Zhang Chengwu, Yang Anqi, Qin Bing, Zhao Wei, Kong Chuipeng, Qin Chuanyu
Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin University, Changchun 130021, China; Jilin Provincial Key Laboratory of Water Resources and Environment, Jilin University, Changchun 130021, China; National and Local Joint Engineering Laboratory for Petrochemical Contaminated Site Control and Remediation Technology, Jilin University, Changchun 130021, China.
Sinopec Research Institute of Petroleum Processing Co., LTD, Beijing 100083, China.
J Hazard Mater. 2024 Dec 5;480:136174. doi: 10.1016/j.jhazmat.2024.136174. Epub 2024 Oct 16.
It has been reported that tripolyphosphate (TPP) can effectively enhance the activation of O by Fe(II) to remove organic pollutants in the environment. However, the influence of solution pH on the generation and conversion of reactive oxygen species (ROS) and their degradation of pollutants in the Fe(II)/O/TPP system needs further investigation. In this study, we demonstrated that O and •OH were the main ROS responsible for degradation in the system at different pH conditions, and their formation rates were calculated using a steady-state model. Experiments combined with density functional theory (DFT) calculations showed that the p-nitrophenol (PNP) degradation pathway in the Fe(II)/O/TPP system is regulated by solution pH. Specifically, at pH = 3, the existence of Fe(II) in the solution is dominated by [Fe(II)(HTPP)], which leads to a rapid conversion from O and HO• to generate •OH, and PNP is primarily oxidatively degraded. However, at pH = 5/7, [Fe(II)(TPP)] is taking the lead with which O is accumulated in the solution due to the slow conversion to •OH in this condition, and the PNP is mainly reductively degraded. This study proposes a new strategy to achieve the targeted oxidative/reductive removal of different types of pollutants by simply varying the solution pH in the Fe(II)/O/TPP system.
据报道,三聚磷酸(TPP)能有效增强Fe(II)对O的活化作用,以去除环境中的有机污染物。然而,溶液pH值对Fe(II)/O/TPP体系中活性氧物种(ROS)的产生、转化及其对污染物的降解影响尚需进一步研究。在本研究中,我们证明了在不同pH条件下,O和•OH是该体系中负责降解的主要ROS,并使用稳态模型计算了它们的生成速率。结合密度泛函理论(DFT)计算的实验表明,Fe(II)/O/TPP体系中对硝基苯酚(PNP)的降解途径受溶液pH值调控。具体而言,在pH = 3时,溶液中Fe(II)主要以[Fe(II)(HTPP)]形式存在,这导致O和HO•迅速转化生成•OH,PNP主要通过氧化降解。然而,在pH = 5/7时,[Fe(II)(TPP)]占主导,由于在此条件下向•OH的转化缓慢,O在溶液中积累,PNP主要通过还原降解。本研究提出了一种新策略,即通过简单改变Fe(II)/O/TPP体系中的溶液pH值,实现对不同类型污染物的靶向氧化/还原去除。