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 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
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. |
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ISSN: | 1096-0953 |
DOI: | 10.1016/j.envres.2020.109665 |