CN1263925A - Long-afterglow photoluminescent composition and its preparing process - Google Patents
Long-afterglow photoluminescent composition and its preparing process Download PDFInfo
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- CN1263925A CN1263925A CN 00103309 CN00103309A CN1263925A CN 1263925 A CN1263925 A CN 1263925A CN 00103309 CN00103309 CN 00103309 CN 00103309 A CN00103309 A CN 00103309A CN 1263925 A CN1263925 A CN 1263925A
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- long
- src
- oxide
- afterglow
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Abstract
A long-afterglow photoluminescent composition is prepared from metallic oxide as matrix, less rare-earth compound (Eu : Dy) as activating agent and H3BO4 as fusing agent through high-temp calcine. Its advantages are no poison and radioactivity, high brightness, long afterglow up to 8-12 hr, and long service life. It can be used to make different luminous products.
Description
The invention discloses a kind of photic long-afterglow material and preparation method thereof, belong to field of light emitting materials.
As everyone knows, existing luminescent material, fluorescent material makes it constantly luminous for a long time by the radiant of luminous substrate (fluorescent substance) ZNS:Cu powder adding artificial radioactivity isotropic substance hard iron 147Pm tritium 3H and thorium 2882TH, and luminosity is decided by contained radioactive species and quantity.This radiant luminescent material is mainly used in the coating compass, and numeral on the instrument clock and watch and pointer guarantee that these instrument show in night and dark place and can observe.This radioactive luminescent material has destruction to tissue and environment, carrying out coating processing back and necessary security measure in use can use, the range of application and the consumption that often need the regulation strictness, its application region is restricted, and existing sulfide embedded photoluminescent material (as Cu and the coactivated ZNS of CO) twilight sunset was lacked 1-2 hours, and the cost height, complicated process of preparation, drawbacks such as life-span weak point.
The objective of the invention is provides a kind of any radioactivity essence that do not use at the above-mentioned weak point that exists, xln by the generating structure novelty makes it have high brightness, reach 8-12 hours time of persistence, and can reach the long after glow luminous material in 10 years work-ing life.
For achieving the above object, I am through concentrating one's attention on the research experiment discovery with aluminium oxide Al for many years
2O
3With Strontium carbonate powder SrC
2O
3, for matrix is mixed rare earth compound EU
2O
3Dy
2O
3In crystal, form luminescence center as its activator, carry out and promote the crystallization process of product easily, in reactant, add fusing assistant boric acid H for making building-up reactions
3BO
4And SrCl
26H
2O mixes the mol ratio of above-mentioned several starting compounds by the chemical constitution requirement of material equably, then in suitable atmosphere and certain roasting temperature, the high-brightness long persistence embedded photoluminescent material.
Below in conjunction with example in detail content of the present invention:
Implement 1
Raw materials used kind of long-afterglow photoluminescent and consumption are:
Al
2O
3 820g SrC
2O
3 140g
H
3BO
4 56g Eu
2O
3 1.8g
Dy
2O
3 2.2g
With Al
2O
3And SrC
2O
3With mixing Eu behind the mechanical mill mixing
2O
3And Dy
2O
3Adding H
3BO
4The mixing crucible of packing into is sent in the retort furnace with 1280 ℃ of calcinations 2 hours under certain atmosphere, take out cooling back, and 200 mesh sieves are crossed in the block ball mill pulverizing of luminescent material, long-afterglow luminescent powder, can add in paint, printing ink, plastics, the rubber, make all kinds of light emitting articles.
Example 2
Al
6O
11Chromatographic aluminium oxide 420g
SrC
2O
3 510g H
3BO
4 26g
SrCl
26H
2O 26g Eu
2O
3 2.5g
Dy
2O
3 3.5g
With Al
6O
11Chromatographic aluminium oxide is put into the retort furnace roasting and is taken out and SrC after 2 hours
2O
3The machinery mixing mixes Eu
2O
3Dy
2O
3Activator adds SrCl again
26H
2O and H
3BO
4Pack into behind the mixing when putting in the crucible retort furnace more than 1200 ℃ in certain atmosphere roasting take out after 2 hours, ball mill pulverizing cross 200 mesh sieves blue light emitting material.
