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将超音速分子束-超热表面电离与飞行时间质谱联用,用于饮用水中多环芳烃的痕量检测,以减少样品制备和分析时间。

Supersonic molecular beam-hyperthermal surface ionisation coupled with time-of-flight mass spectrometry applied to trace level detection of polynuclear aromatic hydrocarbons in drinking water for reduced sample preparation and analysis time.

作者信息

Davis S C, Makarov A A, Hughes J D

机构信息

HD Technologies Ltd., Manchester, UK.

出版信息

Rapid Commun Mass Spectrom. 1999;13(4):247-50. doi: 10.1002/(SICI)1097-0231(19990228)13:4<247::AID-RCM448>3.0.CO;2-U.

Abstract

Analysis of sub-ppb levels of polynuclear aromatic hydrocarbons (PAHs) in drinking water by high performance liquid chromatography (HPLC) fluorescence detection typically requires large water samples and lengthy extraction procedures. The detection itself, although selective, does not give compound identity confirmation. Benchtop gas chromatography/mass spectrometry (GC/MS) systems operating in the more sensitive selected ion monitoring (SIM) acquisition mode discard spectral information and, when operating in scanning mode, are less sensitive and scan too slowly. The selectivity of hyperthermal surface ionisation (HSI), the high column flow rate capacity of the supersonic molecular beam (SMB) GC/MS interface, and the high acquisition rate of time-of-flight (TOF) mass analysis, are combined here to facilitate a rapid, specific and sensitive technique for the analysis of trace levels of PAHs in water. This work reports the advantages gained by using the GC/HSI-TOF system over the HPLC fluorescence method, and discusses in some detail the nature of the instrumentation used.

摘要

采用高效液相色谱(HPLC)荧光检测法分析饮用水中多环芳烃(PAHs)亚皮克级水平,通常需要大量水样以及冗长的萃取程序。检测本身虽具有选择性,但无法确认化合物的身份。台式气相色谱/质谱联用仪(GC/MS)系统在更灵敏的选择离子监测(SIM)采集模式下运行时会丢弃光谱信息,而在扫描模式下运行时灵敏度较低且扫描速度过慢。本文将超热表面电离(HSI)的选择性、超音速分子束(SMB)GC/MS接口的高柱流速容量以及飞行时间(TOF)质量分析的高采集速率相结合,以实现一种快速、特异且灵敏的技术,用于分析水中痕量水平的多环芳烃。本研究报告了使用GC/HSI-TOF系统相对于HPLC荧光法所获得的优势,并详细讨论了所用仪器的特性。

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