Ng K L, Glód B K, Dicinoski G W, Haddad P R
Australian Centre for Research on Separation Science, School of Chemistry, University of Tasmania, Hobart.
J Chromatogr A. 2001 Jun 22;920(1-2):41-9. doi: 10.1016/s0021-9673(01)00608-2.
Previous models for the retention behaviour of carboxylic acids in ion-exclusion chromatography are applicable only when the degree of ionisation of the analyte is constant over the entire chromatographic peak. When solutions of sulfuric acid are used as eluents, this condition applies only when the eluent concentration is considerably higher than that of the analyte. Since it is common for dilute solutions of sulfuric acid to be used as eluents, a retention model which accounts for unbuffered eluents has been developed. This model also considers the effects on retention of hydrophobic adsorption of the undissociated and dissociated forms of the analyte onto the stationary phase substrate, as well as the effects of organic solvents added to the eluent. The derivation of this model is presented and it has been evaluated using a comprehensive set of retention data obtained using three different sulfonated stationary phases over a range of eluent conditions. The adsorption coefficients calculated from the model are in accordance with expected trends and showed that both the undissociated and dissociated forms of the analyte acids were retained by hydrophobic adsorption effects, although this adsorption was much stronger for the undissociated analytes.
先前关于羧酸在离子排斥色谱中保留行为的模型仅适用于分析物的电离程度在整个色谱峰上保持恒定的情况。当使用硫酸溶液作为洗脱剂时,此条件仅在洗脱剂浓度远高于分析物浓度时才适用。由于通常使用稀硫酸溶液作为洗脱剂,因此已开发出一种考虑了未缓冲洗脱剂的保留模型。该模型还考虑了分析物未离解和离解形式在固定相基质上的疏水吸附对保留的影响,以及添加到洗脱剂中的有机溶剂的影响。本文给出了该模型的推导过程,并使用在一系列洗脱剂条件下通过三种不同磺化固定相获得的一组全面的保留数据对其进行了评估。从模型计算得到的吸附系数符合预期趋势,表明分析物酸的未离解和离解形式均通过疏水吸附作用被保留,尽管未离解分析物的这种吸附要强得多。