Nanoparticles In Environmental Matrices Research Articles

Quantitative separation of polystyrene nanoparticles in environmental matrices with picogram detection limits using capillary electrophoresis.

We developed a capillary electrophoresis method to separate polystyrene particles (PSPs) with different sizes or different surface functionalities. Separations were performed in buffer and 100 mg L-1 clay or 100 mg L-1 Suwanee River humic acid. In all solutions, PSPs were baseline or near-baseline resolved in less than 15 minutes.

Insights on the Dynamics and Toxicity of Nanoparticles in Environmental Matrices.

The manufacturing rate of nanoparticles (10–100 nm) is steadily increasing due to their extensive applications in the fabrication of nanoproducts related to pharmaceuticals, cosmetics, medical devices, paints and pigments, energy storage etc. An increase in research related to nanotechnology is also a cause for the production and disposal of nanomaterials at the lab scale. As a result, contamination of environmental matrices with nanoparticles becomes inevitable, and the understanding of the risk of nanoecotoxicology is getting larger attention. In this context, focusing on the environmental hazards is essential. Hence, this manuscript aims to review the toxic effects of nanoparticles on soil, water, aquatic, and terrestrial organisms. The effects of toxicity on vertebrates, invertebrates, and plants and the source of exposure, environmental and biological dynamics, and the adverse effects of some nanoparticles are discussed.

Single-particle ICP-TOFMS with online microdroplet calibration for the simultaneous quantification of diverse nanoparticles in complex matrices

Online microdroplet calibration is used to determine the mass and particle number concentration of inorganic nanoparticles (NPs) without the use of NP standards. This approach can be applied directly to quantify NPs in environmental matrices.

Detection of nanoparticles in Dutch surface waters

Nano-enabled consumer products are a likely source of nanoparticles in the environment and a number of studies have shown the release of nanoparticles from commercial products. Predicted environmental concentrations have been calculated but there is a need for real measurement data to validate these calculations. However, the detection of engineered nanoparticles in environmental matrices is challenging because of the low predicted environmental concentrations which may be in the ng/L range. In this study nanosized Ag, CeO2 and TiO2 have been measured in multiple surface water samples collected along the rivers Meuse and IJssel in the Netherlands using single-particle ICP-MS as measurement technique. Validation of the analytical method showed its capability to quantitatively determine nanoparticles at low concentrations. Concentration mass detection limits for Ag, CeO2 and TiO2 were 0.1ng/L, 0.05ng/L and 10ng/L respectively. Size detection limits for Ag, CeO2 and TiO2 were 14, 10 and 100nm. The results of the study confirm the presence of nano-sized Ag and CeO2 particles and micro-sized TiO2 particles in these surface waters. n-Ag was present in all samples in concentrations ranging from 0.3 to 2.5ng/L with an average concentration of 0.8ng/L and an average particle size of 15nm. n-CeO2 was found in all samples with concentrations ranging from 0.4 to 5.2ng/L with an average concentration of 2.7ng/L and an average particle size of 19nm. Finally, μ-TiO2 was found in all samples with a concentration ranging from 0.2 to 8.1μg/L with an average concentration of 3.1μg/L and an average particle size of 300nm. The particle sizes that were found are comparable with the particle sizes that are used in nanomaterial applications and consumer products. The nanoparticle concentrations confirm the predicted environmental concentrations values in water for all three nanoparticles.

Express It in Numbers: Efforts to Quantify Engineered Nanoparticles in Environmental Matrices Advance

ADVERTISEMENT RETURN TO ISSUEViewpointNEXTExpress It in Numbers: Efforts to Quantify Engineered Nanoparticles in Environmental Matrices AdvanceDesiree L. Plata*†, P. Lee Ferguson†‡, and Paul Westerhoff§View Author Information† ‡ †Department of Civil and Environmental Engineering, ‡Nicholas School of the Environment, Duke University, Durham, North Carolina 27708, United States§ School of Sustainable Engineering and The Built Environment, Arizona State University, Tempe, Arizona 85287-5306, United States*E-mail: [email protected]Cite this: Environ. Sci. Technol. 2012, 46, 22, 12243–12245Publication Date (Web):November 20, 2012Publication History Received12 December 2011Accepted16 July 2012Published online20 November 2012Published inissue 20 November 2012https://doi.org/10.1021/es302789nCopyright © 2012 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1208Altmetric-Citations6LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (2 MB) Get e-AlertsSUBJECTS:Carbon nanotubes,Geological materials,Materials,Nanomaterials,Nanoparticles Get e-Alerts

Single Particle Inductively Coupled Plasma-Mass Spectrometry: A Performance Evaluation and Method Comparison in the Determination of Nanoparticle Size

Sizing engineered nanoparticles in simple, laboratory systems is now a robust field of science; however, application of available techniques to more complex, natural systems is hindered by numerous challenges including low nanoparticle number concentrations, polydispersity from aggregation and/or dissolution, and interference from other incidental particulates. A new emerging technique, single particle inductively coupled plasma-mass spectrometry (spICPMS), has the potential to address many of these analytical challenges when sizing inorganic nanoparticles in environmental matrices. However, to date, there is little beyond the initial feasibility studies that investigates the performance characteristics and validation of spICPMS as a nanoparticle sizing technique. This study compares sizing of four silver nanoparticle dispersions (nominal diameters of 40, 60, 80, and 100 nm) by spICPMS to four established sizing techniques: dynamic light scattering, differential centrifugal sedimentation, nanoparticle tracking analysis, and TEM. Results show that spICPMS is able to size silver nanoparticles, across different sizes and particle number concentrations, with accuracy similar to the other commercially available techniques. Furthermore, a novel approach to evaluating particle coincidence is presented. In addition, spICPMS size measurements were successfully performed on nanoparticles suspended in algal growth media at low concentrations. Overall, while further development of the technique is needed, spICPMS yields important advantages over other techniques when sizing nanoparticles in environmentally relevant media.