N, S co-doped magnetic mesoporous carbon nanosheets for activating peroxymonosulfate to rapidly degrade tetracycline: Synergistic effect and mechanism

被引:93
|
作者
He, Dongdong [1 ]
Zhu, Ke [1 ]
Huang, Jin [1 ]
Shen, Yaqian [1 ]
Lei, Lele [1 ]
He, Hongmei [1 ]
Chen, Wenjin [1 ]
机构
[1] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Peoples R China
关键词
N; S co-doping; Peroxymonosulfate; Tetracycline; Singlet oxygen and electron transfer; POLLUTANTS DEGRADATION; BIFUNCTIONAL MATERIAL; ENHANCED ACTIVATION; OXIDATION; REMOVAL; PERFORMANCE; GRAPHENE; NITROGEN; WATER; CONTAMINANTS;
D O I
10.1016/j.jhazmat.2021.127569
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heteroatoms doped carbon materials are widely used in the advanced oxidation process (AOPs) to remove organic pollutants in water due to the synergies effect between different heteroatoms. In this study, a novel kind of N, S co-doped magnetic mesoporous carbon nanosheets (Fe@NS-C) was prepared by simple one-step pyrolysis. Further, the influence of doping amount of S (L-methionine) and N (melamine) on catalytic activity was studied, the optimized sample Fe@NS-C-2-12/PMS showed a satisfying degradation ( 91.07%) for high concentrations of tetracycline (80 mg/L TC) in 10 min, which was attributed to the proper ratio of S content to N content (S(at.%)/ N(at.%) = 0.2097) in the sample could better play its synergistic effect by XPS analysis. The Fe@NS-C-2-12/ PMS system also exhibited satisfactory degradation effects in a wide pH range (3-10) and the existence of inorganic ions and humic acid. Then, the degradation mechanisms were mainly through the non-radical pathway (1O2 and electron transfer) and the major active sites were pyridinic N compared to thiophene S, C--O, and FeNx. This study could inspire the design of high-performance active and low-cost heteroatomic doping nanomagnetic catalysts for PMS-based waste treatment.
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页数:14
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