化学
催化作用
单线态氧
羟基自由基
化学工程
水溶液
碳化
无机化学
激进的
吸附
氧气
有机化学
工程类
作者
Shijun Zhu,Wei Wang,Yongpeng Xu,Zhigao Zhu,Zhiquan Liu,Fuyi Cui
标识
DOI:10.1016/j.cej.2019.02.011
摘要
Abstract Iron sludge produced numerously from drinking water treatment plants can be recycled to create catalyst for peroxymonosulfate (PMS) activation. In this study, iron sludge-derived catalysts were synthesized via one-step pyrolysis process by self-reduction in argon atmosphere. The crystallite structures and catalytic performance of these catalysts were strongly dependent on the pyrolytic temperature. The product carbonized at 900 °C (Fe0/Fe3C) exhibited a superior catalytic behavior with 99% ciprofloxacin (CIP, 10 mg/L) degradation in 20 min due to the synergistic effect of Fe0 and graphitic carbon. The influences of reaction parameters on the CIP degradation were further investigated and the Fe0/Fe3C-PMS process had a wide efficient pH range from 3 to 9. The catalyst also exhibited excellent magnetic property and could be easily separated with external magnetic field. Radical quenching study and electron paramagnetic resonance (EPR) tests indicated that sulfate radical (SO4 −), hydroxyl radical ( OH), superoxide radical (O2 −) and singlet oxygen (1O2) contributed to the degradation of CIP. This study extended the application of Fe0/Fe3C to catalytic oxidation of other typical refractory organic contaminants and confirmed its excellent catalytic activity. Overall, this study provided a cost-effective iron sludge reuse method to develop an environment-friendly catalyst for decontamination of organics pollutants, and also to relieve detrimental influences on aqueous environment by discharging the iron sludge.
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