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利用电子捕获-串联质谱法测定空气中颗粒物和土壤中硝基取代的多环芳烃的亚部分-每十亿分含量。

Sub-parts-per-billion determination of nitro-substituted polynuclear aromatic hydrocarbons in airborne particulate matter and soil by electron capture-Tandem mass spectrometry.

机构信息

Dipartimento di Chimica Analitica, Università di Torino, Via Pietro Giuria, 5, 10125, Torino, Italy.

出版信息

J Am Soc Mass Spectrom. 1996 Dec;7(12):1255-65. doi: 10.1016/S1044-0305(96)00106-7.

Abstract

A procedure for the determination of nitro-substiruted polynuclear aromatic hydrocarbons (nitro-PAH) on crude air-particulate and soil extracts is introduced. Elimination of purification and fractionation procedures was made possible by the use of both a selective ionization method, such as electron-capture chemical ionization, and a specific fragmentation process, in an experiment of tandem mass spectrometry (gas chromatography-electron capture tandem mass spectrometry). Different mass spectrometric procedures were compared. The best performance was observed when the nitro-PAH molecular ions M were mass-selected by the first analyzer under multiple reaction monitoring conditions and then fragmented to NO 2 (-) (m/z 46). Detection limits were on the order of hundreds of femtograms, as determined in extracts of real environmental samples. This corresponds approximately to 5-15 pg of nitro-PAH per cubic meter of air sampled. Calibration curves were linear over 3 orders of magnitude. Applications to contamination from motor vehicle combustion and the iron industry are briefly discussed.

摘要

介绍了一种用于测定粗空气颗粒物和土壤提取物中硝基取代多环芳烃(硝基-PAH)的方法。通过使用选择性电离方法(如电子俘获化学电离)和特定的碎裂过程,在串联质谱(气相色谱-电子俘获串联质谱)实验中,实现了净化和分级程序的消除。比较了不同的质谱程序。当硝基-PAH 分子离子 M 在多反应监测条件下通过第一分析仪进行质量选择,然后碎裂为 NO 2 (-)(m/z 46)时,观察到最佳性能。在实际环境样品的提取物中,检测限为数百飞克。这大约相当于每立方米采集的空气中含有 5-15 皮克的硝基-PAH。校准曲线在 3 个数量级上呈线性。简要讨论了机动车燃烧和钢铁工业污染的应用。

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