CN1664050A - Method for post-treatment of fluorescent materials - Google Patents
Method for post-treatment of fluorescent materials Download PDFInfo
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- CN1664050A CN1664050A CN 200510038372 CN200510038372A CN1664050A CN 1664050 A CN1664050 A CN 1664050A CN 200510038372 CN200510038372 CN 200510038372 CN 200510038372 A CN200510038372 A CN 200510038372A CN 1664050 A CN1664050 A CN 1664050A
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- fluorescent material
- phosphor powder
- deionized water
- ball milling
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Abstract
A method of final treatment for phosphor powder, relating to the final treatment for low-hydrolytic phosphor powder, comprising: (1) getting the stock according to the element in the composite of the phosphor powder, mixing and incandescing or deacidizing at 1200-1700DEG C, washing the incandesce product with deionized water heated at above 60DEG C until boiling at least one time, 10 minutes to 2 hours for every time and stirring at the same time and treating with supersonic wave, stewing, removing the floater on the surface of the suspension; (2) ball grinding and diffusing for 0.5~ 5 hours the washed phosphor powder; (3) washing the phosphor powder until being neutral, dewatering, drying, riddling and getting the needed phosphor powder. The method increases the process of washing with heat deionized water and treatment with supersonic wave, which can remove the residue on the surface of the phosphor powder and improve the dispersibility of phosphor powder.
Description
Technical field
The present invention relates to a kind of post-treating method of fluorescent material.Especially to a kind of not post-treating method of the fluorescent material of facile hydrolysis that is applicable to.
Background technology
In illumination and demonstration field, fluorescent material plays crucial effects.The preparation of fluorescent material generally need be passed through high temperature sintering, and that the result who brings is exactly a powder granule after the calcination is thick, have sintering or hard aggregation phenomenon, and often remaining unreacted raw material and fusing assistant etc. completely, influences the performance of fluorescent material.For reducing the fluorescent material particle diameter, improving luminescent properties, need carry out processing such as Ball milling, washing to firing product.
As the method for preparing aluminate green fluorescent powder in the U.S. Pat 5989455 is with raw material and an amount of fusing assistant solid phase mixing such as aluminum oxide, barium carbonate, manganous carbonate, Strontium carbonate powder, magnesium oxide, calcination under 1200～1600 ℃ the temperature in nitrogen/hydrogen weak reducing atmosphere is then then carried out firing product Ball milling, washing, drying, is sieved.The method for preparing aluminate green fluorescent powder among the Chinese patent CN1381547A is to dry grind after various raw materials and fusing assistant are mixed or water mill 4～15 hours, dry back is calcination 2～10 hours under 1300～1450 ℃ the temperature under weak reducing atmosphere, carries out Ball milling, hot wash, filtration, oven dry then.Wherein the post-treating method about the high temperature sintering product is Ball milling, washing, drying and other steps, and finds that in experiment the deionized water of normal temperature or lesser temps is difficult to remove fully the resistates of high temperature sintering.
Summary of the invention
Technical problem: the present invention proposes a kind of post-treating method of fluorescent material, has increased the hot deionized water washing and add ultrasonic processing technique before Ball milling is handled, and removes the residual substance of phosphor surface, improves the dispersiveness of fluorescent material.
Technical scheme: a kind of not post-treating method of the fluorescent material of facile hydrolysis that is applicable to that the present invention proposes comprises following step:
1, press the composition of the fluorescent material of required processing, take by weighing various raw materials by each amount of element that its molecular formula embodied, mix the back in 1200～1700 ℃ of high temperature sinterings or reduction, with firing product more than 60 ℃ in the ebullient deionized water washing at least once each 10 minutes to 2 hours, stir simultaneously and add ultrasonication, leave standstill after stopping to stir, remove the material of suspension liquid surface flotation.
2, the fluorescent material after the hot wash was carried out weak Ball milling 0.5～5 hour.
3, with the fluorescent material after the Ball milling with deionized water wash to neutral, get final product after dewatering, dry, sieving required fluorescent material.
