亚硝酸盐
环境化学
硝酸盐
降级(电信)
过氧亚硝酸盐
硝化作用
化学
有机化学
计算机科学
电信
酶
超氧化物
作者
Xiuwei Ao,Xi Zhang,Wenjun Sun,Karl G. Linden,Emma M. Payne,Ted Mao,Zifu Li
出处
期刊:Water Research
[Elsevier]
日期:2024-02-05
卷期号:253: 121259-121259
被引量:40
标识
DOI:10.1016/j.watres.2024.121259
摘要
The effectiveness of UV-based advanced oxidation processes (UV-AOPs) in degrading trace organic contaminants (TrOCs) can be significantly influenced by the ubiquitous presence of nitrate (NO3−) and nitrite (NO2−) in water and wastewater. Indeed, NO3−/NO2− can play multiple roles of NO3−/NO2− in UV-AOPs, leading to complexities and conflicting results observed in existing research. They can inhibit the degradation of TrOCs by scavenging reactive species and/or competitively absorbing UV light. Conversely, they can also enhance the elimination of TrOCs by generating additional •OH and reactive nitrogen species (RNS). Furthermore, the presence of NO3−/NO2− during UV-AOP treatment can affect the transformation pathways of TrOCs, potentially resulting in the nitration/nitrosation of TrOCs. The resulting nitro(so)-products are generally more toxic than the parent TrOCs and may become precursors of nitrogenous disinfection byproducts (N-DBPs) upon chlorination. Particularly, since the impact of NO3−/NO2− in UV-AOPs is largely due to the generation of RNS from NO3−/NO2− including NO•, NO2•, and peroxynitrite (ONOO–/ONOOH), this review covers the generation, properties, and detection methods of these RNS. From kinetic, mechanistic, and toxicologic perspectives, future research needs are proposed to advance the understanding of how NO3−/NO2− can be exploited to improve the performance of UV-AOPs treating TrOCs. This critical review provides a comprehensive framework outlining the multifaceted impact of NO3−/NO2− in UV-AOPs, contributing insights for basic research and practical applications of UV-AOPs containing NO3−/NO2−.
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