Institute of Environmental Engineering, School of Metallurgy and Environment, Central South University, Changsha, 410083, China; Chinese National Engineering Research Center for Control & Treatment of Heavy Metal Pollution, Changsha, 410083, China.
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, 43210, USA.
Water Res. 2024 Sep 1;261:122023. doi: 10.1016/j.watres.2024.122023. Epub 2024 Jul 1.
The roles of superoxide radical (O) in the domains of physiological, physical, and material chemistry are becoming increasingly recognized. Although extensive efforts have been directed to understand O functions in diverse aquatic systems, there is a lack of systematic and in-depth review for its kinetics and mechanisms in various environmental scenarios. This review aims to bridge this gap through discussion of O generation pathways under both natural and controlled conditions. The merits and limitations of the generation and detection methods under various conditions are compared, with emphasis on different approaches for the determination of O-triggered reaction kinetics. We summarize the reaction rate constants of O with organic contaminants covering a wide diversity of structures and reactivity. The comparison indicates that O exhibits weak reactivity with most contaminants and lacks selectivity towards compounds with different functional groups, except with quinones which exhibit higher reactivity compared to non-quinones. Further, the reaction mechanisms, namely single electron transfer, nucleophilic substitution, hydrogen atom abstraction, and radical-adduct formation, are critically evaluated. Various environmental implications of O are highlighted including maintenance of biogeochemical iron cycle, synthesis of nanoparticles for antibacterial purposes, desorption of contaminants from heterogeneous interfaces, and synergetic degradation of contaminants.
超氧自由基 (O) 在生理、物理和材料化学领域的作用正日益受到重视。尽管人们已经做出了大量努力来理解不同水生系统中 O 的功能,但对于其在各种环境场景中的动力学和机制,仍缺乏系统和深入的综述。本综述旨在通过讨论自然和控制条件下 O 的生成途径来填补这一空白。比较了不同条件下生成和检测方法的优缺点,并重点介绍了不同方法确定 O 引发反应动力学的方法。我们总结了 O 与有机污染物的反应速率常数,涵盖了广泛的结构和反应性。比较表明,O 与大多数污染物的反应活性较弱,并且对具有不同官能团的化合物缺乏选择性,除了与醌类相比,非醌类的反应活性更高。此外,还对反应机制,即单电子转移、亲核取代、氢原子提取和自由基加成,进行了批判性评估。强调了 O 的各种环境影响,包括维持生物地球化学铁循环、合成用于抗菌目的的纳米粒子、从多相界面解吸污染物以及污染物的协同降解。