电子顺磁共振
化学
碳化
激进的
电化学
催化作用
过氧二硫酸盐
表面改性
吸附
光化学
化学工程
有机化学
物理化学
电极
物理
核磁共振
工程类
作者
Yang Yu,Ning Li,Xukai Lu,Beibei Yan,Guanyi Chen,Yanshan Wang,Xiaoguang Duan,Zhanjun Cheng,Shaobin Wang
标识
DOI:10.1016/j.jhazmat.2021.126735
摘要
Renewable wood sponge with lamellar structure, compressibility and three-dimensional porous frameworks exhibits excellent functionalization application potential in various fields. Herein, cobalt and nitrogen (Co/N) co-doped carbonized wood sponge (CoNCWS800) was prepared successfully for peroxymonosulfate (PMS) activation to degrade sulfamethoxazole (SMX). The CoNCWS800 material exhibited admirable catalytic activity in PMS activation to oxidize SMX molecules (99.7% within 60 min). Electron paramagnetic resonance (EPR) analysis, quenching tests and electrochemical experiments confirmed the existence of both radical (SO4·-,·OH and O2·-) and non-radical (1O2 and direct charge transfer) pathways during the SMX degradation process. Co species were verified as major contributors for the generation of multiple radicals via activating PMS. Surface defective structure and ketonic CO groups performed the positive linear correlation with reaction kinetic constants, revealing the critical role of the two active sites in PMS activation via non-radical process. This study provides a unique insight in PMS activation mechanism via both radical and non-radical pathways of wood sponge-based functional materials.
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