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Journal ArticleDOI

Temperature dependence of retention in reversed-phase liquid chromatography. 1. Stationary-phase considerations.

Lynn A. Cole, +1 more
- 01 Jul 1992 - 
- Vol. 64, Iss: 13, pp 1324-1327
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TLDR
Thermodynamic constants for the transfer of a solute from the mobile phase to the stationary phase and comparison of these values to previously reported values indicated that the chromatographic retention process is not well-modeled by bulk-phase oil-water partitioning processes, providing additional support that partitioning is the relevant model of retention.
Abstract
The retention mechanism in reversed-phase liquid chromatography (RPLC) has been examined over a wide temperature range with emphasis on the role of the mobile phase. van't Hoff plot shapes were used to assess the retention mechanism, and the data showed evidence of the hydrophobic effect when water-rich and/or hydrogen-bonded mobile phases such as methanol/water were used. However, different van't Hoff plot shape was observed with acetonitrile/water mobile phases, indicating a change in the retention mechanism. These data showed that the hydrophobic effect, which had previously been proposed as the driving force for retention, is not a satisfactory explanation for the retention process in all RPLC systems.

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Citations
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Journal ArticleDOI

Retention behavior of small polar compounds on polar stationary phases in hydrophilic interaction chromatography.

TL;DR: The retention of the acids on the amino phase decreased with increasing salt concentration in the mobile phase due to the ion-exchange effect, and the retention process was endothermic as opposed to exothermic on other phases.
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Hydrophobic interaction chromatography of proteins.

TL;DR: The different proposed theories for the retention mechanism of proteins in HIC are presented and the main parameters to consider for the optimization of fractionation processes by HIC and the stationary phases available were described.
Journal ArticleDOI

Immobilized-artificial-membrane chromatography: measurements of membrane partition coefficient and predicting drug membrane permeability

TL;DR: For 23 structurally unrelated compounds, solute capacity factors measured on IAM columns correlate very well with the solute equilibrium partition coefficients measured in fluid liposome systems (r = 0.907), which indicates that solute partitioning between the IAM bonded phase and the aqueous mobile phase is similar to the solutesome-aqueous phase.
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Membrane partitioning: Distinguishing bilayer effects from the hydrophobic effect

TL;DR: It is shown through measurements of the heat capacity changes associated with the partitioning of tryptophan side-chain analogs into lipid bilayers and into bulk cyclohexane that the hydrophobic effect plays a crucial role regardless of the large negative enthalpy.
Journal ArticleDOI

Effect of temperature in reversed phase liquid chromatography.

TL;DR: The problem of temperature control for thermostating columns which may represent a significant source of peak broadening is discussed: by taking into account the three main parameters such as heat transfer, pressure drop and band broadening resulting from the preheating tube, suitable rules are set up for a judicious choice of the column internal diameter.
References
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Journal ArticleDOI

Dominant forces in protein folding

TL;DR: The present review aims to provide a reassessment of the factors important for folding in light of current knowledge, including contributions to the free energy of folding arising from electrostatics, hydrogen-bonding and van der Waals interactions, intrinsic propensities, and hydrophobic interactions.
Journal ArticleDOI

Solvophobic interactions in liquid chromatography with nonpolar stationary phases

TL;DR: In this article, the solvophobic theory of solvent interaction with non-polar stationary phases in liquid chromatography is examined on the basis of solvophobia theory and a detailed analysis of the effect of the solvent on this process yields an expression for the capacity factor with essentially no adjustable constants.
Journal ArticleDOI

The molecular mechanism of retention in reversed-phase liquid chromatography

John G. Dorsey, +1 more
- 01 Mar 1989 - 
TL;DR: A review of the current understanding of retention of small molecules in reversed-phase liquid chromatography from both a theoretical and experimental perspective can be found in this paper, where the authors discuss the synthetic methodologies for the preparation of reversed phase stationary phases and deal next with the partitioning processes and stationary-phase structural details.
Journal ArticleDOI

Preparation and Chromatographic Properties of Some Chemically Bonded Phases for Reversed-Phase Liquid Chromatography

TL;DR: In this paper, the chromatographic activity of the silica surface is discussed on the basis of TMS-phases with various surface coverages, and it is observed that logarithmic retention data for homologous series and different RPphases-partially taken from the literature-form a set of straight lines with a common intersection point.
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