Role of interfacial electron transfer reactions on sulfamethoxazole degradation by reduced nontronite activating H_(2)O_(2)

It has been documented that organic contaminants can be degraded by hydroxyl radicals(•OH)produced by the activation of H2O2 by Fe(II)-bearing clay.However,the interfacial electron transfer reactions between structural Fe(Ⅱ)and H_(2)O_(2) for•OH generation and its effects on contaminant remediation are unclear.In this study,we first investigated the relation between•OH generation sites and sulfamethoxazole(SMX)degradation by activating H2O2 using nontronite with different reduction extents.SMX(5.2–16.9μmol/L)degradation first increased and then decreased with an increase in the reduction extent of nontronite from 22% to 62%,while the•OH production increased continually.Passivization treatment of edge sites and structural variation results revealed that interfacial electron transfer reactions between Fe(Ⅱ)and H2O2 occur at both the edge and basal plane.The enhancement on basal plane interfacial electron transfer reactions in a high reduction extent rNAu-2 leads to the enhancement on utilization efficiencies of structural Fe(Ⅱ)and H_(2)O_(2) for•OH generation.However,the•OH produced at the basal planes is less efficient in oxidizing SMX than that of at edge sites.Oxidation of SMX could be sustainable in the H_(2)O_(2)/rNAu-2 system through chemically reduction.The results of this study show the importance role of•OH generation sites on antibiotic degradation and provide guidance and potential strategies for antibiotic degradation by Fe(Ⅱ)-bearing clay minerals in H2O2-based treatments.