傅里叶变换红外光谱
扫描电子显微镜
降级(电信)
催化作用
核化学
石墨烯
热液循环
材料科学
氧化物
复合数
化学
化学工程
纳米技术
复合材料
有机化学
冶金
工程类
电信
计算机科学
作者
Junfeng Wu,Jing Bai,Zhaodong Wang,Zuwen Liu,Yanli Mao,Biao Liu,Jinhui Zhang
标识
DOI:10.1080/09593330.2020.1779353
摘要
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 S2O82- 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 SO4-⋅ 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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