Phosphorescent phosphor

TECHNICAL FIELD
The present invention relates to an europium-activated silicate type phosphorescent phosphor which is excellent in weather resistance, has a long afterglow characteristic and exhibits blue to green emission under excitation with ultraviolet rays and/or visible light rays, and which is useful as a light source or a display in a dark place such as indoor or outdoor or in water.
BACKGROUND ART
A phosphorescent phosphor is a phosphor which continues to emit fluorescence even after termination of excitation after some excitation is imparted to the phosphor to emit fluorescence. For a phosphorescent phosphor, along with diversification and high functionalization of display, multi-coloring, long afterglow and improved weather resistance of a phosphorescent phosphor are desired. With conventional phosphorescent phosphors, the types of colors of the fluorescence and afterglow were limited, the weather resistance was poor, and the afterglow time was short.
As a blue-emitting phosphorescent phosphor, a (Ca,Sr)S:Bi phosphor is known. As a yellowish green-emitting phosphorescent phosphor, a ZnS:Cu phosphor is known, and as a red-emitting phosphorescent phosphor, a (Zn,Cd)S:Cu phosphor is known.
However, the above-mentioned (Ca,Sr)S:Bi phosphor is not practically used at present, since the chemical stability of the host material is extremely poor, and the luminance and afterglow characteristics are inadequate. On the other hand, the (Zn,Cd)S:Cu phosphor is not practically used at present, since Cd which is a toxic substance, occupies almost a half of the host material, and the luminance and afterglow characteristics are not satisfactory. ZnS:Cu is also susceptible to decomposition by ultraviolet rays in the presence of moisture and is likely to be blackened, and the afterglow characteristics are also unsatisfactory, but it is inexpensive and is used mostly for face plates of clocks or for indoor use such as emergency escape signs.
DISCLOSURE OF THE INVENTION
The present invention is to overcome the above drawbacks and to provide a phosphorescent phosphor which has a long afterglow characteristic and blue to green emission and which is further chemically stable and excellent in weather resistance.
Namely, the present invention is a phosphorescent phosphor which has the following construction and which exhibits blue to green emission.
(1) In an Eu-activated silicate phosphorescent phosphor, a phosphorescent phosphor represented by a compositional formula m(Sr.sub.1-a M.sup.1.sub.a)O.n(Mg.sub.1-b M.sup.2.sub.b)O.2(Si.sub.1-c Ge.sub.c)O.sub.2 : Eu.sub.x Ln.sub.y, wherein M.sup.1 is at least one element selected from Ca and Ba, M.sup.2 is at least one element selected from Be, Zn and Cd, and the coactivator Ln is at least one element selected from Sc, Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, B, Al, Ga, In, Tl, Sb, Bi, As, P, Sn, Pb, Ti, Zr, Hf, V, Nb, Ta, Mo, W, Cr and Mn, and wherein a, b, c, m, n, x and y are within the following ranges, and said phosphor contains at least one halogen element selected from F, Cl, Br and I in an amount within a range of from 1.times.10.sup.-5 to 1.times.10.sup.-1 g.multidot.atm/mol of the host material:
0.ltoreq.a.ltoreq.0.8
0.ltoreq.b.ltoreq.0.2
0.ltoreq.c.ltoreq.0.2
1.5.ltoreq.m.ltoreq.3.5
0.5.ltoreq.n.ltoreq.1.5
1.times.10.sup.-5 .ltoreq.x.ltoreq.1.times.10.sup.-1
1.times.10.sup.-5 .ltoreq.y.ltoreq.1.times.10.sup.-1.
(2) The phosphorescent phosphor according to the above (1), wherein the above value m satisfies a condition represented by 1.7.ltoreq.m.ltoreq.3.3.
(3) The phosphorescent phosphor according to the above (1) or (2), wherein the above coactivator Ln is at least one element selected from Dy, Nd, Tm, Sn, In and Bi.
(4) The fluorescent phosphor according to any one of the above (1) to (3), which exhibits thermoluminescence at a temperature of at least room temperature, when heated after excitation with ultraviolet rays and/or visible light rays within a range of from 140 to 450 nm.
The present inventors have conducted a study primarily on a phosphor host material of (Sr,M.sup.1)O--(Mg,M.sup.2) O--(Si,Ge)O.sub.2 type (M.sup.1 =at least one of Ca and Ba, and M.sup.2 =at least one of Be, Zn and Cd), whereby they have found that a phosphor host material suitable for a long afterglow characteristic is present in the compositional region shown by the hatched lines in FIG. 1.
