLECK Ill 3,
THERMIONIC EMITTER AND METHOD OF MAKING SAME Filed Sept. 1, 1961 FIG.4.
INVENTOR: JOHN H. AFFLECK,1I[.
HIS ATTORNEY.
United States Patent 3,229,147 THERR'HONIC EMITTER AND NZETHOD 0F DIAKING SAlyiE John H. Afileck III, Schenectady, N.Y., assignor to General Electric Company, a corporation of New York Filed Sept. 1, 1961, Ser. No. 135,547 11 Claims. (Cl. 313337) My invention relates to electron emitters and pertains more particularly to a new and improved thermionic emitter of the dispenser type and a new and improved method of making same.
Dispenser-type emitters usually comprise a porous refractory metal matrix impregnated with an activator compound adapted upon thermal dissociation of the compound to provide an elemental alkaline earth metal which migrates to the surface of the matrix and thus is available as an emissive film. Much of the effort devoted to the development of dispenser-type emitters heretofore has been for the provision of systems characterized by low effective work functions and, thus, adapted for high density electron emission within a given operating temperature range. Much development effort has also been directed toward the provision of emitters characterized by low evaporation rates of the activator material in the mentioned operating range, thereby to provide for prolonged operating life.
Disclosed and claimed in my copending US. application Serial No. 135,549, now Patent No. 3,176,180, filed concurrently herewith and assigned to the same assignee as the present invention are thermionic emitters and a method of manufacturing same which are adapted for providing dispenser type emitters characterized by low effective work functions and reduced evaporation rates. My present invent-ion contemplates improved emitters and a method of manufacturing same effective for affording a dispenser type emitter characterized by a low eifective work function and further reduced evaporation rates.
Accordingly, a primary object of my invention is to provide a new and improved thermionic emitter of the dispenser type.
Another object of my invention is to provide new and improved dispenser-type emitters characterized by low effective work functions and low evaporation rates of the activator materials during operation of the devices incorporating the emitters.
Another object of my invention is to provide new and improved dispenser-type emitters involving a new and improved system of constituents effective for thermally controlling the rate of production of an activator material in the matrix and thereby controlling the rate of evaporation of the activator.
Another object of my invention is to provide new and improved thermionic emitters of the dispenser type which are adapted for prolonged high density emission operation.
Another object of my invention is to provide new and improved thermionic emitters of the dispenser type which can be easily manufactured and which are not subject to the evolution of undesirable gases during manufacture or subsequent use.
Still another object of my invention is to provide a new and improved method of manufacturing a dispensertype thermionic emitter.
Further objects and advantages of my invention will become apparent as the following description proceeds and the features of novelty which characterize my invention will be pointed out with particularity in the claims annexed to and forming part of this specification.
Briefly, my invention contemplates a new and improved emitter of the dispenser type comprising a compressed Patented Jan. 11, 1966 ice fused body of powdered constituents consisting essentially of (l) a refractory matrix material selected prefera'bly from the group consisting of tungsten, tantalum and molybdenum and the silicides, carbides and borides of these materials and combinations thereof; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitan'ate; and (3) a reducing agent selected from the group consisting of aluminum, zirconium and titanium and combinations thereof. The emitter is preferably manufactured by admixing uniformly the powdered constituents and then compressing the mixture with a predetermined pressure effective for fusing the powdered constituents into a compressed coherent body having a consistency and internal structure whereby the body is adapted for uniform migration to the surface thereof of elemental activator upon chemical reduction of the activator compound. The reducing agent and operating temperature control the rate of activator production in the body and thus control the rate of evaporation of the activator.
For a better understanding of my invention reference may be had to the accompanying drawing wherein:
FIGURE 1 is a sectional view of a dispenser type emitter constructed according to an embodiment of my invention;
FIGURE 2 is a fragmentary somewhat schematic illustration of apparatus and the method employable in manufacturing my improved emitter;
FIGURE 3 is a fragmentary sectional view illustrating another modified form of my invention; and
FIGURE 4 is a fragmentary sectionalized view illustrating still another modified form of my invention.
Referring to the drawing, there is shown in FIGURE 1 a thermionic emitter of the dispenser type generally designated 10 and constructed according to an embodiment of my invention. The emitter 10 is supported in a flared end of a cathode holder 11 which can be formed of a refractory metal such as tungsten, tantalum or molybdenum. It is to be understood that the cathode holder 11 need not be flared and can comprise a straightw-alled cylindrical or tubular member of any desired cross-sectional configuration. A heating element 12 is contained in the holder 11 and is adapted when energized to heat the emitter 10, thereby to effect a desired reaction between an activator compound and a reducing agent contained in the emitter 1t) and for thereby effecting reduction of the activator compound and production of elemental barium for migration thereof to an active surface of the emitter designated 13.
