EP0156454A1 - Thermionic electron emitter - Google Patents
Thermionic electron emitter Download PDFInfo
- Publication number
- EP0156454A1 EP0156454A1 EP85300230A EP85300230A EP0156454A1 EP 0156454 A1 EP0156454 A1 EP 0156454A1 EP 85300230 A EP85300230 A EP 85300230A EP 85300230 A EP85300230 A EP 85300230A EP 0156454 A1 EP0156454 A1 EP 0156454A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkaline earth
- layer
- electron emitter
- thermionic electron
- thermionic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000012190 activator Substances 0.000 claims abstract description 29
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052762 osmium Inorganic materials 0.000 claims abstract description 24
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000010937 tungsten Substances 0.000 claims abstract description 24
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 22
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 20
- 239000000956 alloy Substances 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims description 19
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 14
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 claims description 14
- 229910052788 barium Inorganic materials 0.000 claims description 8
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- 239000011733 molybdenum Substances 0.000 claims description 4
- 229910052712 strontium Inorganic materials 0.000 claims description 4
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052810 boron oxide Inorganic materials 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910000820 Os alloy Inorganic materials 0.000 description 7
- 229910001080 W alloy Inorganic materials 0.000 description 7
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 7
- 229910052741 iridium Inorganic materials 0.000 description 6
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 5
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 5
- 239000000292 calcium oxide Substances 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052707 ruthenium Inorganic materials 0.000 description 3
- 238000005275 alloying Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 229910052702 rhenium Inorganic materials 0.000 description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910000575 Ir alloy Inorganic materials 0.000 description 1
- 229910001182 Mo alloy Inorganic materials 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- MGRWKWACZDFZJT-UHFFFAOYSA-N molybdenum tungsten Chemical compound [Mo].[W] MGRWKWACZDFZJT-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 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
-
- 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
- H01J1/14—Solid thermionic cathodes characterised by the material
- H01J1/146—Solid thermionic cathodes characterised by the material with metals or alloys as an emissive material
Definitions
- This invention relates to a thermionic electron emitter.
- a known form of thermionic cathode commonly referred to as "M" type, is disclosed in U.S. Patent 3,373,307.
- the cathode comprises a matrix of tungsten or tungsten-molybdenum in reactive relationship with an alkaline earth activator which supplies free barium or barium oxide to the-emitting surface of the matrix.
- a thin porous coating of a refractory metal having a work function higher than that of tungsten is applied to the emitting surface by sputtering, for example.
- the coating is selected from the group of osmium, iridium, ruthenium, and rhenium, although osmium is preferred.
- the resultant cathode exhibits increased electron emission at the same temperature, or the same electron emission at a lower temperature, as compared with emission from a cathode without the layer.
- the coating comprises a thin porous layer of an alloy of osmium and iridium or osmium and ruthenium which serves to prolong the life of the cathode and reduces manufacturing difficulties due to the tendency for osmium to form an extremely toxic oxide.
- U.S. Patent 4 165 473 discloses a type of thermionic cathode different to "M"-type, the "mixed matrix” type.
- a preferred example of this cathode comprises particles of pure iridium mixed in fixed proportions with particles of pure tungsten. The particles are sintered to form a compacted porous matrix. The matrix is filled with an active material in the form of an alkaline earth aluminate. Some alloying occurs at the particle boundaries, but for optimum results such alloying must be incomplete.
- the emission of such a cathode is greater than that of an "M"-type cathode, the optimum proportions of iridium and tungsten being 20% iridium and 80% tungsten.
- the iridium and tungsten mixture may--be replaced by pure iridium, osmium, ruthenium, or rhenium or mixtures thereof or by a mixture of tungsten and one of those metals.
- European Patent Application 80300910 (Publication No. 19992) describes an improved form of dispenser cathode having the advantage of enhanced electron emission and prolonged life.
- This form of cathode comprises an electron emissive layer formed of an alloy of tungsten and osmium, and an associated alkaline earth activator.
