Degradation of Acetaminophen via UVA-induced advanced oxidation processes (AOPs). Involvement of different radical species: HO , SO4− and HO2/O2−

International audience; In this work, UVA radiation that is part of solar light is taken as the irradiation source and radicals (HOradical dot, SO4radical dot− and HO2radical dot/O2radical dot−) are generated through activation of hydrogen peroxide (H2O2), sodium persulfate (Na2S2O8) and Bismuth catalyst (BiOCl), respectively. The distinguished performance in removing acetaminophen (ACTP), a model pharmaceutical pollutant, by these three radicals was compared for the first time. Effect of pH, halide ions concentration and interfacial mechanism have been investigated in detail. Interestingly, results show that heterogeneous UVA/BiOCl process has higher degradation efficiency than homogeneous UVA/H2O2 and UVA/Na2S2O8 systems whatever the solution’s pH. To explain these results, second order reaction rate constant (kradical, ACTP) have been determined with laser flash photolysis (LFP) or radical scavenging experiments. The strongly interfacial-depended HO2radical dot/O2radical dot− radicals have the lowest second order rate constant with ACTP but highest steady state concentration. BiOCl is much easier activated by UVA, and outstanding ACTP mineralization can be achieved. Combination of BiOCl and Na2S2O8 exhibits synergistic effects rather than antagonism effects with H2O2. This study highlights the relative effective utilization of solar light through interfacial directed BiOCl photocatalysis and its synergistic effects with traditional oxidants.