Suu Agnes, Jalukse Lauri, Liigand Jaanus, Kruve Anneli, Himmel Daniel, Krossing Ingo, Rosés Martí, Leito Ivo
Institute of Chemistry, University of Tartu , 14a Ravila Street, 50411 Tartu, Estonia.
Anal Chem. 2015 Mar 3;87(5):2623-30. doi: 10.1021/ac504692m. Epub 2015 Feb 23.
This work introduces a conceptually new approach of measuring pH of mixed-solvent liquid chromatography (LC) mobile phases. Mobile phase pH is very important in LC, but its correct measurement is not straightforward, and all commonly used approaches have deficiencies. The new approach is based on the recently introduced unified pH (pH(abs)) scale, which enables direct comparison of acidities of solutions made in different solvents based on chemical potential of the proton in the solutions. This work represents the first experimental realization of the pH(abs) concept using differential potentiometric measurement for comparison of the chemical potentials of the proton in different solutions (connected by a salt bridge), together with earlier published reference points for obtaining the pH(abs) values (referenced to the gas phase) or pH(abs)(H₂O) values (referenced to the aqueous solution). The liquid junction potentials were estimated in the framework of Izutsu's three-component method. pH(abs) values for a number of common LC and LC-MS mobile phases have been determined. The pH(abs) scale enables for the first time direct comparison of acidities of any LC mobile phases, with different organic additives, different buffer components, etc. A possible experimental protocol of putting this new approach into chromatographic practice has been envisaged and its applicability tested. It has been demonstrated that the ionization behavior of bases (cationic acids) in the mobile phases can be better predicted by using the pH(abs)(H₂O) values and aqueous pKa values than by using the alternative means of expressing mobile phase acidity. Description of the ionization behavior of acids on the basis of pH(abs)(H₂O) values is possible if the change of their pKa values with solvent composition change is taken into account.
这项工作介绍了一种在概念上全新的测量混合溶剂液相色谱(LC)流动相pH值的方法。流动相pH值在液相色谱中非常重要,但其准确测量并非易事,所有常用方法都存在缺陷。新方法基于最近引入的统一pH(pH(abs))标度,该标度能够根据溶液中质子的化学势直接比较在不同溶剂中配制的溶液的酸度。这项工作首次通过差分电位测量实现了pH(abs)概念的实验验证,用于比较不同溶液(通过盐桥连接)中质子的化学势,同时结合了早期发表的用于获取pH(abs)值(以气相为参考)或pH(abs)(H₂O)值(以水溶液为参考)的参考点。液接电位在Izutsu的三组分方法框架内进行估算。已测定了多种常见液相色谱和液相色谱 - 质谱流动相的pH(abs)值。pH(abs)标度首次实现了对任何具有不同有机添加剂、不同缓冲成分等的液相色谱流动相酸度的直接比较。设想了一种将这种新方法应用于色谱实践的可能实验方案并测试了其适用性。结果表明,与使用表示流动相酸度的其他方法相比,使用pH(abs)(H₂O)值和水溶液pKa值能更好地预测流动相中碱(阳离子酸)的电离行为。如果考虑酸的pKa值随溶剂组成变化的情况,基于pH(abs)(H₂O)值描述酸的电离行为是可行的。