Kinetic performance limits of constant pressure versus constant flow rate gradient elution separations. Part I: Theory

被引:21
作者
Broeckhoven, K. [1 ]
Verstraeten, M. [1 ]
Choikhet, K. [2 ]
Dittmann, M. [2 ]
Witt, K. [2 ]
Desmet, G. [1 ]
机构
[1] Vrije Univ Brussel, Dept Chem Engn CHIS IR, B-1050 Brussels, Belgium
[2] Agilent Technol Germany GmbH, D-76337 Waldbronn Bw, Germany
基金
比利时弗兰德研究基金会;
关键词
Constant pressure; Kinetic plot method; Peak capacity; Plate height; Numerical simulation; Pressure effects; SOLVENT-PROGRAMMED CHROMATOGRAPHY; PHASE LIQUID-CHROMATOGRAPHY; FUNDAMENTAL EQUATION; PEAK COMPRESSION; TEMPERATURE; RETENTION; COLUMNS; REPRESENTATION; EXPRESSIONS; RESOLUTION;
D O I
10.1016/j.chroma.2010.12.086
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report on a general theoretical assessment of the potential kinetic advantages of running LC gradient elution separations in the constant-pressure mode instead of in the customarily used constant-flow rate mode. Analytical calculations as well as numerical simulation results are presented. It is shown that, provided both modes are run with the same volume-based gradient program, the constant-pressure mode can potentially offer an identical separation selectivity (except from some small differences induced by the difference in pressure and viscous heating trajectory), but in a significantly shorter time. For a gradient running between 5 and 95% of organic modifier, the decrease in analysis time can be expected to be of the order of some 20% for both water-methanol and water-acetonitrile gradients, and only weakly depending on the value of V-G/V-0 (or equivalently t(G)/t(0)). Obviously, the gain will be smaller when the start and end composition lie closer to the viscosity maximum of the considered water-organic modifier system. The assumptions underlying the obtained results (no effects of pressure and temperature on the viscosity or retention coefficient) are critically reviewed, and can be inferred to only have a small effect on the general conclusions. It is also shown that, under the adopted assumptions, the kinetic plot theory also holds for operations where the flow rate varies with the time, as is the case for constant-pressure operation. Comparing both operation modes in a kinetic plot representing the maximal peak capacity versus time, it is theoretically predicted here that both modes can be expected to perform equally well in the fully C-term dominated regime (where H varies linearly with the flow rate), while the constant pressure mode is advantageous for all lower flow rates. Near the optimal flow rate, and for linear gradients running from 5 to 95% organic modifier, time gains of the order of some 20% can be expected (or 25-30% when accounting for the fact that the constant pressure mode can be run without having to leave a pressure safety margin of 5-10% as is needed in the constant flow rate mode). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1153 / 1169
页数:17
相关论文
共 44 条
[1]  
[Anonymous], 1965, DYNAMICS CHROMATOGRA
[2]   Influence of pressure and temperature on the physico-chemical properties of mobile phase mixtures commonly used in high-performance liquid chromatography [J].
Billen, Jeroen ;
Broeckhoven, Ken ;
Liekens, Anuschka ;
Choikhet, Konstantin ;
Rozing, Gerard ;
Desmet, Gert .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1210 (01) :30-44
[3]   The kinetic plot method applied to gradient chromatography: Theoretical framework and experimental validation [J].
Broeckhoven, K. ;
Cabooter, D. ;
Lynen, F. ;
Sandra, P. ;
Desmet, G. .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (17) :2787-2795
[4]   Investigation of the validity of the kinetic plot method to predict the performance of coupled column systems operated at very high pressures under different thermal conditions [J].
Cabooter, Deirdre ;
Lestremau, Francois ;
de Villiers, Andre ;
Broeckhoven, Ken ;
Lynen, Frederic ;
Sandra, Pat ;
Desmet, Gert .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (18) :3895-3903
[5]   Effect of Pressure, Particle Size, and Time on Optimizing Performance in Liquid Chromatography [J].
Carr, Peter W. ;
Wang, Xiaoli ;
Stoll, Dwight R. .
ANALYTICAL CHEMISTRY, 2009, 81 (13) :5342-5353
[6]   Probing the kinetic performance limits for ion chromatography. I. Isocratic conditions for small ions [J].
Causon, Tim J. ;
Hilder, Emily F. ;
Shellie, Robert A. ;
Haddad, Paul R. .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (31) :5057-5062
[7]   Probing the kinetic performance limits for ion chromatography. II. Gradient conditions for small ions [J].
Causon, Tim J. ;
Hilder, Emily F. ;
Shellie, Robert A. ;
Haddad, Paul R. .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (31) :5063-5068
[8]   ROLE OF THE TEMPERATURE IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING PYROCARBON-CONTAINING ADSORBENTS [J].
COLIN, H ;
DIEZMASA, JC ;
GUIOCHON, G ;
CZAJKOWSKA, T ;
MIEDZIAK, I .
JOURNAL OF CHROMATOGRAPHY, 1978, 167 (DEC) :41-65
[9]   Practical constraints in the kinetic plot representation of chromatographic performance data: Theory and application to experimental data [J].
Desmet, G ;
Clicq, D ;
Nguyen, DTT ;
Guillarme, D ;
Rudaz, S ;
Veuthey, JL ;
Vervoort, N ;
Torok, G ;
Cabooter, D ;
Gzil, P .
ANALYTICAL CHEMISTRY, 2006, 78 (07) :2150-2162
[10]   Geometry-independent plate height representation methods for the direct comparison of the kinetic performance of LC supports with a different size or morphology [J].
Desmet, G ;
Clicq, D ;
Gzil, P .
ANALYTICAL CHEMISTRY, 2005, 77 (13) :4058-4070