EP0603014B1 - Electrodeless lamp bulb - Google Patents

Electrodeless lamp bulb Download PDF

Info

Publication number
EP0603014B1
EP0603014B1 EP19930310312 EP93310312A EP0603014B1 EP 0603014 B1 EP0603014 B1 EP 0603014B1 EP 19930310312 EP19930310312 EP 19930310312 EP 93310312 A EP93310312 A EP 93310312A EP 0603014 B1 EP0603014 B1 EP 0603014B1
Authority
EP
European Patent Office
Prior art keywords
lamp
iodide
rare earth
fill
bulb
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
EP19930310312
Other languages
German (de)
French (fr)
Other versions
EP0603014A1 (en
Inventor
Alfred E. Feuersanger
Charles William Struck
William M. Keeffe
Michael J. Shea
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.)
Flowil International Lighting Holding BV
Original Assignee
Flowil International Lighting Holding BV
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 Flowil International Lighting Holding BV filed Critical Flowil International Lighting Holding BV
Publication of EP0603014A1 publication Critical patent/EP0603014A1/en
Application granted granted Critical
Publication of EP0603014B1 publication Critical patent/EP0603014B1/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
    • H01J61/125Selection of substances for gas fillings; Specified operating pressure or temperature having an halogenide as principal component
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J65/00Lamps without any electrode inside the vessel; Lamps with at least one main electrode outside the vessel
    • H01J65/04Lamps in which a gas filling is excited to luminesce by an external electromagnetic field or by external corpuscular radiation, e.g. for indicating plasma display panels

