Department of Environmental Science, School of Geography and Tourism, Shaanxi Normal University, Xi'an 710119, China; Institut de Chimie des Milieux et des Matériaux IC2MP UMR 7285 CNRS, Université de Poitiers, France.
Nanyang Environment & Water Research Institute (NEWRI), Nanyang Technological University, 1 Cleantech Loop, CleanTech One, #06-08, 637141, Singapore.
Water Res. 2021 Oct 1;204:117634. doi: 10.1016/j.watres.2021.117634. Epub 2021 Sep 7.
The UV/chlorine process as a potential tertiary municipal wastewater treatment alternative for removing refractory PPCPs has been widely investigated. However, the role of effluent organic matter (EfOM) on the radical chemistry and toxicity alteration is unclear. The elimination of two model PPCPs, primidone (PRM) and caffeine (CAF), by the co-exposure of UV and free chlorine was investigated to elucidate the impact of EfOM. Experimental results indicated that both OH and reactive chlorine species (RCS) were importantly involved in the decay of PRM at acidic condition, while ClO played dominant role at alkaline pH. The decay of CAF was dominated by ClO under all conditions. Chlorine dose, initial contaminant concentration, solution pH, and water matrix affect the process efficiency at varying degree resulting from their specific effect on the radical speciation in the system. Presence of EfOM isolate remarkably inhibited the decay of PRM and CAF by preferentially scavenging RCS and particularly ClO. Good correlations (linear for PRM and exponential for CAF) between UV absorbance at 254 nm and the observed pseudo first-order rate constants (k') for all EfOM solutions were obtained, demonstrating the importance of aromatic moieties in inhibiting the degradation of targeted contaminants by UV/chlorine process. Degradation of PRM/CAF in reconstituted effluent spiked with the major effluent constituents (i.e., EfOM isolates, Cl, HCO, and NO) was comparable to the results obtained with the real WWTP effluent and fit well to the correlation between k' and UV absorbance at 254 nm, suggesting that EfOM isolates can be used to determine the efficiency of UV/chlorine process in real effluent. EfOM serves as the main precursor of adsorbable organic chlorine in the UV/chlorine treatment. Bioassays indicated that chlorine-containing compounds could induce oxidative stress, mitochondrial dysfunction, and increase the cell DNA damage. Among evaluated treatment conditions, the nature of EfOM, hydrophobic versus transphilic fraction, is likely the predominant factor affecting the cytotoxicity. Meanwhile the UV/chlorine treatment can significantly reduce the cytotoxicity of EfOM isolates. However, adding high level of selected contaminants (e.g., PRM and CAF) can inhibit this phenomenon due to the competition with reactive radicals.
紫外线/氯工艺作为一种潜在的三级城市废水处理替代方法,已被广泛研究用于去除难降解的 PPCPs。然而,出水有机物(EfOM)对自由基化学和毒性变化的作用尚不清楚。本研究通过共暴露于紫外线和自由氯来考察两种模型 PPCPs(扑米酮(PRM)和咖啡因(CAF))的去除,以阐明 EfOM 的影响。实验结果表明,在酸性条件下,OH 和反应性氯物种(RCS)均重要参与 PRM 的衰减,而在碱性 pH 下,ClO 起主要作用。在所有条件下,CAF 的衰减均由 ClO 主导。氯剂量、初始污染物浓度、溶液 pH 和水基质以特定方式影响系统中的自由基种类,从而在不同程度上影响处理效率。EfOM 分离物的存在显著抑制了 PRM 和 CAF 的衰减,这是由于其优先清除 RCS,特别是 ClO。对于所有 EfOM 溶液,在 254nm 处的紫外线吸光度与观察到的拟一级速率常数(k')之间存在良好的相关性(对于 PRM 为线性,对于 CAF 为指数),这表明芳香族基团在抑制 UV/氯工艺降解目标污染物方面的重要性。用主要出水成分(即 EfOM 分离物、Cl、HCO 和 NO)加标后的再生出水降解 PRM/CAF 的结果与真实 WWTP 出水的结果相当,且与 k'和 254nm 处紫外线吸光度之间的相关性拟合良好,这表明 EfOM 分离物可用于确定实际出水中 UV/氯工艺的效率。EfOM 是 UV/氯处理中可吸附有机氯的主要前体。生物测定表明,含氯化合物会引发氧化应激、线粒体功能障碍,并增加细胞 DNA 损伤。在所评估的处理条件中,EfOM 的性质(疏水性与亲脂性部分)可能是影响细胞毒性的主要因素。同时,UV/氯处理可以显著降低 EfOM 分离物的细胞毒性。然而,由于与反应性自由基的竞争,添加高水平的选定污染物(例如 PRM 和 CAF)可能会抑制这种现象。