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共存阳离子和阴离子对含铁矿物吸附抗生素的影响。

Effect of Co-Existing Cations and Anions on the Adsorption of Antibiotics on Iron-Containing Minerals.

机构信息

State Key Laboratory of Water Resources and Hydropower Engineering Science, Wuhan University, Wuhan 430072, China.

Hubei Key Laboratory of Water System Science for Sponge City Construction, Wuhan University, Wuhan 430072, China.

出版信息

Molecules. 2022 Nov 19;27(22):8037. doi: 10.3390/molecules27228037.

Abstract

The adsorption of antibiotics on minerals is an important process in their environment behavior. The adsorption behavior of antibiotics on iron-containing minerals and the effect of co-existing cations and anions were studied in this work. Magnetite, hematite, goethite and kaolin were selected as the representative minerals and characterized by SEM, XRD and BET. A total of eight antibiotics, including three quinolones, three sulfonamides and two mycins were chosen as the research targets. Results showed a higher adsorption amount of quinolones than that of sulfonamides and mycins on the surface of iron-containing minerals in most mineral systems. The adsorption isotherms of quinolones can be well fitted using the Freundlich models. The effects of five cations and five anions on the adsorption of quinolones were investigated, among which Mg, Ca, HCO and HPO mainly showed significant inhibition on the adsorption, while the effects of K, Na, NH, Cl, NO and SO showed less. Natural surface water samples were also collected and used as media to investigate the adsorption behavior of quinolones on iron-containing minerals. The buffering capacity of the natural water kept the reaction solution at circumneutral conditions, and the adsorption amount was mostly promoted in the goethite system (from 0.560.78 μmol/g to 0.521.43 μmol/g), but was inhibited in the other systems (magnetite: from 1.131.33 μmol/g to 0.450.76 μmol/g; hematite: from 0.520.65 μmol/g to 0.020.18 μmol/g; kaolin: from 1.981.99 μmol/g to 0.901.40 μmol/g). The results in this work help to further understand the transportation and fate of antibiotics in an aqueous environment.

摘要

抗生素在矿物上的吸附是其环境行为中的一个重要过程。本工作研究了抗生素在含铁矿物上的吸附行为及共存阳离子和阴离子的影响。选择磁铁矿、赤铁矿、针铁矿和高岭土作为代表性矿物,并通过 SEM、XRD 和 BET 进行了表征。选择了 8 种抗生素,包括 3 种喹诺酮类、3 种磺胺类和 2 种霉素作为研究目标。结果表明,在大多数矿物体系中,喹诺酮类在含铁矿物表面的吸附量高于磺胺类和霉素。喹诺酮类的吸附等温线可以用 Freundlich 模型很好地拟合。研究了 5 种阳离子和 5 种阴离子对喹诺酮类吸附的影响,其中 Mg、Ca、HCO 和 HPO 主要表现出明显的抑制作用,而 K、Na、NH、Cl、NO 和 SO 的影响较小。还采集了天然地表水样品作为介质,研究了喹诺酮类在含铁矿物上的吸附行为。天然水的缓冲能力使反应溶液保持在近中性条件下,吸附量在针铁矿体系中大多得到促进(从 0.560.78 μmol/g 增加到 0.521.43 μmol/g),但在其他体系中受到抑制(磁铁矿:从 1.131.33 μmol/g 减少到 0.450.76 μmol/g;赤铁矿:从 0.520.65 μmol/g 减少到 0.020.18 μmol/g;高岭土:从 1.981.99 μmol/g 减少到 0.901.40 μmol/g)。本工作的结果有助于进一步了解抗生素在水相环境中的迁移和归宿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f68/9693120/447f356a2cb6/molecules-27-08037-g001.jpg

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