A Dual Column pH Switchable Water Stationary Phase System for Separation Control in Supercritical Fluid Chromatography

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Emmanuel A. Nai, Kevin B. Thurbide
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引用次数: 0

Abstract

A dual column system comprised of a pH switchable water stationary phase column and a conventional non-polar capillary column is introduced for use in Supercritical Fluid Chromatography (SFC). By removing or adding NH4OH to the system hydration source, the water stationary phase pH can be rapidly switched between acidic (measured at pH∼3) and basic (measured at pH∼9) in seconds, while the operating character of the conventional column is unchanged. This switch modulates the velocity of ionizable analytes about 20-fold in the system, whereas non-ionizable analytes are not affected. In this way, the retention time of acids and/or bases can be reproducibly altered (<1% RSD; n = 3) in SFC separations. As a result, analyte selectivity and resolution can be readily controlled during analyses. For example, a selectivity reversal (alpha from 0.4 to 1.6) and a resolution increase (from 0 to 13) are demonstrated. Rapid stationary phase pH switching also allows multiple acids, bases, and/or neutral analytes to be determined simultaneously. Applications demonstrate that this method can greatly simplify complex mixture analysis in SFC by helping to separate target analytes from interfering matrix components.

用于超临界流体色谱分离控制的双柱 pH 值可切换水固定相系统
介绍了一种用于超临界流体色谱(SFC)的双柱系统,该系统由 pH 值可切换的水固定相柱和传统的非极性毛细管柱组成。通过在系统水合源中移除或添加 NH4OH,水固定相的 pH 值可在几秒钟内在酸性(pH∼3 时测量)和碱性(pH∼9 时测量)之间快速切换,而传统色谱柱的工作特性保持不变。这种切换可将系统中可电离分析物的速度调节约 20 倍,而不可电离分析物则不受影响。这样,酸和(或)碱的保留时间就可以发生可重现的改变 (
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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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