US2714685A - Low pressure fluorescent and discharge lamps - Google Patents

Low pressure fluorescent and discharge lamps Download PDF

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US2714685A
US2714685A US243612A US24361251A US2714685A US 2714685 A US2714685 A US 2714685A US 243612 A US243612 A US 243612A US 24361251 A US24361251 A US 24361251A US 2714685 A US2714685 A US 2714685A
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krypton
xenon
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Meister George
Thomas H Heine
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CBS Corp
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Westinghouse Electric Corp
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    • 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
    • H01J61/18Selection of substances for gas fillings; Specified operating pressure or temperature having a metallic vapour as the principal constituent
    • H01J61/20Selection of substances for gas fillings; Specified operating pressure or temperature having a metallic vapour as the principal constituent mercury vapour

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  • the principal object of our invention is to produce low pressure iluorescent and discharge lamps having a filling of a mixture of mercury and rare gases of such a composition that fluorescence is eliiciently excited in the phosphor.
  • Another object of our invention is to produce a low pressure fluorescent or discharge lamp comprising a mixture of rare gases in which xenon is mixed with krypton and mercury in the proportion to get good emciency at practical pressures.
  • a further object of our invention is to produce a uorescent or discharge lamp which has characteristics such as above outlined, whereby it is better than a lamp having only one rare gas admixed with mercury vapor because it has a higher ultra-violet and corresponding luminous eiiiciency.
  • Figure l is an elevational view, with parts in longitudinal section of a lamp embodying our invention.
  • Figure 2 is a graph showing the variation in arc or visible light output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
  • Figure 3 is a graph showing the variations in ultraviolet output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
  • Figure 4 is a graph showing the variations in fluorescent light output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
  • mercury vapor admixed with an inert or rare gas, such as argon at low pressure is commercially employed for the generation of ultra-Violet radiations which may excite phosphors to give off visible radiations in fluorescent discharge lamps.
  • the efliciency of such a low pressure mercury discharge fluorescent lamp depends upon the mercury pressure and the wattage in the discharge. It has been shown that at a constant bulb temperature and a given current, the inert gas with the greater atomic weight and lower ionization potential has a higher eiiciency than an inert gas of lower atomic weight and higher ionization potential. Thus, of the gases tried, krypton was better than argon or neon.
  • the assembled tube with coated phosphor sections was sealed onto an exhaust system which had a cooling trap, surrounded by Dry Ice throughout the experiment.
  • a liter reservoir for allowing proper diiusion of gas mixtures was provided into which could be introduced the spectroscopically pure inert or noble gases which were The system also was equipped with a McLeod gauge to read pressures.
  • the lamp was exhausted and baked at 475 C. for about one hour.
  • the cathodes were processed until no more gas was liberated.
  • the water-jacket was put into place so that the Vycor sections of the jacket and lamp Vycor sections coincided and was firmly fastened to keep it in a iixed position.
  • the annular space between the lamp and jacket could be flushed with water at any desired temperature, which was read on a thermometer placed in the water surrounding the lampi.
  • a voltage stabilizer was used to control the voltage input on the iilament transformers, the discharge transformer, and the ultra-violet meter.
  • U. radiation was set in position. opposite the Vycor section.
  • the photovoltaic cells were placed in position opposite the Vycor section and the phosphor sections. They were checked before and after a set of readings with a standard incandescent lamp, also using a voltage stabilizer in the circuit. All stands were securely fastened so as to keep all positions xed during a run.
  • the lamp was seasoned for several days before any readings were taken. This seasoning was done in mercury vapor alone, continuously exhausting during the entire period. During operation of the lamp, water was flushed up and down the tube until the water temperature was 45 C. All the data were subsequently taken at this temperature. The temperature was checked before and after each current reading. As each current setting was made, the ultra-violet output of the arc, the voltage, the visible light output of the arc, and the light output of the phosphor were read in that order. These zero gas pressure data were again obtained as a reference check after each change of inert gas or inert gas mixtures. After all the preliminary data were obtained, then this lamp was operated at difierent inert gas pressures and mixtures of inert gases.
  • the inert gases investigated were xenon, krypton, and mixtures 3 of xenon and krypton. These gas mixtures were varied s ARC CHARACTERISTICS as topman Suclem dma to Show any dlfferelen Char'
  • the arc efficiency vs. composition curves of the dis- .acterlsuc and ca di me was dlffused at least Ours to charge at constant current and constant temperature show msure umfonil mlxing' r that at all pressures from 1 to 5 mm.
