US2899592A - coppola - Google Patents
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- Publication number
- US2899592A US2899592A US2899592DA US2899592A US 2899592 A US2899592 A US 2899592A US 2899592D A US2899592D A US 2899592DA US 2899592 A US2899592 A US 2899592A
- Authority
- US
- United States
- Prior art keywords
- barium
- refractory metal
- cathode
- metal
- alloy
- 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.)
- Expired - Lifetime
Links
- 239000003870 refractory metal Substances 0.000 claims description 48
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 19
- 229910052721 tungsten Inorganic materials 0.000 claims description 19
- 239000010937 tungsten Substances 0.000 claims description 19
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 17
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 claims description 9
- 239000011876 fused mixture Substances 0.000 claims description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 4
- CSSYLTMKCUORDA-UHFFFAOYSA-N barium(2+);oxygen(2-) Chemical compound [O-2].[Ba+2] CSSYLTMKCUORDA-UHFFFAOYSA-N 0.000 claims 1
- 229910052788 barium Inorganic materials 0.000 description 31
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 27
- 229910052751 metal Inorganic materials 0.000 description 23
- 239000002184 metal Substances 0.000 description 23
- 239000000463 material Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 18
- 229910052750 molybdenum Inorganic materials 0.000 description 18
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 17
- 239000011733 molybdenum Substances 0.000 description 17
- 229910045601 alloy Inorganic materials 0.000 description 16
- 239000000956 alloy Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 230000008020 evaporation Effects 0.000 description 9
- 238000001704 evaporation Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- -1 eg. Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 229910052726 zirconium Inorganic materials 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 229910052735 hafnium Inorganic materials 0.000 description 5
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 5
- 239000010955 niobium Substances 0.000 description 5
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 4
- 229910052758 niobium Inorganic materials 0.000 description 4
- 238000005245 sintering Methods 0.000 description 4
- 229910052715 tantalum Inorganic materials 0.000 description 4
- 230000004913 activation Effects 0.000 description 3
- 238000005275 alloying Methods 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910001080 W alloy Inorganic materials 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- QKYBEKAEVQPNIN-UHFFFAOYSA-N barium(2+);oxido(oxo)alumane Chemical compound [Ba+2].[O-][Al]=O.[O-][Al]=O QKYBEKAEVQPNIN-UHFFFAOYSA-N 0.000 description 2
- 230000001427 coherent effect Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000005247 gettering Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- MGRWKWACZDFZJT-UHFFFAOYSA-N molybdenum tungsten Chemical compound [Mo].[W] MGRWKWACZDFZJT-UHFFFAOYSA-N 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 229910001029 Hf alloy Inorganic materials 0.000 description 1
- 241000183024 Populus tremula Species 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- UUXFWHMUNNXFHD-UHFFFAOYSA-N barium azide Chemical compound [Ba+2].[N-]=[N+]=[N-].[N-]=[N+]=[N-] UUXFWHMUNNXFHD-UHFFFAOYSA-N 0.000 description 1
- UXFOSWFWQAUFFZ-UHFFFAOYSA-L barium(2+);diformate Chemical compound [Ba+2].[O-]C=O.[O-]C=O UXFOSWFWQAUFFZ-UHFFFAOYSA-L 0.000 description 1
- FZTPSPNAZCIDGO-UHFFFAOYSA-N barium(2+);silicate Chemical compound [Ba+2].[Ba+2].[O-][Si]([O-])([O-])[O-] FZTPSPNAZCIDGO-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 229910000753 refractory alloy Inorganic materials 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 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
- My invention relates to a thermionic dispenser cathode.
- a supply of alkalne earth material is disposed within a body of refractory metal, eg., tungsten, molybdenum, tantalum, hafnium, or niobium, having a porous wall portion through which alkalne earth metal producedby a reaction between the alkalne earth material and the refractory metal can pass and form an emissive layer on a surface of the body.