Definitions

  • This invention relates a lamp bulb. More particularly, this invention relates to a lamp bulb for electrodeless lamps having a metal iodide fill with improved colour rendering.
  • the first practical microwave light sources often called electrodeless lamps, were described by a group at GTE Laboratories in 1975. Using an electrodeless lamp and a termination fixture, having an inner and outer conductor, it is excited by high frequency power at 915 or 2450 MHz, or in the possible frequency range from 100 MHz to 300 GHz.
  • Microwave-powered lamps are comprised of a gas discharge in a sealed envelope containing a chemical fill of mercury, metal halides and starting gas, such as argon.
  • the microwave power from a (solid state, magnetron or other tube) power source is coupled over a transmission line (e.g. waveguide, coaxial line or microstrip line).
  • Impedance matching efficiently couples the EM-field into the chemical fill to start, develop, and maintain the discharge for efficient generation of light.
  • the light emitting plasma discharge, the lamp fill, the arc tube and the field coupler comprise the effective impedance matched load (field coupled lamp load) that the power supplying microwave transmission line sees.
  • US-A-4,427,921 describes such an application of high frequency power to an electrodeless lamp containing metal iodide or iodine.
  • Optical emission is described as being dominated from excited iodine atoms which emit ultraviolet light at 206.2 pm. Additional emissions are described as being produced in the visible and ultraviolet portions of the spectrum from radiative transitions in I, I 2 , HgI 2 , HgI, Cd, CdI 2 , CdI, etc., depending on the composition of the fill material.
  • the use of rare earth fills in electroded lamps results in "very high wall loadings ... resulting in a rapid decrease in colour temperature ... and a very short effective lifetime of about 200 hours".
  • the improved electrodeless lamp is set forth in column 6, lines 50 to 55, "mercury is needed for a high pressure discharge, argon is used to initiate the discharge, and a rare-earth halide is used to achieve atomic plus molecular emission”.
  • the results are described as being improved with the addition of cesium halide, but only mercury, argon, and a rare-earth halide are described as necessary.
  • the improved fill includes a rare earth compound, i.e., dysprosium iodide, holmium iodide.
  • GTE's Metalarc M100/U lamp with a NaIScI 3 CsI chemistry, has a colour rendering index (CRI) of 65, an initial lumens per watt (LPW) of 85, and a 10,000 hour lifetime.
  • the above chemistry can be modified by the replacement of the element cesium with lithium to form a chemistry of NaIScI 3 LiI.
  • the resulting lamp has an improved CRI of 73 while still maintaining the 10,000 hour life and the 85 LPW efficacy.
  • a CRI of 73 must be further improved for the excellent colour rendering needed for showroom lighting, displays in stores, and decorative illumination, both for indoor and outdoor use. Without such further improvement, their colour rendering properties limit their commercial use in certain colour-critical applications.
  • the colour rendering index of light source is a measure of the degree of colour shift objects undergo when illuminated by the light source as compared with the colour of those same objects when illuminated by a reference source of comparable colour temperature.
  • the CRI rating consists of a General Index, Ra, based on a set of eight test-colour samples that have been found adequate to cover the colour gamut.
  • the colour appearance of a lamp is described by its chromaticity coordinates which can be calculated from the spectral power distribution according to standard methods.
  • Luminous efficacy of a source of light is the quotient of the total luminous flux emitted by the total lamp power input as expressed in lumens per watt (LPW or lm/W).
  • An electroded lamp having a fill containing mercury, an inert starting gas, sodium and/or lithium iodide, scandium iodide and a small concentration of a rare earth is known from US-A-3,979,624. This document suggests that the molar ratio of alkali metal halide to scandium halide should be from 1.7:1 to 5:1.
  • An electrodeless lamp having a fill containing mercury, an inert gas, calcium halide, a sodium halide and a rare earth halide is known from EP-A-0,271,911, over which claim 1 is characterised.
  • the calcium halide is present to increase the red emission and thereby lower the lamp's colour temperature.
  • an electrodeless lamp having a lamp bulb comprising a sealed envelope containing a fill material for supporting a gas discharge, said fill material comprising an inert starting gas, mercury, and alkali metal iodides, and at least one iodide of a rare earth, characterised in that the alkali metal iodides consist substantially of sodium iodide and lithium iodide, the fill further comprises scandium iodide, and in that the molar ratio of said iodide of a rare earth to scandium iodide is between 1:1 to 30:1.
  • the lamp bulb comprises a sealed transparent envelope with a continuous wall and containing a chemical fill.
  • the bulb may be operable at a desirable wall temperature conducive to long life while emitting the visible radiation.
  • the chemical fill comprises an inert starting gas, mercury, alkali metal iodides, scandium iodide, and at least one iodide of a rare earth.
  • the alkali metal iodides comprise substantially sodium iodide and lithium iodide.
  • the iodide of a rare earth and scandium iodide are preferably present in amounts sufficient to form a complex for increasing the density of the rare earth in the discharge gas during lamp operation to effect a colour rendering index greater than about 80 and a colour temperature between about 3000 to about 5000 Kelvin. Due to the increased density of the rare earth in the discharge gas at lower temperatures of operation, the wall temperature of the gas discharge tube is desirably maintained at a temperature to enhance the life of the bulb.
  • FIG. 1 shows a representation of a microwave lamp system showing a schematic representation of the bulb during operation.
  • FIGS. 2A-2D show a process for preparing bulbs by a three part construction.
  • FIG. 2A shows bulb components.
  • FIG. 2B and FIG. 2C show construction steps.
  • FIG. 2D shows the completed tube.
  • FIG. 1 shows a microwave lamp bulb in accordance with an embodiment of the invention.
  • a bulb 1 is a transparent envelope containing a chemical fill 4 within an exterior wall 3. The fill forms a gas discharge during lamp operation.
  • the wall material is preferably a fused silica or ceramic alumina (PCA). Yttria or sapphire which is a single crystalline alumina may be used. Since the bulb 1 is utilized in an electrodless lamp, the continuous wall has an internal surface uninterrupted by an electrically conducting path extending through the wall 3 as is found in conventional electroded bulbs.
  • the purpose of the metal halide chemical fill 4 is to generate sufficient optical rare earth emissions without chemical interaction with wall 3.
  • the arc tube can have various shapes, however, a cylindrical arc tube with hemispherical end chambers is most practical. A football shape is more difficult to fabricate, but it will have a desirable increased end-temperature.
  • a chemical fill which forms an electrical discharge sustaining gas for emitting radiation is disposed within the transparent envelope.
  • the chemical fill contains a base chemistry of an inert starting gas, mercury, alkali metal iodides, and scandium iodide.
  • the desired base chemistry contributes to the desirable lamp characteristics of low wall temperature, high LPW, moderate CRI, and long life.
  • the lamp emission due to the base chemistry is approximately on the black body chromaticity locus.
  • the chemical fill comprises at least one iodide of a rare earth element which is at least partially vapourized during lamp operation.
  • the iodide of a rare earth and scandium iodide are present in a molar ratio sufficient to form a complex for increasing the concentration of the rare earth in the discharge gases during lamp operation at a low arc tube wall temperature. Due to the formation of the complex, the vapour phase concentration of the rare earth is increased at the arc tube wall temperature beyond what is obtainable using the rare earth iodide alone.
  • the wall temperature of the arc tube in the lamp of the present invention is preferably maintained between 690 and 960 degrees Celsius, more preferably between 690 and 730 degrees Celsius.
