化学
日冕(行星地质学)
吸附
高分子
环境化学
壬基酚
生物污染
化学工程
电晕放电
吸附
有机化学
膜
天体生物学
生物化学
物理
工程类
物理化学
电极
维纳斯
作者
Shengkai Xu,Meiling Zhu,Lihua Fan,Yao Yao,Tianchi Cao,Rong Ji,Thilo Hofmann,Tong Zhang,Wei Chen
标识
DOI:10.1021/acs.est.5c02378
摘要
The dynamic interactions between nanoplastics and environmental macromolecules, particularly the formation of eco-corona, have received growing attention. There is increasing evidence that eco-corona plays a critical role in determining the fate, transport, and impact of nanoplastics. In this study, we show that even a low mass of eco-corona formed on nanoplastics significantly affects the cotransport of nanoplastics and organic contaminants in porous media. Specifically, eco-corona formation promotes the transport of 4-nonylphenol with polystyrene nanoplastics, especially when the eco-corona forms after contaminant adsorption to nanoplastics. Spectroscopic evidence indicates that 4-nonylphenol molecules are sequestered between the nanoplastics and the eco-corona due to the simultaneous binding to surface O-functional groups of the nanoplastics and to the polar macromolecules preferentially acquired by the nanoplastics. Transport modeling and supplementary adsorption/desorption experiments confirm that this binding configuration effectively inhibits or retards the release of 4-nonylphenol from the nanoplastics-eco-corona complex. Conversely, for 2,2',4,4'-tetrabromodiphenyl ether, an eco-corona inhibits its cotransport with nanoplastics by blocking the porous domains of the nanoparticles, which are the preferred binding sites for nonpolar, nonionic, hydrophobic compounds. The dynamic interplays between nanoplastics, macromolecules, and contaminants have important implications for predicting the spread, release, and bioaccumulation of plastic additives in aquatic environments.
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