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胶束电动色谱中的阴离子-两性离子混合胶束:十二烷基硫酸钠-N-十二烷基-N,N-二甲基铵-3-丙烷-1-磺酸

Anionic-zwitterionic mixed micelles in micellar electrokinetic chromatography: sodium dodecyl sulfate-N-dodecyl-N,N-dimethylammonium-3-propane-1-sulfonic acid.

作者信息

Ahuja E S, Preston B P, Foley J P

机构信息

Department of Chemistry, Villanova University, PA 19085-1699.

出版信息

J Chromatogr B Biomed Appl. 1994 Jul 15;657(2):271-84. doi: 10.1016/0378-4347(94)00364-5.

Abstract

A zwitterionic surfactant, N-dodecyl-N,N-dimethylammonium-3-propane-1- sulfonic acid (SB-12), was used in combination with an anionic surfactant, sodium dodecyl sulfate (SDS), to form a novel pseudostationary phase for use in micellar electrokinetic chromatography. This mixed micellar system was characterized in terms of analyte retention, selectivity, efficiency, elution range, and resolution; and compared to results obtained using only SDS. A typically used SDS concentration, 20 mM, was chosen as a reference to which comparisons could be drawn. With 20 mM SDS, the optimum concentration range of 10-20 mM SB-12 provided efficiencies that were 2-4 times greater than with SDS alone, with minimal (< 15%) changes in the elution range and electroosmotic flow. The addition of 40 and 60 mM SB-12 also resulted in efficiencies on average of 600,000-800,000 theoretical plates/m, but at a significant reduction in the elution range and peak capacity. Retention factors (k') for the various neutral analytes increased by 20% with addition of 10 mM SB-12 and by approximately 60% with addition of 40 and 60 mM SB-12, while operating currents remained constant as SB-12 was added. Geometrical isomers p-nitrotoluene and m-nitrotoluene, that co-eluted with 20 mM SDS, were baseline resolved with the addition of 10 mM SB-12; in addition, methylene selectivity was greatest at this composition. No capillary wall interactions or coating effects were observed with the SDS-SB-12 mixed micellar system, in contrast to previously studied anionic-non-ionic mixed micellar system, SDS-Brij 35. Consequently, migration times were very repeatable (< or = 1.2% R.S.D.).

摘要

一种两性离子表面活性剂N-十二烷基-N,N-二甲基铵-3-丙烷-1-磺酸(SB-12)与一种阴离子表面活性剂十二烷基硫酸钠(SDS)联合使用,形成一种用于胶束电动色谱的新型假固定相。该混合胶束体系在分析物保留、选择性、效率、洗脱范围和分离度方面进行了表征,并与仅使用SDS获得的结果进行了比较。选择了典型的SDS浓度20 mM作为可进行比较的参考。对于20 mM的SDS,10 - 20 mM SB-12的最佳浓度范围提供的效率比单独使用SDS时高2 - 4倍,洗脱范围和电渗流的变化最小(< 15%)。添加40 mM和60 mM SB-12也导致平均效率为600,000 - 800,000理论塔板数/米,但洗脱范围和峰容量显著降低。添加10 mM SB-12时,各种中性分析物的保留因子(k')增加了20%,添加40 mM和60 mM SB-12时增加了约60%,同时随着SB-12的添加,工作电流保持恒定。与20 mM SDS共洗脱的几何异构体对硝基甲苯和间硝基甲苯,添加10 mM SB-12后实现了基线分离;此外,在此组成下亚甲基选择性最大。与先前研究的阴离子 -非离子混合胶束体系SDS - Brij 35不同,SDS - SB-12混合胶束体系未观察到毛细管壁相互作用或涂层效应。因此,迁移时间具有非常高的重复性(<或 = 1.2%相对标准偏差)。

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