- a thermionic electron emitter including an electron emissive layer formed solely of an alloy containing osmium in the proportion, expressed in atomic percent, in the range from 32 percent to 34 percent inclusive, the balance being of tungsten; and an alkaline earth activator.
- said electron emissive layer comprises a coating of said alloy provided on a porous refractory medium impregnated with said alkaline earth activator.
- the alkaline earth activator may be confined on the side of said porous refractory medium remote from said layer.
- said electron emissive layer is porous and is impregnated with said alkaline earth activator.
- said alkaline earth activator may be confined on the side of said porous, electron emissive layer remote from the electron emissive surface of said layer.
- the alkaline earth activator may be a mixture of barium oxide, or a compound of barium, reducible on heating to said oxide; an oxide, or a compound which decomposes on heating to the oxide, of an alkaline earth metal other than barium and at least one of aluminium or boron oxide.
- the alkaline earth metal other than barium may be a metal selected from the group consisting of calcium, strontium and magnesium.
- a method of making a thermionic electron emitter comprising the steps of forming an alloy of the kind defined in said one aspect of the invention and incorporating said alloy and an alkaline earth activator in the emitter.
- a thermionic cathode including a thermionic electron emitter of the kind defined in accordance with the said one aspect of the present invention.
- European Patent Application No. 80300910 discloses a particularly useful thermionic electron emitter including an electron emissive layer, formed of an alloy of tungsten or molybdenum and osmium, and an associated alkaline earth activator. It was considered that optimum results would be achieved if the proportions of alloy constituents used fall in a preferred range - namely 20 to 30% osmium and 80 to 70% tungsten. Another composition considered to be useful was 40% osmium and 60% tungsten. While materials having these preferred compositions are found to have beneficial electron emissive properties the inventors have now discovered that, contrary to expectation; a superior material, with greatly enhanced electron emissive properties, is produced if the composition lies outside the above-mentioned preferred range.
- the alloy comprises osmium in the range (expressed in atomic percent) from 32 percent to 34 percent inclusive, the balance being of tungsten.
- the inventors find that this striking improvement in electron emission is achieved for alloy compositions lying in the above-defined, relatively narrow range (i.e. from 32 percent osmium to 34 percent osmium inclusive, the proportions being expressed as atomic percentages).
- Figure 2 of the drawings shows a cross-sectional view through a thermionic cathode 10 including a cylindrical body 1 of molybdenum, for example, containing a heating element 2 in a cavity 3 of the body, and a thermionic electron emitter constructed in accordance with one example of the present invention.
- the emitter in this example, comprises a porous plug 4 of tungsten or another suitable refractory medium, such as molybdenum, which is impregnated with an alkaline earth activator, and an electron emissive layer 5 in the form of a coating provided at the exposed surface of the plug.
- Layer 5 comprises an alloy of 67 atomic percent tungsten and 33 atomic percent osmium formed at the exposed surface of the plug by cosputtering osmium and tungsten in the desired proportions.
- the alloy could be formed -by co-evaporating the constituent metals or by co-precipating the metals from reducible compounds thereof.
- the thickness of layer 5 is around 4000 Angstrom Units, although alternatively a thickness in the range 2000 Angstrom Units to 25,000 Angstrom Units, for example, could be used.
- the alkaline earth activator in this example comprises a mixture of barium oxide, calcium oxide and aluminium oxide in the molecular proportions 3:;:1 respectively, although, as will be described in greater detail hereinafter other constituents and proportions may usefully be employed.
- the alkaline earth activator is contained within a cavity 6 behind the porous plug 4.
- the thermionic electron emitter comprises a porous layer 7 of the tungsten/osmium alloy impregnated with an alkaline earth activator - again a mixture of barium oxide, aluminium oxide and calcium oxide, in the molecular proportions 3:1:1 respectively is used.
- the alloy contains 33 atomic percent osmium and 67 atomic percent tungsten.
- the emitter of Figure 4 may be constructed by initially pressing a mixture of the powdered alloy constituents (W and Os) in the desired proportions at, for example, 10 tons per square inch.
