Simultaneous analysis of butene isomer mixtures using process mass spectrometry

被引:5
作者
Bennett, KH
Cook, KD [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Univ Tennessee, Measurement & Control Engn Ctr, Knoxville, TN USA
[3] Transylvania Univ, Dept Chem, Lexington, KY USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S1044-0305(00)00182-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The feasibility of simultaneous analysis of mixtures containing two to four butene isomers and up to six total components using process mass spectrometry is assessed. As for typical (nonisomeric) applications of process mass spectrometry, simultaneous analysis is based on the assumption that the electron ionization mass spectra of mixtures are Linear combinations of the spectra of the individual constituents. Limits of detection for binary isomer mixtures are on the order of 0.1% to 10%, Limited by the ability to distinguish small differences between similar spectra. As spectral and mixture complexity increase, both accuracy and precision decrease. Not surprisingly the similarity of the spectra of stereoisomers cis- and trans-2-butene is greater than that of the other (nonstereoisomeric) isomer pairs, and mixtures containing both cis- and trans-2-butene are the most difficult to quantitate. However, even for mixtures of all four butenes, accuracy (root-mean-square error = 2.43%), precision (average coefficient of variation = 6.72%), and linearity (correlation coefficient of a plot of measured versus actual concentration r(2) = 0.985 +/- 0.002) are reasonably good. (J Am Soc Mass Spectrom 2000, 11, 1079-1085) (C) 2000 American Society for Mass Spectrometry.
引用
收藏
页码:1079 / 1085
页数:7
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