Analytes In Reversed-phase Liquid Chromatography Research Articles

Mobile-Phase Contributions to Organic-Solvent Excess Adsorption and Surface Diffusion in Reversed-Phase Liquid Chromatography.

Fast transport of retained analytes in reversed-phase liquid chromatography occurs through surface diffusion in the organic-solvent (OS)-enriched interfacial "ditch" region between the hydrophobic stationary phase and the water (W)-OS mobile phase. Through molecular dynamics simulations that recover the OS excess adsorption isotherms of a typical C18-stationary phase for methanol and acetonitrile, we explore the relation between OS properties, OS excess adsorption, and surface diffusion. The emerging molecular-level picture attributes the mobile-phase contribution to surface diffusion to the hydrogen-bond capability and the eluting power of the OS. The higher affinity of methanol for the formation of W-OS hydrogen bonds at the soft, hydrophobic surface presented by the bonded-phase (C18) chains reduces the OS excess and the related viscosity drop in the ditch. The lower eluting power of methanol, however, translates to increased bonded-phase contacts for analytes, which can increase their mobility gain from surface diffusion above the gain observed with acetonitrile.

Surface Diffusion of Aromatic Hydrocarbon Analytes in Reversed-Phase Liquid Chromatography

In reversed-phase liquid chromatography (RPLC), retained analytes can diffuse faster along the hydrophobic surface of the stationary phase than when dissolved in the water (W)–acetonitrile (ACN) mobile phase. We investigate the surface diffusion of four typical aromatic hydrocarbon analytes in RPLC through molecular dynamics simulations in a slit-pore RPLC model consisting of a silica-supported, end-capped, C18 stationary phase and a 70/30 (v/v) W/ACN mobile phase. Our data show that the lateral (surface-parallel) diffusive mobility of the analytes goes through a maximum in the ACN ditch, an ACN-rich border layer around the terminal part of the bonded-phase chains, because the solvent composition there is more conducive to analyte mobility than the W-rich mobile phase. At their lateral mobility maximum, analytes have contacts with 12–15 bonded-phase groups, 5–6 ACN and 1–2 W molecules. The lateral mobility gain from surface diffusion decreases with analyte polarity first and size second (like and unlike r...

Retention prediction and separation optimization of ionizable analytes in reversed-phase liquid chromatography by organic modifier gradients in different eluent pHs

The influence of eluent pH on retention of ionizable analytes during organic modifier gradients in reversed-phase high performance liquid chromatography is studied. Two approaches are examined for the retention prediction of solutes under organic modifier gradient conditions at any constant mobile phase pH: In the first approach an analytical solution of the fundamental equation of gradient elution in linear organic modifier gradients for monoprotic acids/bases under certain assumptions is proposed. The second approach is based on an empirical model arising from the evaluation of the gradient retention data. Both approaches were successfully applied to describe the retention behavior of 16 OPA derivatives of amino acids obtained in 19 simple mono-linear organic modifier gradient runs performed between two given acetonitrile contents with different gradient duration and at different eluent pHs, in a particular pH range where amino acids behave as weak monoprotic acids. Further, this study provides a reliable way for optimizing gradient separations of ionogenic compounds with respect to mobile phase pH.

Simple models for the effect of aliphatic alcohol additives on the retention in reversed-phase liquid chromatography

Four retention models for the effect of aliphatic alcohol additives on the retention of analytes in reversed-phase liquid chromatography have been developed following either a semi-thermodynamic treatment or an empirical approach. Their performance was tested using the experimental retention times of six non-polar analytes (alkylbenzenes) and ten o-phthalaldehyde derivatives of amino acids under different isocratic chromatographic runs when a small amount of ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol or 1-heptanol was added to methanol/water mixtures containing a constant amount of methanol. It was shown that for the structurally simple alkylbenzenes all the models can be adopted for retention prediction with good results. In contrast, just one out of four models, that with the fewest approximations, predicts satisfactorily the retention properties of amino acids derivatives. However, the most interesting feature is that this model can predict the effect of an alcohol-additive on the retention properties of solutes, even if this additive was not used in chromatographic runs done for the fitting procedure, provided that it belongs to the same homologous series of alkanols. This feature is also observed in all models described the retention of alkylbenzenes.

Retention prediction and hydrophobicity estimation of weak acidic compounds by reversed-phase liquid chromatography using acetic and perchloric acids as ion suppressors

Simple acids are usually applied to suppress the ionization of weakly ionizable acidic analytes in reversed-phase liquid chromatography. The purpose of this study is to investigate the retention behavior of various weak acidic compounds (monoprotic, diprotic, triprotic, and tetraprotic acids) using acetic or perchloric acid as ion suppressor in a binary hydroorganic mobile phase. The apparent n-octanol-water partition coefficient (K(ow)") was proposed to calibrate the n-octanol-water partition coefficient (K(ow)) of weak acidic compound. LogK(ow)" was found to have a better linear correlation with logk(w), the logarithm of the retention factor obtained by extrapolating to neat aqueous fraction of the mobile phase, for all weakly ionizable acidic compounds. This straightforward relationship offers a potential medium for direct measurement of K(ow) data of weak acidic analytes and can be used to predict retention behavior of these compounds in the ion suppression reversed-phase liquid chromatographic mode.

