Dean Tricia H, Jezorek John R
Department of Chemistry and Biochemistry, The University of North Carolina at Greensboro, Greensboro, NC 27402-6170, USA.
J Chromatogr A. 2004 Mar 5;1028(2):239-45. doi: 10.1016/j.chroma.2003.11.068.
We demonstrate in this report that a conventional silica-based strong anion-exchange column can exhibit reversed-phase chromatographic behavior simultaneously with ion-exchange in a methanol-aqueous phthalate mobile phase. Reversed-phase behavior is shown for PAHs in relatively high methanol-content mobile phases, while polar organics exhibit reversed-phase behavior in 0-10% (v/v) methanol-water eluents. At low concentrations (0-10% v/v) methanol has little or no effect on anion retention, while the anions exhibit only slight increases in retention in 60-80% (v/v) methanol at near-neutral pH values. Likewise, pH changes used to manipulate anion retention have essentially no effect on PAH retention, and cause only small decreases in retention for most of the polar organics studied. Little or no pH-effect was seen on a phenyl column (no exchange group) or with acetate mobile phase. It is shown that manipulation of pH and methanol content allows the grouping of neutral organic analytes early in a chromatogram, followed by the anions, with no class overlap. Several example chromatograms are given, including that of a red wine sample. Column efficiency was good for anions but only modest for organics.
我们在本报告中证明,在甲醇 - 邻苯二甲酸盐水相流动相中,传统的硅胶基强阴离子交换柱在进行离子交换的同时可呈现反相色谱行为。在甲醇含量相对较高的流动相中,多环芳烃呈现反相行为,而极性有机物在0 - 10%(v/v)甲醇 - 水流动相中呈现反相行为。在低浓度(0 - 10% v/v)时,甲醇对阴离子保留几乎没有影响,而在接近中性pH值的60 - 80%(v/v)甲醇中,阴离子的保留仅略有增加。同样,用于控制阴离子保留的pH变化对多环芳烃的保留基本没有影响,并且对大多数所研究的极性有机物而言,仅导致保留略有下降。在苯基柱(无交换基团)或使用乙酸盐流动相时,未观察到pH效应。结果表明,通过控制pH和甲醇含量,可以在色谱图早期对中性有机分析物进行分组,随后是阴离子,且无类别重叠。给出了几个示例色谱图,包括一个红酒样品的色谱图。该柱对阴离子的柱效良好,但对有机物的柱效一般。