Abstract
ABSTRACT We reported the preparation of NGO-Fe3O4 by simple hydrothermal-co-precipitation. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). It was demonstrated that norfloxacin (NOR) could be effectively degraded by the UV/NGO-Fe3O4/PDS system. The degradation efficiency reached 100% within 13 min (the concentration of NOR and were 100 mg L−1 and 1 mM, respectively; m(NGO-Fe3O4): m(PDS) = 4: 1; pH: 3.0). In addition, NGO-Fe3O4 showed stable catalytic activity in recycling. The analysis found that the in-situ generated ·OH was the main active free radicals but also participated in the NOR degradation. Based on the identified intermediates, the NOR degradation pathways were proposed with UV/NGO-Fe3O4/PDS system.
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