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在模拟天然水和实际地表水中共沉淀作用下,探究诺氟沙星在微塑料上的不同吸附机制。

Mechanistic insight into different adsorption of norfloxacin on microplastics in simulated natural water and real surface water.

机构信息

Institute of Ecological and Environmental Sciences, Sichuan Agricultural University, Chengdu, Sichuan, 611130, China.

Department of Chemical Engineering, Northwest University for Nationalities, Lanzhou, Gansu, 730030, China.

出版信息

Environ Pollut. 2021 Sep 1;284:117537. doi: 10.1016/j.envpol.2021.117537. Epub 2021 Jun 5.

Abstract

Microplastics (MPs) as carriers of various contaminants have attracted more attentions in water environments. However, the interactions between typical MPs and norfloxacin (NOR) in natural water environments were still not systematically studied. In this study, the adsorption of NOR onto four typical types of MPs (polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC)) was investigated in simulated natural water and real surface water, and the adsorption mechanisms were deeply explored to provide fundamental understandings of the MPs-NOR complicated pollution. The results showed that the kinetics of NOR onto all MPs obeyed pseudo-second-order model, and was greatly slowed down at lower temperature or higher salinity. The intrinsic structure and surface area of MPs played important roles in the adsorption behaviors of NOR on these four types of MPs. The adsorption isotherm of NOR onto all MPs could be well described by linear model, with the K values following the order of PVC > PS > PE > PP (i.e. 6.229-11.901 L/μg) in simulated natural water. However, in surface water the adsorption isotherms of NOR on all MPs could be well fitted by Freundlich model. For all MPs, the adsorption of NOR was quite pH-dependent due to the electrostatic interactions. Furthermore, the salinity and the presence of dissolved organic matter (DOM) had significantly hindered the NOR adsorption. More importantly, compared with adsorption behaviors in simulated natural water, the competition of coexisting substances such as cations and NOM for adsorption sites and higher water pH dramatically reduced the adsorption of NOR onto all types of MPs in Jiang'an River, with the reduction rate of 19.7-41.2%. Finally, the mechanism studies indicated that the electrostatic attractions played a key role in the adsorption of NOR onto MPs, and π-π, H-bonding, polar-polar, and Van Der Waals interactions were also involved in adsorption processes.

摘要

微塑料(MPs)作为各种污染物的载体,在水环境中受到了更多的关注。然而,在自然水环境中,典型的 MPs 与诺氟沙星(NOR)之间的相互作用仍未得到系统研究。在这项研究中,考察了 NOR 在模拟天然水和实际地表水四种典型类型 MPs(聚乙烯(PE)、聚丙烯(PP)、聚苯乙烯(PS)和聚氯乙烯(PVC))上的吸附行为,并深入探讨了吸附机制,为 MPs-NOR 复杂污染提供了基础认识。结果表明,NOR 在所有 MPs 上的动力学均符合准二级模型,在较低温度或较高盐度下会大大减慢。 MPs 的固有结构和表面积在 NOR 对这四种类型 MPs 的吸附行为中起着重要作用。NOR 在所有 MPs 上的吸附等温线可以很好地用线性模型来描述,在模拟天然水中,K 值的顺序为 PVC>PS>PE>PP(即 6.229-11.901 L/μg)。然而,在地表水所有 MPs 上 NOR 的吸附等温线可以很好地用 Freundlich 模型来拟合。对于所有 MPs,由于静电相互作用,NOR 的吸附对 pH 非常敏感。此外,盐度和溶解有机物(DOM)的存在显著阻碍了 NOR 的吸附。更重要的是,与在模拟天然水中的吸附行为相比,共存物质(如阳离子和 NOM)对吸附位点的竞争以及较高的水 pH 极大地降低了 NOR 在所有类型 MPs 上的吸附,降低率为 19.7-41.2%。最后,机制研究表明,静电吸引在 NOR 吸附到 MPs 上起着关键作用,π-π、氢键、偶极-偶极和范德华相互作用也参与了吸附过程。

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