Patent Application
20130214206
The present invention relates to luminescent materials, more particularly, relates to a modified tungstate fluorescent powders. The present invention also relates to preparation methods of tungstate fluorescent powders.
In recent years, it has been found that WO42− can be used as broadband blue light emission group; thus, there is also strong interest in luminescence properties of cathode ray equipped with tungstate, and considerable efforts is being directed toward it. Nowadays, it is widely used in the fields of the photoluminescence, microwave applications, optical fiber, scintillation crystal, humidity sensor, magnetic properties, and catalyst. For example, calcium tungstate is good fluorescent powder used in X-ray intensifying screen. However, WO42− can be used as broadband blue light emission group, the prominent drawback of it is that the luminous intensity is low.
Solving the above problems, the present invention provides tungstate fluorescent powders represented by general formula of RWO4:xM; wherein, R is one or two metal elements of Ca, Sr and Ba; M is one or two metal nano-particles of Ag, Au, Pt and Pd; x is molar ratio of M nano-particles to RWO4, x is in the range of 0<x≦1×10−3.
The other purpose of the present invention is to provide a preparation method of tungstate fluorescent powders, comprising:
Firstly, preparation of M nano-particles collosol
1) weighing and dissolving compound used as source of M in solvent to prepare and dilute solution containing M ions; wherein, M is one or two kinds of metal nano-particles of Ag, Au, Pt and Pd, the compound used as source of M is one or two of silver nitrate, chloroauric acid, chloroplatinic acid and palladium chloride, the solvent is water or mixed solvent of ethanol and water in volume ratio of 1:7˜4:1;
2) while magnetically stirring, dissolving assistant agent in said solution containing M ions of 1), and obtaining a mass concentration of assistant agent in the obtained M nano-particles collosol, which is in the range of 1.5×10−4 g/mL˜2.1×10−3 g/mL; wherein, the assistant agent is at least one of polyvinyl pyrrolidone (PVP), sodium citrate, cetyl trimethyl ammonium bromide, sodium dodecyl sulfate and sodium dodecyl sulfonate;
3) weighing and dissolving matters of reducing agent in solvent to prepare a reducing agent solution having a molar concentration in the range of 1×10−3 mol/L˜1×10−2 mol/L; the matters of reducing agent is hydrazine hydrate, ascorbic acid or sodium borohydride; the solvent is water or mixed solution of ethanol and water in volume ratio of 1:9˜2:1;
4) while magnetically stirring, adding the reducing solution obtained from 3) into the solution obtained from 2) according to the molar ratio of reducing agent to metal ions which is in the range of 1.2:1˜4.8:1 to carry out redox reaction for 10˜45 min, then obtaining M nano-particles collosol; 5) weighing and adding surface treating agent into the M nano-particles collosol prepared in 4), stirring for 3˜24 h, then obtaining the surface treated M nano-particles collosol, wherein mass concentration of the surface treating agent in M nano-particles collosol is in the range of 0.001 g/mL˜0.1 g/mL; the surface treating agent is polyvinyl pyrrolidone (PVP).
Secondly, preparation of RWO4:xM fluorescent powders
As for the preparation of RWO4:xM fluorescent powders, the two following methods can be employed:
Method 1: Pechini Sol-Gel Method
6) adding R salts (e.g. R(NO3)2) solution and tungstate (e.g. (NH4)2WO4 or (NH4)10H2(W2O7)6) solution into a beaker (wherein, the molar ratio of R2+ to WO42− is in the range of 1:1˜1:1.25) according to the general formula RWO4:xM (wherein, R is one or two metal elements of Ca, Sr and Ba, 0<x≦0.5); then adding ethanol, stirring thoroughly to obtain mixed solution containing R ions and tungstate ions; then adding mixed solution of ethanol and water containing citric acid that acts as a chelating agent, and adding polyethylene glycol (PEG, having relative molecular mass of 2000˜20000, preferably 10000, the mass concentration of PEG is in the range of 0.01˜0.1 g/ml) that acts as a cross-linking agent according to the volume of solution at that moment; then regulating the pH value of the mixed solution to keep in the range of 2˜4 to obtain chelate solution; wherein, citric acid is citric acid monohydrate, molar ratio of the citric acid to total amount of R ions of the mixed solution is in the range of 1:1˜6:1; because a few of tungstate ions are volatilized during the calcination, therefore, the tungstate raw materials should be in excess by 1%˜25% when preparing tungstate solution;
7) adding the surface treated M nano-particles collosol of 5) into the chelate solution of 6) according to the molar ratio x (0<x≦1×10−3) of M nano-particles to RWO4 in the general formula of RWO4:xM; after drying at 80˜150° C., the gel is obtained; placing the gel into high temperature furnace, heat treating at 600˜900° C. for 0.5˜7 h, cooling to room temperature, after grinding, tungstate flourescent powders represented by general formula of RWO4:xM is obtained.
