US2728870A - Electroluminescent lamp - Google Patents
Electroluminescent lamp Download PDFInfo
- Publication number
- US2728870A US2728870A US310612A US31061252A US2728870A US 2728870 A US2728870 A US 2728870A US 310612 A US310612 A US 310612A US 31061252 A US31061252 A US 31061252A US 2728870 A US2728870 A US 2728870A
- Authority
- US
- United States
- Prior art keywords
- particles
- phosphor
- lamp
- dielectric
- electroluminescent
- 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
- 239000002245 particle Substances 0.000 claims description 22
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims 1
- 239000004033 plastic Substances 0.000 description 12
- 229920003023 plastic Polymers 0.000 description 12
- 238000000576 coating method Methods 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 10
- 239000003989 dielectric material Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- NUKZAGXMHTUAFE-UHFFFAOYSA-N hexanoic acid methyl ester Natural products CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S116/00—Signals and indicators
- Y10S116/35—Electroluminescent dials
Definitions
- the present invention relates to electroluminescent lamps, that is to lamps 1n which light is produced by electrical excitation of a phosphor.
- Such lamps have two spaced electrodes, between which are electroluminescent phosphor particles suspended or embedded in a dielectric material.
- Plastic materials are generally used as the embedding dielectric.
- the phosphor particles are longer in one dimension than in another, and the heating of the plastic allows the phosphor particles embedded therein sufiicient freedom of motion to allow them to line up in the direction of the field when voltage is applied to the electrodes.
- the dielectric constant of the embedding material is smaller than that of phosphor particle, as is the case with most plastics, the field in the phosphor particles will be a maximum when the particles are aligned in the direction of the field, and will be a minimum when it is aligned in a direction transverse to the field.
- the phosphor particles may actually move around in the dielectric material as the field is varied and reversed, as on alternating current, for example. Such continued motion of the particles is undesirable.
- the use of fairly hard plastic, which holds the phosphor particles rigidly in place, such as the thermosetting resins for example, will keep the particles lined up properly after they are once oriented by the field in the above-described manner.
- some advantage is obtained by our invention even when the dielectric is of the cellulose type.
- Fig. 1 shows a view, partly in section, of one embodiment of the invention
- Fig. 2 is a box diagram showing the sequence of steps in the process of one embodiment of the invention.
- the glass plate 1 carries a transparent conductive coating 2, over which is the coating 3 of phosphor particles embedded in a dielectric material, with a metal coating 4 over at least part of said phosphor-dielectric coating 3 and out of electrical contact with said conductive coating 2.
- the transparent conductive coating can be of stannous chloride, applied as in copending application Serial Num- 2,728,870 Patented Dec. 27, 1955 her 120,398, filed October 8, 1949, by Eric L. Mager, now Patent No. 2,624,857, although other transparent conductive coatings can be used.
- the metal coating 4 is of aluminum, although other metals can be used, and is applied as in the copending Mager application.
- the phosphor suspended in the dielectric material was zinc sulphide containing small amounts of lead, copper and chlorine for activation, as shown in copending application, Serial Number 230,713, filed June 8, 1951, by Keith H. Butler and Horace H. Homer, although other phosphors can be used.
- the ballmill was then washed with 50 ml. each of ethyl acetate, butyl acetate and methyl Cellosolve acetate and ml. of Tolvol which were then added to the phosphor suspension.
- the mixture was then applied by spraying over the conductive layer 2 of a piece of glass 1, so that the coating 3 had a weight of approximately 0.1 gram per square inch of surface.
- the coated glass was then allowed to air dry for one hour, allowing evaporation of a larger portion of the solvents. After air drying, the piece was baked at a temperature of approximately for 15 minutes.
- the coated glass was then placed in a vacuum bell-jar and a thin layer 4 of aluminum applied over the phosphor-resin coating 3 by evaporation.
- the lamp was then heated in an ambient temperature of F. for 30 minutes with a voltage of 450 volts, 60 cycles per second, A. C., connected between the conducting surface 2 and the metal coating 4. The lamp was then cooled.
- the first lamp in the above list had a dielectricphosphor layer about 2 mils thick; in the others, the layer was about 4 mils thick.
- the heat and voltage may be applied before or after the normal baking of the phosphor-dielectric layer in manufacture.
- the treatment can be used with lamps using various plastic dielectric materials, including glass, melamine-alkyds, epoxy resins (Shell Chemical Co.), and others of both the thermoplastic and thermosetting types, although the latter is preferable.
- the following test shows the effect of the voltage applied during the heating period, the measurements being made at 600 volts after the lamp had cooled.
