US2622221A - Fluorescent discharge lamp - Google Patents

Fluorescent discharge lamp Download PDF

Info

Publication number
US2622221A
US2622221A US630339A US63033945A US2622221A US 2622221 A US2622221 A US 2622221A US 630339 A US630339 A US 630339A US 63033945 A US63033945 A US 63033945A US 2622221 A US2622221 A US 2622221A
Authority
US
United States
Prior art keywords
fluorescent
light
mercury
gas
xenon
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
Application number
US630339A
Inventor
Norman C Beese
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CBS Corp
Original Assignee
Westinghouse Electric Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Westinghouse Electric Corp filed Critical Westinghouse Electric Corp
Priority to US630339A priority Critical patent/US2622221A/en
Application granted granted Critical
Publication of US2622221A publication Critical patent/US2622221A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00Gas-discharge or vapour-discharge lamps
    • H01J61/02Details
    • H01J61/12Selection of substances for gas fillings; Specified operating pressure or temperature
    • H01J61/16Selection of substances for gas fillings; Specified operating pressure or temperature having helium, argon, neon, krypton, or xenon as the principle constituent
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00Gas-discharge or vapour-discharge lamps
    • H01J61/70Lamps with low-pressure unconstricted discharge having a cold pressure < 400 Torr
    • H01J61/76Lamps with low-pressure unconstricted discharge having a cold pressure < 400 Torr having a filling of permanent gas or gases only

