Pietrogrande Maria Chiara, Mercuriali Mattia, Pasti Luisa
Department of Chemistry, University of Ferrara, Via L. Borsari, 46, I-44100 Ferrara, Italy.
Anal Chim Acta. 2007 Jun 26;594(1):128-38. doi: 10.1016/j.aca.2007.05.020. Epub 2007 May 21.
Identification and characterization of homologous series by GC-MS analysis provide very relevant information on organic compounds in complex mixtures. A chemometric approach, based on the study of the autocovariance function, EACVF(tot), is described as a suitable tool for extracting molecular-structural information from the GC signal, in particular for identifying the presence of homologous series and quantifying the number of their terms. A data pre-processing procedure is introduced to transform the time axis in order to display a strictly homogenous retention pattern: n-alkanes are used as external standard to stretch or shrink the original chromatogram in order to build up a linear GC retention scale. This addition can be regarded as a further step in the direction of a signal processing procedure for achieving a systematic characterization of complex mixture from experimental chromatograms. The EACVF(tot) was computed on the linearized chromatogram: if the sample presents terms of homologous series, the EACVF(tot) plot shows well-defined deterministic peaks at repeated constant interdistances. By comparison with standard references, the presence of such peaks is diagnostic for the presence of the ordered series, their position can be related to the chemical structure of the compounds, their height is the basis for estimating the number of terms in the series. The power of the procedure can be magnified by studying SIM chromatograms acquired at specific m/z values characteristic of the compounds of interest: the EACVF(tot) on these selective signals makes it possible to confirm the results obtained from an unknown mixture and check their reliability. The procedure was validated on standard mixtures of known composition and applied to an unknown gas oil sample. In particular, the paper focuses on the study of two specific classes of compounds: n-alkanes and oxygen-containing compounds, since their identification provides information useful for characterizing the chemical composition of many samples of different origin. The robustness of the method was tested in experimental chromatograms obtained under unfavorable conditions: chromatograms acquired in non-optimal temperature program conditions and chromatographic data affected by signal noise.
通过气相色谱 - 质谱联用(GC - MS)分析鉴定和表征同系物系列,可为复杂混合物中的有机化合物提供非常相关的信息。一种基于自协方差函数EACVF(tot)研究的化学计量学方法,被描述为从GC信号中提取分子结构信息的合适工具,特别是用于识别同系物系列的存在并量化其项数。引入了一种数据预处理程序来变换时间轴,以显示严格均匀的保留模式:正构烷烃用作外标来拉伸或收缩原始色谱图,以建立线性GC保留尺度。这种添加可被视为信号处理程序朝着从实验色谱图实现复杂混合物系统表征方向迈出的进一步步骤。EACVF(tot)是在线性化的色谱图上计算的:如果样品呈现同系物系列的项,则EACVF(tot)图在重复的恒定间距处显示出定义明确的确定性峰。通过与标准参考进行比较,此类峰的存在可诊断有序系列的存在,其位置可与化合物的化学结构相关,其高度是估计系列中项数的基础。通过研究在感兴趣化合物的特定m/z值下采集的选择离子监测(SIM)色谱图,可以增强该程序的功效:这些选择性信号上的EACVF(tot)使得能够确认从未知混合物中获得的结果并检查其可靠性。该程序在已知组成的标准混合物上进行了验证,并应用于未知的瓦斯油样品。特别是,本文重点研究了两类特定的化合物:正构烷烃和含氧化合物,因为它们的鉴定为表征许多不同来源样品的化学成分提供了有用的信息。该方法的稳健性在不利条件下获得的实验色谱图中进行了测试:在非最佳温度程序条件下采集的色谱图以及受信号噪声影响的色谱数据。