Beneficial effect: advantage of the present invention is:
(1) preparation technology is simple, is easy to realize;
The fusing assistant of the surface remnants that are difficult to remove when the hot deionized water washing can be removed normal temperature or ordinary hot deionized water wash in conjunction with the supersound process process more than (2) 60 ℃, unreacted raw material etc., make the fluorescent material performance higher, and make fluorescent material easier dispersion when ball milling;
(3) present technique is applicable to all not aftertreatments of the fluorescent material of facile hydrolysis, and is as aluminate substrate lamp powder and PDP fluorescent material, rare earth oxide class fluorescent material etc., widely applicable.
Embodiment
Embodiment 1
This example is to fluorescent material lamp or plasma display blue colour fluorescent powder Ba
0.9Eu
0.1MgAl
10O
17Fluorescent material intermediate product in the preparation process is handled.This intermediate product is meant by Ba
0.9Eu
0.1MgAl
10O
17Proportioning take by weighing various raw materials, mix the product of back at 1200～1700 ℃ of high temperature sinterings and reduction back gained.
Firing product is added in the ebullient deionized water, add stirring and supersound process 30 minutes, after staticly settling, strike off the material of suspension liquid surface flotation.In suspension liquid, add high purity aluminium oxide ball or glass sphere, Ball milling 2 hours.Slurry behind the ball milling is extremely neutral with deionized water wash, dehydration, oven dry is crossed 400 mesh sieves and is promptly obtained efficient blue colour fluorescent powder, medium particle diameter 2～4 μ m.
Embodiment 2
This example is plasma display green emitting phosphor Ba
0.5Sr
0.5MgMn
0.2Al
11O
19Fluorescent material intermediate product in the preparation process is handled.This intermediate product is meant by Ba
0.5Sr
0.5MgMn
0.2Al
11O
19Proportioning take by weighing various raw materials, mix the product of back at 1200～1700 ℃ of high temperature sinterings and reduction back gained.
Firing product added to add in the ebullient deionized water stirred supersound process 30 minutes, after staticly settling, strike off the material of suspension liquid surface flotation.In suspension liquid, add high purity aluminium oxide ball or glass sphere, Ball milling 2 hours.Slurry behind the ball milling is extremely neutral with deionized water wash, dehydration, oven dry is crossed 400 mesh sieves and is promptly obtained efficient green fluorescent material, medium particle diameter 2～4 μ m.
Embodiment 3
This example is to three-color fluorescent lamp fluorescent material Y
2O
3: the fluorescent material intermediate product in the Eu preparation process is handled.This intermediate product is meant by Y
2O
3: the proportioning of Eu takes by weighing various raw materials, mixes the product of back gained behind 1200～1500 ℃ of high temperature sinterings.
Stir supersound process 30 minutes with adding in the high temperature sintering product adding ebullient deionized water, after staticly settling, strike off the material of suspension liquid surface flotation.In suspension liquid, add high purity aluminium oxide ball or glass sphere, Ball milling 1 hour.Slurry behind the ball milling is extremely neutral with deionized water wash, dehydration, oven dry is sieved and is promptly obtained high efficiency red fluorescent material, medium particle diameter 5～7 μ m.
Embodiment 4
This example is to three-color fluorescent lamp green emitting phosphor Ce
0.67Tb
0.33MgAl
11O
19Fluorescent material intermediate product in the preparation process is handled.This intermediate product is meant by Ce
0.67Tb
0.33MgAl
11O
19Proportioning take by weighing various raw materials, mix the product of back at 1200～1700 ℃ of high temperature sinterings and reduction back gained.
Firing product added to add in the ebullient deionized water stirred supersound process 30 minutes, after staticly settling, strike off the material of suspension liquid surface flotation.In suspension liquid, add high purity aluminium oxide ball or glass sphere, Ball milling 1 hour.Slurry behind the ball milling is extremely neutral with deionized water wash, dehydration, oven dry, sieving promptly obtains green-fluorescent powder for lamp, medium particle diameter 5～7 μ m.
Embodiment 5
This example is to PDP red fluorescence powder (Y, Gd) BO
3: the fluorescent material intermediate product in the Eu preparation process is handled.This intermediate product is meant by (Y, Gd) BO
3: the proportioning of Eu takes by weighing various raw materials, mixes the product of back gained behind 800～1200 ℃ of high temperature sinterings.
