Effect of first-dimension undersampling on effective peak capacity in comprehensive two-dimensional separations

被引:153
作者
Davis, Joe M. [1 ]
Stoll, Dwight R. [1 ]
Carr, Peter W. [1 ]
机构
[1] So Illinois Univ, Dept Chem & Biochem, Carbondale, IL 62901 USA
关键词
D O I
10.1021/ac071504j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The objective of this work is to establish a means of correcting the theoretical maximum peak capacity of comprehensive two-dimensional (2D) separations to account for the deleterious effect of undersampling first-dimension peaks. Simulations of comprehensive 2D separations of hundreds of randomly distributed sample constituents were carried out, and 2D statistical overlap theory was used to calculate an effective first-dimension peak width based on the number of observed peaks in the simulated separations. The distinguishing feature of this work is the determination of the effective first-dimension peak width using the number of observed peaks in the entire 2D separation as the defining metric of performance. We find that the ratio of the average effective first-dimension peak width after sampling to its width prior to sampling (defined as <beta >) is a simple function of the ratio of the first-dimension sampling time (t(s)) to the first-dimension peak standard deviation prior to sampling ((1)sigma): <beta > =root 1+0.21(t(s)/(1)sigma)(2) This is valid for 2D separations of constituents having either randomly distributed or weakly correlated retention times,. over the range of 0.2 <= t(s)/(1)sigma <= 16. The dependence of <beta > on t(s)/(1)sigma or from this expression is in qualitative agreement with previous work based on the effect of undersampling on the effective width of a single first-dimension peak, but predicts up to 35% more broadening of first-dimension peaks than is predicted by previous models. This simple expression and accurate estimation of the effect of undersampling first-dimension peaks should be very useful in making realistic corrections to theoretical 2D peak capacities, and in guiding the optimization of 2D separations.
引用
收藏
页码:461 / 473
页数:13
相关论文
共 38 条
[1]   Recent developments in comprehensive two-dimensional gas chromatography (GC X GC) - IV. Further applications, conclusions and perspectives [J].
Adahchour, M. ;
Beens, J. ;
Vreuls, R. J. J. ;
Brinkman, U. A. Th. .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2006, 25 (08) :821-840
[2]   Recent developments in comprehensive two-dimensional gas chromatography (GC x GC) III. Applications for petrochemicals and organohalogens [J].
Adahchour, M. ;
Beens, J. ;
Vreuls, R. J. J. ;
Brinkman, U. A. Th. .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2006, 25 (07) :726-741
[3]   Recent developments in comprehensive two-dimensional gas chromatography (GC X GC) I. Introduction and instrumental set-up [J].
Adahchour, M. ;
Beens, J. ;
Vreuls, R. J. J. ;
Brinkman, U. A. Th .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2006, 25 (05) :438-454
[4]   Recent developments in comprehensive two-dimensional gas chromatography (GC x GC) II. Modulation and detection [J].
Adahchour, M ;
Beens, J ;
Vreuls, RJJ ;
Brinkman, UAT .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2006, 25 (06) :540-553
[5]   Comprehensive two-dimensional gas chromatography: metrics, potentials, limits [J].
Blumberg, LM .
JOURNAL OF CHROMATOGRAPHY A, 2003, 985 (1-2) :29-38
[6]  
Bracewell RN, 1986, FOURIER TRANSFORM IT, P31999
[7]  
Crank J., 1979, MATH DIFFUSION
[8]   Statistical-overlap theory for elliptical zones of high aspect ratio in comprehensive two-dimensional separations [J].
Davis, JM .
JOURNAL OF SEPARATION SCIENCE, 2005, 28 (04) :347-359
[9]   Comprehensive multi-dimensional liquid chromatographic separation in biomedical and pharmaceutical analysis: a review [J].
Dixon, Steven P. ;
Pitfield, Ian D. ;
Perrett, David .
BIOMEDICAL CHROMATOGRAPHY, 2006, 20 (6-7) :508-529
[10]   EVALUATION OF THE NUMBER OF COMPONENTS IN MULTICOMPONENT LIQUID CHROMATOGRAMS OF PLANT-EXTRACTS [J].
DONDI, F ;
KAHIE, YD ;
LODI, G ;
REMELLI, M ;
RESCHIGLIAN, P ;
BIGHI, C .
ANALYTICA CHIMICA ACTA, 1986, 191 :261-273