US3200279A - Electroluminescent element employing chrome iron plates - Google Patents
Electroluminescent element employing chrome iron plates Download PDFInfo
- Publication number
- US3200279A US3200279A US86485A US8648561A US3200279A US 3200279 A US3200279 A US 3200279A US 86485 A US86485 A US 86485A US 8648561 A US8648561 A US 8648561A US 3200279 A US3200279 A US 3200279A
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- layer
- metal
- carrier
- electroluminescent
- electroluminescent element
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL 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
- C03C4/00—Compositions for glass with special properties
- C03C4/12—Compositions for glass with special properties for luminescent glass; for fluorescent glass
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23D—ENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
- C23D3/00—Chemical treatment of the metal surfaces prior to coating
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/20—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/26—Light sources with substantially two-dimensional radiating surfaces characterised by the composition or arrangement of the conductive material used as an electrode
Definitions
- This invention relates to electroluminescent elements comprising a layer of glassenamel in which the electroluminescent material is embedded and which is provided, on one side, with a metallic carrier and, on its other side, with a conductive layer which is permeable to the radiation emitted by the electroluminescent layer upon applying a potential between the carrier and the conductive layer.
- the term conductive layer is to be understood herein to mean an electrode galvanically led to the exterior and provided with a terminal.
- the electrolumines cent materials employed may be, for instance, activated Zinc-sulphides and zinc sulphide-selenides.
- the surface layer of the metal carrier consists of a metal which can give rise to an oxide layer which is coherent in itself and satisfactorily coherent with the metal.
- Metals having such a property are Zr, Ti, Ta, Al and Cr.
- the glassenamel with its coefiicient of expansion matched satisfactorily adheres to the surface layer, since during enamelling the metal of the surface layer gives rise to an oxidic transition layer of high mutual coherence which enhances the adhesion of the glass-enamel, whilst the oxide layer, as previously mentioned, also satisfactorily adheres to the metal.
- the assembly comprising the carrier and its particular metal surface layer, the oxide layer and the enamel layer containing electroluminescent material constitutes a system of good coherence.
- the oxide layer according to the period of heating and the atmosphere, has a thiclmess of about 4000 Angstrom and has a uniform colour. it is a dense layer protecting the underlying metal against further oxidation.
- the oxides of the relevent metals are little reactive in contrast to the metals themselves.
- the metal layer provided does not itself exhibit slags and cavities which would have an unfavourable influence upon the electroluminescent system, whilst the layer sufficiently covers any cavities and slags of the metal carrier. Consequently, extremely high requirements need not be imposed upon the basic layer in this respect.
- the oxide layer provided may have a high purity so that no other metal ions are present, which may poison the zinc-sulphide systems, whilst other elements causing difiiculty, such as carbon and silicon, cannot come into contact with the enamel layer either.
- the surface of the carrier shows no errors which may give rise to annealing colours produced upon heating. Consequently, the carrier is free from spots. After enamelling the layer has a comparatively high reflective capacity.
- the surface layer has a thickness of at least several hundreds of ice Angstrom according to the basic layer and the spontaneous formation of oxide.
- the carrier will be formed so that it consists, for the greater part, of a cheap material, the core of the metal carrier then being of iron.
- the surface layer is provided on metal carrier which may be provided, if desired, with one or more metal layers in order to improve the adhesion. Such intermediate layers are matched to the ultimate surface layer.
- metal carrier consisting of iron and a surface layer of chromium, use is made of a nickel layer and/ or a copper layer.
- the light output usually decreases upon increasing thickness of the glassenamel layer, this thickness is not chosen greater than necessary and is preferably from 20 to microns. More particularly the glassenamel layer is built up of a partial layer adjacent the metal carrier and containing titanium dioxide pigment and a partial layer remote from the metal carrier and containing the electroluminescent material. With suitably chosen dimensions and concentrations, such a structure affords the advantage that the light output is higher than in a device having a glassenamel layer which is of the same thickness, but contains electroluminescent material only.