Firing product added to add in the ebullient deionized water stirred supersound process 30 minutes, after staticly settling, strike off the material of suspension liquid surface flotation.In suspension liquid, add high purity aluminium oxide ball or glass sphere, Ball milling 1 hour.Slurry behind the ball milling is extremely neutral with deionized water wash, dehydration, oven dry is sieved and is promptly obtained the PDP red fluorescence powder, medium particle diameter 2～4 μ m.
Embodiment 6
This example is to fluorescent material lamp or plasma display blue colour fluorescent powder Ba
0.9Eu
0.1MgAl
10O
17Fluorescent material intermediate product in the preparation process is handled.This intermediate product is meant by Ba
0.9Eu
0.1MgAl
10O
17Proportioning take by weighing various raw materials, mix the product of back at 1200～1700 ℃ of high temperature sinterings and reduction back gained.
In the deionized water with 60 ℃ of firing product addings, add and stirred supersound process 1 hour, all the other conditions obtain efficient blue colour fluorescent powder with example 1, medium particle diameter～4 μ m.
Embodiment 7
This example is to fluorescent material lamp or plasma display blue colour fluorescent powder Ba
0.9Eu
0.1MgAl
10O
17Fluorescent material intermediate product in the preparation process is handled.This intermediate product is meant by Ba
0.9Eu
0.1MgAl
10O
17Proportioning take by weighing various raw materials, mix the product of back at 1200～1700 ℃ of high temperature sinterings and reduction back gained.
In the deionized water with 90 ℃ of firing product addings, add and stirred supersound process 45 minutes, all the other conditions obtain efficient blue colour fluorescent powder with example 1, medium particle diameter 2～4 μ m.
Claims (1)
1, a kind of post-treating method of fluorescent material is characterized in that this method is:
1), press the composition of the fluorescent material of required processing, take by weighing various raw materials by each amount of element that its molecular formula embodied, mix the back in 1200～1700 ℃ of high temperature sinterings or reduction, with firing product more than 60 ℃ in the ebullient deionized water washing at least once each 10 minutes to 2 hours, stir simultaneously and add ultrasonication, leave standstill after stopping to stir, remove the material of suspension liquid surface flotation;
2), the fluorescent material after the hot wash was carried out weak Ball milling 0.5～5 hour;
3), with the fluorescent material after the Ball milling with deionized water wash to neutral, get final product after dewatering, dry, sieving required fluorescent material.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200510038372 CN1277898C (en) | 2005-02-21 | 2005-02-21 | Method for post-treatment of fluorescent materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200510038372 CN1277898C (en) | 2005-02-21 | 2005-02-21 | Method for post-treatment of fluorescent materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1664050A true CN1664050A (en) | 2005-09-07 |
| CN1277898C CN1277898C (en) | 2006-10-04 |
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ID=35035367
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200510038372 Expired - Fee Related CN1277898C (en) | 2005-02-21 | 2005-02-21 | Method for post-treatment of fluorescent materials |
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| Country | Link |
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| CN (1) | CN1277898C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101298559B (en) * | 2008-04-29 | 2010-12-01 | 彩虹集团电子股份有限公司 | Preparation of rare earth tricolor mixing phosphor for CCFL |
| CN101565618B (en) * | 2009-06-01 | 2012-10-10 | 彩虹集团电子股份有限公司 | Method for preparing red phosphor for CCFL |
-
2005
- 2005-02-21 CN CN 200510038372 patent/CN1277898C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101298559B (en) * | 2008-04-29 | 2010-12-01 | 彩虹集团电子股份有限公司 | Preparation of rare earth tricolor mixing phosphor for CCFL |
| CN101565618B (en) * | 2009-06-01 | 2012-10-10 | 彩虹集团电子股份有限公司 | Method for preparing red phosphor for CCFL |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1277898C (en) | 2006-10-04 |
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| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20050907 Assignee: Jiangsu Borui Photoelectric Co., Ltd. Assignor: Southeast University Contract record no.: 2010990000155 Denomination of invention: Method for post-treatment of fluorescent materials Granted publication date: 20061004 License type: Exclusive License Record date: 20100330 |
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Granted publication date: 20061004 Termination date: 20200221 |
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| CF01 | Termination of patent right due to non-payment of annual fee |