CROSS REFERENCE TO OTHER APPLICATIONS
[0001] U.S. Ser. No. 473,895, filed March 10, 1983, entitled "Unsaturated Vapor Pressure
Type High Pressure Sodium Lamp" in the name of the Inventor and assigned to the Assignee
of the present invention relates to high pressure sodium lamps.
TECHNICAL FIELD
[0002] This invention relates to high intensity sodium vapor discharge devices and more
particularly to emissive materials for high intensity sodium vapor discharge devices.
BACKGROUND ART
[0003] High pressure sodium lamps having an elongated arc tube filled with large amounts
of sodium and mercury and disposed within an evacuated glass envelope are well known
in the art. Also well known is the fact that sodium loss has long been a problem in
such lamps. Moreover, such undesirable features as increased voltage drop across the
lamp and a reduction in the period of useful "life" have been traced to this undesired
loss of sodium. Thus, it is a common practice to load or "saturate" high pressure
sodium lamps with large amounts of sodium in order to compensate for the uncontrolled
sodium losses during operational use of the discharge device.
[0004] One known attempt to reduce the sodium loss problem is an effort to reduce the level
of oxygen impurity of the lamp which, in turn, reduces the sodium loss since there
is a shortage of oxygen for combination with the sodium. Such an effort is set forth
in U.S. Patent No. 4,075.530 by Furukubo et al wherein a decomposable material, NaN
3, is located in an adjacent exhaust tube, heated to decompose the NaN
3 and cooled to condense to a resultant material while the undesired nitrogen gas is
withdrawn. Obviously, such a process is relatively cumbersome of apparatus and expensive
of labor and materials.
[0005] Another known attempt to reduce sodium loss in high pressure sodium lamps is set
forth in the above-mentioned filed application bearing U.S. Ser. No. 473,895. Therein,
a getter is located within the arc tube of the discharge device and provides a metal
oxide having a free energy of formation per mole of oxygen more negative than sodium
oxide. However, the numerous advantages provided do not come without cost since the
getter must be added to the structure.
OBJECTS AND SUMMARY OF THE INVENTION
[0006] An object of the present invention is to provide an enhanced high pressure sodium
lamp. Another object of the invention is to improve the stability of a high pressure
sodium lamp. Still another object of the invention is to reduce the sodium losses
in a high pressure sodium lamp. A further object of the invention is to provide an
improved unsaturated vapor high pressure sodium lamp.
[0007] These and other objects, advantages and capabilities are achieved in one aspect of
the invention by a high pressure sodium lamp having an elongated ceramic tube filled
with sodium and noble gases with leads extending therethrough and coupled to electrodes
therein. The leads are connected to electrical conductors within an envelope, and
at least one of the electrodes within the arc tube includes therein or has an emissive
material thereon which has a free energy of formation per mole of oxygen more negative
than that of barium oxide (BaO).
BRIEF DESCRIPTION OF THE DRAWINGS
[0008]
FIG. 1 is an elevational view of a high pressure sodium lamp of the invention; and
FIG. 2 is a comparison chart illustrating the sodium loss with time in a high pressure
sodium lamp utilizing various electron emissive materials.
BEST MODE FOR CARRYING OUT THE INVENTION
[0009] For a better understanding of the present invention, together with other and further
objects, advantages and capabilities thereof, reference is made to the following disclosure
and appended claims in conjunction with the accompanying drawings.
[0010] Referring to FIG. 1 of the drawings, a high pressure sodium lamp includes an elongated
outer glass envelope 3 attached to a normal screw-type base 5. The lamp has a glass
stem portion 7 hermetically sealed to the envelope 3, and a pair of electrical leads
9 and 11 are sealed into and pass through the glass stem portion 7 of the lamp. An
electrically conductive support member 13 is affixed to one of the electrical leads
9 and extends along the longitudinal axis of the envelope 3. A pair of cross-members
15 and 17 are attached to opposite ends and extend normal to the longitudinal axis
of the electrically conductive support member 13.
[0011] An elongated arc tube 19 of a light transmissive ceramic material, such as polycrystalline
alumina for example, is supported within the outer glass envelope 3 by a pair of electrical
conductors 21 and 23 sealed into opposite ends thereof. These electrical conductors
21 and 23 extend outwardly from the arc tube 19 and are attached to and supported
by the cross members 15 and 17 respectively. Affixed to the other end of each of the
electrical conductors 21 and 23 and spacedly arrayed within the arc tube 19 is a pair
of electrodes which will be explained in detail hereinafter.
[0012] Also, heat insulating sleeves 29 and 31 are wrapped about the opposite ends of the
arc tube 19 in the vicinity of the electrodes 25 and 27. The glass envelope 3 is evacuated
and one or more getters 24, preferably barium, are positioned therein. Moreover, a
lamp fill gas, preferably sodium and mercury, is disposed within the arc tube 19.
This lamp fill gas may be of an amount sufficient to "saturate" or provide an excess
amount of sodium therein, but preferably only sufficient fill gas is added to provide
a lamp of the unsaturated vapor type. In other words, the "saturated" lamp includes
a gas phase saturated with sodium and mercury and a pool of excess sodium and mercury
while the "unsaturated" does not include a pool of excess sodium and mercury.
[0013] Additionally, it has been observed that high pressure sodium lamps employing the
usual di-barium calcium tungstate emission material tend to exhibit an excessive loss
of sodium during operation. Moreover, it is believed that decomposition of the emissive
material liberates oxygen which, in turn, undesirably combines with the sodium and
the alumina of the arc tube to form a non-volatile compound.
