4.7 Article

Heteroaggregation of nanoplastics with oppositely charged minerals in aquatic environment: Experimental and theoretical calculation study

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 428, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.131191

Keywords

Nanoplastics; Mineral; Heteroaggregation; DLVO; DFT

Funding

  1. National Natural Science Foundation of China [41972037]
  2. Basic and Applied Basic Research Foundation of Guangdong Province [2019B1515120015]
  3. Guangdong Special Support Program for Local Innovative and Research Teams Project [2019BT02L218]
  4. Guangdong Science and Technology Program [2020B121201003]
  5. Guangdong special Support Program for Millions of Leading Engineering Talents [201626011]
  6. Fundamental Research Funds for the Central Universities, SCUT [2020ZYGXZR070]

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This study investigated the aggregation behaviors of polystyrene nanoplastics (PSNPs) in aqueous phase with different environmental factors. It was found that pH had little effect on the fate of individual PSNPs under natural aquatic conditions, while high ionic strength (IS) caused homoaggregation. The results also revealed that electrostatic interaction directly influenced the stability of PSNPs in aquatic environments.
The transport, fate, and toxic effects of nanoplastics (NPs) would be affected by various environmental factors. In this study, the aggregation behaviors of polystyrene nanoplastics (PSNPs) with or without the presence of oppositely charged minerals (Mg/Al layered double hydroxides (LDH) and kaolin) in aqueous phase were investigated through settling experiment, and the influencing factors including pH and ionic strength (IS) were also analyzed systematically. Our results revealed that pH had a negligible effect on the fate of individual PSNPs under natural aquatic conditions, while high IS would cause homoaggregation. The positively charged LDH decreased the stability of PSNPs, while negatively charged kaolin had a weak effect on it, suggesting that electrostatic interaction was directly related to the stability of PSNPs in aquatic environment. Further experiments of PSNPs with other metal oxides with different surface charges (Al2O3 and SiO2) confirmed the importance of electrostatic interaction for PSNPs-minerals heteroaggregation. Transmission electron microscopic (TEM), Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, and Density function theory (DFT) calculations were combined for the first time to explain the heteroaggregation mechanism, demonstrating that there were expected to exist hydrogen bond and van der Waals interaction in addition to the dominant force of electrostatic interaction. Our findings are expected to shed light on the environmental behavior of PSNPs in a complex aquatic environment.

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