Tuning of Persulfate Activation from a Free Radical to a Nonradical Pathway through the Incorporation of Non-Redox Magnesium Oxide

• Published in: Environmental science & technology Vol. 54; no. 4; pp. 2476 - 2488
• Main Authors: Jawad, Ali, Zhan, Kun, Wang, Haibin, Shahzad, Ajmal, Zeng, Zehua, Wang, Jia, Zhou, Xinquan, Ullah, Habib, Chen, Zhulei, Chen, Zhuqi
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 18.02.2020
• Subjects: Anions; Catalysts; Copper; Degradation; Electron transfer; Electron Transport; Free radicals; Heavy metals; Intermediates; Iron oxides; Kinetics; Magnesium; Magnesium Oxide; Metals; Organic matter; Oxidation; Oxidation process; Oxidation-Reduction; Peroxides; Phenols; Pollutant removal; Pollutants; pollution control; Reaction kinetics; Superconductors (materials); technology; thermodynamics
• ISSN: 0013-936X; 1520-5851; 1520-5851
• DOI: 10.1021/acs.est.9b04696

Nonradical-based advanced oxidation processes for pollutant removal have attracted much attention due to their inherent advantages. Herein we report that magnesium oxides (MgO) in CuOMgO/Fe3O4 not only enhanced the catalytic properties but also switched the free radical peroxymonosulfate (PMS)-activated process into the 1O2 based nonradical process. CuOMgO/Fe3O4 catalyst exhibited consistent performance in a wide pH range from 5.0 to 10.0, and the degradation kinetics were not inhibited by the common free radical scavengers, anions, or natural organic matter. Quantitative structure–activity relationships (QSARs) revealed the relationship between the degradation rate constant of 14 substituted phenols and their conventional descriptor variables (i.e., Hammett constants σ, σ–, σ+), half-wave oxidation potential (E 1/2), and pK a values. QSARs together with the kinetic isotopic effect (KIE) recognized the electron transfer as the dominant oxidation process. Characterizations and DFT calculation indicated that the incorporated MgO alters the copper sites to highly oxidized metal centers, offering a more suitable platform for PMS to generate metastable copper intermediates. These highly oxidized metals centers of copper played the key role in producing O2 •– after accepting an electron from another PMS molecule, and finally 1O2 as sole reactive species was generated from the direct oxidation of O2 •– through thermodynamically feasible reactions.