[0014] As to the electrodes 25 and 27, a material having a free energy of formation more
negative than about -180 K cal/mole at 1200° or more negative than barium oxide (BaO)
is a preferred electrode emissive material. For example, thorium oxide (Th0
2) coatings, as well as coatings selected from the following emissive material coatings,
are appropriate: scandium oxide (Sc
2O
3): yttrium oxide (Y
2O3); beryllium oxide (BeO); lanthanum oxide (La
2O
3); cerium oxide (Ce 0 ) and hafnium oxide (HfO
2). Moreover, tungsten containing one or more of these emissive materials as inclusions
in the tungsten, such as thoriated tungsten, is also an appropriate material for the
electrodes 25 and 27.
[0015] As a specific example of the advantages of the above- described configuration, a
comparison was made for sodium content of unsaturated high pressure sodium lamps.
A series of 400-watt unsaturated vapor high pressure sodium lamps having a volume
of about 5 cubic centimeters were filled with relatively low amounts of sodium, about
6 X 10
-5 gms, xenon in the range of about 15 to 300 Torr and about 1.8 mgs. of mercury. Moreover,
one series of lamps employed tungsten electrodes with a coating of emissive materials
commonly employed in sodium vapor lamps known as di-barium calcium tungstate. The
other series of lamps employed a similar tungsten electrodes but utilized a coating
of thorium oxide (ThO
2) as the emissive material.
[0016] A comparison test, FIG. 2, was conducted wherein neither of the test groups included
any gettering within the group. A comparison can readily be seen in the chart of FIG.
2 wherein the test group (A) employed thorium oxide (ThO
2) as the emissive material and the control group (B) employed di-barium calcium tungstate
as the emissive material. Operating under the same conditions, the test group (A),
using Th0
2 as the emissive material, maintained a substantially constant level of sodium over
an extended time period. On the other hand, the control group (B) using di-barium
calcium tungstate as an emissive material indicated an almost complete loss of sodium
content within a relatively short operating time, about 400 minutes.
[0017] Thus, test results have indicated that high pressure sodium lamps, saturated and
preferably unsaturated, are enhanced by the utilization of an emissive material having
a free energy of formation per mole of oxygen more negative than that of barium oxide
(BaO). Also, observation of unsaturated high pressure sodium lamps made with both
di-barium calcium tungstate and with thorium oxide emissive materials indicates a
very definite reduction in end blackening when thorium oxide is used as the emissive
material. Both tests are indicative of the reduced loss of sodium within lamps employing
an emissive material with a free energy of formation per mole of oxygen more negative
than about -180 K cal/mole at about 1200° C.
[0018] While there has been shown and described what is at present considered the preferred
embodiments of the invention, it will be obvious to those skilled in the art that
various changes and modifications may be made therein without departing from the invention
as defined by the appended claims.
1. A high intensity sodium vapor discharge device comprising:
an elongated envelope having a pair of electrical leads sealed therein and passing
therethrough:
an elongated arc tube having a fill of noble gas and disposed within said envelope;
and
a pair of electrodes sealed within said arc tube and connected to an electrical conductor
passing through said arc tube and connected to one of said electrical leads with at
least one of said pair of electrodes including thereon or therein emissive material
having a free energy of formation per mole oxygen more negative than the free energy
of formation of barium oxide (BaO).
2. The high intensity sodium vapor discharge device of Claim 1 wherein said discharge
device is an unsaturated vapor type high pressure discharge device.
3. The high intensity sodium vapor discharge device of Claim 1 wherein said at least
one of said pair of electrodes has a coating of thorium oxide.
4. The high intensity sodium vapor discharge device of Claim 1 wherein said at least
one of said pair of electrodes is of a thoriated tungsten material.
5. The high intensity sodium vapor discharge device of Claim 1 wherein at least one
of said pair of electrodes has a coating thereon of a material selected from the group
consisting of scandium oxide (Sc2O3); yttrium oxide (Y2O3); beryllium oxide (BeO); lanthanum oxide (La2O3); cerium oxide (Ce 0 ) and hafnium oxide (HfO2).
6. A high intensity sodium vapor discharge device comprising:
a light transmittable envelope having a pair of electrically conductive leads sealed
therein and passing therethrough:
a ceramic arc tube disposed within said envelope and having a fill of sodium and noble
gases: and
a pair of spaced electrodes within said ceramic arc tube. each of said pair of electrodes
attached to an electrical conductor sealed into and passing through the end of said
ceramic arc tube and connected to one of said pair of electrically conductive leads
of said envelope, at least one of said electrodes including emissive material thereon
or therein having a free energy of formation per mole oxygen more negative than about
-180 K cal/mole at about 1200° C.
7. The high intensity sodium vapor discharge device of Claim 6 wherein said discharge
device is of an unsaturated high intensity sodium vapor discharge device.
8. The high intensity sodium vapor discharge device of Claim 7 wherein at least one
of said pair of electrodes is of a thoriated tungsten material.
9. The high intensity sodium vapor discharge device of Claim 6 wherein at least one
of said pair of electrodes has a coating of thorium oxide thereon.
10. The high intensity sodium vapor discharge device of Claim 7 wherein at least one
of said pair of electrodes has a coating thereon of a material selected from the group
consisting of thorium oxide (ThO2); scandium oxide (Sc203): yttrium oxide (Y2O3); beryllium oxide (BeO); lanthanum oxide (La203); cerium oxide (Ce203) and hafnium oxide (HfO2).