EP0298558B1 - Method of manufacturing a scandat cathode - Google Patents
Method of manufacturing a scandat cathode Download PDFInfo
- Publication number
- EP0298558B1 EP0298558B1 EP88201392A EP88201392A EP0298558B1 EP 0298558 B1 EP0298558 B1 EP 0298558B1 EP 88201392 A EP88201392 A EP 88201392A EP 88201392 A EP88201392 A EP 88201392A EP 0298558 B1 EP0298558 B1 EP 0298558B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cathode
- scandium
- hydride
- approximately
- manufacturing
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000000034 method Methods 0.000 claims description 15
- 229910052706 scandium Inorganic materials 0.000 claims description 14
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims description 14
- -1 scandium hydride Chemical compound 0.000 claims description 12
- 229910000046 scandium hydride Inorganic materials 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 238000005245 sintering Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 4
- 230000008018 melting Effects 0.000 claims description 4
- 229910052788 barium Inorganic materials 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001553 barium compounds Chemical class 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 12
- 229910052721 tungsten Inorganic materials 0.000 description 7
- 239000010937 tungsten Substances 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 238000010849 ion bombardment Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- HYXGAEYDKFCVMU-UHFFFAOYSA-N scandium oxide Chemical compound O=[Sc]O[Sc]=O HYXGAEYDKFCVMU-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- FQNGWRSKYZLJDK-UHFFFAOYSA-N [Ca].[Ba] Chemical compound [Ca].[Ba] FQNGWRSKYZLJDK-UHFFFAOYSA-N 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/04—Manufacture of electrodes or electrode systems of thermionic cathodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/04—Manufacture of electrodes or electrode systems of thermionic cathodes
- H01J9/042—Manufacture, activation of the emissive part
- H01J9/047—Cathodes having impregnated bodies
-
- 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
- the invention relates to a method of manufacturing a dispenser cathode comprising a barium compound for dispensing barium to an emissive surface of a porous cathode body substantially comprising a metal melting at a high temperature.
- the invention also relates to an electron tube provided with a cathode manufactured by such a method.
- a characteristic feature of dispenser cathodes is that there is a functional separation between the electron emissive surface on the one hand and a store of the emitter material for realizing a sufficiently low work function on the emissive surface on the other hand.
- the emitter material is present in the pores of the porous metal cathode body.
- European Patent Specification No. 0,091,161 describes how such cathodes can be improved on sensitivity to and recovery after ion bombardment by compressing the cathode body (notably the top layer) from a mixture of tungsten powder and scandium oxide and by subsequently sintering it.
- the compressing operation is generally performed in two steps. Firstly, the tungsten portion of the cathode body is slightly pre-compressed. Subsequently, the top layer powder is evenly distributed over a surface of the tungsten portion whereafter the definitive compressing operation is performed.
- European Patent Specification 0.179.513 describes a method in which the porous body is obtained from a mixture of scandium hydride-tungsten powder and tungsten powder.
- the scandium hydride-tungsten powder is obtained by compressing tungsten powder into a porous plug, into the pores if which scandium is drawn. After cooling in hydrogen the plug becomes brittle due to the fact that scandium is partly converted into scandiumhydride.
- the plug is then pulverized and the fragments are heated in a hydrogen atmosphere. After cooling substantially all the scandium is converted into scandium hydride. The fragments are then ground to a powder consisting of tungsten grains having scandium hydride in their pores.
- a method according to the invention is characterized in that the cathode body is compressed from a quantity of metal powder which is mixed with scandium or scandium hydride whereafter the body is sintered and the cathode is provided with emitter material.
- the quantity of scandium hydride in the quantity of metal powder is preferably 0.3-0.7 % by weight.
- Such a method is more advantageous because compressing is only to be performed in one operation and the distribution of the top-layer powder is no longer necessary. Also the method of preparing scandium hydride/tungsten grains can be dispensed with. After the introduction of the impregnant the cathode bodies manufactured by means of such a method can undergo mechanical treatments such as turning or other types of shaping without any detrimental effects.
- this sintering operation is preferably performed at a temperature which is lower than the melting point of scandium (1539°C).
- the sintering temperature must be chosen to be as high as possible in order to obtain a sufficiently robust cathode body.
- a preferred embodiment of a method according to the invention is therefore characterized in that the sintering temperature is between 1430°C and 1500°C.
