US3586898A - Aluminum chloride discharge lamp - Google Patents

Aluminum chloride discharge lamp Download PDF

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US3586898A
US3586898A US825661A US3586898DA US3586898A US 3586898 A US3586898 A US 3586898A US 825661 A US825661 A US 825661A US 3586898D A US3586898D A US 3586898DA US 3586898 A US3586898 A US 3586898A
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lamp
aluminum
filling
envelope
iodide
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US825661A
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Dimitrios M Speros
William E Smyser
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General Electric Co
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00—Gas-discharge or vapour-discharge lamps
    • H01J61/02—Details
    • H01J61/12—Selection of substances for gas fillings; Specified operating pressure or temperature
    • H01J61/125—Selection of substances for gas fillings; Specified operating pressure or temperature having an halogenide as principal component

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  • the filling also preferably contains aluminum tri-iodide, mercury for a buffer gas, and an inert gas to facilitate starting.
  • the invention relates to a high intensity discharge lamp containing a filling of aluminum trichloride.
  • the high pressure mercury vapor lamp has in recent years been improved in color rendition and light output by the addition of certain metal iodides to the basic filling of mercury and a rare gas.
  • the addition of, for instance, NaI, Tll and [M has been the most favored and the most widely used.
  • NaI, Tll and [M has been the most favored and the most widely used.
  • the presence of Nal assures a very substantial increase in efficiency and the combination of metals, by their resonance lines, complete the mercury radiation in the blue, green and yellow range of the spectrum. Notwithstanding, the color rendition, consisting essentially of lines superimposed on a weak continuum, though much improved is not equivalent to natural daylight.
  • a quartz or vitreous silica envelope, tungsten electrodes and a filling of argon, mercury and Alcl it is found that the silica envelope reacts and devitrifies rapidly and the tungsten electrodes are destroyed in as little as minutes. Even during its operative period, the lamp is unstable due to the rapidly changing electrode configuration as tungsten is transported from cooler to hotter regions of the electrode.
  • the instability is aggravated by the introduction of impurities such as SiCl resulting from the reaction between AlCl and Si0, into the arc, changes in light transmission due to early devitrification of the silica envelope, and changes in vapor pressure of components due to alteration of the thermal configuration within the lamp.
  • the object of the invention is to provide an improved aluminum chloride lamp which is long lived, stable in character, and which overcomes the above-described shortcomings.
  • M is the total concentration of the metal and Cl is the total concentration of chlorine.
  • excess metal suitably aluminum, may be placed in the lamp.
  • some iodide of the metal namely All may be added to the lamp filling and this further reduces the attack upon the electrodes. 7
  • FIG. 1 illustrates an aluminum chloride lamp in an alumina ceramic arc tube embodying the invention.
  • FIG. 2 shows the spectral output of an aluminum chloride are.
  • the first line in the table gives the equilibrium pressure of tungsten chlorides that will form in the presence of 10 torr or 1 micron of C1 in the absence of Al or other getter metal.
  • the reaction considered in this case is:
  • aluminum trichloride may dissociate directly and release chlorine according to the following reaction:
  • AlC1 AlC1+2Cl VI The aluminum being present in excess tends to combine with any chlorine so released and thus reduces the extent of attack on the tungsten electrodes.
  • the reverse of reaction lll above occurs and the excess aluminum metal may often be seen depositing in dendritic crystals or dark film.
  • reaction ll Chlorine liberated from AlCl by oxygen containing trace impurities (reaction ll) may attack the tungsten electrodes before it can diffuse to the excess aluminum and be gettered by it. However if there is aluminum triiodide in the lamp filling, the following reaction may take place:
  • the rate of attack of iodine on tungsten is much less than that of chlorine.
  • the iodine eventually diffuses to the excess pool of aluminum to regenerate the aluminum tri-iodide.
  • the composition of the lamp atmosphere should remain constant with only some of the excess aluminum being consumed in gettering oxygen containing trace impurities.
  • the presence of the iodide may enhance such regenerative transport cycles as may occur and thereby help to keep the lamp walls clean of tungsten deposits.
  • a lamp arc tube 1 embodying the invention is shown in FIG. 1 of the drawing and comprises an envelope 2 of ceramic tubing consisting of sintered high density polycrystalline alumina. This material tends to be translucent rather than clear like quartz but has exceedingly high light transmittance so that it is quite adaptable to lamp purposes. A central portion of the tube has been cut out to shorten the figure, and the internal construction can be seen in the sectioned portion.
  • the arc tube is about 65 millimeters long and 7 millimeters in internal diameter, the gap between electrodes being about 40 millimeters.
  • a niobium tube 5 penetrates into the thimble and is used as an exhaust tube during manufacture after which it is closed off.
  • a thermionic electrode 6 is mounted in each end of the arc tube and is supported through the niobium tube 5 from the end cap 3. As illustrated, the electrode 6 comprises an inner tungsten wire coil wound around a rodlike tungsten shank and an outer tungsten coil wound around the inner coil, the tungsten shank being seized in the niobium tube 5.
  • the filling of the arc tube consists of AlCl aluminum, mercury, argon and optionally All ln the illustrated lamp, quantities are 1 mg. AlCl 0.5 to 1 mg. Al, 5 mg. Hg, and argon at 20 torr.
  • the are tube operates with its ends at a temperature of better than 600 C. and this means that protection of the metal end caps from oxidation must be provided.
  • the arc tube is not operated in air but is mounted within an evacuated outer jacket (not shown).
  • the illustrated lamp operated at 200 volts with a current of l.6 amperes on alternating current and a reignition peak of about 600 volts was observed. To further reduce attack on the electrodes, 0.1 mg.
  • the aluminum chloride lamp may also be made using a fused silica or quartz arc tube provided with an internal protective coating of A1 0; to protect the silica against attack by the AlCl
  • A1 0 One way of coating the silica with A1 0 is to expose the hot tube to a mixture of AlCl vapor and an oxidizing gas mixture, suitably CO diluted with argon. The following reaction then takes place:
  • aluminum chloride lamps made from alumina-coated fused silica envelopes having volumes ranging from 0.2 to 1 cc. contained 2.2 mg. A1, 3.9 mg. HgCI and Ar at 40 torr. The are gap was about 4 mm. At a loading of 600 watts, current 5.1 amperes and voltage 148 volts, the efficiency was 75 lumens per watt.
  • the niobium end caps may be sealed directly to the tubing by machining them to a close fit and fitting them to the ends of the tubing in a vacuum at a very high temperature.
  • the seal areas may be coated with A1 0 in order to protect the calcia from attack by A101
  • the spectral output of the aluminum chloride lamp is represented by curve 11. Dotted line curve 12 shows the solar spectrum for purposes of comparison, and curve 13 is the eye sensitivity curve.
  • a high-intensity arc lamp comprising a light-transmissive envelope ofa material nonreactive with aluminum trichloride at an elevated temperature, tungsten electrodes sealed into the ends thereof, and a filling within said envelope comprising aluminum trichloride, aluminum, and an inert gas to facilitate starting.
  • a lamp as in claim 1 wherein the filling also includes aluminum tri-iodide.
  • a lamp as in claim 1 wherein the filling includes aluminum tri-iodide. and mercury.

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  • Discharge Lamp (AREA)
  • Vessels And Coating Films For Discharge Lamps (AREA)

Abstract

A metal halide high intensity lamp containing A1C13 and providing a continuous spectrum. Excess aluminum in the filling gives thermodynamic stability against attack of the tungsten electrodes and other lamp metals by chlorine, and an alumina envelope is used which does not react with A1C13. The filling also preferably contains aluminum tri-iodide, mercury for a buffer gas, and an inert gas to facilitate starting.

Description

United States Patent Dimitrios M. Speros Painesville;
William E. Smyser, Chagrin Falls, both of, Ohio May 19, [969 June 22, 1971 General Electric Company lnventors Appl. No. Filed Patented Assignee ALUMINUM CHLORIDE DISCHARGE LAMP 5 Claims, 2 Drawing Figs.
US. Cl 1. 313/229, 313/174, 313/184, 313/223 lnt.C1 .n H0lj 61/18 Field olSearch 313/184,
[56] References Cited UNITED STATES PATENTS 3,319,119 5/1967 Rendina 313/225 X 3,377,498 4/1968 Koury et al. 313/229 X Primary ExaminerRaymond F. Hossfeld Attorneys-Ernest W. Legree, Henry P. Truesdell, Frank L. Neuhauser, Oscar B. Waddell and Melvin M. Goldenberg ABSTRACT: A metal halide high intensity lamp containing AlCl and providing a continuous spectrum. Excess aluminum in the filling gives thermodynamic stability against attack of the tungsten electrodes and other lamp metals by chlorine, and an alumina envelope is used which does not react with AlC1 The filling also preferably contains aluminum tri-iodide, mercury for a buffer gas, and an inert gas to facilitate starting.
' PATENTEU JUN22 mi sww gm m i m P 0 05m u SE A m INKTM/TH l T WW9 ALUMINUM CHLORIDE DISCHARGE LAMP CROSS-REFERENCES TO RELATED APPLICATIONS Application Ser. No. 825,722 concurrently filed by D. M.
Speros, W. E. Smyser and R. M. Caldwell, entitled Metal Halide Discharge Lamp" and similarly assigned.
BACKGROUND OF THE INVENTION The invention relates to a high intensity discharge lamp containing a filling of aluminum trichloride.
The high pressure mercury vapor lamp has in recent years been improved in color rendition and light output by the addition of certain metal iodides to the basic filling of mercury and a rare gas. The addition of, for instance, NaI, Tll and [M has been the most favored and the most widely used. The presence of Nal assures a very substantial increase in efficiency and the combination of metals, by their resonance lines, complete the mercury radiation in the blue, green and yellow range of the spectrum. Notwithstanding, the color rendition, consisting essentially of lines superimposed on a weak continuum, though much improved is not equivalent to natural daylight.
A discharge through aluminum trichloride vapor results in emission consisting almost entirely of a continuum closely matching solar radiation. However when it is attempted to make a lamp in the usual fashion utilizing a quartz or vitreous silica envelope, tungsten electrodes and a filling of argon, mercury and Alcl it is found that the silica envelope reacts and devitrifies rapidly and the tungsten electrodes are destroyed in as little as minutes. Even during its operative period, the lamp is unstable due to the rapidly changing electrode configuration as tungsten is transported from cooler to hotter regions of the electrode. The instability is aggravated by the introduction of impurities such as SiCl resulting from the reaction between AlCl and Si0, into the arc, changes in light transmission due to early devitrification of the silica envelope, and changes in vapor pressure of components due to alteration of the thermal configuration within the lamp.
The object of the invention is to provide an improved aluminum chloride lamp which is long lived, stable in character, and which overcomes the above-described shortcomings.
SUMMARY OF THE INVENTION Our invention is predicated on a thermodynamic analysis which shows that in an aluminum chloride discharge the attack upon the metals such as the tungsten electrodes contained in the lamp envelope can be reduced by a large factor if the following condition is made to prevail in the lamp:
where M is the total concentration of the metal and Cl is the total concentration of chlorine. In order to realize this condition, excess metal, suitably aluminum, may be placed in the lamp. In addition, some iodide of the metal, namely All may be added to the lamp filling and this further reduces the attack upon the electrodes. 7
