催化作用
吸附
过硫酸盐
化学
分子
化学工程
X射线光电子能谱
无机化学
光化学
有机化学
工程类
作者
Sijin Zuo,Shengcai Zhu,Jiaying Wang,Weiping Liu,Juan Wang
标识
DOI:10.1016/j.apcatb.2021.120783
摘要
A N/O-codoped carbon-based catalyst (N/O-C-8) designed with dual reaction sites (pyridinic N and carbonyl group) was fabricated in this work, for persulfate based advanced oxidation reaction. The pyridinic N served as the adsorption site for target molecule, via series of high resolution XPS analysis and DFT calculation. Meanwhile, the carbonyl group functioned as the persulfate activation site, to generate oxidative 1O2. Engineering and isolating the two reaction sites on catalyst surface can greatly shorten the migration distance from 1O2 to target organic molecule, resulting in good catalytic removal efficiency. As demonstrated, during a 4-hour continuous flow experiment, our catalyst showed stable and efficient removal of tetracycline, with a flow rate of 4 mL/min. The study provides keen insights into the design of effective non-metal based catalysts for practical water remediation.
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