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电解质和天然有机物特性对聚苯乙烯纳米塑料聚集和沉降的影响

Impact of electrolyte and natural organic matter characteristics on the aggregation and sedimentation of polystyrene nanoplastics.

作者信息

Zhang Y, Gutierrez L, Benedetti M F, Croué J P

机构信息

IC2MP (UMR CNRS 7285), Université de Poitiers, 1 rue Marcel Doré, 86000 Poitiers, France; Université Paris Cité, Institut de physique du globe de Paris, CNRS, F-75005 Paris, France.

IC2MP (UMR CNRS 7285), Université de Poitiers, 1 rue Marcel Doré, 86000 Poitiers, France; Department of Green Chemistry and Technology, Ghent University, Coupure Links 653, 9000 Gent, Belgium; Facultad del Mar y Medio Ambiente, Universidad del Pacifico, Ecuador.

出版信息

Sci Total Environ. 2024 Dec 10;955:177131. doi: 10.1016/j.scitotenv.2024.177131. Epub 2024 Oct 30.

Abstract

Nanoplastics are increasingly pervasive in ecosystems worldwide, raising concerns about their persistence and mobility in the environment. Our study focused on the interactions between polystyrene nanoplastics (PS NPs, D:~200 nm) and Natural Organic Matter (NOM) uniquely isolated from water bodies under different electrolyte and temperature conditions (i.e., effectively mimicking a wide range of environmental scenarios). The selected dissolved NOM (DOM) fractions of varied physical chemical characteristics and geographical origins include: the hydrophobic acid (HPOA) fraction from the South Platte River (SPR HPOA, USA), the biopolymer/colloid fractions from Cazaux Lake (CL BIOP, France), and the dissolved fraction of the biofilm recovered from a nanofiltration-fouled module at the Méry-sur-Oise drinking water treatment plant (NF BIOP, France). The biopolymers (NF BIOP and CL BIOP) clearly hindered PS NPs aggregation through steric effects, forming a protective eco-corona, enhancing PS NPs stability, and inhibiting sedimentation in the long term, compared to HPOA. The temperature impacted the homo and hetero-aggregation of PS NPs differently, illustrating the complex interplay between thermal effects and NOMs stabilizing interactions. Furthermore, the seldom-explored aspect of the sequential introduction of reactants into the solution during aggregation experiments (i.e., which simulates a realistic scenario: the transport of PS NPs from one aquatic system to another of different compositions) was also investigated. This study provides essential insights into the dynamic behavior of PS NPs in environmental matrices and crucial knowledge for predicting nanoplastic interactions in complex ecosystems.

摘要

纳米塑料在全球生态系统中日益普遍,这引发了人们对其在环境中的持久性和流动性的担忧。我们的研究聚焦于聚苯乙烯纳米塑料(PS NPs,直径约200纳米)与从水体中独特分离出的天然有机物(NOM)在不同电解质和温度条件下的相互作用(即有效模拟广泛的环境场景)。所选的具有不同物理化学特性和地理来源的溶解态NOM(DOM)组分包括:南普拉特河(美国)的疏水酸(HPOA)组分、卡佐湖(法国)的生物聚合物/胶体组分,以及从瓦兹河畔梅里饮用水处理厂的纳滤污染膜组件中回收的生物膜溶解组分(法国)。与HPOA相比,生物聚合物(NF BIOP和CL BIOP)通过空间位阻效应明显阻碍了PS NPs的聚集,形成了保护性的生态冠层,增强了PS NPs的稳定性,并长期抑制了沉降。温度对PS NPs的同聚和异聚有不同影响,说明了热效应与NOM稳定相互作用之间的复杂相互作用。此外,还研究了聚集实验期间将反应物顺序引入溶液这一很少被探索的方面(即模拟了一个现实场景:PS NPs从一个水生系统运输到另一个不同组成的系统)。这项研究为PS NPs在环境基质中的动态行为提供了重要见解,并为预测复杂生态系统中的纳米塑料相互作用提供了关键知识。

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