Preparation method of magnetic core-shell type nanoparticle surface uranyl molecularly imprinted polymer
A technology for imprinting polymers and nanoparticles, which can be used in the fields of alkali metal compounds, radioactive pollutants, chemical instruments and methods, etc. It can solve the problems of uneven distribution of MIP imprinting sites, difficult elution of template molecules, and low mass transfer efficiency. , achieve good selectivity, facilitate magnetic separation, and improve extraction efficiency
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Embodiment 1
[0023] This example is intended to illustrate the present invention " magnetic Fe 3 o 4 Core-SiO 2 Feasibility of preparing uranyl molecularly imprinted polymers on the surface of shell nanoparticles,
[0024] 1. Preparation of magnetic nanoparticles:
[0025] Take 5mmol sodium citrate, 0.2mol NaNO 3 And 20mmol NaOH, dissolved in 100mL distilled water, placed in a boiling water bath to keep the temperature, quickly add 2mol L -1 5 mL of ferrous sulfate solution, the color of the solution turned black rapidly, and the reaction was stirred for 1.5 hours. Take it out and cool it, separate the solid product with a magnet, wash it with distilled water until the clear liquid is neutral, and dry it in a vacuum oven at 50°C to obtain a magnetic Fe 3 o 4 Nanoparticles.
[0026] 2.Fe 3 o 4 @SiO 2 preparation:
[0027] Weigh the 0.5g Fe prepared above 3 o 4 The magnetic nanoparticles were dispersed in a flask filled with 80mL ethanol and 20mL distilled water, and ultrasonica...
Embodiment 2
[0033] In order to remove the template molecule uranium, the prepared U-MIP was eluted with 10ml 0.5mol / L HCl for 1.5h, and the magnetic Fe was detected by UV / Vis spectrophotometer 3 o 4 Core-SiO 2 Whether the uranyl molecularly imprinted polymer template molecules on the surface of shell nanoparticles have been completely cleared. Then wash 2-3 times with ultrapure water, and the obtained magnetic Fe 3 o 4 Core-SiO 2 The uranyl molecularly imprinted polymer on the surface of the shell nanoparticles was dried in a drying oven at 60°C. 10 mg of dried U-MIP (U-NIP) was weighed and placed in 10 ml of uranyl solutions of different concentrations. The mixture was kept stirring at room temperature for 90 min, and the UNIP was separated with a magnet, and the concentration of uranium in the supernatant was measured with a UV / Vis spectrophotometer. By the formula Q=[V×(C 0 –C e )] / m to calculate the equilibrium adsorption capacity of U-MIP (or U-NIP) (Q / μmolg -1 ). C 0 and ...
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