The critical impacts of pyrochar during 2,4,6-trichlorophenol photochemical remediation process: Cooperation between...

The widespread use of polychlorophenols poses enormous environmental challenges. Biochar has the potential to accelerate the transformation of polychlorophenols. But the biochar-triggered photochemical decomposition mechanism of polychlorophenols still remains unclear. Herein, the photochemical behavior of pyrochar was comprehensively investigated in 2,4,6-trichlorophenol (TCP) remediation. Researches revealed that persistent free radicals (PFRs) and oxygenated functional groups (OFGs) on the surface of pyrochar cooperatively promoted ROS generation for TCP degradation. PFRs performed a key role of electron-donating and energy transfer in ROS conversion, especially in the activation of H₂O₂ into •OH. The hydroxyl groups of photosensitive components of pyrochar were photo-excited and provided electrons for enhanced ROS formation as well. With photogenerated ROS involved, more TCP was decomposed through dechlorination under light irradiation than that in the dark, in which ¹O₂, •OH, and •O₂^- were the dominant active species. During this process, stronger light intensities (3 W/m²) and shorter light wavelengths (400 nm) can provide more energy for the activation of PFRs and OFGs, promoting the decomposition of TCP. This work casts a new light on the environmental roles of pyrochar in the photochemical removal of polychlorophenol pollutants.