Heterogeneous transition metal activation of peroxymonosulfate (PMS)-based advanced oxidation processes is limited by low cycling efficiency, secondary contamination, and high toxicity. In this study, a non-transition metal porous nano-MgO catalyst from natural dolomite was synthesized and PMS activation was performed to degrade tetracycline (TC). The nano-MgO/PMS system could achieve TC degradation of 88.09 % within 20 min under the optimum parameters (nano-MgO dosage of 0.2 g·L−1, PMS concentration of 0.3 mM), exceeding the efficiency of the PMS-alone system (11.66 %) by 7-fold, which was related to large specific surface area (41.19 m2·g−1) and defect structure of porous nano-MgO catalysts. As revealed by the quenching tests and electron paramagnetic resonance (EPR) analysis, different from transition metal activation PMS where radicals are generated, singlet oxygen (1O2) was essential in the nano-MgO/PMS oxidation process. Notably, the density functional theory (DFT) calculations demonstrated that nano-MgO with surface hydroxyl groups and oxygen vacancies exhibited the longer O-O bond length (1.47 Å), stronger adsorption energy of PMS (-4.07 eV), and faster electron transfer (0.91 e) than the only nano-MgO with surface hydroxyl groups, proving the surface hydroxyl groups and oxygen vacancies active sites in nano-MgO could synergistically mediate the PMS activation process. Furthermore, the proposed three TC degradation pathways and the toxicity evaluation of intermediates suggested that nano-MgO/PMS system have good ecological safety. This work offers an innovative approach for the cost-effective preparation of porous magnesium oxide with highly efficiency, offering a new perspective for understanding the PMS activation mechanism induced by non-transition metal.
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