- the resistivity to breakdown in a structure according to the invention has been found to be approximately the same ineither case.
- a partial layer containing titanium-dioxide pigment which has a thickness of from 5 to 50 microns, its content of titanium-dioxide pigment being from 5% to 20% by volume.
- the partial layer containing electroluminescent material preferably has a thickness of from 15 to 50 microns and has a content of electroluminescent material of from 20% to 50% by volume.
- those glassenamels are preferred which chemically attack the surface layer of the carrier to the least possible extent, since otherwise due to diffusion of metal into the glassenamel the light output would decline as a result of the disadvantageous influence of the metal of the surface layer upon the electroluminescent material.
- Such attack takes place if the enamel contains many alkaline oxides relative to the acid oxides, and hence in the case of alkaline enamels. Consequently, use is preferably made of glass enamels having a low alkalinity.
- the alkalinity of a glass may be determined, for example, in the following manner.
- a glass powder (so-called frit) is manufactured by pouring molten enamel into water, whereby it is burst into many pieces. The acidity of the water is then a measure of that of the glassenamel.
- a glassenamel of low alkalinity has, for example, a composition of 5 mol. percent of Li O 10 mol. percent of Na O 6 mol. percent of CaO 4.5 mol. percent of SrO 14.5 mol. percent of ZnO 3.5 mol. percent of Ti0 3.5 mol. percent of A1 0 3 23.0 mol. percent of SiO 30.0 mol. percent of B
- FIGURES 1 and 2 are diagrammatic cross-sections of electroluminescent elements, in which the mutual thicknesses of the layers are not shown to scale.
- FIGURE 1 is a cross-sectional view of an electroluminescent element according to the invention, comprising an iron carrier 1 provided with a chromium layer 2 on which is a chromiumoxide film 3 which has been proucked before and during enamelling the carrier.
- the chromiunrplated carrier is covered with a layer 4 of electroluminescent zinc-sulphide embedded in glassenamel, which has been activated, for example, with copper, silver, gold or manganese and co-activated with aluminium or chlorine.
- the layer 4 is covered with a conductive transparent layer 5 consisting of tin-oxide, which is covered for protection with a glass layer 6.
- the carrier 1 is provided with a terminal 7 and the conductive transparent layer 5 with a terminal 8.
- FIGURE 2 is also a cross-sectional view of an electroluminescent element according to the invention, comprising an iron carrier 11 provided with a nickel layer 12 and a chromium layer 13 on which is a chromium oxide film 14 which has been produced before and during enamelling the carrier.
- the carrier is covered with a glass-enamel layer 15 which is built up of two partial layers, that is to say a partial layer 16 adjacent the carrier and containing titanium-oxide pigment and a partial layer 17 adjacent the carrier and containing electroluminescent zinc-sulphide.
- the layer 15 is covered with a conductive transparent layer 18 of conducting tin-oxide.
- the carrier 11 is provided with a terminal 19 and the conductive transparent layer 18 with a terminal 20.
- the chromium-plated iron carrier has a thickness of 0.3 mm.
- the nickel layer provided by electrodeposition has a thickness of about 2 microns and the chromium layer provided by electro-deposition has a thickness of about 1 micron.
- the partial layer 16 has a thickness of 45 microns and a content of titanium-dioxide pigment of 10% by volume.
- the partial layer 17, which contains 35% by volume of activated zinc-sulphide, has a thickness of microns.
- the chromeoxide film 14 has a thickness of 0.2 micron.
- An electroluminescent element comprising a layer of glass-enamel in which the electroluminescent material is embedded and which is provided, on one side, with a metal carrier and, on its other side, with a conductive layer which is permeable to the radiation emitted by the electroluminescent layer upon applying a potential between the carrier and the conductive layer, characterized in that the surface layer of the metal carrier consists of a metal which can give rise to an oxide layer which is coherent in itself and satisfactorily adherent to the metal, said metal being selected from the group consisting of Zr, Ti, Ta, Al and Cr.
- the electroluminescent element of claim 8 wherein the partial layer containing the electroluminescent material has a thickness of from 15 to 50 microns.
