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在快速砂滤器中动态基质加载下探索有机微量污染物的生物降解。

Exploring organic micropollutant biodegradation under dynamic substrate loading in rapid sand filters.

机构信息

Environmental Technology, Wageningen University & Research, P.O. Box 17, 6700 AA Wageningen, The Netherlands.

Evides Water Company N.V., Schaardijk 150, 3063 NH Rotterdam, The Netherlands.

出版信息

Water Res. 2022 Aug 1;221:118832. doi: 10.1016/j.watres.2022.118832. Epub 2022 Jul 7.

Abstract

Microbial removal of trace organic micropollutants (OMPs) from drinking water sources remains challenging. Nitrifying and heterotrophic bacteria in rapid sand filters (RSFs) are capable of biodegrading OMPs while growing on ammonia and dissolved organic matter (DOM). The loading patterns of ammonia and DOM may therefore affect microbial activities as well as OMP biodegradation. So far, there is very limited information on the effect of substrate loading on OMP biodegradation at environmentally relevant concentrations (∼ 1 µg/L) in RSFs. We investigated the biodegradation rates of 16 OMPs at various substrate loading rates and/or empty bed contact times (EBCT). The presence of DOM improved the biodegradation of paracetamol (41.8%) by functioning as supplementary carbon source for the heterotrophic degrader, while hindering the biodegradation of 2,4-D, mecoprop and benzotriazole due to substrate competition. Lower loading ratios of DOM/benzotriazole benefited benzotriazole biodegradation by reducing substrate competition. Higher ammonia loading rates enhanced benzotriazole removal by stimulating nitrification-based co-metabolism. However, stimulating nitrification inhibited heterotrophic activity, which in turn inhibited the biodegradation of paracetamol, 2,4-D and mecoprop. A longer EBCT promoted metformin biodegradation as it is a slowly biodegradable compound, but suppressed the biodegradation of paracetamol and benzotriazole due to limited substrate supply. Therefore, the optimal substrate loading pattern is contingent on the type of OMP, which can be chosen based on the priority compounds in practice. The overall results contribute to understanding OMP biodegradation mechanisms at trace concentrations and offer a step towards enhancing microbial removal of OMPs from drinking water by optimally using RSFs.

摘要

从饮用水源中去除痕量有机微污染物 (OMPs) 仍然具有挑战性。在快速砂滤器 (RSF) 中,硝化细菌和异养细菌能够在氨和溶解有机物 (DOM) 上生长的同时生物降解 OMPs。因此,氨和 DOM 的负荷模式可能会影响微生物活性以及 OMP 的生物降解。到目前为止,关于在 RSF 中环境相关浓度 (∼1µg/L) 下底物负荷对 OMP 生物降解的影响,信息非常有限。我们研究了在各种底物负荷率和/或空床接触时间 (EBCT) 下 16 种 OMP 的生物降解速率。DOM 的存在通过作为异养降解物的补充碳源,提高了对扑热息痛的生物降解率 (41.8%),而由于底物竞争,阻碍了 2,4-D、甲草胺和苯并三唑的生物降解。DOM/苯并三唑的较低负荷比有利于苯并三唑的生物降解,因为它减少了底物竞争。较高的氨负荷率通过刺激硝化作用的共代谢增强了苯并三唑的去除。然而,硝化作用的刺激抑制了异养活性,从而抑制了扑热息痛、2,4-D 和甲草胺的生物降解。较长的 EBCT 促进了二甲双胍的生物降解,因为它是一种缓慢生物降解的化合物,但由于底物供应有限,抑制了扑热息痛和苯并三唑的生物降解。因此,最佳的底物负荷模式取决于 OMP 的类型,可以根据实际中的优先化合物进行选择。总体结果有助于理解痕量浓度下 OMP 的生物降解机制,并朝着通过优化使用 RSF 从饮用水中增强微生物去除 OMPs 的方向迈出了一步。

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