US2348045A - Electron discharge device and method of manufacture - Google Patents
Electron discharge device and method of manufacture Download PDFInfo
- Publication number
- US2348045A US2348045A US425378A US42537842A US2348045A US 2348045 A US2348045 A US 2348045A US 425378 A US425378 A US 425378A US 42537842 A US42537842 A US 42537842A US 2348045 A US2348045 A US 2348045A
- Authority
- US
- United States
- Prior art keywords
- finely divided
- electron
- electron emission
- silica
- binder
- 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
- 238000000034 method Methods 0.000 title description 11
- 238000004519 manufacturing process Methods 0.000 title description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 91
- 239000000463 material Substances 0.000 description 70
- 230000002401 inhibitory effect Effects 0.000 description 50
- 239000000377 silicon dioxide Substances 0.000 description 36
- 239000011230 binding agent Substances 0.000 description 31
- 238000000576 coating method Methods 0.000 description 23
- 229910052751 metal Inorganic materials 0.000 description 21
- 239000002184 metal Substances 0.000 description 21
- 239000011248 coating agent Substances 0.000 description 20
- 239000008119 colloidal silica Substances 0.000 description 19
- 239000007788 liquid Substances 0.000 description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 239000002245 particle Substances 0.000 description 14
- 229910052799 carbon Inorganic materials 0.000 description 10
- 150000002739 metals Chemical class 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 230000008901 benefit Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 6
- 229910052721 tungsten Inorganic materials 0.000 description 6
- 239000010937 tungsten Substances 0.000 description 6
- -1 ClzOs) Chemical compound 0.000 description 5
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 238000010943 off-gassing Methods 0.000 description 5
- 229910052726 zirconium Inorganic materials 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 229910001936 tantalum oxide Inorganic materials 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- 229910052715 tantalum Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 229960004029 silicic acid Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- WTKKCYNZRWIVKL-UHFFFAOYSA-N tantalum Chemical compound [Ta+5] WTKKCYNZRWIVKL-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- QSGNKXDSTRDWKA-UHFFFAOYSA-N zirconium dihydride Chemical compound [ZrH2] QSGNKXDSTRDWKA-UHFFFAOYSA-N 0.000 description 1
- 229910000568 zirconium hydride Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J19/00—Details of vacuum tubes of the types covered by group H01J21/00
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2893/00—Discharge tubes and lamps
- H01J2893/0001—Electrodes and electrode systems suitable for discharge tubes or lamps
- H01J2893/0012—Constructional arrangements
- H01J2893/0019—Chemical composition and manufacture
- H01J2893/0022—Manufacture
- H01J2893/0023—Manufacture carbonising and other surface treatments
Definitions
- Electron discharge devices of which amplifying and rectifying tubes are examples,
- the electron emissive means usually comprises a cathode which is adapted to be heated and which is formed of or coated with a thermionically active material capable of emitting electrons when heated, Usually one or more grids or control electrodes are also disposed in the envelope of the device.
- the present invention provides in the element enclosing envelope of an electron discharge device an anode, grid, or other element having a surface formed of one or more finely divided electron emission inhibiting materials firmly held in place by a binder of silica derived from a colloidal silica solution.
- Such electron emission inhibiting material may be of a type which reacts with electron emissive material deposited from the cathode on the surface embodying the invention to form non-emissive material; or which otherwise neutralizes such deposited emissive material; or which, because of its dark or black color has a high heat radiation capacity and thus lowers the temperature of the surface and hence its electron emissivity; or which inhibits electronic emission because of its high work function or for other reasons; or which operates in a plurality of these ways.
- the invention also provides methods of forming such surfaces. Outstanding advantages are provided by the present invention when the finely divided electron emission inhibiting material and the silica binder are in the form of a surface coating on the desired element, particularly on the anode or grid.
- an anode or grid or other element in the envelope of the electron discharge devic may be formed substantially entirely of a finely divided electron emission inhibiting material and a silica binder.
- the invention affords particular advantages by providing in an electron discharge device an anode or grid, or both, formed of a metal body having at least part of its surface coated with a layer of finely divided electron emission inhibiting material held in place by a binder of silica.
- the metal body provides strength and good heat conductivity, and if formed of the refractory metals usually employed, such as molybdenum or tungsten, good heat resistance also.
- the silica binder has little or no deleterious effect on the electron emission inhibiting properties of the finely divided material; indeed, in some cases it appears to aid in the electron emission inhibiting properties. Moreover, when the silica binder is employed in the proportions deemed most advantageous according to the invention in a coating on a conductive electrode of a device the conductivity of the electrode is not harmfully reduced.
- the silica binder has great resistance to decomposition and firmly holds in place the finely divided particles of the electron emission inhibiting material even when subjected to the high temperatures usually reached in the outgassing of the electron discharge device and often reached in operation of the electron discharge device.
- the silica binder moreover, does not emit electrons even at high temperatures. Moreover, it is nongas occluding and hence does not discharge gases to the electron discharge device during operation of the device.
- finely divided electron emission inhibiting materials which may be employed with a binder of silica according to the invention are the oxides of certain metals, such as the oxides of chromium (particularly ClzOs), tantalum (particularly TaaOs), zirconium (particularly ZrOz), tungsten (particularly W03), platinum, titanium, and nickel.