- Figure 1 is a longitudinal cross-section of a cathode according to the invention.
- the cathode body 1 is compressed from a mixture of tungsten powder and approximately 0.5% by weight of scandium or scandium-hydride. After compressing at a pressure of approximately 3.5 atmosphere and sintering in hydrogen for approximately one hour at 1450°, the cathode body of scandium and tungsten has a porosity of approximately 20%.
- the cathode body 1 now has, for example, a thickness of 0.5 mm and a diameter of approximately 1.8 mm.
- the cathode body 1 is impregnated in a hydrogen atmosphere with barium calcium aluminate (for example, 5BaO; 2Al2O3; 3CaO or 4BaO; 1Al2O3; 1CaO), compressed in a holder 2 and welded onto the cathode shank 3.
- barium calcium aluminate for example, 5BaO; 2Al2O3; 3CaO or 4BaO; 1Al2O3; 1CaO
- the cathode shank 3 accommodates a coiled cathode filament 4 comprising a helically wound metal core 5 and an aluminium oxide insulating layer 6.
- the emission of the emissive surface 7 of such a cathode was approximately 100 A/cm2 at 950°C obtained at a pulse load at 1000 V in a diode with a cathode-anode distance of 0.3 mm.
- Such an emission is comparable to that of a cathode with a top layer of tungsten and scandium oxide as described in European Patent Application No. 0,178,716 (PHN 11,169) which is more difficult to manufacture.
- the recovery after ion bombardment was comparable to that of the cathode described in that Application with a cathode body sintered at approximately 1900°C (approximately 65%). In a cathode according to the invention, sintered at 1500°C this recovery was poorer and was approximately 58%.
- the impregnant absorption was approximately 4.5%.
- this absorption decreased to approximately 2% which shortens the life time of the cathode.
- the quantity of absorbed impregnant is sufficient; the recovery after ion bombardment did not show any significant change in this range.
- a cylinder 20 with an emissive surface 21 in which a heating element is provided and which is shown in an elevational view in Figure 2 can also be turned from a tungsten body compressed in accordance with the method as described hereinbefore.
- the cathodes according to the invention may be used in electron tubes such as, for example magnetrons, transmitter tubes, etc., but also in cathode-ray tubes for e.g. television applications and electron microscopy.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Solid Thermionic Cathode (AREA)
- Powder Metallurgy (AREA)
Description
- The invention relates to a method of manufacturing a dispenser cathode comprising a barium compound for dispensing barium to an emissive surface of a porous cathode body substantially comprising a metal melting at a high temperature.
- The invention also relates to an electron tube provided with a cathode manufactured by such a method.
- A characteristic feature of dispenser cathodes is that there is a functional separation between the electron emissive surface on the one hand and a store of the emitter material for realizing a sufficiently low work function on the emissive surface on the other hand. The emitter material is present in the pores of the porous metal cathode body.
- A method of the type mentioned in the opening paragraph is described in United States Patent No. 4,077,393. This patent describes how a cathode body with a porosity of approximately 20% compressed from tungsten powder and subsequently sintered is impregnated with a mixture which comprises calcium oxide, aluminium oxide and scandium oxide in addition to barium oxide.
- European Patent Specification No. 0,091,161 describes how such cathodes can be improved on sensitivity to and recovery after ion bombardment by compressing the cathode body (notably the top layer) from a mixture of tungsten powder and scandium oxide and by subsequently sintering it. To obtain a cathode body with a thin top layer (approximately 0.1 mm) which is as homogeneous as possible the compressing operation is generally performed in two steps. Firstly, the tungsten portion of the cathode body is slightly pre-compressed. Subsequently, the top layer powder is evenly distributed over a surface of the tungsten portion whereafter the definitive compressing operation is performed.
- European Patent Specification 0.179.513 describes a method in which the porous body is obtained from a mixture of scandium hydride-tungsten powder and tungsten powder. The scandium hydride-tungsten powder is obtained by compressing tungsten powder into a porous plug, into the pores if which scandium is drawn. After cooling in hydrogen the plug becomes brittle due to the fact that scandium is partly converted into scandiumhydride. The plug is then pulverized and the fragments are heated in a hydrogen atmosphere. After cooling substantially all the scandium is converted into scandium hydride. The fragments are then ground to a powder consisting of tungsten grains having scandium hydride in their pores.