Method 2: Hydrothermal Method
6′) adding tungstate (e.g. (NH4)2WO4 or Na2WO4) solution into a beaker according the molar ratio x (0<x≦1×10−3) of M nano-particles to RWO4 in the general formula of RWO4:xM, then adding the surface treated M nano-particles collosol of 5), stirring for 10 min˜60 min to obtain mixed solution; wherein R is one or two metal elements of Ca, Sr and Ba;
7′) dripping R salts (e.g. R(NO3)2) solution, whose amount is as much as that of tungstate of 6′), into the mixed solution of 6′) to regulate the pH value of mixed solution to keep it in the range of 8˜12, stirring for 0.5˜4 h, then obtaining alkaline mixed solution;
8′) transferring alkaline mixed solution of 7′) to hydrothermal reactor, keeping the temperature constant at 120˜250° C. for 12˜72 h, cooling, taking out and filtrating, rinsing (e.g. rinsing with water, alcohols), drying to obtain powders;
9′) placing dry powders in high temperature furnace, heat treating at 500˜900° C. for 0.5˜7 h, cooling to room temperature, after grinding, tungstate fluorescent powders represented by general formula of RWO4:xM is obtained.
Compared to the prior art, the present invention has the following features:
1. The present invention is to dope fluorescent powders with metal particles, improves luminous intensity of fluorescent powders by plasma resonance;
2. The present invention is simple, pollution-free, easy to control, low demand in equipment, beneficial to industry production, can be widely used in the field of producing fluorescent powders.
The present invention provides tungstate fluorescent powders represented by general formula of RWO4:xM; wherein, R is one or two metal elements of Ca, Sr and Ba; M is one or two metal nano-particles of Ag, Au, Pt and Pd; x is molar ratio of M nano-particles to RWO4, x is in the range of 0<x≦1×10−3.
As shown in
Step S1, Preparation of M Nano-Particles Collosol
1) weighing and dissolving compound used as source of M in solvent to prepare and dilute solution containing M ions; wherein, M is one or two kinds of metal nano-particles of Ag, Au, Pt and Pd, the compound used as source of M is one or two of silver nitrate, chloroauric acid, chloroplatinic acid and palladium chloride, the solvent is water or mixed solvent of ethanol and water in volume ratio of 1:7˜4:1;
2) while magnetically stirring, dissolving assistant agent in said solution containing M ions of 1), and obtaining a mass concentration of assistant agent in the obtained M nano-particles collosol, which is in the range of 1.5×10−4 g/mL˜2.1×10−3 g/mL; wherein, the assistant agent is at least one of polyvinyl pyrrolidone (PVP), sodium citrate, cetyl trimethyl ammonium bromide, sodium dodecyl sulfate and sodium dodecyl sulfonate;
3) weighing and dissolving matters of reducing agent in solvent to prepare a reducing agent solution having a molar concentration of 1×10−3 mol/L˜1×10−2 mol/L; the matters of reducing agent is hydrazine hydrate, ascorbic acid or sodium borohydride; the solvent is water or mixed solution of ethanol and water in volume ratio of 1:9˜2:1;
4) while magnetically stirring, adding the reducing solution obtained from 3) into the solution obtained from 2) according to the molar ratio of reducing agent to metal ions which is in the range of 1.2:1˜4.8:1 to carry out redox reaction for 10˜45 min, then obtaining M nano-particles collosol; 5) weighing and adding surface treating agent into the M nano-particles collosol prepared in 4), stirring for 3˜24 h, then obtaining the surface treated M nano-particles collosol, wherein mass concentration of the surface treating agent is in the range of 0.001 g/mL˜0.1 g/mL; the surface treating agent is polyvinyl pyrrolidone (PVP).
Step S2: Preparation of RWO4:xM Fluorescent Powders
As for the preparation of RWO4:xM fluorescent powders, the two following methods can be employed:
Method 1: Pechini Sol-Gel Method
6) adding R salts (e.g. R(NO3)2) solution and tungstate (e.g. (NH4)2WO4 or (NH4)10H2(W2O7)6) solution into a beaker (wherein, the molar ratio of R2+ to WO42− is in the range of 1:1˜1:1.25) according to the general formula RWO4:xM (wherein, R is one or two metal elements of Ca, Sr and Ba, 0<x≦0.5); then adding ethanol, stirring thoroughly to obtain mixed solution of containing R ions and tungstate ions; then adding mixed solution of ethanol and water containing citric acid that acts as a chelating agent, and adding polyethylene glycol (PEG, having relative molecular mass of 2000˜20000, preferably 10000, the mass concentration of PEG is in the range of 0.01˜0.1 g/ml) that acts as a cross-linking agent according to the volume of solution at that moment; then regulating the pH value of the mixed solution to keep in the range of 2˜4 to obtain chelate solution; wherein, citric acid is citric acid monohydrate, molar ratio of the citric acid to total amount of R ions of the mixed solution is in the range of 1:1˜6:1; because a few of tungstate ions are volatilized during the calcination, therefore, the tungstate raw materials should be in excess by 1%˜25% when preparing tungstate solution;
7) adding the surface treated M nano-particles collosol of 5) into the chelate solution of 6) according to the molar ratio x (0<x≦1×10−3) of M nano-particles to RWO4 in the general formula of RWO4:xM; after drying at 80˜150° C., the gel is obtained; placing the gel into high temperature furnace, heat treating at 600˜900° C. for 0.5˜7 h, cooling to room temperature, after grinding, tungstate flourescent powders represented by general formula of RWO4:xM is obtained.
Method 2: Hydrothermal Method
6′) adding tungstate (e.g. (NH4)2WO4 or Na2WO4) solution into a beaker according the molar ratio x (0<x≦1×10−3) of M nano-particles to RWO4 in the general formula of RWO4:xM, then adding the surface treated M nano-particles collosol of 5), stirring for 10 min˜60 min to obtain mixed solution; wherein R is one or two metal elements of Ca, Sr and Ba;
7′) dripping R salts (e.g. R(NO3)2) solution, whose amount is as much as that of tungstate of 6′), into the mixed solution of 6′) to regulate the pH value of mixed solution to keep in the range of 8˜12, stirring for 0.5˜4 h, then obtaining alkaline mixed solution;
8′) transferring alkaline mixed solution of 7′) to hydrothermal reactor, keeping the temperature constant at 120˜250° C. for 12˜72 h, cooling, taking out and filtrating, rinsing (e.g. rinsing with water, alcohols), drying to obtain powders;
9′) placing dry powders in high temperature furnace, heat treating at 500˜900° C. for 0.5˜7 h, cooling to room temperature, after grinding, tungstate fluorescent powders represented by general formula of RWO4:xM is obtained.
Further description of the present invention will be illustrated, which combined with preferred embodiments in the drawings.
Weighing and dissolving 5.18 mg of chloroplatinic acid (H2PtCl6.6H2O) in 17 mL of deionized water; after chloroplatinic acid dissolved completely, weighing and dissolving 8 mg of sodium citrate and 12 mg of sodium dodecyl sulfonate in the aqueous solution of chloroplatinic acid under the condition of magnetic stirring; weighing and dissolving 0.38 mg of sodium borohydride in mixed solution of 9 mL of deionized water and 1 mL of ethanol, obtaining 10 mL of 1×10−3 mol/L aqueous solution of sodium borohydride, preparing 10 mL of 1×10−2 mol/L hydrazine hydrate solution at the same time; under the condition of magnetic stirring, adding 0.4 mL aqueous solution of sodium borohydride into the aqueous solution of chloroplatinic acid, stirring and reacting for 5 min, and then adding 2.6 mL of 1×10−2 mol/L hydrazine hydrate solution into the aqueous solution of chloroplatinic acid, continue to react for 40 min, then obtaining 20 mL of Pt nano-particles collosol containing 5×10−4 mol/L of Pt; then adding 2.0 mg of PVP into Pt nano-particles collosol, magnetically stirring for 12 h. The surface-treated Pt nano-particles were obtained.
