摘要
The application of MoS 2 to enhance Co(II)/peroxymonosulfate (Co(II)/PMS) system for organic pollutants degradation was developed, and the mechanism for pH dependent catalytic activity in the MoS 2 co-catalyzed Co(II)/PMS processes was systematically investigated. It was found that MoS 2 presented enhancement effect for Co(II)/PMS system in the tested pH range from 4.0 to 7.0, especially at pH 5.5 and 6.0. The pseudo first order reaction rates for Rhodamine B (RhB) degradation in MoS 2 -Co 2+ /PMS system at pH 5.5 and 6.0 were 3.2 and 1.8 times that in Co 2+ /PMS system (Co 2+ 2 μmol L −1 , PMS 0.2 mmol L −1 , MoS 2 0.5 g L −1 ). The redox recycle of Co 3+ /Co 2+ was promoted by Mo(IV) and S(-II) on MoS 2 surface and regenerated Co 2+ induced homogeneous activation of PMS for the robust production of free radical with the major of hydroxyl radicals . Increasing MoS 2 dosage, Co 2+ and PMS concentration can linearly raise RhB degradation rate in MoS 2 -Co(II)/PMS system. Moreover, MoS 2 exhibited excellent catalytic and chemical stability in recyclability and reuse for catalytic decontamination in MoS 2 -Co(II)/PMS system. This work gains new insight into the enhancement effect of MoS 2 in the meal ions/PMS system, and provides a high performance wastewater treatment process of Co(II)/PMS at low concentrated Co 2+ .
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