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Determination of transformation products of per- and polyfluoroalkyl substances at trace levels in agricultural plants

机译:农业植物中痕量水平的血液和多氟烷基物质转化产物的测定

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Per- and polyfluoroalkyl substances (PFASs) are ubiquitous in the environment. However, only a limited number of predominantly persistent perfluoroalkyl acids (PFAAs) have been analyzed in edible plants so far. We present a generic trace analytical method that allows for quantification of 16 intermediate fluorotelomer alcohol (FTOH)- or perfluoroalkane sulfonamidoethanol (FASE)-based transformation products as well as 18 PFAAs in plants. Additionally, 36 suspected intermediate PFAS transformation products were qualitatively analyzed. The ultrasound-assisted solid-liquid extraction of wheat and maize grain, maize leaves, Jerusalem artichoke and ryegrass (1-5 g plant sample intake) was followed by a clean-up with dispersive solid-phase extraction using graphitized carbon adsorbent (5-10 mg per sample) and chemical analysis by reversed phase liquid chromatography-tandem mass spectrometry. The method was based on matrix matched and extracted calibration and displayed good precision with relative standard deviations in triplicate analyses typically below 15% for all quantified analytes and matrices. An average deviation of 12% between quantified concentrations obtained by matrix matched and extracted calibration and a method based on isotopically labelled internal standards underlines the good trueness of the method. The method quantification limits for the majority of analytes in all plant samples were in the low ng/kg concentration range on a dry weight basis. Plant matrices were analyzed from crops grown on agricultural fields that have been contaminated with PFASs. FTOH- and/or FASE-based intermediate transformation products were detected in all samples with N-ethyl perfluorooctane sulfonamidoacetic acid (EtFOSAA) and perfluorooctane sulfonamide (FOSA) as the prevailing compounds in concentrations up to several hundred ng/kg in maize leaves. The 9:3 Acid (a transformation product of 10:2 FTOH) was tentatively identified. In accordance with these findings, the final degradation products perfluorooctane sulfonic acid (PFOS) and perfluorodecanoic acid (PFDA) were frequently detected. For perfluoroalkyl carboxylic acids (PFCAs), according to earlier findings, short chain homologues generally displayed the highest levels (up to 98 pg/kg for perfluorobutanoic acid (PFBA) in maize leaves). However, maize grain was an exception showing the highest concentrations for long chain PFCAs, whereas PFBA was not detected. The uptake of high levels of PFASs into plants is of concern since these may be used as animal feed or represent a direct exposure medium for humans. (C) 2020 Elsevier B.V. All rights reserved.
机译:每氟氟烷基物质(PFASS)在环境中普遍存在。然而,到目前为止,仅在可食用的植物中分析了有限数量的主要持续的全氟烷基酸(PFAAs)。我们提出了一种通用的痕量分析方法,其允许定量16个中间氟羧醇(FTOH) - 或全氟烷烃磺胺酰氯乙醇(ZHASE)的转化产物以及18种植物中的18个PFAAs。另外,36种疑似中间PFAS转化产物进行了定性分析。小麦和玉米籽粒,玉米叶,耶路撒冷朝鲜蓟和黑麦草(1-5g植物样品摄入量)的超声辅助固液提取,然后用石墨化碳吸附剂的分散固相提取清除(5-通过反相液相色谱 - 串联质谱法,每种样品10mg)和化学分析。该方法基于矩阵匹配和提取的校准,并显示出良好的精度,其三重分析中的相对标准偏差通常低于15%的所有量化分析物和矩阵。通过基质匹配和提取的校准获得的量化浓度与基于同位素标记的内标的方法的平均偏差和基于同位素标记的内标的方法强调了该方法的良好特征。所有植物样品中大多数分析物的方法量化限制在低Ng / kg浓度范围内为干重基础。植物矩阵从被污染的农业领域种植的作物分析了杂粮。在所有用N-乙基全氟辛烷磺胺酰胺乙酸(ETFOSAA)和全氟辛烷磺酰胺(FOSA)的所有样品中检测到FTAH-和/或基于源的中间转化产物,作为玉米叶中浓度的浓度为浓度的常年化合物。暂时鉴定9:3酸(10:2 FTOH的转化乘积)。根据这些发现,经常检测到最终降解产物全氟辛烷磺酸(PFOS)和全氟二癸酸(PFDA)。对于全氟烷基羧酸(PFCAS),根据前面的结果,短链同源物通常呈现出最高水平(玉米叶片的全氟丁酸(PFBA)最高水平(高达98pg / kg)。然而,玉米谷物是显示长链PFCAS最高浓度的例外,而PFBA未被检测到。由于这些可以用作动物饲料或者是用于人类的直接暴露培养基,因此对植物的高水平施用是令人担忧的。 (c)2020 Elsevier B.v.保留所有权利。

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