PubMed · 491238
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T Wada, G Inamoto. 1979-06-29. [Electrolyte loading and restriction tests].. https://pubmed.ncbi.nlm.nih.gov/491238/
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Ionizable planar interfaces and linear polyelectrolytes show markedly different proton-binding behavior. Planar interfaces protonate in a single broad step, whereas polyelectrolytes mostly undergo a two-step protonation. Such contrasting behavior is explained using a discrete-charge Ising model. This model is based on an approximation of the ionizable groups by point charges that are treated within a linearized Poisson-Boltzmann approximation. The underlying reason as to why planar interfaces exhibit mean-field-like behavior, whereas linear polyelectrolytes usually do not, is related to the range of the site-site interaction potential. For a planar interface, this interaction potential is much more long ranged if compared with that of the cylindrical geometry as appropriate to a linear polyelectrolyte. The model results are in semi-quantitative agreement with experimental data for fatty-acid monolayers, water-oxide interfaces, and various linear polyelectrolytes.
This paper presents a rapid and reliable micellar electrokinetic capillary chromatography (MEKC) method to separate major prostaglandins and thromboxane B2. The running buffer was modified with sodium dodecyl sulfate (SDS). The effects of the SDS concentration on the migration behavior of analytes was also examined. Moreover, the influences of electrolyte concentration and capillary temperature on the separation were investigated. In optimum conditions, seven major prostaglandins and thromboxane B2 could be separated within 8 min. The relative standard deviations of the migration times (reproducibility) of the analytes were less than 0.82%.
The combination of capillary isotachophoresis and capillary zone electrophoresis may enhance greatly the performance of analytical capillary electrophoresis with respect to both separation power and the concentration sensitivity. The concentrating effects and the separation power of isotachophoresis allow the analysis of diluted samples and the elimination of interferences due to bulk components. The separation process of zone electrophoresis enables one to resolve the stack of trace analytes and detect the resulting individual zones with high sensitivity. The transition of isotachophoresis into zone electrophoresis plays the key role in the overall performance of this hyphenated technique. This article describes the dynamics of the conversion of isotachophoresis into zone electrophoretic mode and shows that the key role is played by the segments of the leading and terminating zones from the isotachophoretic stage. The magnitude of these segments directly effects the detection time as well as the separation width of the peaks of analytes. It is shown that these effects are also important in the analyses by capillary zone electrophoresis where isotachophoresis is induced by the sample itself. Finally, the paper presents a list of recommended, user-friendly, electrolyte systems which enable one to simply predict the performance of the combination isotachophoresis-zone electrophoresis.