  • the followmg mixtures were used d much as 50% xenon to krypton causes an almost linear reduction in the visible eiiiciency. However, at l mm.
  • the voltage-composition curves are vastly 40 gg (.l- 100 l diierent from those of the Krypton-argon and krypton- 25 75 04 i02 ⁇ .i neon series.
  • gg .l- 100 l diierent from those of the Krypton-argon and krypton- 25 75 04 i02 ⁇ .i neon series.
  • xenon concentration 0 100 0.2 9&8 they do not proceed in any regular progressive manner but *i ShoW a ShaI'P inflection at about 20% Xenon eSPeCaUY
  • the maximum occurs at 1 mm. gas pres- With 2, 4 and 5 nIngas Pressure UP to this Xenon con' 45 sure for pure krypton and then shifts gradually down centration, the voltage at each pressure is practically conto 0 2 mm gas Pressure for pure Xenon This is in con.
  • the voltage for pure xenon is practically independent pure krypton up to approximately 2 mm. for pure neon. of the gas PIeSSne for L 3, 4 and 5 nnnand annonnfS to In the case of krypton-argon there was no shift in gas aPPl'oXlInatelY 95% of the Voltage of Pore kTyphon at 2 pressure for maximum efficiency. In connection with min, Whlle for 2 nnn gas Pressure it S approximately these maximum arc eiciencies, it should be noted that 905%.
  • the highest fluorescent output eciency is obtained at approximately l, mrn. gas pressure for pure xenon and for mixtures down to about xenon-40% krypton. Below this composition the highest iluorescent eticiency occurs at 2 mm. gas pressure, and the etliciency thus progressively decreases as the pressure increases. It is to be noted, also, that the uorescent eiliciency for pure krypton is approximately that for pure xenon at 1 mm. gas pressure.
  • the fluorescent output eiciency for pure krypton is better than that for pure xenon at all pressures except at l mm. gas pressure and lower where xenon is slightly better than pure krypton.
  • the fluorescent output for mixtures far exceeds that of pure xenon so that at 5 mm.
  • the uorescent efficiency is only that ⁇ of xenon at l mm.
  • the relative decrease in lluorescent output efiiciency is approximately the same as with the ultra-violet elliciency. It can be seen that there again is a correlation between ultraviolet etlciency and fluorescent output efficiency in these xenon-krypton mixtures.
  • the arc, ultraviolet and iluorescent eiciencies at 2 mm. gas pressure all follow the same general course when plotted against the atomic number of the gases.
  • the maximum efficiency at 2 mm. gas pressure is obtained with krypton while the relative ultraviolet and iuorescent eciencies for argon and xenon are about the same.
  • the arc eiiiciency for pure xenon is relatively poorer than for any of the other gases. From these collective data it can be concluded that for the most eflicient uorescent or ultraviolet lamps at 2 mm. gas pressure, krypton or krypton-rich mixtures should be used provided there are no unusual maxima produced by the inert-gas mixtures.
  • the ultraviolet and fluorescent eiiciencies showed good ⁇ correlation and there was very little spread in the relative eiciencies in the pressure range of 1 to 4 mm.
  • the maxima in the curves for the fluorescent eiliciency corresponded to the maxima in the ultraviolent eciency curves.
  • These eliciency curves did not show any corresponding relation to the arc efliciency curves.
  • the present krypton-xenon gas mixtures there not only is a correlation between the ultraviolet and uorescent eflciency curves, but there also is reasonably good correspondence with the arc efficiency curves at pressures ranging from 1 to 5 mm.
  • the arc eiciency for visible light was highest at 1 mm. gas pressure for pure krypton, and at 0.4 mm. gas pressure for pure xenon and krypton-xenon mixtures having more than 30% of xenon.
  • the efficiencies for pure xenon and xenongrich mixtures showed a very rapid decrease with increasing pressure, 1 to 5 mm., comparable to the ultra-violet and fluorescent efticiency curves.
  • the high eiciency values at l mrn. gas pressure agree in general with the data obtained with krypton-argon and krypton-neon series.
  • Fluorescent lamps of the positiveV column type exhibit these experimental data.
