Nitrogen Vacancy-Modulated Peroxymonosulfate Nonradical Activation for Organic Contaminant Removal via High-Valent Cobalt-Oxo Species

被引:199
作者
Jiang, Jingjing [1 ,2 ]
Zhao, Ziqing [1 ,2 ]
Gao, Jiaying [1 ,2 ]
Li, Tianren [1 ,2 ]
Li, Mingyu [1 ,2 ]
Zhou, Dandan [3 ]
Dong, Shuangshi [1 ,2 ]
机构
[1] Jilin Univ, Key Lab Groundwater Resources & Environm, Minist Educ, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Jilin Prov Key Lab Water Resources & Environm, Changchun 130021, Jilin, Peoples R China
[3] Northeast Normal Univ, Sch Environm, Engn Lab Water Pollut Control & Resources Recover, Changchun 130117, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
nitrogen vacancy; peroxymonosulfate; high-valent cobalt-oxo species; selectivity; organic contaminants; DEGRADATION; COMPOSITES; POLLUTANTS; OXIDATION; CLEAVAGE; FENTON; METAL;
D O I
10.1021/acs.est.2c01913
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Rapid generation of high-valent cobalt-oxo species (Co(IV)???O) for the removal of organic contaminants has been challenging because of the low conversion efficiency of Co(III)/Co(II) and the high activation energy barrier of the Co(II)-oxidant complex. Herein, we introduced nitrogen (N) vacancies into graphite carbon nitride imbedded with cobalt carbonate (CCH/CN-V-n) in a peroxymonosulfate (PMS)/visible light system to break the limitations of a conventional two-electron transfer path. These N vacancies enhanced the electron distribution of the Co 3d orbital and lowered the energy barrier to cleave the O-O bond of PMS in the Co(II)-PMS complex, achieving the modulation of major active species from O-1(2) to Co(IV)???O. The developed synergistic system that exhibited adsorption and oxidation showed remarkable selectivity and contaminant removal performance in inorganic (Cl-, NO3-, HCO3-, and HPO4-) organic (HA) and even practical aqueous matrices (tap water and secondary effluent). This study provides a novel mechanistic perspective to modulate the nonradical path for refractory contaminant treatment via defect engineering.
引用
收藏
页码:5611 / 5619
页数:9
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