- electroluminescent element of claim 9 wherein the content of electroluminescent material in the relevant partial layer is from 20% to 50% by volume.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Glass Compositions (AREA)
Description
Aug. 10, 1965 w. WESTERVELD ETAL 3,200,279
I ELECTROLUMINESCENT ELEMENT EMPLOYING CHROME IRON PLATES Filed Feb. 1, 1961 FIGJ III/Ill 'I/IIII IIIII INVENTOR WILLEM WESTERVELD LOUIS M. NIJLAND BY HENRI H. JANSSEN AGENT United States Patent 3,26%,279 ELECTRQLUMINEdCENT ELEMENT EMPLGYING CHRGME IRON PLATES Willem Westerveld, Louis Marius Nijland, and Henri Hubert llansseus, all of Emmasingel, Eindhoven, Nethcrlands, assiguors to North American Philips Company, Inc, New York, N.Y., a corporation of Delaware Filed Feb. 1, 1963i, Ser. No. 86,435 Claims priority, application Netherlands, Feb. 4, 1960,
248, Claims. (Cl. 313-103) This invention relates to electroluminescent elements comprising a layer of glassenamel in which the electroluminescent material is embedded and which is provided, on one side, with a metallic carrier and, on its other side, with a conductive layer which is permeable to the radiation emitted by the electroluminescent layer upon applying a potential between the carrier and the conductive layer. The term conductive layer is to be understood herein to mean an electrode galvanically led to the exterior and provided with a terminal. The electrolumines cent materials employed may be, for instance, activated Zinc-sulphides and zinc sulphide-selenides.
It is known to use metal plates or" iron, copper or nickelplated or copper-plated iron as substrata for electrolumiescent elements in which the electroluminescent material is embedded in glassenamel. However, disadvantages then involved are the comparatively poor adhesion to iron or copper of glassenamels which are readily fusible and endured by Zinc sulphides, the poor light output of the element and the low breakdown voltage. However, nickelplating and copper-plating of the iron has not been found sufficient to meet these disadvantages. An element according to the invention provides a solution in which the said disadvantages are avoided.
According to the invention, the surface layer of the metal carrier consists of a metal which can give rise to an oxide layer which is coherent in itself and satisfactorily coherent with the metal. Metals having such a property are Zr, Ti, Ta, Al and Cr. The glassenamel with its coefiicient of expansion matched satisfactorily adheres to the surface layer, since during enamelling the metal of the surface layer gives rise to an oxidic transition layer of high mutual coherence which enhances the adhesion of the glass-enamel, whilst the oxide layer, as previously mentioned, also satisfactorily adheres to the metal. The assembly comprising the carrier and its particular metal surface layer, the oxide layer and the enamel layer containing electroluminescent material constitutes a system of good coherence. With other metals the enamel layer and the oxide film are readily liable to loosen. The oxide layer, according to the period of heating and the atmosphere, has a thiclmess of about 4000 Angstrom and has a uniform colour. it is a dense layer protecting the underlying metal against further oxidation. The oxides of the relevent metals are little reactive in contrast to the metals themselves. The metal layer provided does not itself exhibit slags and cavities which would have an unfavourable influence upon the electroluminescent system, whilst the layer sufficiently covers any cavities and slags of the metal carrier. Consequently, extremely high requirements need not be imposed upon the basic layer in this respect. The oxide layer provided may have a high purity so that no other metal ions are present, which may poison the zinc-sulphide systems, whilst other elements causing difiiculty, such as carbon and silicon, cannot come into contact with the enamel layer either. The surface of the carrier shows no errors which may give rise to annealing colours produced upon heating. Consequently, the carrier is free from spots. After enamelling the layer has a comparatively high reflective capacity. The surface layer has a thickness of at least several hundreds of ice Angstrom according to the basic layer and the spontaneous formation of oxide.
Of the above-mentioned metals chromium is preferred, since the said properties are then most pronounced and this material also has good refiexion properties. More particularly the carrier will be formed so that it consists, for the greater part, of a cheap material, the core of the metal carrier then being of iron.