Chromatographic retention prediction and octanol–water partition coefficient determination of monobasic weak acidic compounds in ion-suppression reversed-phase liquid chromatography using acids as ion-suppressors

Although simple acids, replacing buffers, have been widely applied to suppress the ionization of weakly ionizable acidic analytes in reversed-phase liquid chromatography (RPLC), none of the previously reported works focused on the systematic studies about the retention behavior of the acidic solutes in this ion-suppression RPLC mode. The subject of this paper was therefore to investigate the retention behavior of monobasic weak acidic compounds using acetic, perchloric and phosphoric acids as the ion-suppressors. The apparent octanol–water partition coefficient (K″ow) was proposed to calibrate the octanol–water partition coefficient (Kow) of these weak acidic compounds, which resulted in a better linear correlation with log kw, the logarithm of the hypothetical retention factor corresponding to neat aqueous fraction of hydroorganic mobile phase. This log K″ow−log kw linear correlation was successfully validated by the results of monocarboxylic acids and monohydrating phenols, and moreover by the results under diverse experimental conditions for the same solutes. This straightforward relationship not only can be used to effectively predict the retention values of weak acidic solutes combined with Snyder–Soczewinski equation, but also can offer a promising medium for directly measuring Kow data of these compounds via Collander equation. In addition, the influence of the different ion-suppressors on the retention of weak acidic compounds was also compared in this RPLC mode.

A new approach to the determination of column overload characteristics in reversed-phase liquid chromatography

Column overloading is very common during the separations of basic analytes in analytical scale reversed-phase liquid chromatography (RPLC). Due to the complex interactions of ionic analytes with stationary and mobile phases, only a very small amount of ionized sample compared to the amount of nonpolar solute can be injected before the peak shape is distorted by non-linear chromatographic processes. Often the amount that can be injected before overload is observed is so small that the signal is quite noisy, thereby making the measured plate count imprecise and possibly inaccurate. The purpose of the present study was to develop a practical method for the precise measurement of the plate count and a column overload parameter using a simple but mathematically rigorous model of Langmuirian non-linear chromatography. An “overload profile”, i.e. a plot of apparent plate count versus amount injected, is characterized by two parameters: the limiting plate count ( N 0) and the column sample loading capacity ( ω 0.5). The limiting plate count is the plate count that should be observed when the amount of sample injected is so small that a linear isotherm pertains. The column sample loading capacity, which is taken as the sample load that leads to a plate count equal to half of the limiting plate count, is a measure of the maximum amount of sample that can be injected into that column. The approach was tested by applying it to the study of cationic analytes in RPLC. We show that N 0 under constant conditions (column length, flow rate, mobile phase composition, etc.) is almost independent of column type (manufacturer); however, different column types (at the same length, diameter and flow rate) exhibit clear differences in their sample loading capacity ( ω 0.5). We believe that for most well packed type B columns, the column sample loading capacity and not the limiting plate count is the more important property that accounts for most of the apparent differences in peak width when different types of columns are examined.

Exact peak compression factor in linear gradient elution: I. Theory

The only existing expression for the peak compression factor in linear gradient elution chromatography assumes that the linear-solvent-strength model (LSSM) applies to the retention of the compound studied, that the column efficiency is independent of the mobile phase composition, and that, during gradient elution, the relative retention factor of a compound inside its band varies linearly with the distance from the band center. Because the retention factors of many analytes in reversed-phase liquid chromatography do not rigorously follow the LSSM, we extend the theoretical approach of Poppe et al. to the prediction of peak compression factors in linear gradient elution chromatography for any retention model, when column efficiency varies with the mobile phase composition. Only the contribution of the chromatographic column to the peak compression was taken into account, the contribution of the dwell volume being neglected. A second restriction is the linearity of the relative retention factor as a function of the position along the band width inside the column. These constraints could be the sources for the difference observed between experimental and theoretical values of peak compression factors. When the retention factor varies steeply with the mobile phase composition, such as with proteins or large peptides in RP-HPLC, it is found that the thermodynamic compression term, which tends to sharpen the peak, is coupled with the column dispersion term, which tends to broaden the peak. This coupling term acts as an apparent dispersion term, contributing to broaden the peak. This result is consistent with the measurements of peak compression factors found in the literature.

Retention prediction of analytes in reversed-phase high-performance liquid chromatography based on molecular structure : IV. Branched and unsaturated alkylbenzenes

As part of a study to predict the retention of analytes in reversed-phase liquid chromatography the effects of isomerisation and unsaturation in alkyl chain substituents on an aromatic ring have been examined. The contributions of the presence of branching and of olefinic groups have been related to the eluent composition in methanol-buffer and acetonitrile-buffer eluents. These results have been applied to a comparison of the influence on retention of primary, secondary and tertiary hydroxyl groups in isomeric phenylpropanols.