Intraparticle mass transfer kinetics on molecularly imprinted polymers of structural analogues of a template

被引:29
作者
Kim, H
Kaczmarski, K
Guiochon, G [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[3] Rzeszow Univ Technol, Fac Chem, PL-35959 Rzeszow, Poland
基金
美国国家科学基金会;
关键词
Fmoc-L-tryptophan imprinted polymers; frontal analysis; tri-Langmuir isotherm model; lumped pore diffusion model; intraparticle mass transfer; peak profiles; surface diffusion model; isosteric heat of adsorption;
D O I
10.1016/j.ces.2005.08.012
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The intraparticle mass transfer kinetics of the structural analogues of a template on a Fmoc-L-Tryptophan (Fmoc-L-Trp) imprinted polymer (MIP) and on the corresponding non-imprinted polymer (NIP) were quantitatively studied using the lumped pore diffusion model (POR) of chromatography. The best equilibrium isotherm models of these compounds were used to calculate the high-concentration band profiles of different substrates on the MIP and the NIP with the POR model. These profiles were compared to experimental band profiles. The numerical values of the intraparticle pore and surface diffusion coefficients were adjusted to determine those that minimized the differences between calculated and experimental profiles. The results of this exercise show that surface diffusion is the dominant intraparticle mass transfer process for the substrates on the polymers and that the energetic heterogeneity of the surface should be considered in accounting for the surface diffusion of the L-enantiomers on the MIP. The surface diffusion coefficient increases with decreasing overall affinity of each substrate for the polymers. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1122 / 1137
页数:16
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