催化作用
双酚A
化学
降级(电信)
电子顺磁共振
普鲁士蓝
动力学
碳纤维
核化学
化学工程
多相催化
材料科学
有机化学
物理化学
复合材料
工程类
环氧树脂
物理
复合数
电信
量子力学
电化学
核磁共振
计算机科学
电极
作者
Chuanyi Guo,Chaofa Chen,Jiaying Lu,Du Fu,Cheng‐Zong Yuan,Xi‐Lin Wu,Kwun Nam Hui,Jianrong Chen
标识
DOI:10.1016/j.jcis.2021.04.092
摘要
Stable and recyclable catalysts are crucial to the peroxymonosulfate (PMS) based advanced oxidation process (AOPs) for wastewater treatment. Herein, nitrogen-rich carbon wrapped Fe3C (Fe3[email protected]) on carbon felt (CF) substrate was synthesized by using Prussian blue (PB) loaded CF as the precursors. The obtained Fe3[email protected]/CF catalyst was applied for degradation of bisphenol A (BPA) via the heterogeneous catalytic activation of PMS. Results showed that ~91.7%, 95.2%, 98.1% and 99.1% of BPA (20 mg/L) were eliminated in the Fe3[email protected]/CF + PMS system within 4, 10, 20 and 30 min, respectively. The fast degradation kinetics is attributed to the production of abundant reactive species (OH, SO4− and 1O2) in the Fe3[email protected]/CF + PMS system, as demonstrated by the electron paramagnetic resonance spectroscopy and quench experiments. The Fe3[email protected]/CF catalyst was stable and can be easily recycled by using an external magnet. The results indicated that the nanoconfined Fe3C endowed Fe3[email protected]/CF with high stability and magnetic property and enabled the efficient electron transfer for PMS activation. This study provides a cost-effective approach for the fabrication of stable and recyclable Fe3[email protected]/CF catalyst, and shed a new light on the rational design of multifunctional catalyst for advanced water remediation.
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