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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Trace determination of sulphur mustard and related compounds in water by headspace-trap gas chromatography-mass spectrometry
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Trace determination of sulphur mustard and related compounds in water by headspace-trap gas chromatography-mass spectrometry

机译:顶空捕集-气相色谱-质谱法测定水中的硫芥菜及相关化合物

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A method for trace determination of sulphur mustard (HD) and some of its cyclic decomposition compounds in water samples has been developed using headspace-trap in combination with gas chromatography-mass spectrometry (GC-MS). Factorial design was used for optimisation of the method. The trap technology allows enrichment and focusing of the analytes on an adsorbent, hence the technique offers better sensitivity compared to conventional static headspace. A detection limit of 1 ng/ml was achieved for HD, while the cyclic sulphur compounds 1,4-thioxane, 1,3-dithiolane and 1,4-dithiane could be detected at a level of 0.1 ng/ml. The method was validated for the stable cyclic compounds in the concentration range from the limit of quantification (LOQ: 0.2-0.4 ng/ml) to hundred times LOQ. The within and between assay precisions at hundred times LOQ were 1-2% and 7-8% relative standard deviation, respectively. This technique requires almost no sample handling, and the total time for sampling and analysis was less than 1 h. The method was successfully employed for muddy river water and sea water samples.
机译:使用顶空捕集-气相色谱-质谱联用(GC-MS),开发了一种痕量测定水样中芥子气(HD)及其某些环状分解化合物的方法。使用析因设计来优化方法。捕集阱技术可使分析物富集并集中在吸附剂上,因此与传统的静态顶空相比,该技术具有更高的灵敏度。 HD的检出限为1 ng / ml,而环状硫化合物1,4-噻烷,1,3-二硫杂环戊烷和1,4-二噻吩的检出限为0.1 ng / ml。在定量限(LOQ:0.2-0.4 ng / ml)到LOQ的100倍范围内,对稳定的环状化合物进行了方法验证。百倍LOQ时的内部和之间测定精度分别为相对标准偏差的1-2%和7-8%。该技术几乎不需要样品处理,并且采样和分析的总时间少于1小时。该方法已成功用于泥泞的河水和海水样品。

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