CN1415695A - Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation - Google Patents

Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation Download PDF

Info

Publication number
CN1415695A
CN1415695A CN 02155321 CN02155321A CN1415695A CN 1415695 A CN1415695 A CN 1415695A CN 02155321 CN02155321 CN 02155321 CN 02155321 A CN02155321 A CN 02155321A CN 1415695 A CN1415695 A CN 1415695A
Authority
CN
China
Prior art keywords
mole
calcination
vacuum ultraviolet
barium
oxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 02155321
Other languages
Chinese (zh)
Other versions
CN1189535C (en
Inventor
尤洪鹏
洪广言
吴雪艳
吴琼
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Changchun Institute of Applied Chemistry of CAS
Original Assignee
Changchun Institute of Applied Chemistry of CAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Changchun Institute of Applied Chemistry of CAS filed Critical Changchun Institute of Applied Chemistry of CAS
Priority to CNB021553211A priority Critical patent/CN1189535C/en
Publication of CN1415695A publication Critical patent/CN1415695A/en
Application granted granted Critical
Publication of CN1189535C publication Critical patent/CN1189535C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Luminescent Compositions (AREA)

Abstract

A vacuum ultraviolet ray activated blue fluorescent aluminate powder has a formula. Ba1-xEuxMgAl10O17, where x=0.02-0.2, and is prepared by choosing raw materials and coflux, generating reduction atmosphere, and controlling reaction temp and time. It can be used for plasma flat display or gas lamp.

