Dai Jun, Carr Peter W, McCalley David V
Bristol-Myers Squibb, Princeton, NJ 08540, USA.
J Chromatogr A. 2009 Mar 20;1216(12):2474-82. doi: 10.1016/j.chroma.2009.01.036. Epub 2009 Jan 17.
Column overloading is very common during the separations of basic analytes in analytical scale reversed-phase liquid chromatography (RPLC). Due to the complex interactions of ionic analytes with stationary and mobile phases, only a very small amount of ionized sample compared to the amount of nonpolar solute can be injected before the peak shape is distorted by non-linear chromatographic processes. Often the amount that can be injected before overload is observed is so small that the signal is quite noisy, thereby making the measured plate count imprecise and possibly inaccurate. The purpose of the present study was to develop a practical method for the precise measurement of the plate count and a column overload parameter using a simple but mathematically rigorous model of Langmuirian non-linear chromatography. An "overload profile", i.e. a plot of apparent plate count versus amount injected, is characterized by two parameters: the limiting plate count (N(0)) and the column sample loading capacity (omega(0.5)). The limiting plate count is the plate count that should be observed when the amount of sample injected is so small that a linear isotherm pertains. The column sample loading capacity, which is taken as the sample load that leads to a plate count equal to half of the limiting plate count, is a measure of the maximum amount of sample that can be injected into that column. The approach was tested by applying it to the study of cationic analytes in RPLC. We show that N(0) under constant conditions (column length, flow rate, mobile phase composition, etc.) is almost independent of column type (manufacturer); however, different column types (at the same length, diameter and flow rate) exhibit clear differences in their sample loading capacity (omega(0.5)). We believe that for most well packed type B columns, the column sample loading capacity and not the limiting plate count is the more important property that accounts for most of the apparent differences in peak width when different types of columns are examined.
在分析规模的反相液相色谱法(RPLC)中分离碱性分析物时,柱过载现象非常常见。由于离子分析物与固定相和流动相之间存在复杂的相互作用,与非极性溶质的量相比,在峰形因非线性色谱过程而变形之前,只能注入非常少量的离子化样品。通常,在观察到过载之前能够注入的量非常小,以至于信号相当嘈杂,从而使得测得的塔板数不精确且可能不准确。本研究的目的是使用一个简单但数学上严谨的朗缪尔非线性色谱模型,开发一种精确测量塔板数和柱过载参数的实用方法。一个“过载曲线”,即表观塔板数与注入量的关系图,由两个参数表征:极限塔板数(N(0))和柱样品负载量(ω(0.5))。极限塔板数是当注入的样品量非常小以至于适用线性等温线时应观察到的塔板数。柱样品负载量被视为导致塔板数等于极限塔板数一半的样品负载量,它是可以注入该柱的最大样品量的一种度量。通过将该方法应用于RPLC中阳离子分析物的研究来对其进行测试。我们表明,在恒定条件下(柱长、流速、流动相组成等),N(0)几乎与柱类型(制造商)无关;然而,不同类型的柱(在相同长度、直径和流速下)在其样品负载量(ω(0.5))方面表现出明显差异。我们认为,对于大多数装填良好的B型柱,柱样品负载量而非极限塔板数是在检查不同类型的柱时,解释峰宽表观差异大部分的更重要特性。