Preparation method of composite luminescent fiber nanomaterial
A technology of luminescent fibers and composite nanoparticles, which is applied in fiber processing, filament/thread forming, textiles and papermaking, etc. It can solve the problems of difficulty in preparing oriented fiber bundles or single nanofibers, and achieve luminous intensity and anti-light Enhanced bleaching ability, high luminous efficiency, and increased fluorescence lifetime
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Embodiment 1
[0042] ① 0.106g of rare earth complex Eu(DBM) prepared by wet chemical method 3 Phen was dissolved in 25.0g N,N dimethylformamide, and after ultrasonic dispersion for 30 minutes, 2.40g SDS (dissolved in 96.0g water to make a solution) was added to the solution. After the solution was homogenized, styrene monomer was added. 3.32g, adjust the ultrasonic radiation power to 600W to initiate the polymerization reaction, the reaction temperature is 25℃, the reaction time is 1.5h, the rare earth complex Eu(DBM) 3 Phen is embedded in the polymer to form a core-shell structure Eu (DBM) 3 PhenPS complex; the whole reaction needs to be in high purity N 2 Under protection.
[0043] ②The compound obtained in step ① was demulsified with absolute ethanol, separated by centrifugation, washed repeatedly with deionized water and absolute ethanol, and dried under vacuum at 80°C for 8.0 hours to obtain Eu(DBM) 3 PhenPS composite nano-particle powder;
[0044] ③The 1.0g Eu(DBM) prepared in step ② 3 Phen...
Embodiment 2
[0046] ① 0.106g of rare earth complex Tb(acac) prepared by wet chemical method 3 Dissolve Phen in 25.0g N,N dimethylformamide, continue to add 2.40g SDS (dissolved in 96.0g water to make a solution), ultrasonically disperse for 30min, after the solution is homogenized, add styrene monomer 5.32g, adjust the ultrasonic radiation power to 800W to initiate the polymerization reaction, the reaction temperature is 40℃, the reaction time is 1.5h, the rare earth complex Tb(acac) 3 Phen is embedded in polymer to form core-shell structure Tb(acac) 3 PhenPS complex; the whole reaction needs to be in high purity N 2 Under protection.
[0047] ②The compound obtained in step ① was demulsified with absolute ethanol, centrifuged, washed with deionized water and absolute ethanol 4 times, and dried under vacuum at 80°C for 8.0 hours to obtain Tb(acac) 3 PhenPS composite nano-particle powder;
[0048] ③The 1.0g Tb(acac) prepared in step ② 3 PhenPS composite nano-particle powder is uniformly dissolved ...
Embodiment 3
[0050] ① 0.1g of rare earth doped nanocrystalline YVO prepared by hydrothermal method 4 :Dy 3+ Disperse to 100ml with a concentration of 2×10 -3 mol / L citric acid solution, then add 48.0g N,N-dimethylformamide, ultrasonic dispersion for 1h, continue to add 0.204g azobisisobutyronitrile and 0.109g potassium persulfate to this solution, ultrasonic dispersion After 30 minutes, after the solution is homogenized, add 5.32g of styrene monomer, adjust the ultrasonic radiation power to 500W to initiate the polymerization reaction, the reaction temperature is 90℃, the reaction time is 3.0h, and the rare earth doped nanocrystalline YVO 4 :Dy 3+ Embedded in polymer to form core-shell structure YVO 4 :Dy 3+ PS complex; the whole reaction needs to be in high purity N 2 Under protection.
[0051] ②The compound obtained in step ① was demulsified with absolute ethanol, centrifuged, washed with deionized water and absolute ethanol 4-6 times, and dried in vacuum at 80°C for 8.0 hours to obtain YVO 4...
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