The emitter 10 comprises a compressed fused body of powdered constituents of approximately 325 mesh and consisting essentially of (1) a refractory matrix material preferably selected from the group consisting of tungsten, tantalum and molybdenum, the silicides, carbides and borides of tungsten, tantalum and molybdenum and combinations thereof; (2) an activator compound selected from the group consisting of barium orthosilicate (Ba SiOQ and barium orthotitanate (Ba TiO.,) and combinations thereof, and (3) a reducing agent selected from the group consisting of aluminum, zirconium and titanium.
More specifically, the emitter 10 is preferably formed of a uniform, compressed fused mixture of powders of one of the mentioned refractory materials, one of the mentioned activator compounds and one of the reducing agents. However, it is to be understood that combinations of the refractory materials as well as combinations of the active compounds can be employed .in practicing my invention. Additionally, while aluminum, zirconium and titanium can be effectively employed as the reducing agent in practicing my invention, aluminum is preferred. Also, in the embodiment incorporating barium orthotitanate the use of titanium as a reducing agent should be avoided.
The above-discussed mixture is compressed at approximately 70 to 80 tons per square inch to a desired shape and whereby the particles constituting the powdered constituents are fused together to provide a coherent unitary body. In the present disclosure the term fused is used to mean that the particles constituting the body are blended together or joined as the result of pressure applied to the mixture in much the same way that metal members can be joined or fused by the application of pressure in the manner generally referred to in the art as cold welding.
Illustrated in FIGURE 2 is apparatus whereby the device of FIGURE 1 can be constructed. This apparatus comprises a female die 14 adapted for holding the cathode holder 11 firmly in an inverted position against a smooth surface die 15 while a quantity of the mixture of the above-discussed metal powders designated 16 is compressed by activation of a ramrod 17. The rod 17 is actuated with a force effective for compressing the mixture at the mentioned 70 to 80 tons per square inch. In this manner, the desired plug-like form of the emitter illustrated in FIGURE 1 is obtained and the emitter is formed as a compressed fused body having a desired consistency and porosity which contributes .to the effectiveness of the emitter in providing a desired low effective work function and insuring uniform coverage of the active surface 13 with elemental barium during energization of a heater 12.
Upon heating of the emitter in a vacuum, as by incorporation of the emitter in a vacuum discharge device and energization of the heater 12, the reducing agent in the emitter is effective for chemically reducing the activator compound and thereby producing elemental barium for diffusion through the body and migration uniformly to the active surface 13. Thus is provided an emitter having a refractory matrix bearing an active surface 13 substantially uniformly covered with elemental barium for providing a high density source of electrons and characterized by a substantially reduced effective work function. Additionally, in this structure the amount of barium produced is dependent upon the chemical reduction of the activator compound by the reducing agent. Thus, only through the continued operation of the device and energization of the heater 12 can the reducing agent be rendered effective for chemically reducing the barium compound and thus producing elemental barium. As a result, the amount of barium appearing at the active surface 13 is controlled and, thus, is not subject to rapid evaporation. However, the reducing agent is effective when heated for continuously causing the production of barium from the activator compound and, thus, the device is adapted for continuous replenishment of the active surface with barium to maintain the active surface for high density emission operation and a substantially reduced effective work function. Included below are the reactions obtained in the present device when tungsten is the refractory metal and aluminum is utilized as the reducing agent and whereby the production of barium results:
It will be understood that, while the foregoing reactions indicate the use of tungsten (W) as the refractory matrix material, any one of the above-mentioned matrix materials can be substituted therefor. Additionally, while in the reactions indicated above aluminum (Al) is indicated as the reducing agent employed, any one of the above-noted reducing agents may be alternatively employed except, however, in the case of barium orthotitanate where the use of titanium as a reducing agent should be avoided.
