首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >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
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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

机译:超音速分子束高温表面电离与飞行时间质谱联用,可用于饮用水中痕量痕量多核芳烃的痕量检测,从而减少了样品制备和分析时间

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摘要

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. Copyright (C) 1999 John Wiley & Sons, Ltd. [References: 5]
机译:通过高效液相色谱(HPLC)荧光检测分析饮用水中多核芳烃(PAH)的亚ppb水平通常需要大量的水样和冗长的提取程序。检测本身尽管具有选择性,但不能提供化合物身份确认。在更敏感的选定离子监测(SIM)采集模式下运行的台式气相色谱/质谱(GC / MS)系统会丢弃光谱信息,并且在扫描模式下运行时灵敏度较低,并且扫描速度太慢。将高温表面电离(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结合起来,可以促进了一种快速,特异性和灵敏的技术来分析水中痕量PAHs。这项工作报告了使用GC / HSI-TOF系统相对于HPLC荧光方法所获得的优势,并详细讨论了所用仪器的性质。版权所有(C)1999 John Wiley&Sons,Ltd. [参考:5]

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