Dielectric friction in capillary electrophoresis: mobility of organic anions in mixed methanol-water media.

Abstract

The mobilities of a series of organic carboxylates and sulfonates, ranging in charge from -1 to -4, were investigated by capillary electrophoresis using buffers containing 0 to 75% (v/v) methanol. Effective mobilities were measured at a series of ionic strengths, and were extrapolated to zero ionic strength using Pitts' equation to yield absolute mobilities. Generally, higher-charged ions were more strongly influenced by ionic strength, as predicted by the Pitts' equation. Some differences in the ionic strength effects for anions of like charge were observed and were consistent with the relaxation effect. The absolute mobilities of anions were altered by the addition of methanol to the buffer. Analytes with higher charge-to-size ratios were slowed to a greater extent than were ions with lower charge-to-size. As a result, dramatic changes in relative mobility were observed, such as a reversal in migration order between anions of -1 and -4 charge at 75% methanol and 20 mM ionic strength. The mobility changes caused by the addition of methanol are attributed to dielectric friction. Mobilities in the methanol-water solutions were found to depend on analyte charge-to-size and solvent dielectric relaxation time (tau) and were inversely dependent upon solvent dielectric constant (epsilon), as predicted by the Hubbard-Onsager mobility model.