Description

The preparation method of vacuum ultraviolet rays activated blue aluminate fluorescent powder
Technical field
The present invention relates to the preparation method of the aluminate blue fluorescent body that a kind of vacuum ultraviolet rays excites.
Background technology
In recent years, vacuum ultraviolet rays excites down luminescent device to obtain development widely, and its mechanism is by rare gas Xe, Ne-Xe, the vacuum ultraviolet rays excited fluophor visible emitting that produces thereby Ar etc. discharge.Vacuum ultraviolet rays excites down luminescent device Chromatic color large-screen high-resolution degree plasma panel display (PDP), non-mercury florescent lamp etc., PDP utilizes vacuum ultraviolet rays to excite different fluor generations red, green, thereby the light color image display of blue three kinds of different colours, it is little that PDP has a volume, thin thickness and image fidelity, and the advantage of easily making flat pannel display such as big area, and PDP makes the digitizing that shows image by the regulation and control of 8 byte digital gray scales, representing the developing direction of following information and demonstration, will be at digitized high definition television (HDTV), all many-sides such as graphoscope are widely used.And non-mercury florescent lamp utilizes the vacuum ultraviolet rays excited fluophor luminous, because its discharge gas is rare gas, mostly excites with the mercury ionizing ray with at present used luminescent lamp and to compare, and can not cause environmental pollution in the process of producing and using.Therefore, it is with possible green illumination light source as future.For this reason, people are developing and are utilizing Xe, Ne-Xe, the non-mercury florescent lamp that the vacuum ultraviolet rays that noble gas discharges such as Ar produce excites.
Since the seventies, people have been developed some high-efficiency vacuum ultraviolet rays excited fluorescent bodies.As be used for the three-color phosphor of PDP: red-emitting phosphors (Y, Gd) BO 3: Eu, green-emitting phosphor Zn 2SiO 4: Mn and BaAl 12O 19: Mn, blue emitting phophor BaMgAl 10O 17: Eu and BaMgAl 14O 23: Eu etc.These vacuum ultraviolet luminescent materials the preparation method be the important directions that people study always.
Divalent europium activates barium magnesium aluminate, its structure is the beta-alumina structure, divalent europium replaces barium ion in aluminate, under the vacuum-ultraviolet light irradiation, the matrix absorption vacuum ultraviolet rays is also given divalent europium transmission ofenergy, the electronics of europium ion is on the higher excited level, and electronics relaxes towards on the minimum excited level by radiationless then, and last electronics transits to ground state from minimum excited level and launches blue light.Need reducing atmosphere owing to obtain divalent europium, the formation of barium magnesium aluminate needs reaction at high temperature, and therefore, its preparation will be carried out in high temperature reduction atmosphere.The reducing atmosphere that generally adopts is the mixed gas of nitrogen and hydrogen at present.High efficient luminous material Ba is disclosed as U.S. Pat 6096243 1-xEu xMgAl 10O 17Preparation method, the atmosphere that it adopts are the mixed gass of nitrogen and hydrogen.Adopt the mixed gas calcination conditional request strictness of nitrogen and hydrogen, calcination time is long, and whole preparation cycle is long, and preparation cost is higher, and in preparation process owing to the existence of hydrogen, set off an explosion easily.Middle Chinese patent CN1190115A discloses BaMgAl 14O 23: the preparation method of Eu, this patent directly cover carbon dust on the starting material, and this preparation method's causes the Prevent Carbon Contamination of the part of fluorescent material, thereby cause the waste of starting material in preparation process because carbon dust is directly to contact with starting material.Therefore, this preparation method can not satisfy demand of practical production well.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of vacuum ultraviolet rays activated blue aluminate fluorescent powder.Adopt two crucible graphite or carbon reduction method preparation, wanting the reductive sample to be placed in the interior crucible, and put non-tight lid at interior crucible, graphite or carbon are put between outer crucible and the crucible, outer crucible covers sealing cover, puts into High Temperature Furnaces Heating Apparatus then, and calcination at high temperature produces reducing atmosphere, with the sample reduction, thereby make needed high efficient luminous material.
The chemical formula that the present invention relates to the barium magnesium aluminate blue emitting phophor is:
Ba 1-xEu xMgAl 10O 17
0.04≤x≤0.2 wherein
The starting material that adopted are: europium sesquioxide; Barium oxide maybe can transform one or both compounds in the barium carbonate of corresponding oxide or the barium oxalate; Magnesium oxide maybe can transform in magnesium hydroxide, magnesiumcarbonate or the magnesium oxalate of corresponding oxide one or more; Aluminum oxide maybe can transform in the aluminium hydroxide of corresponding oxide one or both;
Fusing assistant is 0~6% mole of boric acid, Neutral ammonium fluoride, aluminum fluoride, magnesium fluoride or barium fluoride, and wherein one or more or do not add fusing assistant;
To put into graphite or carbon calcination between outer crucible and the interior crucible, calcination temperature is 1400~1700 ℃; Calcination time is 1~8 hour; The calcination number of times is for once or secondary; Cooling is taken out, and gets powdery phosphor through crushing screening, and 147nm excites down, and luminosity is greater than 100.
Adopt the present invention to prepare high-efficiency vacuum ultraviolet rays activated barium magnesium aluminate blue emitting phophor following characteristics arranged:
1, when the above-mentioned luminescent material of preparation, crucible is a high temperature sintering in air, and preparation technology is simple, and is safe and reliable, and working condition is controlled easily, and is with short production cycle, and cost is low.
2, owing to adopt two crucible reduction, sample and graphite or carbon are separated, can either prevent the pollution of graphite or carbon effectively, can effectively go back raw sample again simultaneously, therefore can obtain high efficient luminous material.
3, can heat continuously, a large amount of save energy reduce production costs.
Embodiment
Embodiment 1
Take by weighing BaCO 30.09 mole, Al 2O 30.5 mole, 0.1 mole of MgO, Eu 2O 30.005 mole, H 3BO 30.005 mole utilizes ball mill to carry out abundant ground and mixed, puts into a less alumina crucible, cover the non-tight lid, then it is put into a bigger alumina crucible, its China ink or carbon are put between outer crucible and the crucible, outer crucible covers sealing cover, puts into High Temperature Furnaces Heating Apparatus, 1450 ℃, calcination 5 hours, cooling is taken out, and removes carbon, after the Ball milling, the after scouring that sieves, oven dry then, sieve and promptly obtain efficient blue emitting phophor, it is 104 that 147nm excites down luminosity.
Embodiment 2
Take by weighing BaCO 30.09 mole, Al 2O 30.5 mole, 0.1 mole of MgO, Eu 2O 30.005 mole, NH 40.015 mole of F, other condition is with embodiment 1, and the fluor that is obtained brightness under 147nm excites is 103.
Embodiment 3
Take by weighing BaC 2O 42H 20.08 mole of O, Al (OH) 31 mole, Mg (OH) 20.1 mole, Eu 2O 30.01 mole, H 3BO 30.002 mole, AlF 30.004 mole, other condition are with embodiment 1, the fluor that is obtained brightness under 147nm excites is 102.
Embodiment 4
Take by weighing BaCO 30.095 mole, BaC 2O 42H 20.01 mole of O, Al 2O 30.5 mole, 0.1 mole of MgO, Eu 2O 30.002 mole, H 3BO 30.003 mole, BaF 20.002 mole, other condition are with embodiment 1, the fluor that is obtained brightness under 147nm excites is 101.
Embodiment 5
Take by weighing 0.09 mole of BaO, Al 2O 30.5 mole, 0.09 mole of MgO, Mg (OH) 20.01 mole, Eu 2O 30.005 mole, H 3BO 30.005 mole, calcination temperature is 1400 ℃, and calcination is 8 hours, and other condition is with embodiment 1, and the fluor that is obtained brightness under 147nm excites is 103.
Embodiment 6
Take by weighing BaCO 30.09 mole, Al 2O 30.5 mole, 0.05 mole of MgO, (MgCO 3) 4Mg (OH) 25H 20.01 mole of O, Eu 2O 30.005 mole, MgF 20.006 mole, other condition are with embodiment 1, the fluor that is obtained brightness under 147nm excites is 105.
Embodiment 7
Take by weighing BaCO 30.09 mole, Al 2O 30.5 mole, (MgCO 3) 4Mg (OH) 25H 2The O0.02 mole, Eu 2O 30.005 mole, in 1400 ℃ of calcinations 3 hours, other condition was with embodiment 1, took out to grind, and then calcination 3 hours under 1600 ℃ of reducing atmospheres, and the fluor that is obtained excites down at 147nm that brightness is 108.
Embodiment 8
Take by weighing BaCO 30.09 mole, Al (OH) 31 mole, Mg (OH) 20.1 mole, Eu 2O 30.005 mole, utilize ball mill to carry out abundant ground and mixed, the mixture that is obtained is put into a less alumina crucible adds a cover, it is being put into bigger crucible then, add a cover after putting into carbon or graphite, put into High Temperature Furnaces Heating Apparatus, in 1700 ℃ of calcinations 2 hours, other condition is with embodiment 1, and the luminosity of gained fluor is 106.

Claims (1)

1. the preparation method of a vacuum ultraviolet rays activated blue aluminate fluorescent powder, the chemical formula of described fluor is:
Ba 1-xEu xMgAl 10O 17
0.04≤x≤0.2 wherein,
The starting material that adopt are: europium sesquioxide; Barium oxide maybe can transform one or both compounds in the barium carbonate of corresponding oxide or the barium oxalate; Magnesium oxide maybe can transform in magnesium hydroxide, magnesiumcarbonate or the magnesium oxalate of corresponding oxide one or more; Aluminum oxide is or/and can be converted into the aluminium hydroxide of corresponding oxide;
Fusing assistant be 0~6% mole of boric acid, Neutral ammonium fluoride, aluminum fluoride, magnesium fluoride or barium fluoride wherein one or more, or do not add fusing assistant;
To put into graphite or carbon calcination between outer crucible and the interior crucible, calcination temperature is 1400~1700 ℃; Calcination time is 1~8 hour; Calcination 1-2 time; Cooling is taken out, and gets powdery phosphor through crushing screening, and 147nm excites down, and luminosity is greater than 100.
CNB021553211A 2002-12-10 2002-12-10 Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation Expired - Fee Related CN1189535C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB021553211A CN1189535C (en) 2002-12-10 2002-12-10 Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB021553211A CN1189535C (en) 2002-12-10 2002-12-10 Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation

Publications (2)

Publication Number Publication Date
CN1415695A true CN1415695A (en) 2003-05-07
CN1189535C CN1189535C (en) 2005-02-16

Family

ID=4752598

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB021553211A Expired - Fee Related CN1189535C (en) 2002-12-10 2002-12-10 Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation

Country Status (1)

