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Chinese Journal of Applied Ecology ›› 2020, Vol. 31 ›› Issue (1): 333-339.doi: 10.13287/j.1001-9332.202001.035

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Mechanism underlying photocatalyzed degradation of methyl orange by layered black phosphorus

HAN Ya-qi1,2, LEI Lei1,2, YANG Chen3, ZHANG Si-yu1*, ZHAO Qing1, ZHANG Xue-jiao1   

  1. 1Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, China;
    2 University of Chinese Academy of Sciences, Beijing 100049, China;
    3School of Resources and Civil Engineering, Northeastern University, Shenyang 110004, China
  • Received:2019-05-01 Online:2020-01-15 Published:2020-01-15
  • Contact: E-mail: syzhang@iae.ac.cn
  • Supported by:
    This work was supported by the National Natural Science Foundation of China (21607165, 41603120,41703107,418773891), the National Key Research and Development Program of China (2016YFD0800305), the Youth and Middle-aged Science and Technology Innovation Talent Team of Shenyang (RC170020) and the Youth Innovation Promotion Association of China (2017242).

Abstract: A large amount of azo dye wastewater is discharged into the environment, with serious risks to ecosystems and human health. Therefore, the development of treatment technology of azo dye wastewater was of practical significance. Photocatalytic methods showed promising application prospects due to easy to implement and effective. In this study, layered black phosphorus nanosheet (LBP) was used as a catalyst through liquid phase exfoliation method. Methyl orange (MO) was employed as a model azo dye to investigate the catalytic mechanism of LBP. The dominant transient species involved in the photocatalytic reaction was probed by quenching and fluorescence probe experiments. Degradation pathways of MO were proposed according to degradation products identified by the liquid chromatography-mass spectrometry. The results showed that degradation rate (kobs) of MO at acidic condition (pH=3.0) or alkaline condition (pH=11.0) was higher than that at neutral condition (pH=7.0). Degradation pathways of MO included that the azo bond was attacked by hydroxyl radicals (·OH) photogenerated by the LBP, and the intermediate products were further oxidized by ·OH to produce N, N-dimethyl-4-(2-p-phenylmethylhydrazine) aniline, 2-(dimethylamino)-5-((4(dimethylamino) phenyl) diazenyl) phenol and N, N-dimethyl-4-nitroaniline.