Enhanced activation of peroxymonosulfate by nitrogen-doped graphene/TiO2 under photo-assistance for organic pollutants degradation: Insight into N doping mechanism

被引:44
作者
Zhao, Ya [1 ]
Wang, Guanlong [1 ]
Li, Lujie [1 ]
Dong, Xiaoli [1 ]
Zhang, Xiufang [1 ]
机构
[1] Dalian Polytech Univ, Sch Light Ind & Chem Engn, Dalian 116034, Peoples R China
基金
中国国家自然科学基金;
关键词
Peroxymonosulfate activation; Photo-assistance; Nitrogen doped graphene; TiO2; Bisphenol A; ADVANCED OXIDATION; POROUS CARBON; EFFICIENT DEGRADATION; PERFORMANCE; SULFATE; RADICALS; OXIDE; PHOTOCATALYSIS; GENERATION; REDUCTION;
D O I
10.1016/j.chemosphere.2019.125526
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Production of sulfate radical from peroxymonosulfate (PMS) activation by carbon-based catalysts is a promising strategy to degrade pollutants. However, the electron-transfer ability of carbon catalysts, which is critical in PMS activation, still needs to be improved. In this study, a novel photo-assisted PMS activation system (PPAS) was constructed on a nitrogen-doped graphene/TiO2 (NG/TiO2), in which the photogenerated electrons excited from TiO2 could be utilized by NG for enhanced PMS activation on it. Moreover, the N content was varied to firstly investigate the role of N doping on PPAS. Under photo-assistance, the NG/TiO2 displayed significantly enhanced PMS activation for removal of organic pollutants. 100% bisphenol A (BPA) can be removed within 1 h. The results show that the degradation kinetic constant of BPA by the NG/TiO2 PPAS was 24 times higher than that under PMS alone, and was 1.4 times higher than that of rGO/TiO2 PPAS. The singlet oxygen (O-1(2)) and sulfate radical (SO4 center dot-) were the main reactive species in PPAS. The outstanding performance of NG/TiO2 system was ascribed to the two main reasons: on one hand, the N doping decreased the schottky barrier formed between NG and TiO2, which favored the electron transfer from TiO2 to NG. On the other hand, the N doping enhanced the adsorption and electron-transfer ability of NG towards PMS. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:10
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