Our thermodynamic analysis has also indicated that aluminum trichloride is incompatible with a fused quartz arc chamber due to the possibility of reaction between AlCl and Sim. It is therefore necessary to provide an envelope material which is not attacked by AlCl and we have found that high density alumina ceramic is such a material and that AICI, will not react with A1 0 Alternatively, if it is desired to use a fused silica envelope, the silica must be protected by an internal coating ofAlll DESCRIPTION OF DRAWING FIG. 1 illustrates an aluminum chloride lamp in an alumina ceramic arc tube embodying the invention.
FIG. 2 shows the spectral output of an aluminum chloride are.
DETAILED DESCRIPTION A measure of the severity of the attack by the chlorides on tungsten is the equilibrium pressure of gaseous tungsten species that will form in the lamp. The results of thermodynamic analysis based upon data obtained from JANAF tables and their supplements are given in Table 1 below. The JANAF Therrnochemical Tables are a compendium of thermochemical data made under joint ArmyNavy-Air Force sponsorship and is a US. Department of Commerce publication distributed by Clearing House for Federal Scientific and Technical Information.
The first line in the table gives the equilibrium pressure of tungsten chlorides that will form in the presence of 10 torr or 1 micron of C1 in the absence of Al or other getter metal. The reaction considered in this case is:
The second line of the table gives the results for the case in which only AlCl exists in the lamp. The reaction then will take the form:
The third line of the table gives the results for the case in which both AlCl and Al exist in the lamp. The reaction then will be:
Finally the last line of the table gives the results for the case in which, in addition to AlCl and Al, All also exists in the lamp. The reaction then is the same as in III above but with the partial pressure of A1( g) being equal to that from the dissociation:
The table shows dramatically the suppression of the attack by the utilization of excess metal and excess metal plus iodide.
Because of uncertainties in the data, the results of table I should be taken in a qualitative rather than an absolute sense,
The trace of free chlorine would then enter a transport cycle involving the lamp metals and causing a rapid attack on the electrodes. However by having excess aluminum present, either the oxygen impurity or the trace of free chlorine is gettered and the transport cycle is prevented.
2. At high temperatures, aluminum trichloride may dissociate directly and release chlorine according to the following reaction:
AlC1 AlC1+2Cl VI The aluminum being present in excess tends to combine with any chlorine so released and thus reduces the extent of attack on the tungsten electrodes. When the lamp is turned off and cooled, the reverse of reaction lll above occurs and the excess aluminum metal may often be seen depositing in dendritic crystals or dark film.
The beneficial effect of the addition of aluminum tri-iodide to the lamp filling in further reducing attack of electrodes is probably accounted for by the following three factors:
1. Chlorine liberated from AlCl by oxygen containing trace impurities (reaction ll) may attack the tungsten electrodes before it can diffuse to the excess aluminum and be gettered by it. However if there is aluminum triiodide in the lamp filling, the following reaction may take place:
Even though there may be some iodine temporarily present in the lamp filling as the lamp warms up, the rate of attack of iodine on tungsten is much less than that of chlorine. Of course, the iodine eventually diffuses to the excess pool of aluminum to regenerate the aluminum tri-iodide. Thus the composition of the lamp atmosphere should remain constant with only some of the excess aluminum being consumed in gettering oxygen containing trace impurities.
2. The presence of aluminum tri-iodide in the lamp atmosphere further increases the concentration of aluminum thereby decreasing the chlorine concentration and this further reduces the attack on the lamp electrodes. Thus the iodine may be said to volatilize the excess metal and thereby reduce the rate of attack of chlorine on electrodes.
. The presence of the iodide may enhance such regenerative transport cycles as may occur and thereby help to keep the lamp walls clean of tungsten deposits.
A lamp arc tube 1 embodying the invention is shown in FIG. 1 of the drawing and comprises an envelope 2 of ceramic tubing consisting of sintered high density polycrystalline alumina. This material tends to be translucent rather than clear like quartz but has exceedingly high light transmittance so that it is quite adaptable to lamp purposes. A central portion of the tube has been cut out to shorten the figure, and the internal construction can be seen in the sectioned portion. By way of example, in a 400 watt size of lamp, the arc tube is about 65 millimeters long and 7 millimeters in internal diameter, the gap between electrodes being about 40 millimeters. The ends of the tube are closed by thimblelike niobium closures or end caps 3,3 hermetically sealed to the ceramic by an aluminaealcia sealing composition shown at 4. A niobium tube 5 penetrates into the thimble and is used as an exhaust tube during manufacture after which it is closed off. A thermionic electrode 6 is mounted in each end of the arc tube and is supported through the niobium tube 5 from the end cap 3. As illustrated, the electrode 6 comprises an inner tungsten wire coil wound around a rodlike tungsten shank and an outer tungsten coil wound around the inner coil, the tungsten shank being seized in the niobium tube 5.
The filling of the arc tube consists of AlCl aluminum, mercury, argon and optionally All ln the illustrated lamp, quantities are 1 mg. AlCl 0.5 to 1 mg. Al, 5 mg. Hg, and argon at 20 torr. The are tube operates with its ends at a temperature of better than 600 C. and this means that protection of the metal end caps from oxidation must be provided. In a practical lamp, the arc tube is not operated in air but is mounted within an evacuated outer jacket (not shown). The illustrated lamp operated at 200 volts with a current of l.6 amperes on alternating current and a reignition peak of about 600 volts was observed. To further reduce attack on the electrodes, 0.1 mg. ofAll may be added to the filling; the amount of mercury may be reduced to offset the increase in arc drop from the addition ofAll The aluminum chloride lamp may also be made using a fused silica or quartz arc tube provided with an internal protective coating of A1 0; to protect the silica against attack by the AlCl One way of coating the silica with A1 0 is to expose the hot tube to a mixture of AlCl vapor and an oxidizing gas mixture, suitably CO diluted with argon. The following reaction then takes place:
but
By way of example, aluminum chloride lamps made from alumina-coated fused silica envelopes having volumes ranging from 0.2 to 1 cc. contained 2.2 mg. A1, 3.9 mg. HgCI and Ar at 40 torr. The are gap was about 4 mm. At a loading of 600 watts, current 5.1 amperes and voltage 148 volts, the efficiency was 75 lumens per watt.
In the case of an alumina envelope, the niobium end caps may be sealed directly to the tubing by machining them to a close fit and fitting them to the ends of the tubing in a vacuum at a very high temperature. Where the alternative method previously described of sealing a niobium end cap by a sealing composition or glass consisting primarily of alumina and calcia is used, the seal areas may be coated with A1 0 in order to protect the calcia from attack by A101 In FIG. 2 of the drawing, the spectral output of the aluminum chloride lamp is represented by curve 11. Dotted line curve 12 shows the solar spectrum for purposes of comparison, and curve 13 is the eye sensitivity curve. It will be observed that the spectrum is a strong continuum with a great number of relatively weak lines or bands superposed. The amplitude is high in the region of the eye sensitivity curve so that a high luminous efficiency may be expected from the discharge. Measurements have confirmed efficiencies of lumens per watt and up.
What we claim as new and desire to secure by Letters Patent of the United States is:
l. A high-intensity arc lamp comprising a light-transmissive envelope ofa material nonreactive with aluminum trichloride at an elevated temperature, tungsten electrodes sealed into the ends thereof, and a filling within said envelope comprising aluminum trichloride, aluminum, and an inert gas to facilitate starting.
2. A lamp as in claim 1 wherein the filling also includes aluminum tri-iodide.
3. A lamp as in claim 1 wherein the filling includes aluminum tri-iodide. and mercury.
4. A lamp as in claim 1 wherein the envelope is high density polycrystalline alumina.
5. A lamp as in claim 1 wherein the envelope is fused silica coated internally with a protective layer of aluminum oxide.

