用于全氟化合物分子筛选的微等离子体电离/轨道阱质谱的初步演示

IF 3.1 2区 化学 Q2 CHEMISTRY, ANALYTICAL Journal of Analytical Atomic Spectrometry Pub Date : 2024-08-27 DOI:10.1039/D4JA00157E
Joseph V. Goodwin, Claudia Masucci, Davide Bleiner and R. Kenneth Marcus
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引用次数: 0

摘要

全氟烷基和多氟烷基(PFAS)持久性有机污染物的快速测定日益受到关注,但在仪器方面仍具有挑战性。传统技术需要对目标物种有一定的初步了解,而且往往需要耗时的多步骤程序。通常情况下,样品污染的浓度和成分范围是未知的。这就限制了对新材料环境足迹水平和最终结果的研究。液体取样-大气压辉光放电(LS-APGD)是一种微等离子体电离源,可提供有关分析物的原子和分子(CAM)综合信息。为了扩展电离源的应用范围,LS-APGD 与 Orbitrap 傅立叶变换质谱仪 (FT-MS) 联用,以鉴定其分析全氟辛烷磺酸化合物的能力,包括全氟辛酸 (PFOA) 和全氟辛基磺酸 (PFOS),以及全氟磺酰胺、丙烯酸酯和端基醇 (FTOH)。总的来说,这些化合物带来了令人难以置信的分析挑战,因为它们存在于不同的基质中,无处不在(包括实验室),缺乏通用的电离方法,而且在质谱分析之前必须进行复杂的预浓缩/分离。这里所做的努力为此类分析设定了基本特征,但需要注意的是,本实验室并不具备高灵敏度 PFAS 分析的条件,这为今后更深入的发展创造了机会。各化合物类型的质谱特征非常一致,其中 PFOA、PFOS、磺酰胺类化合物和丙烯酸酯类化合物的质谱特征以各自的 M-H(去质子化)假分子离子为主。FTOH 化合物是通过确定共同的特征碎片途径来确定的。光谱的简易性和高质 量分辨率/精确度表明,可以在不进行化学分离的情况下进行测定。对所有物种都实现了线性响应曲线,在不进行预浓缩的情况下,60 μL 输液的检测限分别为 20 pg mL-1 (PFOA)和 310 pg mL-1 (PFOS)。与既有的电喷雾离子化 (ESI-MS) 方法相比,CAM/Orbitrap 耦合方法对所有 PFAS 化合物都具有物种选择性,而且无需事先进行色谱分离或预浓缩,就能对混合物进行鉴别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Initial demonstration of microplasma ionization/Orbitrap mass spectrometry for molecular screening of perfluorinated compounds†

The rapid determination of per and polyfluoroalkyl (PFAS) persistent organic pollutants is of growing interest but remains instrumentally challenging. Traditional techniques require some preliminary knowledge of the target species and often time-consuming multistep procedures. Often, the concentration and compositional range of sample contamination is unknown. This is a limitation in investigating the level and fate of a new material's environmental footprint. The liquid sampling – atmospheric pressure glow discharge (LS-APGD) is a microplasma ionization source which provides combined atomic and molecular (CAM) information about analytes. To extend upon the demonstrated applications of the ionization source, the LS-APGD was coupled to an Orbitrap Fourier transform mass spectrometer (FT-MS) to characterize its capabilities towards the analysis of PFAS compounds, including perfluorooctanoic acid (PFOA) and perfluorooctyl sulfonic (PFOS) acid, extending to the perfluoro sulfonamides, acrylates, and telomer alcohols (FTOH). Across the board, these compounds pose incredible analytical challenges regarding the diverse matrices where they are found, their ubiquitous nature (including the laboratory), the lack of a universal ionization method, and the necessity for complex preconcentration/separation prior to MS analysis. The efforts here set the basic characteristics for such analyses, with the caveat that this laboratory is not outfitted for high-sensitivity PFAS analysis, setting up opportunities for more in-depth developments in the future. The mass spectral features for the respective compound types are very uniform, with those of PFOA, PFOS, sulfonamides, and acrylates dominated by their respective M–H (deprotonated) pseudomolecular ions. FTOH compounds were determined by identifying a common characteristic fragmentation pathway. The simplicity of the spectra and high mass resolution/accuracy suggest that determinations might be made without chemical separations. Linear response curves are realized for all species, with limits of detection of 20 pg mL−1 (PFOA) and 310 pg mL−1 (PFOS) obtained, without pre-concentration, for 60 μL infusions. In contrast to the established electrospray ionization (ESI-MS) methods, the CAM/Orbitrap coupling provides species selectivity across the entire breadth of the PFAS compounds and the potential for mixture discrimination without prior chromatographic separation or preconcentration.

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来源期刊
CiteScore
6.20
自引率
26.50%
发文量
228
审稿时长
1.7 months
期刊介绍: Innovative research on the fundamental theory and application of spectrometric techniques.
期刊最新文献
Back cover Evaluation of miniaturized ultrasonic nebulization for high-efficiency sampling in characterization of silver nanoparticles by single particle inductively coupled plasma mass spectrometry† Atomic spectrometry update: review of advances in the analysis of metals, chemicals and materials Assessing the performance of handheld LIBS for predicting soil organic carbon and texture in European soils† Research on a bimodal fusion detection method for surface defects of metal AM components based on LIBS
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