  • the lamp of said gure comprises an elongated translucent vitrous envelope 11, with heated filamentary electrodes 12 and 13, one in each end portion, and containing the selected noble gas mixture and some mercury, indicated by the globule 14. If a uorescent lamp, the selected phosphor 15 is applied to the inner surface of the envelope.
  • the experimental lamp described contained a 3500 white phosphor of zinc beryllium silicate and magnesium tungstate
  • the phosphor for commercial use may be any one which efciently uses and, therefore, has a high absorption of, ultra-violet radiations in the region of 2537 A.
  • U. that is, the mercury resonance radiation, and consequently a strong ultra-violet response giving'a good light output.
  • Another example of phosphors which may be employed are the halo phosphates described in the British Patent No. 578,192.
  • a discharge lamp comprising a translucent vitreous 8 envelope, a pair of electrodes in said envelope, andy a contained mixture of xenon and krypton at a pressure between 3A; and 11/2 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being between and 80%, and that of the Krypton being between 30% and 20% of the gas mixture.
  • a discharge lamp comprising an elongated translucent vitreous envelope, an electrode in each end portion of said envelope, and a contained mixture of Xenon and krypton at a pressure of about 1 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being about and that of krypton being about 25% so that the generation of ultra-violet radiation is approximately at a maximum when operating at a temperature between 40 and 50 C.
  • a discharge lamp comprising a translucent vitreous envelope, a pair of electrodes in said envelope, and a contained mixture of xenon and krypton at a pressure of between 1 and .4 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being between 70% and 80% and that of krypton being between 30% and 20% so that the generation of visible light is approximately at a maximum.
  • a discharge lamp comprising a translucent vitreous envelope, a pair of electrodes in said envelope, and a contained mixture of xenon and krypton at a pressure of between 1 and .4 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being about 75 and that of the krypton being about 25% so that the generation of visible light is approximately at a maximum.

Description

Aug. 2, 1955 G. MEISTER ET AL LOW PRESSURE FLUORESCENT AND DISCHARGE LAMPS Filed Aug. 25
TTORNE United States Patent O LOW PRESSURE FLUORESCENT AND DISCHARGE LAMPS Application August 25, 1951, Serial No. 243,612 4 Claims. (Cl. 313-185) H. Heine, Cedar Westinghouse Electric Cor- Pa., a corporation of Penn- This invention relates to low pressure discharge lamps and, more particularly, to such employing only mixtures of rare gases and mercury as the filling material.
The principal object of our invention generally considered, is to produce low pressure iluorescent and discharge lamps having a filling of a mixture of mercury and rare gases of such a composition that fluorescence is eliiciently excited in the phosphor.
Another object of our invention is to produce a low pressure fluorescent or discharge lamp comprising a mixture of rare gases in which xenon is mixed with krypton and mercury in the proportion to get good emciency at practical pressures.
A further object of our invention is to produce a uorescent or discharge lamp which has characteristics such as above outlined, whereby it is better than a lamp having only one rare gas admixed with mercury vapor because it has a higher ultra-violet and corresponding luminous eiiiciency.
Other objects and advantages of the invention will become apparent as the description proceeds.
Referring to the drawing:
Figure l is an elevational view, with parts in longitudinal section of a lamp embodying our invention.
Figure 2 is a graph showing the variation in arc or visible light output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
Figure 3 is a graph showing the variations in ultraviolet output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
Figure 4 is a graph showing the variations in fluorescent light output as the composition of the contained gas is changed, each curve having applied thereto a numeral indicating pressure in millimeters of the enclosed gas.
As is well known, mercury vapor admixed with an inert or rare gas, such as argon at low pressure is commercially employed for the generation of ultra-Violet radiations which may excite phosphors to give off visible radiations in fluorescent discharge lamps.
The electrical characteristics of such low pressure mercury discharges are known. It has been shown that, at a given lamp temperature, pressure and current, as the atomic weight of the inert gas increases, the voltage gradient in the mercury discharge and the voltage drop at the electrodes decrease.
The efliciency of such a low pressure mercury discharge fluorescent lamp depends upon the mercury pressure and the wattage in the discharge. It has been shown that at a constant bulb temperature and a given current, the inert gas with the greater atomic weight and lower ionization potential has a higher eiiciency than an inert gas of lower atomic weight and higher ionization potential. Thus, of the gases tried, krypton was better than argon or neon.
employed.
