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梯度洗脱分离:为什么陡梯度曲线会发生扭曲,以及它对反相液相色谱中分辨率的影响。

Separations by gradient elution: why are steep gradient profiles distorted and what is their impact on resolution in reversed-phase liquid chromatography.

机构信息

Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600, USA.

Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600, USA.

出版信息

J Chromatogr A. 2014 May 30;1344:66-75. doi: 10.1016/j.chroma.2014.04.010. Epub 2014 Apr 18.

Abstract

The formation of a concentration shock layer of either methanol or acetonitrile used as the modifier in steep RPLC aqueous/organic gradients was predictable from their excess adsorption isotherm and was directly observed from their elution profiles recorded in UV absorption. A discontinuity of the concentration profile of the organic modifier arises and grows along the column. Its effects on the peak shapes and the resolution levels achieved in steep gradient chromatography were measured in the recorded chromatograms of a sample mixture containing 14 different analytes uniformly distributed across the gradient retention window. The results showed severe peak shape deformation for some compounds and a significant degradation of the baseline resolution of weakly (when using acetonitrile) and moderately (when using methanol) retained analytes. Solutions to limit this loss of resolution may lie in changing the initial gradient conditions or in adjusting the curvature of the gradient profile at the column inlet.

摘要

在陡峭的反相高效液相色谱水/有机溶剂梯度中,甲醇或乙腈作为改性剂形成浓度激波层,可以根据它们的过剩吸附等温线来预测,并可以从它们在紫外吸收中记录的洗脱曲线中直接观察到。有机改性剂的浓度曲线出现不连续,并沿柱生长。在记录的包含 14 种不同分析物的样品混合物的色谱图中,测量了其对峰形和在陡峭梯度色谱中达到的分辨率水平的影响,这些分析物均匀分布在梯度保留窗口中。结果表明,对于某些化合物,峰形严重变形,对于弱保留(使用乙腈时)和中等保留(使用甲醇时)的分析物,基线分辨率显著降低。限制这种分辨率损失的解决方案可能在于改变初始梯度条件或调整柱入口处梯度曲线的曲率。

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