CN1903977A - Preparation method of aluminate base blue fluorescent powder - Google Patents
Preparation method of aluminate base blue fluorescent powder Download PDFInfo
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- CN1903977A CN1903977A CN 200610052735 CN200610052735A CN1903977A CN 1903977 A CN1903977 A CN 1903977A CN 200610052735 CN200610052735 CN 200610052735 CN 200610052735 A CN200610052735 A CN 200610052735A CN 1903977 A CN1903977 A CN 1903977A
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- citric acid
- gel
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- fluorescent powder
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Abstract
The present invention relates to a preparation method of aluminate base blue fluorescent powder. Said method includes the following steps: using aluminium nitrate, barium carbonate, basic magnesium carbonate and europium oxide according to a certain ratio, making them be dissolved in citric acid solution, regulating solution volume to make concentration of aluminium nitrate be 0.2-I mol/L, regulating pH value to 4.5-7, heat-insulating for 10-30 hr at 70-85 deg.C, making said solution be converted into sol and gel; heat-insulating for 3-4 hr at 110-150 deg.C to make gel be converted into dried gel, and self-spread and burned to obtain black powder, finally calcining said powder for 1-3 hr in reduction gas containing 5-10% of hydrogen gas and 90-95% of nitrogen gas at 1050-1250 deg.C so as to oblain the invented fluorescent powder.
Description
Technical field
The present invention relates to the preparation method of divalent europium activated aluminate base blue colour fluorescent powder, refer in particular to be applied to the plasma flat-plate display screen blue colour fluorescent powder (as BaMgAl
10O
17: Eu
2+, BaMgAl
14O
23: Eu
2+) the preparation method.
Background technology
In recent years, the fast development of the emitting components technology that vacuum-ultraviolet light (VUV) excites is to the demands for higher performance of three primary colors fluorescent powder.As the used three primary colors fluorescent powder of plasma flat-plate display screen (PDP): comprise red fluorescence powder (Y, Gd) BO
3: Eu
3+, green emitting phosphor Zn
2SiO
4: Mn
2+, BaAl
12O
19: Mn
2+, blue colour fluorescent powder BaMgAl
10O
17: Eu
2+, BaMgAl
14O
23: Eu
2+Deng, differ greatly with the Working environment of common lamp phosphor, bearing the impact more much better than, and higher luminous efficiency will arranged, therefore to the demands for higher performance of fluorescent material than common phosphors.
Divalent europium activated aluminate base blue colour fluorescent powder is as BaMgAl
10O
17: Eu
2+, BaMgAl
14O
23: Eu
2+, its structure is β-Al
2O
3Structure, Eu
2+Enter crystalline structure and replace the part barium ion, under the irradiation of vacuum-ultraviolet light, the matrix absorption transmission ofenergy is given Eu
2+, make the electronics acquisition energy of europium ion launch blue light by energy level transition.
The traditional preparation method of aluminate base blue colour fluorescent powder mainly is a high temperature solid-state method, as U.S. Pat 3937998, US6096243, Chinese patent CN85100242 etc. are described be with required raw materials of compound according to the element ratio mixed grinding after, behind the long-time sintering of high temperature, obtain fluorescent material.Because sintering temperature is higher, makes that the crystal property of fluorescent material is bad.Follow-up study such as Chinese patent CN1091149, CN1129727, CN1188788, CN1190115, CN1203208, CN1415695 etc. are by adding fusing assistant such as boride, halogenide, basic metal and alkali-metal salt etc. in raw material, significantly reduced sintering temperature, but the adding of fusing assistant, make that the synthetic fluorescent powder grain is bigger than normal, must and sieve and to use through ball milling, long ball milling has reduced the performance of fluorescent material; The surface property thermal degradation when causes the light-emitting phosphor decrease in efficiency, and stability reduces, and all detrimentally affect can be arranged to optical throughput, light decay; CN1197831 adopts sol-gel method to prepare aluminate base blue colour fluorescent powder, can directly use without ball milling, but comparatively expensive and easy evaporable organic compound has been adopted in this invention, and the production cycle is longer; CN1334309 uses nitrate, carbonate, acetate or oxide compound to be raw material, and sol-gel method synthesized the fluorescent material that need not ball milling, but for the fluorescent material that contains Sr, Ba, aluminum nitrate dissolving back need be added ammoniacal liquor, make Al
3+Change Al (OH) into
3Active colloidal shape precipitation, and, remove NO wherein with the washing of precipitate filtration
3 -, being dissolved in citric acid with other raw material then and being mixed with solution, this process operations complexity can't accurately be controlled the proportioning of feed composition, and there is the composition deviation in the fluorescent material that obtains, has reduced the fluorescent material performance.
