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在强酸性阳离子交换柱上同时展现阳离子交换和反相机制

Demonstration of simultaneous cation-exchange and reversed-phase mechanisms on a strong-acid cation-exchange column.

作者信息

Gu R F, Jezorek J R

机构信息

Department of Chemistry and Biochemistry, The University of North Carolina at Greensboro, 27402-6170, USA.

出版信息

J Chromatogr A. 2001 Jun 1;919(1):21-8. doi: 10.1016/s0021-9673(01)00786-5.

Abstract

It is demonstrated in this report that a conventional strong-acid cation-exchange column can exhibit reversed-phase chromatographic behavior simultaneously with ion-exchange. Adjusting the pH to control cation retention has no effect on the retention of neutral organic analytes. Likewise, changes in the methanol content of the mobile phase to adjust organic analyte retention causes only a small decrease in retention of metal ions in the 0 to 10% (v/v) methanol range, and no significant effect beyond that. Linear calibration behavior of both metal cations and neutral organic analytes is found on this column over three-order of magnitude. Examples of simultaneous metal cation-neutral organic separations in both the isocratic and gradient modes are shown, with conductivity detection for the metal ions and UV for the organic analytes. An isocratic separation of metal ions and neutrals in a vitamin pill is also demonstrated.

摘要

本报告表明,传统的强酸阳离子交换柱可同时呈现反相色谱行为和离子交换行为。调节pH以控制阳离子保留对中性有机分析物的保留没有影响。同样,改变流动相中的甲醇含量以调节有机分析物保留,在0至10%(v/v)甲醇范围内只会使金属离子的保留略有降低,超过该范围则无显著影响。在此柱上发现金属阳离子和中性有机分析物在三个数量级范围内均呈现线性校准行为。展示了等度和梯度模式下金属阳离子与中性有机物同时分离的示例,其中金属离子采用电导检测,有机分析物采用紫外检测。还展示了维生素片中金属离子和中性物质的等度分离。

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