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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Chromatographic retention prediction and octanol-water partition coefficient determination of monobasic weak acidic compounds in ion-suppression reversed-phase liquid chromatography using acids as ion-suppressors
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Chromatographic retention prediction and octanol-water partition coefficient determination of monobasic weak acidic compounds in ion-suppression reversed-phase liquid chromatography using acids as ion-suppressors

机译:酸作为离子抑制剂的离子抑制反相液相色谱中一元弱酸性化合物的色谱保留预测和辛醇-水分配系数测定

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摘要

Although simple acids, replacing buffers, have been widely applied to suppress the ionization of weakly ionizable acidic analytes in reversed-phase liquid chromatography (RPLC), none of the previously reported works focused on the systematic studies about the retention behavior of the acidic solutes in this ion-suppression RPLC mode. The subject of this paper was therefore to investigate the retention behavior of monobasic weak acidic compounds using acetic, perchloric and phosphoric acids as the ion-suppressors. The apparent octanol-water partition coefficient (K-ow '') was proposed to calibrate the octanol-water partition coefficient (K-ow) of these weak acidic compounds, which resulted in a better linear correlation with log k(w), the logarithm of the hypothetical retention factor corresponding to neat aqueous fraction of hydroorganic mobile phase. This log Kow '' - log k(w) linear correlation was successfully validated by the results of monocarboxylic acids and monohydrating phenols, and moreover by the results under diverse experimental conditions for the same solutes. This straightforward relationship not only can be used to effectively predict the retention values of weak acidic solutes combined with Snyder-Soczewinski equation, but also can offer a promising medium for directly measuring K-ow data of these compounds via Collander equation. In addition, the influence of the different ion-suppressors on the retention of weak acidic compounds was also compared in this RPLC mode.
机译:尽管用简单的酸代替缓冲剂已广泛用于抑制反相液相色谱(RPLC)中弱电离的酸性分析物的电离,但以前报道的工作都没有集中于系统研究酸性溶质在色谱柱中的保留行为。此离子抑制RPLC模式。因此,本文的主题是研究使用乙酸,高氯酸和磷酸作为离子抑制剂的一元弱酸性化合物的保留行为。为了校正这些弱酸性化合物的辛醇-水分配系数(K-ow),提出了表观的辛醇-水分配系数(K-ow),这导致与log k(w)的线性关系更好,假设保留因子的对数,对应于有机溶剂流动相的纯净水相。通过单羧酸和一水合酚的结果以及在相同溶质的不同实验条件下的结果成功验证了该log Kow-log k(w)线性相关性。这种直接的关系不仅可以用于结合Snyder-Soczewinski方程来有效预测弱酸性溶质的保留值,而且可以为通过Collander方程直接测量这些化合物的Kow数据提供有希望的介质。此外,在此RPLC模式下,还比较了不同离子抑制剂对弱酸性化合物保留的影响。

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