Definitions

  • This invention relates to fluorescent discharge lamps and, more particularly, to such employing only mixtures of rare gases as the filling material.
  • the principal object of my invention is to produce a fluorescent lamp having a filling of a mixture of rare gases of such a composition that fluorescence is efficiently excited in the phosphor.
  • Another object of my invention is to produce a fluorescent discharge lamp comprising a mixture of rare gases in which either helium or neon is selected as a carrying gas to make it possible to get good elciency at practical pressures, and either krypton or Xenon is selected to determine the intensity of the light generated by increasing the amounts of fluorescent-exciting radiations produced by the mixture.
  • a further object of my invention is to produce a iluorescent lamp which has such characteristics that as the gas cleans up during life the generated light may increase, compensating for losses, including that of phosphor efficiency, whereby a practically constant output is obtained.
  • Fig. 1 is a graph showing the variation in fluorescent light output from manganese-activated zinc silicate as a function of the gas pressure in the pure rare gases helium, neon, argon, krypton and xenon.
  • Fig. 2 is a graph showing the increase in maximum iiuorescent light from a manganese-activated zinc silicate phosphor with increasing atomic number or atomic weight of the exciting gas.
  • Fig. 3 is a graph showing the amount of rare gas in percentage which should be added to helium to produce a nat fluorescent response over a large pressure range.
  • Fig. 4 is a graph showing the light produced by a fluorescent lamp having a phosphor of manganese-activated zinc silicate excited by various argon-helium gas mixtures.
  • Fig. 5 is a graph similar to Fig. li, but showing the light so produced when employing various krypton-helium gas mixtures.
  • Fig. 6 is a graph similar to Fig. 4, but showing the light so generated when using various xenonhelium gas mixtures.
  • Fig. '7 is a graph similar to Fig. 4 but showing the light so generated when using various krypton-neon gas mixtures.
  • mercury vapor is commercially employed for the generation of radiations which excite phosphors to give off visible radiations in fluorescent discharge lamps.
  • This material has many inherent properties that make it well suited for that purpose. Important ones are the ecient production of useful ultra-violet radiations, the high quantum utilization of the energy of such in exciting phosphors, the fact that it has a suitable vapor pressure at room temperature, lasting indenitely and giving a cool operating lamp of relatively low intrinsic brightness, that its glow does not seriously affect the color of the resultant light, that phosphors are available to produce almost any desired color using such vapor, and its ease to use in the manufacture of practical commercial lamps.
  • the light from such a device depends upon the ecient production of ultra-violet resonance radiations from the mercury vapor, and its efficient utilization by the phosphor. It is possible to convert approximately half the wattage into useful ultra-violet radiations at 2537 A. U. This energy can be utilized by suitable phosphors with nearly 100% quantum conversion.
  • all lamps utilizing mercury vapor are temperature-dependent and require, for best results, an envelope temperature which is between 40 and C. While this is an easy requirement in designing a lamp for normal room-temperature operation, it prevents fluorescent lamps from being used outdoors in cold climates, or any place where the ambient is abnormally low. This is one of the most serious defects inherent in such lamps.
  • inert gases such as helium, neon, argon, krypton and xenon
  • inert gases such as helium, neon, argon, krypton and xenon
  • the discharge tube with the phosphor-coated plate within it was evacuated as a normal lamp and then various gaseous mixtures and gases ad mitted. 'Ihe electrodes were heated during all measurements. Most of the time, alternating current of -about 100 milliamperes was used.
  • Fig. 1 shows the relationship between the uorescent light derived from such phosphor, when excited by the ve rare gases mentioned, from pressures ranging from a small fr ction of a millimeter oi mercury to more milli meters.
  • the data for the curves there illustrated was taken by maintaining a uniform alternati. ff current of 100 milliamperes through the discharge tube. It will be seen that xenon is the most eincient of the gases and that it, Krypton and argon, have their maximum efficiencies at pressures well below 1/2 millimeter, while neon and helium have their maximum efciencies at considerably higher pressures.
  • Fig. 2 shows the increase in maximum fluorescent light from such a phosphor with increasing atomic number of the exciting gas or vapor.
  • the wave lengths of the resonant radiations of the rare gases and mercury Vapor also increases with atomic weight to 2537 AU. for mercury.
  • Fig. 4 shows that with a mixture of 6.9% argon in helium, lthe variation in fluorescent light is small over a pressure range from about l to 3 millimeters of mercury.
  • This gure also shows the variation in fluorescent light with other selected gas compositions over considerable pressure ranges, as Well as showing the increase in light by the addition of that from the rare gases for two mixtures of the gases employed.
  • Fig. 5 shows the situation when lrrypton gas is diluted with helium, to maintain the relatively high output of krypton to a total gas pressure of several millimeters.
  • This gure shows that with a mixture of 3.8% Krypton in helium, a nearly constant intensity of fluorescent light is derived from a manganese-activated zinc silicate phosphor over a pressure range of l to 3 millimeters of mercury.
  • the uorescent light is almost as great as the maximum value obtained from lrrypton alone, while the contribution ci light from the rare gas is much less than that produced by helium alone.
  • the optimum effect is restricted to certain gas ratios of percentage compositions, as will be seen by comparing the 3.8% krypton curves with the other curves illustrated.
  • Fig. 6 shows a set of curves for xenon-helium gas mixtures, corresponding with those of Fig. 5 for Krypton-helium gas mixtures. This figure, however, shows that the optimum percentage of xenon is between 2 and 21/2% rather than about 4%, while the optimum pressure ci the mixture is between 1 and 2 mm. of mercury.
  • Fig. 7 shows the fluorescent light from a manganese-activated zinc silicate phosphor excited by two Krypton-neon gas mixtures.
  • a 9.2% krypton, 90.8% neon mixture there is an almost constant ratio of fluorescent light to total light over an extended range of pressures, although the total light is not constant.
  • the fluorescent output is quite constant over a considerable pressure range, but the contribution from neon increases very rapidly with decreasing pressures, so the result in color is greatly aiected by gas pressure.
  • a fluorescent discharge lamp comprising a transparent envelope phosphor-coated on its interior surface and containing, as a lling, a mixture of only rare gases consisting of helium and xenon, the total pressure of the mixture being between 1/2 mm. and 3 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%.
  • a uorescent discharge lamp comprising a transparent envelope coated on its interior surface with a phosphor consisting of manganeseactivated zinc silicate and containing, as a filling, a. mixture of only rare gases consisting of helium and xenon, the total pressure of the mixture being between 1/2 mm. and 3 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%.
  • a fluorescent discharge lamp comprising a transparent envelope phosphor-coated on its interior surface and containing, as a lling, a mixture of only rare gases consisting of helium as the carrying gas and xenon as the light-intensitydetermining gas, the total pressure of the mixture being between 1 and 2 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%, so that when the lamp operates said xenon generates radiation at its resonance frequency and eiciently activates the phosphor.

