Sunlight-driven degradation of diethyl phthalate via magnetically modified biochar catalysts in water: Internal electron transfer mechanism
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Updated: Sep 29, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Kexin Yi1, Ming Lei2, Liang Peng2
1College of Resources and Environment, Hunan Agricultural University, Changsha, 410128, PR China; College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, PR China.
Abstract:
This study presents a one-step synthetic approach for magnetic biochar (MBC) photo-degradation of diethyl phthalate (DEP). The results showed that MBC exhibited better catalytic property for DEP degradation than BC, and its catalytic performance was influenced by the amount of Fe doping. Electron paramagnetic resonance (EPR), quenching experiments, and chemical probe studies confirmed the presence of persistent free radicals (PFRs), hydroxyl radicals (·OH), and superoxide anion radical (·O2-) in both of BC and MBC. Solar light promoted the formation of PFRs in BC system, which transferred electrons to oxygen to form ·O2-, thus yielding ·OH. On the other hand, electron transfer occurred between PFRs and Fe3+ for MBC, Fe2+ played an important role in activation of O2 and ·O2- production. Subsequently, photo-Fenton reaction was primarily responsible for ·OH formation. This work compared the different generation pathways for ROS between BC and MBC and provides new insight into the possible mediatory roles of BC in O2 activation under solar light by transition metals.
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