Namely, a phosphor represented by the compositional formula m(Sr.sub.1-a,M.sup.1.sub.a)O.n(Mg.sub.1-b,M.sup.2.sub.b)O.2(Si.sub.1-c,Ge.sub.c)O.sub.2, wherein m and n are within ranges of 1.5.ltoreq.m.ltoreq.3.5, and 0.5.ltoreq.n.ltoreq.1.5, is suitable.
And, in the present invention, the above phosphor host material is activated with Eu and at the same time, co-activated with Ln (at least one element selected from Sc, Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, B, Al, Ga, In, Tl, Sb, Bi, As, P, Sn, Pb, Ti, Zr, Hf, V, Nb, Ta, Mo, W, Cr and Mn), and a halog en element (at least one element selected from F, Cl, Br and I) is incorporated, whereby it has been successful to optimize the luminescence center (Eu) and the incorporated elements, and it has been successful to obtain a blue to green-emitting phosphorescent phosphor which has a very long afterglow characteristic and which is chemically stable and excellent in weather resistance. Among the above co-activators Ln, Dy, Nd, Tm, Sn, In and Bi are particularly excellent.
In the compositional formula of the present invention, the substitution amount a of Sr is suitably within a range of 0.ltoreq.a.ltoreq.0.8, preferably 0.ltoreq.a.ltoreq.0.4. If it exceeds 0.8, the effect of improving the afterglow characteristic tends to be small. The substitution amount b of M.sup.2 element is suitably within a range of 0.ltoreq.b.ltoreq.0.2, preferably 0.ltoreq.b.ltoreq.0.1. If it exceeds 0.2, the effect of improving the afterglow characteristic tends to be small. The amount C of Ge substituted for Si is suitably within a range of 0.ltoreq.c.ltoreq.0.2, preferably 0.ltoreq.c.ltoreq.0.1. If it exceeds 0.2, the effect of improving the afterglow characteristic tends to be small, and the luminance also tends to decrease.
Further, the above m and n values determining the compositional ratio of m(Sr.sub.1-a,M.sup.1.sub.a)O, n(Mg.sub.1-b,M.sup.2.sub.b)O and 2(Si.sub.1-c,Ge.sub.c)O.sub.2, as components constituting the host material of the phosphor, are suitably within ranges of 1.5.ltoreq.m.ltoreq.3.5 and 0.5.ltoreq.n.ltoreq.1.5, preferably 1.7.ltoreq.m.ltoreq.3.3 and 0.7.ltoreq.n.ltoreq.1.3. If they depart from such ranges, a compound other than the desired compound will be formed, or the starting material oxides will remain, whereby the luminance will decrease.
The incorporated amount x (g.multidot.atm) of the activator Eu is suitably within a range of 1.times.10.sup.-5 .ltoreq.x.ltoreq.1.times.10.sup.1, preferably 1.times.10.sup.-4 .ltoreq.x.ltoreq.5.times.10.sup.-2. If it is less than 1.times.10.sup.-5, the numbers of the luminescence center tend to diminish, and the desired luminance can not be obtained. Further, if it exceeds 1.times.10.sup.-1, concentration quenching takes place, whereby the luminance decreases, and the afterglow characteristic decreases.
The incorporated amount y (g.multidot.atm) of the co-activator element Ln is suitably within a range of 1.times.10.sup.-5 .ltoreq.y.ltoreq.1.times.10.sup.-1, preferably 1.times.10.sup.-4 .ltoreq.y.ltoreq.5.times.10.sup.-2. If it is less than 1.times.10.sup.-5, no effect for the afterglow characteristic tends to be obtained, and if it exceeds 1.times.10.sup.-1, the co-activator element undergoes light emission, whereby an emission in a range of blue to green can not be obtained.
The halogen element incorporated to the phosphor of the present invention serves partially as a flux for crystal growth and for diffusion of the luminescence center and the co-activator element Ln and improves the luminance and the afterglow characteristic. The incorporated amount z(g.multidot.atm) of the halogen element is suitably 1.times.10.sup.-5 .ltoreq.z.ltoreq.1.times.10.sup.-1, preferably 1.times. .sup.4 .ltoreq.z.ltoreq.1.times.10.sup.2 as a value analyzed after the washing treatment, etc. If it exceeds 1.times.10.sup.-1, the phosphor tends to sinter, whereby treatment into a powder tends to be difficult, and if it is less than 1.times.10.sup.-5, a drawback such as a decrease in the afterglow and spontaneous emission luminance, tends to result.