- oxides of certain metals such as the oxides of chromium (particularly ClzOs), tantalum (particularly TaaOs), zirconium (particularly ZrOz), tungsten (particularly W03), platinum, titanium, and nickel.
- emissive material such as barium or barium oxide vaporized or thrownoff from the cathode and deposited on the surface of the invention, to form a stable material which has little or no electron emission capacity even at the temperatures reached in outgassing or operation of the electron discharge device.
- Most, if not all, of such electron emission inhibiting oxides also have high work'functions and hence inhibit secondary emission for this reason also.
- Oxides of the above type are black or in anyevent darker in color than bare metals. Therefore such oxides also may act to inhibit electron emission by reducing the temperature of the an-* ode, grid or other part of which they form the graphitic form, and a binder of silica, may also be employed on the. surfaces of grids, anodes or other parts in the envelopes of electron discharge devices from which electronic emission is undesired, In such case, carbon appears to reduce electronic emission primarily by reducing the temperature of the surface due to the high black body heat radiation constant, although carbon also appears to react, in at least some cases, with electron emitting material vaporized or thrown off from the cathode to form non-emitting substances and in this way also inhibit electronic emission.
- the present invention also provides on anodes, grids or other parts in the envelopes of electron discharge devices surfaces formed of a silica binder firmly holding in place finely divided particles of metals ha ving the property of inhibiting electronic emission.
- metals may be the nobel metals, such as gold, platinum, iridium, palladiam, osmium,- ruthenium and rhodium, which appear to operate, by reaction or otherwise, to neutralize electronic emission effects of electron emitting material deposited on such surface on the cathode.
- Such metals also have high work functions which inhibit secondary emission.
- a metal such as zirconium, which in its finely divided state is black or dark in .color and hence has a high black body heat radiation constant, may also be held in place by a binder of silica according. to the invention to form a surface of an anode, grid or other part from which electron emission is undesired.
- Metals such as zirconium appear also to inhibit electronic emission by reaction or similar means with electron emitting materials deposited on the surface from the cathode.
- Zirconium and similar metals also have. gas. absorption properties which are advantageous in electron discharge devices for removing traces of undesired gases from the interior of such devices. Electron discharge devices having surfaces formed of finely divided zirconium or similar gas absorbing metals and a silica binder are described and claimed in copending application Serial No. 425,377, filed January 1, 1942, by
- electron emission inhibiting surfaces may be formed of more than one finely divided electron emission inhibiting material and a silica binder.
- coatings employing more than one electron emission inhibiting oxide may be-employed;
- carbon may be mixed with one of the metal oxides useful for inhibiting electronic emission and both held in place by a silica binder.
- Combinations of carbon and zirconium oxide and'carbon and molybdenum oxide in a silica binder may be employed to advantage.
- mixtures of carbon and finely divided metal, or of a finely divided metal oxide and Ranely divided metal, with or without finely-divided carbon, in a silica binder may be employed.
- a coating material is made of a suspension of the finely divided electron emission inhibiting material in a liquid also containing colloidal hydratedsilica.
- the coating material may be applied to the electrode by spraying, painting, dipping' or by other suitable means,
- the liquid in which the colloidal silica and finely divided electron inhibiting material is suspended is a volatile. liquid, such as water, alcohol or the like. After being, coated the electrode or other part may, if desired, b'bair dried or heated to evaporate the liquid;
- a liquid binder comprising a colloidal silica solution, in which the finely divided particles of the electron emission inhibiting material are advantageously suspended to form the material of 1 formed by merely a'gitatingthe organic silicatev with a suitable amount .of water. It is advantageous to include in the water a small amount of an acid, such as hydrochloric acid, since this facilitates the hydrolysis.
- the hydrolysis is conveniently carried out in the presence of a solvent,
- the finely divided. electron emission inhibiting material may then be mixed withthe colloidal silica solution and the desired surface formed. If desired, water or a suitable organic solvent may be added before, during or after the addition of the finely divided electron emission inhibiting material further to reduce the concentration of the colloidal silica or, if desired, to reduce the consistency of the suspension of finely divided particles in the liquid to a point permitting ready application as by spraying.
- the following are examples of advantageous methods of forming on electrodes coatings of a finely divided electron emission inhibition material and a silica binder.
- Example 1 Ethyl silicate, a commercially obtainable material, was mixedwith 0.06N dilute hydrochloric acid in the proportion of milliliters of ethyl silicate to 2 milliliters of the dilute acid, the mixture being agitated until the reaction was complete. The resulting colloidal solution of silica was then diluted to 50 milliliters with ethyl alcohol, although any one of many other volatile solvents, such as amyl acetate, could have been employed. Finely divided tantalum oxide powder in the amount of grams was moistened with water or alcohol and added to 20 milliliters of the binding liquid containing colloidal silica described above. This suspension was agitated until it was thoroughly mixed.
- a coating of the material was applied to the electrode to be coated by a standard spraying procedure. Since the coated electrode was not immediately incorporated into the tube assembly, it was air dried, although it could have been heated, to evaporate the water in alcohol to cause the colloidal silica to deposit and form a bin lng m teriai firmly holding the tantalum oxide in place. The coated electrode was then incorporated into tube assembly in the envelope of the tube and the'tube heated and outgassed. Any of the other electron emission inhibiting oxides indicated above could be substituted for the tantalum oxide in this example.
- Example 2 liters of 0.06 normal hydrochloric acid-solution and the mixture agitated until hydrolysis was complete. A 2% per cent solution of colloidal silica was then made by diluting to 50 milliliters.
- the final coating material was prepared by mixing ten grams of Aquadag," a commercial product consisting of a paste of finely divided graphitic carbon with 10 milliliters of the above colloidal silica solution and 50 milliliters of water. The grid of a tube was then sprayed with the resulting material, air dried and incorporated in a vacuum tube assembly where it was subjected to the usual heating and outgassing operation.
- Aquadag a commercial product consisting of a paste of finely divided graphitic carbon with 10 milliliters of the above colloidal silica solution and 50 milliliters of water.
- the amount of silica which is employed as a binder depends upon the severity of the treatment to which the electrodes are subjected in handling and construction of the tube and under the outgassing and operating conditions of the tube. It is advantageous, in general, to employ as small an amount of silica as possible, since in this manner any possibilities of inhibition of the action of the electron emission inhibiting material are reduced.
- the proportion of the silica in the coating material should be less than the proportion of the finely divided electron emission inhibiting material, and, in general, it is advantageous to employ silica in an amount which is from about 2 per cent to about 10 per cent by weight of the finely divided electron emission inhibiting material.
- the amount of the volatile suspending liquid or liquids employed may vary widely, but it is desirable that it be in such proportion as to permit ready application to the surface.
- the finely divided electron emission inhibiting material may be of any one of various particle sizes, although in general the more finely divided the material is, the better is its activity.
- the particle size should not be so large that the material does not remain suspended in the binding liquid for a sufilcient period to permit application of the material to the parts which it is desired to coat in the coating processes employed.
- the drawing illustrates one form of electron discharge device in connection with which the present invention may be advantageously employed.
- Said device is a three-electrode electron discharge tube comprising a cathode I, control grid 2, and an anode 3, which are contained in a sealed glass envelope 4 which is shown as broken away to reveal the electrodes in the tube.
- the electrodes are supported in said envelope by any suitable means, such as that shown comprising insulators 5 of which only the upper one is shown and brackets 6 which are supported from the base I. Leads 8 passing through said base provide electrical connection to the electrodes of the tube in the known manner.
- the cathode is shown as a directly heated filament formed of thermionic emitting material such as thoriated tungsten.
- the anode and grid may be formed of a suitable metal, such as nickel, tungsten, molybdenum, iron or the like, and are preferably formed of a refractory metal such as tungsten or molybdenum.
- both the anode 3 and the grid 2 have a surface coating which comprises a finely divided electron emission inhibition material, suchas carbon, tantalum oxide, tungsten oxide, molybdenum oxide, or the like, held in place on the electrode by means of a binder which is substantially pure silica. Either one of said electrodes alone could be so coated.
- the illustrated anode 3 is coated on both its interior surface which faces the cathode, and its exterior surface.
- the coating inhibits electron emission primarily by increasing the heat radiation of the anode, it may be advantageous to apply the coating only to the exterior surface of the anode; if the coating inhibits electron emission by reacting with or otherwise neutralizing electron emissive material deposited on the anode from the cathode, it may be advantageous to apply the coating only to the interior surface ofthe anode.
- the electrode to be provided with such a coating material is, after being constructed or formed, coated with a suspension of the finely divided electron emission inhibiting material and colloidal silica which is applied by spraying, painting, *dipping or other suitable means.
- electron discharge devices of both the gas-filled or high vacuum types may be provided according to the invention with anodes, grids or other parts in their envelopes having surfaces of finely divided electron emission inhibiting materials and a silica binder.
- the invention is applicable to amplifying tubes and rectifying tubes including those of the mercury vapor type, since surfaces of the kind contemplated by the present invention, particularly when employed on anodes or on grids, provide marked advantages in such tubes.
- the present invention contemplates electron discharge devices in which the grid alone, or the anode alone, or both such electrodes are provided with surfaces embodying the invention. Moreover, only a portion of the surface area of a grid or anode may be provided with a surface according to the invention.
- colloidal silica solution employed as a binder in the formation of the surface of the invention may be pro pared in other ways than those indicated.
- Mixtures of finely divided electron emission inhibitmg materials, as well as other finely divided electron emission inhibiting materials than those indicated above, may be employed with a silica binder, in surfaces of anodes, grids or other parts in the envelopes/of electron discharge devices embodying the invention.
- liquid employed to form the surfaces of the invention may be prepared in other ways than those indicated.
- silica and the electron inhibiting material may be simultaneously suspended in the liquid. It is also possible to grind to the desired particle size the electron emission inhibiting material while it is in a colloidal silica solution.
- an organic silicate may be hydrolyzed in the presence of the finely divided material; thus, ethyl silicate may be hydrolyzed in the presence of "Aquadag.”
- the present invention includes a process in which a surface is formed of a silica binder firmly holding in place finely divided particles of a material which after a subsequent treatment is transformed into an electron emission inhibiting material.
- a surface is formed of a silica binder firmly holding in place finely divided particles of a material which after a subsequent treatment is transformed into an electron emission inhibiting material.
- an anode or a grid may be provided with a surface coating of tantalum or zirconium hydride held in place by. a binder of finely divided silica, and the hydride decomposed to the metal by subsequent heating in an inert atmosphere, as during the outgassing of the tube.
