Experimental and theoretical study of kinetic and mechanism of hydroxyl radical-mediated degradation of sulfamethazine
2020
Zheng, Xie | Chen, Shijie | Gao, Lingwei | Liu, Yucheng | Shen, Fenghua | Liu, Hui
Hydroxyl radical (•OH)-based advanced oxidation technologies (AOTs) is an effective and clean way to remove sulfonamide antibiotics in water at ambient temperature and pressure. In this study, we systematically investigated the degradation kinetics of sulfamethazine (SMT) by •OH with a combination of experimental and theoretical approaches. The second-order rate constant (k) of SMT with •OH was experimentally determined to be 5.27 ± 0.06 × 10⁹ M⁻¹ s⁻¹ at pH 4.5. We also calculated the thermodynamic and kinetic behaviors for the reactions by density functional theory (DFT) using the B3LYP/6-31G*. The results revealed that •OH addition pathways at the methylene (C4) site on the pyridine ring and the ortho sites (C12 and C14) of the amino group on the benzene ring dominate the reaction, especially C14 site on the benzene ring accounted for 43.95% of SMT degradation kinetics. The theoretical k value which was calculated by conventional transition state theory is 3.96 × 10⁹ M⁻¹ s⁻¹, indicating that experimental observation (5.27 ± 0.06 × 10⁹) is correct. These results could further help AOTs design in treating sulfonamide during wastewater treatment processes.
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