- the mixture, so pressed, is then sintered (e.g. at 2500°C for 30 minutes) to achieve a porosity of approximately 20% and the sinter then furnaced at a temperature, and for a time, sufficient to allow full osmium/tungsten interdiffusion to occur (e.g. at a temperature in the range 1800° to 2000°C for 5 to 10 hours).
- the porous layer of tungsten/osmium alloy, thus formed, is then impregnated with the alkaline earth activator. Impregnation techniques are well known in the art and are described, for example, in US 3,201,639.
- the emitter of Figure 4 may be constructed by an alternative method involving pressing a powder of an alloy of tungsten and osmium (in the proportions 33 atomic percent osmium and 67 atomic percent tungsten), sintering the powder, so pressed (e.g. at 2500 0 C for 30 mins.) to achieve a porosity of about 20% and then impregnating the porous layer, so formed, with the alkaline earth activator.
- the alkaline earth activator is contained within a cavity 8 behind the porous alloy layer, formed as described hereinbefore.
- the present invention encompasses a thermionic electron emitter including an alloy of osmium and tungsten in the proportions of 33 + 1 atomic percent and 67 + 1 atomic percent respectively (i.e. tungsten in the proportion (expressed in atomic percent) in the range from 66 percent to 68 percent inclusive and osmium in the proportion (expressed in atomic percent) in the range from 34 percent to 32 percent inclusive).
- an alkaline earth activator in the form of barium oxide, calcium oxide and aluminium oxide in the molecular proportions 3:1 ⁇ 2:1 respectively has been described, other proportions and materials may be used.
- the barium oxide, calcium oxide and aluminum oxide may be in the proportions 4:1:1 or 5:3:2 respectively.
- another oxide of an alkaline earth metal other than barium
- the oxide of strontium or magnesium or a mixture of the oxides of any two or more of calcium, strontium and magnesium could be used.
- the carbonates of the alkaline earth metals, mentioned hereinbefore, which decompose on heating to the oxide could be used.
- aluminium oxide boron oxide may be used.
Landscapes
- Solid Thermionic Cathode (AREA)
Abstract
Description
- This invention relates to a thermionic electron emitter.
- A known form of thermionic cathode, commonly referred to as "M" type, is disclosed in U.S. Patent 3,373,307. The cathode comprises a matrix of tungsten or tungsten-molybdenum in reactive relationship with an alkaline earth activator which supplies free barium or barium oxide to the-emitting surface of the matrix. A thin porous coating of a refractory metal having a work function higher than that of tungsten is applied to the emitting surface by sputtering, for example. The coating is selected from the group of osmium, iridium, ruthenium, and rhenium, although osmium is preferred. The resultant cathode exhibits increased electron emission at the same temperature, or the same electron emission at a lower temperature, as compared with emission from a cathode without the layer.
- In a development of the "M" type cathode disclosed in US Patent 3,497,757 the coating comprises a thin porous layer of an alloy of osmium and iridium or osmium and ruthenium which serves to prolong the life of the cathode and reduces manufacturing difficulties due to the tendency for osmium to form an extremely toxic oxide.
- Another development of the "M"-type cathode is described in an article entitled "Surface and Emission Characteristics of the Impregnated Dispenser Cathode" (Jones, MacNealy, and Swanson) in "Applications of Surface Science 2 (1979)" pages 232-257, North-Holland Publishing Company. This development is an IDC (impregnated dispenser cathode) made by Spectra-Mat Inc. of Watsonville California USA. This cathode has a sputter coating of osmium-rhuthenium alloy, the coating having a random columnar structure. This cathode has improved emission which is attributed, at least in part, to the geometric form of the surface structure.
- U.S.