- Other modifications will be apparent to those skilled in the art.
- a non-emissive electrode adapted to be disposed within the sealed envelope of an electron discharge device comprising a metal body portion having a surface coated with an electron emission inhibiting layer which is electrically conductive through the layer and which comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said finely divided electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
- An electron discharge device comprising a sealed envelope, electron emissive means in said envelope, and a metal element in and separated from said envelope and adapted to be heated having a surface coated with a layer which is electrically conductive through the layer and which comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
- An electron discharge device comprising a sealedenvelope, electron emissive means in said envelope, and a non-emissive electrode in and separated from said envelope comprising a metal body portion having a surface coated with a layer which is electrically conductive through the layer and which comprises a mixture of finely divided carbon and a finely divided metal oxide having electron emission inhibiting properties and a binder firmly holding the particles of said carbon and said metal oxide which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
- An electron discharge device comprising a sealed envelope, electron emissive means in said envelope, and a non-emissive electrode in and separated from said envelop comprising a metal body portion having a surface coated with a layer which is electrically conductive through the layer and which'comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
- the method of forming a coating on a surface of an element of an electron discharge device comprising hydrolyzing an organic silicate to form a solution of colloidal silica, adding a finely divided electron emission inhibiting material to said solution to form a suspension in a volatile liquid of said material and colloidal silica in an amount between about 2 per cent to about 10 per cent by weight of said electron emission inhibiting material, applying said suspension to said surface, and evaporating said liquid to form a coating in which the particles of said finely divided electron emission inhibiting material are firmly bound by silica.
Landscapes
- Cold Cathode And The Manufacture (AREA)
Description
Patented May 2, 1944 ELECTRON DISCHARGE DEVICE AND METHOD OF MANUFACTURE Leland A. Wooten, Maplewood, N. J., assignor to Bell Telephone Laboratories, Incorporated, New York, N. Y., a corporation 01' New York Application January 1, 1942, Serial No. 425,378
9 Claims. 250-177) Although the surfaces of the present invention may be provided on various portions of electron discharge devices within their element-enclosing envelopes, for the purposes of illustration the advantages of such a surface on the anode or control grid of such a device will be discussed hereinafter. Electron discharge devices, of which amplifying and rectifying tubes are examples,
' usually contain in an evacuated or gas-filled envelope electron emissive means and an anode to which the electrons migrate. The electron emissive means usually comprises a cathode which is adapted to be heated and which is formed of or coated with a thermionically active material capable of emitting electrons when heated, Usually one or more grids or control electrodes are also disposed in the envelope of the device.
In most electron discharge devices of this type electron emission from the grid or anode is undesired and should be avoided to as great an extent as possible. When an electrode from which electronic emission is undesired emits electrons in suflicient quantities the operation of the electron discharge device is deleteriously ailected.
The present invention provides in the element enclosing envelope of an electron discharge device an anode, grid, or other element having a surface formed of one or more finely divided electron emission inhibiting materials firmly held in place by a binder of silica derived from a colloidal silica solution. Such electron emission inhibiting material may be of a type which reacts with electron emissive material deposited from the cathode on the surface embodying the invention to form non-emissive material; or which otherwise neutralizes such deposited emissive material; or which, because of its dark or black color has a high heat radiation capacity and thus lowers the temperature of the surface and hence its electron emissivity; or which inhibits electronic emission because of its high work function or for other reasons; or which operates in a plurality of these ways. The invention also provides methods of forming such surfaces. Outstanding advantages are provided by the present invention when the finely divided electron emission inhibiting material and the silica binder are in the form of a surface coating on the desired element, particularly on the anode or grid. The present invention, however, also contemplates that an anode or grid or other element in the envelope of the electron discharge devic may be formed substantially entirely of a finely divided electron emission inhibiting material and a silica binder. The invention affords particular advantages by providing in an electron discharge device an anode or grid, or both, formed of a metal body having at least part of its surface coated with a layer of finely divided electron emission inhibiting material held in place by a binder of silica. In such case the metal body provides strength and good heat conductivity, and if formed of the refractory metals usually employed, such as molybdenum or tungsten, good heat resistance also.
The silica binder, surprisingly, has little or no deleterious effect on the electron emission inhibiting properties of the finely divided material; indeed, in some cases it appears to aid in the electron emission inhibiting properties. Moreover, when the silica binder is employed in the proportions deemed most advantageous according to the invention in a coating on a conductive electrode of a device the conductivity of the electrode is not harmfully reduced. The silica binder has great resistance to decomposition and firmly holds in place the finely divided particles of the electron emission inhibiting material even when subjected to the high temperatures usually reached in the outgassing of the electron discharge device and often reached in operation of the electron discharge device. The silica binder, moreover, does not emit electrons even at high temperatures. Moreover, it is nongas occluding and hence does not discharge gases to the electron discharge device during operation of the device.
These and other advantages of the invention will be apparent from the following discussion.
As examples of finely divided electron emission inhibiting materials which may be employed with a binder of silica according to the invention are the oxides of certain metals, such as the oxides of chromium (particularly ClzOs), tantalum (particularly TaaOs), zirconium (particularly ZrOz), tungsten (particularly W03), platinum, titanium, and nickel. Most, if not all, or such oxides inhibit electron emission by reacting with the electron, emissive material such as barium or barium oxide vaporized or thrownoff from the cathode and deposited on the surface of the invention, to form a stable material which has little or no electron emission capacity even at the temperatures reached in outgassing or operation of the electron discharge device. Most, if not all, of such electron emission inhibiting oxides also have high work'functions and hence inhibit secondary emission for this reason also.
Oxides of the above type are black or in anyevent darker in color than bare metals. Therefore such oxides also may act to inhibit electron emission by reducing the temperature of the an-* ode, grid or other part of which they form the graphitic form, and a binder of silica, may also be employed on the. surfaces of grids, anodes or other parts in the envelopes of electron discharge devices from which electronic emission is undesired, In such case, carbon appears to reduce electronic emission primarily by reducing the temperature of the surface due to the high black body heat radiation constant, although carbon also appears to react, in at least some cases, with electron emitting material vaporized or thrown off from the cathode to form non-emitting substances and in this way also inhibit electronic emission.
The present invention also provides on anodes, grids or other parts in the envelopes of electron discharge devices surfaces formed of a silica binder firmly holding in place finely divided particles of metals ha ving the property of inhibiting electronic emission. These metals may be the nobel metals, such as gold, platinum, iridium, palladiam, osmium,- ruthenium and rhodium, which appear to operate, by reaction or otherwise, to neutralize electronic emission effects of electron emitting material deposited on such surface on the cathode. Such metals also have high work functions which inhibit secondary emission. A metal, such as zirconium, which in its finely divided state is black or dark in .color and hence has a high black body heat radiation constant, may also be held in place by a binder of silica according. to the invention to form a surface of an anode, grid or other part from which electron emission is undesired. Metals such as zirconium appear also to inhibit electronic emission by reaction or similar means with electron emitting materials deposited on the surface from the cathode. Zirconium and similar metals also have. gas. absorption properties which are advantageous in electron discharge devices for removing traces of undesired gases from the interior of such devices. Electron discharge devices having surfaces formed of finely divided zirconium or similar gas absorbing metals and a silica binder are described and claimed in copending application Serial No. 425,377, filed January 1, 1942, by
both of which processes result in some alloying of the metal with the base metal of the coated electrode, with a consequent loss of electron emission inhibiting or other desired properties.
According to the present invention electron emission inhibiting surfaces may be formed of more than one finely divided electron emission inhibiting material anda silica binder. Thus, coatings employing more than one electron emission inhibiting oxide may be-employed; If it is desired to increase the conductivity of the surface coating, carbon may be mixed with one of the metal oxides useful for inhibiting electronic emission and both held in place bya silica binder. Combinations of carbon and zirconium oxide and'carbon and molybdenum oxide in a silica binder may be employed to advantage. Similarly, mixtures of carbon and finely divided metal, or of a finely divided metal oxide and afinely divided metal, with or without finely-divided carbon, in a silica binder may be employed.
when a surface coating of the material of the invention is applied to an anode, grid or other part of an electron disch'argedevice, a coating material is made of a suspension of the finely divided electron emission inhibiting material in a liquid also containing colloidal hydratedsilica. The coating material may be applied to the electrode by spraying, painting, dipping' or by other suitable means, The liquid in which the colloidal silica and finely divided electron inhibiting material is suspended is a volatile. liquid, such as water, alcohol or the like. After being, coated the electrode or other part may, if desired, b'bair dried or heated to evaporate the liquid;
, A liquid binder comprising a colloidal silica solution, in which the finely divided particles of the electron emission inhibiting material are advantageously suspended to form the material of 1 formed by merely a'gitatingthe organic silicatev with a suitable amount .of water. It is advantageous to include in the water a small amount of an acid, such as hydrochloric acid, since this facilitates the hydrolysis. The hydrolysis is conveniently carried out in the presence of a solvent,
such as ethyl alcohol, in which the water necessary for the reaction and the ethyl silicate are mutually soluble. The finely divided. electron emission inhibiting material may then be mixed withthe colloidal silica solution and the desired surface formed. If desired, water or a suitable organic solvent may be added before, during or after the addition of the finely divided electron emission inhibiting material further to reduce the concentration of the colloidal silica or, if desired, to reduce the consistency of the suspension of finely divided particles in the liquid to a point permitting ready application as by spraying.
The following are examples of advantageous methods of forming on electrodes coatings of a finely divided electron emission inhibition material and a silica binder.
Example 1 Ethyl silicate, a commercially obtainable material, was mixedwith 0.06N dilute hydrochloric acid in the proportion of milliliters of ethyl silicate to 2 milliliters of the dilute acid, the mixture being agitated until the reaction was complete. The resulting colloidal solution of silica was then diluted to 50 milliliters with ethyl alcohol, although any one of many other volatile solvents, such as amyl acetate, could have been employed. Finely divided tantalum oxide powder in the amount of grams was moistened with water or alcohol and added to 20 milliliters of the binding liquid containing colloidal silica described above. This suspension was agitated until it was thoroughly mixed. A coating of the material was applied to the electrode to be coated by a standard spraying procedure. Since the coated electrode was not immediately incorporated into the tube assembly, it was air dried, although it could have been heated, to evaporate the water in alcohol to cause the colloidal silica to deposit and form a bin lng m teriai firmly holding the tantalum oxide in place. The coated electrode was then incorporated into tube assembly in the envelope of the tube and the'tube heated and outgassed. Any of the other electron emission inhibiting oxides indicated above could be substituted for the tantalum oxide in this example.
Example 2 liters of 0.06 normal hydrochloric acid-solution and the mixture agitated until hydrolysis was complete. A 2% per cent solution of colloidal silica was then made by diluting to 50 milliliters.
with water. The final coating material was prepared by mixing ten grams of Aquadag," a commercial product consisting of a paste of finely divided graphitic carbon with 10 milliliters of the above colloidal silica solution and 50 milliliters of water. The grid of a tube was then sprayed with the resulting material, air dried and incorporated in a vacuum tube assembly where it was subjected to the usual heating and outgassing operation.
The amount of silica which is employed as a binder depends upon the severity of the treatment to which the electrodes are subjected in handling and construction of the tube and under the outgassing and operating conditions of the tube. It is advantageous, in general, to employ as small an amount of silica as possible, since in this manner any possibilities of inhibition of the action of the electron emission inhibiting material are reduced. The proportion of the silica in the coating material should be less than the proportion of the finely divided electron emission inhibiting material, and, in general, it is advantageous to employ silica in an amount which is from about 2 per cent to about 10 per cent by weight of the finely divided electron emission inhibiting material. The amount of the volatile suspending liquid or liquids employed may vary widely, but it is desirable that it be in such proportion as to permit ready application to the surface.
The finely divided electron emission inhibiting material may be of any one of various particle sizes, although in general the more finely divided the material is, the better is its activity. The particle size, however, should not be so large that the material does not remain suspended in the binding liquid for a sufilcient period to permit application of the material to the parts which it is desired to coat in the coating processes employed.
The drawing illustrates one form of electron discharge device in connection with which the present invention may be advantageously employed. Said device is a three-electrode electron discharge tube comprising a cathode I, control grid 2, and an anode 3, which are contained in a sealed glass envelope 4 which is shown as broken away to reveal the electrodes in the tube. The electrodes are supported in said envelope by any suitable means, such as that shown comprising insulators 5 of which only the upper one is shown and brackets 6 which are supported from the base I. Leads 8 passing through said base provide electrical connection to the electrodes of the tube in the known manner.
In the illustrated embodiment the cathode is shown as a directly heated filament formed of thermionic emitting material such as thoriated tungsten.
In the illustrated embodiment of the invention, the anode and grid may be formed of a suitable metal, such as nickel, tungsten, molybdenum, iron or the like, and are preferably formed of a refractory metal such as tungsten or molybdenum. In this embodiment, moreover, both the anode 3 and the grid 2 have a surface coating which comprises a finely divided electron emission inhibition material, suchas carbon, tantalum oxide, tungsten oxide, molybdenum oxide, or the like, held in place on the electrode by means of a binder which is substantially pure silica. Either one of said electrodes alone could be so coated. The illustrated anode 3 is coated on both its interior surface which faces the cathode, and its exterior surface. It could be coated on only one of said surfaces. Thus, if the coating inhibits electron emission primarily by increasing the heat radiation of the anode, it may be advantageous to apply the coating only to the exterior surface of the anode; if the coating inhibits electron emission by reacting with or otherwise neutralizing electron emissive material deposited on the anode from the cathode, it may be advantageous to apply the coating only to the interior surface ofthe anode.
In the manufacture of this tube the electrode to be provided with such a coating material is, after being constructed or formed, coated with a suspension of the finely divided electron emission inhibiting material and colloidal silica which is applied by spraying, painting, *dipping or other suitable means.
Various modifications may be made in the methods and electron discharge devices indicated above. Thus electron discharge devices of both the gas-filled or high vacuum types may be provided according to the invention with anodes, grids or other parts in their envelopes having surfaces of finely divided electron emission inhibiting materials and a silica binder. The invention is applicable to amplifying tubes and rectifying tubes including those of the mercury vapor type, since surfaces of the kind contemplated by the present invention, particularly when employed on anodes or on grids, provide marked advantages in such tubes. As indicated above, the present invention contemplates electron discharge devices in which the grid alone, or the anode alone, or both such electrodes are provided with surfaces embodying the invention. Moreover, only a portion of the surface area of a grid or anode may be provided with a surface according to the invention.
The colloidal silica solution employed as a binder in the formation of the surface of the invention, and which, after removal of the liquid provides the resulting silica binder, may be pro pared in other ways than those indicated. Mixtures of finely divided electron emission inhibitmg materials, as well as other finely divided electron emission inhibiting materials than those indicated above, may be employed with a silica binder, in surfaces of anodes, grids or other parts in the envelopes/of electron discharge devices embodying the invention.
The mixtures of colloidal silica, finely divided electron emission inhibiting materials, and
liquid employed to form the surfaces of the invention may be prepared in other ways than those indicated. Thus, instead of preparing the finely divided material and addingit to a prepared colloidal solution of silica, both silica and the electron inhibiting material may be simultaneously suspended in the liquid. It is also possible to grind to the desired particle size the electron emission inhibiting material while it is in a colloidal silica solution. As another alternative method, an organic silicate may be hydrolyzed in the presence of the finely divided material; thus, ethyl silicate may be hydrolyzed in the presence of "Aquadag."
Moreover, the present invention includes a process in which a surface is formed of a silica binder firmly holding in place finely divided particles of a material which after a subsequent treatment is transformed into an electron emission inhibiting material. For example, an anode or a grid may be provided with a surface coating of tantalum or zirconium hydride held in place by. a binder of finely divided silica, and the hydride decomposed to the metal by subsequent heating in an inert atmosphere, as during the outgassing of the tube. Other modifications will be apparent to those skilled in the art.
It is intended that the patent shall cover by suitable expression in the appended claims whatever features of patentable novelty reside in the invention.
What is claimed is:
1. A non-emissive electrode adapted to be disposed within the sealed envelope of an electron discharge device comprising a metal body portion having a surface coated with an electron emission inhibiting layer which is electrically conductive through the layer and which comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said finely divided electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
2. An electron discharge device comprising a sealed envelope, electron emissive means in said envelope, and a metal element in and separated from said envelope and adapted to be heated having a surface coated with a layer which is electrically conductive through the layer and which comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
3. An electron discharge device comprising a sealedenvelope, electron emissive means in said envelope, and a non-emissive electrode in and separated from said envelope comprising a metal body portion having a surface coated with a layer which is electrically conductive through the layer and which comprises a mixture of finely divided carbon and a finely divided metal oxide having electron emission inhibiting properties and a binder firmly holding the particles of said carbon and said metal oxide which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
4. An electron discharge device comprising a sealed envelope, electron emissive means in said envelope, and a non-emissive electrode in and separated from said envelop comprising a metal body portion having a surface coated with a layer which is electrically conductive through the layer and which'comprises finely divided electron emission inhibiting material and a binder firmly holding the particles of said electron emission inhibiting material which is substantially only chemically combined silicon and oxygen in the form of silica derived from drying of a solution of colloidal silica.
5 An electron discharge device as in claim 4 in which said electron emission inhibiting material is finely divided carbon.
6. An electron discharge device as in claim 4 in which said electron emission inhibiting material is a finely divided oxide of tantalum.
7. An electron discharge device as in claim 4 in which said electron emission inhibiting material is a finely divided oxide of tungsten.
8. The method of forming a coating on a surface of an element of an electron discharge devicecomprising applying to said surface a suspension in a volatile liquid of a finely divided electron emission inhibiting material and colloidal hydrated silica in an amount betweenabout 2 per cent to about 10 per cent by weight of the electron emission inhibiting material, and evaporating said liquid to form a coating in which the particles of said finely divided electron emission inhibiting material are firmly bound by silica.
9. The method of forming a coating on a surface of an element of an electron discharge device comprising hydrolyzing an organic silicate to form a solution of colloidal silica, adding a finely divided electron emission inhibiting material to said solution to form a suspension in a volatile liquid of said material and colloidal silica in an amount between about 2 per cent to about 10 per cent by weight of said electron emission inhibiting material, applying said suspension to said surface, and evaporating said liquid to form a coating in which the particles of said finely divided electron emission inhibiting material are firmly bound by silica.
LELAND A. WOOTEN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US425378A US2348045A (en) | 1942-01-01 | 1942-01-01 | Electron discharge device and method of manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US425378A US2348045A (en) | 1942-01-01 | 1942-01-01 | Electron discharge device and method of manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2348045A true US2348045A (en) | 1944-05-02 |
Family
ID=23686294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US425378A Expired - Lifetime US2348045A (en) | 1942-01-01 | 1942-01-01 | Electron discharge device and method of manufacture |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2348045A (en) |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417730A (en) * | 1942-11-30 | 1947-03-18 | Eitel Mccullough Inc | Electron tube and method of making same |
| US2417461A (en) * | 1945-08-31 | 1947-03-18 | Eitel Mccullough Inc | Electron tube and method of making same |
| US2417460A (en) * | 1945-07-25 | 1947-03-18 | Eitel Mccullough Inc | Nonemissive electrode for electron tube and method of making the same |
| US2557372A (en) * | 1948-02-21 | 1951-06-19 | Westinghouse Electric Corp | Manufacture of thoria cathodes |
| US2666864A (en) * | 1950-01-20 | 1954-01-19 | Westinghouse Electric Corp | Image intensifier tube |
