Open-tubular admicellar electrochromatography of charged analytes

Abstract

Fundamental studies on the separation of cationic and anionic analytes in open-tubular admicellar electrochromatography (OT-AMEC) using cetyltrimethylammonium bromide (CTAB) and fused silica capillaries are presented. OT-AMEC was compared with open-tubular admicellar liquid chromatography (OT-AMLC) by running the two methods using the same mobile phases. The mobile phases were buffered at pH ≥ 6 and contained a low concentration (above the critical surface aggregation concentration and below the critical micelle concentration) of CTAB. The stationary pseudophase of CTAB admicelles were formed at the solid surface and liquid interface inside the capillary by simply conditioning the capillary with the mobile phase. Separations were performed in a 30 cm (21.5 cm to UV detector) long and 50 μm inner diameter capillary, using low pressure (50 mbar) in OT-AMLC and high voltage (15 kV at negative polarity) in OT-AMEC. The appropriate equations for the experimental estimation of retention factor (k) values of analytes were discussed. For anionic analytes, k in OT-AMEC were carefully determined by considering the observed interaction between CTAB monomers and tested analytes. The calculated k for each analyte was found similar in OT-AMLC and OT-AMEC, although the mechanism of retention was not entirely different due to the contribution of electrophoresis in OT-AMEC. Studies on the addition of a typical (i.e., acetonitrile) and atypical modifier (i.e., nonyl-β-glucoside) into the mobile phase, and sample focusing with >10x improvement in peak height under isocratic conditions were also conducted.