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Determination of Endocrine Disrupting Compounds in Marine Water by Nanoliquid Chromatography/Direct-Electron Ionization Mass Spectrometry

机译:纳米液相色谱/直接电离质谱法测定海水中的内分泌干扰物

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摘要

We present a new method for the determination of 29 endocrine-disrupting compounds in marine water. This method is based on a solid-phase extraction preconcentration technique, followed by a nanoscale liquid chromatography/direct-electron ionization (EI) mass spectrometric analysis. Direct-EI is a novel technique for the rapid conversion of a GC/MS into an efficient and reliable LC/MS for EI detection. The capability to acquire EI mass spectra of the analytes, and to operate in selected ion monitoring mode during real sample analyses, allows certain identification and precise quantification. In addition, this method is not influenced by the polarity of the analytes and does not require different detection modes (positive and negative) for identification with API techniques. Limits of detection of the method span from 0.4 to 118.7 ng(centre dot)L~(-1), corresponding to an instrumental detection limit of 0.005-1.260 ng. Linear regression and recovery experiment data, together with their standard deviations, are also presented. Marine water samples were collected along the middle-western Adriatic Coast (Italy), near the shore and at the mouth of rivers and canals.
机译:我们提出了一种测定海水中29种内分泌干扰化合物的新方法。该方法基于固相萃取预浓缩技术,然后进行纳米级液相色谱/直接电离(EI)质谱分析。 Direct-EI是一种将GC / MS快速转换为高效可靠的EI检测LC / MS的新颖技术。采集分析物的EI质谱,并在实际样品分析过程中以选定的离子监测模式运行的能力,可以实现一定的识别和精确的定量。此外,该方法不受分析物极性的影响,并且不需要使用不同的检测模式(阳性和阴性)进行API技术鉴定。该方法的检出限范围为0.4至118.7 ng(中心点)L〜(-1),对应的仪器检出限为0.005-1.260 ng。还显示了线性回归和恢复实验数据以及它们的标准偏差。沿中亚得里亚海海岸(意大利),海岸附近以及河流和运河口收集了海水样品。

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