The present invention relates to a green light-emitting fluorescent material and a fluorescent lamp therewith, and more particularly to a green light-emitting fluorescent material having a short afterglow time and a fluorescent lamp therewith.
For the fluorescent material in the general fluorescent lamp and the three emission bands type cold-cathode fluorescent lamp using the mercury emission line as an excitation source, a mixture of fluorescent materials of three colors, namely, red light-emitting, green light-emitting and blue light-emitting fluorescent materials is currently in use. Among these fluorescent materials, the green light-emitting fluorescent material is known to have the emission characteristics which particularly affect the light flux and the color rendering properties of the fluorescent lamp itself. As for such a green light-emitting fluorescent material, a Tb activated phosphate fluorescent material LaPO4: Ce, Tb has been widely used due to its high emission intensity (For instance, see Patent Literature 1 and Patent Literature 2). [Patent Literature 1] Japanese Patent application Laid-open No.3837/2002 [Patent Literature 2] Japanese Patent application Laid-open No.56812/2002
The LaPO4: Ce, Tb fluorescent material has an emission peak at a wavelength of 548 nm, providing a sharp emission line, but its afterglow lasts disadvantageously long.
In the lighting system equipped with the fluorescent lamp in which the inner surface of the tube is coated with the fluorescent material, the inverter electronic driver circuit at a frequency of 45 Khz, which makes little flicker, has recently become in wide use, replacing the conventional driver circuit at a frequency of 50/60 Hz with a stabilizer. Further, in the driver circuit of the cold-cathode mercury fluorescent lamp used for the back lighting in the liquid crystal display apparatus, the inverter electronic driver circuit has been also being used. The use of such an inverter electronic driver circuit at a frequency of 45 Khz certainly increases the repetitive lighting frequency of the fluorescent lamp, but because the conventional LaPO4: Ce, Tb fluorescent material has an afterglow that is long in duration, a problem of slow response arises for the fluorescent lamp wherein the LaPO4: Ce, Tb fluorescent material is used, and a green light-emitting fluorescent material with a short afterglow time has been being earnestly sought after.
In light of the above problems, an object of the present invention is to provide a green light-emitting fluorescent material which efficiently absorbs lights, has a short afterglow time and emits a green light when an ultraviolet light at a wavelength of 254 nm sent forth by the mercury discharge is used as an excitation source, and a fluorescent lamp with a short response time.
The present invention relates to a fluorescent material which efficiently absorbs an ultraviolet light in a wavelength region around 240 nm and has green light-emitting characteristics of having main emission peaks at 548 nm, 487 nm and 585 nm with short afterglow properties. The present invention, further, relates to a fluorescent lamp whose afterglow is made, through the use of such a fluorescent material, much shorter in duration than the conventional ones.
Further,
Referential numerals used in the drawings are described below.
Referential numeral 11 indicates a glass tube; referential numeral 12, an electrode and referential numeral 13, a fluorescent material film.
A green light-emitting fluorescent material of the present invention is a fluorescent material comprising, at least, calcium, yttrium, aluminum and oxygen, with terbium as an activator at an emission center. This green light-emitting fluorescent material has a composition expressed by the general formula CaY1-xTbxAlO4 (wherein 0.005≦x≦0.5), and efficiently absorbs an ultraviolet light in a wavelength region around 240 nm and, being excited, emits a light. Further, this green light-emitting fluorescent material shows emission characteristics of having the main peak at a wavelength of 548 nm and sub-peaks at wavelengths of 487 nm and 585 nm and characteristically its afterglow is shorter in duration than that of the conventional green light-emitting fluorescent materials.
Further, a green light-emitting fluorescent material of the present invention is the afore-mentioned fluorescent material wherein gadolinium and/or lanthanum is, in part, substituted for yttrium and has a composition expressed by the general formula CaY1-x-yTbxReyAlO4 (wherein Re is at least one sort of elements selected between Gd and La, and 0.005≦x≦0.5, 0.1≦y≦0.7). Further, this green light-emitting fluorescent material also efficiently absorbs an ultraviolet light in a wavelength region around 240 nm and, being excited, emits a light. Further, this green light-emitting fluorescent material shows emission characteristics of having the main peak at a wavelength of 548 nm and sub-peaks at wavelengths of 487 nm and 585 nm and characteristically its afterglow is still shorter in duration and its emission intensity is still higher than the afore-mentioned green light-emitting fluorescent material.
Further, a green light-emitting fluorescent material of the present invention has a composition expressed by the general formula CaGd1-x-yLayTbxAlO4 (wherein 0.005≦x≦0.5, 0≦y≦1−x). This green light-emitting fluorescent material corresponds to the afore-mentioned green light-emitting fluorescent material expressed by the general formula CaY1-xTbxAlO4 wherein gadolinium and/or lanthanum is substituted for the whole of yttrium, and its crystal structure is different from that of afore-mentioned two green light-emitting fluorescent materials. Because of that, the structure of the excitation band is changed to show a higher efficiency for the mercury emission line at a wavelength of 254 nm. With regard to the emission characteristics including the afterglow characteristic, which are almost similar to those of the afore-mentioned two green light-emitting fluorescent materials, this green light-emitting fluorescent material has the main emission peak at a wavelength of 548 nm and sub-peaks at wavelengths of 487 nm and 585 nm, and has excellent short afterglow property, its afterglow time being approximately ⅓ or so of that of the conventional green light-emitting fluorescent materials.
A fluorescent lamp of the present invention is a fluorescent lamp with a fluorescent material film being formed on the inner surface of a glass tube in which mercury and an inert gas are sealed, wherein the fluorescent material film contains at least the afore-mentioned green light-emitting fluorescent material of the present invention. Further, the fluorescent lamp may have a fluorescent material film formed of a mixture of three sorts of fluorescent materials, with a red light-emitting and a blue light-emitting fluorescent material being added to the green light-emitting fluorescent material of the present invention.
The present inventors examined various fluorescent materials in search of the one that can be used in the mercury fluorescent lamp in which the inert gas containing the mercury vapor is sealed in the inside of the glass tube, and, with an ultraviolet light at a wavelength of 254 nm set forth by mercury being used as an excitation source, can efficiently absorb the light in a wavelength region of that excitation light from the source and emit the visible light in a wavelength region of green color, and found out that a fluorescent material comprising aluminate as the mother material and utilizing terbium as an activator at an emission center meets the above conditions. Now, referring to respective examples, First Embodiment, Second Embodiment and Third Embodiment of the present invention relating to a green light-emitting fluorescent material and Fourth Embodiment of the present invention relating to a mercury fluorescent lamp utilizing such a green light-emitting material are described in detail below.
Among afore-mentioned green light-emitting fluorescent materials comprising aluminate as the mother material and utilizing terbium as an activator at the emission center, a green light-emitting fluorescent material having a composition expressed by the general formula CaY1-xTbxAlO4 (wherein 0.005≦x≦0.5) is particularly favored, and confirmed to have a shorter afterglow time than the conventional ones.
The emission intensity characteristics of the fluorescent material CaY0.9Tb0.1AlO4, which corresponds to the afore-mentioned green light-emitting fluorescent material CaY1-xTbxAlO4 in the case of a composition value of x=0.1, are shown, together with the excitation intensity characteristics, in
As is evident from
In comparison of afterglow characteristics between the green light-emitting fluorescent material with the above composition CaY0.9Tb0.1AlO4 (the composition value of x=0.1) and the conventional green light-emitting fluorescent material LaPO4:Ce, Tb, the afterglow times (the time between the instant at which the excitation is terminated and the instant at which the emission intensity falls to 1/10 of its initial magnitude) for a CaY0.9Tb0.1AlO4 fluorescent material of the present example and a conventional LaPO4:Ce, Tb fluorescent material are 2.8 ms and 7.7 ms, respectively, as given in
Next, a method of manufacturing a green light-emitting fluorescent material of the present invention is described, taking one with the above composition (the composition value of x=0.1) as an example. The green light-emitting fluorescent material CaY0.9Tb0.1AlO4 of the present example can be prepared by either the solid-state reaction method or the coprecipitation method, for instance, by baking the starting material in a weakly reducing atmosphere. As an example, the starting material, a CaCO3 reagent with a purity of 99.99% or higher, Y2O3 with a purity of 99.99% or higher, an α-Al2O3 reagent with a purity of 99.99% or higher and Tb4O7 reagent with a purity of 99.9% or higher are mixed so as to be in the above composition ratio, in other words, CaCO3, Y2O3, α-Al2O3 and Tb4O7 are mixed in such a way that Ca, Y, Al and Tb may be at the molar ratio of 1:0.9:1:0.1. After that, blending dry or wet, they are baked at approximately 1200-1500° C. for some hours (approximately three hours) and thereby a green light-emitting fluorescent material CaY0.9Tb0.1AlO4 can be obtained.