The surface layer is provided on metal carrier which may be provided, if desired, with one or more metal layers in order to improve the adhesion. Such intermediate layers are matched to the ultimate surface layer. With a metal carrier consisting of iron and a surface layer of chromium, use is made of a nickel layer and/ or a copper layer.
Since for given operating voltage, for example the mains voltage, the light output usually decreases upon increasing thickness of the glassenamel layer, this thickness is not chosen greater than necessary and is preferably from 20 to microns. More particularly the glassenamel layer is built up of a partial layer adjacent the metal carrier and containing titanium dioxide pigment and a partial layer remote from the metal carrier and containing the electroluminescent material. With suitably chosen dimensions and concentrations, such a structure affords the advantage that the light output is higher than in a device having a glassenamel layer which is of the same thickness, but contains electroluminescent material only. In addition, there is a smaller possibility of the electroluminescent material being chemically attacked by the metal carrier, whilst the light emitted by the electroluminescent material is reflected by the partial layer containing the titanium-dioxide pigment. In contrast to known analogous layers containing organic binders instead of glassenamel, the resistivity to breakdown in a structure according to the invention has been found to be approximately the same ineither case. Preference is given to a partial layer containing titanium-dioxide pigment which has a thickness of from 5 to 50 microns, its content of titanium-dioxide pigment being from 5% to 20% by volume. Such a thin layer is sufficient, since due to the dense oxide-layer it is difficult for metal ions to penetrate the enamel layer. The partial layer containing electroluminescent material preferably has a thickness of from 15 to 50 microns and has a content of electroluminescent material of from 20% to 50% by volume.
As regards the glassenamel in which the electroluminescent material is embedded, those glassenamels are preferred which chemically attack the surface layer of the carrier to the least possible extent, since otherwise due to diffusion of metal into the glassenamel the light output would decline as a result of the disadvantageous influence of the metal of the surface layer upon the electroluminescent material. Such attack takes place if the enamel contains many alkaline oxides relative to the acid oxides, and hence in the case of alkaline enamels. Consequently, use is preferably made of glass enamels having a low alkalinity. The alkalinity of a glass may be determined, for example, in the following manner. A glass powder (so-called frit) is manufactured by pouring molten enamel into water, whereby it is burst into many pieces. The acidity of the water is then a measure of that of the glassenamel. A glassenamel of low alkalinity has, for example, a composition of 5 mol. percent of Li O 10 mol. percent of Na O 6 mol. percent of CaO 4.5 mol. percent of SrO 14.5 mol. percent of ZnO 3.5 mol. percent of Ti0 3.5 mol. percent of A1 0 3 23.0 mol. percent of SiO 30.0 mol. percent of B In order that the invention may be readily carried into effect, it will now be described in detail, by way of example, with reference to the accompanying drawing, in which:
FIGURES 1 and 2 are diagrammatic cross-sections of electroluminescent elements, in which the mutual thicknesses of the layers are not shown to scale.
FIGURE 1 is a cross-sectional view of an electroluminescent element according to the invention, comprising an iron carrier 1 provided with a chromium layer 2 on which is a chromiumoxide film 3 which has been pro duced before and during enamelling the carrier. The chromiunrplated carrier is covered with a layer 4 of electroluminescent zinc-sulphide embedded in glassenamel, which has been activated, for example, with copper, silver, gold or manganese and co-activated with aluminium or chlorine. On the side remote from the carrier 1, the layer 4 is covered with a conductive transparent layer 5 consisting of tin-oxide, which is covered for protection with a glass layer 6. The carrier 1 is provided with a terminal 7 and the conductive transparent layer 5 with a terminal 8.
FIGURE 2 is also a cross-sectional view of an electroluminescent element according to the invention, comprising an iron carrier 11 provided with a nickel layer 12 and a chromium layer 13 on which is a chromium oxide film 14 which has been produced before and during enamelling the carrier. The carrier is covered with a glass-enamel layer 15 which is built up of two partial layers, that is to say a partial layer 16 adjacent the carrier and containing titanium-oxide pigment and a partial layer 17 adjacent the carrier and containing electroluminescent zinc-sulphide. The layer 15 is covered with a conductive transparent layer 18 of conducting tin-oxide. The carrier 11 is provided with a terminal 19 and the conductive transparent layer 18 with a terminal 20.
In a particular structure of an element as shown in FIGURE 2, the chromium-plated iron carrier has a thickness of 0.3 mm., the nickel layer provided by electrodeposition has a thickness of about 2 microns and the chromium layer provided by electro-deposition has a thickness of about 1 micron. The partial layer 16 has a thickness of 45 microns and a content of titanium-dioxide pigment of 10% by volume. The partial layer 17, which contains 35% by volume of activated zinc-sulphide, has a thickness of microns. The chromeoxide film 14 has a thickness of 0.2 micron.
What is claimed is:
1. An electroluminescent element comprising a layer of glass-enamel in which the electroluminescent material is embedded and which is provided, on one side, with a metal carrier and, on its other side, with a conductive layer which is permeable to the radiation emitted by the electroluminescent layer upon applying a potential between the carrier and the conductive layer, characterized in that the surface layer of the metal carrier consists of a metal which can give rise to an oxide layer which is coherent in itself and satisfactorily adherent to the metal, said metal being selected from the group consisting of Zr, Ti, Ta, Al and Cr.
2. The electroluminescent element of claim 1, wherein the metal carrier is made of chromium-plated metal.
3. The electroluminescent element of claim 1, wherein the core of the metal carrier consists of iron.
4. The electroluminescent element of claim 3, wherein the metal carrier consists of iron covered with an inter mediate layer of a metal selected from the group consisting of nickel and copper which intermediate layer is covered with a chromium layer.
5. The electroluminescent element of claim 1, wherein the glass-enamel layer has a thickness of from 20 to 80 microns.
6. The electroluminescent element of claim 1, wherein the glass-enamel layer is built up of a partial layer adjacent the metal carrier and containing titanium-dioxide pigment and a partial layer remote from the metal carrier and containing the electroluminescent material.
7. The electroluminescent element of claim 6, wherein the partial layer containing the titanium-dioxide pigment has a thickness of from 5 to 50 microns.
8. The electroluminescent element of claim 7, wherein the content of titanium-dioxide pigment in the relevant partial layer is from 5% to 20% by volume.
9. The electroluminescent element of claim 8, wherein the partial layer containing the electroluminescent material has a thickness of from 15 to 50 microns.
10. The electroluminescent element of claim 9, wherein the content of electroluminescent material in the relevant partial layer is from 20% to 50% by volume.
References Cited by the Examiner UNITED STATES PATENTS 2,866,117 12/58 Walker et al. 2,911,553 11/59 Joorman et al. 2,922,912 1/ Miller.
FOREIGN PATENTS 733,260 7/55 Great Britain.
OTHER REFERENCES Problems in Electroluminescent Television Display, Robert M. Bowie, Sylvania Technologist, XVI, No. 3, July 1958, pages 82 to 85.
Materials Technology for Electron Tubes, by Walter H. Kohl, Reinhold Publishing Corp, 330 W. 42nd St., New York, N.Y., Chapter 4, Glass to Metal Seals.
GEORGE N. WESTBY, Primary Examiner.
RALPH G. NILSON, Examiner.
Claims (1)
1. AN ELECTROLUMINESCENT ELEMENT COMPRISING A LAYER OF GLASS-ENAMEL IN WHICH THE ELECTROLUMINESCENT MATERIAL IS EMBEDDED AND WHICH IS PROVIDED, ON ONE SIDE, WITH A METAL CARRIER AND, ON ITS OTHER SIDE, WITH A CONDUCTIVE LAYER WHICH IS PERMEABLE TO THE RADIATION EMITTED BY THE ELECTROLUMINESCENT LAYER UPON APPLYING A POTENTIAL BETWEEN THE CARRIER AND THE CONDUCTIVE LAYER, CHARACTERIZED IN THAT THE SURFACE LAYER OF THE METAL CARRIER CONSISTS OF A METAL WHICH CAN GIVE RISE TO AN OXIDE LAYER WHICH IS COHERENT IN ITSELF AND SATISFACTORILY ADHERENT TO THE METAL, SAID METAL BEING SELECTED FROM THE GROUP CONSISTING OF ZR, TI, TA, AL AND CR.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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NL248090 | 1960-02-04 |
Publications (1)
Publication Number | Publication Date |
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US3200279A true US3200279A (en) | 1965-08-10 |
Family
ID=19752160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US86485A Expired - Lifetime US3200279A (en) | 1960-02-04 | 1961-02-01 | Electroluminescent element employing chrome iron plates |
Country Status (6)
Country | Link |
---|---|
US (1) | US3200279A (en) |
CH (1) | CH414013A (en) |
ES (1) | ES264564A1 (en) |
FR (1) | FR1284117A (en) |
GB (1) | GB997783A (en) |
OA (1) | OA00770A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4455506A (en) * | 1981-05-11 | 1984-06-19 | Gte Products Corporation | Contrast enhanced electroluminescent device |
US5955837A (en) * | 1996-10-15 | 1999-09-21 | U.S. Philips Corporation | Electroluminescent illumination system with an active layer of a medium having light-scattering properties for flat-panel display devices |
US20030094896A1 (en) * | 2001-11-21 | 2003-05-22 | Paul Valentine | Light emitting ceramic device and method for fabricating the same |
US20040217702A1 (en) * | 2003-05-02 | 2004-11-04 | Garner Sean M. | Light extraction designs for organic light emitting diodes |
US20220268871A1 (en) * | 2021-02-24 | 2022-08-25 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12143182B1 (en) * | 2023-10-17 | 2024-11-12 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009001109A1 (en) * | 2009-02-24 | 2010-08-26 | KÜHN EMAIL GmbH | Method for enameling magnesium-containing aluminum alloy, comprises applying a buffer layer in the form of a passivation on metal base, where the passivation is applied in flow-less manner and is cooled at room temperature |
Citations (4)
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---|---|---|---|---|
GB733260A (en) * | 1952-04-12 | 1955-07-06 | Sylvania Electric Prod | Improvements in electroluminescent lamps |
US2866117A (en) * | 1955-04-15 | 1958-12-23 | British Thomson Houston Co Ltd | Electroluminescent panel |
US2911553A (en) * | 1955-04-01 | 1959-11-03 | Philips Corp | Electro-luminescent element |
US2922912A (en) * | 1959-01-05 | 1960-01-26 | Miller John Dawson | Indicia bearing electrolluminescent panel and method of manufacture |
-
1961
- 1961-02-01 US US86485A patent/US3200279A/en not_active Expired - Lifetime
- 1961-02-01 ES ES0264564A patent/ES264564A1/en not_active Expired
- 1961-02-01 CH CH116961A patent/CH414013A/en unknown
- 1961-02-01 FR FR851333A patent/FR1284117A/en not_active Expired
- 1961-02-03 GB GB4153/61A patent/GB997783A/en not_active Expired
-
1964
- 1964-12-12 OA OA50839A patent/OA00770A/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB733260A (en) * | 1952-04-12 | 1955-07-06 | Sylvania Electric Prod | Improvements in electroluminescent lamps |
US2911553A (en) * | 1955-04-01 | 1959-11-03 | Philips Corp | Electro-luminescent element |
US2866117A (en) * | 1955-04-15 | 1958-12-23 | British Thomson Houston Co Ltd | Electroluminescent panel |
US2922912A (en) * | 1959-01-05 | 1960-01-26 | Miller John Dawson | Indicia bearing electrolluminescent panel and method of manufacture |
Cited By (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4455506A (en) * | 1981-05-11 | 1984-06-19 | Gte Products Corporation | Contrast enhanced electroluminescent device |
US5955837A (en) * | 1996-10-15 | 1999-09-21 | U.S. Philips Corporation | Electroluminescent illumination system with an active layer of a medium having light-scattering properties for flat-panel display devices |
US20030094896A1 (en) * | 2001-11-21 | 2003-05-22 | Paul Valentine | Light emitting ceramic device and method for fabricating the same |
US6825054B2 (en) | 2001-11-21 | 2004-11-30 | Paul Valentine | Light emitting ceramic device and method for fabricating the same |
US7719186B2 (en) | 2001-11-21 | 2010-05-18 | Paul Valentine | Light emitting ceramic device |
US20040217702A1 (en) * | 2003-05-02 | 2004-11-04 | Garner Sean M. | Light extraction designs for organic light emitting diodes |
US20230378650A1 (en) * | 2021-02-24 | 2023-11-23 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240006765A1 (en) * | 2021-02-24 | 2024-01-04 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20220268869A1 (en) * | 2021-02-24 | 2022-08-25 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11664594B2 (en) | 2021-02-24 | 2023-05-30 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11670855B2 (en) | 2021-02-24 | 2023-06-06 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11695209B2 (en) | 2021-02-24 | 2023-07-04 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11721900B2 (en) | 2021-02-24 | 2023-08-08 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11742578B2 (en) * | 2021-02-24 | 2023-08-29 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11742579B2 (en) | 2021-02-24 | 2023-08-29 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11777215B2 (en) * | 2021-02-24 | 2023-10-03 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11784412B2 (en) | 2021-02-24 | 2023-10-10 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11791557B2 (en) * | 2021-02-24 | 2023-10-17 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20230361471A1 (en) * | 2021-02-24 | 2023-11-09 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11817636B2 (en) * | 2021-02-24 | 2023-11-14 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11824280B2 (en) | 2021-02-24 | 2023-11-21 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11824279B2 (en) | 2021-02-24 | 2023-11-21 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20220268871A1 (en) * | 2021-02-24 | 2022-08-25 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11843188B2 (en) | 2021-02-24 | 2023-12-12 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240006766A1 (en) * | 2021-02-24 | 2024-01-04 | Bluehalo, Llc | System and method for a digitally beamformed phased array f |
US20220268870A1 (en) * | 2021-02-24 | 2022-08-25 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11870159B2 (en) | 2021-02-24 | 2024-01-09 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240047876A1 (en) * | 2021-02-24 | 2024-02-08 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240047877A1 (en) * | 2021-02-24 | 2024-02-08 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240047875A1 (en) * | 2021-02-24 | 2024-02-08 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240063542A1 (en) * | 2021-02-24 | 2024-02-22 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11955727B2 (en) | 2021-02-24 | 2024-04-09 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US11996634B2 (en) | 2021-02-24 | 2024-05-28 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12009606B2 (en) * | 2021-02-24 | 2024-06-11 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12021317B2 (en) * | 2021-02-24 | 2024-06-25 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US20240213674A1 (en) * | 2021-02-24 | 2024-06-27 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12034228B2 (en) | 2021-02-24 | 2024-07-09 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12062862B2 (en) * | 2021-02-24 | 2024-08-13 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12062861B2 (en) | 2021-02-24 | 2024-08-13 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12080958B2 (en) * | 2021-02-24 | 2024-09-03 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12088021B2 (en) * | 2021-02-24 | 2024-09-10 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12113302B2 (en) * | 2021-02-24 | 2024-10-08 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12119563B2 (en) * | 2021-02-24 | 2024-10-15 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12126096B2 (en) * | 2021-02-24 | 2024-10-22 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
US12143182B1 (en) * | 2023-10-17 | 2024-11-12 | Bluehalo, Llc | System and method for a digitally beamformed phased array feed |
Also Published As
Publication number | Publication date |
---|---|
GB997783A (en) | 1965-07-07 |
FR1284117A (en) | 1962-02-09 |
ES264564A1 (en) | 1961-04-01 |
OA00770A (en) | 1967-11-15 |
CH414013A (en) | 1966-05-31 |
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