Sonolytic degradation of benzophenone-3 in water matrices: Reaction mechanism, transformation products,
Neus Lopez-Arago1, Alexandra A Ioannidi2, Maria Antonopoulou3
1Chemical Engineering Department, University of Patras, Caratheodory 1, University Campus, GR-26504 Patras, Greece; Chemical Engineering Department, Universidad Autónoma de Madrid, Ctra. Colmenar km 15, 28049 Madrid, Spain.
Abstract:
The degradation of the UV filter benzophenone-3 (BP-3) by low-frequency ultrasound was investigated in different aqueous matrices. BP-3 sonodegradation followed pseudo-first-order kinetics, achieving >97 % removal of 500 μg L-1 of BP-3 within 120 min in ultrapure water (UPW), using a 20 kHz ultrasound horn at 71 W L-1. Varying the initial pH from 3 to 6 and 9 had only a slight effect on the process efficacy, with corresponding kinetic constant rates of 0.029, 0.030, and 0.041 min-1, respectively. Experiments conducted in different water matrices showed a decrease in the apparent rate constant from 0.030 min-1 in ultrapure water to 0.027 min-1 in drinking water and 0.015 min-1 in secondary effluent. Similarly, the presence of 250 mg L-1 of chlorides or 10 mg L-1 of humic acid reduced the degradation rate to 0.016 and 0.020 min-1, respectively, while 250 mg L-1 of hydrogen carbonate had no significant effect. The presence of nano- or microplastics led to a moderate decrease in BP-3 removal, particularly with smaller particles. Electron paramagnetic resonance (EPR) spectroscopy confirmed that fewer hydroxyl radicals were available in the presence of plastics. Twelve transformation products were identified by UHPLC-TOF/MS, resulting mainly from hydroxylation, demethylation, and ring-cleavage. According to the ecotoxicity analysis using the ECOSAR software, most of the transformation products were less toxic than the parent compound, enhancing the environmental feasibility of the process.
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