Abstract

Fe3O4 nanoparticles were prepared by continuously pumping aqueous solutions of FeCl3/FeCl2 and NaOH into a rotating packed bed (RPB), where 0.148mol/L of FeCl3·6H2O, 0.075mol/L of FeCl2·4H2O, and 0.888mol/L of NaOH co-precipitated. A rotational speed of 1800rpm, liquid flow rates of 500mL/min, and a temperature of 60°C were adopted. Fe3O4 nanoparticles that were prepared in this manner had an average diameter of 6.4nm, a maximal saturation magnetization of 50emu/g, and a BET surface area of 173m2/g. The rate of production of Fe3O4 nanoparticles was 17kg/day.The H2O2-activating capacity of Fe3O4 nanoparticles that were prepared using the RPB, measured using the decolorization of Rhodamine B (RhB), was related to the Fe3O4 dosage, the H2O2 concentration, and the temperature. At pH 5 and 80°C with an Fe3O4 dosage of 0.30g/L and an H2O2 concentration of 0.11mol/L, the Fe3O4 nanoparticles that were prepared using the RPB were observed to activate H2O2 and to have a decolorization efficiency of approximately 100% in 75min with an observed decolorization rate constant of 0.0592min−1. The decolorization of RhB in the Fe3O4–H2O2 process was consistent with the pseudo-first-order kinetic model.

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