Description

N. C. BEESE FLUORESCENT DISCHARGE L AMP Dec. 16, 1952 2 Sl-iEETS--SI-IEET 2 Filed Nov. 23, 1945 Rw Y. 7. mf. m R V m M l B s m M W H K -P m M m m M 0 r IW m r r @w ,M U m n www Patented Dec. 16, 1952 FLUORESCENT DISCHARGE LAMP Norman C. Beese, Verona, N. J., assignor to Westinghouse Electric Corporation, East Pittsburgh, Pa., a corporation of Pennsylvania Application November 23, 1945, Serial No. 630,339
3 Claims.
This invention relates to fluorescent discharge lamps and, more particularly, to such employing only mixtures of rare gases as the filling material.
The principal object of my invention, generally considered, is to produce a fluorescent lamp having a filling of a mixture of rare gases of such a composition that fluorescence is efficiently excited in the phosphor.
Another object of my invention is to produce a fluorescent discharge lamp comprising a mixture of rare gases in which either helium or neon is selected as a carrying gas to make it possible to get good elciency at practical pressures, and either krypton or Xenon is selected to determine the intensity of the light generated by increasing the amounts of fluorescent-exciting radiations produced by the mixture.
A further object of my invention is to produce a iluorescent lamp which has such characteristics that as the gas cleans up during life the generated light may increase, compensating for losses, including that of phosphor efficiency, whereby a practically constant output is obtained.
Other objects and advantages of the invention will become apparent as the description proceeds.
Referring to the drawing:
Fig. 1 is a graph showing the variation in fluorescent light output from manganese-activated zinc silicate as a function of the gas pressure in the pure rare gases helium, neon, argon, krypton and xenon.
Fig. 2 is a graph showing the increase in maximum iiuorescent light from a manganese-activated zinc silicate phosphor with increasing atomic number or atomic weight of the exciting gas.
Fig. 3 is a graph showing the amount of rare gas in percentage which should be added to helium to produce a nat fluorescent response over a large pressure range.
Fig. 4 is a graph showing the light produced by a fluorescent lamp having a phosphor of manganese-activated zinc silicate excited by various argon-helium gas mixtures.
Fig. 5 is a graph similar to Fig. li, but showing the light so produced when employing various krypton-helium gas mixtures.
Fig. 6 is a graph similar to Fig. 4, but showing the light so generated when using various xenonhelium gas mixtures.
Fig. '7 is a graph similar to Fig. 4 but showing the light so generated when using various krypton-neon gas mixtures.
As is well known, mercury vapor is commercially employed for the generation of radiations which excite phosphors to give off visible radiations in fluorescent discharge lamps. This material has many inherent properties that make it well suited for that purpose. Important ones are the ecient production of useful ultra-violet radiations, the high quantum utilization of the energy of such in exciting phosphors, the fact that it has a suitable vapor pressure at room temperature, lasting indenitely and giving a cool operating lamp of relatively low intrinsic brightness, that its glow does not seriously affect the color of the resultant light, that phosphors are available to produce almost any desired color using such vapor, and its ease to use in the manufacture of practical commercial lamps.
The light from such a device depends upon the ecient production of ultra-violet resonance radiations from the mercury vapor, and its efficient utilization by the phosphor. It is possible to convert approximately half the wattage into useful ultra-violet radiations at 2537 A. U. This energy can be utilized by suitable phosphors with nearly 100% quantum conversion. However, all lamps utilizing mercury vapor are temperature-dependent and require, for best results, an envelope temperature which is between 40 and C. While this is an easy requirement in designing a lamp for normal room-temperature operation, it prevents fluorescent lamps from being used outdoors in cold climates, or any place where the ambient is abnormally low. This is one of the most serious defects inherent in such lamps.
