Metal halide lamps typically include a quartz arc tube having metal electrodes and a lamp fill material including halides of sodium, scandium or one or more of the rare earth metals, or combinations thereof. In addition, thorium oxide ThO2 and scandium Sc or cadmium Cd metals may be added to improve lumen maintenance.
Lumen depreciation and voltage rise in metal halide lamps are due in part to arc tube blackening, sodium loss or a loss of chemical species from halide reaction with the arc tube wall or electrodes.
Early metal halide lamps used pure tungsten electrodes which suffered from sputtering of the tungsten from the electrodes onto the arc tube wall during start-up, a high evaporation rate and the lack of a regenerative cycle during normal operation. Electrode material may also be chemically transported to the arc tube wall as halides.
Wall blackening has long been addressed by the doping of the electrodes with a suitable electron emissive material. The dopant reduces the work function of the electrode and results in a shorter glow-to-arc transition period and a lower electrode tip temperature. This in turn reduces the sputtering and evaporation of tungsten which causes blackening of the arc tube and lumen depreciation. Thorium oxide ThO2 in concentrations of 1% to 2% by weight is commonly used as the dopant, but is radioactive and difficult to manufacture.
The need for metal halide lamps with high efficacy, good lumen maintenance and long life is ever increasing. This has led to the development in recent years of sodium scandium metal halide lamps in which the arc tubes have a high wall loading to improve their performance. The increased arc tube loading has resulted in an increased voltage rise over the life of the lamp, a higher rate of lumen depreciation and a shorter lamp life.
In quartz metal halide lamps containing rare earth halides such as ScI3 and thoriated electrodes, a continuous increase in ThI4 content in the fill has been observed as the lamps are burned, thereby resulting in a continuous drop in light output over the life of the lamp. The present invention addresses the continuous increase of ThI4 in metal halide lamps with thoriated electrodes by eliminating the doping of the electrodes. The elimination of ThO2 in the electrodes reduces the chemical reaction of ScI3 in the fill with the ThO2 in the electrodes, and thus reduces the amount of ThI4 formed. The reduction of ThI4 reduces the operating voltage of the lamp.
Accordingly, it is an object of the present invention to obviate many of the deficiencies in the prior art and to provide a novel high pressure metal halide arc tube and lamp with good lumen maintenance and long life by eliminating the doping in the electrodes.
This and many other objects and advantages of the present invention will be readily apparent to one skilled in the art to which the invention pertains from a perusal of the claims, the appended drawings, and the following detailed description of the preferred embodiments.
With reference to the figures where like elements have been given like numerical designations to facilitate an understanding of the present invention, metal halide lamps 10 generally include light emitting chemicals at a specific pressure that are hermetically sealed within an arc tube 12 formed from light transmitting material such as ceramics or quartz glass. The arc tube 12 may comprise a pinched body or a formed body as illustrated in
As shown in
Experiments were conducted using 350 watt pulse-start quartz metal halide lamps using a NaI-ScI3-ThI4 dose and excess Sc. One set of lamps had pure tungsten electrodes whereas a second set of lamps included thoriated tungsten electrodes. The lamps were burned for 5000 hours in a base-up orientation and lamps were removed from each set at specific intervals for analysis.
As indicated earlier, lamp performance depends on the availability of chemical species in the arc tube. Scandium iodide ScI3, for example, can be consumed by reaction with the quartz wall (SiO2) of the arc tube as well as by reaction with the thorium oxide (ThO2.) in the electrodes, i.e., the loss of ScI3 as shown in
arc tube wall: 4ScI3+7SiO2→3SiI4+2Sc2Si2O7 (1)
electrodes: 4ScI3+3ThO2→2Sc2O3+3ThI4 (2)
The increase in ThI4 content in lamps having thoriated tungsten electrodes and the constant value of ThI4 in lamps having pure tungsten electrodes demonstrates the significance of reaction (2) in the depletion of ScI3.
In an experiment to measure lumen maintenance at buffer gas pressures between 30 torr and 400 torr, the performance of 350 Watt sodium scandium lamps using pure tungsten electrodes was compared with similar lamps using thoriated tungsten electrodes containing 2% ThO2. Lamps were cycled for 2 minutes on and 30 minutes off in a vertical orientation, and
Further tests were conducted to determine if the performance of metal halide lamps with pure tungsten electrodes could be improved using high frequency ballasts. The performance of 350 Watt sodium scandium pulse start lamps with excess scandium and ThI4 using pure tungsten electrodes was compared with similar lamps using thoriated tungsten electrodes. Lamps were operated on a 10 hours on and 1 hour off cycle in a vertical orientation on a high frequency (100 kHz) ballast. Pure tungsten electrode lumen maintenance was experimentally determined to be significantly better than thoriated electrode lumen maintenance. It is to be understood that the frequency of the ballast will depend upon the lamp requirements and may have a frequency greater than 100 kHz.
While preferred embodiments of the present invention have been described, it is to be understood that the embodiments described are illustrative only and that the scope of the invention is to be defined solely by the appended claims when accorded a full range of equivalence, many variations and modifications naturally occurring to those of skill in the art from a perusal hereof.
This application claims the priority of U.S. Provisional Application Ser. No. 60/488,348 entitled “Dopant-Free Tungsten Electrodes in Metal Halide Lamps and Methods” filed Jul. 21, 2003.
Number | Date | Country | |
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60488348 | Jul 2003 | US |