A silicon-based photocatalytic magnetic molecular imprinting material and its preparation method
A technology of magnetic molecular imprinting and photocatalysis, applied in chemical instruments and methods, catalysts for physical/chemical processes, chemical elements of heterogeneous catalysts, etc. and other problems, to achieve the effect that the processing capacity is not easy to reduce, easy to reuse, and environmentally friendly.
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[0024] The preparation method of the silicon-based photocatalytic magnetic molecular imprinting material of the present invention comprises the following steps:
[0025] Step 1: Add ammonium fluorotitanate and boric acid into a beaker filled with 100mL of deionized water according to the ratio of raw materials, stir at a speed of 280~300r / min for 30min at 30~35°C; then add ammonium fluorosilicate according to the ratio of raw materials , stirred at a speed of 280-300r / min for 30min; then added oxytetracycline according to the raw material ratio, and stirred at a speed of 280-300r / min for 30min; then added zinc acetate and FeCl at a time according to the raw material ratio 2 , FeCl 3 , Potassium sodium tartrate and sodium hydroxide, stirred at a speed of 450-500r / min for 60min, and left for 4-6h to obtain a mixed solution;
[0026] Above-mentioned reaction process is all carried out under anaerobic state (nitrogen purging);
[0027] Step 2: put the mixed solution in a water b...
Embodiment 1
[0033] Put 1.98g of ammonium fluorotitanate and 1.55g of boric acid into a beaker filled with 100mL of deionized water, stir for 30min at a speed of 300r / min at a temperature of 30-35°C; then add 0.356g of ammonium fluorosilicate , stirred at a speed of 300r / min for 30min; then added 1.96g of oxytetracycline and continued to stir at a speed of 300r / min for 30min, and then added 0.45g of zinc acetate and 0.6g of FeCl 2 , 1.8g of FeCl 3 , 1g sodium potassium tartrate and 5g sodium hydroxide, stirred at a speed of 500r / min for 60min, and left for 4h. Above reaction is carried out under nitrogen purging;
[0034] Place the beaker in a water bath and heat at 45-50°C for 20 hours;
[0035] After the heating is completed, discard the upper liquid, gently scrape off the loose powder at the bottom of the beaker, rinse with distilled water and absolute ethanol for 3 times, then centrifuge at 3500r / min for 5min, pour off the supernatant to obtain the powder material ;
[0036] Put th...
Embodiment 2
[0038] Oxytetracycline was detected at 0.01 mg / L in the effluent of a city sewage plant. The material obtained in Example 1 was added to the sewage at 50 mg / L. After 30 minutes of photocatalytic reaction with a UV lamp (300W), no oxygen was detected in the effluent. Tetracycline, indicating that oxytetracycline is degraded.
[0039] After the powder is collected by a magnet, it is dried in a vacuum oven at 70°C for 3 hours, and can be reused 10 times, and the oxytetracycline can be degraded.
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