  • the improved chemical fill comprising the base chemistry and at least one rare earth iodide may enhance the colour rendering index of the lamp. Due to the presence of the rare earth atoms in the discharge gas, the lamp has a colour rendering index greater than 80. Preferably, the colour rendering index is greater than 85 and more preferably greater than 90.
  • High colour rendering indices on the order of about 90, are easier to realize at high correlated colour temperatures (CCT).
  • CCT correlated colour temperatures
  • the present invention achieves high Ra at relatively low CCT between 3000 and 4000 Kelvin.
  • the amount of rare earth in the gas discharge is sufficient to produce an enhanced colour rendering index while maintaining the relatively low arc tube wall temperature that is conducive to long lamp life.
  • the formation of complex molecules of the rare earth with scandium iodide results in an increased density of rare earth atoms in the gas discharge.
  • rare earth is present in an amount sufficient to complex with scandium iodide in order to increase the density of the rare earth atoms in the vapour during lamp operation to the desired level.
  • the molar ratio of the rare earth iodide to scandium iodide in the fill is between 1:1 to 30:1, and more preferably between 5:1 to 20:1.
  • the rare earths are selected from the group consisting of La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and mixtures thereof.
  • the choice of rare earth depends on the desired radiation characteristics.
  • the preferred rare earths for enhanced CRI are the iodides of cerium (Ce), praseodymium (Pr), neodymium (Nd), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), and lutetium (Lu).
  • the rare earth iodide is present as a single rare earth iodide selected from the above preferred group. Even more preferred are the rare earth iodides of cerium, praseodymium, dysprosium, holmium, and thulium.
  • a charge of mercury is present in a sufficient amount so as to establish the electrical characteristics of the lamp by desirably increasing the electric field strength to sustain a desirable power loading.
  • Such an amount should provide an operating mercury pressure between 10 kPa (1 atmosphere) to about 1 MPa (100 atmospheres), and preferably between about 10 kPa (1 atmosphere) to about 200 kPa (20 atmospheres).
  • an inert ionizable starting gas such as argon is contained within the transparent envelope. It is contemplated that other noble gases can be substituted for argon provided an appropriate pressure is maintained that is conducive to starting the lamp.
  • the scandium iodide and the alkali metal iodides are present in the fill and in the discharge gas during lamp operation.
  • These ingredients form a base chemistry which is conducive to the low wall temperature and long lamp life.
  • These ingredients also improve colour quality by adding a variety of lines to the emission spectrum and are preferably present in amounts for producing emission with its colour substantially on the black body radiator chromaticity locus.
  • the molar ratio of sodium iodide to scandium iodide is preferably between 5:1 to 25:1.
  • the ratio of sodium iodide to lithium iodide is preferably between 1:1 to 5:1.
  • the alkali metal iodides adjust the current-voltage characteristics, improve the colour quality, and contribute to lumen output of the lamp through strong emissions.
  • the scandium iodides significantly improves the "efficacy" in lumens per watt (LPW) and the CRI.
  • the addition of rare earth iodides further improves the LPW to greater than 90 and preferably greater than 100, and, also, improves the CRI to greater than 80 while maintaining CCT between 3000 and 5000 Kelvin.
  • the selection of fill ingredients results in a desirable colour temperature between 3000 K and 5000 K, more preferably between about 3000 to about 4000 Kelvin.
  • the molar ratios of the ingredients are selected also so that the resulting emission colour is near the highly desirable black body (BB) chromaticity locus at this desired colour temperature.
  • scandium, thorium, cadmium, or zinc may be added to the fill as metals or alloys to adjust the metal/iodine ratio in the lamp and to getter oxygen impurities.
  • the preferred additive is scandium.
  • the scandium metal weight dosage is preferably about 100 micrograms per cubic centimeter of arc tube volume at all wattages.
  • the total fill weight varies with lamp operating power between about 4 and about 20mg.
  • the 100 watt lamp fill is preferably between about 4mg and about 8 mg, and more preferably between about 5.5 and about 6.5 mg.
  • a microwave power source 7 may be solid state, magnetron or some other tube coupled over a transmission line 9 in the form of a waveguide, coaxial line or microstrip line.
  • the impedance matching network 11 and EM-field coupler 13 delivers power to the bulb 1.
  • a - A is the impedance reference plane.
  • the light emitting plasma discharge, the lamp fill 4, the bulb 1 and the field coupler 13 comprise the effective impedance matched load (field coupled lamp load) that the power supplying microwave transmission line sees.
  • the lamp is powered by high frequency (microwave) excitation of the discharge that is the matched load of a microwave circuit (for maximum power transfer) operating in the frequency range from 100 MHz to 300 GHz.
  • the lamp is impedance matched to the impedance of the transmission line 9 from the driving source for such load circuit conditions the lamp represents when it is operating in equilibrium at lamp design input power.
  • the range of design input power for the microwave lamps is typically from 10 Watt to 1 kWatt.
  • the arc tube wall temperature at the center is preferably in the range of 690 to 730 degrees Celsius. This, of course, depends on the lamp design parameters such as mercury pressure, arc tube wall thickness and wall-loading (W/cm 2 ) of the arc tube.
  • bulb 1 is a high purity fused silica with zero hydroxyl ion content, such as GTE-Sylvania water free fused silica or General Electric GE 214A hydroxyl free fused silica.
  • the bulb 1 is formed from tubing having a size (I.D. and O.D.) which is determined according to the desired and allowable wall loading for the particular discharge lamp.
  • the quartz tube 43 is first attached to a quartz rod or support member 45.
  • a funnel 47 is inserted into the resulting assembly. The charge of chemical fill is introduced through the funnel 47.
  • FIG. 2C shows the quartz tube 43 necked down at a constriction 49 for evacuaation and sealing.
  • FIG. 4D shows the completed bulb 1 which includes support 45 which may be used to hold and positioned the bulb 1 in the EM-field coupling structure.
  • the bulb blanks as shown in Fig. 2B are prepared for filling by baking them in a furnace at temperatures of 1000°C and ultra high vacuum by attaching them to a vacuum system. This is done by means of a NUPRO R B series valve (SS 8BG TSW) that is equipped with a quick-connect (CAJON, Ultra-Torr) for attaching the fill tube of bulb blank to the valve.
  • the baked bulb still under vacuum is put into an argon filled drybox and opened to the argon.
  • the bulb is then is filled with the liquid and solid components of the fill, the valve is again closed, and then the bulb is transferred from the drybox and attached to the gas fill system.
  • the bulb After the argon is pumped out, the bulb is filled to the desired pressure with a noble gas such as argon, xenon or a Penning mixture and then tipped off.
  • a noble gas such as argon, xenon or a Penning mixture and then tipped off.
  • the backfilled gas serves as the starting gas in the lamp.
  • the following fill is for a bulb with a volume of 1.25 cm 3 and the total fill weight is 19 mg. Typical fill weights are from about 4 to about 50 mg/cm 3 .
  • a preferred embodiment of the present invention may provide a lamp bulb with increased colour rendering index for an electrodeless high intensity discharge lamp utilizing the NaIScI 3 LiI chemistry while maintaining the efficacy and long life characteristic of such lamps; may improve the colour rendering properties of the emitted light while maintaining a long bulb life; may increase the density of the rare earth species above the density obtainable with a rare earth iodide alone; may increase the density of the rare earth atoms in the gas discharge by forming a complex molecule containing the rare earth element; and may have a low wall temperature of the gas discharge envelope which is conducive to a long lamp life.

Description

  • This invention relates a lamp bulb. More particularly, this invention relates to a lamp bulb for electrodeless lamps having a metal iodide fill with improved colour rendering.
  • High frequency electromagnetic field excitation of gas discharges has been studied and applied for many years. Originally, microwaves were applied in gas discharge devices such as Noise Sources, Transmit-Receive (TR) Tubes, and, generally, as Gas Discharge Circuit Elements. The interaction of microwaves with gas discharges was treated by S. C. Brown, Introduction to Electrical Discharges in Gases, John Wiley & Sons, Inc., New York, (1966). An early application to lamps is given in "Microwave Discharge Cavities Operating at 2450 MHz" by F. C. Fehsenfeld et al., Rev. Sci. Instruments, 36, No. 3, (March 1965), where,in a resonant discharge cavity power, is transferred from the source to the lamp. The lamp is substantially enclosed by the resonant cavity impeding the transmission of light from the gas discharge source.
  • The first practical microwave light sources, often called electrodeless lamps, were described by a group at GTE Laboratories in 1975. Using an electrodeless lamp and a termination fixture, having an inner and outer conductor, it is excited by high frequency power at 915 or 2450 MHz, or in the possible frequency range from 100 MHz to 300 GHz. This work is described and covered in the following patents: US-A-3,942,058; US-A-3,942,068; US-A-3,943,401; US-A-3,943,402; US-A-3,943,403; US-A-3,943,404; US-A-3,993,927; US-A-3,995,195; US-A-3,997,816; US-A-4,001,631; US-A-4,001,632; US-A-4,002,944; US-A-4,041,352; US-A-4,053,814; US-A-4,065,701; US-A-4,070,603; US-A-4,178,534; and US-A-4,266,162.
  • The possible frequency bands available for microwave lamp operation are regulated by the Federal Communications Commission, Rules and Regulations, Vol. II, Part 18, Industrial, Scientific, and Medical Equipment, Federal Communication Commission, July 1981. See 18.13, page 180. Guidelines for threshold limit values for microwave radiation are published by the American Conference of Governmental Industrial Hygienists, Threshold Limit Values and Biological Exposure Indices for 1989-1990; American Conference of Governmental Industrial Hygienists, Cincinnati, Ohio, pp. 108-111.
  • Microwave-powered lamps are comprised of a gas discharge in a sealed envelope containing a chemical fill of mercury, metal halides and starting gas, such as argon. The microwave power from a (solid state, magnetron or other tube) power source is coupled over a transmission line (e.g. waveguide, coaxial line or microstrip line). Impedance matching efficiently couples the EM-field into the chemical fill to start, develop, and maintain the discharge for efficient generation of light. The light emitting plasma discharge, the lamp fill, the arc tube and the field coupler comprise the effective impedance matched load (field coupled lamp load) that the power supplying microwave transmission line sees.
  • US-A-4,427,921 describes such an application of high frequency power to an electrodeless lamp containing metal iodide or iodine. Optical emission is described as being dominated from excited iodine atoms which emit ultraviolet light at 206.2 pm. Additional emissions are described as being produced in the visible and ultraviolet portions of the spectrum from radiative transitions in I, I2, HgI2, HgI, Cd, CdI2, CdI, etc., depending on the composition of the fill material.
  • US-A-4,206,387 al describes scandium iodide and sodium iodide chemical fills for an electrodeless lamp to provide high efficacy (about 100LPW) but only fair colour rendering (CRI=65). As set forth, the use of rare earth fills in electroded lamps results in "very high wall loadings ... resulting in a rapid decrease in colour temperature ... and a very short effective lifetime of about 200 hours". The improved electrodeless lamp, is set forth in column 6, lines 50 to 55, "mercury is needed for a high pressure discharge, argon is used to initiate the discharge, and a rare-earth halide is used to achieve atomic plus molecular emission". The results are described as being improved with the addition of cesium halide, but only mercury, argon, and a rare-earth halide are described as necessary. The improved fill includes a rare earth compound, i.e., dysprosium iodide, holmium iodide.
  • Because of their superior efficacy and operating life, conventional electroded lamps utilizing a chemical fill of alkali and scandium iodides are highly desirable. GTE's Metalarc M100/U lamp, with a NaIScI3CsI chemistry, has a colour rendering index (CRI) of 65, an initial lumens per watt (LPW) of 85, and a 10,000 hour lifetime. The above chemistry can be modified by the replacement of the element cesium with lithium to form a chemistry of NaIScI3LiI. The resulting lamp has an improved CRI of 73 while still maintaining the 10,000 hour life and the 85 LPW efficacy. However, a CRI of 73 must be further improved for the excellent colour rendering needed for showroom lighting, displays in stores, and decorative illumination, both for indoor and outdoor use. Without such further improvement, their colour rendering properties limit their commercial use in certain colour-critical applications.
  • Certain advantages are attendant with the electrodeless lamp, or microwave powered lamp as compared to the conventional electroded lamp. The absence of conduction current electrodes, i.e., the elimination of tungsten from the inside of the gas discharge tube, reduces significantly the limitations imposed by the high temperature chemical reactions of the active light producing lamp fill with the container and electrical lamp materials. The electrode feedthroughs (eg. press seals) that can lead to lamp defects are also not required. In addition, lamp efficacy is improved, compared to equivalent electroded lamps, by absence of the electrical and thermal conduction losses generated in lamps with conduction electrodes. Electrolysis of fill species, such as sodium, is reduced to give good colour stability. The improved lamp performance may be more easily achieved without increase of wall temperatures.
  • These advantages, of themselves, do not improve the CRI of electrodeless lamps. With rare earth fills they also do not allow low enough temperatures at the wall of the gas discharge tube to promote long life. Further improvements in chemical fills for high frequency microwave powered lamps are desirable, especially fills which desirably contribute to improved colour rendering, superior efficacy, and longer operating life.
  • Certain terms as used in this specification have meanings which are generally accepted in the lighting industry. These terms are described in the IES LIGHTING HANDBOOK, Reference Volume, 1984, Illuminating Engineering Society of North America. The colour rendering index of light source (CRI) is a measure of the degree of colour shift objects undergo when illuminated by the light source as compared with the colour of those same objects when illuminated by a reference source of comparable colour temperature. The CRI rating consists of a General Index, Ra, based on a set of eight test-colour samples that have been found adequate to cover the colour gamut. The colour appearance of a lamp is described by its chromaticity coordinates which can be calculated from the spectral power distribution according to standard methods. See CIE, Method of Measuring and Specifying Colour Rendering Properties of Light Sources (2nd ed.), Publ. CIE No. 13.2 (TC-3,2), Bureau Central de la CIE, Paris, 1974. The CIE standard chromaticity diagram includes the colour points of black body radiators at various temperatures. The locus of blackbody chromaticities on the x,y-diagram is known as the Planckian locus. Any emitting source represented by a point on this locus may be specified by a colour temperature. A point near but not on this Planckian locus has a correlated colour temperature (CCT) because lines can be drawn from such points to intersect the Planckian locus at this colour temperature such that all points look to the average human eye as having nearly the same colour. Luminous efficacy of a source of light is the quotient of the total luminous flux emitted by the total lamp power input as expressed in lumens per watt (LPW or lm/W).