2,714,685 Patented Aug. 2, 1955 The early data was mainly taken on the individual inert gases mixed with mercury. We have investigated the use of mixtures of inert gases with mercury for discharge lamps, as a continuation of the subject matter described and claimed in our application Serial No. 102,016, led June 29, 1949, and owned by the assignee of the present application.
In order to obtain as much information as possible on one experimental lamp, a special tube was designed in which the central portion consisted of a 5 inch section of glass identified by the Corning trademark Vycor (as further identied in the Rentschler Patent No. 2,469,410, dated May 10, 1949) and of 1.5 inches inside diameter which was sealed to a 1.5 inch diameter glass tube, identified by the Corning trademark Pyrex, at each end. The Pyrex sections could be coated with phosphors. Independently heated oxide coated cathodes were used and spaced about 24 inches apart, producing a so-called positive column lamp. In addition, a water-jacket three inches in diameter was designed to lit around the lamp in which the central portion again was a 5 inch Vycor section sealed with white wax to a Pyrex section at each end. With this construction it was possible to measure the light output of the phosphors, the ultra-violet output of the arc discharge, and the light output of the arc, at diiferent gas pressures and controlled temperatures with corresponding voltages and power input.
The assembled tube with coated phosphor sections was sealed onto an exhaust system which had a cooling trap, surrounded by Dry Ice throughout the experiment. A liter reservoir for allowing proper diiusion of gas mixtures was provided into which could be introduced the spectroscopically pure inert or noble gases which were The system also was equipped with a McLeod gauge to read pressures.
The lamp was exhausted and baked at 475 C. for about one hour. The cathodes were processed until no more gas was liberated. The water-jacket was put into place so that the Vycor sections of the jacket and lamp Vycor sections coincided and was firmly fastened to keep it in a iixed position. The annular space between the lamp and jacket could be flushed with water at any desired temperature, which was read on a thermometer placed in the water surrounding the lampi. A voltage stabilizer was used to control the voltage input on the iilament transformers, the discharge transformer, and the ultra-violet meter.
The ultra-violet meter containing a tantalurn cell to read the 2537 A. U. radiation was set in position. opposite the Vycor section. The photovoltaic cells were placed in position opposite the Vycor section and the phosphor sections. They were checked before and after a set of readings with a standard incandescent lamp, also using a voltage stabilizer in the circuit. All stands were securely fastened so as to keep all positions xed during a run.
The lamp was seasoned for several days before any readings were taken. This seasoning was done in mercury vapor alone, continuously exhausting during the entire period. During operation of the lamp, water was flushed up and down the tube until the water temperature was 45 C. All the data were subsequently taken at this temperature. The temperature was checked before and after each current reading. As each current setting was made, the ultra-violet output of the arc, the voltage, the visible light output of the arc, and the light output of the phosphor were read in that order. These zero gas pressure data were again obtained as a reference check after each change of inert gas or inert gas mixtures. After all the preliminary data were obtained, then this lamp was operated at difierent inert gas pressures and mixtures of inert gases. The inert gases investigated were xenon, krypton, and mixtures 3 of xenon and krypton. These gas mixtures were varied s ARC CHARACTERISTICS as topman Suclem dma to Show any dlfferelen Char' The arc efficiency vs. composition curves of the dis- .acterlsuc and ca di me was dlffused at least Ours to charge at constant current and constant temperature show msure umfonil mlxing' r that at all pressures from 1 to 5 mm. the addition of as The followmg mixtures were used d much as 50% xenon to krypton causes an almost linear reduction in the visible eiiiciency. However, at l mm. gas Krypton Xenon pressure, between 50% Xenon and 75% Xenon, as shown f by Fig. 2, a definite plateau develops to interrupt the smooth drop. This plateau generally becomes less pronounced as the gas pressure increases from 1 to 5 mm.
