Activation of peroxymonosulfate by magnetic Fe3S4/biochar composites for the efficient degradation of 2,4,6-trichlorophenol: Synergistic effect and mechanism

生物炭 催化作用 X射线光电子能谱 化学 电子顺磁共振 介电谱 降级(电信) 碳纤维 电化学 化学工程 光化学 材料科学 热解 有机化学 复合材料 复合数 物理化学 电信 物理 电极 核磁共振 计算机科学 工程类
作者
Hui Li,Siyang Li,Lide Jin,Lu Zhen,Minghui Xiang,Chen Wang,Wenbing Wang,Jin Zou,Chunyang Li,Haijiao Xie
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:10 (1): 107085-107085 被引量:30
标识
DOI:10.1016/j.jece.2021.107085
摘要

The synergistic catalytic degradation of metal carbon-based composites is a feasible strategy to improve the efficiency of advanced oxidation processes (AOPs) by means of green chemistry. In this work, Fe3S4 nanoparticles were anchored on the surface of peanut shell biochar to prepare magnetic Fe3S4/biochar (Fe3S4/BC) composites, which were applied to activate peroxymonosulfate (PMS) to degrade 2,4,6-trichlorophenol (2,4,6-TCP). The addition of biochar not only reduced the aggregation of Fe3S4 nanoparticles, but also accelerated the electron transfer rate, and the constructed C-O-Fe bridges accelerated the regeneration of Fe(Ⅱ), which made Fe3S4/BC have better catalytic performance than pure Fe3S4 even though the use of metal sulfides was reduced. Fe on the surface of Fe3S4/BC was the catalytic reaction center. The dominant role of sulfate radical (SO4·-) and hydroxyl radical (HO·) on the degradation of 2,4,6-TCP was verified by electron paramagnetic resonance (EPR) and free radical quenching experiments. The mechanism of C-O-Fe bridges was verified by density functional theory (DFT) calculation. The mechanism of PMS activation by Fe3S4/BC was elucidated by electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS). Based on the detection results of intermediate products, the possible degradation pathways to 2,4,6-TCP were proposed. This work provides new insights into the synergistic catalytic mechanism of metal carbon-based sulfides and promotes the development of environmentally friendly and efficient metal carbon-based catalysts.
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