McCormick T J, Foley J P, Riley C M, Lloyd D K
Department of Chemistry, Drexel University, Philadelphia, Pennsylvania 19104, USA.
Anal Chem. 2000 Jan 15;72(2):294-301. doi: 10.1021/ac9903398.
One of the limitations that has restricted the applicability of micellar liquid chromatography (MLC) is the weak eluting power of micellar mobile phases compared to conventional hydro-organic mobile phases used in reversed-phase liquid chromatography. This may be the result of Donnan or steric exclusion of the micelles from the pores of the stationary phase, within which nearly all (> or = 99%) of the stationary phase resides and the analytes spend most of their time. To determine whether wide-pore stationary phases would overcome this limitation in MLC, several C8 and C18 stationary phases ranging from 100 to 4000 A were investigated using a diverse set of test solutes and micellar solutions of anionic, neutral, and cationic surfactants as mobile phases. With the larger pore size stationary phases, the eluting power of the MLC mobile phases was enhanced with all surfactant types, the greatest effect being with the neutral surfactant. Differences in retention behavior were observed between various solute types and between the C8 and C18 stationary phases. These differences appear to be related to the relative hydrophobicity of the solutes and to differences in the surfactant-modified stationary phases. Partitioning behavior of representative solutes on the large-pore C8 and C18 columns was shown to follow the three-phase partitioning model for MLC. Methylene group selectivity data showed only minor differences in the stationary-phase characteristics between the small- and large-pore size C18 columns. The true eluting power of micellar mobile phases was revealed with wide-pore stationary phases and was demonstrated by the separation and elution of an extended series of alkylphenones on C18 columns.
限制胶束液相色谱法(MLC)应用的一个因素是,与反相液相色谱中使用的传统水-有机流动相相比,胶束流动相的洗脱能力较弱。这可能是由于胶束被固定相孔隙中的唐南效应或空间排阻作用,几乎所有(≥99%)的固定相都存在于这些孔隙中,分析物也大部分时间处于其中。为了确定大孔径固定相是否能克服MLC中的这一限制,使用了多种测试溶质以及阴离子、中性和阳离子表面活性剂的胶束溶液作为流动相,研究了一系列孔径从100到4000 Å的C8和C18固定相。对于孔径较大的固定相,所有类型的表面活性剂都增强了MLC流动相的洗脱能力,其中对中性表面活性剂的影响最大。在不同溶质类型之间以及C8和C18固定相之间观察到了保留行为的差异。这些差异似乎与溶质的相对疏水性以及表面活性剂改性固定相的差异有关。代表性溶质在大孔径C8和C18柱上的分配行为表明遵循MLC的三相分配模型。亚甲基选择性数据显示,小孔径和大孔径C18柱在固定相特性上只有微小差异。大孔径固定相揭示了胶束流动相的真正洗脱能力,这通过在C18柱上分离和洗脱一系列烷基苯酮得以证明。