Transformations of citrate and Tween coated silver nanoparticles reacted with Na2S
- 1. Center for Environmental Nanoscience and Risk, Department of Environmental Health Sciences, Arnold School of Public Health, University of South Carolina, Columbia, SC 29028 (United States)
- 2. School of Biochemistry, University of Bristol, Bristol BS8 1TD (United Kingdom)
- 3. School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham B15 2TT (United Kingdom)
- 4. School of Physics and Astronomy, University of Birmingham, Birmingham B15 2TT (United Kingdom)
Description
Silver nanoparticles (Ag NPs) are susceptible to transformations in environmental and biological media such as aggregation, oxidation, dissolution, chlorination, sulfidation, formation/replacement of surface coatings following interaction with natural organic matter (NOM). This paper investigates the impact of surface coating and Suwannee River fulvic acid (SRFA) on the transformations and behavior of Ag NPs (citrate coated and Tween coated; cit-Ag NPs and Tween-Ag NPs, respectively), following reaction with different concentrations of Na2S solution (as a source of sulfide species, H2S and HS−). These transformations and the dominant mechanisms of transformations were investigated using UV–vis and scanning transmission electron microscopy coupled with electron energy loss spectroscopy. Here, we have shown that Ag NP surface coating impacts their dissolution following dilution in ultrahigh purity water, with higher extent of dissolution of Tween-Ag NPs compared with cit-Ag NPs. Tween-Ag NPs are susceptible to dissolution following their sulfidation at low S/Ag molar ratio. Suwannee River fulvic acid (SRFA) slows down the dissolution of Tween-Ag NPs at low sulfide concentrations and reduces the aggregation of cit-Ag NP in the presence of sodium sulfide. Sulfidation appears to occur by direct interaction of sulfide species with Ag NPs rather than by indirect reaction of sulfide with dissolved Ag species subsequent to dissolution. Furthermore, the sulfidation process results in the formation of partially sulfidized Ag NPs containing unreacted (metallic) subgrains at the edge of the NPs for Tween-Ag NPs in the presence of high sulfide concentration (2000 nM Na2S), which occurred to less extent at lower Na2S concentration for Tween-Ag NPs and at all concentrations of Na2S for cit-Ag NPs. Thus, sulfidized Ag NPs may preserve some of the properties of the Ag NPs such as their potential to shed Ag+ ions and their toxic potential of Ag NPs. - Graphical abstract: Ag NPs may preserve some of the original properties of Ag0 even following sulfidation
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2014.09.035Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2014.09.035;
- PII
- S0048-9697(14)01345-X;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 502
- Journal Issue
- Complete
- Journal Page Range
- p. 344-353
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47012668
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CHLORINATION; CITRATES; CONCENTRATION RATIO; DISSOLUTION; ENERGY-LOSS SPECTROSCOPY; FULVIC ACIDS; HYDROGEN SULFIDES; NANOPARTICLES; SILVER; SILVER IONS; SODIUM SULFIDES; SULFIDATION; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CARBOXYLIC ACID SALTS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; DIMENSIONLESS NUMBERS; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; HALOGENATION; HYDROGEN COMPOUNDS; IONS; METALS; MICROSCOPY; ORGANIC ACIDS; ORGANIC COMPOUNDS; PARTICLES; SODIUM COMPOUNDS; SPECTROSCOPY; SULFIDES; SULFUR COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.