Chair of Environmental Chemistry & Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, 7 Gagarin St., PL 87-100 Toruń, Poland.
J Chromatogr A. 2013 Feb 22;1278:89-97. doi: 10.1016/j.chroma.2012.12.077. Epub 2013 Jan 10.
In the current work, a 14 different types of stationary phases with specific structural properties (eight commercially available stationary phases and six home-made) have been studied. We used the minor disturbance method to measure the excess adsorption isotherms of water onto surface of chemically bonded stationary phases from water-acetonitrile mixtures. The presence of polar and hydrophobic groups in the structures of adsorbents as well as changes in the mobile phase composition causes the excess adsorption of given solvent when its concentration in the mobile phase is low. The excess adsorption of water is observed in acetonitrile-rich mobile phase and the excess adsorption of acetonitrile is observed in water-rich mobile phase. The maximum excess of adsorbed water is connected with a negative excess of adsorbed acetonitrile. However, the scale of these excess adsorption depend on the type of the stationary bonded phases. The retention factors of three test solutes (tryptophan, glycine and proline) are correlated with the maximum amount of excessively adsorbed water on the stationary bonded phase surface. Linear dependence of retention factor with excess amount of water suggest, that the amount of adsorbed water ("hydrophilic pillow") play an important role in the retention mechanism in HILIC. All tested stationary phases were divided into several groups according to the retention factors of 16 different biologically active compounds (selected amino acids, pesticides, vitamin B6). Principal component analysis (PCA) and cluster analysis (CA) analysis were used in column comparison and grouping. CA results indicated that all stationary phases may be generally grouped into several clusters, due to structure and properties of stationary phases. Interesting results were obtained also with the use of PCA. Presented methodologycan provide useful information on the hydrophilic properties of various polar columns and their suitability for HILIC applications.
在当前的工作中,研究了 14 种具有特定结构特性的固定相(8 种市售固定相和 6 种自制固定相)。我们使用微扰法测量了从水-乙腈混合物到化学键合固定相表面的水的过剩吸附等温线。吸附剂结构中存在极性和疏水性基团以及流动相组成的变化导致当流动相中的浓度低时,给定溶剂的过剩吸附。在富含乙腈的流动相中观察到水的过剩吸附,而在富含水的流动相中观察到乙腈的过剩吸附。吸附的水的过剩量与吸附的乙腈的过剩量呈负相关。然而,这些过剩吸附的规模取决于固定相的类型。三种测试溶质(色氨酸、甘氨酸和脯氨酸)的保留因子与固定相表面上过度吸附的水的最大量相关。保留因子与过量水之间的线性关系表明,吸附水的量(“亲水枕头”)在 HILIC 中的保留机制中起着重要作用。所有测试的固定相根据 16 种不同生物活性化合物(选择的氨基酸、农药、维生素 B6)的保留因子分为几组。主成分分析(PCA)和聚类分析(CA)用于柱比较和分组。CA 结果表明,由于固定相的结构和性质,所有固定相通常可以分为几个簇。使用 PCA 也可以得到有趣的结果。所提出的方法可以提供有关各种极性柱的亲水性能及其在 HILIC 应用中的适用性的有用信息。