Song Zhao, Zhang Yu, Zhang Xue, Zhou Xu, Chen Yidi, Duan Xiaoguang, Ren Nanqi
State Key Laboratory of Urban Water Resource and Environment, Shenzhen Key Laboratory of Organic Pollution Prevention and Control, School of Civil and Environmental Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, P R China.
School of Electronic and Information Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Water Res. 2023 Aug 15;242:120274. doi: 10.1016/j.watres.2023.120274. Epub 2023 Jun 26.
Peracetic acid is an emerging oxidant and disinfectant for wastewater purification. In this study, we first developed a comprehensive and accurate model to elucidate the reaction mechanisms and simulate reaction kinetics of peracetic acid (PAA, CHC(=O)OOH) activated by chloride (Cl) based on experimental results and literature. A diversity of experiments methods (e.g., quenching experiments, probe compounds degradation, electron paramagnetic resonance (EPR) measurements) and kinetic modeling were used to determine the reactive species. As a result, carbon-centered radicals and free chlorine reactive species (Cl and HClO) were devoted to BPA degradation in the PAA/Cl system. The carbon-centered radicals CHC(=O)OO, CHC(=O)O, CHOO, and CH greatly accelerated BPA degradation with their corresponding kinetics of k = 2 × 10 M s, k = 2 × 10 M s, k = 2 × 10 M s and k = 2 × 10 M s. Dissolved Cl(l) species was also important for BPA degradation with k of 2 × 10 M s, much higher than HClO/ClO of k = 1.2 × 10 M s and k- = 9 × 10 M s. While free chlorine tends to transform BPA to estrogenic chlorinated organic products, the primary degradation of BPA by carbon-centered radicals results in chlorine-free products, reducing the production of disinfection byproducts during the treatment of saline wastewater. This study improves the knowledge of reaction kinetics and mechanism and reactive species generation in the PAA/Cl system.
过氧乙酸是一种新兴的用于废水净化的氧化剂和消毒剂。在本研究中,我们首先基于实验结果和文献,开发了一个全面且准确的模型,以阐明过氧乙酸(PAA,CHC(=O)OOH)被氯离子(Cl)活化的反应机理并模拟其反应动力学。采用了多种实验方法(如猝灭实验、探针化合物降解、电子顺磁共振(EPR)测量)和动力学建模来确定反应活性物种。结果表明,碳中心自由基和游离氯反应活性物种(Cl和HClO)对PAA/Cl体系中双酚A(BPA)的降解有贡献。碳中心自由基CHC(=O)OO、CHC(=O)O、CHOO和CH极大地加速了BPA的降解,其相应的反应动力学常数分别为k = 2×10 M s、k = 2×10 M s、k = 2×10 M s和k = 2×10 M s。溶解的Cl(l)物种对BPA降解也很重要,其k值为2×10 M s,远高于HClO/ClO的k = 1.2×10 M s和k- = 9×10 M s。虽然游离氯倾向于将BPA转化为具有雌激素活性的氯化有机产物,但碳中心自由基对BPA的主要降解产生无氯产物,减少了含盐废水处理过程中消毒副产物的产生。本研究增进了对PAA/Cl体系中反应动力学、反应机理和反应活性物种生成的认识。