Environment Research Institute, Shandong University, Qingdao 266237, China.
Atmospheric Chemistry Department (ACD), Leibniz-Institute for Tropospheric Research (TROPOS), Leipzig 04318, Germany.
J Hazard Mater. 2022 Apr 5;427:127941. doi: 10.1016/j.jhazmat.2021.127941. Epub 2021 Nov 27.
Benzophenone-3 (BP-3) is a widespread emerging organic pollutant. However, little is known about the synergistic effect of various reactive oxygen species (ROS) in natural waters and wastewater treatment plants on its transformation. In this study, the indirect photochemical behavior of BP-3 in the natural aquatic environments and the degradation process in the AOPs system were investigated by theoretical chemistry calculations. Besides the potential eco-toxicity effects, health effects, and bioaccumulation of the transformation products were assessed by computational toxicology. Results of transformation mechanism and kinetics showed that OH· and O are the keys to the transformation of BP-3, whereas the role of HO· and O can be ignored. AOPs based on OH· and O could lead to the rapid transformation of BP-3, while the transformation of BP-3 in natural waters is slow, and even environmental persistence can be observed. However, dissolved organic matter (DOM) promotes the indirect phototransformation of BP-3 in natural waters. A variety of transformation products are generated under the synergistic effects of ROS, HO, and O. Assessments of environmental risks indicated that the potential eco-toxicity and health effects of the main products are significantly lower than that of the parent BP-3. More importantly, low bioaccumulation of transformation products would not enlarge their eco-toxicity and health effects. This study not only gives valuable insights into the indirect phototransformation of BP-3 in natural waters but also provides theoretical support for the feasibility of BP-3 degradation in industrial wastewater by AOPs based on OH· and O.
二苯甲酮-3(BP-3)是一种广泛存在的新兴有机污染物。然而,关于天然水体和废水处理厂中各种活性氧(ROS)的协同作用对其转化的影响,人们知之甚少。在这项研究中,通过理论化学计算研究了 BP-3 在自然水生态环境中的间接光化学行为及其在 AOPs 体系中的降解过程。除了评估潜在的生态毒性效应、健康效应和转化产物的生物累积性外,还通过计算毒理学进行了评估。转化机制和动力学的结果表明,OH·和 O 是 BP-3 转化的关键,而 HO·和 O 的作用可以忽略不计。基于 OH·和 O 的 AOPs 可以导致 BP-3 的快速转化,而 BP-3 在天然水中的转化则较慢,甚至可以观察到环境持久性。然而,溶解有机物(DOM)促进了 BP-3 在天然水中的间接光转化。在 ROS、HO 和 O 的协同作用下,会生成多种转化产物。环境风险评估表明,主要产物的潜在生态毒性和健康效应明显低于母体 BP-3。更重要的是,转化产物的低生物累积性不会扩大其生态毒性和健康效应。本研究不仅深入了解了 BP-3 在天然水中的间接光转化,还为基于 OH·和 O 的 AOPs 降解工业废水中 BP-3 的可行性提供了理论支持。