And, the phosphorescent phosphor of the present invention exhibits thermoluminescence at a temperature fat least room temperature, when the phosphor is heated after excitation with ultraviolet rays and/or visible light rays within a range of from 140 to 450 nm.
The phosphorescent phosphor of the present invention is synthesized as follows.
With respect to the materials for the phosphor, the host material-constituting elements Sr, M.sup.1 (M.sup.1 =at least one of Ca and Ba), Mg, M.sup.2 (M.sup.2 =Be, Zn, Cd), Si and Ge, and activator Eu and co-activator Ln, are used in the form of the respective oxides or in the form of salts such as carbonates, nitrates or chlorides which can readily be converted to oxides by baking. Further, the halogen elements are used in the form of ammonium salts, alkali metal salts or halogenated compounds of the above-mentioned constituting elements (the host material-constituting elements, activator element Eu or co-activator element Ln). And, they are sampled so that the composition will be stoichiometrically within the above compositional formula and thoroughly mixed in a wet system or in a dry system. Rare earth materials may be mixed to one another by co-precipitation. This mixture is filled in a heat resistant container such as an alumina crucible and baked at least once at a temperature of from 800 to 1400.degree. C. for from 1 to 12 hours in a reducing atmosphere of hydrogen-containing neutral gas or in a reducing atmosphere consisting of carbon element-containing gas, e.g. CO.sub.x gas, CS.sub.2 gas etc. When baking is carried out in a plurality of times, the final baking step is carried out necessarily in a reducing atmosphere. This baked product is pulverized and then subjected to washing with a weak mineral acid, washing with water, drying, sieving, etc., to obtain the phosphorescent phosphor of the present invention.
FIG. 2 is an X-ray diffraction pattern, whereby the crystal structure of the phosphorescent phosphor Sr.sub.1.995 Mgsi.sub.2 O.sub.7 :Eu.sub.0.005, Dy.sub.0.025, Cl.sub.0.025 synthesized in Example 1, was confirmed. FIG. 3 is an X-ray diffraction pattern whereby the crystal structure of the phosphorescent phosphor Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03, Dy.sub.0.025, Cl.sub.0.025 synthesized in Example 2, was confirmed. Even when a part of Sr, Mg or Si in these phosphor compositions, was substituted by other elements within the range defined in the Claims, substantially the same results were obtained.
FIG. 4 shows emission spectra, under excitation with ultraviolet rays of 365 nm, of the phosphorescent phosphor (curve a) of Example 1, the phosphorescent phosphor Sr.sub.1.195 Ca.sub.0.8 MgSi.sub.2 O.sub.7 :Eu.sub.0.005,Dy.sub.0.025,Br.sub.0.025 (curve b), synthesized in Example 3 and the phosphorescent phosphor Sr.sub.0.995 BaMgSi.sub.2 O.sub.7 :Eu.sub.0.005,Dy.sub.0.025,Br.sub.0.025 (curve b) synthesized in Example 5, and the respective emission peak wavelengths were 470 nm, 500 nm and 450 nm. Further, FIG. 5 shows emission spectra, under excitation with ultraviolet rays of 365 nm, of the phosphorescent phosphor (curve a) of Example 2, the phosphorescent phosphor Sr.sub.2.07 Ca.sub.0.9 Mgsi.sub.2 O.sub.8 :Eu.sub.0.03,Dy.sub.0.025,Cl.sub.0.025 (curve b) synthesized in Example 4 and the phosphorescent phosphor Sr.sub.2.375 Ba.sub.0.6 MgSi.sub.2 O.sub.8 :Eu.sub.0.025 Dy.sub.0.3.Br.sub.0.015 (curve c) synthesized in Example 6, and the respective emission peak wavelengths were 460 nm, 471 nm and 450 nm. Even if a part of these phosphor compositions, was substituted by other elements within the range defined in the Claims, substantially the same results were obtained.