For the purpose of demonstrating the effective work functions and activator evaporation rates obtainable with the present invention, I have listed in the chart below some of the emitter systems tested at a given operating temperature of l250 K. and the emission and evaporation properties observed:
It is to be understood that, while I have not listed in the above chart all of the systems falling within the purview of my invention as disclosed above, the other systems which are encompassed by my invention including, for example, those involving the admixture of activator compounds with molybdenum and the carbides, silicides and borides of tungsten, tantalum and molybdenum are equally effective in providing a low effective work function and low evaporation rate emitters having characteristics comparable to those indicated in the chart. Additionally, it is to be noted that the above chart shows no evaporation rate for one of the systems. Such datum was not prepared; however, it is expected that such datum would not be substantially different from that noted in respect to the other systems indicated.
Further, while the activator compound was in each case in the systems included in the above chart 9.5% and the reducing agent was 0.5% of the composition of the system under test, it is to be understood that the percentage compositions of the systems can vary and still be characterized by desirably low effective work function and evaporation rates, although the indicated percentage composition in the chart has been found highly satisfactory.
Additionally, in conducting the test whereby the abovelisted information was obtained the temperature 1250 K. was arbitrarily selected for test purposes, and the effective work functions and the activator evaporation rates indicated are those calculated for this temperature. The effective work functions and evaporation rates will vary, of course, with different temperatures and can be determined by use of calculations well-known to those skilled in the art.
However, it can be seen from the data included in the above chart that the described systems are adapted for affording work functions which are considerably lower than the work functions of most metals. Additionally, the effective work functions approach closely the work functions of alkaline earth oxide cathodes which latter type cathodes have lower work functions but are limited in applications since they cannot withstand high operating temperatures and electron bombardment Without deteriora mg.
Illustrated in FIGURE 3 is a modified form of my Invention in which the emitter is generally designated 20. In this embodiment a base member 21 is provided which is preferably formed of a refractory metal such as tungsten, stantalum or molybdenum. The base member 21 carries as a coating thereon a body of the compressed fused mixture employed in forming the emitter 10 in FIGURE 1. In this embodiment the coating 22 is fused to the base member 21 and the formation of the coating 22 and the fusion thereof to the base member can be effected by the use of die means similar in function to that illustrated in FIGURE 2. Provided for cooperating with the emitter 20 is a heating element 23. Upon energization of the heating element 23 the base 21 and the coating 22 are heated, whereby the reducing agent in the coating 22 is efiective for reducing chemically the barium orthosilicate or barium orthotitanate in the mixture for producing barium for migration to the outer surface of the coating 22. In this embodiment also, by controlling the operating temperatures of the system, the amount of barium produced is controllable, whereby the device is adapted for relatively low evaporation of the activator. Alternatively, the emitter can be in a tubular form instead of the planar form illustrated.
Illustrated in FIGURE 4 is another modified form of my invention. In this embodiment an emitter generally designated 25 is tubular in form and comprises a unitary compressed fused and self-sustaining cylinder of the mixture employed in manufacturing the plug-like emitter 10 in FIGURE 1 and the emissive coating 22 in FIGURE 3. In this embodiment the member 26 contains a heating element 27 adapted when energ zed for heating the member 26 thereby to provide the desired reaction between the reducing agent and the activator compound in the member 26 for producing elemental barium to enable diffusion thereof through the member 26 and migration to the outer surface thereof. In this embodiment also the evaporation rate of the barium is controlled by the amount of reaction occurring between the activator compound and the reducing agent contained in the matrix and, thus, the amount of barium produced and which can be vaporized is controllable.
While I have shown and described specific embodiments of my invention, I do not desire my invention to be limited to the particular forms shown and described, and I intend by the appended claims to cover all modifications within the spirit and scope of my invention.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. A thermionic emitter comprising a porous refractory matrix and a mixture consisting of an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate and a discrete reducing agent for said activator compound dispersed in said matrix.
2. A thermionic emitter comprising a densely packed fused mixture of powders consisting of a refractory matrix material, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate, and a reducing agent for said activator compound and which is in addition to and not a constituent of said matrix material.
3. A thermionic emitter according to claim 2, wherein said mixture is positioned in one end of a tubular refractory metal support member and said support member contains heating means adapted when energized to effect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
4. A thermionic emitter according to claim 2, wherein said mixture comprises a coating fused to a refractory metal base member associated with heating means adapted when energized to effect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
5. A thermionic emitter according to claim 2, wherein said mixture is in an integral self-sustaining form and contains heating means adapted when energized to elfect a reaction between said activator compound and reducing agent, thereby to produce elemental barium for migration to the surface of said mixture.
