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

• Published in: Analytical chemistry (Washington) 2006-01, Vol.78 (2), p.538-546
• Main Authors: Breadmore, Michael C, Mosher, Richard A, Thormann, Wolfgang
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Chemistry; Chromatographic methods and physical methods associated with chromatography; Computer Simulation; Electrophoresis, Capillary - methods; Exact sciences and technology; Formates - analysis; Hydrogen-Ion Concentration; Ions; Osmolar Concentration; Other chromatographic methods; Sodium Chloride - chemistry; Temperature
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac051420f

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 pK a 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 pK a 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.