首页> 外文期刊>Analytica chimica acta >Determination of hydrazine in drinking water: Development and multivariate optimization of a rapid and simple solid phase microextraction-gas chromatography-triple quadrupole mass spectrometry protocol
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Determination of hydrazine in drinking water: Development and multivariate optimization of a rapid and simple solid phase microextraction-gas chromatography-triple quadrupole mass spectrometry protocol

机译:饮用水中肼的测定:快速简单的固相微萃取-气相色谱-三重四极杆质谱法的发展及多变量优化

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摘要

In this work, the capabilities of solid phase microextraction were exploited in a fully optimized SPME-GC-QqQ-MS analytical approach for hydrazine assay. A rapid and easy method was obtained by a simple derivatization reaction with propyl chloroformate and pyridine carried out directly in water samples, followed by automated SPME analysis in the same vial without further sample handling. The affinity of the different derivatized compounds obtained towards five commercially available SPME coatings was evaluated, in order to achieve the best extraction efficiency. GC analyses were carried out using a GC-QqQ-MS instrument in selected reaction monitoring (SRM) acquisition mode which has allowed the achievement of high specificity by selecting appropriate precursor-product ion couples improving the capability in analyte identification. The multivariate approach of experimental design was crucial in order to optimize derivatization reaction, SPME process and tandem mass spectrometry parameters. Accuracy of the proposed protocol, tested at 60,200 and 800 ng L~(-1), provided satisfactory values (114.2%, 83.6% and 98.6%, respectively), whereas precision (RSD%) at the same concentration levels were of 10.9%, 7.9% and 7.7% respectively. Limit of detection and quantification of 4.4 and 8.3 ng L~(-1) were obtained. The reliable application of the proposed protocol to real drinking water samples confirmed its capability to be used as analytical tool for routine analyses.
机译:在这项工作中,在用于肼测定的完全优化的SPME-GC-QqQ-MS分析方法中利用了固相微萃取的能力。通过直接在水样品中与氯甲酸丙酯和吡啶进行简单的衍生化反应,然后在同一小瓶中进行自动SPME分析,而无需进一步处理样品,即可获得快速简便的方法。为了获得最佳提取效率,评估了获得的不同衍生化合物对五种市售SPME涂层的亲和力。使用GC-QqQ-MS仪器在选定的反应监测(SRM)采集模式下进行了GC分析,通过选择合适的前体产物离子对提高了分析物鉴定的能力,从而实现了高特异性。实验设计的多元方法对于优化衍生化反应,SPME工艺和串联质谱参数至关重要。在60,200和800 ng L〜(-1)下测试的拟议方案的准确性提供了令人满意的值(分别为114.2%,83.6%和98.6%),而在相同浓度水平下的精密度(RSD%)为10.9% ,分别为7.9%和7.7%。检出限和定量限分别为4.4和8.3 ng L〜(-1)。所提出的方案在实际饮用水样品中的可靠应用证实了其可用作常规分析的分析工具的能力。

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