- refractory metal eg., tungsten, molybdenum, tantalum, hafnium, or niobium
- the reaction between the refractory metal and the alkalne earth compound usually proceeds quite rapidly, and in many cases an excessive amount of alkalne earth metal is supplied to the emissive surface and is evaporated which is a disadvantage of the cathode for certain applications.
- A'princpal object of my invention is to provide a thermionic dispenser cathode having a reduced rate of evaporation of alkalne earth metal.
- a still further object of my invention is to provide a cathode in which the porosity of the porous wall is not the controlling factor in determining the rate at which free alkalne earth metal is furnished to the emissive surface of the cathode.
- a further object'of my invention is to provide a thermionic dispenser cathode in which the initial rate of evaporation of alkalne earth metal duringfabrication and activation is reduced.
- Another object of my invention is to facilitate the fabrication of a thermionic dispenser cathode by employing a refractory metal alloy which can be sintered into a body at lower temperatures.
- a further object of my invention is to provide a dispenser cathode employing a more readily machinable refractory metal whereby the cathode can be machined to close tolerances.
- a further object of my invention is to employ a refractory metal alloy in which one of the constituents of the alloy will serve to bind some undesirable gaseous products which may be produced during the operation of the cathode.
- the rate of evaporation of alkalne earth metal in a dispenser cathode can be reduced by substituting for the refractory metal, such as tungsten, in the porous wall of the cathode structure an alloy of at least two refractory metals one of which is active in reducing the alkalne earth material disposed in a cavity within the body and the other of which is more passive during the reaction.
- the refractory metal such as tungsten
- active refractory metal I mean a refractory metal which will react with certain alkalne earth compounds to furnish a supply of free alkalne earth metal in excess of that required to form a satisfactory emitter.
- passive refractory metal I mean a re fractory metal which does not react or only reacts with those alkalne earth compounds to such an extent as to form an insufficient amount of free alkalne earth metal.
- the refractory metals may be either passive or active depending upon which alkalne earth compounds are employed.
- the passive refractory metal serves to limit the amount of active refractory metal'available for reaction with the alkalne earth material in the cavity and also serves to limit the rate at which the active refractory metal is brought into contact with the alkalne earth material because the active refractory metal must diffuse through the passive refractory metal before Contacting the alkalne earth material. Consequently, the alloy must con tain the active and passive refractory metals in amounts suflicient to form the emissive surface while preventing excessive evaporation of alkalne earth metal.
- the refractory metals are more or less active in reducng certain alkalne earth compounds or compositions to' free alkalne earth metal. More particularly, I have found that molybdenum is the least active of the refractory metals in its ability to reduce alkalne earth compounds or compositions to the free alkalne earth metal.
- I mix the alkalne earth material with powdered refractory metal alloy and press the mixture into a body which is sintered to produce a coherent body.
- this reduction I have found, is materially less than if tungsten alone is used as a refractory metal.
- the alloys according to my invention substantially reduce the rate of evaporation of the alkaline earth metal by inhibiting the rate of reduction of the alkaline earth material.
- Fig. 1 is a sectional View of one embodiment of a dispenser cathode according to the invention.
- Fig. 2 is a sectional view of another embodiment of a dispenser cathode according to the invention.
- the dispenser cathode shown in Fig. l comprises a tube 1 composed of refractory metal such as molybdenum having an internal partition 2 for separating the tube into two chambers.
- the lower chamber houses a conventional heater 3 while the upper chamber houses a supply of alkaline earth compounds 4 such as a mixture of barium and strontum carbonates.
- the upper chamber is closed by a porous disc 5 sealed to the end of the tube fl by welding so that the pores in the wall constitute the only passageways connecting the cavity in which the alkaline earth compounds are disposed to the emissive surface 6.
- the porous disc 5 is made of an alloy composed of 25% of tungsten and 75% of molybdenum made by pressing the powdered alloy into a disc and sintering the same at a temperature of about l600 to 1900 C Since the resulting disc is porous, the alkaline earth metal obtained by reaction between the alkaline earth compounds in the cavity passes through the pores of the disc and forms an emissive layer on the surface of the cathode.
- tungsten is the active refractory metal which reacts with the barium and strontum oxides formed by thermal decomposition of the carbonates in the cavity to supply free barium to the emissive surface of the cathode. Since the tungsten is alloyed with molybdenum, not only is the amount of tungsten available for the reaction diminshed but the rate at which it is made available for reaction is limited by its diffusion rate through the molybdenum.
- alkaline earth compounds or mixtures or solid solutions thereof are substituted in the cavity for the barium and strontum carbonates, other refractory alloys may be used.
- the following table lists the most suitable refractory metal that should be used for various alkaline earth compositions in the cavity in order to obtain a suflicient but not excessive supply of barium for the ernissive surface.
- Mo-W up to about 90% of W BaO.
- Mo-Ta up to about Ta,...
- W-Ta up to about 10% MO-rNb, up to about 10% Nb Refractory Metal Alloy Passive Ref. Metal-Active Ref. Metal Alkaliue Earth Materialin cavity W-Nb, up to about 10% Nb Basic and normal barium beyl- ⁇ Basic barium aluminates.
- Mo-Zr less than about 5% Hf Basic barium aluminates. Normal and basic barium hei-yll'atcs.
- the alkaline earth compounds are homogeneously distributed within the porous disc itself.
- the disc 5 in which the alkaline earth compounds are disposed is sealed in one end of a tube 1 of refractory metal such as molybdenum and separated from the heater 3 by a partition 2 of refractory metal.
- the porous disc in which the alkaline earth compounds are disposed can be fabricated as follows.
- the disc may be made by mixing the refractory metal in powdered form with the alkaline earth material, eg., a 5 to 2 mole ratio of a prefired mixture of BaO and Al O This mixture is then pressed and sintered at a temperature of about 1650 to l750 C. for about 30 seconds.
- the resulting body is mechanically coherent and relatively free of entrapped gases.
- a porous disc obtained by pressing and sintering a powdered refractory metal alloy at relatively high temperatures, e.g., l600-1900 C. but in any event no higher than a temperature slightly below the lowest melting point of either the alloy or any of its constituents.
- the porous disc thus obtained which may be machined, if desircd, is then impregnated with a suitable alkaline earth material as described in U.S. application Serial No. 273,607, filed February 27, 1952, now Patent 2,700,000 by R. Levi et al.
- the alkaline earth material to be used must have a meltng point below the temperature at which the porous disc was sintered in order to avoid further sintering thereof during impregnation.
- the alkaline earth material In the cathodes in which the alkaline earth material is homogeneously distributed throughout the porous disc, the alkaline earth material must be selected so that t is readily reducible by the active refractory metal without deleteriously reacting therewith.
- Suitable alkaline earth materials and the criteria governing their selection for that type of cathode are disclosed in U.S. applications Serial Nos. 258,89l, now Patent No. 2,716,716 and 258,892, now Patent 2,700,112 filed November 29, 1951, by R. C. Hughes et al. All of the compositions and mixtures of alkaline earth compounds disclosed therein may be used in the cathode according to my invention and the foregoing advantages erumerated hereinabove will be realized.
- the selection of the particular alkaline earth material will to some extent determine the particular refractory metal alloy that should be used and I have listed in the table below the best combinations of refractory metal alloys and alkaline earth materials.
- the terms pressed powder" and “impreguated” refer, respectively, to cathodes made by mixing the alkaline earth material with the powdered metal alloy and forming a body therefrom, and to a cathode obtained by ntroducing the alkaline earth material into a porous disc by impregratio.
- Normal barium berylliate Mono-barium aluminates.
- Basic barium berylliates ⁇ Barium ortho-silicate.
- the cathode was assembled in an evacuated envelope in which an anode was arranged. All emisson measurements were taken at a cathode Operating temperature of 950 C. brightness pulse-wise with 100 microsecond pulses at the rate of 20 per second at a 1000 volts on the anode. The cathode was held at 1050 C. brightness with 100 volts D.C. on the anode during life.
- said refractory metal alloy consisting of 75% by weight of molybdenum and 25% by weight of tungsten.
- a thermionic cathode comprising a tubular structure consisting of .Iefractory metal, &portion of the wall of said -structure constituting the emissive surface thereof consisting of a sintered body composcd of 90% by weight of an alloy consisting of 75% by weight of molybdenum
- the time required OH the P P for those cathodes was 10 and 25% by weight of tungsten, and 10% by weight of a fraction of that required when pure tungsten or pure molybdenum instead of the alloy was used.
- This invention is not limited to cathodes having the shape shown but is applicable to dispenser cathodes of more complex Construction.
- the cathode for example, could have a cylindrical shape, or it could be a concave or planar type of cathode.
- a thermionic cathode comprisng a structure con sisting of refractory metal, a portion of the wall of said structure constituting the emissive surface thereof consistng of a homogeneously-porous sintered refractory metal alloy, and a supply of a fused mixture of 5 moles of barium oxide and 2 moles of aluminum oxide distributed within and only within the pores of said wall a fused miXture of 5 moles of barium oxide and 2 moles of aluminum oxide, the fused mixture of barium and aluminum oxide being contained within and only within said sintered body.
Landscapes
- Solid Thermionic Cathode (AREA)
- Powder Metallurgy (AREA)
- Discharge Lamp (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US345392XA | 1953-11-18 | 1953-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2899592A true US2899592A (en) | 1959-08-11 |
Family
ID=21877047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US2899592D Expired - Lifetime US2899592A (en) | 1953-11-18 | coppola |
Country Status (7)
Country | Link |
---|---|
US (1) | US2899592A (is") |
BE (1) | BE533455A (is") |
CH (1) | CH345392A (is") |
DE (1) | DE1043519B (is") |
FR (1) | FR1113555A (is") |
GB (1) | GB777142A (is") |
NL (1) | NL97571C (is") |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3127537A (en) * | 1960-02-25 | 1964-03-31 | Rca Corp | Cathode mount and alloy therefor |
US3558966A (en) * | 1967-03-01 | 1971-01-26 | Semicon Associates Inc | Directly heated dispenser cathode |
US3693007A (en) * | 1970-05-25 | 1972-09-19 | Egyesuelt Izzolampa | Oxide cathode for an electric discharge device |
US4417173A (en) * | 1980-12-09 | 1983-11-22 | E M I-Varian Limited | Thermionic electron emitters and methods of making them |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1954474A (en) * | 1927-05-20 | 1934-04-10 | Espe Werner | Glow cathode |
US2085605A (en) * | 1934-05-11 | 1937-06-29 | Gen Electric | Thermionic cathode for electric discharge devices |
US2121589A (en) * | 1934-06-28 | 1938-06-21 | Westinghouse Electric & Mfg Co | Emissive incandescent cathode |
US2147447A (en) * | 1936-09-21 | 1939-02-14 | Siemens Ag | Glow cathode |
US2180988A (en) * | 1937-06-16 | 1939-11-21 | Gen Electric | Electrode for electric discharge devices |
US2389060A (en) * | 1943-08-13 | 1945-11-13 | Callite Tungsten Corp | Refractory body of high electronic emission |
US2473550A (en) * | 1947-08-19 | 1949-06-21 | Raytheon Mfg Co | Directly heated cathode |
US2543728A (en) * | 1947-11-26 | 1951-02-27 | Hartford Nat Bank & Trust Co | Incandescible cathode |
US2700118A (en) * | 1951-11-29 | 1955-01-18 | Philips Corp | Incandescible cathode |
US2700000A (en) * | 1952-02-27 | 1955-01-18 | Philips Corp | Thermionic cathode and method of manufacturing same |
US2716716A (en) * | 1951-11-29 | 1955-08-30 | Philips Corp | Cathode containing a supply of an electron-emissive material |
US2741717A (en) * | 1951-06-14 | 1956-04-10 | Siemens Ag | Dispenser type cathode having gettercoated parts |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE707255C (de) * | 1936-09-21 | 1941-06-17 | Siemens Schuckertwerke Akt Ges | Gluehkathode hoher Leistung, insbesondere fuer gas- oder dampfgefuellte Entladungsgefaese |
BE498869A (is") * | 1949-10-25 | |||
DE895479C (de) * | 1951-11-20 | 1953-11-02 | Siemens Ag | Kathode fuer elektrische Entladungsgefaesse |
-
0
- US US2899592D patent/US2899592A/en not_active Expired - Lifetime
- NL NL97571D patent/NL97571C/xx active
- BE BE533455D patent/BE533455A/xx unknown
-
1954
- 1954-11-15 DE DEN9761A patent/DE1043519B/de active Pending
- 1954-11-16 GB GB33173/54A patent/GB777142A/en not_active Expired
- 1954-11-16 CH CH345392D patent/CH345392A/de unknown
- 1954-11-18 FR FR1113555D patent/FR1113555A/fr not_active Expired
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1954474A (en) * | 1927-05-20 | 1934-04-10 | Espe Werner | Glow cathode |
US2085605A (en) * | 1934-05-11 | 1937-06-29 | Gen Electric | Thermionic cathode for electric discharge devices |
US2121589A (en) * | 1934-06-28 | 1938-06-21 | Westinghouse Electric & Mfg Co | Emissive incandescent cathode |
US2147447A (en) * | 1936-09-21 | 1939-02-14 | Siemens Ag | Glow cathode |
US2180988A (en) * | 1937-06-16 | 1939-11-21 | Gen Electric | Electrode for electric discharge devices |
US2389060A (en) * | 1943-08-13 | 1945-11-13 | Callite Tungsten Corp | Refractory body of high electronic emission |
US2473550A (en) * | 1947-08-19 | 1949-06-21 | Raytheon Mfg Co | Directly heated cathode |
US2543728A (en) * | 1947-11-26 | 1951-02-27 | Hartford Nat Bank & Trust Co | Incandescible cathode |
US2741717A (en) * | 1951-06-14 | 1956-04-10 | Siemens Ag | Dispenser type cathode having gettercoated parts |
US2700118A (en) * | 1951-11-29 | 1955-01-18 | Philips Corp | Incandescible cathode |
US2716716A (en) * | 1951-11-29 | 1955-08-30 | Philips Corp | Cathode containing a supply of an electron-emissive material |
US2700000A (en) * | 1952-02-27 | 1955-01-18 | Philips Corp | Thermionic cathode and method of manufacturing same |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3127537A (en) * | 1960-02-25 | 1964-03-31 | Rca Corp | Cathode mount and alloy therefor |
US3558966A (en) * | 1967-03-01 | 1971-01-26 | Semicon Associates Inc | Directly heated dispenser cathode |
US3693007A (en) * | 1970-05-25 | 1972-09-19 | Egyesuelt Izzolampa | Oxide cathode for an electric discharge device |
US4417173A (en) * | 1980-12-09 | 1983-11-22 | E M I-Varian Limited | Thermionic electron emitters and methods of making them |
Also Published As
Publication number | Publication date |
---|---|
FR1113555A (fr) | 1956-03-30 |
BE533455A (is") | |
NL97571C (is") | |
DE1043519B (de) | 1958-11-13 |
GB777142A (en) | 1957-06-19 |
CH345392A (de) | 1960-03-31 |
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