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Mass spectrometric analysis of chemical warfare agents and their degradation products in soil and synthetic samples

机译:土壤和合成样品中化学战剂及其降解产物的质谱分析

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A packed capillary liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) method was developed for the identification of chemical warfare agents, their degradation products and related compounds in synthetic tabun samples and in soil samples collected from a former mustard storage site. A number of organophosphorus and organosulfur compounds that had not been previously characterized were identified, based on acquired high-resolution ESI-MS data. At lower sampling cone voltages, the ESI mass spectra were dominated by protonated, sodiated and protonated acetonitrile adducts and/or their dimers that could be used to confirm the molecular mass of each compound. Structural information was obtained by inducing product ion formation in the ESI interface at higher sampling cone voltages. Representative ESI-MS mass spectra for previously uncharacterized compounds were incorporated into a database as part of an on-going effort in chemical warfare agent detection and identification. The same samples were also analyzed by capillary column gas chromatography (GC)-MS in order to compare an established method with LC-ESI-MS for chemical warfare agent identification. Analysis times and full-scanning sensitivities were similar for both methods, with differences being associated with sample matrix, ease of ionization and compound volatility. GC-MS would be preferred for organic extracts and must be used for the determination of mustard and relatively non-polar organosulfur degradation products, including 1,4-thioxane and 1,4-dithiane, as these compounds do not ionize during ESI-MS. Diols, formed following hydrolysis of mustard and longer-chain sulfur vesicants, may be analyzed using both methods with LC-ESI-MS providing improved chromatographic peak shape. Aqueous samples and extracts would, typically, be analyzed by LC-ESI-MS, since these analyses may be conducted directly without the need for additional sample handling and/or derivatization associated with GC-MS determinations. Organophosphorus compounds, including chemical warfare agents, related compounds and lower volatility hydrolysis products may all be determined during a single LC-ESI-MS analysis. Derivatization of chemical warfare agent hydrolysis products and other compounds with hydroxyl substitution would be required prior to GC-MS analysis, giving LC-ESI-MS a definite advantage over GC-MS for the analysis of samples containing chemical warfare agents and/or their hydrolysis products.
机译:建立了填充毛细管液相色谱-电喷雾电离质谱(LC-ESI-MS)方法,用于鉴定化学战剂,其降解产物和相关化合物,这些化学战剂来自合成芥末样品和从以前的芥菜储存地点收集的土壤样品中。根据获得的高分辨率ESI-MS数据,鉴定出许多以前未表征的有机磷和有机硫化合物。在较低的采样锥电压下,ESI质谱以质子化,质子化和质子化的乙腈加合物和/或其二聚体为主导,可用于确认每种化合物的分子量。通过在较高的采样锥电压下诱导ESI界面中的产物离子形成来获得结构信息。先前未表征的化合物的代表性ESI-MS质谱已纳入数据库,这是化学战剂检测和识别方面正在进行的工作的一部分。还通过毛细管柱气相色谱法(GC)-MS分析了相同的样品,以便将建立的方法与LC-ESI-MS进行化学战剂鉴定进行比较。两种方法的分析时间和全扫描灵敏度相似,不同之处在于样品基质,电离的容易程度和化合物的挥发性。 GC-MS将是有机提取物的首选,并且必须用于测定芥子油和相对非极性的有机硫降解产物,包括1,4-噻吨和1,4-二噻吩,因为这些化合物在ESI-MS过程中不会电离。芥子油和长链硫表面活性剂水解后形成的二元醇可以使用LC-ESI-MS两种方法进行分析,以提供改善的色谱峰形。水样品和提取物通常将通过LC-ESI-MS分析,因为这些分析可以直接进行,而无需进行额外的样品处理和/或与GC-MS测定相关的衍生化。包括化学战剂,相关化合物和较低挥发性水解产物在内的有机磷化合物都可以在一次LC-ESI-MS分析中测定。在进行GC-MS分析之前,需要对化学战剂水解产物和其他具有羟基取代基的化合物进行衍生化处理,这使得LC-ESI-MS在分析包含化学战剂和/或其水解的样品方面具有优于GC-MS的绝对优势产品。

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