Many investigations have been carried out in an endeavor to use inert gases, such as helium, neon, argon, krypton and xenon, as a substitute for mercury vapor in exciting phosphors within a discharge lamp. It is known that most of the fluorescent light given olf by phosphors is that caused by resonant radiation, which can be produced more efficiently than any other type of ultra-Violet radiation. It has been estimated that no more than 30% of the energy supplied to a neon discharge lamp is converted to the neon resonance radiation at 740 A. U. This value is appreciably below that for mercury vapor, which utilizes about 50% of the wattage supplied to the lamp. Hence, the maximum theoretical efficiency of fluorescent light produced by neon resonance radiation is below that for mercury vapor at suitable temperatures, but neon and other rare gases are not dependent on relatively high temperatures for their efficient operation..
In accordance with my work on the development of a mercury-free fluorescent lamp, I have investigated the response of many phosphors to various inert gases and mixtures in a similar manner in a positive-column discharge lamp, that is, one with a transparent glass envelope and containing fluorescent material as a coating on its interior surface. Most of the work was done with a special lamp in which a glass plate 7/8 wide and 10" long, coated with patches of different uorescent materials, each about '7/8 sq., was placed. The fluorescent powders were mixed with a nitro-cellulose binder, painted on the glass plate, and when dry the plate was baked in air yat over 500 C. to remove the binder. This simulated the phosphor coating in a fluorescent lamp. The discharge tube with the phosphor-coated plate within it was evacuated as a normal lamp and then various gaseous mixtures and gases ad mitted. 'Ihe electrodes were heated during all measurements. Most of the time, alternating current of -about 100 milliamperes was used.
Light measurements were made with a telescope 21/2 in diameter and 10 long, using a hand magnifier to form an image of the fluorescent patches on 4a Lange photovoltaic cell iitted with an eye-sensitivity filter. A telescope was moved along a horizontal bar parallel to the nuorescent plate so that the various phosphors could be measured. The cell was removable from the telescope so that each spot could be centered with a ground-glass screen. One of the patches was aluminum oxide which did not fluoresce and was used to correct for the visible light of the discharge. galvanometer shunted with a resistance box, so that `a greater range of intensities could be measured. The final results were calculated on the basis of a 500 ohm galvanometer shunt resistance. After completing the work with the rare gases, mercury vapor was distilled into the tube so as to have a direct comparison with mercury resonance excitation. I have found that manganese-activated zinc silicate gives the best response to resonant radiations from the rare f gases and mixtures.
Fig. 1 shows the relationship between the uorescent light derived from such phosphor, when excited by the ve rare gases mentioned, from pressures ranging from a small fr ction of a millimeter oi mercury to more milli meters. The data for the curves there illustrated was taken by maintaining a uniform alternati. ff current of 100 milliamperes through the discharge tube. It will be seen that xenon is the most eincient of the gases and that it, Krypton and argon, have their maximum efficiencies at pressures well below 1/2 millimeter, while neon and helium have their maximum efciencies at considerably higher pressures. The relationship between the maximum output of the rare gases argon, krypton and xenon, as compared with mercury is further illustrated by Fig. 2, which shows the increase in maximum fluorescent light from such a phosphor with increasing atomic number of the exciting gas or vapor. The wave lengths of the resonant radiations of the rare gases and mercury Vapor also increases with atomic weight to 2537 AU. for mercury.
As in the case of mercury vapor, which has its maximum eciency at a pressure oi a few microns and which efliciency may be maintained by diluting it with rare gas at several millimeters pressure, I have found that by diluting one of the gases such as argon, krypton and xenon, with The photronic cell was connected to a 'l one of the gases helium and neon, it is possible to maintain the relatively high output of the gas selected from the rst three with a total gas pressure of from one to several millimeters. Such a phenomenon is shown graphically in Fig. 3 which indicates that about '7% of argon, about 4% Krypton, or about 2% of xenon, should be added to heiium to give a flat fluorescent response over a large pressure range.