Claims (4)

  1. 2. A lamp as in claim 1 wherein the filling also includes aluminum tri-iodide.
  2. 3. A lamp as in claim 1 wherein the filling includes aluminum tri-iodide. and mercury.
  3. 4. A lamp as in claim 1 wherein the envelope is high density polycrystalline alumina.
  4. 5. A lamp as in claim 1 wherein the envelope is fused silica coated internally with a protective layer of aluminum oxide.
US825661A 1969-05-19 1969-05-19 Aluminum chloride discharge lamp Expired - Lifetime US3586898A (en)

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS48100992A (en) * 1972-04-04 1973-12-19
US3882345A (en) * 1971-11-22 1975-05-06 Gen Electric Metal halide discharge lamp containing tin and sodium halides
US3882343A (en) * 1970-10-06 1975-05-06 Gen Electric Tin chloride molecular radiation lamp
US3898504A (en) * 1970-12-09 1975-08-05 Matsushita Electronics Corp High pressure metal vapor discharge lamp
US3911308A (en) * 1974-02-07 1975-10-07 Matsushita Electronics Corp High-pressure metal-vapor discharge lamp
US3958145A (en) * 1973-03-06 1976-05-18 U.S. Philips Corporation High pressure, mercury vapor, metal halide discharge lamp
US4436762A (en) 1982-07-26 1984-03-13 Gte Laboratories Incorporated Low pressure plasma discharge formation of refractory coatings
US4480213A (en) * 1982-07-26 1984-10-30 Gte Laboratories Incorporated Compact mercury-free fluorescent lamp
US4492898A (en) * 1982-07-26 1985-01-08 Gte Laboratories Incorporated Mercury-free discharge lamp
US4495435A (en) * 1982-07-26 1985-01-22 Gte Laboratories Incorporated Plasma switch
US4636692A (en) * 1984-09-04 1987-01-13 Gte Laboratories Incorporated Mercury-free discharge lamp
US4647821A (en) * 1984-09-04 1987-03-03 Gte Laboratories Incorporated Compact mercury-free fluorescent lamp
US4710679A (en) * 1985-12-06 1987-12-01 Gte Laboratories Incorporated Fluorescent light source excited by excimer emission
EP0714551B1 (en) * 1993-08-16 1997-08-20 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Metal-halide discharge lamp for photographic-lighting purposes
US20060091812A1 (en) * 2002-11-26 2006-05-04 Koninklijke Philips Electronics, N.V. High-pressure discharge lamp with mercury chloride having a limited chlorine content
US20090096342A1 (en) * 2007-10-12 2009-04-16 General Electric Company. Highly emissive material, structure made from highly emissive material, and method of making the same
US20090098389A1 (en) * 2007-10-12 2009-04-16 General Electric Company. Highly emissive material, structure made from highly emissive material, and method of making the same

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50115519U (en) * 1974-03-07 1975-09-20
JPH03152852A (en) * 1989-11-08 1991-06-28 Matsushita Electric Works Ltd Discharge lamp of high brightness and electrodeless discharge lamp device
US5256940A (en) * 1989-11-08 1993-10-26 Matsushita Electric Works, Ltd. High intensity discharge lamp device
DE10216092A1 (en) * 2002-04-11 2003-10-30 Schott Glas Composite material used for envelope for HID lamps comprises a substrate material in the form of quartz and a barrier coating applied on one side of the substrate material using impulse-CVD

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3882343A (en) * 1970-10-06 1975-05-06 Gen Electric Tin chloride molecular radiation lamp
US3898504A (en) * 1970-12-09 1975-08-05 Matsushita Electronics Corp High pressure metal vapor discharge lamp
US3882345A (en) * 1971-11-22 1975-05-06 Gen Electric Metal halide discharge lamp containing tin and sodium halides
JPS48100992A (en) * 1972-04-04 1973-12-19
US3958145A (en) * 1973-03-06 1976-05-18 U.S. Philips Corporation High pressure, mercury vapor, metal halide discharge lamp
US3911308A (en) * 1974-02-07 1975-10-07 Matsushita Electronics Corp High-pressure metal-vapor discharge lamp
US4436762A (en) 1982-07-26 1984-03-13 Gte Laboratories Incorporated Low pressure plasma discharge formation of refractory coatings
US4480213A (en) * 1982-07-26 1984-10-30 Gte Laboratories Incorporated Compact mercury-free fluorescent lamp
US4492898A (en) * 1982-07-26 1985-01-08 Gte Laboratories Incorporated Mercury-free discharge lamp
US4495435A (en) * 1982-07-26 1985-01-22 Gte Laboratories Incorporated Plasma switch
US4636692A (en) * 1984-09-04 1987-01-13 Gte Laboratories Incorporated Mercury-free discharge lamp
US4647821A (en) * 1984-09-04 1987-03-03 Gte Laboratories Incorporated Compact mercury-free fluorescent lamp
US4710679A (en) * 1985-12-06 1987-12-01 Gte Laboratories Incorporated Fluorescent light source excited by excimer emission
EP0714551B1 (en) * 1993-08-16 1997-08-20 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Metal-halide discharge lamp for photographic-lighting purposes
US5691601A (en) * 1993-08-16 1997-11-25 Patent-Treuhand-Gesellschaft F. Elektrische Gluehlampen Mbh Metal-halide discharge lamp for photooptical purposes
US20060091812A1 (en) * 2002-11-26 2006-05-04 Koninklijke Philips Electronics, N.V. High-pressure discharge lamp with mercury chloride having a limited chlorine content
US7282862B2 (en) * 2002-11-26 2007-10-16 Koninklijke Philips Electronics, N.V. High-pressure discharge lamp with mercury chloride having a limited chlorine content
US20080007179A1 (en) * 2002-11-26 2008-01-10 Koninklijke Philips Electronics, N.V. High-pressure discharge lamp with mercury chloride having a limited chlorine content
US20090096342A1 (en) * 2007-10-12 2009-04-16 General Electric Company. Highly emissive material, structure made from highly emissive material, and method of making the same
US20090098389A1 (en) * 2007-10-12 2009-04-16 General Electric Company. Highly emissive material, structure made from highly emissive material, and method of making the same
US7768207B2 (en) * 2007-10-12 2010-08-03 General Electric Company Highly emissive material, structure made from highly emissive material, and method of making the same

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GB1253948A (en) 1971-11-17
DE2023772B2 (en) 1974-01-17
DE2023772C3 (en) 1974-08-22
DE2023772A1 (en) 1970-12-10
BE750474A (en) 1970-11-16
JPS4915414B1 (en) 1974-04-15
FR2047427A5 (en) 1971-03-12

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