首页> 外文期刊>Chromatographia >INFLUENCE OF TEMPERATURE AND MOBILE PHASE COMPOSITION ON RETENTION PROPERTIES OF OLIGOMERIC BONDED PHASES IN REVERSED-PHASE LIQUID CHROMATOGRAPHY (RPLC)
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INFLUENCE OF TEMPERATURE AND MOBILE PHASE COMPOSITION ON RETENTION PROPERTIES OF OLIGOMERIC BONDED PHASES IN REVERSED-PHASE LIQUID CHROMATOGRAPHY (RPLC)

机译:反相液相色谱(RPLC)中温度和移动相组成对低聚物键合相保留特性的影响

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The effect of temperature and mobile phase composition (methanol-water) on the retention behaviour of an oligomeric series of n-octylsilyl bonded phases in reversed-phase liquid chromatography has been investigated. Plots of In k against 1/T (van't Hoff plot) and the enthalpy of transfer (Delta H degrees) yields linear relationships under the conditions studied. The Delta H degrees values of the aromatic hydrocarbons and n-alkyl benzoates are higher than those of the polar compounds due to their higher level of interaction with the stationary phase. A linear plot of Delta H degrees vs. Delta S degrees suggest that the retention process, which is essentially controlled by non-specific (dispersive) interactions between the solutes and the bonded ligands, is identical for all cases evaluated. The existence of similar retention mechanisms is confirmed by the constant value of the enthalpy-entropy compensation temperature of the columns for a given class of compounds. As expected, decreasing the methanol content (% v/v) of the mobile phase results in increased eluite retention times. The methylene and phenyl selectivities are found to be independent of the carbon content of the stationary phases and varied only with the eluent composition. In addition to their high stability under aggressive mobile phase conditions as previously reported, the results of this study generally showed that the solute retention process on oligomeric phases are similar to those exhibited by the conventional reversed phases. [References: 31]
机译:研究了温度和流动相组成(甲醇-水)对反相液相色谱中低级系列正辛基甲硅烷基键合相的保留行为的影响。在所研究的条件下,In k对1 / T的曲线(范霍夫曲线)和转移焓(ΔH度)产生线性关系。芳香烃和苯甲酸正烷基酯的Delta H度值高于极性化合物,因为它们与固定相的相互作用程度更高。 Delta H度对Delta S度的线性图表明,保留过程主要由溶质和键合配体之间的非特异性(分散)相互作用控制,在所有评估的情况下都是相同的。对于给定类别的化合物,通过色谱柱的焓-熵补偿温度的恒定值可以确认是否存在类似的保留机理。如预期的那样,降低流动相的甲醇含量(%v / v)会增加洗脱液的保留时间。发现亚甲基和苯基的选择性与固定相的碳含量无关,并且仅随洗脱液组成而变化。除了先前报道的在侵蚀性流动相条件下的高稳定性外,这项研究的结果还普遍表明,低聚物相上的溶质保留过程与常规反相显示的相似。 [参考:31]

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