Co@MoS2 Nanocatalyst: Enhanced Activation of Peroxymonosulfate for Effective Degradation of Sulfadiazine

Author:

Wang Sai12ORCID,Wu En-Ni1ORCID,Meng Liang3ORCID,Wang Zhen-Jun4ORCID,Wang Tuan-Tuan12ORCID

Affiliation:

1. State Key Laboratory of Marine Resource, Utilization in South China Sea, Hainan University, Haikou 570228, P. R. China

2. School of Ecology and Environment, Hainan University, Haikou 570228, P. R. China

3. University of Shanghai for Science and Technology, Shanghai 200093, P. R. China

4. School of Environmental and Geographical Sciences, Shanghai Normal University, Shanghai 200233, P. R. China

Abstract

To improve the activation efficiency of PMS to efficiently degrade antibiotic sulfadiazine (SD), herein, a Co@MoS2 catalyst was prepared by a one-step hydrothermal process. The unique petal-like structure of MoS2 enables the transition metal Co to achieve high dispersion and avoid agglomeration. Mo(IV) and unsaturated S accelerate the electron transfer between Co[Formula: see text] and Co[Formula: see text] to improve the cycling efficiency and thus realize the efficient activation of PMS. The results of active substance quenching experiment and ESR analysis show that the main active substance for the efficient degradation of SD by Co@MoS2 is the non-radical 1O2, while the other three radicals [Formula: see text], ⋅OH and [Formula: see text] contribute significantly to the efficient degradation of SD. And after 5 cycles, the degradation could still be as high as 90%. The strong consolidation of Co on the petal-shaped sheet of MoS2 ensures the stability of Co@MoS2 catalyst.

Funder

Key R&D Program of Hainan Province

National Key R&D Program of China

National Natural Science Foundation of China

Natural Science Foundation of Hainan Province

Open Project of State Key Laboratory of Marine Resource Utilization in South China Sea

Hainan University Start-up Funding for Scientific Research

Publisher

World Scientific Pub Co Pte Ltd

Subject

Condensed Matter Physics,General Materials Science

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