Effective peroxymonosulfate activation by natural molybdenite for enhanced atrazine degradation: Role of sulfur vacancy, degradation pathways and mechanism

In this study, natural molybdenite (MoS₂) was applied to activate peroxymonosulfate (PMS) for the removal of atrazine (ATZ) and its degradation mechanism was investigated. Molybdenite exhibits superior catalytic performance. The best condition for atrazine degradation efficiency (>99%) was obtained with molybdenite concentration of 0.4 g/L, PMS concentration of 0.1 mM, and ATZ concentration of 12 μM within 10 min under experimental conditions. Electron paramagnetic resonance (EPR) test and chemical probe test further proved that HO^• and SO₄^•- played important roles in the molybdenite/PMS system, and SO₄^•- was dominant. Meanwhile, Electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) tests showed that sulfur vacancies and edge sulfur played important roles in the system. Edge sulfur was conducive to Mo⁴⁺ exposure, while sulfur vacancy facilitated electron transfer and reduced Mo⁶⁺ back to Mo⁴⁺. Combined with DFT calculation, the role of sulfur in the degradation process was verified. Besides, five ATZ degradation pathways were proposed. Finally, the degradation ability of the molybdenite/PMS system for different pollutants and in actual water bodies was also explored. This work provided ideas for exploring the degradation of organic contaminants by natural minerals.