对气相挥发性有机化合物进行特定化合物同位素分析的溶剂采样法现场演示

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-02-01 DOI:10.1016/j.jconhyd.2024.104310
Daniel Bouchard , Daniel Hunkeler , Massimo Marchesi , Ramon Aravena , Tim Buscheck
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引用次数: 0

摘要

在一项受控实地研究中,采用了基于溶剂的取样方法来收集气相挥发性有机化合物 (VOC) 并进行特定化合物同位素分析 (CSIA)。这种基于溶剂的方法使用甲醇作为沉淀物,在土壤空气和废气采样过程中积聚石油碳氢化合物。对于收集到的每个气体样本,都会对地下合成碳氢化合物源排放的五种挥发性有机化合物(苯、甲苯、邻二甲苯、环戊烷和辛烷)进行碳同位素分析(δ13C)。气态挥发性有机化合物(从土壤气体和排出气体中收集)的 δ13C 值与源材料(非水相液体 - NAPL)中存在并溶解在地下水中的相同挥发性有机化合物的测量值进行了比较,以评估基于溶剂的取样方法在提供准确同位素测量值方面的可靠性。由于 NAPL 源仅由 12 种挥发性有机化合物组成,因此避免了与分析程序有关的潜在偏差(如共洗脱),从而强调了与现场有关的偏差。这次实地评估证明了溶剂型方法有能力进行精确的 δ13C 测量。在 41 个比较点中,有 39 个点的气态值和 NAPL 值之间的同位素差异为 < 1 ‰,因此根据常见的同位素不确定性误差 ±0.5 ‰,被认为不存在统计学差异。此外,目前的实地研究是首次报告从同一样品中获得的多达五种气相挥发性有机化合物的δ13C 测量结果的实地研究,这似乎对挥发性有机化合物的归宿或法医研究很有意义。这种采样方法可以进行多种挥发性有机化合物同位素测量,有助于加强气态挥发性有机化合物与可疑排放源之间的联系评估。因此,本文介绍的实地结果支持在挥发性有机化合物蒸汽研究框架内应用这种采样方法进行 CSIA 评估。
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Field demonstration for the solvent-based sampling method to perform compound-specific isotope analysis on gas-phase VOC

The solvent-based sampling method for collecting gas-phase volatile organic compounds (VOCs) and conducting compound-specific isotope analysis (CSIA) was deployed during a controlled field study. The solvent-based method used methanol as a sink to accumulate petroleum hydrocarbons during the sampling of soil air and effluent gas. For each gaseous sample collected, carbon isotope analysis (δ13C) was conducted for a selection of five VOCs (benzene, toluene, o-xylene, cyclopentane and octane) emitted by a synthetic hydrocarbon source emplaced in the subsurface. The δ13C values obtained for gaseous VOCs (collected from soil gas and effluent gas) were compared to measurements obtained for the same VOCs present in the source material (none aqueous phase liquid - NAPL) and dissolved in groundwater to evaluate the reliability of the solvent-based sampling method in providing accurate isotope measurements. Since the NAPL source was composed of only 12 VOCs, potential bias related to the analytical procedure (such as co-elution) were avoided, hence emphasizing on field-related bias. This field evaluation demonstrated the capacity of the solvent-based method to produce precise and accurate δ13C measurements. The isotopic discrepancies between the gaseous and the NAPL values were < 1 ‰ for 39 out of the 41 comparison points, thus deemed not statistically different based on a common isotopic uncertainty error of ±0.5 ‰. Moreover, the current field study is the first field study to report δ13C measurements for up to five gas-phase VOCs obtained from the same sample, which appears to be of interest for VOC fate or forensic studies. The possibility to use several VOC isotopic measurements enabled by the sampling method would contribute to strengthen the connection assessment between gaseous VOCs and the suspected emitting source. Accordingly, the field results presented herein support the application of this sampling methodology to conduct CSIA assessment in the frame of VOC vapor studies.

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