In HPLC, the nonlinear behavior of the retention factor k' with temperature (dependence of ln k' on 1/T) can be attributed to the multiple interactions of a unique analyte in the separation process and/or to the existence in solution of multiple forms of the analyte (also leading to different free enthalpies of interaction). In this study, several examples of nonlinear retention-temperature dependence are evaluated for both reversed-phase (RP) and hydrophilic interaction chromatography (HILIC) separations. The potential explanation for nonlinear retention-temperature behavior is evaluated for each example, some caused by multiple interactions in the separation system of a unique analyte and others by multiple forms of the analyte. In cases where the analyte does not have more forms and the separation is based predominantly on one type of interaction (e.g., hydrophobic interaction in RP-HPLC), the dependence is linear, as expected. By studying the changes in the chemical structure of a compound as a function of pH it is possible to decide, in many cases, if a unique form or multiple forms of a compound are present in the solution. The use of this information allows us to determine when the lack of linearity (when present) is caused by multiple interactions in the separation system (for one form of the compound) and when more forms are causing the lack of linearity. The approximation with a quadratic form for the nonlinear dependence has been verified in most cases to be good, and only minor improvements were obtained when using higher polynomial dependencies.
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