在线耦合超临界流体萃取-液相色谱-气相色谱-质谱法分析有机酸

Masahiko Shimmo, Tuulia Hyötyläinen, Kari Hartonen, Marja-Liisa Riekkola
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引用次数: 19

摘要

建立了超临界流体萃取-液相色谱-气相色谱-质谱联用(SFE-LC-GC-MS)在线联用系统,并将其应用于所选有机酸的定量分析。在SFE中,分析物在改性剂三乙胺和丙酮的存在下与五氟苯溴原位衍生化,使其极性更小,挥发性更强,可溶于超临界CO2。研究了影响衍生化和萃取的参数。在GC分析之前,LC有效地去除了多余的试剂。含3%乙酸乙酯的戊烷适用于SFE固相阱和LC-GC的洗脱。采用柱上界面和部分同步溶剂蒸发,可转移1600 μL的LC。整个分析在封闭系统中进行了2小时。该方法在5 ~ 200 ng范围内呈线性,检出限在3 ng左右。方法的相对标准偏差为5 ~ 20%。采用在线SFE-LC-GC-MS系统对芬兰赫尔辛基地区用特氟龙过滤器采集的气溶胶样品进行了分析。苯甲酸和丁酸在纳克/立方米的水平上被鉴定出来,但没有观察到蒎酸。隐含了人为排放对该地区气溶胶形成的重要性。©2001 John Wiley &[J]微型电子公司,2001年9月13日:202-210
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On-line coupled supercritical fluid extraction–liquid chromatography–gas chromatography–mass spectrometry for the analysis of organic acids

An on-line coupled supercritical fluid extraction–liquid chromatography–gas chromatography–mass spectrometry (SFE-LC-GC-MS) system was constructed and applied for the quantitative analysis of selected organic acids. In SFE the analytes were derivatized in situ with pentafluorobenzyl bromide in the presence of the modifiers triethylamine and acetone to make them less polar, more volatile, and soluble in supercritical CO2. Parameters that affect derivatization and extraction were studied. Excess reagent was efficiently removed by LC prior to GC analysis. Pentane containing 3% ethyl acetate was suitable for elution of both the SFE solid phase trap and LC-GC. A LC fraction of 1600 μL could be transferred using an on-column interface and partially concurrent solvent evaporation. The whole analysis took place for 2 h in a closed system. The method was linear in the range 5–200 ng, with detection limits around 3 ng. The relative standard deviations of the method were 5–20%. The on-line SFE-LC-GC-MS system was applied for the analysis of aerosol samples collected with Teflon filters in Helsinki, Finland. Benzoic acid and butyric acid were identified at the level of nanograms per cubic meter, but pinonic acid was not observed. The importance of anthropogenic emissions for aerosol formation in the region is implied. © 2001 John Wiley & Sons, Inc. J Micro Sep 13: 202–210, 2001

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