US2660686A - Fluorescent screen - Google Patents

Fluorescent screen Download PDF

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US2660686A
US2660686A US34060A US3406048A US2660686A US 2660686 A US2660686 A US 2660686A US 34060 A US34060 A US 34060A US 3406048 A US3406048 A US 3406048A US 2660686 A US2660686 A US 2660686A
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glass
layer
screen
phosphor
support
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US34060A
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Charles W Putnam
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CBS Corp
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Westinghouse Electric Corp
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Priority to BE515307D priority patent/BE515307A/xx
Application filed by Westinghouse Electric Corp filed Critical Westinghouse Electric Corp
Priority to US34060A priority patent/US2660686A/en
Priority to GB13441/49A priority patent/GB669584A/en
Priority to US146373A priority patent/US2660539A/en
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J29/00Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
    • H01J29/02Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
    • H01J29/10Screens on or from which an image or pattern is formed, picked up, converted or stored
    • H01J29/36Photoelectric screens; Charge-storage screens
    • H01J29/38Photoelectric screens; Charge-storage screens not using charge storage, e.g. photo-emissive screen, extended cathode
    • H01J29/385Photocathodes comprising a layer which modified the wave length of impinging radiation
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/062Glass compositions containing silica with less than 40% silica by weight
    • C03C3/064Glass compositions containing silica with less than 40% silica by weight containing boron
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/062Glass compositions containing silica with less than 40% silica by weight
    • C03C3/064Glass compositions containing silica with less than 40% silica by weight containing boron
    • C03C3/066Glass compositions containing silica with less than 40% silica by weight containing boron containing zinc
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/12Silica-free oxide glass compositions
    • C03C3/253Silica-free oxide glass compositions containing germanium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J29/00Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
    • H01J29/02Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
    • H01J29/10Screens on or from which an image or pattern is formed, picked up, converted or stored
    • H01J29/18Luminescent screens
    • H01J29/22Luminescent screens characterised by the binder or adhesive for securing the luminescent material to its support, e.g. vessel

