1. Degradation of diclofenac sodium by peroxymonosulfate activated with a sulfur-doped chitosan ferrocarbon material: Synergistic interaction of free radical and nonfree radical pathways.
- Author
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Wu, Yajie, Zheng, Junli, Liu, Jiaxin, Lin, Qintie, Zeng, Chen, Liu, Yuxin, Luo, Hao, Luo, Yang, Pan, Jieyi, and Xie, Haijiao
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ORGANIC compounds removal (Water purification) , *CARBON content of water , *DENSITY functional theory , *RADICALS (Chemistry) , *FREE radicals - Abstract
[Display omitted] The synthesis of efficient and stable peroxymonosulfate (PMS) catalysts by doping naturally degradable and functional group-rich chitosan (CS) with nonmetallic atoms remains challenging. In this study, an environmentally friendly electron-rich S-doped CS ferrocarbon material (Fe-S-CN) was synthesized via the sol–gel method, and the resulting material exhibited excellent catalytic activity (up to 98.6 % diclofenac sodium (DCF) removal in 5 min), wide pH applicability, environmental tolerance and renewability. Moreover, Fe-S-CN synergistically activated PMS via both the radical pathway (superoxide radical (O 2 •−)) and the nonradical pathway (single-linear oxygen (1O 2) and electron transfer processes (ETP)) to efficiently mineralize DCF. O 2 •− originates from the self-decomposition of PMS, whereas 1O 2 is due to the oxidation of PMS and further conversion of O 2 •−. In addition, Fe species, graphitic N and thiophene S are the major active sites in Fe-S-CN. The susceptibility sites of DCF and its possible degradation pathways in the Fe-S-CN/PMS system were inferred in conjunction with density functional theory (DFT) calculation. The present study creates a promising scenario for the synergistic effect of easily overlooked heteroatom doping in chitosan iron–carbon materials in the removal of difficult-to-biodegrade organic matter from water bodies. [ABSTRACT FROM AUTHOR]
- Published
- 2025
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