Abstract
Catalytic activation of peroxymonosulfate (PMS) for purifying organic wastewater has been widely studied. CoSe microcubes were prepared by a facile one-step ions exchange method, which exhibited efficient redox reactions on account of the 3d configuration of Co2+ in combination with Se. Required only 1 min, 20 mg/L PhH (Phenazopyridine Hydrochloride) was decomposed completely by CoSe-10/PMS under UV–Visible light. The influence of Se ratio, pH, temperature, PMS dosage, catalyst loading and inorganic ion on PhH degradation was investigated. The degradation efficiencies of PhH by CoSe-10/PMS in tap water, river-water and reservoir water were evaluated, all of the removal efficiencies were higher than 95%. In addition, the 1O2, h+, O2·−, ·OH and SO4·− were verified in reaction by the electron paramagnetic resonance (EPR) experiments and scavenging test. After four runs, the removal efficiency of CoSe-10 was declined from 97.40 to 95.80%. Moreover, the possible cleavage paths of PhH were firstly analyzed with HPLC-MS. This work presents a strategy to prepare CoSe-10 photocatalyst with remarkable photocatalytic performance for the removal of PhH in water.
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Funding
This work was supported by the Ningxia Natural Science Foundation Project (Grant No. 2021AAC03242) and the Engineering Research Center of Liupanshan (Grant No. HGZD22-07). The Key Research Plan Projects of Ningxia (Grant No. 2021BEB04003).
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All the persons have made substantial contributions to the work reported. The first draft of the manuscript was written by ZLL, SYY and XNQ. Material preparation was performed by SYY. Data processing was performed by SYY, XRL, SL and ZRZ. Writing—Reviewing was performed by SYY and ZQW, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Li, Z., Yuan, S., Liu, X. et al. CoSe as highly efficient catalyst for photo-assisted activation of peroxymonosulfate for rapid degradation of phenazopyridine hydrochloride. J Mater Sci: Mater Electron 34, 1378 (2023). https://doi.org/10.1007/s10854-023-10781-4
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DOI: https://doi.org/10.1007/s10854-023-10781-4