Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
641875 | Separation and Purification Technology | 2013 | 7 Pages |
In this study, core–shell Fe–Fe2O3 nanostructures (FNs) were used to effectively activate sodium persulfate (Na2S2O8) to induce sulfate radicals (SO4-) oxidation of methyl orange (MO) in aqueous solution (FNs/Na2S2O8). In this FNs/Na2S2O8 system, an enhanced degradation of MO was achieved in comparison with the Fe2+/Na2S2O8Fe2+/Na2S2O8 system using ferrous ions as persulfate activator under neutral pH condition. An acid pH and a high persulfate to FNs molar ratio (Na2S2O8:FNs) were favorable to the MO oxidation in the FNs/Na2S2O8 process. We characterized the prepared FNs and the used FNs during the FNs/Na2S2O8 process via X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) systematically. On the basis of the degradation and characterization results, we proposed a mechanism for the degradation of MO in the FNs/Na2S2O8 process, which involved in situ homogenous and heterogeneous activation of persulfate simultaneously.
► FNs could activate Na2S2O8 to generate sulfate radicals effectively. ► FNs/Na2S2O8 system showed an enhanced activity on degradation of MO. ► Sulfate radicals were responsible for degradation of MO in the FNs/Na2S2O8 system.