FIG. 6 is one wherein using the phosphorescent phosphor of Example 1, the region of the excited spectrum was measured and shown. FIG. 7 is one wherein using the phosphorescent phosphor of Example 2, the region of the excited spectrum was measured and shown. In the measurement of the region of the excited spectrum, the intensity of 460 nm (output light) was plotted when the exciting wavelength of light irradiated to the sample, was varied while the spectrum wavelength on the output side of the spectrophotometer, is fixed at 460 nm, whereby the ordinate represents the relative emission intensity of 460 nm, and the abscissa represents the wavelength of the scanning exciting light. Even if a part of this phosphor composition was substituted by other elements within the range as defined in the Claims, substantially the same results were obtained.
In FIG. 8, the phosphorescent phosphor of Example 1 (the emission spectrum peak wavelength: 470 nm), the phosphorescent phosphor of Example 3 (the emission spectrum peak wavelength: 500 nm), the phosphorescent phosphor of Example 5 (the emission spectrum peak wavelength: 450 nm), the phosphorescent phosphor of Comparative Example 1 (Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005, the emission spectrum peak wavelength: 470 nm) and the phosphorescent phosphor of Comparative Example 3 (ZnS:Cu, the emission spectrum peak wavelength: 516 nm) were irradiated with 300 lux for 30 minutes by means of a day light color fluorescent lamp, and the afterglow characteristics upon expiration of 2 minutes after termination of the irradiation, were measured. Further, in FIG. 9, the phosphorescent phosphor of Example 2 (the emission spectrum peak wavelength: 460 nm), the phosphorescent phosphor of Example 4 (the emission spectrum peak wavelength: 471 nm), the phosphorescent phosphor of Example 6 (the emission spectrum peak wavelength: 450 nm), the phosphorescent phosphor of Comparative Example 2 (Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03, the emission spectrum peak wavelength: 460 nm) and the phosphorescent phosphor of Comparative Example 3 (ZnS:Cu, the emission spectrum peak wavelength: 516 nm) were irradiated with 300 lux for 30 minutes by means of a day light color fluorescent lamp, and the afterglow characteristics upon expiration of 2 minutes after termination of irradiation, were measured. In each case, the measuring method was such that, as described above, the sample was irradiated with a 30 W day light color fluorescent lamp, and the afterglow of the phosphor after switching off the lamp, was determined by measuring the luminance of the afterglow by a luminance meter provided with a filter adjusted to luminosity curve.
As is evident from FIGS. 8 and 9, the phosphorescent phosphor having an emission spectrum peak wavelength of 470 nm of Example 1 has an extremely remarkable afterglow characteristic as compared with Comparative Example 1. Further, it is evident that the phosphorescent phosphor having an emission spectrum peak wavelength of 460 nm of Example 2 has an extremely remarkable afterglow characteristic as compared with Comparative Example 2. Further, it is evident that the phosphorescent phosphors of Examples 4 and 6 have excellent afterglow characteristics as compared with the ZnS:Cu yellowish green-emitting phosphor of Comparative Example 3 which corresponds to a commercial product, although the emission colors are different. Furthermore, the respective phosphorescent phosphors of Examples 3, 4, 5 and 6 also have excellent afterglow characteristics as compared with the ZnS:Cu yellowish green-emitting phosphor of Comparative Example 3 which corresponds to a commercial product, although the emission colors are different.
FIG. 10 is a graph showing the results, when the respective phosphorescent phosphors of Examples 1, 3 and 5 were irradiated with 300 lux for 15 seconds by a day light color fluorescent lamp, and the thermoluminescence characteristic (glow curve) upon expiration of 1 minute after termination of irradiation was measured at a temperature raising rate of about 8 to 10.degree. C./sec by means of TLD reader (KYOKKO TLD-1300 improved type), manufactured by Kasei Optonix, Ltd. FIG. 11 is a graph showing the results, when the phosphorescent phosphors of Examples 2, 4 and 6 were irradiated with 300 lux for 15 seconds by a day light color fluorescent lamp as described above, and the thermoluminescence characteristic (glow curve) upon expiration of 1 minute after termination of irradiation, was measured by TLD reader (KYOKKO TLD-1300 improved type) manufactured by Kasei Optonix, Ltd. As is evident from curves a to c in FIG. 10 and curves a to c in FIG. 11, the phosphorescent phosphors of Examples 1 to 6 exhibit thermoluminescence when heated at the above-mentioned temperature-raising speed within a temperature range of at least room temperature.