- the heating period was 30 minutes at 180 F. at both voltages shown, and the Initial readings were taken before the heat was applied at 600 volts.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Electroluminescent Light Sources (AREA)
Description
Dec. 27, 1955 w, c, LE ETAL 2,728,870
ELECTROLUMINESCENT LAMP Filed Sept. 20, 1952 HEA T/NG VOLTAGE APPL/CAT/ON COOL IIVG INVENTORS: WARREN C. GUNGLE ROBERT E. CLEARY ATTORNEY United States Patent ELECTROLUMINESCENT LAMP Warren Calvin Gungle, Peabody, and Robert Emmett Cleary, Danvers, Mass, assignors to Sylvania Electr1c Products Inc., Salem, Mass, a corporation of Massachusetts Application September 20, 1952, Serial No. 310,612
4 Claims. (Cl. 313108) The present invention relates to electroluminescent lamps, that is to lamps 1n which light is produced by electrical excitation of a phosphor.
Such lamps have two spaced electrodes, between which are electroluminescent phosphor particles suspended or embedded in a dielectric material. Plastic materials are generally used as the embedding dielectric. We have found that when the plastic dielectric in such a lamp is heated to a temperature above its softening point but below its decomposition point, andvoltage below the breakdown voltage of the lamp is applied to the lamp while the plastic dielectric is so heated, a remarkable increase in brightness of the lamp and decrease of current through the lamp will be found during its subsequent operation.
The phosphor particles are longer in one dimension than in another, and the heating of the plastic allows the phosphor particles embedded therein sufiicient freedom of motion to allow them to line up in the direction of the field when voltage is applied to the electrodes. When the dielectric constant of the embedding material is smaller than that of phosphor particle, as is the case with most plastics, the field in the phosphor particles will be a maximum when the particles are aligned in the direction of the field, and will be a minimum when it is aligned in a direction transverse to the field.
The simultaneous application of heat and voltage lines up the particles in the direction of the field, and they are set in that position when the phosphor cools. The application also tends to break up any agglomerates present into separate phosphor particles.
When a soft dielectric substance such as nitrocellulose is used as the embedding medium, the phosphor particles may actually move around in the dielectric material as the field is varied and reversed, as on alternating current, for example. Such continued motion of the particles is undesirable. The use of fairly hard plastic, which holds the phosphor particles rigidly in place, such as the thermosetting resins for example, will keep the particles lined up properly after they are once oriented by the field in the above-described manner. However, some advantage is obtained by our invention even when the dielectric is of the cellulose type.
Other objects, features and advantages of the invention will be apparent from the following specification, taken in connection with the accompanying drawings, in which Fig. 1 shows a view, partly in section, of one embodiment of the invention, and Fig. 2 is a box diagram showing the sequence of steps in the process of one embodiment of the invention.
In Fig. 1, the glass plate 1 carries a transparent conductive coating 2, over which is the coating 3 of phosphor particles embedded in a dielectric material, with a metal coating 4 over at least part of said phosphor-dielectric coating 3 and out of electrical contact with said conductive coating 2.
The transparent conductive coating can be of stannous chloride, applied as in copending application Serial Num- 2,728,870 Patented Dec. 27, 1955 her 120,398, filed October 8, 1949, by Eric L. Mager, now Patent No. 2,624,857, although other transparent conductive coatings can be used. The metal coating 4 is of aluminum, although other metals can be used, and is applied as in the copending Mager application.
The phosphor suspended in the dielectric material was zinc sulphide containing small amounts of lead, copper and chlorine for activation, as shown in copending application, Serial Number 230,713, filed June 8, 1951, by Keith H. Butler and Horace H. Homer, although other phosphors can be used.
160 grams of phosphor powder, having particles whose average dimension is about 10 microns, was ground for one hour in a quart ballmill together with 28 grams of a vinyl chloride-acetate copolymer known commercially as VAGH resin, in a 10% solution by weight of methyl ethyl ketone and butyl acetate. The ketone and acetate were in proportion by weight of 1 to 9. This mixture was milled for one hour.
After milling the above suspension 72 grams of a 55% solution by weight of melamine formaldehyde resin inbutanol and 196 grams of a 50% solution by weight of soya-modified alkyd resin in xylol was added to the above suspension.
The ballmill was then washed with 50 ml. each of ethyl acetate, butyl acetate and methyl Cellosolve acetate and ml. of Tolvol which were then added to the phosphor suspension.
The mixture was then applied by spraying over the conductive layer 2 of a piece of glass 1, so that the coating 3 had a weight of approximately 0.1 gram per square inch of surface. The coated glass was then allowed to air dry for one hour, allowing evaporation of a larger portion of the solvents. After air drying, the piece was baked at a temperature of approximately for 15 minutes. The coated glass was then placed in a vacuum bell-jar and a thin layer 4 of aluminum applied over the phosphor-resin coating 3 by evaporation.
