Steiner Steven A, Watson Dawn M, Fritz James S
Department of Chemistry and Engineering Physics, University of Wisconsin-Platteville, Platteville, WI 53818, USA.
J Chromatogr A. 2005 Aug 26;1085(1):170-5. doi: 10.1016/j.chroma.2005.01.070.
A background electrolyte (BGE) containing a 100 mM concentration of an alkylammonium cation with ethyl, propyl or butyl groups provides an excellent medium for separation of anions by capillary electrophoresis (CE). Two major effects were noted. Use of one of a series of alkylammonium cations in the BGE at a selected pH provides a simple and effective way to vary and control electroosmotic flow (EOF) over a broad range. It is believed that the alkylammonium cations are coated onto the capillary surface through a reversible dynamic equilibrium. Secondly, alkylammonium cations modify the electrophoretic migration of sample anions and the electroosmotic migration of neutral organic analytes by association interaction. This selective interaction results in improved anion separations and permits the simultaneous separation of neutral analytes. The degree of association interaction varies with the bulk and hydrophobicity of the alkylammonium cations. Incorporation of an aliphatic amine salt of moderate molecular weight in the running electrolyte provides a valuable new way to vary the migration times of sample anions and to optimize their resolution. The interactions between alkylammonium cations and sample anions or neutral organics appear to take place entirely within the liquid phase and do not require a polymeric or micellar pseudo phase.
含有浓度为100 mM的乙基、丙基或丁基烷基铵阳离子的背景电解质(BGE)为通过毛细管电泳(CE)分离阴离子提供了极佳的介质。注意到两个主要影响。在选定的pH值下,在BGE中使用一系列烷基铵阳离子中的一种,提供了一种简单有效的方法,可在很宽的范围内改变和控制电渗流(EOF)。据信,烷基铵阳离子通过可逆的动态平衡被包覆在毛细管表面。其次,烷基铵阳离子通过缔合相互作用改变样品阴离子的电泳迁移和中性有机分析物的电渗迁移。这种选择性相互作用导致阴离子分离得到改善,并允许同时分离中性分析物。缔合相互作用的程度随烷基铵阳离子的体积和疏水性而变化。在运行电解质中加入中等分子量的脂肪胺盐,为改变样品阴离子的迁移时间和优化其分离度提供了一种有价值的新方法。烷基铵阳离子与样品阴离子或中性有机物之间的相互作用似乎完全发生在液相内,不需要聚合物或胶束假相。