Now, with a green light-emitting fluorescent material of the present invention with a composition expressed by the general formula CaY1-x,TbxAlO4 (wherein 0.005≦x≦0.5), if the composition value x is less than the minimum value of x=0.005, a sufficient emission intensity cannot be attained. On the other hand, if the composition value x is greater than the maximum value of x=0.5, its emission intensity drops due to the concentration quenching and its use becomes less practicable. For these reasons, a range of the composition value x of the present invention is defined to be 0.005≦x≦0.5.
Further, the present inventors found out that, in the case of the afore-mentioned green light-emitting fluorescent material having a composition expressed by the general formula CaY1-xTbxAlO4, it is possible to shorten the afterglow time and raise the emission intensity by substituting gadolinium (Gd) and/or lanthanum (La) for one of the compositional elements, yttrium, in part.
In particular, a green light-emitting fluorescent material having a composition expressed by the general formula CaY1-x-yTbxReyAlO4 (wherein Re is at least one sort of elements selected between Gd and La, and 0.005≦x≦0.5, 0.1≦y≦0.7) is favored and it was confirmed such a fluorescent material has a shorter afterglow time and a higher emission intensity than the fluorescent material of Example 1.
Referring to Example 2, a green light-emitting fluorescent material expressed by the general formula CaY1-x-yTbxReyAlO4 is described below. This Example 2 is a green light-emitting fluorescent material in the case of being expressed by the above general formula wherein x=0.1, Re=Gd and y=0.30, in other words, by the compositional formula CaY0.6Tb0.1Gd0.3AlO4. The characteristics of emission intensity and excitation intensity of the green light-emitting material of the present example are shown in
As is evident from
In
Next, referring to Example 3, another green light-emitting fluorescent material expressed by the general formula CaY1-x-y,Tbx,ReyAlO4 is described below. This Example 3 is a green light-emitting fluorescent material in the case of being expressed by the above general formula wherein x=0.1, Re=La and y=0.30, in other words, by the compositional formula CaY0.6Tb0.1La0.3AlO4.
Making measurements of the excitation and the emission spectra for the green light-emitting fluorescent material of the present example, the present inventors confirmed the green light-emitting fluorescent material of the present example has the same emission structure as Example 1 and Example 2, that is, the green light-emitting characteristics of having the main peak at an emission wavelength of 548 nm and sub-peaks at emission wavelengths of 487 nm and 585 nm. Moreover, the emission intensity with excitation of an ultraviolet light at a wavelength of 254 nm was observed to be higher than the fluorescent materials of Example 1 and Example 2.
The excitation spectrum of the green light-emitting fluorescent material of Example 3 is shown in
With reference to
Next, the investigation of the afterglow time of the green light-emitting fluorescent material of Example 3 with the excitation light at a wavelength of 266 nm was made and the results, as given in Table 1, indicate its afterglow time is 2.5 ms, having almost the middle value between the values of Example 1 (2.8 ms) and Example 2 (2.2 ms).
The green light-emitting fluorescent materials of Example 2 (substitution of Gd for Y) and Example 3 (substitution of La for Y), that is, the green light-emitting fluorescent materials with respective compositions CaY1-x-yTbxReyAlO4 (Re is either Gd or La) may be prepared, as in Example 1, by either the solid-state reaction method or the coprecipitation method, for instance, by baking the starting material in a weakly reducing atmosphere. As an example, a method of manufacturing a fluorescent material in the case that x=0.1 and y=0.30, in other words, when expressed by the compositional formula CaY0.6Tb0.1Re0.3AlO4 (Re is either Gd or La) is described below.