Patent 4 165 473 discloses a type of thermionic cathode different to "M"-type, the "mixed matrix" type. A preferred example of this cathode comprises particles of pure iridium mixed in fixed proportions with particles of pure tungsten. The particles are sintered to form a compacted porous matrix. The matrix is filled with an active material in the form of an alkaline earth aluminate. Some alloying occurs at the particle boundaries, but for optimum results such alloying must be incomplete. The emission of such a cathode is greater than that of an "M"-type cathode, the optimum proportions of iridium and tungsten being 20% iridium and 80% tungsten. The iridium and tungsten mixture may--be replaced by pure iridium, osmium, ruthenium, or rhenium or mixtures thereof or by a mixture of tungsten and one of those metals. - European Patent Application 80300910 (Publication No. 19992) describes an improved form of dispenser cathode having the advantage of enhanced electron emission and prolonged life. This form of cathode comprises an electron emissive layer formed of an alloy of tungsten and osmium, and an associated alkaline earth activator.
- It is an object of this invention to provide a further form of thermionic electron emitter.
- In accordance with one aspect of the invention there is provided a thermionic electron emitter including an electron emissive layer formed solely of an alloy containing osmium in the proportion, expressed in atomic percent, in the range from 32 percent to 34 percent inclusive, the balance being of tungsten; and an alkaline earth activator.
- In an embodiment said electron emissive layer comprises a coating of said alloy provided on a porous refractory medium impregnated with said alkaline earth activator. Alternatively, the alkaline earth activator may be confined on the side of said porous refractory medium remote from said layer.
- In another embodiment said electron emissive layer is porous and is impregnated with said alkaline earth activator. Alternatively said alkaline earth activator may be confined on the side of said porous, electron emissive layer remote from the electron emissive surface of said layer.
- The alkaline earth activator may be a mixture of barium oxide, or a compound of barium, reducible on heating to said oxide; an oxide, or a compound which decomposes on heating to the oxide, of an alkaline earth metal other than barium and at least one of aluminium or boron oxide. The alkaline earth metal other than barium may be a metal selected from the group consisting of calcium, strontium and magnesium.
- According'to a further aspect of the invention there is provided a method of making a thermionic electron emitter comprising the steps of forming an alloy of the kind defined in said one aspect of the invention and incorporating said alloy and an alkaline earth activator in the emitter.
- According to a yet further aspect of the invention there is provided a thermionic cathode including a thermionic electron emitter of the kind defined in accordance with the said one aspect of the present invention.
- In order that the invention may be carried into effect embodiments thereof are now described, by way of example only, by reference to the accompanying drawings of which:
- Figure 1 shows how electron emission density of-a thermionic electron emitter varies as a function of alloy composition and
- Figures 2 to 5 show thermionic cathodes having different forms of electron emitter constructed in accordance with the present invention.
- Over the past few years an extensive programme of axperimental and theoretical research has been carried out by the inventors with the aim of producing a thermionic electron emitter which, as compared with hitherto known electron emitters of the kind described, for example, in the above-mentioned United States Patents, has enhanced electron emissive properties.
- As described hereinbefore, European Patent Application No. 80300910 (Publication No. 19992) discloses a particularly useful thermionic electron emitter including an electron emissive layer, formed of an alloy of tungsten or molybdenum and osmium, and an associated alkaline earth activator. It was considered that optimum results would be achieved if the proportions of alloy constituents used fall in a preferred range - namely 20 to 30% osmium and 80 to 70% tungsten. Another composition considered to be useful was 40% osmium and 60% tungsten. While materials having these preferred compositions are found to have beneficial electron emissive properties the inventors have now discovered that, contrary to expectation; a superior material, with greatly enhanced electron emissive properties, is produced if the composition lies outside the above-mentioned preferred range.
- The inventors have found, in accordance with the present invention, that greatly enhanced electron emission is achieved if the alloy comprises osmium in the range (expressed in atomic percent) from 32 percent to 34 percent inclusive, the balance being of tungsten.
- The relative proportions of the alloy constituents used is found to be remarkably critical. This fact is demonstrated in Figure 1 of the drawings which shows how the zero field electron emission density e is found to vary as a function of alloy composition - assuming a cathode operating temperature of 1340K. It will be apparent that the electron emission density exhibits a striking peak, centred on an osmium composition of 33 atomic percent; in comparison, the electron densities achieved at compositions of 25 atomic percent osmium or 40 atomic percent osmium, for example, are relatively small.