Preparation of 0.01 mol of CaWO4:1×10−3Pt
Pipetting 10 mL of 1 mol/L Ca(NO3)3 solution, 10.1 mL of 1 mol/L (NH4)2WO4 solution (excess 1%) and adding into a beaker, then adding 20 mL of ethanol, stirring thoroughly to obtain mixed solution of nitrate, adding citric acid of 5 mL-water-20 mL-ethanol (containing 2.1014 g of citric acid monohydrate; the molar ratio of the citric acid to total amount of ions of the mixed solution is 1:1) and 0.65 g of PEG (0.01 g/ml, PEG having a relative molecular mass of 2000) into the mixed solution, stirring thoroughly, regulating the pH value of reaction solution to about 2; taking 20 mL of the above-mentioned treated metal particles solution, heating in a water bath at 60° C. while stirring for 16 h to obtain collosol; completely drying the collosol at 80° C. to obtain gel; placing the gel into high temperature furnace, calcining at 600° C. for 7 h, cooling to room temperature, fluorescent powders CaWO4:1×10−3Pt were obtained after grinding.
Weighing and dissolving 4.12 mg of chloroauric acid (AuCl3.HCl.4H2O) in mixed solvent of 2.8 mL of water and 5.6 mL of ethanol; after chloroauric acid dissolved completely, weighing and dissolving 14 mg of sodium citrate and 6 mg of cetyl trimethyl ammonium bromide in the aqueous solution of chloroauric acid under the condition of magnetic stirring; weighing and dissolving 1.9 mg of sodium borohydride and 17.6 mg of ascorbic acid in 10 mL of deionized water, respectively, obtaining 10 mL of 5×10−3 mol/L aqueous solution of sodium borohydride and 10 mL of 1×10−2 mol/L aqueous solution of ascorbic acid; under the condition of magnetic stirring, adding 0.04 mL aqueous solution of sodium borohydride into the aqueous solution of chloroauric acid, stirring and reacting for 5 min, and then adding 1.56 mL of 1×10−2 mol/L aqueous solution of ascorbic acid into the aqueous solution of chloroauric acid, continue to react for 30 min, then obtaining 10 mL of Au nano-particles collosol containing 1×10−3 mol/L of Au; adding 0.006 g of PVP into 6 mL of obtained Au nano-particles collosol, and magnetically stirring for 8 h. The surface-treated Au nano-particles were obtained.
Preparation of 0.01 mol of SrWO4:5×10−4Au
Pipetting 10 mL of 1 mol/L Sr(NO3)3 solution, 12.5 mL of 1 mol/L (NH4)2WO4 solution (excess 25%) and adding into a beaker, then adding 20 mL of ethanol, stirring thoroughly to obtain mixed solution of nitrate, adding citric acid of 5 mL-water-20 mL-ethanol (containing 4.2028 g of citric acid monohydrate; the molar ratio of the citric acid to total amount of ions of the mixed solution is 2:1) and 2.025 g of PEG (0.03 g/ml, PEG having a relative molecular mass of 6000) into the mixed solution, stirring thoroughly, regulating the pH value of reaction solution to about 3; taking 5 mL of the above-mentioned treated metal particles solution, heating in a water bath at 90° C. while stirring for 2 h to obtain collosol; completely drying the collosol at 150° C. to obtain gel; placing the gel into high temperature furnace, calcining at 900° C. for 0.5 h, cooling to room temperature, fluorescent powders SrWO4:5×10−4Au were obtained after grinding.
weighing and dissolving 3.40 mg of silver nitrate (AgNO3) in 18.4 mL of deionized water; after silver nitrate dissolved completely, weighing and dissolving 22 mg of sodium citrate and 20 mg of PVP in the aqueous solution of silver nitrate under the condition of magnetic stirring; weighing and dissolving 5.7 mg of sodium borohydride in mixed solvent of 2 mL of deionized water and 8 mL of ethanol, obtaining 10 ml of 1.5×10−2 mol/L aqueous solution of sodium borohydride; under the condition of magnetic stirring, adding 1.6 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride into the aqueous solution of silver nitrate at once, continue to react for 10 min, then obtaining 20 mL of Ag nano-particles collosol containing 1×10−3 mol/L of Ag; adding 1 g of PVP into the Ag nano-particles collosol, and magnetically stirring for 6 h. The surface-treated Ag nano-particles were obtained.
