Biochar (BC)-activated peracetic acid (PAA)-based advanced oxidation processes (AOPs) were increasingly considered as cost-efficient and eco-friendly water treatment technologies for the removal of organic pollutants. However, the specific role of intrinsic carbon, nitrogen species and structure properties played in activation mechanism is still vague. In this study, the waste tea residues-based biochar (WTBC) was prepared by thermal carbonization and applied to activate PAA for the degradation of bisphenol A (BPA). The product carbonized at 800 °C (WTBC800) possessed larger specific surface area (342.57 m2/g), more abundant porous structure and massive defects state (ID/IG = 3.53), and exhibited a superior activation performance with 83.7% BPA removal within 120 min. Adsorption and non-radical oxidation pathways e.g., the mediated electron transfer process (ETP) and singlet oxygen (1O2) generation were evidenced to play the dominant roles in the BPA degradation through the formation of metastable complex WTBC-PAA*. The graphitic carbon, functional nitrogen species, defects structure and persistent free radicals (PFRs) in WTBC were proposed to contribute to the activation of PAA. Overall, relatively higher dosages of WTBC (0–0.5 g/L) and PAA (0–1.5 mM) facilitated the BPA degradation. The solution pH and water matrix (e.g., Cl−, NO3−, HCO3− and SO42−) presented a negligible effect on the BPA degradation in WTBC/PAA system. This study not only proposes a sustainable approach for organic pollutants removal in wastewater, but also promotes the resource re-utilization of agricultural waste.
Zhu et al. (Sun,) studied this question.