it is interesting to note that the arc visible output eiciencies for pure xenon show approximately the same large decrease as later observed in the ultraviolet and fluorescent-composition curves, shown respectively in Fig- All data illustrated in the accompanying composition i ures 3 and 4. On the other hand, pure krypton at all prescurves are for a constant lamp current of 500 milliamperes sures from 1 to 5 mm. maintain a high eiciency showing and for a constant temperature of 45 C. for dilterent a drop of only 6% over that pressure range. These pressure parameters ranging from below 1 to 5 mm. curves, for pressures downl only to 1 mm. compare with Krypton at 2 mm. gas pressure is taken as the 100% refn the Curves previously published on the Krypton-argon se' @rence point' ries which I ilso showed the highs eiiiiency atl 1 v pressure. owever, at pressures e ow mm., s. own y VOLTAGE CHARACTERISTICS Figure 2 for a pressure of 0.4 mm., the efficiency of a 25% Curves plotted to compare the voltage with the corre- Krypton 75% xenon mixture reaches a maximum which sponding composition at constant current and temperature ,.5 is higher than the corresponding values for other presfor krypton-xenon mixtures show that the lowest voltage M suies. The following table presents the maximum visible is obtained with 2 mm. gas pressure throughout the entire output eiiiciencies and the pressures at which they occur range of composition from 100% krypton to 100% xenon. for representative mixtures with krypton at 2 mm., as These curves, therefore, generally agree with previous shown in Figure 2, taken as the 100% reference point data obtained with the krypton-argon and krypton-neon (Table 2). mixtures. However, in the neon-rich Krypton-neon mix- Table 2 tures, the lowest voltage was obtained with 1 mm. gas pressure. The reason for this difference is that with these MAXIMUM ARC EFFXCIENCY inert gases there is a pronounced voltage minimum at about 2 mrn. with krypton and xenon, but for the lower 3F Composition atomic number gases, higher ionization potentials, this Pressure, Efficiency,
mm. of Hg Percent voltage minimum vanishes and instead a plateau develops, Kr Xe especially with neon at about 2 mm. gas pressure with a l l i l ai i subsequent decrease in voltage below this pressure. 100 0 1.0
The voltage-composition curves, furthermore, are vastly 40 gg (.l- 100 l diierent from those of the Krypton-argon and krypton- 25 75 04 i02`.i neon series. When the xenon concentration is increased, 0 100 0.2 9&8 they do not proceed in any regular progressive manner but *i ShoW a ShaI'P inflection at about 20% Xenon eSPeCaUY It is noted that the maximum occurs at 1 mm. gas pres- With 2, 4 and 5 nIngas Pressure UP to this Xenon con' 45 sure for pure krypton and then shifts gradually down centration, the voltage at each pressure is practically conto 0 2 mm gas Pressure for pure Xenon This is in con. stant. While this inflection is not pronounced with 1 and tragt to the characteristics previously published on kryp- 3 fnfngas PfeSSnle, it S moet pronounced With 5 nnlngas ton-neon mixtures which showed that the` gas pressure pressure. for maximum eiiiciency gradually rose from V1 nini. for
The voltage for pure xenon is practically independent pure krypton up to approximately 2 mm. for pure neon. of the gas PIeSSne for L 3, 4 and 5 nnnand annonnfS to In the case of krypton-argon there was no shift in gas aPPl'oXlInatelY 95% of the Voltage of Pore kTyphon at 2 pressure for maximum efficiency. In connection with min, Whlle for 2 nnnn gas Pressure it S approximately these maximum arc eiciencies, it should be noted that 905%. A'lSo, l[he voltages for 1 and 3 InnngaS PfeSSnfeS they do not occur at the pressure for minimum voltage are aPPl'oXlIhatelY the Sane throughout 'Che kfYpon-Xenon which is the case with ultra-violet and iluorescent output series at each pressure and vary only from about 95% at efficiencies, pure xenon to about 105.5% at pure krypton.