Definitions

  • My invention relates to radiation-emitting screens and, in particular, it relates to a process for making light-emitting screens which produce a visible replica of the intensity distribution in an X-ray field.
  • One use for my invention is in electr cal discharge tubes in which electron images corresponding to a light image generated on a fluorescent screen by X-rays are first produced, and then a second light image which is an intensified replica of the initial light image is produced by incidence of the electron ima e on a second fluorescent screen.
  • an electrical discharge device this type is shown and claimed in Lloyd P. Hunter and Richard Longini ?atent 2,555,5 l5 for an Image intensifier, issued June 5, 1951.
  • an electron image is produced which is a replica of an X-ray picture on a fluorescent screen; the electrons are then accelerated to high velocity and into incidence upon a screen comprising a cathode ray phosphor, and the light image produced on the latter is observed.
  • the photo-electric surface comprises materials such as cesium which. are active chemically and hav a vapor of a substantial pressure and which likely to react chemically with the components in the fluorescent screen during processing. It is, accordingly, necessary to provide some protective coating for the fluorescent material which is capable of preventing this reaction.
  • One object of my invention is, accordingly, to provide a novel type of fluorescent screen in which the fluorescent material is provided with a coating which is substantially transparent to incident light and is capable of preventing chemical reaction between the phosphor of the screen and cesium vapor.
  • Another object of my invention is to provide a protective coating for the particles comprised in a fluorescent screen which shall prevent chemical reaction between them and vapors present in the space around them.
  • Still another object of my invention is to provide an improved form of fluorescent screen in which chemical reaction between the fluorescent materials and an adjacent layer of chemically active material is prevented.
  • a still more specific object of my invention is to provide a method of protecting zinc sulphide from chemical reaction with photo-electrically active materials.
  • a still further object of my invention is to provide a method of preventin chemical reaction between fluorescent zinc sulphide and th components of cesiated antimony located in a common container therewith.
  • Still another object 01" my invention is to provide a fluorescent screen which is much less difficult to outgas than are prior art screens in which the individual fine particles of fluorescent material are exposed to the atmosphere of an evacuated container, and which contains a minimum of adsorbed vapors likely to gradually exude into such atmosphere during operative life of the tube.
  • Figure 1 shows a view in longitudinal section of an electrical discharge tube containing a fluorescent screen protected in accordance with the principles of my invention
  • Fig. 2 is an enlarged view in section of the screen forming a wall portion of 1;
  • Fig. 3 is a longitudinal section of a container in which the plate 5 is placed at an intermediate point in the fabrication.
  • the fluorecent screen in accordance with my invention, comprises a layer 5A made up of particles of a fluorescent material or phosphor, such, for example, as zinc sulphide or silver-activated zinc sulphide, which is embedded in glass plate 5 positioned within a container 4 of glass or other suitable material.
  • the container i may be a vacuum-tight enclosure, such as the tube l in the above-mentioned Hunter and Longini application.
  • the enclosure t may contain during the process of its manufacture a substantial pressure of the vapor or some photo-electric material, such, for example, as cesium used to produce a layer 8 of cesiated antimony deposited in close contiguity to the layer 5A.
  • a layer 9 of an electron phosphor such as zinc sulphide which may be provided with chemical protection such as is described and claimed in the Patent 2,586,304 of J. W. Coltman and R. L. Longini for Protection of Electron Phosphors, issued February 19, 1952.
  • an electron phosphor such as zinc sulphide
  • the fluorescent layer 5A is embedded in the glass of the plate 5 by a procedure which will now be described.
  • the final desired product is a glass plate 5 with a layer 5A of fluorescent material or phosphor sunk into the upper surface until all the phosphor particles are completely enclosed in the glass.
  • the method of achieving this result is as follows:
  • a glass must be used for the plate 5 which will not be detrimental to the phosphor.