- The inventors find that this striking improvement in electron emission is achieved for alloy compositions lying in the above-defined, relatively narrow range (i.e. from 32 percent osmium to 34 percent osmium inclusive, the proportions being expressed as atomic percentages).
- Figure 2 of the drawings shows a cross-sectional view through a
thermionic cathode 10 including a cylindrical body 1 of molybdenum, for example, containing aheating element 2 in acavity 3 of the body, and a thermionic electron emitter constructed in accordance with one example of the present invention. - The emitter, in this example, comprises a
porous plug 4 of tungsten or another suitable refractory medium, such as molybdenum, which is impregnated with an alkaline earth activator, and an electronemissive layer 5 in the form of a coating provided at the exposed surface of the plug.Layer 5 comprises an alloy of 67 atomic percent tungsten and 33 atomic percent osmium formed at the exposed surface of the plug by cosputtering osmium and tungsten in the desired proportions. Alternatively, the alloy could be formed -by co-evaporating the constituent metals or by co-precipating the metals from reducible compounds thereof. - Typically, the thickness of
layer 5 is around 4000 Angstrom Units, although alternatively a thickness in the range 2000 Angstrom Units to 25,000 Angstrom Units, for example, could be used. - The alkaline earth activator in this example comprises a mixture of barium oxide, calcium oxide and aluminium oxide in the molecular proportions 3:;:1 respectively, although, as will be described in greater detail hereinafter other constituents and proportions may usefully be employed.
- In another example of the invention, shown in Figure 3 of the drawings, the alkaline earth activator is contained within a cavity 6 behind the
porous plug 4. - In a yet further example of the invention, shown in Figure 4 of the drawings, the thermionic electron emitter comprises a
porous layer 7 of the tungsten/osmium alloy impregnated with an alkaline earth activator - again a mixture of barium oxide, aluminium oxide and calcium oxide, in the molecular proportions 3:1:1 respectively is used. As before, in this example, the alloy contains 33 atomic percent osmium and 67 atomic percent tungsten. - The emitter of Figure 4 may be constructed by initially pressing a mixture of the powdered alloy constituents (W and Os) in the desired proportions at, for example, 10 tons per square inch. The mixture, so pressed, is then sintered (e.g. at 2500°C for 30 minutes) to achieve a porosity of approximately 20% and the sinter then furnaced at a temperature, and for a time, sufficient to allow full osmium/tungsten interdiffusion to occur (e.g. at a temperature in the range 1800° to 2000°C for 5 to 10 hours). The porous layer of tungsten/osmium alloy, thus formed, is then impregnated with the alkaline earth activator. Impregnation techniques are well known in the art and are described, for example, in US 3,201,639.
- The emitter of Figure 4 may be constructed by an alternative method involving pressing a powder of an alloy of tungsten and osmium (in the proportions 33 atomic percent osmium and 67 atomic percent tungsten), sintering the powder, so pressed (e.g. at 25000C for 30 mins.) to achieve a porosity of about 20% and then impregnating the porous layer, so formed, with the alkaline earth activator.
- In yet a further example of the invention, illustrated in Figure 5, the alkaline earth activator is contained within a
cavity 8 behind the porous alloy layer, formed as described hereinbefore. - Although the examples, described hereinbefore, concern use of an alloy of tungsten and osmium in the proportions 67 atomic percent and 33 atomic percent respectively, the present invention, as described hereinbefore, encompasses a thermionic electron emitter including an alloy of osmium and tungsten in the proportions of 33 + 1 atomic percent and 67 + 1 atomic percent respectively (i.e. tungsten in the proportion (expressed in atomic percent) in the range from 66 percent to 68 percent inclusive and osmium in the proportion (expressed in atomic percent) in the range from 34 percent to 32 percent inclusive).