A statement was made that the voltage in these low ULTRAVIOLET CHARACTERISTICS pressure mercury discharges containing inert gases varies directly with the ionization potential of the gas. This ret" lation is shown by plotting the voltage against the atomic number of the gas which is correlated to the ionization potential. This correlation is further shown when the relative percentage voltage values and ionization poten- The ultra-violet (U. V.) eiciency vs. composition curves at constant current and constant temperature for krypton-xenon mixtures (Fig. 3) show that as the percentage of xenon is increased at 1 mm. gas pressure (and also at .75 and 1.5 mm. and intermediate pressures), unlike at higher pressures, there is a gradual rise in the tial val'IiIe1 aile tabulated with krypton as the reference G5 U V efciency until a maximum is reached at 25% oint a p e krypton75% xenon. This maximum corresponds for 1 Table 1 mm. to the maximum observed in the published data for krypton-neon mixtures Where the composition was Gas Atomic Percent ronimion krypton25% neon. Higher concentration of xenon in P Number Voltage Potrltlal ement krypton reduces the eiciency again until for pure xenon at 1 mm. pressure the efficiency is about the same g 2 as that of pure krypton at 1 mm. pressure. 3s 100 13` 9 100 Raising the gas pressure of pure krypton from 1 mm. 54 91 12.1 87 75 up to 2 mm. increases the eiciency over 4% up to the highest possible for pure krypton. At this constant pressure ofA 2 mm., increasing the percentage `of xenon has practically no eiect on the eliciency up to 80% xenon. For mixtures containing less than about 60% xenon, the highest U. V. efficiency is obtained at 2 mm. gas pressure. This compares with the published data on the krypton-argon and krypton-neon mixtures where the highest ultraviolet efficiency was obtained at 2 mm. gas pressure for pure gases and all mixtures. At xenon concentrations higher `than about 60%, the eiciency at 2 mm. gas pressure goes below that .obtained for l mm. gas pressure. After this cross-over a decline in ethciency occurs for compositions containing more than about 80% xenon. v
All the curves for 3, 4 and 5 mm. gas pressure with pure krypton show ultraviolet eiciencies higher than the eciency at 1 mm. However, as the concentration of xenon is increased, the efficiencies cross the l mm. curve and decrease more rapidly for the higher pressures so that with pure xenon there is a decrease in elliciency over the narrow pressure range from 1 to 5 mm. It should be noted that for this same pressure range, the ultraviolet eciencies for pure krypton change only 4%. The corresponding range of eiciencies in pure neon and pure argon for these pressures is approximately the same as for pure krypton.
FLUORESCENT CHARACTERISTICS In general the lluorescent output efficiency vs. cornposition curves at constant current and temperature for krypton-xenon mixtures (Fig. 4) have the same general shape and relative output as the ultraviolet eiiiciency vs. composition curves at the corresponding gas pressures.
The highest fluorescent output eciency is obtained at approximately l, mrn. gas pressure for pure xenon and for mixtures down to about xenon-40% krypton. Below this composition the highest iluorescent eticiency occurs at 2 mm. gas pressure, and the etliciency thus progressively decreases as the pressure increases. It is to be noted, also, that the uorescent eiliciency for pure krypton is approximately that for pure xenon at 1 mm. gas pressure.
The fluorescent output eiciency for pure krypton is better than that for pure xenon at all pressures except at l mm. gas pressure and lower where xenon is slightly better than pure krypton. As the pressure increases from l to 5 mm., the fluorescent output for mixtures far exceeds that of pure xenon so that at 5 mm. the uorescent efficiency is only that `of xenon at l mm. The relative decrease in lluorescent output efiiciency is approximately the same as with the ultra-violet elliciency. It can be seen that there again is a correlation between ultraviolet etlciency and fluorescent output efficiency in these xenon-krypton mixtures. This observation is in agreement with the data published in the krypton-argon and krypton-neon mixtures where a similar relation was found. These curves also have a maximum at 1 mm. gas pressure (and also at .75 and 1.5 mm. and intermediate pressures) at approximately 75% xenon- 25% krypton, and therefore, coincide with the ultraviolet eiciency data. ln the data for the krypton-neon mixture, a similar more pronounced peak was observed at about this composition where the mixture was 75% krypton- 25% neon.
COLLECTIVE DATA With the addition of pure xenon to the published data on the other pure gases, krypton, argon, and neon, the characteristics for all the pure inert gases except helium have been obtained.
The relative voltages for the above gases for 2 mm. gas pressure when compared show that the lowest voltage is obtained with xenon and the highest voltage with neon. The other two gases, krypton and argon, have intermediate values but in progressive sequence with potential of mercury while 6 their atomic numbers and ionization potentials (Table 1).
The arc, ultraviolet and iluorescent eiciencies at 2 mm. gas pressure all follow the same general course when plotted against the atomic number of the gases. The maximum efficiency at 2 mm. gas pressure is obtained with krypton while the relative ultraviolet and iuorescent eciencies for argon and xenon are about the same. The arc eiiiciency for pure xenon is relatively poorer than for any of the other gases. From these collective data it can be concluded that for the most eflicient uorescent or ultraviolet lamps at 2 mm. gas pressure, krypton or krypton-rich mixtures should be used provided there are no unusual maxima produced by the inert-gas mixtures. With krypton-argon and krypton-neon gas mixtures, the ultraviolet and fluorescent eiiciencies showed good `correlation and there was very little spread in the relative eiciencies in the pressure range of 1 to 4 mm. The maxima in the curves for the fluorescent eiliciency corresponded to the maxima in the ultraviolent eciency curves. These eliciency curves, however, did not show any corresponding relation to the arc efliciency curves. With the present krypton-xenon gas mixtures, there not only is a correlation between the ultraviolet and uorescent eflciency curves, but there also is reasonably good correspondence with the arc efficiency curves at pressures ranging from 1 to 5 mm.
