二苯甲酮
降级(电信)
机制(生物学)
环境化学
化学
转化(遗传学)
光化学
物理
生物化学
工程类
量子力学
电信
基因
作者
Neus Lopez-Arago,Alexandra Α. Ioannidi,Μαρία Αντωνοπούλου,Macarena Muñoz,Zacharias Frontistis,Zahara M. de Pedro,Dionissios Mantzavinos,José A. Casas
标识
DOI:10.1016/j.scitotenv.2025.180087
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI