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High-speed electroseparations inside silica colloidal crystals.

Abstract

Crystals made from 200 nm silica colloids are hardened and chemically modified with chlorodimethyloctadecylsilane for use in electrically driven, reversed-phase separations. A van Deemter plot reveals extremely narrow peak widths for the separation of a cationic hydrophobic dye, DiI, with both the A and C terms 10-fold smaller than those for a conventional HPLC column. Electrically driven separations are demonstrated to be achieved in less than 10 s for three dyes differing in hydrophobicity and also for three peptides differing in electrophoretic mobility. The results show that these media are promising for high-speed separations.

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Suping Zheng, Eric Ross, Michael A Legg, Mary J Wirth. 2006-07-19. High-speed electroseparations inside silica colloidal crystals.. https://doi.org/10.1021/ja062676l

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The renormalized jellium model for spherical and cylindrical colloids.

Starting from a mean-field description for a dispersion of highly charged spherical or (parallel) rodlike colloids, we introduce the simplification of a homogeneous background to include the contribution of other polyions to the static field created by a tagged polyion. The charge of this background is self-consistently renormalized to coincide with the polyion effective charge, the latter quantity thereby exhibiting a nontrivial density dependence, which directly enters into the equation of state through a simple analytical expression. The good agreement observed between the pressures calculated using the renormalized jellium and Monte Carlo simulations confirms the relevance of the renormalized jellium model for theoretical and experimental purposes and provides an alternative to the Poisson-Boltzmann cell model since it is free of some of the intrinsic limitations of this approach.

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