  • An electroded lamp having a fill containing mercury, an inert starting gas, sodium and/or lithium iodide, scandium iodide and a small concentration of a rare earth is known from US-A-3,979,624. This document suggests that the molar ratio of alkali metal halide to scandium halide should be from 1.7:1 to 5:1.
  • An electrodeless lamp having a fill containing mercury, an inert gas, calcium halide, a sodium halide and a rare earth halide is known from EP-A-0,271,911, over which claim 1 is characterised. The calcium halide is present to increase the red emission and thereby lower the lamp's colour temperature.
  • It is known from WO-A-93/18541 to provide an electroded lamp having a chemical fill in the discharge tube comprising an inert starting gas, mercury, alkali metal iodides, scandium iodide and at least one iodide of a rare earth. This document has a priority date of 3 March 1992 and a publication date of 16 September 1993, and accordingly falls within the terms of Article 54(3) EPC.
  • According to the present invention there is provided an electrodeless lamp having a lamp bulb comprising a sealed envelope containing a fill material for supporting a gas discharge, said fill material comprising an inert starting gas, mercury, and alkali metal iodides, and at least one iodide of a rare earth, characterised in that the alkali metal iodides consist substantially of sodium iodide and lithium iodide, the fill further comprises scandium iodide, and in that the molar ratio of said iodide of a rare earth to scandium iodide is between 1:1 to 30:1.
  • Preferably, the lamp bulb comprises a sealed transparent envelope with a continuous wall and containing a chemical fill. During operation of the bulb by energization of the chemical fill with a high frequency electromagnetic field, the bulb may be operable at a desirable wall temperature conducive to long life while emitting the visible radiation.
  • The chemical fill comprises an inert starting gas, mercury, alkali metal iodides, scandium iodide, and at least one iodide of a rare earth. The alkali metal iodides comprise substantially sodium iodide and lithium iodide. The iodide of a rare earth and scandium iodide are preferably present in amounts sufficient to form a complex for increasing the density of the rare earth in the discharge gas during lamp operation to effect a colour rendering index greater than about 80 and a colour temperature between about 3000 to about 5000 Kelvin. Due to the increased density of the rare earth in the discharge gas at lower temperatures of operation, the wall temperature of the gas discharge tube is desirably maintained at a temperature to enhance the life of the bulb.
  • An embodiment of the present invention will now be discussed by way of example only and with reference to the accompanying drawings, in which:
  • FIG. 1 shows a representation of a microwave lamp system showing a schematic representation of the bulb during operation.
  • FIGS. 2A-2D show a process for preparing bulbs by a three part construction. FIG. 2A shows bulb components. FIG. 2B and FIG. 2C show construction steps. FIG. 2D shows the completed tube.
  • FIG. 1 shows a microwave lamp bulb in accordance with an embodiment of the invention. A bulb 1 is a transparent envelope containing a chemical fill 4 within an exterior wall 3. The fill forms a gas discharge during lamp operation. The wall material is preferably a fused silica or ceramic alumina (PCA). Yttria or sapphire which is a single crystalline alumina may be used. Since the bulb 1 is utilized in an electrodless lamp, the continuous wall has an internal surface uninterrupted by an electrically conducting path extending through the wall 3 as is found in conventional electroded bulbs.
  • The purpose of the metal halide chemical fill 4 is to generate sufficient optical rare earth emissions without chemical interaction with wall 3. The arc tube can have various shapes, however, a cylindrical arc tube with hemispherical end chambers is most practical. A football shape is more difficult to fabricate, but it will have a desirable increased end-temperature.
  • A chemical fill which forms an electrical discharge sustaining gas for emitting radiation is disposed within the transparent envelope. The chemical fill contains a base chemistry of an inert starting gas, mercury, alkali metal iodides, and scandium iodide. The desired base chemistry contributes to the desirable lamp characteristics of low wall temperature, high LPW, moderate CRI, and long life. The lamp emission due to the base chemistry is approximately on the black body chromaticity locus.
  • In addition to the appropriate base chemistry, the chemical fill comprises at least one iodide of a rare earth element which is at least partially vapourized during lamp operation. The iodide of a rare earth and scandium iodide are present in a molar ratio sufficient to form a complex for increasing the concentration of the rare earth in the discharge gases during lamp operation at a low arc tube wall temperature. Due to the formation of the complex, the vapour phase concentration of the rare earth is increased at the arc tube wall temperature beyond what is obtainable using the rare earth iodide alone. The wall temperature of the arc tube in the lamp of the present invention is preferably maintained between 690 and 960 degrees Celsius, more preferably between 690 and 730 degrees Celsius.
  • In accordance with the principles of the present invention, the improved chemical fill comprising the base chemistry and at least one rare earth iodide may enhance the colour rendering index of the lamp. Due to the presence of the rare earth atoms in the discharge gas, the lamp has a colour rendering index greater than 80. Preferably, the colour rendering index is greater than 85 and more preferably greater than 90.
  • High colour rendering indices, on the order of about 90, are easier to realize at high correlated colour temperatures (CCT). In a preferred embodiment, the present invention achieves high Ra at relatively low CCT between 3000 and 4000 Kelvin.
  • During lamp operation, the amount of rare earth in the gas discharge is sufficient to produce an enhanced colour rendering index while maintaining the relatively low arc tube wall temperature that is conducive to long lamp life. The formation of complex molecules of the rare earth with scandium iodide results in an increased density of rare earth atoms in the gas discharge.
  • In preferred embodiments of the present invention, rare earth is present in an amount sufficient to complex with scandium iodide in order to increase the density of the rare earth atoms in the vapour during lamp operation to the desired level. The molar ratio of the rare earth iodide to scandium iodide in the fill is between 1:1 to 30:1, and more preferably between 5:1 to 20:1.