It can also be seen from the curves that these ultraviolet and iiuorescent eilciencies for pure xenon are comparable within a few percent with those of pure krypton at low gas pressures of 1 to 2 mm. but with pure xenon they progressively and rapidly decrease as the gas pressure is increased to 5 mm. The arc efficiencies, however, decrease rapidly from 1 to 5 mm. gas pressure for pure xenon and xenon-rich mixtures. Apparently there must be some property directly associated with xenon gas because the general shape of the eciency curves agrees for all compositions of krypton-xenon gas mixtures.
In comparing some of the properties of the inert gases that may have a direct bearing on this phenomenon, it was noted that the metastable levels of xenon lie below the ionization potential of mercury. With neon and argon the `rnetastable levels are above the ionization with krypton there is one above and one below. When these gases, therefore, are excited by collision with electrons, they can influence the mercury discharge by collisions of the second kind. However, when the electrons collide with xenon atoms, all the energy is lost to the xenon and there is apparently no subsequent eiect on the mercury atoms thus accounting for the results obtained.
SUMMARY 9 microns corresponding to a wall temperature of 45 and fluorescent output eciency at 1 mm. gas pressure for 25 krypton-75% xenon. This indicates that for best results, the proportion should range between 80% xenon and 30-20% krypton, with the pressure about l or between 3%: and 11/2 mm. for an operating temperature near or at 45 C.; that is, between 40 and 50 C. This maximum eiciency was found at a similar composition in the krypton-neon gas mixture at 2 mm. gas pressure where the higher atomic number gas constituent, krypton, in the mixture was The voltage of the lamp was lowest at 2 mm. gas pressure for krypton and xenon and also for the kryptonxenon mixtures. This lowest voltage was also generally observed with the krypton-argon and krypton-neon mixtures. The voltages in the krypton-xenon series have a very narrow spread going from pure krypton to pure xenon.
The arc eiciency for visible light was highest at 1 mm. gas pressure for pure krypton, and at 0.4 mm. gas pressure for pure xenon and krypton-xenon mixtures having more than 30% of xenon. The efficiencies for pure xenon and xenongrich mixtures showed a very rapid decrease with increasing pressure, 1 to 5 mm., comparable to the ultra-violet and fluorescent efticiency curves. The high eiciency values at l mrn. gas pressure agree in general with the data obtained with krypton-argon and krypton-neon series.
The highest ultraviolet and fluorescent eiciencies occurred at 2 mm. gas pressure for all krypton-xenon mixtures containing more than 40% krypton. These highest efciencies are observed where the voltage is lowest. They, therefore agree with those found in the kryptonargon, and krypton-neon series. The ultraviolet and fluorescent eiciencies in pure xenon and xenon-rich mixtures showed a very rapid decrease with increasing pressure, 1 to 5 mm., which was not observed in the kryptonargon or krypton-neon series.
The collective data on the characteristics of insert gases and their mixtures at 2 mm. gas pressure in the presence of low pressure mercury vapor show that the highest arc, ultraviolet and fluorescent efliciencies are obtained with krypton or krypton-rich mixtures and the lowest voltage is obtained with pure xenon.
Fluorescent lamps of the positiveV column type, one of which is illustrated in Figure 1, exhibit these experimental data. The lamp of said gure comprises an elongated translucent vitrous envelope 11, with heated filamentary electrodes 12 and 13, one in each end portion, and containing the selected noble gas mixture and some mercury, indicated by the globule 14. If a uorescent lamp, the selected phosphor 15 is applied to the inner surface of the envelope.
Although the experimental lamp described contained a 3500 white phosphor of zinc beryllium silicate and magnesium tungstate, the phosphor for commercial use may be any one which efciently uses and, therefore, has a high absorption of, ultra-violet radiations in the region of 2537 A. U., that is, the mercury resonance radiation, and consequently a strong ultra-violet response giving'a good light output. Another example of phosphors which may be employed are the halo phosphates described in the British Patent No. 578,192.
