Characterization of C 18-bonded liquid chromatographic stationary phases by Raman spectroscopy: : the effect of temperature

Abstract

This study represents the first time that both the mobile phase composition and the temperature are simultaneously controlled to examine silica-bonded octadecylsilyl (C 18) ligands spectroscopically at typical liquid chromatographic (LC) mobile phase flow-rates and back-pressures. Raman spectroscopy is used to characterize the behavior of the C 18 bonded ligands equilibrated at temperatures from 45 to 2°C in neat, single-component, mobile phase solvents including: water, acetonitrile, methanol, and chloroform. In addition, the effect of stationary phase ligand bonding density is examined by using two different monomeric reversed-phase liquid chromatographic (RPLC) stationary phases, a 2.34 and a 3.52 μmol m −2 Microporasil C 18 stationary phase, under identical conditions. The direct, on-column, spectroscopic analysis used in this study allows direct evaluation of the temperature-dependent behavior of the bonded C 18 ligands. The temperature-dependent ordering of the stationary phase ligands is examined to determine if the ligands undergo a phase transition from a less-ordered “liquid-like” state at higher temperatures to a more-ordered “solid-like” state at lower temperatures. A discrete phase transition was not observed, but rather a continual ordering as temperature was lowered.