Accuracy and precision of adsorption isotherm parameters measured by dynamic HPLC methods

被引:31
作者
Gritti, F
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
基金
美国国家科学基金会;
关键词
adsorption equilibrium; frontal analysis; mobile phase composition; accuracy; precision; adsorption isotherms; phenol;
D O I
10.1016/j.chroma.2004.05.067
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The fluctuations of the column temperature, the composition and the flow rate of the mobile phase affect the accuracy and precision of the adsorption isotherm parameters measured by dynamic HPLC methods. Experimental data were acquired by frontal analysis (FA) for phenol in equilibrium between C-18-bonded Symmetry and a methanol:water mixture (20:80, v/v), at 303 K and a flow rate of 1 mL/min. The fluctuations of the experimental parameters were 0.1 K for the temperature, 0.1% for the mobile phase composition and 0.00 1 mL/min for the flow rate. The best isotherm model was shown to be the tri-Langmuir isotherm. Random errors were calculated and shown to agree with experimental results. Overloaded band profiles of phenol were acquired at low (sample size, 100 muL, concentration 3 g/L) and high (same sample size, concentration 60 g/L) loadings, at seven temperatures (298, 300, 302, 303, 304, 306, and 308 K), for seven mobile phase compositions (methanol 16, 18, 19, 20, 21, 22, and 24%), and with seven mobile phase flow rates (0.95, 0.97, 0.99, 1.00, 1.01, 1.03, and 1.05 mL/min), always keeping two experimental parameters at the values selected for the FA runs. Assuming that the isotherm model stays the same, the inverse method (IM) was used to derive the isotherm parameters in each case. Temperature affects the equilibrium constants according to Van't Hoff law. A temperature change of I K around 303 K causes a relative variation of 1.5% of the high-energy adsorption constant b(3) and of 0.6% of the saturation capacity q(3). The isotherm parameters are very sensitive to the mobile phase composition, especially the highest energy mode. Both adsorption constants b(2) and b(3) follow the linear strength solvent model (LSSM). A methanol volume fraction change of 1% causes a relative decrease of 3.2 and 5.0% of b(2) and b(3), respectively and a 2% decrease of the saturation capacity q(3). Finally, flow rate changes affect only the saturation capacities. A flow rate change of 1% causes a 2% change in the saturation capacity parameters. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 170
页数:12
相关论文
共 28 条
[1]   CONTINUOUS FLOW SYSTEMS - DISTRIBUTION OF RESIDENCE TIMES [J].
DANCKWERTS, PV .
CHEMICAL ENGINEERING SCIENCE, 1953, 2 (01) :1-13
[2]   DETERMINATION OF ISOTHERMS FROM CHROMATOGRAPHIC PEAK SHAPES [J].
DOSE, EV ;
JACOBSON, S ;
GUIOCHON, G .
ANALYTICAL CHEMISTRY, 1991, 63 (08) :833-839
[3]   Repeatability and reproducibility of high-concentration data in reversed-phase liquid chromatography -: III.: Isotherm reproducibility on Kromasil C18 [J].
Felinger, A ;
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1024 (1-2) :21-38
[4]   Numerical determination of the competitive isotherm of enantiomers [J].
Felinger, A ;
Cavazzini, A ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2003, 986 (02) :207-225
[5]   Adsorption isotherms of nonionic surfactants in SBA-15 measured by micro-column chromatography [J].
Findenegg, G. H. ;
Eltekov, A. Y. .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1150 (1-2) :236-240
[6]   Effect of the ionic strength of salts on retention and overloading behavior of ionizable compounds in reversed-phase liquid chromatography I.: XTerra-C18 [J].
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1033 (01) :43-55
[7]   Heterogeneity of the surface energy on unused C18-chromolith adsorbents in reversed-phase liquid chromatography [J].
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (01) :105-119
[8]   Band splitting in overloaded isocratic elution chromatography III. Modeling of adsorbate-adsorbate interactions by a two-component extension of a BET kinetic isotherm model [J].
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (01) :121-137
[9]   Physical origin of peak tailing on C18-bonded silica in reversed-phase liquid chromatography [J].
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (01) :75-88
[10]   Reproducibility of low and high concentration data in reversed-phase liquid chromatography II.: Overloaded band profiles on Chromolith-C18 [J].
Gritti, F ;
Guiochon, G .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1021 (1-2) :25-53