Atlthough preferred embodiments of our invention have been disclosed, it will be understood that modifications may be made within the spirit and scope of the appended claims.
We claim:
l. A discharge lamp comprising a translucent vitreous 8 envelope, a pair of electrodes in said envelope, andy a contained mixture of xenon and krypton at a pressure between 3A; and 11/2 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being between and 80%, and that of the Krypton being between 30% and 20% of the gas mixture.
2. A discharge lamp comprising an elongated translucent vitreous envelope, an electrode in each end portion of said envelope, and a contained mixture of Xenon and krypton at a pressure of about 1 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being about and that of krypton being about 25% so that the generation of ultra-violet radiation is approximately at a maximum when operating at a temperature between 40 and 50 C.
3. A discharge lamp comprising a translucent vitreous envelope, a pair of electrodes in said envelope, and a contained mixture of xenon and krypton at a pressure of between 1 and .4 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being between 70% and 80% and that of krypton being between 30% and 20% so that the generation of visible light is approximately at a maximum.
4. A discharge lamp comprising a translucent vitreous envelope, a pair of electrodes in said envelope, and a contained mixture of xenon and krypton at a pressure of between 1 and .4 mm. of mercury, admixed with mercury vapor, the proportion of the xenon being about 75 and that of the krypton being about 25% so that the generation of visible light is approximately at a maximum.
References Cited in the le of this patent UNITED STATES PATENTS 1,726,107 Hertz Aug. 27, 1929 1,876,083 Spaeth Sept. 6, 1932 1,882,032 Oosterhuis Oct. 11, 1932 1,882,609 Howe Oct. 11, 1932 1,906,119 Spencer Apr. 25, 1933 1,908,647 Spaeth May 9, 1933 1,994,381 Beck Mar. 12, 1935 2,007,919 Braselton July 9, 1935 2,007,926 Braselton Iuly 9, 1935 2,007,934 Braselton July 9, 1935 2,022,219 Ruben Nov. 26, 1935 2,094,450 Geffcken et al. Sept. 28, 1937 2,407,379 Morehouse Sept. 10, 1946 2,421,571 Leyshon June 3, 1947 2,473,642 Found et al. June 21, 1949 2,492,619 Casellini et al. Dec. 27, 1949

Claims (1)

1. A DISCHARGE LAMP COMPRISING A TRANSLUCENT VITREOUS ENVELOPE, A PAIR OF ELECTRODES IN SAID ENVELOPE, AND A CONTAINED MIXTURE OF XENON AND KRYPTON AT A PRESSURE BETWEEN 3/4 AND 1 1/2 MM. OF MERCURY, ADMIXED WITH MERCURY VAPOR, THE PROPORTION OF THE XENON BEING BETWEEN 70% AND 80%, AND THAT OF THE KRYPTON BEING BETWEEN 30% AND 20% OF THE GAS MIXTURE.
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US3453427A (en) * 1966-05-27 1969-07-01 Xerox Corp Electric lamp for uniformly charging the photoconductive insulating layer of a xerographic plate
US3780329A (en) * 1971-11-12 1973-12-18 Matsushita Electronics Corp 40 watt fluorescent lamp
US3780330A (en) * 1971-11-12 1973-12-18 Matsushita Electronics Corp 20 watt fluorescent lamp
US4879469A (en) * 1988-05-13 1989-11-07 University Of North Carolina Mixed media for kinestatic charge detectors
US8421333B2 (en) 2011-03-07 2013-04-16 Osram Sylvania Inc. Energy saving gas discharge lamp including a xenon-based gaseous mixture

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US3453427A (en) * 1966-05-27 1969-07-01 Xerox Corp Electric lamp for uniformly charging the photoconductive insulating layer of a xerographic plate
US3780329A (en) * 1971-11-12 1973-12-18 Matsushita Electronics Corp 40 watt fluorescent lamp
US3780330A (en) * 1971-11-12 1973-12-18 Matsushita Electronics Corp 20 watt fluorescent lamp
US4879469A (en) * 1988-05-13 1989-11-07 University Of North Carolina Mixed media for kinestatic charge detectors
US8421333B2 (en) 2011-03-07 2013-04-16 Osram Sylvania Inc. Energy saving gas discharge lamp including a xenon-based gaseous mixture
US8579670B2 (en) 2011-03-07 2013-11-12 Osram Sylvania Inc. Energy saving gas discharge lamp including a xenon-based gaseous mixture

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