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DOI | 10.1039/c7en00952f |
Where is the nano? Analytical approaches for the detection and quantification of TiO2 engineered nanoparticles in surface waters | |
Gondikas, Andreas1,2,7; von der Kammer, Frank1,2; Kaegi, Ralf3; Borovinskaya, Olga4; Neubauer, Elisabeth1,2; Navratilova, Jana1,2,8; Praetorius, Antonia1,2,5; Cornelis, Geert6; Hofmann, Thilo1,2 | |
发表日期 | 2018-02-01 |
ISSN | 2051-8153 |
卷号 | 5期号:2页码:313-326 |
英文摘要 | Detecting and quantifying engineered nanoparticles (ENPs) in complex environmental matrices requires the distinction between natural nanoparticles (NNPs) and ENPs. The distinction of NNPs and ENPs for regulatory purposes calls for cost-efficient methods, but is hampered by similarities in intrinsic properties, such as particle composition, size, density, surface chemistry, etc. Titanium dioxide (TiO2) ENPs, for instance, are produced in very large quantities but Ti also commonly occurs naturally in nano-scale minerals. In this work, we focus on utilizing particle size and composition to identify ENPs in a system with a significant background concentration of the target metal. We have followed independent approaches involving both conventional and state-of-the-art analytical techniques to detect and quantify TiO2 ENPs released into surface waters from sunscreen products and to distinguish them from Ti-bearing NNPs. To achieve this, we applied single particle inductively coupled plasma mass spectrometry with single-element (spICPMS) and multi-element detection (time-of-flight) spICP-TOFMS, together with transmission electron microscopy (TEM), automated scanning electron microscopy (autoSEM), and bulk elemental analyses. A background concentration of Ti-bearing NPs (approximately 5 x 10(3) particles per ml), possibly of natural origin, was consistently observed outside the bathing season. This concentration increased by up to 40% during the bathing season. Multi-element analysis of individual particles using spICP-TOFMS revealed that Al, Fe, Mn, and Pb are often present in natural Ti-bearing NPs, but no specific multi-element signatures were detected for ENPs. Our data suggests that TiO2 ENPs enter the lake water during bathing activities, eventually agglomerating and sedimenting. We found adhesion of the TiO2 ENPs to the air-water interface for short time periods, depending on wind conditions. This study demonstrates that the use of spICP-TOFMS and spICPMS in combination with other conventional analytical techniques offers significant advantages for discriminating between NNPs and ENPs. The quantitative data produced in this work can be used as input for modeling studies or as a benchmark for analysis protocols and model validations. |
语种 | 英语 |
WOS记录号 | WOS:000425492800007 |
来源期刊 | ENVIRONMENTAL SCIENCE-NANO |
来源机构 | 美国环保署 |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/61106 |
作者单位 | 1.Univ Vienna, Dept Environm Geosci, A-1090 Vienna, Austria; 2.Univ Vienna, Environm Sci Res Network, A-1090 Vienna, Austria; 3.Eawag, Dept Proc Engn, CH-8600 Dubendorf, Switzerland; 4.TOFWERK, CH-3600 Thun, Switzerland; 5.Univ Vienna, Res Platform Nanonorms Nat, A-1090 Vienna, Austria; 6.Swedish Univ Agr Sci, Dept Soil & Environm, S-75651 Uppsala, Sweden; 7.Gothenburg Univ, Dept Marine Sci, S-45178 Kristineberg, Fiskebackskil, Sweden; 8.US EPA, Natl Exposure Res Lab, Res Triangle Pk, NC 27709 USA |
推荐引用方式 GB/T 7714 | Gondikas, Andreas,von der Kammer, Frank,Kaegi, Ralf,et al. Where is the nano? Analytical approaches for the detection and quantification of TiO2 engineered nanoparticles in surface waters[J]. 美国环保署,2018,5(2):313-326. |
APA | Gondikas, Andreas.,von der Kammer, Frank.,Kaegi, Ralf.,Borovinskaya, Olga.,Neubauer, Elisabeth.,...&Hofmann, Thilo.(2018).Where is the nano? Analytical approaches for the detection and quantification of TiO2 engineered nanoparticles in surface waters.ENVIRONMENTAL SCIENCE-NANO,5(2),313-326. |
MLA | Gondikas, Andreas,et al."Where is the nano? Analytical approaches for the detection and quantification of TiO2 engineered nanoparticles in surface waters".ENVIRONMENTAL SCIENCE-NANO 5.2(2018):313-326. |
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