The lamp was then heated in an ambient temperature of F. for 30 minutes with a voltage of 450 volts, 60 cycles per second, A. C., connected between the conducting surface 2 and the metal coating 4. The lamp was then cooled.
The results of tests on several such lamps are given below, the current being given in milliamperes and the surface brightness in footlamberts. The applied voltage was 600 volts, 60 cycles per second, alternating current, in each case. Current readings under such conditions are shown only for three of the lamps, but brightness read- The above shows that the current is reduced and the brightness increased by the treatment.
The first lamp in the above list had a dielectricphosphor layer about 2 mils thick; in the others, the layer was about 4 mils thick.
The heat and voltage may be applied before or after the normal baking of the phosphor-dielectric layer in manufacture. The treatment can be used with lamps using various plastic dielectric materials, including glass, melamine-alkyds, epoxy resins (Shell Chemical Co.), and others of both the thermoplastic and thermosetting types, although the latter is preferable.
The following test shows the effect of the voltage applied during the heating period, the measurements being made at 600 volts after the lamp had cooled. The heating period was 30 minutes at 180 F. at both voltages shown, and the Initial readings were taken before the heat was applied at 600 volts.
Table 2 Current, Mil- Brightness,
Iiamperes Footlamberts Initial... 10.0 5.0 200 volts 8. 5 5. 2 450 volts 6. 6.0
2. The lamp of claim 1, in which the material of the dielectric is hard enough to maintain the particles in alignment against the action of the electric field during operation.
3. The combination of claim 1, in which the dielectric is a thermosetting plastic.
4. The method of increasing the brightness of electroluminescent lamps having a layer of electroluminescent phosphor particles in a plastic dielectric medium, said electroluminescent phosphor particles being longer in one dimension than in another, said method comprising heating the plastic to a temperature above its softening point but below its decomposition point, and simultaneously applying to the plastic, an electric field in the same direction as the operating field and of sufiicient strength to align the particles in its own direction, and then cooling the plastic While the particles are aligned so that the plastic will set and hold the particles rigidly in their aligned position.
References Cited in the file of this patent UNITED STATES PATENTS 2,559,279 Charles July 3, 1951 2,566,349 Mager Sept. 4, 1 2,624,857 Mager Jan. 6, 1953 OTHER REFERENCES G. Destriau: New Phenomenon of Electrophotoluminescence Philosophical Mag, vol. 38, 1947, pp. 700-702, 7ll-7l3 and 723 (copy in Sci. Library).
Claims (1)
1. AN ELECTROLUMINESCENT LAMP COMPRISING TWO ELECTRODES AND A LAYER THEREBETWEEN OF ELECTROLUMINESCENT PHOSPHOR PARTICLES EMBEDDED IN A SOLID DIELECTRIC, THE ELECTROLUMINESCENT PHOSPOR PARTICLES BEING ALIGNED IN THE DIRECTION IN WHICH A FIELD WOULD BE PRODUCED BY THE APPLICATION OF VOLTAGE BETWEEN SAID ELECTRODES.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US310612A US2728870A (en) | 1952-09-20 | 1952-09-20 | Electroluminescent lamp |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US310612A US2728870A (en) | 1952-09-20 | 1952-09-20 | Electroluminescent lamp |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2728870A true US2728870A (en) | 1955-12-27 |
Family
ID=23203322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US310612A Expired - Lifetime US2728870A (en) | 1952-09-20 | 1952-09-20 | Electroluminescent lamp |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2728870A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2824992A (en) * | 1955-01-17 | 1958-02-25 | Sylvania Electric Prod | Electroluminescent lamp |
| US2840741A (en) * | 1954-11-01 | 1958-06-24 | Westinghouse Electric Corp | Electroluminescent cell |
| US2872567A (en) * | 1954-12-24 | 1959-02-03 | Thorn Electrical Ind Ltd | Instrument panel illuminator |
| US2887601A (en) * | 1956-08-01 | 1959-05-19 | Itt | Polarized electroluminescent phosphors and dielectrics |
| US2915661A (en) * | 1953-02-19 | 1959-12-01 | Westinghouse Electric Corp | Color television screen |
| US2964666A (en) * | 1956-09-21 | 1960-12-13 | Philips Corp | Electroluminescent element |
| US2991384A (en) * | 1957-07-16 | 1961-07-04 | Sylvania Electric Prod | Electroluminescent device |
| US3008065A (en) * | 1958-02-26 | 1961-11-07 | Ncr Co | Electroluminescent indicators |
| US3040201A (en) * | 1960-03-03 | 1962-06-19 | Westinghouse Electric Corp | Method of processing electroluminescent phosphor and electroluminescent device |
| US3178580A (en) * | 1959-07-02 | 1965-04-13 | Ibm | Means for producing radiation induced electroluminescence |
| US3214635A (en) * | 1962-04-10 | 1965-10-26 | Westinghouse Electric Corp | Information display screen |
| US3341915A (en) * | 1963-02-19 | 1967-09-19 | Westinghouse Electric Corp | Method of manufacturing electroluminescent lamps |
| US3883743A (en) * | 1973-12-13 | 1975-05-13 | Rudolf J Hradcovsky | Film negative display system |
| US4240992A (en) * | 1978-04-03 | 1980-12-23 | Westinghouse Electric Corp. | Technique for fabricating radiation sensitive dosimeters |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2559279A (en) * | 1947-03-27 | 1951-07-03 | Cie Generale De T S F | Manufacture of electroluminescent screens |
| US2566349A (en) * | 1950-01-28 | 1951-09-04 | Sylvania Electric Prod | Electroluminescent lamp |
| US2624857A (en) * | 1949-10-08 | 1953-01-06 | Sylvania Electric Prod | Electroluminescent lamp |
-
1952
- 1952-09-20 US US310612A patent/US2728870A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2559279A (en) * | 1947-03-27 | 1951-07-03 | Cie Generale De T S F | Manufacture of electroluminescent screens |
| US2624857A (en) * | 1949-10-08 | 1953-01-06 | Sylvania Electric Prod | Electroluminescent lamp |
| US2566349A (en) * | 1950-01-28 | 1951-09-04 | Sylvania Electric Prod | Electroluminescent lamp |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2915661A (en) * | 1953-02-19 | 1959-12-01 | Westinghouse Electric Corp | Color television screen |
| US2840741A (en) * | 1954-11-01 | 1958-06-24 | Westinghouse Electric Corp | Electroluminescent cell |
| US2872567A (en) * | 1954-12-24 | 1959-02-03 | Thorn Electrical Ind Ltd | Instrument panel illuminator |
| US2824992A (en) * | 1955-01-17 | 1958-02-25 | Sylvania Electric Prod | Electroluminescent lamp |
| US2887601A (en) * | 1956-08-01 | 1959-05-19 | Itt | Polarized electroluminescent phosphors and dielectrics |
| US2964666A (en) * | 1956-09-21 | 1960-12-13 | Philips Corp | Electroluminescent element |
| US2991384A (en) * | 1957-07-16 | 1961-07-04 | Sylvania Electric Prod | Electroluminescent device |
| US3008065A (en) * | 1958-02-26 | 1961-11-07 | Ncr Co | Electroluminescent indicators |
| US3178580A (en) * | 1959-07-02 | 1965-04-13 | Ibm | Means for producing radiation induced electroluminescence |
| US3040201A (en) * | 1960-03-03 | 1962-06-19 | Westinghouse Electric Corp | Method of processing electroluminescent phosphor and electroluminescent device |
| US3214635A (en) * | 1962-04-10 | 1965-10-26 | Westinghouse Electric Corp | Information display screen |
| US3341915A (en) * | 1963-02-19 | 1967-09-19 | Westinghouse Electric Corp | Method of manufacturing electroluminescent lamps |
| US3883743A (en) * | 1973-12-13 | 1975-05-13 | Rudolf J Hradcovsky | Film negative display system |
| US4240992A (en) * | 1978-04-03 | 1980-12-23 | Westinghouse Electric Corp. | Technique for fabricating radiation sensitive dosimeters |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2728870A (en) | Electroluminescent lamp | |
| US3173050A (en) | Electroluminescent cell | |
| US2566349A (en) | Electroluminescent lamp | |
| US3172862A (en) | Organic electroluminescent phosphors | |
| US2755406A (en) | Electroluminescent lamp | |
| US2721950A (en) | Electroluminescent cell | |
| US2880346A (en) | Electroluminescent device | |
| US3205393A (en) | Electroluminescent lamp with a dielectric reflective material | |
| US2937353A (en) | Photoconductive devices | |
| US3274024A (en) | Energy converter | |
| US3059118A (en) | Light amplification and storage device | |
| US2709765A (en) | Electroluminescent structure | |
| US3350610A (en) | Electric charge storage elements | |
| US2894854A (en) | Electroluminescent device | |
| US3149281A (en) | Electroluminescent voltage measuring device | |
| US3015036A (en) | Image storage device | |
| US3580738A (en) | Plastics materials with conductive surfaces | |
| US2964666A (en) | Electroluminescent element | |
| US2847386A (en) | Electroluminescent materials | |
| US2921218A (en) | Electroluminescent devices | |
| US3185650A (en) | Phosphor-dielectric composition | |
| US3104339A (en) | Electroluminescent device | |
| US2878394A (en) | Light amplifier and storage device | |
| US3242368A (en) | Low-voltage hole-injection electroluminescence in cadmium sulphide | |
| US2755400A (en) | Electroluminescent lamp |