Firstly, for the starting material, a CaCO3 reagent with a purity of 99.99% or higher, Y2O3 with a purity of 99.99% or higher, an α-Al2O3 reagent with a purity of 99.99% or higher, a Tb4O7 reagent with a purity of 99.9% or higher and Re2O3 (Re is either Gd or La) are mixed so as to be in the above composition ratio. In other words, in case of Example 2, CaCO3, Y2)3, α-Al2O3, Tb4O7 and Gd2O3 are mixed in such a way that Ca, Y, Al, Tb and Gd may be at the molar ratio of 1:0.6:1:0.1:0.3. In case of Example 3, using La2O3 in place of Gd2O3, the mixture is made in such a way that Ca, Y, Al, Tb and La may be at the molar ratio of 1:0.6:1:0.1:0.3.
After that, blending dry or wet, they are baked at approximately 1200-1500° C. for approximately three hours or so and thereby a green light-emitting fluorescent material with one of the above compositions can be obtained.
Now, with a green light-emitting fluorescent material with a composition expressed by the general formula CaY1-x-yTbxReyAlO4 (wherein Re is either Gd or La, and 0.005≦x≦0.5, 0.1≦y≦0.7 ), if the composition value x is less than the minimum value of x=0.005, a sufficient emission intensity cannot be attained. On the other hand, if the composition value x is greater than the maximum value of x=0.5, its emission intensity drops due to the concentration quenching and its use becomes less practicable. Further, when the composition value y is less than the minimum value of y=0.1, the effects shown in Example 2 or Example 3, that is, the effects that the emission intensity with the mercury emission line becomes increased and the afterglow time becomes shortened cannot be obtained. On the other hand, if the composition value y is greater than the maximum value of y=0.7, the crystal structure of the green light-emitting fluorescent material expressed by the general formula CaY1-x-yTbxReyAlO4 (wherein Re is Gd and/or La) changes. For these reasons, the composition values of the green light-emitting fluorescent material according to the present embodiment are determined as above.
Further, while Example 2 and Example 3 are examples wherein Gd alone or La alone is substituted for Y, the present inventors established that even in the case that both Gd and La are substituted for Y, the same afore-mentioned effects as Example 2 and Example 3 have over Example 1 can be obtained.
The present inventors conducted further investigations and came to a conclusion that the complete replacement of yttrium with gadolinium and/or lanthanum which is, in Second Embodiment, substituted for yttrium in part, the emission characteristics equivalent to those of a green light-emitting fluorescent material expressed by the above general formula CaY1-xTbxAlO4 (wherein 0.005≦x≦0.5), and a green light-emitting fluorescent material expressed by the general formula CaY1-x-yTbxReyAlO4 (wherein 0.005≦x≦0.5, Re=Gd or La and 0.1≦y≦0.7) can be obtained.
In particular, a green light-emitting fluorescent material having a composition expressed by the general formula CaGd1-x-yLayTbxAlO4 (wherein 0.005≦x≦0.5, 0≦y≦1−x ) is favored.
The crystal structure of the green light-emitting fluorescent material of the present embodiment is different from that of the green light-emitting fluorescent materials of First Embodiment and Second Embodiment and, thus, as described below, the structure of the excitation band is changed to show a higher efficiency for excitation at 254 nm. On the other hand, the emission characteristics including afterglow characteristic show little difference. Referring to Examples 4-7, the green light-emitting fluorescent materials of the present embodiment are described below.
Example 4 is a green light-emitting fluorescent material of the general formula CaGd1-x-yLayTbxAlO4 wherein x=0.1 and y=0.0, that is, CaGd0.9Tb0.1AlO4.
Example 5 is a green light-emitting fluorescent material of the same general formula CaGd1-x-yLayTbxAlO4 wherein x=0.1 and y=0.3, that is, CaGd0.6La0.3Tb0.1AlO4.
Example 6 is a green light-emitting fluorescent material of the same general formula CaGd1-x-yLayTbxAlO4wherein x=0.1 and y=0.6, that is, CaGd0.3La0.6Tb0.1AlO4.
Example 7 is a green light-emitting fluorescent material of the same general formula CaGd1-x-yLayTbxAlO4 wherein x=0.1 and y=0.9, that is, CaLa0.9Tb0.1AlO4.
As is evident from
Meanwhile, with respect to the emission, as is clear from in
Next, in
From
Next, a method of manufacturing a green light-emitting fluorescent material of the present embodiment is described below. A green light-emitting fluorescent material with the afore-mentioned compositions CaGd1-x-yLayTbxAlO4 may be prepared by either the solid-state reaction method or the coprecipitation method, for instance, by baking the starting material in a weakly reducing atmosphere.