6. A thermionic emitter, comprising a body of compressed fused powdered constituents consisting essentially of: (1) a refractory matrix material selected from the group consisting of tungsten, tantalum and molybdenum, and the silicides, borides and carbides of tungstens, tantalum and molybdenum; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and (3) a discrete reducing agent selected from the group consisting of aluminum, zirconium and titanium.
7. A thermionic emitter according to claim 6, wherein the activator compound constitutes approximately 9.5% and said reducing agent comprises approximately 0.5% by weight of said mixture.
8. The method of manufacturing a thermionic emitter comprising the steps of providing a powdered mixture consisting essentially of a refractory material, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate and a discrete reducing agent, and compressing said mixture at a pressure of between about tons to tons per square inch into a densely packed coherent body until the particles of the constituents are fused together, thereby to provide a .porous matrix formed of said refractory material and having said activator compound and reducing agent dispersed in the pores of said matrix.
9. The method of manufacturing a thermionic emitter comprising the steps of providing a powdered mixture consisting essentially of (l) a refractory matrix material selected from the group consisting of tungsten, tantalum and molybdenum, and the silicides, borides and carbides of tungsten, tantalum and molybdenum; (2) an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and (3) a discrete reducing agent selected from the group consisting of aluminum, Zirconium and titanium and combinations thereof, and compressing said mixture at a pressure of between approximately 70 and 80 tons per square inch for effecting a densely packed body wherein the particles of the constituents are fused, thereby to provide a porous matrix formed of said refractory material and having said reducing agent dispersed in the pores of said matrix.
It A thermionic emitter comprising a densely packed fused mixture of powders consisting of a refractory metal selected from the group consisting of tungsten, tantalum and molybdenum, an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate, and aluminum.
11. A thermionic emitter comprising a densely packed fused mixture of powders consisting of materials selected from the group consisting of tantalum, tungsten and molybdenum; an activator compound selected from the group consisting of barium orthosilicate and barium orthotitanate; and aluminum, and said activator compound and aluminum comprising approximately 9.5% and approximately 0.5%, respectively, by weight of said mixture.
References Cited by the Examiner UNITED STATES PATENTS 2,175,345 10/1939 Gaidies et al. 2,813,220 11/ 1957 Coppola 313-346 2,899,992 8/1959 Coppola 313-3461 3,010,826 11/1961 Koppius 313346 X GEORGE N. WESTBY, Primary Examiner.
RALPH G. NILSON, Examiner.
Claims (1)
1. A THERMIONIC EMITTER COMPRISING A POROUS REFRACTORY MATRIX AND A MIXTURE CONSISTING OF AN ACTIVATOR COMPOUND SELECTED FROM THE GROUP CONSISTING OF BARIUM ORTHOSILICATE AND BARIUM ORTHOTITANATE AND A DISCRETE REDUCING AGENG FOR SAID ACTIVATOR COMPOUND DISPERSED IN SAID MATRIX.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3258636D US3258636A (en) | 1961-09-01 | Electron emitter with activator of sill cide, boride or carbide of solid solu- tion of barium and at least one other alkaline earth metal | |
US135549A US3176180A (en) | 1961-09-01 | 1961-09-01 | Dispenser cathode |
US135547A US3229147A (en) | 1961-09-01 | 1961-09-01 | Thermionic emitter and method of making same |
FR907697A FR1335736A (en) | 1961-09-01 | 1962-08-24 | thermionic emitter and its manufacturing method |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13554861A | 1961-09-01 | 1961-09-01 | |
US135549A US3176180A (en) | 1961-09-01 | 1961-09-01 | Dispenser cathode |
US135547A US3229147A (en) | 1961-09-01 | 1961-09-01 | Thermionic emitter and method of making same |
Publications (1)
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US3229147A true US3229147A (en) | 1966-01-11 |
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US3258636D Expired - Lifetime US3258636A (en) | 1961-09-01 | Electron emitter with activator of sill cide, boride or carbide of solid solu- tion of barium and at least one other alkaline earth metal | |