The development of this information is illustrated in Fig. 4, which shows that with a mixture of 6.9% argon in helium, lthe variation in fluorescent light is small over a pressure range from about l to 3 millimeters of mercury. This gure also shows the variation in fluorescent light with other selected gas compositions over considerable pressure ranges, as Well as showing the increase in light by the addition of that from the rare gases for two mixtures of the gases employed.
Fig. 5 shows the situation when lrrypton gas is diluted with helium, to maintain the relatively high output of krypton to a total gas pressure of several millimeters. This gure shows that with a mixture of 3.8% Krypton in helium, a nearly constant intensity of fluorescent light is derived from a manganese-activated zinc silicate phosphor over a pressure range of l to 3 millimeters of mercury. The uorescent light is almost as great as the maximum value obtained from lrrypton alone, while the contribution ci light from the rare gas is much less than that produced by helium alone. The optimum effect is restricted to certain gas ratios of percentage compositions, as will be seen by comparing the 3.8% krypton curves with the other curves illustrated.
Fig. 6 shows a set of curves for xenon-helium gas mixtures, corresponding with those of Fig. 5 for Krypton-helium gas mixtures. This figure, however, shows that the optimum percentage of xenon is between 2 and 21/2% rather than about 4%, while the optimum pressure ci the mixture is between 1 and 2 mm. of mercury.
Fig. 7 shows the fluorescent light from a manganese-activated zinc silicate phosphor excited by two Krypton-neon gas mixtures. With a 9.2% krypton, 90.8% neon mixture, there is an almost constant ratio of fluorescent light to total light over an extended range of pressures, although the total light is not constant. With .4% krypton and 99.6% neon, the fluorescent output is quite constant over a considerable pressure range, but the contribution from neon increases very rapidly with decreasing pressures, so the result in color is greatly aiected by gas pressure.
For comparison, mercury was distilled into the lamp after completing the work with the rare gases and mixtures. The efficiency in total fiuorescent light was always greater with mercury excitation than with rare gas excitation. To obtain a pink fluorescent light, it might be desirable to use neon gas to excite the phosphor, since its orange-red color could be utilized and the efiiciency of such a lamp would be quite comparable with a mercury-activated lamp giving a similar color. I have also found that the light given of by a phosphor when excited by various ultra-violet sources is very dependent upon chemical composition, the degree of purity, the amount of activator, and the physical processes through which it has passed.
Although preferred embodiments oi my invention have been disclosed, it will be understood that modifications may be made within the spirit and scope of the appended claims, and that the phosphor or fluorescent mattei' reported in accordance with the specication was always manganese-activated zinc silicate in order to make for consistent comparisons.
I claim:
1. A fluorescent discharge lamp comprising a transparent envelope phosphor-coated on its interior surface and containing, as a lling, a mixture of only rare gases consisting of helium and xenon, the total pressure of the mixture being between 1/2 mm. and 3 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%.
2. A uorescent discharge lamp comprising a transparent envelope coated on its interior surface with a phosphor consisting of manganeseactivated zinc silicate and containing, as a filling, a. mixture of only rare gases consisting of helium and xenon, the total pressure of the mixture being between 1/2 mm. and 3 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%.
3. A fluorescent discharge lamp comprising a transparent envelope phosphor-coated on its interior surface and containing, as a lling, a mixture of only rare gases consisting of helium as the carrying gas and xenon as the light-intensitydetermining gas, the total pressure of the mixture being between 1 and 2 mm. of mercury, and the percentage, by volume, of the xenon ranging from 2 to 21/2%, so that when the lamp operates said xenon generates radiation at its resonance frequency and eiciently activates the phosphor.
NORMAN C. BEESE.
REFERENCES CITED The following references are of record in the le of this patent:
UNITED STATES PATENTS Number Name Date 1,882,609 Howe Oct. 11, 1932 1,949,069 Balear Feb. 27, 1934 1,977,688 Miesse Oct. 23, 1934 2,135,732 Randall et al Nov. 8, 1938 2,207,174 Jenkins July 9, 1940 2,346,522 Gessel Apr. 11, 1944 2,351,270 Lemmers June 13, 1944 2,374,677 Goldstein et al May 1, 1945 2,409,769 Leyshon Oct. 22, 1946 2,476,616 Morehead July 19, 1949

Claims (1)

1. A FLUORESCENT LAMP COMPRISING A TRANSPARENT ENVELOPE PHOSPHOR-COATED ON ITS INTERIOR SURFACE AND CONTAINING, AS A FILLING, A MIXTURE OF ONLY RARE GASES CONSISTING OF HELIUM AND XENON, THE TOTAL PRESSURE OF THE MIXTURE BEING BETWEEN 1/2 MM. AND 3 MM. OF MERCURY, AND THE PERCENTAGE, BY VOLUME, OF THE XENON RANGING FROM 2 TO 2 1/2%.
US630339A 1945-11-23 1945-11-23 Fluorescent discharge lamp Expired - Lifetime US2622221A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US630339A US2622221A (en) 1945-11-23 1945-11-23 Fluorescent discharge lamp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US630339A US2622221A (en) 1945-11-23 1945-11-23 Fluorescent discharge lamp

Publications (1)

Publication Number Publication Date
US2622221A true US2622221A (en) 1952-12-16

Family

ID=24526774

Family Applications (1)

Application Number Title Priority Date Filing Date
US630339A Expired - Lifetime US2622221A (en) 1945-11-23 1945-11-23 Fluorescent discharge lamp

Country Status (1)

Country Link
US (1) US2622221A (en)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2802129A (en) * 1952-08-21 1957-08-06 Westinghouse Electric Corp Low pressure fluorescent and discharge lamps
US2966602A (en) * 1956-06-27 1960-12-27 Sylvania Electric Prod High output fluorescent lamp
US2976448A (en) * 1959-02-26 1961-03-21 Egyesuelt Izzolampa Fluorescent lamp
US3012165A (en) * 1959-05-11 1961-12-05 Gen Electric Fluorescent lamp gas filling
US3052813A (en) * 1959-06-30 1962-09-04 Sylvania Electric Prod Helium-argon lamp
US3444415A (en) * 1965-12-10 1969-05-13 Microdot Inc Fluorescent discharge lamp
US3536945A (en) * 1966-02-14 1970-10-27 Microdot Inc Luminescent gas tube including a gas permeated phosphor coating
US3814971A (en) * 1973-03-01 1974-06-04 Gen Electric Fill gas mixture for glow lamps
US4000436A (en) * 1973-05-31 1976-12-28 Dai Nippon Toryo Co., Ltd. Gaseous discharge luminous device
US4027191A (en) * 1970-12-16 1977-05-31 Schaufele Robert F Phosphor geometry for color displays from a multiple gaseous discharge display/memory panel
US4032813A (en) * 1974-08-19 1977-06-28 Duro-Test Corporation Fluorescent lamp with reduced wattage consumption having electrode shield with getter material
US4032814A (en) * 1974-08-19 1977-06-28 Duro-Test Corporation Fluorescent lamp with reduced wattage consumption
US4039889A (en) * 1976-02-25 1977-08-02 General Electric Company Blue-white glow lamp
US4107571A (en) * 1973-10-22 1978-08-15 Hitachi, Ltd. Light emitting device having luminescent screen with self activated blue light emitting phosphor
US4171501A (en) * 1973-10-22 1979-10-16 Hitachi, Ltd. Light emitting devices based on the excitation of phosphor screens
FR2441920A1 (en) * 1978-11-17 1980-06-13 Philips Nv LOW PRESSURE MERCURY VAPOR DISCHARGE LAMP
US4731560A (en) * 1970-08-06 1988-03-15 Owens-Illinois Television Products, Inc. Multiple gaseous discharge display/memory panel having improved operating life
US4794308A (en) * 1970-08-06 1988-12-27 Owens-Illinois Television Products Inc. Multiple gaseous discharge display/memory panel having improved operating life
US4882520A (en) * 1987-04-02 1989-11-21 Kabushiki Kaisha Toshiba Rare gas arc lamp having hot cathode
US5159237A (en) * 1987-08-10 1992-10-27 Mitsubishi Denki Kabushiki Kaisha Green-light-emitting rare gas discharge lamp
US5173642A (en) * 1990-06-06 1992-12-22 Mitsubishi Denki Kabushiki Kaisha Rare gas discharge fluorescent lamp device
US5866984A (en) * 1996-02-27 1999-02-02 General Electric Company Mercury-free ultraviolet discharge source
US20050133740A1 (en) * 2003-12-19 2005-06-23 Gardner William G. Variable wavelength ultraviolet lamp

