Luminous metal organic framework material for uranyl ion detection in water and preparation method thereof
A metal-organic framework and uranyl ion technology, which is applied in the field of luminescent metal-organic framework materials and their preparation, achieves the effects of simple preparation, strong selectivity, and good application prospects
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Embodiment 1
[0023] Weigh 2mL of N,N'-dimethylformamide into 10mL of deionized water, add 0.026g of terbium nitrate hexahydrate and 0.035g of 4,4'-biphenyldicarboxylic acid in turn while stirring, add three Ethylamine adjusted the pH of the mixed solution to 7.5, and stirred at room temperature for 30 minutes; then put the mixed solution into a reaction kettle with a polytetrafluoroethylene lining, crystallized at 140°C for 72 hours, cooled naturally to room temperature, filtered, After washing three times with ethanol and drying, the terbium metal-organic framework was obtained. Select a terbium metal-organic framework single crystal with a suitable size, use a German Bruker ApexCCD single crystal X-ray diffractometer, use graphite as a monochromator, and use MoKα Target, the test temperature is (293±2)K, in the range of 1.87°figure 1 .
[0024] The prepared terbium metal-organic framework was dispersed in aqueous solution, which exhibited strong green fluorescence, and the main emiss...
Embodiment 2
[0026] Weigh 4mL of N,N'-dimethylformamide and add it to 12mL of ethylene glycol, then add 0.026g of terbium nitrate hexahydrate and 0.048g of 4,4'-biphenyldicarboxylic acid in turn while stirring, using Adjust the pH of the mixed solution with ammonia water to about 9.0, and stir at room temperature for 10 minutes; then put the mixed solution into a reaction kettle with a polytetrafluoroethylene lining, crystallize at 150°C for 72 hours, cool naturally to room temperature, filter, and use After washing with ethanol three times and drying, the terbium metal-organic framework was obtained; figure 2 As shown, the X-ray powder diffraction peak position of the obtained sample is basically consistent with the peak position simulated by X-ray single crystal diffraction.
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