Country Link
CN (1) CN1189535C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009012651A1 (en) * 2007-07-23 2009-01-29 Rhodia China Co., Ltd. Process for the preparation of an yttrium and rare earth mixed oxide
CN102212368A (en) * 2010-04-02 2011-10-12 财团法人工业技术研究院 Blue-light fluorescent material, white-light emitting device using same and solar battery
CN102277171A (en) * 2011-09-09 2011-12-14 太原理工大学 Method for preparing up-conversion white light fluorescent powder
CN106367067A (en) * 2016-08-30 2017-02-01 内蒙古科技大学 Aluminate blue fluorescent powder and preparation method thereof
CN113831916A (en) * 2021-10-11 2021-12-24 中国人民解放军陆军工程大学 Preparation method of rare earth doped long-afterglow luminescent material
CN114874769A (en) * 2022-03-17 2022-08-09 宝鸡文理学院 Preparation method of thermoluminescent color-changing fluorescent powder

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009012651A1 (en) * 2007-07-23 2009-01-29 Rhodia China Co., Ltd. Process for the preparation of an yttrium and rare earth mixed oxide
CN102212368A (en) * 2010-04-02 2011-10-12 财团法人工业技术研究院 Blue-light fluorescent material, white-light emitting device using same and solar battery
CN102212368B (en) * 2010-04-02 2014-05-07 财团法人工业技术研究院 Blue-light fluorescent material, white-light emitting device using same and solar battery
CN102277171A (en) * 2011-09-09 2011-12-14 太原理工大学 Method for preparing up-conversion white light fluorescent powder
CN106367067A (en) * 2016-08-30 2017-02-01 内蒙古科技大学 Aluminate blue fluorescent powder and preparation method thereof
CN113831916A (en) * 2021-10-11 2021-12-24 中国人民解放军陆军工程大学 Preparation method of rare earth doped long-afterglow luminescent material
CN114874769A (en) * 2022-03-17 2022-08-09 宝鸡文理学院 Preparation method of thermoluminescent color-changing fluorescent powder
CN114874769B (en) * 2022-03-17 2024-02-27 宝鸡文理学院 Preparation method of thermoluminescent color-changing fluorescent powder

Also Published As

Publication number Publication date
CN1189535C (en) 2005-02-16

Similar Documents

Publication Publication Date Title
KR100858269B1 (en) Method of producing aluminate fluorescent substance, a fluorescent substance and a device containing a fluorescent substance
CN102115667B (en) Borate green luminescent material and preparation method thereof
WO2006072919A2 (en) Illumination system comprising barium magnesium aluminate phosphor
WO2005001875A1 (en) Plasma display
CN1189535C (en) Method for preparing blue luminescent powder of aluminate activated by vacuum ultraviolet radiation
JP2007526390A (en) Luminescent material that emits green light and plasma display panel using the same
US7410599B2 (en) Stable green phosphor and plasma display panel using the same
CN1366017A (en) Vacuum ultraviolet ray excited green barium magnesium aluminate as fluorescent substance and its preparing process
KR20010062527A (en) Phosphor for vacuum ultraviolet excited light emitting device
KR100742552B1 (en) Vacuum ultraviolet ray-excited light-emitting phosphor
US7486010B2 (en) Plasma display device and method of preparing phosphor
CN101029229A (en) Vacuum-ultraviolet-excited aluminate green luminophore andits production
CN100383217C (en) Phosphor for vacuum ultravilet ray-excited light-emitting element
JP2002180041A (en) Fluorescent particle
CN102191051A (en) Borate luminescent material and preparation method thereof
CN1644648A (en) Fluorescent powder of aluminium borate and its preparation
JP3956434B2 (en) Aluminate phosphor
JPS5943507B2 (en) Method for manufacturing blue-emitting phosphor
CN1219848C (en) Vacuum ultraviolet excited green aluminate fluorescent powder and its preparing process
CN1818015A (en) Rare-earth luminescent materials for plasma planar plate display and non-mercury fluorescent light and production thereof
CN1405268A (en) Method for preparing green fluorophor of aluminate excited by vacuum ultravoilet rays
JP2003292950A (en) Fluorescent substance and method of producing the same
JP2005146071A (en) Vacuum ultraviolet-excited green luminescent material and light emitting device
JP2001123164A (en) Phosphor for vacuum ultraviolet-excitable luminous element
JP2001123163A (en) Phosphor for vacuum ultraviolet-excitable luminous element

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee