Geng X, Regnier F E
J Chromatogr. 1985 Sep 20;332:147-68. doi: 10.1016/s0021-9673(01)83293-3.
This paper proposes a retention model which predicts that the displacement of non-polar solutes from a reversed-phase chromatographic column is accompanied by the adsorption of a stoichiometric number (Z) of solvent molecules. The number of solvent molecules involved in this process is a function of both solute and solvent contact surface areas. Increasing solute contact surface area would increase Z whereas increasing solvent contact surface area would decrease the Z value for a specific solute. The experimental observations presented are consistent with this model. Further predictions of the model are that (1) plots of log k' versus the inverse log of solvent concentration will be non-linear at solvent concentrations where the surface of a reversed-phase support is not fully solvated, and (2) only a portion of the total non-polar surface area of a molecule actually contacts the surface of a reversed-phase support. Non-linearity in plots of log k' versus the inverse log of solvent concentration was in fact observed at solvent concentrations where solvation of the reversed-phase support is incomplete.
本文提出了一种保留模型,该模型预测反相色谱柱中非极性溶质的置换伴随着化学计量数(Z)的溶剂分子的吸附。参与此过程的溶剂分子数量是溶质和溶剂接触表面积的函数。增加溶质接触表面积会增加Z,而增加溶剂接触表面积会降低特定溶质的Z值。所呈现的实验观察结果与该模型一致。该模型的进一步预测是:(1)在反相载体表面未完全溶剂化的溶剂浓度下,log k'与溶剂浓度的负对数的关系图将呈非线性;(2)分子的总非极性表面积中只有一部分实际接触反相载体的表面。实际上,在反相载体溶剂化不完全的溶剂浓度下,观察到log k'与溶剂浓度的负对数关系图呈非线性。