The phosphorescent phosphor of the present invention exhibits a very high luminance afterglow characteristic as described above and is excellent in weather resistance and chemically stable, and even when compared with the conventional ZnS type phosphorescent phosphors, it makes application possible not only to indoors but also to a wide range of applications outdoors. For example, it may be coated on the surfaces of various articles, or it may be mixed in plastics, rubbers, polyvinyl chlorides, synthetic resins or glass and may be applied widely in the form of molded products or fluorescent films, for example, for various signs for traffic safety (such as traffic armbands, traffic control gloves, reflectors of vehicles, reflector flags, signals, road signs, emergency ropes, footgears, safety umbrellas, sticks for blind persons, stickers, knapsacks, raincoats or safety covers), indicators (such as telephone dial covers, switches, slip prevention of stair case, escape guide signals, tires, mannequins, fire extinguishers, keys, doors, fluorescent lamps or display tapes), ornaments (such as artificial flowers, accessories or interior plates), various leisure articles (such as floats for fishing, toys, golf balls, ropes, kites, artificial trees or puzzles), clocks (such as face plates, hands or scales), office articles and office appliances (such as writing means, cardboards, scales, marker pens, seals, liquid crystal back lights, solar cells, calculators, printers or inks), educational articles and appliances (such as constellation plates, planet models, transparency, keyed instruments or maps) and building materials (such as concrete, guard rails, scales for construction work, scaffoldings for manholes, tiles, decorative laminated sheets, measuring apparatus or tape measures).
Especially when the phosphorescent phosphor of the present invention is used alone or as a blue to bluish green-emitting component phosphor for a high color rendering fluorescent lamp, and this is coated on a tubular wall of the fluorescent lamp and used as a fluorescent film for the fluorescent lamp, it continues to emit fluorescence with high luminance for a long period of time even when the lamp is suddenly off due to e.g. power breakdown, and thus it is useful also as an emergency fluorescent lamp.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a graph showing a ternary state diagram of a (Sr,M.sup.1)O--(Mg,M.sup.2)O--(Si,Ge)O.sub.2 type oxide which is the host material of the phosphorescent phosphor of the present invention.
FIG. 2 is an X-ray diffraction pattern whereby the crystal structure of the phosphorescent phosphor synthesized in Example 1 was confirmed.
FIG. 3 is an X-ray diffraction pattern whereby the crystal structure of the phosphorescent phosphor synthesized in Example 2 was confirmed.
FIG. 4 is a graph showing emission spectra when the phosphorescent phosphors synthesized in Examples 1, 3 and 5 were excited with ultraviolet rays of 365 nm.
FIG. 5 is a graph showing emission spectra when the phosphorescent phosphors synthesized in Examples 2, 4 and 6 were excited with ultraviolet rays of 365 nm.
FIG. 6 is a graph showing the excitation spectrum at each emission spectrum peak of the phosphorescent phosphor of Example 1.
FIG. 7 is a graph showing the excitation spectrum at each emission spectrum peak of the phosphorescent phosphor of Example 2.
FIG. 8 is a graph wherein the afterglow characteristics were compared among the blue to green-emitting phosphorescent phosphors of Examples 1, 3 and 5 and Comparative Example 1 and the yellowish green-emitting phosphorescent phosphor of Comparative Example 3.
FIG. 9 is a graph wherein the afterglow characteristics were compared among the blue to green-emitting phosphorescent phosphors of Examples 2, 4 and 6 and Comparative Example 2 and the yellowish green-emitting phosphorescent phosphor of Comparative Example 3.
FIG. 10 is a graph showing the thermoluminescence characteristics (glow curves) of the phosphorescent phosphors of Examples 1, 3 and 5.
FIG. 11 is a graph showing the thermoluminescence characteristics (glow curves) of the phosphorescent phosphors of Examples 2, 4 and 6.

BEST MODE FOR CARRYING OUT THE INVENTION
The present invention will be described in further detail with reference to the following Examples, but it is by no means restricted by the following Examples unless it exceeds the gist thereof.
EXAMPLE
______________________________________ SrCO.sub.3 29.5 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.09 g Dy.sub.2 O.sub.3 0.47 g NH.sub.4 Cl 2.3 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 115.degree. C. for 2 hours in a reducing atmosphere comprising 98% of nitrogen and 2% of hydrogen, by means of an electric furnace. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005, Dy.sub.0.025 Cl.sub.0.025 and showed an X-ray diffraction pattern of FIG. 2, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 4 (curve a), whereby its emission peak wavelength had a blue-emitting phosphorescence of 470 nm. Further, the excitation spectrum was found to extend to a visible region, as shown in FIG. 6. The afterglow characteristic showed a long afterglow as shown in FIG. 8 (curve a). Further, the glow curve was as shown in FIG. 10. Furthermore, the emission peak wavelength of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the peak temperature value of the glow curve, are shown in Table 1.
EXAMPLE
______________________________________ SrCO.sub.3 43.8 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.53 g Dy.sub.2 O.sub.3 0.47 g NH.sub.4 Cl 2.3 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 1150.degree. C. for 2 hours in a reducing atmosphere comprising 98% of nitrogen and 2% of hydrogen by means of an electric furnace. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.2.97 Mgsi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 and showed an X-ray diffraction pattern of FIG. 3, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 5 (curve a), whereby its emission peak wavelength had a blue-emitting phosphorescence of 460 Further, the excitation spectrum was found to extend to a visible region, as shown in FIG. 7. The afterglow characteristic showed a long afterglow, as shown in FIG. 9 (curve a). Further, the glow curve was as shown in FIG. 11. Furthermore, the emission peak wavelength of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the peak temperature value of the glow curve, are shown in Table
EXAMPLE
______________________________________ SrCO.sub.3 17.6 g CaCO.sub.3 8.0 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.09 g Dy.sub.2 O.sub.3 0.47 g NH.sub.4 Br 3.3 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 1200.degree. C. for 2 hours in a carbon-reducing atmosphere by means of an electric furnace. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.1.195 Ca.sub.0.8 Mgsi.sub.2 O.sub.7 Eu.sub.0.005 Dy.sub.0.025,Br.sub.0.025, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 4 (curve b), whereby its peak wavelength had a green-emitting phosphorescence of 500 nm. Further, the afterglow characteristic showed a long afterglow, as shown in FIG. 8 (curve b). Further, the glow curve was as shown in FIG. 10 (curve b). Furthermore, the emission peak wavelength of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the glow peak temperature, are shown in Table 1.
EXAMPLE
______________________________________ SrCO.sub.3 30.6 g CaCO.sub.3 9.1 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.52 g Dy.sub.2 O.sub.3 0.47 g NH.sub.4 Cl 2.6 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 1200.degree. C. for 2 hours in a reducing atmosphere consisting of carbon element-containing gas, e.g. Co.sub.x gas, CS.sub.2 gas etc. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.2.07 Ca.sub.0.9 Mgsi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.02, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 5 (curve b), whereby its peak had a bluish green-emitting phosphorescence of 471 nm. Further, the afterglow characteristic showed a long afterglow, as shown in FIG. 9 (curve b). Further, the glow curve was as shown in FIG. 11 (curve b). Furthermore, the emission peak wavelength of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the glow peak temperature value, are shown in Table 1.
EXAMPLE
______________________________________ SrCO.sub.3 14.7 g BaCO.sub.3 19.7 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.09 g Dy.sub.2 O.sub.3 0.47 g NH.sub.4 Br 2.68 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 1200.degree. C. for 3 hours in a reducing atmosphere comprising 97% of nitrogen and 3% of hydrogen, by means of an electric furnace. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.0.995 Ba.sub.1.0 MgSi.sub.2 O.sub.7 :Eu.sub.0.005, Dy.sub.0.025, Br.sub.0.25, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 4 (curve c), whereby its peak had a bluish green-emitting phosphorescence of 450 nm. Further, the afterglow characteristic showed a long afterglow, as shown in FIG. 8 (curve c). Further, the glow curve was as shown in FIG. 10 (curve c). Furthermore, the emission peak value of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the peak temperature value of the glow curve, are shown in Table 1.
EXAMPLE
______________________________________ SrCO.sub.3 35.1 g BaCO.sub.3 11.8 g MgO 4.0 g SiO.sub.2 12.0 g Eu.sub.2 O.sub.3 0.44 g Dy.sub.2 O.sub.3 0.56 g NH.sub.4 Br 1.6 g______________________________________
The above starting materials were thoroughly mixed, packed into an alumina crucible and baked at 1200.degree. C. for 3 hours in a reducing atmosphere comprising 97% of nitrogen and 3% of hydrogen, by means of an electric furnace. The obtained baked product was pulverized and subjected to washing with water, drying and sieving to obtain a phosphorescent phosphor.
This phosphor had a composition of Sr.sub.2.35 Ba.sub.0.6 MgSi.sub.2 O.sub.8 :Eu.sub.0.025 Dy.sub.0.3 Br.sub.0.015, and the emission spectrum under excitation with ultraviolet rays of 365 nm was as shown in FIG. 5 (curve c), whereby its peak had a bluish-emitting phosphorescence of 450 nm. Further, the afterglow characteristic showed a long afterglow, as shown in FIG. 9 (curve c). Further, the glow curve was as shown in FIG. 11 (curve c). Furthermore, the emission peak value of the phosphor, the afterglow characteristic (the emission intensity ratio of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the peak temperature value of the glow curve, are shown in Table 1.
EXAMPLES 7 to 22
In the same manner as in Example 1, the hosphorescent phosphors of Examples 7 to 22 having compositions as disclosed in Tables 1 and 2, were obtained. The emission peak values of the phosphors of Examples 7 to 22, the afterglow characteristics (the emission intensity ratios of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the glow peak temperature values are shown in Tables 1 and 2.
EXAMPLES 23 to 37
In the same manner as in Example 2, phosphorescent phosphors of Examples 23 to 37 having the compositions as disclosed in Table 4, were obtained. The emission peak values of the phosphors of Examples 23 to 37, the afterglow characteristics (the emission intensity ratios of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green-emitting phosphorescent phosphor being 100%) and the glow peak temperature values, were shown in Tables 3 and 4.
COMPARATIVE EXAMPLES 1 and 3
A Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 phosphorescent phosphor of Comparative Example 1 was obtained in the same manner as in Example 1 except that incorporation of the coactivator element Ln and the halogen element was omitted.
COMPARATIVE EXAMPLE 2
A Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 phosphorescent phosphor of Comparative Example 2 was obtained in the same manner as in Example 2 except that incorporation of the coactivator element Ln and the halogen element was omitted.
COMPARATIVE EXAMPLE 3
A ZnS:Cu yellowish green-emitting phosphorescent phosphor (LC-G1) manufactured by Kasei Optonix, Ltd. was used as a reference sample, and this was used as a phosphor of Comparative Example 3.
The emission peak wavelengths of the respective phosphors of these Comparative Examples 1 to 3, the afterglow characteristics (the emission intensity ratios of the emission intensities upon expiration of 2 minutes and 60 minutes after termination of irradiation, as compared with a ZnS:Cu yellowish green phosphorescent phosphor being 100%) and the peak values of the glow curves, are shown in Table 4.
INDUSTRIAL APPLICABILITY
By adopting the above-described construction, the present invention makes it possible to present for the first time a blue to green-emitting phosphorescent phosphor which is chemically stable and which exhibits high luminance and a far longer afterglow as compared with a commercially available ZnS type yellowish green-emitting phosphorescent phosphor, and thus substantially contributes to multi-coloring and diversification of display.
TABLE 1__________________________________________________________________________ Afterglow characteristics Emission 5 minutes 60 minutes Glow peakChemical compositional formula peak (nm) later later (.degree. C.)__________________________________________________________________________Ex. 1 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Cl.sub.0.02 5 470 480 1540 90Ex. 2 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 460 250 800 90Ex. 3 Sr.sub.1.995 Ca.sub.0.8 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Br.sub.0.025 500 180 250 70Ex. 4 Sr.sub.2.07 Ca.sub.0.9 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.02 471 155 350 85Ex. 5 Sr.sub.1.995 Ba.sub.1.0 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Br.sub.0.025 450 195 440 100Ex. 6 Sr.sub.2.375 Ba.sub.0.6 MgSi.sub.2 O.sub.8 :Eu.sub.0.025 Dy.sub.0.03 Br.sub.0.015 450 150 200 80Ex. 7 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 470 60 180 85Ex. 8 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Cl.sub.0.05 470 870 2530 95Ex. 9 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Br.sub.0.03 470 705 1830 95Ex. 10 Sr.sub.1.97 MgSi.sub.2 O.sub.7 :Eu.sub.0.03 Dy.sub.0.025 F.sub.0.01 470 195 280 80__________________________________________________________________________
