Rare earth blue red light conversion material and preparation thereof
A fluorescent material, red light technology, applied in luminescent materials, chemical instruments and methods, etc., can solve the problem of not matching the maximum absorption peak position, and achieve the effect of good luminous intensity, good compatibility and fine particle size
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Embodiment 1
[0022] 0.4mmolSm 2 o 3 , 0.05mmolTb 4 o 7 Dissolve in 10ml of concentrated hydrochloric acid (concentration: 33%), heat to remove the hydrochloric acid to obtain rare earth chlorides, dissolve the rare earth chlorides in 30ml of distilled water to obtain rare earth chloride solutions. Separately, 3 mmol of N-phenylanthranilic acid and 1 mmol of 1,10-phenanthroline were weighed and dissolved in 20 ml of ethanol, respectively. Transfer the rare earth chloride into the flask, install magnetic stirring, and reflux device. After fully stirring and mixing, add the ethanol solution of N-phenylanthranilic acid, then add 1,10-phenanthroline ethanol solution after fully stirring, adjust the pH value to 6-7 with ammonia water, heat to 80°C, and A large amount of white powdery precipitate formed. After refluxing for 3-4 hours, hot filter, wash the precipitate with 80°C hot distilled water three times, and vacuum dry (80°C, 0.05MPa) to obtain the light converting agent.
[0023] The ...
Embodiment 2
[0025] 0.3mmolSm 2 o 3 , 0.0375mmolTb 4 o 7 In concentrated hydrochloric acid, heat to remove the hydrochloric acid to obtain rare earth chlorides, and dissolve the rare earth chlorides in 30ml distilled water to obtain rare earth chloride solutions. Separately, 3 mmol of N-phenylanthranilic acid and 1 mmol of 1,10-phenanthroline were weighed and dissolved in 20 ml of ethanol, respectively. Transfer the rare earth chloride into the flask, install magnetic stirring, and reflux device. After fully stirring and mixing, add the ethanol solution of N-phenylanthranilic acid, then add the ethanol solution of 1,10-phenanthroline after fully stirring, adjust the pH value to 6-7 with ammonia water, heat to 80°C, A large amount of white powdery precipitate formed. After refluxing for 3-4 hours, hot filter, wash the precipitate with 80°C hot distilled water three times, and vacuum dry (80°C, 0.05MPa) to obtain the light converting agent. The composition of the resulting fluorescent ...
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