  • the glass must not dissolve the phosphor, and it must not contain substances that will react with or unfavorably activate the phosphor.
  • the phosphor to be used maybe a silver-activated zinc sulphide which fluoresces blue under excitation. This material as readily purchasa ble upon the market is notably subject to adverse activation by very minute quantities of impurities.
  • the glass for plate 5- is up from chemicals containing impurities less than 0.001%.
  • the glass contains the following components: K20, ZnO, B203.
  • K20 potassium oxide
  • B203 boric oxide
  • I found mixes within the range of O to 40 percent K20, to 60 percent ZnO and 100 to 40 percent B203 to be satisfactory for many purposes.
  • the constituents were fused in a platinum crucible at 1000 C. and poured into an aluminum mold. Besides their purity, these glasses are relatively low-melting, and the compositions mentioned above had a considerable range of thermal expansion coefficients.
  • the glass melt is evacuated in the molten state to remove all occluded gases, formed into a thin plate, annealed, and cooled.
  • the layer A of fluorescent material is settled onto one surface of this plate from a solution containing a suitable binder.
  • binders such as borates, boro-phosphates or silicates of the alkali metals
  • the solution used was approximately 5% by weight potassium borate in water.
  • the potassium borate was roughly of the formula: K2O.3B2O3 or KB305 and very pure. tion is rapidly dried, it first forms an elastic him. which. on further drying becomes hard. Upon heating to fusion, this material forms a glass which will not devitrify under any heat treatment anticipated in this process, and it is a glass which is readily miscible with the glass used for the backing of the phosphor.
  • a homogeneous suspension of phosphor in the 5 percent potassium borate solution is placed in a container with the glass plate in the bottom.
  • the amount of the phosphor mixture poured into the container will, of course, determine'the thickness of the resulting layer.
  • a layer thickness when dried of 12 mils will be found suitable for many purposes.
  • the glass plate with superimposed phosphor layer is then baked at approximately 125 C. to dry the binder.
  • the glass plate is then placed, phosphor layer up, on a support of such a substance as graphite which, when the glass is heated to a softened condition, will maintain the glass shape, and Will not stick to it.
  • This support may have an integral heater, or it should be thin enough and of a material which will readily conduct heat.
  • the temperature is then raised above the softening point of the glass (approximately 900 C'.). This temperature is maintained while the molten glass diffuses up through the phosphor layer until the upper surface of the bonded unit is a continuous, though slightly irregular, glass surface. At this point the glass should be quickly reduced to annealing temperature, annealed and cooled.
  • the cesiated antimony layer may be applied to the surface of the finished plate by methods known in the art.
  • a vacuum-tight container containing a glass support having a fluorescent material completely submerged beneath its surface and a coat ing of photo-electric material on said support.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a glass support having a layer of fluorescent material completely submerged beneath its surface.
  • a vacuumtight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a glass support having a layer of zinc sulphide completely submerged beneath its surface.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
  • a vacuum-tight container having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc .oxide, and 100% to 40% boric oxide, said support having a layer of zinc suiphide submerged within its surface.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium and having a screen comprising a support consisting of 0% to 4.0% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium and having a screen comprising a glass support having a layer of fluorescent material completely submerged beneath its surface.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of 5 cesium and having a screen comprising a glass support having a layer of zinc sulphide completely submerged beneath its surface.
  • An image screen comprising a support consisting of to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
  • An image screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of phosphor submerged beneath its surface.
  • a vacuum-tight container enclosing an atmosphere containing a substantial pressure of a component which is chemically active toward phosphors and having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of at least one of said phosphors submerged beneath its surface.

