Facile synthesis of Mn, Ce co-doped g-C3N4 composite for peroxymonosulfate activation towards organic contaminant degradation

被引:74
作者
Lai, Cui [1 ,2 ]
Yan, Huchuan [1 ,2 ]
Wang, Dongbo [1 ,2 ]
Liu, Shiyu [1 ,2 ]
Zhou, Xuerong [1 ,2 ]
Li, Xiaopei [1 ,2 ]
Zhang, Mingming [1 ,2 ]
Li, Ling [1 ,2 ]
Fu, Yukui [1 ,2 ]
Xu, Fuhang [1 ,2 ]
Yang, Xiaofeng [1 ,2 ]
Huo, Xiuqin [1 ,2 ]
机构
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Hunan Univ, Key Lab Environm Biol & Pollut Control, Minist Educ, Changsha 410082, Peoples R China
基金
湖南省自然科学基金; 中国国家自然科学基金;
关键词
Peroxymonosulfate; Mn-N bond; CeO2; Superoxide radical; Singlet oxygen; Z-SCHEME HETEROJUNCTION; HETEROGENEOUS CATALYST; OXIDATION; OXYGEN;
D O I
10.1016/j.chemosphere.2021.133472
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Peroxymonosulfate (PMS)-based advanced oxidation processes for wastewater treatment have received extensive attention in the past years. Here, a novel Mn, Ce co-modified g-C3N4 (MnCe-CN) composite was successfully synthesized by one-step pyrolysis for activating PMS. The physical and chemical characterization of MnCe-CN/PMS was conducted, indicating that Mn and Ce were evenly distributed on g-C3N4 and existed in the form of Mn-N structure and CeO2, respectively. The MnCe-CN/PMS system could effectively degrade pollutants such as acetaminophen (ACT), methylparaben (MeP), p-nitrophenol (PNP), and 2,4-dichlorophenol (2,4-DCP). Among them, 2,4-DCP could be rapidly degraded, reaching 100% within 30 min. The masking experiments and electrochemical testing results revealed that 2,4-DCP was degraded via superoxide radicals (O-2(-)), singlet oxygen (O-1(2)), and electron transfer path. The cyclic experiments and real water treatment experiments testified that the oxidative system had excellent stability and applicability. This study provides a facile synthetic method to fabricate bimetallic co-modified g-C3N4 for the enhancement of PMS activation.
引用
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页数:11
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