标题: Insights into the mechanism of carbocatalysis for peracetic acid activation: Kinetic discernment and active site identification
作者: Miao, F (Miao, Fei); Yue, XT (Yue, Xiting); Cheng, C (Cheng, Cheng); Chen, XT (Chen, Xuantong); Ren, W (Ren, Wei); Zhang, H (Zhang, Hui)
来源出版物: WATER RESEARCH 卷: 227 文献号: 119346 DOI: 10.1016/j.watres.2022.119346 出版年: DEC 1 2022
摘要: Peracetic-acid-based advanced oxidation processes (PAA-AOPs) on metal-free catalysts have emerged as charming strategies for water contaminant removal. However, the involved reactive species and their corresponding active sites are ambiguous. Herein, using carbon nanotube (CNT) as a model carbocatalyst, we demonstrated that, under neutral conditions, the CNT-PAA* complex was the dominant reactive species to oxidize phenolic compounds via electron-transfer process (ETP), whereas the surface-bound hydroxyl radicals ((OHsurface)-O-center dot) played a minor role on the basis of quenching and electrochemical tests as well as Raman spectroscopy. More importantly, the experimental and density functional theory (DFT) calculation results collaboratively proved that the active site for ETP was the sp(2)-hybridized carbon on the CNT bulk, while that for radical generation was the edge-located hydroxyl group (C-OH), which lowered the energy barrier for cleaving the O-O bond in CNT-PAA* complex. We further discerned the oxidation kinetic constants (k(oxid)) of different pollutants from the apparent kinetic constants in CNT/PAA system. The significant negative linear correlation between lnkoxid and half-wave potential of phenolic compounds suggests that the pollutants with a lower oneelectron oxidation potential (i.e., stronger electron-donating ability) are more easily oxidized. Overall, this study scrutinizes the hybrid radical and non-radical mechanism and the corresponding active sites of the CNT/PAA system, providing insights into the application of PAA-AOPs and the development of ETP in the remediation of emerging organic pollutants.
作者关键词: Nanocarbon; PAA; Nonradical oxidation; Catalytic sites; Environmental remediation
地址: [Miao, Fei; Yue, Xiting; Cheng, Cheng; Chen, Xuantong; Zhang, Hui] Wuhan Univ, Sch Resource & Environm Sci, Dept Environm Sci & Engn, Hubei Key Lab Biomass Resource Chem & Environm Bi, Wuhan 430079, Peoples R China.
[Ren, Wei] Nanchang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Contro, Nanchang 330063, Jiangxi, Peoples R China.
通讯作者地址: Zhang, H (通讯作者),Wuhan Univ, Sch Resource & Environm Sci, Dept Environm Sci & Engn, Hubei Key Lab Biomass Resource Chem & Environm Bi, Wuhan 430079, Peoples R China.
电子邮件地址: eeng@whu.edu.cn
影响因子:13.4
版权所有 © 武汉大学资源与环境科学学院
地址:湖北省武汉市珞喻路129号 邮编:430079
电话:027-68778381,68778284,68778296 传真:027-68778893 邮箱:sres@whu.edu.cn