CN1277982A - Rare-earth activated aluminosilicate long persistence luminescent, and prepn. method therefor - Google Patents
Rare-earth activated aluminosilicate long persistence luminescent, and prepn. method therefor Download PDFInfo
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- CN1277982A CN1277982A CN 00111210 CN00111210A CN1277982A CN 1277982 A CN1277982 A CN 1277982A CN 00111210 CN00111210 CN 00111210 CN 00111210 A CN00111210 A CN 00111210A CN 1277982 A CN1277982 A CN 1277982A
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Abstract
The present invention relates to a rare earth-activated alkali earth metal aluminium silicate long-afterglow luminous material and its preparation method. Its general expression formula is MO.aAl2O3.bSiO2.cL:fx, in which MO is one or several of SrO, CaO, MgO and BaO; L is mineralizing agent, x is rare erath activator, a,b,c and f are mole numbers. The raw materials are proportionally weighed, mixed and calcined in reducing atmosphere at 1200-1450 deg.C for 2-4 hrs; then ground, washed, baked to obtain the said luminous material powder. Characteristics include: simple preparation method high brightness of luminous material, and superlong afterglow.
Description
The invention belongs to material science, particularly a kind of rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material and preparation method thereof.
The rare earth-activated luminous alkali earth metal aluminate luminescent material that grew up in recent years, owing to have the original intensity height, advantage such as time of persistence is long, "dead" harm and extremely people's favor.About this class luminescent material more existing report and patent introductions.Chinese invention patent application publication number CN 1126746A has proposed Eu, Ce, Tb, Dy activated alkali earth metal aluminate long-afterglow photoluminescent; Chinese invention patent application publication number CN 1115779A has then proposed rare earth ion, and (Tb is Dy) with non-rare earth ion (Sb, Sn) coactivated polyion activated luminescent material for Eu, Ce; Chinese invention patent application publication number CN 1152018A discloses a kind of long Persistence and high brightness fluorescent materials and preparation method thereof, and the general expression of luminescent material is: M.N.AL
2-XB
XO
4, wherein M represents alkaline-earth metal, is generally strontium, N represents rare earth element, is generally europium, 0.1≤X≤1.Chinese invention patent application publication number CN 1132777A and United States Patent (USP) (US Patent 5686022) all disclose rare-earth activated luminous alkali earth metal aluminate luminescent material and preparation technology thereof.Chinese invention patent application publication number CN 1194292 discloses a kind of long persistence luminescent silicate material and manufacture method thereof.The main chemical constitution formula of its luminescent material is: aMO.bM ' O.cSiO
2.dR:Eux, Lny, wherein M is selected from one or more elements in strontium (Sr), calcium (Ca), barium (Ba), the zinc (Zn); M ' is selected from one or more elements in magnesium (Mg), cadmium (Cd), the beryllium (Be); Ln is selected from rare earth or transition element, and luminescent material sends the emmission spectrum that peak value is 450-580nm, presents the long-persistence luminous of colors such as orchid, blue green, green, greenish-yellow, Huang.But, above-mentioned rare-earth activated luminous alkali earth metal aluminate luminescent material, the particularly higher luminescent material of alkaline earth metal oxide content, its sintering block hardness is very big, and broken difficulty is strong basicity mostly in water medium, be difficult to direct use in many occasions.Be easy to generate ill effects such as blackening, change ash when for example, in plastics, directly using; Often produce hydrolysis when in water-borne coatings, using, can not form stable coating system, be easy to precipitation; When in low-temp ceramics enamel firing paper and glass enamel firing paper, using, also, be difficult to obtain slick polychromy owing to alumina content in the composition is higher.On the other hand, often are lower than the luminous intensity of rare-earth activated silicate luminescent material and time of persistence rare-earth activated aluminate based luminescent material.
The objective of the invention is to overcome the shortcoming of prior art, provide a kind of easy to use and have rare-earth activated alkaline earth metal aluminosilicate luminescent material of good luminous intensity and preparation method thereof.
The objective of the invention is to be achieved through the following technical solutions:
Rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material of the present invention, general expression is MOaAl
2O
3BSiO
2CL:fX, wherein MO is one or more of SrO, CaO, MgO and BaO; L is a mineralizer, and X is rare-earth activated dose, a, b, c and f representative Al when the mole number of MO is 1
2O
3, SiO
2, mineralizer L and activator X mole number, 0.5≤(a+b)≤5, b=(0.1-10) a, c=0.02～0.5, f=0.003～0.05.
