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首页> 外文期刊>Journal of liquid chromatography and related technologies >COMPARISON OF REVERSED-PHASE AND NORMAL-PHASE COLUMN LIQUID CHROMATOGRAPHIC TECHNIQUES FOR THE SEPARATION OF LOW AND HIGH MOLECULAR WEIGHT COMPOUNDS
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COMPARISON OF REVERSED-PHASE AND NORMAL-PHASE COLUMN LIQUID CHROMATOGRAPHIC TECHNIQUES FOR THE SEPARATION OF LOW AND HIGH MOLECULAR WEIGHT COMPOUNDS

机译:反相和正相柱液相色谱技术分离低分子量和高分子量化合物的比较

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摘要

Liquid chromatography of complex samples often requires gradient elution to separate components with great differences in retention properties. The theory of gradient elution has now been elaborated so that it allows predicting the retention and the resolution of sample compounds not only in reversed-phase, but also in various normal-phase (adsorption chromatography) systems, for almost any combination of gradient profile and relationship between the retention and mobile phase composition. Using this knowledge, parameters of binary or ternary linear and non-linear gradients can be adjusted by predictive calculations for the desired resolution and minimum separation time in various chromatographic systems.In addition to accurate calculations of the gradient elution data, simple procedures can be employed for rapid estimation of the effects of the gradient program on the retention, both in reversed-phase and in normal-phase gradient chromatography. However, these procedures cannot be used for fine-tuning of separation, as they do not take into account possible effects of the gradient program on the elution order.Non-ideal instrumental or phase system effects impair the reproducibility of the retention data and the accuracy of the retention prediction and separation optimization. The most important, are the migration of some compounds during the dwell period, before the start of the gradient and the preferential adsorption of strong solvents, or of the traces of water from the mobile phase on to the column during gradient run. These effects should be accounted for to increase the accuracy of the predicted gradient retention data and of the gradient optimization.Both in reversed-phase and in normal-phase liquid chromatography, the strong solvent affects the retention of macro-molecules much more strongly than the retention of small molecules. Consequently, less steep gradients, and much narrower gradient concentration ranges, are usually required for the separation of polymers and oligomers according to the molar mass distribution, than for the gradient-elution separation of small molecules.
机译:复杂样品的液相色谱通常需要梯度洗脱以分离保留特性差异很大的组分。现在已经详细阐述了梯度洗脱的理论,这样就可以预测几乎在梯度谱图和色谱图的任何组合下,样品化合物的保留和分离度不仅在反相系统中,而且在各种正相(吸附色谱)系统中。保留与流动相组成之间的关系。利用这些知识,可以通过预测计算来调整二元或三元线性和非线性梯度的参数,以在各种色谱系统中获得所需的分离度和最短分离时间。除了准确计算梯度洗脱数据外,还可以使用简单的程序可以快速估算梯度程序对反相和正相梯度色谱中保留率的影响。但是,这些方法不能用于分离的微调,因为它们没有考虑到梯度程序对洗脱顺序的可能影响。非理想的仪器或相系统的影响会损害保留数据的重现性和准确性保留预测和分离优化。最重要的是,在梯度开始之前的保质期内某些化合物的迁移以及强溶剂的优先吸附,或者在梯度运行期间痕量水从流动相到色谱柱的迁移。应该考虑这些影响,以提高预测的梯度保留数据和梯度优化的准确性。在反相和正相液相色谱中,强溶剂对大分子保留的影响远大于对大分子的保留。保留小分子。因此,与小分子的梯度洗脱分离相比,根据摩尔质量分布分离聚合物和低聚物通常需要的梯度较弱,梯度浓度范围更窄。

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