Preparation of 0.01 mol of CaWO4:5×10−5Ag
Pipetting 5 mL of 2 mol/L Ca(NO3)3 solution, 5.5 mL of 2 mol/L (NH4)2WO4 solution (excess 10%) and adding into a beaker, then adding 0.5 mL of ethanol, stirring thoroughly to obtain mixed solution of nitrate, adding citric acid of 5 mL-water-20 mL-ethanol (containing 8.4056 g of citric acid monohydrate; the molar ratio of the citric acid to total amount of ions of the mixed solution is 4:1) and 3.6 g of PEG (0.1 g/ml, PEG having a relative molecular mass of 10000) into the mixed solution, stirring thoroughly, regulating the pH value of reaction solution to about 4; taking 0.5 mL of the above-mentioned treated metal particles solution, heating in a water bath at 85° C. while stirring for 5 h to obtain collosol; completely drying the collosol at 120° C. to obtain gel; placing the gel into high temperature furnace, calcining at 800° C. for 2 h, cooling to room temperature, fluorescent powders CaWO4:5×10−5Ag were obtained after grinding. Fluorescent powders CaWO4 were prepared at the same conditions.
Weighing and dissolving 0.43 mg of palladium chloride (PdCl2.2H2O) in 8.5 mL of deionized water; after palladium chloride dissolved completely, weighing and dissolving 11.0 mg of sodium citrate and 4.0 mg of sodium dodecyl sulfate in the aqueous solution of palladium chloride under the condition of magnetic stirring; weighing and dissolving 3.8 mg of sodium borohydride in mixed solvent of 7.5 mL of deionized water and 2.5 mL of ethanol, obtaining 1×10−2 mol/L reducing aqueous solution of sodium borohydride; under the condition of magnetic stirring, adding rapidly 0.48 mL of 1×10−2 mol/L aqueous solution of sodium borohydride into the aqueous solution of palladium chloride, continue to react for 20 min, then obtaining 10 mL of Pd nano-particles collosol containing 1×10−4 mol/L of Pd; adding 0.5 g of PVP into 10 mL of the obtained Pd nano-particles collosol, and magnetically stirring for 4 h. The surface-treated Pd nano-particles were obtained.
Preparation of 0.01 mol of BaWO4:5×10−5Pd
Pipetting 5 mL of 2 mol/L Ba(NO3)3 solution, 5 mL of 0.2 mol/L (NH4)10H2(W2O7)6 solution (excess 20%) and adding into a beaker, then adding 1 mL of ethanol, stirring thoroughly to obtain mixed solution of nitrate, adding citric acid of 5 mL-water-20 mL-ethanol (containing 12.6084 g of citric acid monohydrate; the molar ratio of the citric acid to total amount of ions of the mixed solution is 6:1) and 2.16 g of PEG (0.06 g/ml, PEG having a relative molecular mass of 20000) into the mixed solution, stirring thoroughly, regulating the pH value of reaction solution to about 3; taking 5 mL of the above-mentioned treated metal particles solution, heating in a water bath at 80° C. while stirring for 12 h to obtain collosol; completely drying the collosol at 120° C. to obtain gel; placing the gel into high temperature furnace, calcining at 700° C. for 5 h, cooling to room temperature, fluorescent powders BaWO4:5×10−5Pd were obtained after grinding.
weighing and dissolving 6.2 mg of chloroauric acid (AuCl3.HCl.4H2O) and 7.8 mg of chloroplatinic acid (H2PtCl6.6H2O) in mixed solvent of 14 mL and 14 mL of ethanol; after dissolved completely, weighing and dissolving 22 mg of sodium citrate and 20 mg of PVP in the mixed solution under the condition of magnetic stirring; weighing and dissolving 5.7 mg of fresh-made sodium borohydride 10 mL of deionized water, obtaining 10 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride; under the condition of magnetic stirring, adding 2 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride into the mixed solution at once, continue to react for 20 min, then obtaining 30 mL of Pt/Au nano-particles collosol containing 1×10−3 mol/L of total metal particles; adding 2 g of PVP into Pt/Au nano-particles collosol, and magnetically stirring for 24 h. The surface-treated Pt/Au nano-particles were obtained.
Preparation of 0.01 mol of Ca0.5Ba0.5WO4:1×10−4Pt/Au
According to the general formula, adding 10 mL of 1 mL/L (NH4)2WO4 solution into a beaker, then adding 1 mL of the above-mentioned treated metal particles solution, stirring for 10 min; then dripping mixed solution of 5 mL of 1 ml/L Ca(NO3)2 and 5 mL of 1 ml/L Ba(NO3)2 into the above solution, regulating pH to 8, stirring for 0.5 h; transferring the solution to hydrothermal reactor, then keeping the temperature constant at 120° C. for 72, after that, cooling, taking out and filtrating, rinsing with water and alcohols, drying; at last, placing the dry products into high temperature furnace, calcining at 500° C. for 7 h, cooling to room temperature, tungstate fluorescent powders Ca0.5Ba0.5WO4:1×10−4Pt/Au were obtained after grinding.
weighing and dissolving 3.40 mg of silver nitrate (AgNO3) in 18.4 mL of deionized water; after silver nitrate dissolved completely, weighing and dissolving 22 mg of sodium citrate and 20 mg of PVP in the aqueous solution of silver nitrate under the condition of magnetic stirring; weighing and dissolving 5.7 mg of sodium borohydride in 10 mL of deionized water, obtaining 10 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride; under the condition of magnetic stirring, adding 1.6 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride into the aqueous solution of silver nitrate at once, continue to react for 10 min, then obtaining 20 mL of Ag nano-particles collosol containing 1×10−3 mol/L of Ag; adding 1 g of PVP into Ag nano-particles collosol, and magnetically stirring for 3 h. The surface-treated Ag nano-particles were obtained.
Preparation of 0.01 mol of CaWO4:5×10−5Ag
According to the general formula, adding 10 mL of 1 mL/L Na2WO4 solution into a beaker, then adding 0.5 mL of the above-mentioned treated metal particles solution, stirring for 60 min; then dripping 10 mL of 1 ml/L Ca(NO3)2 solution into the above solution, regulating pH to 10, stirring for 4 h; transferring the solution to hydrothermal reactor, then keeping the temperature constant at 200° C. for 72, after that, cooling, taking out and filtrating, rinsing with water and alcohols, drying; at last, placing the dry products into high temperature furnace, calcining at 600° C. for 3 h, cooling to room temperature, tungstate fluorescent powders CaWO4:5×10−5Ag were obtained after grinding. Tungstate fluorescent powders CaWO4 were prepared at the same conditions.
weighing and dissolving 3.40 mg of silver nitrate (AgNO3) in mixed solvent of 2.3 mL of ethanol and 16.1 mL of water; after silver nitrate dissolved completely, weighing and dissolving 22 mg of sodium citrate and 20 mg of PVP in the aqueous solution of silver nitrate under the condition of magnetic stirring; weighing and dissolving 5.7 mg of sodium borohydride in mixed solvent of 5 mL of deionized water and 5 mL of ethonal, obtaining 10 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride; under the condition of magnetic stirring, adding 1.6 mL of 1.5×10−2 mol/L aqueous solution of sodium borohydride into the aqueous solution of silver nitrate at once, continue to react for 10 min, then obtaining 20 mL of Ag nano-particles collosol containing 1×10−3 mol/L of Ag; adding 0.5 g of PVP into Ag nano-particles collosol, and magnetically stirring for 6 h. The surface-treated Ag nano-particles were obtained.
Preparation of 0.01 mol of BaWO4:1×10−4Ag
According to the general formula, adding 10 mL of 1 mL/L Na2WO4 solution into a beaker, then adding 1 mL of the above-mentioned treated metal particles solution, stirring for 30 min; then dripping 10 mL of 1 ml/L Ba(NO3)2 solution into the above solution, regulating pH to 12, stirring for 1 h; transferring the solution to hydrothermal reactor, then keeping the temperature constant at 250° C. for 12, after that, cooling, taking out and filtrating, rinsing with water and alcohols, drying; at last, placing the dry products into high temperature furnace, calcining at 900° C. for 0.5 h, cooling to room temperature, tungstate fluorescent powders BaWO4: 1×10−4Ag were obtained after grinding.
While the present invention has been described with reference to particular embodiments, it will be understood that the embodiments are illustrative and that the invention scope is not so limited. Alternative embodiments of the present invention will become apparent to those having ordinary skill in the art to which the present invention pertains. Such alternate embodiments are considered to be encompassed within the spirit and scope of the present invention. Accordingly, the scope of the present invention is described by the appended claims and is supported by the foregoing description.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN10/79767 | 12/14/2010 | WO | 00 | 4/25/2013 |
