Magnusson R, Nordlander T, Östin A
The Swedish Defence Research Agency, FOI CBRN Defence and Security, SE-90182 Umeå, Sweden.
The Swedish Armed Forces, National CBRN Defence Centre, CBRN-Analysis, SE-90176 Umeå, Sweden.
J Chromatogr A. 2016 Jan 15;1429:40-52. doi: 10.1016/j.chroma.2015.12.009. Epub 2015 Dec 8.
Sampling teams performing work at sea in areas where chemical munitions may have been dumped require rapid and reliable analytical methods for verifying sulfur mustard leakage from suspected objects. Here we present such an on-site analysis method based on dynamic headspace GC-MS for analysis of five cyclic sulfur mustard degradation products that have previously been detected in sediments from chemical weapon dumping sites: 1,4-oxathiane, 1,3-dithiolane, 1,4-dithiane, 1,4,5-oxadithiephane, and 1,2,5-trithiephane. An experimental design involving authentic Baltic Sea sediments spiked with the target analytes was used to develop an optimized protocol for sample preparation, headspace extraction and analysis that afforded recoveries of up to 60-90%. The optimized method needs no organic solvents, uses only two grams of sediment on a dry weight basis and involves a unique sample presentation whereby sediment is spread uniformly as a thin layer inside the walls of a glass headspace vial. The method showed good linearity for analyte concentrations of 5-200 ng/g dw, good repeatability, and acceptable carry-over. The method's limits of detection for spiked sediment samples ranged from 2.5 to 11 μg/kg dw, with matrix interference being the main limiting factor. The instrumental detection limits were one to two orders of magnitude lower. Full-scan GC-MS analysis enabled the use of automated mass spectral deconvolution for rapid identification of target analytes. Using this approach, analytes could be identified in spiked sediment samples at concentrations down to 13-65 μg/kg dw. On-site validation experiments conducted aboard the research vessel R/V Oceania demonstrated the method's practical applicability, enabling the successful identification of four cyclic sulfur mustard degradation products at concentrations of 15-308μg/kg in sediments immediately after being collected near a wreck at the Bornholm Deep dumpsite in the Baltic Sea.
在可能倾倒过化学弹药的海域作业的采样团队,需要快速可靠的分析方法来验证疑似物体是否有硫芥泄漏。在此,我们介绍一种基于动态顶空气相色谱 - 质谱联用技术的现场分析方法,用于分析五种环状硫芥降解产物,这些产物此前已在化学武器倾倒场的沉积物中被检测到:1,4 - 氧硫杂环己烷、1,3 - 二硫戊环、1,4 - 二硫环己烷、1,4,5 - 氧二硫杂环戊烷和1,2,5 - 三硫杂环戊烷。采用一种实验设计,即向真实的波罗的海沉积物中添加目标分析物,以开发一种优化的样品制备、顶空萃取和分析方案,回收率高达60 - 90%。优化后的方法无需有机溶剂,以干重计仅使用两克沉积物,且采用独特的样品呈现方式,即将沉积物均匀地铺展在玻璃顶空瓶壁内形成薄层。该方法在分析物浓度为5 - 200 ng/g干重时具有良好的线性、良好的重复性和可接受的残留。加标沉积物样品的方法检测限为2.5至11 μg/kg干重区间,基质干扰是主要限制因素。仪器检测限低一至两个数量级。全扫描气相色谱 - 质谱分析能够利用自动质谱解卷积快速鉴定目标分析物。采用这种方法,可在加标沉积物样品中鉴定出浓度低至13 - 65 μg/kg干重的分析物。在“大洋洲号”研究船上进行的现场验证实验证明了该方法的实际适用性,能够在波罗的海博恩霍尔姆深海倾倒场一艘沉船附近采集沉积物后,立即成功鉴定出浓度为15 - 308 μg/kg的四种环状硫芥降解产物。