Above-mentioned luminescent material middle-weight rare earths activator comprises mol ratio 1: the oxide compound of the europium sesquioxide of (0.5～5) and dysprosium, cerium, neodymium, praseodymium, samarium, terbium, holmium, erbium, thulium, ytterbium at least a or multiple.
Above-mentioned luminescent material middle-weight rare earths activator is a mol ratio 1: the europium sesquioxide of (1～2) and dysprosium oxide.
Used mineralizer is an alkali metal halide or/and ammonium halide salt in the above-mentioned luminescent material, particularly including ammonium chloride or brometo de amonio.
The preparation method of rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material of the present invention comprises the steps:
1) raw material: alkaline earth metal carbonate or oxide compound, aluminum oxide or aluminium hydroxide, SiO 2 powder and mineralizer L, activator X, press MOaAl
2O
3BSiO
2Among the cL:fX 0.5≤(a+b)≤5, b=(0.1-10) a, c=0.02～0.5, after the mole proportioning weighing of f=0.003～0.05, thorough mixing is in the crucible of packing into then, under reducing atmosphere, under 1200～1450 ℃ temperature, burnt till in 2-4 hour in the top temperature insulation;
2) above-mentioned sintered compact is pulverized, with deionized water, dilute hydrochloric acid solution or washing with alcohol, oven dry is prepared into rare-earth activated alkaline earth metal aluminosilicate luminescent material powder.
Above-mentioned steps 1) reducing atmosphere in is hydrogen, ammonia, nitrogen and hydrogen, carbon granules.
The present invention has successfully prepared a kind of novel overlength afterglow luminescent material by selecting suitable aluminosilicate body material, rare-earth activated dose, mineralizer and preparation method.Luminescent material luminosity of the present invention (15 seconds after exciting) reaches 1800mcd/m
2, surpass 12 hours time of persistence, and its luminescent spectrum main peak can change in the 440nm-510nm scope according to composition; In water medium, be neutral; Sintered body structure is loose, is easy to fragmentation.Rare-earth activated alkaline earth metal aluminosilicate luminescent material of the present invention can be used to produce various injection mouldings easily, extrudes, luminescent plastics, luminous rubber such as film, products such as luminescent ceramic, frit for porcelain enamel and marble paper, luminous paint.
The GB/T14633-93 standard-required is pressed in the luminosity of luminescent material of the present invention and the test of time of persistence.
The invention will be further described below in conjunction with embodiment, but not in limitting this.
Embodiment 1. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material, expression MOaAl
2O
3BSiO
2CL:fX, wherein MO is SrO, CaO; L is an ammonium chloride, and X is 1: 2 europium sesquioxide Eu of mol ratio
2O
3With dysprosium oxide Dy
2O
3, a=1.2, b=2.0, c=0.2, f=0.018.
The preparation method is as follows:
Take by weighing SrCO
329.69 gram, CaCO
35.05 gram, Al
2O
3Micro mist 30.75 grams, SiO
2Fine powder 30.18 grams, Eu
2O
3.0.52 restrain Dy
2O
31.12 gram; Take by weighing ammonium chloride .2.69 gram, thorough mixing; Compound is packed in the crucible, under reducing atmosphere (hydrogen and nitrogen),, be incubated 2 hours in 1280 ℃ of calcinings; Sintered compact is pulverized, used washing with alcohol, oven dry makes the luminescent material powder; The rare-earth activated alkaline earth metal aluminosilicate luminescent material that present embodiment is prepared is blue purple, luminosity (15 seconds after exciting) 1100mcd/m
2, being longer than time of persistence 10 hours, luminescent spectrum λ max is 440nm, is neutral in the aqueous solution.
Embodiment 2. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material, expression MOaAl
2O
3BSiO
2CL:fX, wherein MO is SrO, CaO; L is a brometo de amonio, and X is 1: 1 europium sesquioxide Eu of mol ratio
2O
3With dysprosium oxide Dy
2O
3, a=1.9, b=2.0, c=0.35, f=0.018.
The preparation method is as follows:
Take by weighing SrCO
318.52 gram, CaCO
38.36 gram, Al
2O
3Micro mist 40.50 grams, SiO
2Fine powder 25.11 grams, Eu
2O
30.44 gram, Dy
2O
30.93 gram, brometo de amonio 6.14 grams, thorough mixing; Compound is packed in the crucible, under reducing atmosphere (ammonia),, be incubated 2 hours in 1250 ℃ of calcinings; Sintered compact is pulverized, used washing with alcohol, oven dry makes the luminescent material powder; The rare-earth activated alkaline earth metal aluminosilicate luminescent material that present embodiment is prepared is sky blue, luminosity (15 seconds after exciting) 1800mcd/m
2, being longer than time of persistence 10 hours, luminescent spectrum λ max is 460nm, is neutral in the aqueous solution.
Embodiment 3. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material, expression MOaAl
2O
3BSiO
2CL:fX, wherein MO is SrO, BaO; L is a brometo de amonio, and X is 1: 2 europium sesquioxide Eu of mol ratio
2O
3With dysprosium oxide Dy
2O
3, a=1.8, b=2.0, c=0.3, f=0.018.
The preparation method is as follows:
Take by weighing SrCO
314.42 gram, BaCO
319.27 gram, Al
2O
3Micro mist 35.83 grams, SiO
2Fine powder 23.45 grams, Eu
2O
30.41 gram, Dy
2O
30.87 gram; Take by weighing NH
4Br 5.75 grams, thorough mixing;
Compound is packed in the crucible, under reducing atmosphere (hydrogen),, be incubated 2 hours in 1300 ℃ of calcinings; Sintered compact is pulverized, used washing with alcohol, oven dry makes the luminescent material powder; The rare-earth activated alkaline earth metal aluminosilicate luminescent material that present embodiment is prepared is blue green, luminosity (15 seconds after exciting) 1600mcd/m
2, being longer than time of persistence 10 hours, luminescent spectrum λ max is 480nm, is neutral in the aqueous solution.
Embodiment 4. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material, expression MOaAl
2O
3BSiO
2CL:fX, wherein MO is that SrO, MgO: L is an ammonium chloride, X is 1: 2 europium sesquioxide Eu of mol ratio
2O
3With dysprosium oxide Dy
2O
3, a=1.6, b=2.0, c=0.3, f=0.018.
The preparation method is as follows:
Take by weighing SrCO
318.48 gram, MgO 5.05 grams, Al
2O
3Micro mist 40.74 grams, SiO
2Fine powder 30.06 grams, Eu
2O
30.53 gram, Dy
2O
31.12 gram; Take by weighing ammonium chloride 4.02 grams, thorough mixing; Compound is packed in the crucible, under reducing atmosphere,, be incubated 2 hours in 1330 ℃ of calcinings; Sintered compact is pulverized, used washing with alcohol, oven dry makes the luminescent material powder; The rare-earth activated alkaline earth metal aluminosilicate luminescent material that present embodiment is prepared is blue-greenish colour, luminosity (15 seconds after exciting) 1400mcd/m
2, being longer than time of persistence 10 hours, luminescent spectrum λ max is 490nm, is neutral in the aqueous solution.
Embodiment 5. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material, expression MOaAl
2O
3BSiO
2CL:fX, wherein MO is SrO, MgO; L is an ammonium chloride, and X is 1: 2 europium sesquioxide Eu of mol ratio
2O
3With Neodymium trioxide Nd
2O
3, a=0.4, b=0.6, c=0.08, f=0.006.
The preparation method is as follows:
Take by weighing CaCO
330 grams, MgO 19.10 grams, Al (OH)
323.92 gram, SiO
228.18 gram, Eu
2O
30.50 gram, Nd
2O
31.05, take by weighing ammonium chloride 3.76 grams, thorough mixing; Compound is packed in the crucible, under reducing atmosphere,, be incubated 2 hours in 1350 ℃ of calcinings; Sintered compact is pulverized, used washing with alcohol, oven dry makes the luminescent material powder; The rare-earth activated alkaline earth metal aluminosilicate luminescent material that present embodiment is prepared is green, luminosity (15 seconds after exciting) 1200mcd/m
2, being longer than time of persistence 10 hours, luminescent spectrum λ max is 510nm, is neutral in the aqueous solution.