  • Due to their many emission lines, all rare earths may enhance the arc performance of a lamp, at least to some degree and in some respect. The rare earths are selected from the group consisting of La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and mixtures thereof. The choice of rare earth depends on the desired radiation characteristics. The preferred rare earths for enhanced CRI are the iodides of cerium (Ce), praseodymium (Pr), neodymium (Nd), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), and lutetium (Lu). According to one embodiment the rare earth iodide is present as a single rare earth iodide selected from the above preferred group. Even more preferred are the rare earth iodides of cerium, praseodymium, dysprosium, holmium, and thulium.
  • A charge of mercury is present in a sufficient amount so as to establish the electrical characteristics of the lamp by desirably increasing the electric field strength to sustain a desirable power loading. Such an amount should provide an operating mercury pressure between 10 kPa (1 atmosphere) to about 1 MPa (100 atmospheres), and preferably between about 10 kPa (1 atmosphere) to about 200 kPa (20 atmospheres).
  • In addition to mercury, a small charge of an inert ionizable starting gas such as argon is contained within the transparent envelope. It is contemplated that other noble gases can be substituted for argon provided an appropriate pressure is maintained that is conducive to starting the lamp.
  • To achieve the above discussed desirable lamp properties, the scandium iodide and the alkali metal iodides are present in the fill and in the discharge gas during lamp operation. These ingredients form a base chemistry which is conducive to the low wall temperature and long lamp life. These ingredients also improve colour quality by adding a variety of lines to the emission spectrum and are preferably present in amounts for producing emission with its colour substantially on the black body radiator chromaticity locus. The molar ratio of sodium iodide to scandium iodide is preferably between 5:1 to 25:1. The ratio of sodium iodide to lithium iodide is preferably between 1:1 to 5:1.
  • The alkali metal iodides adjust the current-voltage characteristics, improve the colour quality, and contribute to lumen output of the lamp through strong emissions. The scandium iodides significantly improves the "efficacy" in lumens per watt (LPW) and the CRI. The addition of rare earth iodides further improves the LPW to greater than 90 and preferably greater than 100, and, also, improves the CRI to greater than 80 while maintaining CCT between 3000 and 5000 Kelvin.
  • In embodiments of the present invention, the selection of fill ingredients results in a desirable colour temperature between 3000 K and 5000 K, more preferably between about 3000 to about 4000 Kelvin. The molar ratios of the ingredients are selected also so that the resulting emission colour is near the highly desirable black body (BB) chromaticity locus at this desired colour temperature.
  • In addition to the above-mentioned fill ingredients, scandium, thorium, cadmium, or zinc may be added to the fill as metals or alloys to adjust the metal/iodine ratio in the lamp and to getter oxygen impurities. The preferred additive is scandium. For a low wattage metal iodide discharge lamp with a lamp wattage less than 175 watts, e.g., between 40 to 150 watts, the scandium metal weight dosage is preferably about 100 micrograms per cubic centimeter of arc tube volume at all wattages. The total fill weight varies with lamp operating power between about 4 and about 20mg. For example, the 100 watt lamp fill is preferably between about 4mg and about 8 mg, and more preferably between about 5.5 and about 6.5 mg.
  • As illustrated schematicly in FIG. 1, a microwave power source 7 may be solid state, magnetron or some other tube coupled over a transmission line 9 in the form of a waveguide, coaxial line or microstrip line. The impedance matching network 11 and EM-field coupler 13 delivers power to the bulb 1. A - A is the impedance reference plane. The light emitting plasma discharge, the lamp fill 4, the bulb 1 and the field coupler 13 comprise the effective impedance matched load (field coupled lamp load) that the power supplying microwave transmission line sees.
  • The lamp is powered by high frequency (microwave) excitation of the discharge that is the matched load of a microwave circuit (for maximum power transfer) operating in the frequency range from 100 MHz to 300 GHz. The lamp is impedance matched to the impedance of the transmission line 9 from the driving source for such load circuit conditions the lamp represents when it is operating in equilibrium at lamp design input power. The range of design input power for the microwave lamps is typically from 10 Watt to 1 kWatt.
  • When the lamp is fully warmed up and operating in equilibrium at the design power, the arc tube wall temperature at the center is preferably in the range of 690 to 730 degrees Celsius. This, of course, depends on the lamp design parameters such as mercury pressure, arc tube wall thickness and wall-loading (W/cm2) of the arc tube.
  • Preferably, bulb 1 is a high purity fused silica with zero hydroxyl ion content, such as GTE-Sylvania water free fused silica or General Electric GE 214A hydroxyl free fused silica. The bulb 1 is formed from tubing having a size (I.D. and O.D.) which is determined according to the desired and allowable wall loading for the particular discharge lamp.
  • As shown in FIG. 2A, the quartz tube 43 is first attached to a quartz rod or support member 45. As shown in FIG. 2B, a funnel 47 is inserted into the resulting assembly. The charge of chemical fill is introduced through the funnel 47. FIG. 2C shows the quartz tube 43 necked down at a constriction 49 for evacuaation and sealing. FIG. 4D shows the completed bulb 1 which includes support 45 which may be used to hold and positioned the bulb 1 in the EM-field coupling structure.
  • Because the chemical fill is highly hygroscopic, the bulb blanks as shown in Fig. 2B are prepared for filling by baking them in a furnace at temperatures of 1000°C and ultra high vacuum by attaching them to a vacuum system. This is done by means of a NUPROR B series valve (SS 8BG TSW) that is equipped with a quick-connect (CAJON, Ultra-Torr) for attaching the fill tube of bulb blank to the valve. The baked bulb still under vacuum is put into an argon filled drybox and opened to the argon. The bulb is then is filled with the liquid and solid components of the fill, the valve is again closed, and then the bulb is transferred from the drybox and attached to the gas fill system. After the argon is pumped out, the bulb is filled to the desired pressure with a noble gas such as argon, xenon or a Penning mixture and then tipped off. The backfilled gas serves as the starting gas in the lamp. The following fill is for a bulb with a volume of 1.25 cm3 and the total fill weight is 19 mg. Typical fill weights are from about 4 to about 50 mg/cm3.
    Hg 67.30 µmol
    Li 4.03 µmol (as iodide)
    Na 10.20 µmol (as iodide)
    Sc 0.42 µmol (as iodide)
    Tm 6.82 µmol (as iodide)
    I 35.95 µmol (as metal iodide)
    Sc 2.89 µmol (as metal)
    Ar 0.5 to 50 torr (as gas)
  • A preferred embodiment of the present invention may provide a lamp bulb with increased colour rendering index for an electrodeless high intensity discharge lamp utilizing the NaIScI3LiI chemistry while maintaining the efficacy and long life characteristic of such lamps; may improve the colour rendering properties of the emitted light while maintaining a long bulb life; may increase the density of the rare earth species above the density obtainable with a rare earth iodide alone; may increase the density of the rare earth atoms in the gas discharge by forming a complex molecule containing the rare earth element; and may have a low wall temperature of the gas discharge envelope which is conducive to a long lamp life.

