Comparison of Three Types of Mass Spectrometer for High-Performance Liquid Chromatography/Mass Spectrometry Analysis of Perfluoroalkylated Substances and Fluorotelomer Alcohols

质谱法 化学 色谱法 电喷雾 电喷雾电离 离子阱 分析化学(期刊) 检出限 三级四极质谱仪 碎片(计算) 离子 质谱 离子源 选择性反应监测 串联质谱法 有机化学 操作系统 计算机科学
作者
Urs Berger,Ingrid Langlois,Michael Oehme,Roland Kallenborn
出处
期刊:European journal of mass spectrometry [SAGE Publishing]
卷期号:10 (5): 579-588 被引量:82
标识
DOI:10.1255/ejms.679
摘要

The performance of three different types of mass spectrometer (MS) coupled to high performance liquid chromatography (HPLC), was compared for trace analysis of perfluoroalkylated substances (PFAS) and fluorotelomer alcohols (FTOHs). An ion trap MS in the full-scan and product-ion mass spectrometry (MS 2 ) mode, time-of-flight (ToF) high-resolution MS and quadrupole MS in the selected ion mode, as well as triple quadrupole tandem MS were tested. Electrospray ionisation in the negative-ion mode [ESI(–)] was best suited for all instruments and compounds. PFAS could only be separated by a buffered mobile phase, but the presence of buffer suppressed the ionisation of FTOHs. Therefore, two independent chromatographic methods were developed for the two compound classes. Mass spectra and product-ion spectra obtained by in-source and collision-induced dissociation fragmentation are discussed, including ion adduct formation. Product ion yields of PFAS were only in the range of 0.3 to 12%, independent of the applied MS instrument. Ion trap MS 2 gave product ion yields of 20 to 62% for FTOHs, whereas only 4.1 to 5.8% were obtained by triple quadrupole tandem MS. Ion trap MS was best suited for qualitative analysis and structure elucidation of branched isomeric structures of PFAS. Providing typical detection limits of 5 ng injected in MS 2 mode, it was not sensitive enough for selective trace amount quantification. ToF high-resolution MS was the only technique combining high selectivity and excellent sensitivity for PFAS analysis (detection limits of 2 to 10 pg), but lacked the possibilities of MS/MS. Triple-quadrupole tandem MS was the method of choice for quantification of FTOHs with detection limits in the low pg range. It is also well suited for the determination of PFAS, although its detection limits of 10 to 100 pg in tandem MS mode are about one order of magnitude higher than for ToF MS.
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