Oily sludge derived carbons as peroxymonosulfate activators for removing aqueous organic pollutants: Performances and the key role of carbonyl groups in electron-transfer mechanism

过硫酸盐 化学 催化作用 单线态氧 水溶液 污染物 电子转移 热解 苯酚 总有机碳 碳纤维 光化学 化学工程 无机化学 有机化学 氧气 材料科学 复合材料 工程类 复合数
作者
Wenjie Liu,Chunyang Nie,Wenlang Li,Zhimin Ao,Shaobin Wang,Taicheng An
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:414: 125552-125552 被引量:82
标识
DOI:10.1016/j.jhazmat.2021.125552
摘要

In this work, low-cost carbon-based materials were developed via a facile one-pot pyrolysis of oily sludge (OS) and used as catalysts to activate peroxymonosulfate (PMS) for removing aqueous recalcitrant pollutants. By adjusting the pyrolysis temperature, the optimized OS-derived carbocatalyst manifested good performance for PMS activation to abate diverse organic pollutants in water treatment. Particularly, an average removal rate of 0.87 mol phenol per mol PMS per hour at a catalyst dosage of 0.2 g L−1 is attained by the OS-derived carbocatalyst, higher than many other documented catalysts. A series of experimental evidences consolidated that organic pollutants were oxidized mainly via electron-transfer mechanism albeit the detection of singlet oxygen (1O2) from PMS activation driven by the OS-derived carbocatalyst. Specifically, the proportion of carbonyl groups (C˭O) in the carbocatalyst adopted with selective modification treatments to tailor the surface chemistry was found to be linearly correlated with the catalytic activity and theoretical calculations demonstrated that the reactions between C˭O and PMS to form surface reactive complexes were more energetically favorable compared to 1O2 generation. Herein, this study not only offers a new strategy for reusing OS as value-added persulfate activators but also deepens the fundamental understanding on the nonradical regime.
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