- It is an object of the invention to provide a different method of manufacturing such a dispenser cathode which method is simpler and leads to similar results as regards current density and lifetime.
- To this end a method according to the invention is characterized in that the cathode body is compressed from a quantity of metal powder which is mixed with scandium or scandium hydride whereafter the body is sintered and the cathode is provided with emitter material. The quantity of scandium hydride in the quantity of metal powder is preferably 0.3-0.7 % by weight.
- From a manufacturing technical point of view such a method is more advantageous because compressing is only to be performed in one operation and the distribution of the top-layer powder is no longer necessary. Also the method of preparing scandium hydride/tungsten grains can be dispensed with. After the introduction of the impregnant the cathode bodies manufactured by means of such a method can undergo mechanical treatments such as turning or other types of shaping without any detrimental effects.
- In order to prevent as much as possible that scandium is lost during sintering which is preferably performed in a hydrogen atmosphere, this sintering operation is preferably performed at a temperature which is lower than the melting point of scandium (1539°C). However, on the other hand the sintering temperature must be chosen to be as high as possible in order to obtain a sufficiently robust cathode body.
- A preferred embodiment of a method according to the invention is therefore characterized in that the sintering temperature is between 1430°C and 1500°C.
- The invention will now be described in greater detail by way of example with reference to the accompanying drawing, in which:
- Figure 1 is a longitudinal cross-section of a cathode according to the invention and
- Figure 2 is an elevational view of a cylindrical cathode according to the invention.
- Figure 1 is a longitudinal cross-section of a cathode according to the invention. The cathode body 1 is compressed from a mixture of tungsten powder and approximately 0.5% by weight of scandium or scandium-hydride. After compressing at a pressure of approximately 3.5 atmosphere and sintering in hydrogen for approximately one hour at 1450°, the cathode body of scandium and tungsten has a porosity of approximately 20%. The cathode body 1 now has, for example, a thickness of 0.5 mm and a diameter of approximately 1.8 mm.
- Subsequently, the cathode body 1 is impregnated in a hydrogen atmosphere with barium calcium aluminate (for example, 5BaO; 2Al₂O₃; 3CaO or 4BaO; 1Al₂O₃; 1CaO), compressed in a
holder 2 and welded onto thecathode shank 3. Thecathode shank 3 accommodates a coiled cathode filament 4 comprising a helically wound metal core 5 and an aluminiumoxide insulating layer 6. The emission of the emissive surface 7 of such a cathode was approximately 100 A/cm² at 950°C obtained at a pulse load at 1000 V in a diode with a cathode-anode distance of 0.3 mm. Such an emission is comparable to that of a cathode with a top layer of tungsten and scandium oxide as described in European Patent Application No. 0,178,716 (PHN 11,169) which is more difficult to manufacture. The recovery after ion bombardment was comparable to that of the cathode described in that Application with a cathode body sintered at approximately 1900°C (approximately 65%). In a cathode according to the invention, sintered at 1500°C this recovery was poorer and was approximately 58%. For the significance of the recovery percentages and the way in which they have been determined reference is made to the European Patent Application No. 0,178,716 or to the magazine Article "Properties and manufacture of top layer scandate cathodes" in Applied Surface Science 26 (1986), pages 173-195. - In the above-mentioned example the impregnant absorption was approximately 4.5%. Upon raising the quantity of scandium (hydride) in the mixture to be compressed to 1 percent by weight this absorption decreased to approximately 2% which shortens the life time of the cathode. For a quantity of 0.3-0.7% by weight of scandium (hydride) the quantity of absorbed impregnant is sufficient; the recovery after ion bombardment did not show any significant change in this range.
- A
cylinder 20 with anemissive surface 21 in which a heating element is provided and which is shown in an elevational view in Figure 2 can also be turned from a tungsten body compressed in accordance with the method as described hereinbefore. - The cathodes according to the invention may be used in electron tubes such as, for example magnetrons, transmitter tubes, etc., but also in cathode-ray tubes for e.g. television applications and electron microscopy.
Claims (6)
- A method of manufacturing a dispenser cathode comprising a barium compound for dispensing barium to an emissive surface of a porous cathode body substantially comprising a metal melting at a high temperature, characterized in that the cathode body is compressed from a quantity of metal powder which is mixed with scandium or scandium hydride whereafter the body is sintered and the cathode is provided with emitter material.
- A method as claimed in Claim 1, characterized in that the quantity of scandium or scandium hydride in the mixture of metal powder and scandium or scandium hydride is approximately between 0.3 and 0.7 % by weight.
- A method as claimed in Claim 1 or 2, characterized in that the sintering temperature is lower than the melting point of scandium.
- A method as claimed in Claim 3, characterized in that the sintering temperature is between 1430° C and 1500° C.
- A method as claimed in any one of the preceding Claims, characterized in that the cathode body is definitively shaped after it has been provided with emitter material.
- An electron tube provided with a cathode manufactured by means of a method as claimed in Claims 1 to 5
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL8701583A NL8701583A (en) | 1987-07-06 | 1987-07-06 | SCANDAT CATHOD. |
| NL8701583 | 1987-07-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0298558A1 EP0298558A1 (en) | 1989-01-11 |
| EP0298558B1 true EP0298558B1 (en) | 1994-05-25 |
Family
ID=19850259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP88201392A Expired - Lifetime EP0298558B1 (en) | 1987-07-06 | 1988-07-04 | Method of manufacturing a scandat cathode |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0298558B1 (en) |
| JP (1) | JP2685232B2 (en) |
| KR (1) | KR890002949A (en) |
| DE (1) | DE3889696T2 (en) |
| NL (1) | NL8701583A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8902793A (en) * | 1989-11-13 | 1991-06-03 | Philips Nv | SCANDAT CATHOD. |
| DE69411248T2 (en) * | 1993-10-28 | 1999-02-04 | Philips Electronics N.V., Eindhoven | Supply cathode and manufacturing process |
| BE1007676A3 (en) * | 1993-10-28 | 1995-09-12 | Philips Electronics Nv | Method for manufacturing a dispenser cathode |
| BE1007677A3 (en) * | 1993-10-28 | 1995-09-12 | Philips Electronics Nv | Method for manufacturing a dispenser cathode |
| US5407633A (en) * | 1994-03-15 | 1995-04-18 | U.S. Philips Corporation | Method of manufacturing a dispenser cathode |
| US6281626B1 (en) * | 1998-03-24 | 2001-08-28 | Casio Computer Co., Ltd. | Cold emission electrode method of manufacturing the same and display device using the same |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL165880C (en) * | 1975-02-21 | 1981-05-15 | Philips Nv | DELIVERY CATHOD. |
| JPS58154131A (en) * | 1982-03-10 | 1983-09-13 | Hitachi Ltd | Impregnation type cathode |
| NL8201371A (en) * | 1982-04-01 | 1983-11-01 | Philips Nv | METHODS FOR MANUFACTURING A SUPPLY CATHOD AND SUPPLY CATHOD MANUFACTURED BY THESE METHODS |
| NL8403031A (en) * | 1984-10-05 | 1986-05-01 | Philips Nv | METHOD FOR MANUFACTURING A SCANDAL FOLLOW-UP CATHOD AND SCANDAL FOLLOW-UP CATHOD Manufactured By This Method |
| NL8403032A (en) * | 1984-10-05 | 1986-05-01 | Philips Nv | METHOD FOR MANUFACTURING A SCANDAL FOLLOW-UP CATHOD, FOLLOW-UP CATHOD MADE WITH THIS METHOD |
| JPS63254636A (en) * | 1987-04-10 | 1988-10-21 | Hitachi Ltd | Impregnated cathode |
-
1987
- 1987-07-06 NL NL8701583A patent/NL8701583A/en not_active Application Discontinuation
-
1988
- 1988-07-04 DE DE3889696T patent/DE3889696T2/en not_active Expired - Fee Related
- 1988-07-04 JP JP63165191A patent/JP2685232B2/en not_active Expired - Lifetime
- 1988-07-04 EP EP88201392A patent/EP0298558B1/en not_active Expired - Lifetime
- 1988-07-04 KR KR1019880008245A patent/KR890002949A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| JP2685232B2 (en) | 1997-12-03 |
| KR890002949A (en) | 1989-04-12 |
| DE3889696D1 (en) | 1994-06-30 |
| NL8701583A (en) | 1989-02-01 |
| JPH01163941A (en) | 1989-06-28 |
| EP0298558A1 (en) | 1989-01-11 |
| DE3889696T2 (en) | 1994-12-08 |
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