The advanced persulfate oxidation method is known for its efficiency, stability, and capacity to breakdown organic contaminants without secondary contamination. In this study, biochar derived from sludge containing iron and manganese from domestic wastewater treatment was produced via pyrolysis and utilized to activate persulfate for the degradation of benzo(a)pyrene (BaP) in sediments. Results demonstrated that biochar pyrolyzed at 800 °C for 2 hours exhibited the highest catalytic performance. Under optimal conditions: a catalyst concentration of 1 g/L, persulfate concentration of 0.4 mM, and a reaction pH of 3, BaP removal efficiency reached 99.85% after 180 min. Characterization of the biochar showed that it was rich in Fe and Mn oxides, along with functional groups such as C-O-C, C=C, and C=O, which facilitated the adsorption and catalytic degradation of BaP. Quenching experiments revealed that the degradation of BaP was driven by reactive species such as •SO₄⁻ and •OH radicals, as well as singlet oxygen (¹O₂). The integration of radical dand non-radical pathways was essential for effective BaP removal. This research presents an innovative method for managing polycyclic aromatic hydrocarbons (PAHs) contamination in sediments by utilizing sludge-derived biochar in conjunction with activated persulfate.
Wang et al. (Tue,) studied this question.