By literature search, the research of using citric acid complex method to prepare aluminate base blue colour fluorescent powder in recent years mainly contains 121 pages of " silicate journal " 2002 the 1st phases " sol-gel processing synthesizes BaMgAl
10O
17Powder ", in this document, propose, because the nitrate solubleness of Ba is lower, because the evaporation of moisture, the nitrate of Ba is separated out the result in becoming the glue process, makes the colloid instability, has influenced the homogeneity of fluorescent material composition, therefore, needs to remove the NO in the solution
3 -, preparation technology's more complicated.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of aluminate base blue colour fluorescent powder, adopt sol-gel processing to combine, reduced the synthesis temperature of powder, simplify production technique with self-propagating combustion, simple to operate, the blue colour fluorescent powder that obtains can use without ball milling.
The preparation method of a kind of aluminate base blue colour fluorescent powder provided by the invention is characterized in that this method comprises the following steps:
(1), the chemical composition according to prepared aluminate base blue colour fluorescent powder takes by weighing aluminum nitrate, barium carbonate, magnesium basic carbonate, europium sesquioxide; 1.5～3 times according to the aluminum nitrate mole number that takes by weighing take by weighing citric acid;
(2), the citric acid that takes by weighing is mixed with citric acid solution, with citric acid all dissolving be as the criterion;
(3), 4 kinds of raw materials that will take by weighing: aluminum nitrate, barium carbonate, magnesium basic carbonate, europium sesquioxide all are dissolved in the citric acid solution for preparing, and the concentration of controlling aluminum nitrate by the adjustment liquor capacity is 0.2～1mol/L;
(4), the pH value with above-mentioned solution is adjusted into 4.5～7;
(5), with above-mentioned solution adjusted 70～85 ℃ of down insulations 10～30 hours, make it change colloidal sol, gel gradually into;
(6), again with the gel that forms 110～150 ℃ of insulations 3～4 hours down, gel conversion is the concurrent propagating combustion of being conigenous of xerogel, generates black powder;
(7), above-mentioned powder was calcined in 1050～1250 ℃ reducing atmosphere 1～3 hour, reducing atmosphere is the hydrogen of 5～10% volume ratios and the nitrogen of 90～95% volume ratios, can obtain required fluorescent material.
The fluorescent material of the present invention's preparation can be used as three-color fluorescent lamp and various indicating meter such as plasma flat-plate display screen (PDP) blue color component with fluorescent material at vacuum-ultraviolet light (VUV) or ultraviolet ray excited emission blue light down.
The present invention prepares aluminate base blue colour fluorescent powder following characteristics:
1, preparation technology is simple, and easy handling is compared with short production cycle with general sol-gel processing;
2, by adjusting the pH of solution, eliminated in the glue process Ba ionic crystal to separate out the disadvantageous effect of bringing to preparation technology, simplified preparation technology;
3, utilize citric acid and nitrate ion that self-propagating combustion synthesizing aluminate base blue colour fluorescent powder presoma takes place under certain condition, reduced synthesis temperature, shortened the production cycle, reduced production cost.
4, by suitably improving the concentration of hydrogen in the reducing atmosphere, make reaction more complete, improved the luminescent properties of blue powder.
Embodiment
Following examples are preparation blue colour fluorescent powder BaMgAl
10O
17: Eu
2+, can be used for the blue color component of fluorescent material used in kinds of displays part such as the plasma panel (PDP).
