pH-Self-Buffering and Flocculation-Enabled Nonradical Oxidation via Magnesium Hydroxide-Activated Peroxymonosulfate for Selective Organic Pollutant Degradation

Peroxymonosulfate (PMS)-based advanced oxidation is often hindered by pH instability and the lack of post-reaction separation. Herein, commercial magnesium hydroxide (Mg(OH)₂) is introduced as a multifunctional catalyst to address these limitations. Mg(OH)₂ effectively catalyzed PMS decomposition via a nonradical pathway dominated by singlet oxygen (¹O₂) generation, achieving rapid and complete degradation of electron-rich pollutants like bisphenol A (BPA) within 40 min. The system exhibits exceptional pH self-regulation, stabilizing the solution at ~9.8 and maintaining high efficiency across an initial pH range of 3-11. Mechanistic studies confirm ¹O₂ as the primary reactive species with a steady-state concentration of 1.67 × 10^-12 M. The catalyst demonstrates strong resistance to common anions and humic acid, along with excellent stability over four cycles. Furthermore, Mg(OH)₂ enables in situ flocculation and removal of degradation products. This work highlights Mg(OH)₂ as an efficient, stable, and multifunctional activator, offering a integrated strategy for practical wastewater treatment.