TABLE 2__________________________________________________________________________ Afterglow characteristics Emission 5 minutes 60 minutes Glow peakChemical compositional formula peak (nm) later later (.degree. C.)__________________________________________________________________________Ex. 11 Sr.sub.1.97 MgSi.sub.2 O.sub.7 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 470 450 990 90Ex. 12 Sr.sub.1.97 MgSi.sub.2 O.sub.7 :Eu.sub.0.03 Dy.sub.0.02 Cl.sub.0.025 470 330 710 80Ex. 13 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Nd.sub.0.025 Br.sub.0.02 5 470 75 210 70Ex. 14 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Tm.sub.0.025 Br.sub.0.02 5 470 70 200 80Ex. 15 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 In.sub.0.025 Br.sub.0.02 5 470 45 120 75Ex. 16 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Bi.sub.0.025 Br.sub.0.02 5 470 40 110 70Ex. 17 Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Sn.sub.0.025 Br.sub.0.02 5 470 45 110 80Ex. 18 Sr.sub.0.395 Ba.sub.1.8 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Br.sub.0.025 470 45 230 90Ex. 19 Sr.sub.1.995 Mg.sub.0.9 Zn.sub.0.1 Si.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Cl.sub.0.025 470 525 1330 80Ex. 20 Sr.sub.1.995 MgSi.sub.1.96 Ge.sub.0.04 O.sub.7 :Eu.sub.0.005 Dy.sub.0. 025 Cl.sub.0.025 470 330 1200 80Ex. 21 Sr.sub.1.995 Mg.sub.0.97 Cd.sub.0.03 Si.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Cl.sub.0.03 470 420 920 75Ex. 22 Sr.sub.1.995 Mg.sub.0.97 Be.sub.0.03 Si.sub.2 O.sub.7 :Eu.sub.0.005 Dy.sub.0.025 Cl.sub.0.025 470 395 900 80__________________________________________________________________________
TABLE 3__________________________________________________________________________ Afterglow characteristics Emission 5 minutes 60 minutes Glow peakChemical compositional formula peak (nm) later later (.degree. C.)__________________________________________________________________________Ex. 23 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 460 40 150 80Ex. 24 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.05 460 300 800 90Ex. 25 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Br.sub.0.03 460 250 750 95Ex. 26 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 F.sub.0.025 460 300 750 85Ex. 27 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.05 Dy.sub.0.025 Cl.sub.0.025 460 280 700 90Ex. 28 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.05 Dy.sub.0.025 Cl.sub.0.025 460 250 600 80Ex. 29 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Nd.sub.0.025 Cl.sub.0.025 460 230 700 95Ex. 30 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Tm.sub.0.025 Cl.sub.0.025 460 75 185 90Ex. 31 Sr.sub.2.97 Ca.sub.0.9 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 In.sub.0.025 Cl.sub.0.025 460 70 175 95__________________________________________________________________________
TABLE 4__________________________________________________________________________ Afterglow characteristics Emission 5 minutes 60 minutes Glow peakChemical compositional formula peak (nm) later later (.degree. C.)__________________________________________________________________________Ex. 32 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Bi.sub.0.025 Cl.sub.0.025 460 50 120 85Ex. 33 Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 Sn.sub.0.025 Cl.sub.0.025 460 85 210 90Ex. 34 Sr.sub.2.97 Mg.sub.0.9 Zn.sub.0.1 Si.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 460 100 260 90Ex. 35 Sr.sub.2.97 Mg.sub.0.9 Cd.sub.0.1 Si.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 460 60 150 85Ex. 26 Sr.sub.2.97 Mg.sub.0.9 Be.sub.0.1 Si.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.025 460 50 125 90Ex. 37 Sr.sub.2.97 Mg.sub.1.95 Ge.sub.0.05 Si.sub.2 O.sub.8 :Eu.sub.0.03 Dy.sub.0.025 Cl.sub.0.03 460 43 115 80Comp. Sr.sub.1.995 MgSi.sub.2 O.sub.7 :Eu.sub.0.005 470 3 0 80Ex. 1Comp. Sr.sub.2.97 MgSi.sub.2 O.sub.8 :Eu.sub.0.03 460 5 0 90Ex. 2Comp. ZnS:Cu 516 100 100 120Ex. 3__________________________________________________________________________

Number	Date	Country	Kind
8-8630	Jan 1996	JPX
8-54955	Mar 1996	JPX

Number	Name	Date
3544482	Barry	Dec 1970
3676361	Datta	Jul 1972
5231328	Hisamune et al.	Jul 1993
5839718	Hase et al.	Nov 1998

Number	Date	Country
48-37714	Nov 1973	JPX
48-37715	Nov 1973	JPX
50-49178	May 1975	JPX
50-49177	May 1975	JPX
7-11250	Jan 1995	JPX
8-73845	Mar 1996	JPX
8-127772	May 1996	JPX

Phosphorescent phosphor

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