| US2692838A (en) * | 1951-05-26 | 1954-10-26 | Bell Telephone Labor Inc | Process for producing a silica coating |
| US2734857A (en) * | 1951-10-11 | 1956-02-14 | snyder | |
| US2765237A (en) * | 1953-02-27 | 1956-10-02 | Midland Chemical Corp | Coating compositions |
| US2769112A (en) * | 1953-06-11 | 1956-10-30 | Westinghouse Electric Corp | Discharge lamp, mount therefor, and method |
| US2803566A (en) * | 1953-04-28 | 1957-08-20 | S J Chemical Company | Method of coating articles with heatresistant electrically conducting compositions |
| DE1021499B (en) * | 1954-11-16 | 1957-12-27 | Philips Nv | Glow discharge tubes |
| US2840493A (en) * | 1952-11-22 | 1958-06-24 | Westinghouse Electric Corp | Method of emission suppression in vacuum tubes, especially magnetron hats |
| US2864024A (en) * | 1954-11-16 | 1958-12-09 | Philips Corp | Glow-discharge tube |
| US2879406A (en) * | 1955-05-31 | 1959-03-24 | Westinghouse Electric Corp | Electron discharge tube structure |
| US2883347A (en) * | 1955-09-13 | 1959-04-21 | Bell Telephone Labor Inc | Formation of expanded silica spheres |
| DE1099651B (en) * | 1956-10-22 | 1961-02-16 | Werk Fernsehelektronik Veb | Process for coating a control electrode with a substance that reduces its thermal emission, such as silver, gold or tin, in the case of highly stressed electron tubes with an oxide cathode |
| US2978349A (en) * | 1957-07-03 | 1961-04-04 | Eastern Prod Corp | Soil proofing |
| US3504213A (en) * | 1966-08-17 | 1970-03-31 | Tesla Np | Nonemissive carbide elements for grids for power tubes |
| US20090096318A1 (en) * | 2007-10-11 | 2009-04-16 | James Peter Metropoulos | Method and appartus for generating electricity |
-
1942
- 1942-01-01 US US425378A patent/US2348045A/en not_active Expired - Lifetime
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417730A (en) * | 1942-11-30 | 1947-03-18 | Eitel Mccullough Inc | Electron tube and method of making same |
| US2417460A (en) * | 1945-07-25 | 1947-03-18 | Eitel Mccullough Inc | Nonemissive electrode for electron tube and method of making the same |
| US2417461A (en) * | 1945-08-31 | 1947-03-18 | Eitel Mccullough Inc | Electron tube and method of making same |
| US2557372A (en) * | 1948-02-21 | 1951-06-19 | Westinghouse Electric Corp | Manufacture of thoria cathodes |
| US2666864A (en) * | 1950-01-20 | 1954-01-19 | Westinghouse Electric Corp | Image intensifier tube |
| US2692838A (en) * | 1951-05-26 | 1954-10-26 | Bell Telephone Labor Inc | Process for producing a silica coating |
| US2734857A (en) * | 1951-10-11 | 1956-02-14 | snyder | |
| US2840493A (en) * | 1952-11-22 | 1958-06-24 | Westinghouse Electric Corp | Method of emission suppression in vacuum tubes, especially magnetron hats |
| US2765237A (en) * | 1953-02-27 | 1956-10-02 | Midland Chemical Corp | Coating compositions |
| US2803566A (en) * | 1953-04-28 | 1957-08-20 | S J Chemical Company | Method of coating articles with heatresistant electrically conducting compositions |
| US2769112A (en) * | 1953-06-11 | 1956-10-30 | Westinghouse Electric Corp | Discharge lamp, mount therefor, and method |
| DE1021499B (en) * | 1954-11-16 | 1957-12-27 | Philips Nv | Glow discharge tubes |
| US2864024A (en) * | 1954-11-16 | 1958-12-09 | Philips Corp | Glow-discharge tube |
| US2879406A (en) * | 1955-05-31 | 1959-03-24 | Westinghouse Electric Corp | Electron discharge tube structure |
| US2883347A (en) * | 1955-09-13 | 1959-04-21 | Bell Telephone Labor Inc | Formation of expanded silica spheres |
| DE1099651B (en) * | 1956-10-22 | 1961-02-16 | Werk Fernsehelektronik Veb | Process for coating a control electrode with a substance that reduces its thermal emission, such as silver, gold or tin, in the case of highly stressed electron tubes with an oxide cathode |
| US2978349A (en) * | 1957-07-03 | 1961-04-04 | Eastern Prod Corp | Soil proofing |
| US3504213A (en) * | 1966-08-17 | 1970-03-31 | Tesla Np | Nonemissive carbide elements for grids for power tubes |
| US20090096318A1 (en) * | 2007-10-11 | 2009-04-16 | James Peter Metropoulos | Method and appartus for generating electricity |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2348045A (en) | Electron discharge device and method of manufacture | |
| US2368060A (en) | Coating of electron discharge device parts | |
| US4342662A (en) | Getter device | |
| US2895854A (en) | Method of making cathode assemblies and products | |
| US2041802A (en) | Electron emitter | |
| US2173258A (en) | Active metal compound for vacuum tubes | |
| US3563797A (en) | Method of making air stable cathode for discharge device | |
| US2361203A (en) | Electron discharge device and method of manufacture | |
| US2117735A (en) | Getter | |
| US3041209A (en) | Method of making a thermionic cathode | |
| US3108906A (en) | Electric discharge tube | |
| US2226567A (en) | Fluorescent coating | |
| US2226720A (en) | Reduction of undesired emissions of electronic discharge devices | |
| US2769114A (en) | Anode for electron tubes | |
| US2171230A (en) | Insulating coating | |
| US2874077A (en) | Thermionic cathodes | |
| US1670483A (en) | Electron device and method of activation | |
| US1529597A (en) | Electron-emitting device and method of preparation | |
| US2527984A (en) | Method of manufacturing electric discharge tubes | |
| US2156414A (en) | Introducing active metals into envelopes | |
| US2250189A (en) | Method of applying fluorescent material in cathode-ray tube manufacture | |
| US2740914A (en) | Thermionic cathodes | |
| US1835118A (en) | Alkali metal tube | |
| US1865449A (en) | Thermionically inactive electrode | |
| US2356956A (en) | Process of carbonizing |