Activation of H2O2/PDS/PMS by Iron-Based Biochar Derived from Fenton Sludge for Oxidative Removal of 2,4-DCP and As(III)

In this study, the catalytic performance of the Fenton sludge iron-based biochar catalyst (Fe@BC700), generated during the Fenton process, was investigated regarding its role in oxidizing 2,4-dichlorophenol (2,4-DCP) and As(III) from aqueous solutions in peroxymonosulfate (PMS), peroxydisulfate (PDS), and hydrogen peroxide (H2O2) systems. The characteristics of the as-prepared catalyst, operational parameters of H2O2/UV/Fe@BC700, PDS/UV/Fe@BC700, and PMS/UV/Fe@BC700 systems, and the kinetics of 2,4-DCP degradation were evaluated. Fe@BC700 exhibited excellent capabilities for activating persulfate and an outstanding oxidant performance as a heterogeneous photocatalyst under UV irradiation. Among the tested systems, PMS/UV/Fe@BC700 showed the highest oxidation capabilities for both 2,4-DCP and As(III) within 40 min. The total organic carbon (TOC) removal efficiency for 2,4-DCP was up to 95.9% in the PMS/UV/Fe@BC700 system. The presence of free radicals in the PMS/PDS system included ·OH, SO4·−, and ·O2−, which were facilitated by both UV irradiation and the catalyst. The by-products generated during the PMS/UV/Fe@BC700 treatment were identified via LC-MS analysis, which showed that catalytic degradation substantially reduced the chronic and acute toxicity of 2,4-DCP intermediates. The present study demonstrates that the iron-based biochar derived from Fenton sludge exhibited remarkable persulfate activation capabilities and was highly effective in removing 2,4-DCP and As(III).