In situ chemical transformations of silver nanoparticles along the water-sediment continuum.

Citation data:

Environmental science & technology, ISSN: 1520-5851, Vol: 49, Issue: 1, Page: 318-25

Publication Year:
2015
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Citations 14
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Repository URL:
https://ro.uow.edu.au/smhpapers/2848
PMID:
25405257
DOI:
10.1021/es504395m
Author(s):
Khaksar, Maryam; Jolley, Dianne F; Sekine, Ryo; Vasilev, Krasimir; Johannessen, Bernt; Donner, Erica; Lombi, Enzo
Publisher(s):
American Chemical Society (ACS); American Chemical Society
Tags:
Chemistry; Environmental Science; Medicine and Health Sciences; Social and Behavioral Sciences
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article description
In order to accurately assess the potential environmental risk posed by silver nanoparticles (Ag-NPs), their transformation and fate must be investigated in natural systems. This has proven to be very challenging due to the difficulties encountered in retrieving/analyzing NPs dispersed in complex and heterogeneous environmental matrices at relevant (i.e., low) concentrations. In this study, we overcame this challenge by immobilizing functionalized Ag-NPs onto plasma polymerized solid substrates to form "nano in situ deployment devices" (nIDDs). This method allowed us to retrieve and analyze the Ag-NPs after 48 h of direct exposure in freshwater-sediment and saltwater-sediment environments. The type and extent of Ag-NPs transformation was expected to vary along the water-sediment continuum as sediments typically contain steep gradients in solute concentrations and redox potential. To trace the distribution of redox sensitive elements (e.g., Fe, Mn), Diffusive Equilibration in Thin-films (DET) devices were inserted into the sediments alongside the nIDDs. Chemical transformation of the immobilized Ag-NPs across the water-sediment continuum was investigated after retrieval by synchrotron radiation X-ray Absorption Spectroscopy. Linear combination fitting of Ag K-edge X-ray absorption spectra indicated that the chemical transformations of Ag-NPs in both freshwater and saltwater sediments were strongly affected by the redox conditions over the investigated range. Silver bound to reduced sulfur was the principal product of Ag-NP transformations but different extents of transformation were observed for Ag-NPs exposed to different depths in the sediment. These field results add important insights about the transformation of Ag-NPs in heterogeneous environments.