The efficient degradation of sulfisoxazole by singlet oxygen ( 1 O 2 ) derived from activated peroxymonosulfate (PMS) with Co 3 O 4 -SnO 2 /RSBC

Co O -SnO /rice straw biochar (RSBC) was prepared for the first time via calcining oxalate precipitation precursor dispersed on the surface of RSBC and used as a catalyst for activating PMS to degrade sulfisoxazole (SIZ). The results demonstrated that Co O -SnO /RSBC possessed much better catalytic...

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Veröffentlicht in:Environmental research 2020-05, Vol.187, p.109665
Hauptverfasser: Liu, Li, Li, Yunong, Li, Wei, Zhong, Ruixue, Lan, Yeqing, Guo, Jing
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Sprache:eng
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Zusammenfassung:Co O -SnO /rice straw biochar (RSBC) was prepared for the first time via calcining oxalate precipitation precursor dispersed on the surface of RSBC and used as a catalyst for activating PMS to degrade sulfisoxazole (SIZ). The results demonstrated that Co O -SnO /RSBC possessed much better catalytic performance than Co O , Co O -SnO , Co O /RSBC, and SnO /RSBC, which is ascribed to the synergy of Co O , SnO and RSBC. Approximately 98% of SIZ (50 mg/L) was decomposed by PMS (1 mmol/L) activated with Co O -SnO /RSBC (0.1 g/L) within 5 min. The optimal degradation efficiency of SIZ was realized at the initial pH 9. Co O -SnO /RSBC also displayed remarkable stability and reusability, and the degradation rate of SIZ maintained over 90% even after the fifth recycle run. The electron paramagnetic resonance (EPR) technique and quenching experiments proved singlet oxygen ( O ) to be the main reactive oxygen species (ROS) responsible for the SIZ decomposition in the Co O -SnO /RSBC/PMS system. On the basis of the characterization analysis, the identification of the ROS and the SIZ degradation products, the possible mechanism and pathways of the SIZ degradation by a combination of PMS and Co O -SnO /RSBC were further proposed. This study provides not only a new insight into non-radical mechanism for the heterogeneous activating PMS over Co O -SnO /RSBC to degrade organic pollutants but also an eco-friendly synthetic route for exploring novel and efficient catalysts.
ISSN:1096-0953
DOI:10.1016/j.envres.2020.109665