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有机物-针铁矿相互作用对萘啶酸反应迁移的影响:柱实验研究与模拟。

Effects of organic matter-goethite interactions on reactive transport of nalidixic acid: Column study and modeling.

机构信息

College of Resources and Environmental Science, South-Central University for Nationalities, Wuhan, China; Univ Rennes, École Nationale Supérieure de Chimie de Rennes, CNRS, ISCR - UMR6226, F-35000, Rennes, France.

Univ Rennes, École Nationale Supérieure de Chimie de Rennes, CNRS, ISCR - UMR6226, F-35000, Rennes, France.

出版信息

Environ Res. 2020 Dec;191:110187. doi: 10.1016/j.envres.2020.110187. Epub 2020 Sep 10.

DOI:10.1016/j.envres.2020.110187
PMID:32919970
Abstract

The fractionation of natural organic matter (NOM) and its impact on the binding of quinolones to mineral surfaces and transport behavior under flow-through conditions have been scarcely investigated. In this study, the sorption and transport of a widely used quinolone antibiotic, Nalidixic acid (NA), were investigated in goethite-coated sand (GCS) columns over a wide concentration range (5-50 mg/L) of Leonardite humic acid (LHA), a representative NOM. Simultaneous injection of NA and LHA in GCS columns mutually alter transport of each other, i.e. NA mobility and LHA molecular fractionation. Preloading of GCS column with LHA dramatically facilitated the transport behavior of NA, where nonspecific interactions with LHA-covered goethite surfaces controlled NA mobility. Simulations using a two-site nonequilibrium model showed that a modified sorption rate constant was required to accurately describe the breakthrough curves of NA under these conditions. This altered rate constant suggests that nonspecific interactions of NA on bound LHA may take place as an additional binding mechanism affecting adsorption kinetics. NOM fractionation alters sorption mechanisms and kinetics of quinolone antibiotics, which in turn affect their fractionation. These results may have important implications for an accurate assessment of the fate of these types of antibiotics in aquatic environments.

摘要

天然有机物(NOM)的分级及其对喹诺酮类抗生素与矿物表面结合和在流动条件下的输运行为的影响很少被研究。在这项研究中,我们在针铁矿涂覆砂(GCS)柱中研究了一种广泛使用的喹诺酮类抗生素萘啶酸(NA)在莱奥纳德ite 腐殖酸(LHA)(一种代表性的 NOM)浓度范围内(5-50mg/L)的吸附和输运。在 GCS 柱中同时注入 NA 和 LHA 会相互改变彼此的输运,即 NA 的迁移性和 LHA 的分子分级。GCS 柱预先加载 LHA 会极大地促进 NA 的输运行为,其中与 LHA 覆盖的针铁矿表面的非特异性相互作用控制着 NA 的迁移性。使用双位点非平衡模型进行的模拟表明,需要修改吸附速率常数才能准确描述这些条件下 NA 的穿透曲线。这种改变的速率常数表明,NA 在结合的 LHA 上的非特异性相互作用可能作为影响吸附动力学的另一种结合机制发生。NOM 的分级改变了喹诺酮类抗生素的吸附机制和动力学,这反过来又影响了它们的分级。这些结果对于准确评估这些类型的抗生素在水生环境中的命运具有重要意义。

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