Claims (13)

  1. An electrodeless lamp having a lamp bulb comprising a sealed envelope (3) containing a fill material (4) for supporting a gas discharge, said fill material comprising an inert starting gas, mercury, alkali metal iodides, and at least one iodide of a rare earth, characterised in that the alkali metal iodides consist substantially of sodium iodide and lithium iodide, the fill further comprises scandium iodide, and in that the molar ratio of said iodide of a rare earth to scandium iodide is between 1:1 to 30:1.
  2. A lamp as claimed in claim 1, characterised in that the molar ratio of said iodide of a rare earth to scandium iodide is between 5:1 to 20:1.
  3. A lamp as claimed in claim 1 or 2, characterised in that the iodide of a rare earth and the scandium iodide are present in amounts sufficient to form a complex molecule.
  4. A lamp as claimed in any of the preceding claims, characterised in that the molar ratio of said sodium iodide to said scandium iodide is between 5:1 to 25:1.
  5. A lamp as claimed in any of the preceding claims, characterised in that the molar ratio of said sodium iodide to said lithium iodide is between 1:1 to 5:1.
  6. A lamp as claimed in any preceding claim, characterised in that the emission from said bulb has a colour temperature of between 3000-5000 Kelvin.
  7. A lamp as claimed in claim 6, characterised in that the emission from said bulb has a colour temperature of between 3000-4000 Kelvin.
  8. A lamp as claimed in any preceding claim, characterised in that the lamp has a colour rendering index greater than 80.
  9. A lamp as claimed in any of the preceding claims, characterised in that said iodide of a rare earth is selected from the group consisting of the iodides of cerium, praseodymium, neodymium, dysprosium, holmium, erbium, thulium, lutetium and mixtures thereof.
  10. A lamp as claimed in any of the preceding claims, characterised in that said scandium iodide and said alkali metal iodides are present in amounts for producing emission with its colour substantially on the black body radiator chromaticity locus.
  11. A lamp as claimed in any of the preceding claims, characterised in that in use the wall temperature is in the range of 690 to 960 degrees Celsius and said envelope (3) has a wall loading in the range of about 12 to 17 watts/cm2.
  12. A lamp as claimed in claim 11, characterised in that in use the wall temperature is from 690 to 730 degrees Celsius.
  13. A lamp as claimed in any of the preceding claims, characterised in that said envelope (3) has a total concentration of fill between about 4 to about 50 mg/cm3.
EP19930310312 1992-12-18 1993-12-20 Electrodeless lamp bulb Expired - Lifetime EP0603014B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99333492A 1992-12-18 1992-12-18
US993334 1992-12-18

