Synergistic oxytetracycline adsorption and peroxydisulfate-driven oxidation on nitrogen and sulfur co-doped porous carbon spheres

被引:53
|
作者
An, Ning [1 ,2 ,3 ]
Zhao, Min [1 ,2 ,3 ]
Zheng, Xiangyong [1 ,2 ,3 ]
Wang, Qi [1 ,2 ,3 ]
Huang, Xianfeng [1 ,2 ,3 ]
Sun, Bo [1 ,2 ,3 ]
Shen, Yi [4 ]
Wang, Jun [5 ]
Chen, Baoliang [6 ]
Liu, Renlan [1 ,2 ,3 ]
机构
[1] Wenzhou Univ, Coll Life & Environm Sci, Wenzhou 325035, Peoples R China
[2] Wenzhou Univ, Natl & Local Joint Engn Res Ctr Ecol Treatment Te, Wenzhou 325035, Peoples R China
[3] Wenzhou Univ, Zhejiang Prov Engn Lab Ecol Treatment Technol Urb, Wenzhou 325035, Peoples R China
[4] Zhejiang Univ Technol, Coll Environm, Hangzhou 310032, Peoples R China
[5] Tianjin Polytech Univ, Dept Chem Engn, Tianjin 300387, Peoples R China
[6] Zhejiang Univ, Dept Environm Sci, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous carbon spheres; Nitrogen and sulfur co-doped; Peroxydisulfate; Radical and nonradical pathways; Synergistic effect; CATALYTIC-OXIDATION; ORGANIC POLLUTANTS; GRAPHENE; DEGRADATION; ACTIVATION; PERSULFATE; BIOCHAR;
D O I
10.1016/j.jhazmat.2021.127444
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Metal-free carbonaceous catalysts are receiving increasing attention in wastewater treatment. Here, nitrogen and sulfur co-doped carbon sphere catalysts (N,S-CSs(900)-OH) were synthesized using glucose and L-cysteine via a hydrothermal method and high temperature alkali activation. The N,S-CSs(900)-10%-OH exhibited excellent catalytic performance for the degradation of oxytetracycline (OTC). The degradation rate was 95.9% in 60 min, and the reaction equilibrium rate constant was 0.0735 min(-1) (k(0-15) min). The synergistic effect of adsorption-promoting degradation was demonstrated in the removal process of OTC. The excellent adsorption capacity of N,S-CSs(900)-10%-OH ensured the efficient oxidation of OTC. N,S-CSs(900)-10%-OH reduced the activation energy of the OTC degradation reaction (Ea=18.23 kJ/mol). Moreover, the pyrrolic N, thiophene S and carbon skeleton played an important role in the degradation of OTC based on density function theory, and the catalytic mechanism was expounded through radical and nonradical pathways. The active species involved in the reaction were O2(center dot-), O-1(2), SO4 center dot- and center dot OH, of which O-2(center dot-) was the primary reactive species. This study provides a new insight into the reaction mechanism for efficient treatment of organic pollutants using metal-free doped porous carbon materials.
引用
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页数:13
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