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Determination of ~(13)C/~(12)C-ratios of anthropogenic organic contaminants in river water samples by GC-irmMS

机译:气相色谱-红外光谱法测定河水样品中人为有机污染物的〜(13)C /〜(12)C比率

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摘要

This study describes the application of a common analytical procedure adapted for compound-specific stable carbon isotope analyses of riverine contaminants. To evaluate the sensitivity of the analytical method and the precision of the isotopic data obtained, a set of numerous substances at different concentration levels were measured. For most of the anthropogenic contaminants investigated (including chlorinated aliphatics and aromatics, musk fragrances, phthalate-based plasticizers and tetrabutyl tin) acceptable carbon isotope analyses could be obtained down to amounts of approximately 5 ng absolutely applied to the gas chromatograph. These amounts correspond to concentrations in water samples at a natural abundance level of approximately 50-200 ng L~(-1) (low to medium contaminated river systems). However, it has to be considered that the precision and the sensitivity of the analytical method depend partially on the chemical properties of the substances measured. Five recovery experiments were conducted to assess changes in carbon isotope ratios during sample preparation and measurement. The compounds selected for these experiments are known riverine contaminants. Isotopic shifts or higher variations of the isotope ratios as a result of the analytical procedures applied were observed only for a couple of contaminants. Furthermore, compound-specific carbon isotope analyses were performed on eight water extracts of the Rhine river. By comparing the variation of the data of several individual compounds with the deviations obtained from the recovery experiments, it was possible to differentiate contaminants with unaffected isotope ratios and substances with significant alterations of the δ~(13)C-values.
机译:本研究描述了适用于河流污染物化合物特异性稳定碳同位素分析的通用分析程序的应用。为了评估分析方法的灵敏度和获得的同位素数据的准确性,对一组不同浓度水平的多种物质进行了测量。对于所研究的大多数人为污染物(包括氯化脂肪族和芳香族化合物,麝香香料,邻苯二甲酸酯类增塑剂和四丁基锡),可接受的碳同位素分析量低至大约5 ng(绝对用于气相色谱仪)。这些量对应于自然丰度约为50-200 ng L〜(-1)(低至中度污染的河流系统)的水样中的浓度。但是,必须考虑到分析方法的精度和灵敏度部分取决于所测物质的化学性质。进行了五个回收率实验,以评估样品制备和测量过程中碳同位素比的变化。选择用于这些实验的化合物是已知的河流污染物。由于仅采用了两种污染物,观察到的同位素变化或同位素比率的较高变化是所应用分析程序的结果。此外,对莱茵河的八种水提取物进行了化合物特异性碳同位素分析。通过将几种化合物的数据变化与回收率实验得出的偏差进行比较,可以区分出同位素比率不受影响的污染物和δ〜(13)C值发生重大变化的物质。

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