4.7 Article

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

期刊

CHEMOSPHERE
卷 244, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2019.125526

关键词

Peroxymonosulfate activation; Photo-assistance; Nitrogen doped graphene; TiO2; Bisphenol A

资金

  1. Natural Science Foundation of China [21577008, 21878031]
  2. National Natural Science Foundation of China [21906013]
  3. Natural Science Foundation of Liaoning Province of China [20180550678]
  4. Open Foundation of Key Laboratory of Industrial Ecology and Environmental Engineering, MOE [KLIEEE-18-08]

向作者/读者索取更多资源

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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