Claims (5)
1. a rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material is characterized in that, general expression is MOaAl
2O
3BSiO
2CL: fX, wherein MO is one or more of SrO, CaO, MgO and BaO; L is a mineralizer, and X is rare-earth activated dose, a, b, c and f representative Al when the mole number of MO is 1
2O
3, SiO
2, mineralizer L and activator X mole number, 0.5≤(a+b)≤5, b=(0.1-10) a, c=0.02～0.5, f=0.003～0.05.
2. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material as claimed in claim 1, it is characterized in that described rare-earth activated dose of X is mol ratio 1: the oxide compound of the europium sesquioxide of (0.5～5) and dysprosium, cerium, neodymium, praseodymium, samarium, terbium, holmium, erbium, thulium, ytterbium at least a or multiple.
3. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material as claimed in claim 1 or 2 is characterized in that, described rare-earth activated dose is mol ratio 1: the europium sesquioxide of (1～2) and dysprosium oxide.
4. rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material as claimed in claim 1 is characterized in that, described mineralizer is that alkali metal halide is or/and ammonium halide salt, particularly ammonium chloride or brometo de amonio.
5. the preparation method of the described rare-earth activated alkaline earth metal aluminosilicate long after glow luminous material of claim 1 comprises the steps:
1) raw material: alkaline earth metal carbonate or oxide compound, aluminum oxide or aluminium hydroxide, SiO 2 powder and mineralizer L, activator X, press MOaAl
2O
3BSiO
2CL: among the fX 0.5≤(a+b)≤5, b=(0.1-10) a, c=0.02～0.5, after the mole proportioning weighing of f=0.003～0.05, thorough mixing is in the crucible of packing into then, under reducing atmosphere, under 1200～1450 ℃ temperature, burnt till in 2-4 hour in the top temperature insulation;
2) above-mentioned sintered compact is pulverized, with deionized water, dilute hydrochloric acid solution or washing with alcohol, oven dry is prepared into rare-earth activated alkaline earth metal aluminosilicate luminescent material powder.
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|---|---|---|---|
| CN 00111210 CN1130440C (en) | 2000-07-14 | 2000-07-14 | Rare-earth activated aluminosilicate long persistence luminescent, and prepn. method therefor |
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|---|---|---|---|
| CN 00111210 CN1130440C (en) | 2000-07-14 | 2000-07-14 | Rare-earth activated aluminosilicate long persistence luminescent, and prepn. method therefor |
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| CN1130440C CN1130440C (en) | 2003-12-10 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103074059A (en) * | 2012-12-08 | 2013-05-01 | 北京工业大学 | Dysprosium and thulium co-doped silicon phosphoaluminate white phosphor and its preparation method |
| CN103612449A (en) * | 2013-11-15 | 2014-03-05 | 英利能源（中国）有限公司 | Insulating luminescent material, solar battery back plate comprising insulating luminescent material, and solar battery component |
| CN103741203A (en) * | 2014-01-23 | 2014-04-23 | 中国科学院福建物质结构研究所 | Mineralizing agent for growing CuI single crystal by hydrothermal method and CuI crystal growing method |
| CN106277791A (en) * | 2016-08-13 | 2017-01-04 | 华南理工大学 | A kind of high temperature resistant silicon hydrochlorate luminous ceramic glaze and preparation method thereof |
-
2000
- 2000-07-14 CN CN 00111210 patent/CN1130440C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103074059A (en) * | 2012-12-08 | 2013-05-01 | 北京工业大学 | Dysprosium and thulium co-doped silicon phosphoaluminate white phosphor and its preparation method |
| CN103612449A (en) * | 2013-11-15 | 2014-03-05 | 英利能源（中国）有限公司 | Insulating luminescent material, solar battery back plate comprising insulating luminescent material, and solar battery component |
| CN103741203A (en) * | 2014-01-23 | 2014-04-23 | 中国科学院福建物质结构研究所 | Mineralizing agent for growing CuI single crystal by hydrothermal method and CuI crystal growing method |
| CN106277791A (en) * | 2016-08-13 | 2017-01-04 | 华南理工大学 | A kind of high temperature resistant silicon hydrochlorate luminous ceramic glaze and preparation method thereof |
| CN106277791B (en) * | 2016-08-13 | 2019-04-09 | 华南理工大学 | A kind of high temperature resistant silicon hydrochlorate luminous ceramic glaze and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN1130440C (en) | 2003-12-10 |
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