Description

Nov. 24, 1953 c. w. PUTNAM 2,660,686
FLUORESCENT SCREEN Filed June 19, 1948 I I 5/? I 1 .5
WITNESSES: INVENTOR 4%! Charles W Putnam iatcnted Nev. 24,1953
illilTED STATES PATENT OFFlCE FLUDRESCEN'E SCREEN Application June 19, 1948, Serial No. 34,066
13 Claims. l
My invention relates to radiation-emitting screens and, in particular, it relates to a process for making light-emitting screens which produce a visible replica of the intensity distribution in an X-ray field. One use for my invention is in electr cal discharge tubes in which electron images corresponding to a light image generated on a fluorescent screen by X-rays are first produced, and then a second light image which is an intensified replica of the initial light image is produced by incidence of the electron ima e on a second fluorescent screen. Certain subject matter herein disclosed is being claimed in my application Serial No. 146,373, filed February 25, 1950, for a Fluorescent Screen.
One example of an electrical discharge device this type is shown and claimed in Lloyd P. Hunter and Richard Longini ?atent 2,555,5 l5 for an Image intensifier, issued June 5, 1951. In the device just mentioned, an electron image is produced which is a replica of an X-ray picture on a fluorescent screen; the electrons are then accelerated to high velocity and into incidence upon a screen comprising a cathode ray phosphor, and the light image produced on the latter is observed. In the electrical discharge tube just described, the photo-electric surface comprises materials such as cesium which. are active chemically and hav a vapor of a substantial pressure and which likely to react chemically with the components in the fluorescent screen during processing. It is, accordingly, necessary to provide some protective coating for the fluorescent material which is capable of preventing this reaction.
One object of my invention is, accordingly, to provide a novel type of fluorescent screen in which the fluorescent material is provided with a coating which is substantially transparent to incident light and is capable of preventing chemical reaction between the phosphor of the screen and cesium vapor.
Another object of my invention is to provide a protective coating for the particles comprised in a fluorescent screen which shall prevent chemical reaction between them and vapors present in the space around them.
Still another object of my invention is to provide an improved form of fluorescent screen in which chemical reaction between the fluorescent materials and an adjacent layer of chemically active material is prevented.
A still more specific object of my invention is to provide a method of protecting zinc sulphide from chemical reaction with photo-electrically active materials.
A still further object of my invention is to provide a method of preventin chemical reaction between fluorescent zinc sulphide and th components of cesiated antimony located in a common container therewith.
Still another object 01" my invention is to provide a fluorescent screen which is much less difficult to outgas than are prior art screens in which the individual fine particles of fluorescent material are exposed to the atmosphere of an evacuated container, and which contains a minimum of adsorbed vapors likely to gradually exude into such atmosphere during operative life of the tube.
Other objects of my invention will become apparent upon reading the following description, taken in connection with the drawing, in which:
Figure 1 shows a view in longitudinal section of an electrical discharge tube containing a fluorescent screen protected in accordance with the principles of my invention;
Fig. 2 is an enlarged view in section of the screen forming a wall portion of 1; and
Fig. 3 is a longitudinal section of a container in which the plate 5 is placed at an intermediate point in the fabrication.
Referring in detail to the drawing, the fluorecent screen, in accordance with my invention, comprises a layer 5A made up of particles of a fluorescent material or phosphor, such, for example, as zinc sulphide or silver-activated zinc sulphide, which is embedded in glass plate 5 positioned within a container 4 of glass or other suitable material. The container i may be a vacuum-tight enclosure, such as the tube l in the above-mentioned Hunter and Longini application. As is illustrated in said application, the enclosure t may contain during the process of its manufacture a substantial pressure of the vapor or some photo-electric material, such, for example, as cesium used to produce a layer 8 of cesiated antimony deposited in close contiguity to the layer 5A. There is also located on another portion of the wall 6 of the container 4, a layer 9 of an electron phosphor such as zinc sulphide, which may be provided with chemical protection such as is described and claimed in the Patent 2,586,304 of J. W. Coltman and R. L. Longini for Protection of Electron Phosphors, issued February 19, 1952. As has been stated above, there is a likelihood of chemical reaction between the fluorescent material of the layer 5A and photo-electric material just mentioned, and
to prevent such undesired chemical reaction, the fluorescent layer 5A is embedded in the glass of the plate 5 by a procedure which will now be described.
Referring to the drawing, the final desired product is a glass plate 5 with a layer 5A of fluorescent material or phosphor sunk into the upper surface until all the phosphor particles are completely enclosed in the glass. The method of achieving this result is as follows:
A glass must be used for the plate 5 which will not be detrimental to the phosphor. The glass must not dissolve the phosphor, and it must not contain substances that will react with or unfavorably activate the phosphor. For example, the phosphor to be used maybe a silver-activated zinc sulphide which fluoresces blue under excitation. This material as readily purchasa ble upon the market is notably subject to adverse activation by very minute quantities of impurities.
The glass for plate 5- is up from chemicals containing impurities less than 0.001%. The glass contains the following components: K20, ZnO, B203. To give one instance, I have found a mix of 31 percent by weight of potassium oxide (K20) with 69 percent by weight of boric oxide (B203) to be a satisfactory one. However, I found mixes within the range of O to 40 percent K20, to 60 percent ZnO and 100 to 40 percent B203 to be satisfactory for many purposes. The constituents were fused in a platinum crucible at 1000 C. and poured into an aluminum mold. Besides their purity, these glasses are relatively low-melting, and the compositions mentioned above had a considerable range of thermal expansion coefficients.
The glass melt is evacuated in the molten state to remove all occluded gases, formed into a thin plate, annealed, and cooled. The layer A of fluorescent material is settled onto one surface of this plate from a solution containing a suitable binder.
Although a number of binders, such as borates, boro-phosphates or silicates of the alkali metals could probably be used, the one developed for this process has certain desirable features. The solution used was approximately 5% by weight potassium borate in water. The potassium borate was roughly of the formula: K2O.3B2O3 or KB305 and very pure. tion is rapidly dried, it first forms an elastic him. which. on further drying becomes hard. Upon heating to fusion, this material forms a glass which will not devitrify under any heat treatment anticipated in this process, and it is a glass which is readily miscible with the glass used for the backing of the phosphor.
A homogeneous suspension of phosphor in the 5 percent potassium borate solution is placed in a container with the glass plate in the bottom. The amount of the phosphor mixture poured into the container will, of course, determine'the thickness of the resulting layer. A layer thickness when dried of 12 mils will be found suitable for many purposes.
The glass plate with superimposed phosphor layer is then baked at approximately 125 C. to dry the binder.
The glass plate is then placed, phosphor layer up, on a support of such a substance as graphite which, when the glass is heated to a softened condition, will maintain the glass shape, and Will not stick to it. This support may have an integral heater, or it should be thin enough and of a material which will readily conduct heat.
When a thin layer of this solu- The glass and support are then placed in a container which can be evacuated. The chamber is closed and evacuated. The temperature is gradually raised while under vacuum to a point just below the softening point of the glass. The purpose of this treatment is to complete the removal of water from the binder and to outgas the phosphor and the surface of the glass. The vacuum is then broken, allowing the chamber to return to atmospheric pressure. The potassium borate binder protects the phosphor against oxidation. Zinc sulphide ordinarily oxidizes at 600 C. in air.
The temperature is then raised above the softening point of the glass (approximately 900 C'.). This temperature is maintained while the molten glass diffuses up through the phosphor layer until the upper surface of the bonded unit is a continuous, though slightly irregular, glass surface. At this point the glass should be quickly reduced to annealing temperature, annealed and cooled.
The cesiated antimony layer may be applied to the surface of the finished plate by methods known in the art. Patent 2,456,968 of R. L. Longini for a Process for Outgassing Photocells Containing Antimony, issued December 21, 1948, shows one such method.
I claim as my invention:
1. A vacuum-tight container containing a glass support having a fluorescent material completely submerged beneath its surface and a coat ing of photo-electric material on said support.
2. A vacuum-tight container containing a glass support having a layer .of zinc sulphide completely submerged beneath its surface and coated with photo-electric material.
3. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a glass support having a layer of fluorescent material completely submerged beneath its surface.
4. A vacuumtight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a glass support having a layer of zinc sulphide completely submerged beneath its surface.
5. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium during manufacture and having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
6. A vacuum-tight container having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc .oxide, and 100% to 40% boric oxide, said support having a layer of zinc suiphide submerged within its surface.
'7. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium and having a screen comprising a support consisting of 0% to 4.0% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
8. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of cesium and having a screen comprising a glass support having a layer of fluorescent material completely submerged beneath its surface.
9. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of 5 cesium and having a screen comprising a glass support having a layer of zinc sulphide completely submerged beneath its surface.
10. A vacuum-tight container containing a glass support having a layer of zinc sulphide complete- 1y submerged beneath its surface and coated with cesium.
11. An image screen comprising a support consisting of to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of zinc sulphide submerged within its surface.
12. An image screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of phosphor submerged beneath its surface.
13. A vacuum-tight container enclosing an atmosphere containing a substantial pressure of a component which is chemically active toward phosphors and having a screen comprising a support consisting of 0% to 40% potassium oxide, 0% to 60% zinc oxide, and 100% to 40% boric oxide, said support having a layer of at least one of said phosphors submerged beneath its surface.
CHARLES W. PUTNAM.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date Berger June Leverenz Mar. 2, Hartmann Aug. 3, Winninghoff Oct. 5, Germer July 19, Schleede Nov. 15, Fairbrother Apr. 4, Massa et all. Oct. 31, Bruche et al. Nov. 7, Langmuir Apr. 23, Steadman Aug. Bode Apr. 8, Scott et al. Apr. 7, Roberts Oct. 13, Hood et a1. Mar. 30, Hooley May 14, Szegho July 8,
US34060A 1948-06-19 1948-06-19 Fluorescent screen Expired - Lifetime US2660686A (en)

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BE515306D BE515306A (en) 1948-06-19
BE515307D BE515307A (en) 1948-06-19
US34060A US2660686A (en) 1948-06-19 1948-06-19 Fluorescent screen
GB13441/49A GB669584A (en) 1948-06-19 1949-05-19 Improvements in or relating to radiation-emitting screens
US146373A US2660539A (en) 1948-06-19 1950-02-25 Method for producing a fluorescent screen

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2945128A (en) * 1955-12-29 1960-07-12 Westinghouse Electric Corp Fluorescent structures and method of manufacture
US2996623A (en) * 1957-04-11 1961-08-15 Sylvania Electric Prod Electroluminescent image device
US3089956A (en) * 1953-07-10 1963-05-14 Westinghouse Electric Corp X-ray fluorescent screen
US3533827A (en) * 1963-03-11 1970-10-13 Westinghouse Electric Corp Method for phosphor coating and phosphor-coated substrate

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US2072115A (en) * 1932-08-30 1937-03-02 Rca Corp Luminescent screen
US2088595A (en) * 1930-05-24 1937-08-03 Firm Siemens Reiniger Veifa Ge Fluorescent screen
US2094630A (en) * 1931-01-26 1937-10-05 Gen Electric Vapor Lamp Co Vitreous body for electric discharge devices
US2123939A (en) * 1935-04-11 1938-07-19 Germer Edmund Method of applying luminescent colors on bodies consisting of glass or other material
US2137118A (en) * 1933-12-19 1938-11-15 Telefunken Gmbh Fluorescent screen
US2152991A (en) * 1935-03-12 1939-04-04 Gen Electric Method of coating surfaces with powdered materials
US2178238A (en) * 1937-03-17 1939-10-31 Rca Corp Electric discharge device
US2179083A (en) * 1936-08-08 1939-11-07 Aeg Electron image tube
US2198479A (en) * 1937-11-03 1940-04-23 Gen Electric Image reproduction
US2212134A (en) * 1938-11-23 1940-08-20 Steadman Albert Method of producing luminous tubes
US2237288A (en) * 1937-06-07 1941-04-08 Bode Hans Spattling and spraying process
US2278742A (en) * 1937-04-20 1942-04-07 Gen Electric Method of forming luminescent screens
US2298968A (en) * 1940-03-14 1942-10-13 Gen Electric Fluorescent coating and method of manufacture
US2315328A (en) * 1938-11-04 1943-03-30 Corning Glass Works High silica glass article
US2400147A (en) * 1942-07-17 1946-05-14 Corning Glass Works Fluorescent glass composition
US2423626A (en) * 1944-05-20 1947-07-08 Rauland Corp Method of manufacturing screens in cathode-ray tubes

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2088595A (en) * 1930-05-24 1937-08-03 Firm Siemens Reiniger Veifa Ge Fluorescent screen
US1961603A (en) * 1930-11-14 1934-06-05 Firm Jenaer Glaswerk Schott & Heat absorbing glass
US2094630A (en) * 1931-01-26 1937-10-05 Gen Electric Vapor Lamp Co Vitreous body for electric discharge devices
US2072115A (en) * 1932-08-30 1937-03-02 Rca Corp Luminescent screen
US2137118A (en) * 1933-12-19 1938-11-15 Telefunken Gmbh Fluorescent screen
US2152991A (en) * 1935-03-12 1939-04-04 Gen Electric Method of coating surfaces with powdered materials
US2123939A (en) * 1935-04-11 1938-07-19 Germer Edmund Method of applying luminescent colors on bodies consisting of glass or other material
US2179083A (en) * 1936-08-08 1939-11-07 Aeg Electron image tube
US2178238A (en) * 1937-03-17 1939-10-31 Rca Corp Electric discharge device
US2278742A (en) * 1937-04-20 1942-04-07 Gen Electric Method of forming luminescent screens
US2237288A (en) * 1937-06-07 1941-04-08 Bode Hans Spattling and spraying process
US2198479A (en) * 1937-11-03 1940-04-23 Gen Electric Image reproduction
US2315328A (en) * 1938-11-04 1943-03-30 Corning Glass Works High silica glass article
US2212134A (en) * 1938-11-23 1940-08-20 Steadman Albert Method of producing luminous tubes
US2298968A (en) * 1940-03-14 1942-10-13 Gen Electric Fluorescent coating and method of manufacture
US2400147A (en) * 1942-07-17 1946-05-14 Corning Glass Works Fluorescent glass composition
US2423626A (en) * 1944-05-20 1947-07-08 Rauland Corp Method of manufacturing screens in cathode-ray tubes

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3089956A (en) * 1953-07-10 1963-05-14 Westinghouse Electric Corp X-ray fluorescent screen
US2945128A (en) * 1955-12-29 1960-07-12 Westinghouse Electric Corp Fluorescent structures and method of manufacture
US2996623A (en) * 1957-04-11 1961-08-15 Sylvania Electric Prod Electroluminescent image device
US3533827A (en) * 1963-03-11 1970-10-13 Westinghouse Electric Corp Method for phosphor coating and phosphor-coated substrate

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GB669584A (en) 1952-04-02
BE515306A (en)
BE515307A (en)

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