Publications (2)

Publication Number Publication Date
EP0603014A1 EP0603014A1 (en) 1994-06-22
EP0603014B1 true EP0603014B1 (en) 1999-06-16

Family

ID=25539402

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19930310312 Expired - Lifetime EP0603014B1 (en) 1992-12-18 1993-12-20 Electrodeless lamp bulb

Country Status (3)

Country Link
EP (1) EP0603014B1 (en)
CA (1) CA2111426A1 (en)
DE (1) DE69325349T2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5814944A (en) * 1996-01-22 1998-09-29 Matsushita Electric Works, Ltd. High pressure sodium vapor lamp with high color rendering
JP2003249196A (en) * 2002-02-25 2003-09-05 Matsushita Electric Works Ltd Microwave electrodeless discharge lamp lighting device
KR100459448B1 (en) * 2002-04-10 2004-12-03 엘지전자 주식회사 Electrodeless lamp for plasma lighting system
WO2006129102A2 (en) * 2005-06-03 2006-12-07 Ceravision Limited Lamp
WO2010044020A2 (en) * 2008-10-15 2010-04-22 Koninklijke Philips Electronics N.V. Discharge lamp comprising a monoxide radiation emitting material

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US271911A (en) * 1883-02-06 Half to george riplet
US3979624A (en) * 1975-04-29 1976-09-07 Westinghouse Electric Corporation High-efficiency discharge lamp which incorporates a small molar excess of alkali metal halide as compared to scandium halide
JPS54102070A (en) * 1978-01-30 1979-08-11 Mitsubishi Electric Corp Metal vapor discharge lamp
US4206387A (en) * 1978-09-11 1980-06-03 Gte Laboratories Incorporated Electrodeless light source having rare earth molecular continua
CA2090360A1 (en) * 1992-03-03 1993-09-04 Michael J. Shea Metal iodide lamp

Also Published As

Publication number Publication date
DE69325349D1 (en) 1999-07-22
DE69325349T2 (en) 2000-02-24
CA2111426A1 (en) 1994-06-19
EP0603014A1 (en) 1994-06-22

Similar Documents

Publication Publication Date Title
CA1288799C (en) Rare earth halide light source with enhanced red emission
EP0207333B1 (en) Electrodeless high pressure sodium iodide arc lamp
EP0762476B1 (en) Electrodeless HID lamp and electrodeless HID lamp system using the same
EP0542467B1 (en) Arc chamber for a lamp containing a mercury-free fill
JP2003242934A (en) Metal halide lamp
GB2387267A (en) Cermaic metal halide lamp
US4890042A (en) High efficacy electrodeless high intensity discharge lamp exhibiting easy starting
US5363015A (en) Low mercury arc discharge lamp containing praseodymium
US4937503A (en) Fluorescent light source based on a phosphor excited by a molecular discharge
US6501220B1 (en) Thallium free—metal halide lamp with magnesium and cerium halide filling for improved dimming properties
US20040108815A1 (en) Microwave-excited elecrodeles discharge bulb and microwave-excited discharge lamp system
EP0603014B1 (en) Electrodeless lamp bulb
EP0582709B1 (en) Metal iodide lamp
EP1803145B1 (en) Mercury-free compositions and radiation sources incorporating same
US20060132042A1 (en) Mercury-free and sodium-free compositions and radiation source incorporating same
JP3196571B2 (en) Electrodeless discharge lamp
KR20010037340A (en) AN ELECTRODELESS LAMP INCLUDING SnI2
WO2008120172A2 (en) Gas discharge lamp comprising a mercury-free gas fill
EP0583113B1 (en) Discharge lamp arc tube and method of making a discharge lamp arc tube
JPH09120800A (en) Electrodeless high-pressure discharge lamp
JPH10294089A (en) Electrodeless metal halid lamp device
WO2019234454A2 (en) A plasma light source
Lapatovich et al. High intensity discharge device containing oxytrihalides
JPH10294080A (en) Metal halide lamp and its lighting device
JPH10294082A (en) Electrodeless metal halid lamp and its lighting device

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE FR GB NL

17P Request for examination filed

Effective date: 19940708

17Q First examination report despatched

Effective date: 19950531

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE FR GB NL

REF Corresponds to:

Ref document number: 69325349

Country of ref document: DE

Date of ref document: 19990722

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20031229

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20040121

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20040130

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20040227

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20040301

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20041220

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20041231

BERE Be: lapsed

Owner name: *FLOWIL INTERNATIONAL LIGHTING (HOLDING) B.V.

Effective date: 20041231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050701

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050701

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20041220

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20050831

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20050701

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

BERE Be: lapsed

Owner name: *FLOWIL INTERNATIONAL LIGHTING (HOLDING) B.V.

Effective date: 20041231