For example, using, for the starting material, a CaCO3 reagent with a purity of 99.99% or higher, Y2O3 with a purity of 99.99% or higher, an α-Al2O3 reagent with a purity of 99.99% or higher, a Tb4O7 reagent with a purity of 99.9% or higher and Re2O3 (Re is either Gd or La), they are mixed so as to be in the above composition ratio.
In other words, in case of Example 5, CaCO3, Gd2O3, La2O3, α-Al2O3 and Tb4O7 are mixed in such a way that Ca, Gd, La, Al and Tb may be at the molar ratio of 1:0.6:0.3:1:0.1.
After that, blending dry or wet, they are baked at approximately 1200-1500° C. for some hours (approximately three hours) and thereby a green light-emitting fluorescent material of Example 5 can be obtained.
Now, with a green light-emitting fluorescent material of the present embodiment expressed by the above general formula, if the composition value x is less than the minimum value of x=0.005, a sufficient emission intensity cannot be attained. On the other hand, if the composition value x is greater than the maximum value of x=0.5, its emission intensity drops due to the concentration quenching and its use becomes less practicable.
Further, the composition value y, which is described by 0≦y≦1x can be freely determined within this range, once the composition value x is given. For these reasons, the composition values of the green light-emitting fluorescent material according to the present embodiment are determined as above.
Accordingly, the present invention can provide a green light-emitting fluorescent material, which comprises, at least, calcium, yttrium, aluminum and oxygen, and utilizes terbium as an activator at an emission center, and thereby efficiently absorbs an ultraviolet light in a wavelength region around 240 nm and has the main emission peaks at 548 nm, 487 nm and 585 nm, and has an afterglow time as short as approximately ⅓ of the conventional green light-emitting fluorescent material.
Further, in the present invention, obviously through the substitution of gadolinium and/or lanthanum for a part or the whole of yttrium in the above composition with various ratios between gadolinium and lanthanum, the composition thereof can be freely changed so that characteristics in regard of the afterglow and the excitation intensity with the mercury emission line at a wavelength of 254 nm can be appropriately selected, according to the purpose.
Referring to
The fluorescent material of the present invention provides green luminescence so that when the fluorescent film 13 is solely formed of the fluorescent material of the present invention, the fluorescent lamp emits a green light with an afterglow shorter in duration than the conventional ones.
A requirement of a fluorescent lamp that emits white light can be met through the employment of a fluorescent material film formed of a mixture of three sorts of fluorescent materials, that is, red light-emitting, green light-emitting and blue light-emitting fluorescent materials. By utilizing a green light-emitting fluorescent material of the present invention as the green light-emitting fluorescent material among these three sorts of fluorescent materials, that is, red light-emitting, green light-emitting and blue light-emitting fluorescent materials, a fluorescent lamp with green light component whose afterglow is shorter in duration than the conventional ones may be provided.
For the red light-emitting fluorescent material, any conventional material such as Y2O3:Eu or Y (P, V)O4:Eu can be used. As for the blue light-emitting fluorescent material, for instance, BaMgAl10O17:Eu or Sr5(PO4)3 Cl:Eu can be utilized.
While the description in the present embodiment is made so far, taking a straight tube-shaped type fluorescent lamp as an example, the fluorescent lamp can obviously take any form including ring shape, compact type and form with a cap similar to the incadescent lamp. Further, an appropriate choice of the mixing ratio of the three sorts of fluorescent materials, that is, red light-emitting, green light-emitting and blue light-emitting fluorescent materials, enables the fluorescent lamp to emit a light with a hue of a warm color or a cold color.
The present invention is particularly well suited for application to either the mercury fluorescent lamp for general illumination, wherein the inverter electronic driver circuit which makes little flicker is used in place of the driver circuit at a frequency of 50/60 Hz with the stabilizer or the cold-cathode mercury fluorescent lamp used for the back lighting in the liquid-crystal display apparatus.
Number | Date | Country | Kind |
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2003-015013 | Jan 2003 | JP | national |
2003-407452 | Dec 2003 | JP | national |
2004-006254 | Jan 2004 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP04/00591 | 1/23/2004 | WO | 7/22/2005 |