化学
单线态氧
双酚A
电子顺磁共振
催化作用
激进的
蒙脱石
活性炭
核化学
X射线光电子能谱
羟基自由基
无机化学
光化学
氧气
有机化学
化学工程
吸附
环氧树脂
工程类
物理
核磁共振
作者
Shanshan Yang,Pingxiao Wu,Junqin Liu,Meiqing Chen,Zubair Ahmed,Nengwu Zhu
标识
DOI:10.1016/j.cej.2018.04.175
摘要
For eliminating organic pollutants from wastewater, Fe0 or Fe0-composites as catalyst for peroxymonosulfate (PMS) activation have attracted increasing attention in advanced oxidation processes. In this work, a novel Fe0-montmorillonite composites (Fe-Mt-C-H2) have been prepared by thermal reduction and used as an activator for PMS to remove bisphenol A (BPA). The removal efficiency of BPA (25 mg·L−1) and total organic carbon (TOC) were 99.3% and 70.6%, respectively, in the presence of Fe-Mt-C-H2 (0.4 g·L−1) and PMS (1 mM) at pH of 3. Electron paramagnetic resonance (EPR) spectroscopy and radical scavenger studies demonstrated that superoxide radical (O2−) and singlet oxygen (1O2) were the crucial reactive oxygen species (ROS) in the Fe-Mt-C-H2/PMS system rather than sulfate (SO4−) and hydroxyl radical (·OH). Besides, it was found that pH had a great influence on the catalytic oxidation rate of BPA and the Fe-Mt-C-H2 exhibited best catalytic performance and reusability at initial pH of 3. Furthermore, the constituents of the iron surface oxidation layer at different initial pH were investigated with X-ray photoelectron spectroscopy studies, which indicated that the major constituents were Fe3O4 in acidic solution and contained α-Fe2O3, FeO and FeSO4(s) in alkaline or neutral solution. The findings of this study provide new insights into the activation mechanism of PMS by Fe0-composites and exhibit a promising application of Fe-Mt-C-H2 in wastewater treatment.
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