Suppr超能文献

臭氧与化学试剂协同作用(协同氧化)促进自由基形成和微污染物降解的研究进展:综述。

The promotions on radical formation and micropollutant degradation by the synergies between ozone and chemical reagents (synergistic ozonation): A review.

机构信息

Key Laboratory of Microorganism Application and Risk Control of Shenzhen, Guangdong Provincial Engineering Research Center for Urban Water Recycling and Environmental Safety, Institute of Environment and Ecology, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.

College of Architecture & Environment, Sichuan University, Chengdu 610000, China.

出版信息

J Hazard Mater. 2021 Sep 15;418:126327. doi: 10.1016/j.jhazmat.2021.126327. Epub 2021 Jun 8.

Abstract

The combination of ozone (O) and chemical reagents (such as HO) shows synergies on the radical formation and micropollutant degradation. The promoting performance was associated with various parameters including chemical reagents, micropollutants, solution pH, and the water matrix. In this review, we summarized existing knowledge on radical formation pathways, radical yields, and radical oxidation for different synergistic ozonation processes in various water matrices (such as groundwater, surface water, and wastewater). The increase of radical yields by synergistic ozonation processes was positively related to the increase of O-decay, with the increase being 1.1-4.4 folds than ozonation alone (0.2). Thus, synergistic ozonation can promote the degradation rate and efficiency of O-resistant micropollutants (second order rate constant, k < 200 M s), but only slightly affects or even minorly inhibits the degradation of O-reactive micropollutants (k > 200 M s). The water matrices such as the dissolved organic matters, negatively suppressed the degradation of micropollutant by quenching O-oxidation and radical oxidation (i.e. maximum promoting was decreased by 1.3 times), but may positively extend the promoting effects of synergistic ozonation to micropollutants that are more reactive to O (i.e. k was extended from <200 to <2000 M s). The formation of bromate would be increased through increasing radical oxidation by synergistic ozonation, but can be depressed by relative higher HO as the reducing agent of HOBr/OBr intermediate. The increase in bromate formation by O/permononsulfate is a considerable concern due to permononsulfate cannot reduce the HOBr/OBr intermediate.

摘要

臭氧 (O) 与化学试剂(如 HO)的组合在自由基形成和微污染物降解方面表现出协同作用。促进性能与包括化学试剂、微污染物、溶液 pH 值和水基质在内的各种参数有关。在本综述中,我们总结了现有的关于不同水基质(如地下水、地表水和废水)中不同协同臭氧氧化过程的自由基形成途径、自由基产率和自由基氧化的知识。协同臭氧氧化过程中自由基产率的增加与 O 衰减的增加呈正相关,增加幅度比单独臭氧氧化(0.2)高 1.1-4.4 倍。因此,协同臭氧氧化可以提高 O 抗性微污染物的降解速率和效率(二级反应速率常数,k < 200 M s),但对 O 反应性微污染物的降解影响甚微甚至略有抑制(k > 200 M s)。溶解有机物等水基质通过淬灭 O 氧化和自由基氧化,显著抑制了微污染物的降解(最大促进作用降低了 1.3 倍),但可能会将协同臭氧氧化对更反应性的 O 的微污染物的促进作用延长(即 k 从 <200 延长至 <2000 M s)。协同臭氧氧化通过增加自由基氧化会增加溴酸盐的形成,但相对较高的 HO 作为 HOBr/OBr 中间物的还原剂会抑制溴酸盐的形成。O/过一硫酸盐中溴酸盐形成的增加是一个相当大的问题,因为过一硫酸盐不能还原 HOBr/OBr 中间物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验