US135547A Expired - Lifetime US3229147A (en) | 1961-09-01 | 1961-09-01 | Thermionic emitter and method of making same |
US135549A Expired - Lifetime US3176180A (en) | 1961-09-01 | 1961-09-01 | Dispenser cathode |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US3258636D Expired - Lifetime US3258636A (en) | 1961-09-01 | Electron emitter with activator of sill cide, boride or carbide of solid solu- tion of barium and at least one other alkaline earth metal |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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US135549A Expired - Lifetime US3176180A (en) | 1961-09-01 | 1961-09-01 | Dispenser cathode |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3684401A (en) * | 1970-11-17 | 1972-08-15 | Westinghouse Electric Corp | Cathode-getter materials for sputter-ion pumps |
US3824039A (en) * | 1971-03-24 | 1974-07-16 | British Oxygen Co Ltd | Sublimable targets |
US3988075A (en) * | 1972-05-15 | 1976-10-26 | General Electric Company | Nuclear fuel element |
EP0009261A1 (en) * | 1978-09-27 | 1980-04-02 | Siemens Aktiengesellschaft | Storage cathode, particularly metal capillary cathode |
EP0299126A1 (en) * | 1987-07-13 | 1989-01-18 | Syracuse University | Impregnated thermionic cathode |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3529334A (en) * | 1967-08-11 | 1970-09-22 | Isaac S Goodman | Assembling and brazing method |
US3590242A (en) * | 1969-06-12 | 1971-06-29 | Gen Electric | Making fused thorium carbide-tungsten cathodes for electron guns |
JPS5075763A (en) * | 1973-11-07 | 1975-06-21 | ||
US4808137A (en) * | 1988-05-31 | 1989-02-28 | The United States Of America As Represented By The Secretary Of The Army | Method of making a cathode from tungsten and iridium powders using a bariumaluminoiridiate as the impregnant |
KR910006044B1 (en) * | 1988-11-12 | 1991-08-12 | 삼성전관 주식회사 | Manufacturing method of an electron gun for crt |
KR930008611B1 (en) * | 1991-06-13 | 1993-09-10 | 삼성전관 주식회사 | Impregnated Cathode Structure and Manufacturing Method Thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US2175345A (en) * | 1935-07-12 | 1939-10-10 | Gen Electric | Electric gaseous discharge device |
US2813220A (en) * | 1954-12-06 | 1957-11-12 | Philips Corp | Indirectly heated cathode |
US2899992A (en) * | 1959-08-18 | Apparatus for making wood pulp chips | ||
US3010826A (en) * | 1951-03-22 | 1961-11-28 | Philips Corp | Method of making dispenser type cathodes |
Family Cites Families (9)
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US2647216A (en) * | 1950-04-01 | 1953-07-28 | Rca Corp | Dispenser cathode |
US2654045A (en) * | 1951-01-15 | 1953-09-29 | Gen Electric | Thermionic cathode for electric discharge device |
BE512852A (en) * | 1951-07-17 | |||
NL91132C (en) * | 1951-11-29 | |||
NL96177C (en) * | 1952-02-27 | |||
CH315203A (en) * | 1952-03-24 | 1956-07-31 | Siemens Ag | Cathode for electrical discharge vessels |
US2846339A (en) * | 1953-10-21 | 1958-08-05 | Honeywell Regulator Co | Method of forming an electron emitting body |
BE550302A (en) * | 1955-08-15 | |||
BE559450A (en) * | 1956-07-24 |
-
0
- US US3258636D patent/US3258636A/en not_active Expired - Lifetime
-
1961
- 1961-09-01 US US135547A patent/US3229147A/en not_active Expired - Lifetime
- 1961-09-01 US US135549A patent/US3176180A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2899992A (en) * | 1959-08-18 | Apparatus for making wood pulp chips | ||
US2175345A (en) * | 1935-07-12 | 1939-10-10 | Gen Electric | Electric gaseous discharge device |
US3010826A (en) * | 1951-03-22 | 1961-11-28 | Philips Corp | Method of making dispenser type cathodes |
US2813220A (en) * | 1954-12-06 | 1957-11-12 | Philips Corp | Indirectly heated cathode |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3684401A (en) * | 1970-11-17 | 1972-08-15 | Westinghouse Electric Corp | Cathode-getter materials for sputter-ion pumps |
US3824039A (en) * | 1971-03-24 | 1974-07-16 | British Oxygen Co Ltd | Sublimable targets |
US3988075A (en) * | 1972-05-15 | 1976-10-26 | General Electric Company | Nuclear fuel element |
EP0009261A1 (en) * | 1978-09-27 | 1980-04-02 | Siemens Aktiengesellschaft | Storage cathode, particularly metal capillary cathode |
EP0299126A1 (en) * | 1987-07-13 | 1989-01-18 | Syracuse University | Impregnated thermionic cathode |
Also Published As
Publication number | Publication date |
---|---|
US3258636A (en) | 1966-06-28 |
US3176180A (en) | 1965-03-30 |
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