首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Repetitive injection method: A tool for investigation of injection zone formation and its compression in microfluidic liquid chromatography
【24h】

Repetitive injection method: A tool for investigation of injection zone formation and its compression in microfluidic liquid chromatography

机译:重复进样方法:用于研究进样区形成及其在微流控液相色谱中压缩的工具

获取原文
获取原文并翻译 | 示例
           

摘要

Sample introduction in microfluidic liquid chromatography often generates wide zones rather than peaks, especially when a large sample volume (relative to column volume) is injected. Formation of wide injection zones can be further amplified when the sample is dissolved in a strong eluent. In some cases sample breakthrough may occur, especially when the injection is performed into short trapping columns. To investigate the band formation and subsequent zone focusing under gradient elution in situations such as these, we developed the Repetitive Injection Method (RIM), based on the temporally resolved introduction of two discrete peaks to a column, mimicking both the leading and trailing edges of a larger, singly injected sample zone. Using titanium microfluidic 0.32 mm I.D. columns, the results of RIM experiments were practically identical to injection of a correspondingly larger single zone volume. It was also experimentally shown that zone width (spacing between two injected peaks) decreases during gradient elution. We utilized RIM experiments to investigate wide sample zones created by strong sample solvent, and subsequent gradient zone focusing for a series of compounds. This experimental work was compared with computationally simulated chromatograms. The success of sample focusing during injection and gradient elution depends not only on an analyte's absolute retention, but also on how rapidly the analyte's retention changes during the mobile phase gradient. (C) 2015 Elsevier B.V. All rights reserved.
机译:在微流体液相色谱中引入样品通常会产生较宽的区域,而不是峰,特别是在进样量大(相对于色谱柱体积)的样品中。当样品溶解在强洗脱液中时,宽进样区的形成可以进一步放大。在某些情况下,可能会发生样品穿透,特别是在短捕获柱中进样时。为了研究在此类情况下梯度洗脱下的能带形成和随后的区域聚焦,我们开发了重复进样方法(RIM),该方法基于时间分辨将两个离散峰引入色谱柱的过程,模拟了色谱柱的前缘和后缘较大的单次进样区。使用钛微流体0.32毫米内径色谱柱,RIM实验的结果实际上与注入相应更大的单区体积相同。实验还表明,在梯度洗脱过程中,区域宽度(两个注入峰之间的间隔)减小。我们利用RIM实验研究了由强样品溶剂产生的宽样品区,以及随后针对一系列化合物的梯度区聚焦。将该实验工作与计算模拟色谱图进行了比较。进样和梯度洗脱过程中样品聚焦的成功不仅取决于分析物的绝对保留,还取决于分析物的保留在流动相梯度变化的速度有多快。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号