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1882609A (en) * 1928-06-08 1932-10-11 Los Angeles Testing Lab Electroluminous display
US1949069A (en) * 1930-03-29 1934-02-27 Air Reduction Luminescent tube
US1977688A (en) * 1930-03-10 1934-10-23 Gen Scientific Corp Permanent color gaseous conduction tube
US2135732A (en) * 1935-07-30 1938-11-08 Gen Electric Device for producing visible light
US2207174A (en) * 1935-05-30 1940-07-09 Gen Electric Electric discharge lamp
US2346522A (en) * 1942-05-12 1944-04-11 Hartford Nat Bank & Trust Co Fluorescent lamp
US2351270A (en) * 1941-08-01 1944-06-13 Gen Electric Electric discharge device and method of operation
US2374677A (en) * 1943-09-20 1945-05-01 Canadian Radium & Uranium Corp Glow discharge lamp
US2409769A (en) * 1944-07-28 1946-10-22 Sylvania Electric Prod Fluorescent glow lamp
US2476616A (en) * 1943-11-08 1949-07-19 Westinghouse Electric Corp Low-power miniature fluorescent and/or glow lamp

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1882609A (en) * 1928-06-08 1932-10-11 Los Angeles Testing Lab Electroluminous display
US1977688A (en) * 1930-03-10 1934-10-23 Gen Scientific Corp Permanent color gaseous conduction tube
US1949069A (en) * 1930-03-29 1934-02-27 Air Reduction Luminescent tube
US2207174A (en) * 1935-05-30 1940-07-09 Gen Electric Electric discharge lamp
US2135732A (en) * 1935-07-30 1938-11-08 Gen Electric Device for producing visible light
US2351270A (en) * 1941-08-01 1944-06-13 Gen Electric Electric discharge device and method of operation
US2346522A (en) * 1942-05-12 1944-04-11 Hartford Nat Bank & Trust Co Fluorescent lamp
US2374677A (en) * 1943-09-20 1945-05-01 Canadian Radium & Uranium Corp Glow discharge lamp
US2476616A (en) * 1943-11-08 1949-07-19 Westinghouse Electric Corp Low-power miniature fluorescent and/or glow lamp
US2409769A (en) * 1944-07-28 1946-10-22 Sylvania Electric Prod Fluorescent glow lamp