- Furthermore, although an alkaline earth activator in the form of barium oxide, calcium oxide and aluminium oxide in the molecular proportions 3:½:1 respectively has been described, other proportions and materials may be used. For example, the barium oxide, calcium oxide and aluminum oxide may be in the proportions 4:1:1 or 5:3:2 respectively. Furthermore, instead of using calcium oxide, another oxide of an alkaline earth metal (other than barium) may be used; for example, the oxide of strontium or magnesium or a mixture of the oxides of any two or more of calcium, strontium and magnesium. Alternatively the carbonates of the alkaline earth metals, mentioned hereinbefore, which decompose on heating to the oxide, could be used. Instead of using aluminium oxide, boron oxide may be used.
Claims (10)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8404943 | 1984-02-24 | ||
GB8404943 | 1984-02-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0156454A1 true EP0156454A1 (en) | 1985-10-02 |
EP0156454B1 EP0156454B1 (en) | 1987-12-09 |
Family
ID=10557160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19850300230 Expired EP0156454B1 (en) | 1984-02-24 | 1985-01-14 | Thermionic electron emitter |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0156454B1 (en) |
DE (1) | DE3561180D1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0248417A2 (en) * | 1986-06-06 | 1987-12-09 | Kabushiki Kaisha Toshiba | Impregnated cathode |
GB2188771B (en) * | 1986-04-01 | 1990-12-19 | Ceradyne Inc | Dispenser cathode and method of manufacture therefor |
GB2268325A (en) * | 1992-07-01 | 1994-01-05 | Thorn Emi Electronics Ltd | Thermionic cathode structure. |
GB2394117A (en) * | 2002-10-07 | 2004-04-14 | Toshiba Kk | Ion source, ion implantation device, and manufacturing method of semiconductor devices |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4165473A (en) * | 1976-06-21 | 1979-08-21 | Varian Associates, Inc. | Electron tube with dispenser cathode |
EP0019992A1 (en) * | 1979-05-29 | 1980-12-10 | Thorn Emi-Varian Limited | Thermionic electron emitters and methods of making them |
-
1985
- 1985-01-14 DE DE8585300230T patent/DE3561180D1/en not_active Expired
- 1985-01-14 EP EP19850300230 patent/EP0156454B1/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4165473A (en) * | 1976-06-21 | 1979-08-21 | Varian Associates, Inc. | Electron tube with dispenser cathode |
EP0019992A1 (en) * | 1979-05-29 | 1980-12-10 | Thorn Emi-Varian Limited | Thermionic electron emitters and methods of making them |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2188771B (en) * | 1986-04-01 | 1990-12-19 | Ceradyne Inc | Dispenser cathode and method of manufacture therefor |
EP0248417A2 (en) * | 1986-06-06 | 1987-12-09 | Kabushiki Kaisha Toshiba | Impregnated cathode |
EP0248417A3 (en) * | 1986-06-06 | 1989-10-25 | Kabushiki Kaisha Toshiba | Impregnated cathode |
GB2268325A (en) * | 1992-07-01 | 1994-01-05 | Thorn Emi Electronics Ltd | Thermionic cathode structure. |
GB2268325B (en) * | 1992-07-01 | 1996-01-03 | Thorn Emi Electronics Ltd | Thermionic cathode structure |
GB2394117A (en) * | 2002-10-07 | 2004-04-14 | Toshiba Kk | Ion source, ion implantation device, and manufacturing method of semiconductor devices |
GB2394117B (en) * | 2002-10-07 | 2004-09-08 | Toshiba Kk | Ion souce Ion implanting device and manufacturing method of semiconductor devices |
US6825597B2 (en) | 2002-10-07 | 2004-11-30 | Kabushiki Kaisha Toshiba | Ion source, ion implanting device, and manufacturing method of semiconductor devices |
US7144794B2 (en) | 2002-10-07 | 2006-12-05 | Kabushiki Kaisha Toshiba | Ion source, ion implanting device, and manufacturing method of semiconductor devices |
CN1294614C (en) * | 2002-10-07 | 2007-01-10 | 株式会社东芝 | Ion source, ion injection equipment, manufacturing method of semiconductor device |
Also Published As
Publication number | Publication date |
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EP0156454B1 (en) | 1987-12-09 |
DE3561180D1 (en) | 1988-01-21 |
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