Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, HKSAR, P.R.China.
Environmental Microbiome Engineering and Biotechnology Laboratory, Department of Civil Engineering, The University of Hong Kong, HKSAR, P.R.China.
Water Res. 2020 Dec 15;187:116419. doi: 10.1016/j.watres.2020.116419. Epub 2020 Sep 19.
Recent studies have demonstrated that weathering modifies the physicochemical properties and sorption behavior of microplastics (MPs). However, little is known about the effects of such weathering on the simultaneous sorption by MPs of different organic pollutants in multi-solute systems. In this study, the role of cosolute properties in the formation of solute multilayers with a hydrophobic primary solute (4-MBC) on pristine and various weathered polystyrene MPs (PSMPs) was examined. Three weathered PSMPs were studied namely, UV-irradiated PS (UV-PS), microbially degraded PS (MD-NPS), and UV-irradiated PS with subsequent microbial degradation (MD-UV-PS). The weathered PSMPs generally exhibited higher degree of oxygenated functionalities with less surface hydrophobicity than pristine particles. Our findings showed that the formation of solute multilayers with hydrophobic cosolutes was drastically suppressed in UV-PS due to more severe competition at hydrophobic sorption sites. Nevertheless, hydrophilic cosolutes contributed to solute multilayer formation with 4-MBC on PSMPs after UV irradiation, probably due to the stronger sorption of hydrophilic compounds to the oxidized surfaces of these particles via enhanced H-bonding. Strikingly, the sorption of 4-MBC by MD-UV-PS was notably enhanced when hydrophobic cosolutes were present. The observed synergistic sorption indicates that adhered biofilms and/or organic matter on MD-UV-PS could sorb the hydrophobic cosolute molecules, and eventually promote sorption of 4-MBC. Our further toxicity tests revealed that such solute multilayers formed on PSMPs inhibited microalgal growth. These results suggest that the fate and biological effects of MP-mediated chemical exposure could be strongly affected by weathering processes and coexistence of multiple organic contaminants in natural environments.
最近的研究表明,风化会改变微塑料(MPs)的物理化学性质和吸附行为。然而,对于这种风化对多溶质体系中不同有机污染物同时被 MPs 吸附的影响,人们知之甚少。在这项研究中,考察了共溶质性质在疏水性主溶质(4-MBC)与原始和各种风化聚苯乙烯 MPs(PSMPs)形成溶质多层结构中的作用。研究了三种风化 PSMPs,即紫外线照射 PS(UV-PS)、微生物降解 PS(MD-NPS)和紫外线照射后微生物降解 PS(MD-UV-PS)。风化 PSMPs 通常表现出较高的含氧官能团度,表面疏水性低于原始颗粒。我们的研究结果表明,由于疏水性吸附位点的竞争更加激烈,疏水性共溶质在 UV-PS 中形成溶质多层结构的程度大大受到抑制。然而,亲水性共溶质有助于在 PSMPs 上形成与 4-MBC 的溶质多层结构,这可能是由于亲水性化合物通过增强氢键更强烈地吸附到这些颗粒的氧化表面上。值得注意的是,当存在疏水性共溶质时,MD-UV-PS 对 4-MBC 的吸附明显增强。观察到的协同吸附表明,MD-UV-PS 上附着的生物膜和/或有机物可以吸附疏水性共溶质分子,最终促进 4-MBC 的吸附。我们进一步的毒性测试表明,在 PSMPs 上形成的这种溶质多层结构抑制了微藻的生长。这些结果表明,在自然环境中,风化过程和多种有机污染物的共存可能会强烈影响 MPs 介导的化学暴露的命运和生物效应。