化学
钴
纳米颗粒
催化作用
电子顺磁共振
激进的
核化学
热解
光化学
化学工程
无机化学
有机化学
核磁共振
物理
工程类
作者
Mingya Yao,Meng Xie,Shiyong Zhang,Jinpeng Yuan,Lei Zhao,Ru-Song Zhao
标识
DOI:10.1016/j.seppur.2022.122145
摘要
In this work, new covalent organic framework (COF) materials with high crystallinity and large specific surface areas were used as cobalt-loaded supports. Cobalt nanoparticle-embedded nitrogen-doped carbon porous catalysts ([email protected]) were obtained by high-temperature pyrolysis of the COF materials and cobalt salts. With multiple active sites (Co0, pyridine N, and graphitic N), [email protected] exhibited superior catalytic properties for peroxymonosulfate (PMS) activation toward the degradation of sulfamerazine (SMZ). The efficiency of SMZ degradation reached 92.4 % within 10 min and the total organic carbon (TOC) removal rate reached 70.3 % within 30 min. Using radical quenching experiments and electron paramagnetic resonance (EPR) analysis, sulfate radicals (SO4•−), hydroxyl radicals (•OH), and singlet oxygen (1O2) were identified in this system, while 1O2 was the dominant active species for SMZ removal. The degradation intermediates of SMZ in [email protected]/PMS were monitored by high performance liquid chromatography–time of flight mass spectrometry (HPLC–TOFMS).
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