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2802129A (en) * 1952-08-21 1957-08-06 Westinghouse Electric Corp Low pressure fluorescent and discharge lamps
US2966602A (en) * 1956-06-27 1960-12-27 Sylvania Electric Prod High output fluorescent lamp
US2976448A (en) * 1959-02-26 1961-03-21 Egyesuelt Izzolampa Fluorescent lamp
US3012165A (en) * 1959-05-11 1961-12-05 Gen Electric Fluorescent lamp gas filling
US3052813A (en) * 1959-06-30 1962-09-04 Sylvania Electric Prod Helium-argon lamp
US3444415A (en) * 1965-12-10 1969-05-13 Microdot Inc Fluorescent discharge lamp
US3536945A (en) * 1966-02-14 1970-10-27 Microdot Inc Luminescent gas tube including a gas permeated phosphor coating
US4731560A (en) * 1970-08-06 1988-03-15 Owens-Illinois Television Products, Inc. Multiple gaseous discharge display/memory panel having improved operating life
US4794308A (en) * 1970-08-06 1988-12-27 Owens-Illinois Television Products Inc. Multiple gaseous discharge display/memory panel having improved operating life
US4027191A (en) * 1970-12-16 1977-05-31 Schaufele Robert F Phosphor geometry for color displays from a multiple gaseous discharge display/memory panel
US3814971A (en) * 1973-03-01 1974-06-04 Gen Electric Fill gas mixture for glow lamps
US4000436A (en) * 1973-05-31 1976-12-28 Dai Nippon Toryo Co., Ltd. Gaseous discharge luminous device
US4107571A (en) * 1973-10-22 1978-08-15 Hitachi, Ltd. Light emitting device having luminescent screen with self activated blue light emitting phosphor
US4171501A (en) * 1973-10-22 1979-10-16 Hitachi, Ltd. Light emitting devices based on the excitation of phosphor screens
US4032813A (en) * 1974-08-19 1977-06-28 Duro-Test Corporation Fluorescent lamp with reduced wattage consumption having electrode shield with getter material
US4032814A (en) * 1974-08-19 1977-06-28 Duro-Test Corporation Fluorescent lamp with reduced wattage consumption
US4039889A (en) * 1976-02-25 1977-08-02 General Electric Company Blue-white glow lamp
FR2441920A1 (en) * 1978-11-17 1980-06-13 Philips Nv LOW PRESSURE MERCURY VAPOR DISCHARGE LAMP
US4882520A (en) * 1987-04-02 1989-11-21 Kabushiki Kaisha Toshiba Rare gas arc lamp having hot cathode
US5159237A (en) * 1987-08-10 1992-10-27 Mitsubishi Denki Kabushiki Kaisha Green-light-emitting rare gas discharge lamp
US5173642A (en) * 1990-06-06 1992-12-22 Mitsubishi Denki Kabushiki Kaisha Rare gas discharge fluorescent lamp device
US5723952A (en) * 1990-06-06 1998-03-03 Mitsubishi Denki Kabushiki Kaisha Rare gas discharge fluorescent lamp device
US5866984A (en) * 1996-02-27 1999-02-02 General Electric Company Mercury-free ultraviolet discharge source
US20050133740A1 (en) * 2003-12-19 2005-06-23 Gardner William G. Variable wavelength ultraviolet lamp
US7148497B2 (en) 2003-12-19 2006-12-12 Gardner William G Variable wavelength ultraviolet lamp

Similar Documents

Publication Publication Date Title
US2622221A (en) Fluorescent discharge lamp
Kuo et al. A green-emitting phosphor Sr3La (PO4) 3: Ce3+, Tb3+ with efficient energy transfer for fluorescent lamp
JP3714952B2 (en) Dielectric disturbing discharge fluorescent lamp
US3858082A (en) Warm white lamp with normal output and improved color rendition
US5866984A (en) Mercury-free ultraviolet discharge source
Thornton Electroluminescence maintenance
US3839219A (en) Europium activated alkaline earth magnesium aluminium silicate luminescent material
US4085351A (en) Gaseous discharge light emitting element
JP4190995B2 (en) Vacuum ultraviolet-excited ultraviolet phosphor and light emitting device using the same
US2207174A (en) Electric discharge lamp
US6613248B2 (en) Quantum-splitting oxide-based phosphors and method of producing the same
Zhang et al. Luminescence properties of CaZr (PO4) 2: RE (RE= Eu3+, Tb3+, Tm3+) under x-ray and VUV–UV excitation
Kamegaya et al. Basic study on the gas-discharge panel for luminescent color display
US2714682A (en) Low pressure fluorescent and discharge lamps
US4032812A (en) Fluorescent high-pressure mercury-vapor lamp
CN100380569C (en) Dielectric barrier discharge lamp with improved colour reproduction
US2494883A (en) Cascaded fluorescent material
US2802129A (en) Low pressure fluorescent and discharge lamps
JPS5941474B2 (en) gas discharge light emitting device
US4085350A (en) Gaseous discharge light emitting element
JPS5910710B2 (en) gas discharge light emitting device
CN108194844B (en) Deep ultraviolet light source for exciting fluorescent powder by electron beam
JP4272973B2 (en) Vacuum ultraviolet light excited green phosphor material and light emitting device using the same
US4233538A (en) Luminescent lead-activated alkaline earth metal rare earth metal borates and mercury vapor discharge lamp containing the same
JPH1173138A (en) Red light emitting phosphor, and plasma display device and noble gas discharging light emitting device using it