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High-resolution computer simulations of stacking of weak bases using a transient pH boundary in capillary electrophoresis. 1. Concept and impact of sample ionic strength

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Breadmore, MC and Mosher, RA and Thormann, W (2006) High-resolution computer simulations of stacking of weak bases using a transient pH boundary in capillary electrophoresis. 1. Concept and impact of sample ionic strength. Analytical Chemistry, 78 (2). pp. 538-546. ISSN 0003-2700

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Abstract

The dynamics of focusing weak bases using a transient pH boundary was examined via high-resolution computer simulation software. Emphasis was placed on the mechanism and impact that the presence of salt, namely, NaCl, has on the ability to focus weak bases. A series of weak bases with mobilities ranging from 5 × 10-9 to 30 × 10-9 m2/V·s and pKa values between 3.0 and 7.5 were examined using a combination of 65.6 mM formic acid, pH 2.85, for the separation electrolyte, and 65.6 mM formic acid, pH 8.60, for the sample matrix. Simulation data show that it is possible to focus weak bases with a pKa value similar to that of the separation electrolyte, but it is restricted to weak bases having an electrophoretic mobility of 20 × 10-9 m2/V·s or quicker. This mobility range can be extended by the addition of NaCl, with 50 mM NaCl allowing stacking of weak bases down to a mobility of 15 × 10-9 m2/V·s and 100 mM extending the range to 10 × 10-9 m2/V·s. The addition of NaCl does not adversely influence focusing of more mobile bases, but does prolong the existence of the transient pH boundary. This allows analytes to migrate extensively through the capillary as a single focused band around the transient pH boundary until the boundary is dissipated. This reduces the length of capillary that is available for separation and, in extreme cases, causes multiple analytes to be detected as a single highly efficient peak.

Item Type: Article
Journal or Publication Title: Analytical Chemistry
Page Range: pp. 538-546
ISSN: 0003-2700
Identification Number - DOI: 10.1021/ac051420f
Additional Information: Copyright © 2005 American Chemical Society
Date Deposited: 05 Jun 2008 12:39
Last Modified: 18 Nov 2014 03:42
URI: http://eprints.utas.edu.au/id/eprint/6628
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