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观察表面:环境样品和消费品中有机氟化合物的 μ-XRF 映射和氟 K 边 μ-XANES 光谱。

Taking a look at the surface: μ-XRF mapping and fluorine K-edge μ-XANES spectroscopy of organofluorinated compounds in environmental samples and consumer products.

机构信息

Bundesanstalt für Materialforschung und -prüfung (BAM), Unter den Eichen 87, 12205 Berlin, Germany.

Paul Scherrer Institute, Swiss Light Sources, 5232 Villigen PSI, Switzerland.

出版信息

Environ Sci Process Impacts. 2023 Jul 19;25(7):1213-1223. doi: 10.1039/d3em00107e.

DOI:10.1039/d3em00107e
PMID:37335293
Abstract

For the first time, μ-X-ray fluorescence (μ-XRF) mapping combined with fluorine K-edge μ-X-ray absorption near-edge structure (μ-XANES) spectroscopy was applied to depict per- and polyfluoroalkyl substance (PFAS) contamination and inorganic fluoride in sample concentrations down to 100 μg kg fluoride. To demonstrate the matrix tolerance of the method, several PFAS contaminated soil and sludge samples as well as selected consumer product samples (textiles, food contact paper and permanent baking sheets) were investigated. μ-XRF mapping allows for a unique element-specific visualization at the sample surface and enables localization of fluorine containing compounds to a depth of 1 μm. Manually selected fluorine rich spots were subsequently analyzed fluorine K-edge μ-XANES spectroscopy. To support spectral interpretation with respect to inorganic and organic chemical distribution and compound class determination, linear combination (LC) fitting was applied to all recorded μ-XANES spectra. Complementarily, solvent extracts of all samples were target-analyzed LC-MS/MS spectrometry. The detected PFAS sum values range from 20 to 1136 μg kg dry weight (dw). All environmentally exposed samples revealed a higher concentration of PFAS with a chain length > C ( 580 μg kg dw PFOS for Soil1), whereas the consumer product samples showed a more uniform distribution with regard to chain lengths from C to C. Independent of quantified PFAS amounts target analysis, μ-XRF mapping combined with μ-XANES spectroscopy was successfully applied to detect both point-specific concentration maxima and evenly distributed surface coatings of fluorinated organic contaminants in the corresponding samples.

摘要

首次应用μ-X 射线荧光(μ-XRF)成像与氟 K 边μ-X 射线吸收近边结构(μ-XANES)光谱学相结合,描绘了浓度低至 100μgkg 氟化物的全氟和多氟烷基物质(PFAS)污染和无机氟化物。为了证明该方法的基质耐受性,研究了若干受 PFAS 污染的土壤和污泥样品以及选定的消费品样品(纺织品、食品接触纸和永久性烤板)。μ-XRF 成像可在样品表面进行独特的元素特异性可视化,并能够将含氟化合物定位到 1μm 的深度。随后,对手动选择的富含氟的斑点进行氟 K 边μ-XANES 光谱分析。为了支持有关无机和有机化学分布以及化合物类别确定的光谱解释,对所有记录的μ-XANES 光谱均应用线性组合(LC)拟合。此外,对所有样品的溶剂提取物进行 LC-MS/MS 靶向分析。检测到的 PFAS 总和值范围为 20 至 1136μgkg 干重(dw)。所有受环境暴露的样品均显示出更高浓度的 PFAS,其链长>C(Soil1 中的 PFOS 为 580μgkg dw),而消费品样品在 C 至 C 的链长方面显示出更均匀的分布。独立于定量的 PFAS 量进行目标分析,μ-XRF 成像与μ-XANES 光谱学的联合应用成功地检测到相应样品中含氟有机污染物的点状浓度最大值和均匀分布的表面涂层。

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