4.6 Article

Degradation of methylene blue in liquid using high-voltage pulsed discharge plasma synergizing iron-based catalyst-activated persulfate

期刊

出版社

IOP Publishing Ltd
DOI: 10.1088/1361-6463/abecb1

关键词

gas– liquid discharge; iron-based catalyst; persulfate activation; methylene blue degradation; plasma characteristics

资金

  1. National Natural Science Foundation of China [11965018, 51677019, 51967018]
  2. Science and Technology Development Fund of Xinjiang Production and Construction [2019BC009]

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This study utilized high-voltage pulsed Ar gas-liquid discharge combined with iron-based catalyst-activated persulfate to degrade methylene blue in water. Comparison between Fe2+ and nano-Fe3O4 catalysts showed that the plasma process significantly enhanced MB degradation efficiency, with Fe2+ exhibiting better activation performance than Fe3O4. The synergistic mechanism and key reactive species responsible for MB degradation were explored through various experiments, demonstrating the potential of plasma-assisted catalytic degradation.
In this work, high-voltage pulsed Ar gas-liquid discharge synergizing iron-based catalyst-activated persulfate (PS) was employed to degrade methylene blue (MB) in water. The catalytic performances of two types of iron-based catalysts, namely the homogeneous catalyst Fe2+ and the heterogeneous catalyst nano-Fe3O4, were compared. Correspondingly, the plasma gas temperature and excited species were calculated and diagnosed using optical emission spectra. It was found that the introduced plasma process significantly enhanced the degradation efficiency of MB by the PS/Fe2+ and the PS/Fe3O4 systems. After 20 min of treatment, the MB degradation efficiency reaches 97.5% and 83.1% in the hybrid plasma/PS/Fe2+ and plasma/PS/Fe3O4 systems, respectively, which is 37.9% and 35.6% higher than that in the PS/Fe2+ and PS/Fe3O4 systems. The synergistic mechanism and key reactive species responsible for MB degradation in hybrid plasma/PS/Fe2+ and plasma/PS/Fe3O4 were explored using the addition of radical scavengers and control experiments under various conditions. The homogeneous catalyst Fe2+ exhibits better activation performance in PS and plasma than that of the heterogeneous catalyst nano-Fe3O4.

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