Effectiveness and degradation pathways of bisphenol A (BPA) initiated by hydroxyl radicals and sulfate radicals in water: Initial reaction sites based on DFT prediction

Bisphenol A (BPA), one of the widely known endocrine-disrupting chemicals, can be effectively degraded by advanced oxidation processes in water because of the powerful reactive oxygen species. In this study, Fenton, UV/Fenton, and metal ion/peroxymonosulfate (PMS) processes were compared to investigate BPA degradation efficiency and pathways initiated by hydroxyl radicals and sulfate radicals. In contrast to the Fenton system, which only degraded 60% of BPA within 15 min, the UV/Fenton system could degrade greater than 80% of BPA, because more hydroxyl radicals (center dot OH) were generated under the reduction of Fe3+ to Fe2+. The optimized pa-rameters of the UV/Fenton system were as follows: 8 mu mol/L of Fe2+, 80 mu mol/L of H2O2, and a pH value of 3.0. As for the metal ion/PMS system, the BPA degradation efficiency was closely associated with the applied metal ions, and the order was as follows: Co2+/PMS (-100%) > Fe2+/PMS (-80%) > Cu2+/PMS (-79%). The degradation pathways of BPA were theoretically interpreted through density functional theory prediction and degradation products during various processes. Two major initial reaction sites (4C and 6C) for center dot OH initiated using the UV/Fenton system and one initial reaction site (4C) for sulfate radicals (SO4 center dot-) using the metal ion/PMS system were recognized for BPA degradation processes. The degradation products by center dot OH showed a larger average molecular weight than those by SO4 center dot-. These studies are instructive for the application of different advanced oxidation systems in the treatment process of BPA in wastewater.