Embodiment 1
Take by weighing aluminum nitrate 1mol, barium carbonate 0.09mol, magnesium basic carbonate 0.02mol, europium sesquioxide 0.01mol, be dissolved in jointly in the solution that contains citric acid 1.5mol that (preparation of citric acid solution is formulated with citric acid and water 1: 1, as follows), adjust liquor capacity, make that the concentration of aluminum nitrate is 0.2mol/L; The pH value of adjusting solution is 6.5; The solution of configuration is incubated 24 hours down at 70 ℃, and solution changes glassy yellow vitreosol, gel gradually into; Above-mentioned gel is incubated 3 hours down at 150 ℃, and gel changes the concurrent propagating combustion of being conigenous of xerogel gradually into, collects the black powder that obtains; Can obtain BaMgAl in 2.5 hours in 5% hydrogen and 95% nitrogen (volume ratio) reducing gas, calcining under 1150 ℃
10O
17: Eu
2+Blue colour fluorescent powder.The X-ray diffraction result shows d value and the relative intensity and the BaMgAl of product
10O
17Standard card unanimity, the median size of fluorescent material are 3.5 μ m, and emission wavelength is the blue light of 452nm under vacuum ultraviolet ray (147nm) irradiation.
Embodiment 2
Take by weighing aluminum nitrate 1mol, barium carbonate 0.09mol, magnesium basic carbonate 0.02mol, europium sesquioxide 0.01mol, be dissolved in jointly in the solution that contains citric acid 3mol, adjust liquor capacity, make that the concentration of aluminum nitrate is 1mol/L; The pH value of adjusting solution is 6; The solution of configuration is incubated 15 hours down at 85 ℃, and solution changes glassy yellow vitreosol, gel gradually into; Above-mentioned gel is incubated 4 hours down at 130 ℃, and gel changes xerogel gradually into, and the concurrent propagating combustion of being conigenous is collected the black powder art that obtains; Can obtain BaMgAl in 1.5 hours in 10% hydrogen and 90% nitrogen (volume ratio) reducing gas, calcining under 1100 ℃
10O
17: Eu
2+Blue colour fluorescent powder.The X-ray diffraction result shows d value and the relative intensity and the BaMgAl of product
10O
17Standard card unanimity, the median size of fluorescent material are 4.0 μ m, and emission wavelength is the blue light of 454nm under vacuum ultraviolet ray (147nm) irradiation.
Embodiment 3
Take by weighing aluminum nitrate 1mol, barium carbonate 0.09mol, magnesium basic carbonate 0.02mol, europium sesquioxide 0.01mol, be dissolved in jointly in the solution that contains citric acid 2mol, adjust liquor capacity, make that the concentration of aluminum nitrate is 0.8mol/L; The pH value of adjusting solution is 5.5; The solution of configuration is incubated 20 hours down at 80 ℃, and solution changes glassy yellow vitreosol, gel gradually into; Above-mentioned gel is incubated 3.5 hours down at 140 ℃, and gel changes the concurrent propagating combustion of being conigenous of xerogel gradually into, collects the black powder that obtains; Can obtain BaMgAl in 2 hours in 7% hydrogen and 93% nitrogen (volume ratio) reducing gas, calcining under 1200 ℃
10O
17: Eu
2+Blue colour fluorescent powder.The X-ray diffraction result shows d value and the relative intensity and the BaMgAl of product
10O
17Standard card unanimity, the median size of fluorescent material are 4.2 μ m, and emission wavelength is the blue light of 457nm under vacuum ultraviolet ray (147nm) irradiation.
Following examples are preparation blue colour fluorescent powder BaMgAl
14O
23: Eu
2+, can be used for the blue color component of used fluorescent material in kinds of displays part such as the plasma panel (PDP).
Embodiment 4
Take by weighing aluminum nitrate 1.4mol, barium carbonate 0.09mol, magnesium basic carbonate 0.02mol, europium sesquioxide 0.01mol, be dissolved in jointly in the solution that contains citric acid 2.5mol, adjust liquor capacity, make that the concentration of aluminum nitrate is 0.5mol/L; The pH value of adjusting solution is 5; The solution of configuration is incubated 30 hours down at 75 ℃, and solution changes glassy yellow vitreosol, gel gradually into; Above-mentioned gel is incubated 4 hours down at 140 ℃, and gel changes the concurrent propagating combustion of being conigenous of xerogel gradually into, collects the black powder that obtains; Can obtain BaMgAl in 3 hours in 7% hydrogen and 93% nitrogen (volume ratio) reducing gas, calcining under 1200 ℃
14O
23: Eu
2+Blue colour fluorescent powder.The X-ray diffraction result shows d value and the relative intensity and the BaMgAl of product
14O
23: Eu
2+Standard card unanimity, the median size of fluorescent material are 3.1 μ m, and emission wavelength is the blue light of 447nm under ultraviolet ray (147nm) irradiation.
Embodiment 5
Take by weighing aluminum nitrate 1.4mol, barium carbonate 0.09mol, magnesium basic carbonate 0.02mol, europium sesquioxide 0.01mol, be dissolved in jointly in the solution that contains citric acid 2.2mol, adjust liquor capacity, make that the concentration of aluminum nitrate is 0.6mol/L; The pH value of adjusting solution is 6.8; The solution of configuration is incubated 20 hours down at 80 ℃, and solution changes glassy yellow vitreosol, gel gradually into; Above-mentioned gel is incubated 3 hours down at 140 ℃, and gel changes the concurrent propagating combustion of being conigenous of xerogel gradually into, collects the black powder art that obtains; Can obtain BaMgAl in 1.5 hours in 6% hydrogen and 94% nitrogen (volume ratio) reducing gas, calcining under 1250 ℃
14O
23: Eu
2+Blue colour fluorescent powder.The X-ray diffraction result shows d value and the relative intensity and the BaMgAl of product
14O
23: Eu
2+Standard card unanimity, the median size of fluorescent material are 3.8 μ m, and emission wavelength is the blue light of 444nm under ultraviolet ray (147nm) irradiation.
Claims (1)
1, a kind of preparation method of aluminate base blue colour fluorescent powder is characterized in that this method comprises the following steps:
(1), the chemical composition according to prepared aluminate base blue colour fluorescent powder takes by weighing aluminum nitrate, barium carbonate, magnesium basic carbonate, europium sesquioxide; 1.5～3 times according to the aluminum nitrate mole number that takes by weighing take by weighing citric acid;
(2), the citric acid that takes by weighing is mixed with citric acid solution, with citric acid all dissolving be as the criterion;
(3), 4 kinds of raw materials that will take by weighing: aluminum nitrate, barium carbonate, magnesium basic carbonate, europium sesquioxide all are dissolved in the citric acid solution for preparing, and the concentration of controlling aluminum nitrate by the adjustment liquor capacity is 0.2～1mol/L;
(4), the pH value with above-mentioned solution is adjusted into 4.5～7;
(5), with above-mentioned solution adjusted 70～85 ℃ of down insulations 10～30 hours, make it change colloidal sol, gel gradually into;
(6), again with the gel that forms 110～150 ℃ of insulations 3～4 hours down, gel conversion is the concurrent propagating combustion of being conigenous of xerogel, generates black powder;
(7), above-mentioned powder was calcined in 1050～1250 ℃ reducing atmosphere 1～3 hour, reducing atmosphere is the hydrogen of 5～10% volume ratios and the nitrogen of 90～95% volume ratios, can obtain required fluorescent material.
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|---|---|---|---|
| CNB2006100527354A CN100500797C (en) | 2006-08-01 | 2006-08-01 | Preparation method of aluminate base blue fluorescent powder |
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| CNB2006100527354A CN100500797C (en) | 2006-08-01 | 2006-08-01 | Preparation method of aluminate base blue fluorescent powder |
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| CN100500797C CN100500797C (en) | 2009-06-17 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101376806B (en) * | 2008-10-13 | 2011-01-05 | 彩虹集团电子股份有限公司 | Preparation of blue powder for color display tube |
| CN102367384A (en) * | 2011-10-29 | 2012-03-07 | 南昌大学 | Preparation method of flaky aluminate green phosphor |
| CN103789861A (en) * | 2011-12-31 | 2014-05-14 | 四川虹欧显示器件有限公司 | Blue fluorescence fiber used for plasma display panel and preparation method thereof |
-
2006
- 2006-08-01 CN CNB2006100527354A patent/CN100500797C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101376806B (en) * | 2008-10-13 | 2011-01-05 | 彩虹集团电子股份有限公司 | Preparation of blue powder for color display tube |
| CN102367384A (en) * | 2011-10-29 | 2012-03-07 | 南昌大学 | Preparation method of flaky aluminate green phosphor |
| CN103789861A (en) * | 2011-12-31 | 2014-05-14 | 四川虹欧显示器件有限公司 | Blue fluorescence fiber used for plasma display panel and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN100500797C (en) | 2009-06-17 |
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