The foregoing description 1 example, 2 embedded photoluminescent material compositions and existing sulfide (the coactivated ZNS of CU CO) are done the contrast experiment, see that its luminosity increases by 200%, and can reach 8-12 hours time of persistence.
Therefore, the present invention has stronger luminosity and long fluorescent lifetime, can be made into various luminous product with the present invention, as various labels, switching push button, artwork, clock and watch, field instrument or telltale, the advertisement helmet, emergency lighting or the like, be widely used in coating, printing ink (printing sheets, coating) compounding rubber plastic cement, enamel porcelain, weaving, trade mark, clothing item, Fishing device, fire-fighting emergency escape system, debate industries such as knowing military equipment, architectural decoration, textile printing and dyeing.
Claims (4)
1, a kind of long-afterglow photoluminescent composition is by aluminum oxide, Al
2O
3, chromatographic aluminium oxide Al
6O
11, Strontium carbonate powder SRC
2O
3, europium sesquioxide EU
2O
3, dysprosium oxide DY
2O
3With boric acid H
3BO
4Strontium chloride ScCl
26H
2The O compound constitutes, and it is characterized in that: composition and proportioning (portion rate) are as follows:
Aluminum oxide AL
2O
3820g Strontium carbonate powder SrC
2O
3140g
Boric acid H
3BO
456g europium sesquioxide EU
2O
31.8g
Dysprosium oxide Dy
2O
32.2g
2, long-afterglow photoluminescent according to claim 1 is characterized in that: composition and proportioning (portion rate) are as follows:
The neutral chromatography aluminium oxide Al
6O
11420g Strontium carbonate powder SrC
2O
3510g
Strontium oxide SrCl
26H
2O 26g boric acid H
3BO
428g
Europium sesquioxide EU
2O
32.5g dysprosium oxide Dy
2O
33.5g
3, long-afterglow photoluminescent according to claim 1, its feature also is the preparation method, and is as follows:
With Al
2O
3And SrC
2O
3Behind mechanical mixing, mix Eu
2O
3And Dy
2O
3, adding H
3BO
4The mixing crucible of packing into is sent in the retort furnace with 1280 ℃ of roasts 2 hours, and take out the cooling back, and 200 mesh sieves are crossed in the block ball mill pulverizing of luminescent material, long-afterglow luminescent powder.
4, long-afterglow photoluminescent according to claim 1, its feature are that also the preparation method is as follows: with A
16O
11Middle domestic animal chromatographic aluminium oxide is put into 1180 ℃ of roasts of retort furnace and is taken out and SrC after 2 hours
2O
3The machinery mixing mixes Eu
2O
3, Dy
2O
3Add SrCl again
26H
2O and H
3BO
4, mixing pack into put in the crucible retort furnace more than 1200 ℃ in certain atmosphere roast take out after 2 hours, ball mill pulverizing cross 200 mesh sieves the blue light emitting powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 00103309 CN1263925A (en) | 2000-02-29 | 2000-02-29 | Long-afterglow photoluminescent composition and its preparing process |
Applications Claiming Priority (1)
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CN 00103309 CN1263925A (en) | 2000-02-29 | 2000-02-29 | Long-afterglow photoluminescent composition and its preparing process |
Publications (1)
Publication Number | Publication Date |
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CN1263925A true CN1263925A (en) | 2000-08-23 |
Family
ID=4576891
Family Applications (1)
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CN 00103309 Pending CN1263925A (en) | 2000-02-29 | 2000-02-29 | Long-afterglow photoluminescent composition and its preparing process |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100358057C (en) * | 2005-01-18 | 2007-12-26 | 江苏中煤电缆集团有限公司 | Improved rubber sheath insulated luminous cable |
CN103208171A (en) * | 2013-04-01 | 2013-07-17 | 深圳市广安消防装饰工程有限公司 | Self-luminous fire hydrant button |
-
2000
- 2000-02-29 CN CN 00103309 patent/CN1263925A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100358057C (en) * | 2005-01-18 | 2007-12-26 | 江苏中煤电缆集团有限公司 | Improved rubber sheath insulated luminous cable |
CN103208171A (en) * | 2013-04-01 | 2013-07-17 | 深圳市广安消防装饰工程有限公司 | Self-luminous fire hydrant button |
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PB01 | Publication | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |