Shaw Matthew J, Nesterenko Pavel N, Dicinoski Greg W, Haddad Paul R
Australian Centre for Research on Separation Science, School of Chemistry, University of Tasmania, GPO Box 252-75, Hobart 7001, Tasmania, Australia.
J Chromatogr A. 2003 May 16;997(1-2):3-11. doi: 10.1016/s0021-9673(03)00111-0.
The chromatographic behaviour of a commercially available ion-exchange stationary phase (the Dionex IonPac CS12A column) is described for a wide range of transition and heavy metal ions with nitric acid eluents containing chloride and nitrate potassium salts. The separation selectivity was found to arise from simultaneous ion-exchange interactions and chelation with the attached carboxylic and phosphonic acid groups. These interactions were investigated by altering the ionic strength and pH of the eluent and also the column temperature. Strong affinity of the stationary phase towards heavy metal ions, in particular bismuth and the uranyl ion was observed at low pH under chelating ion-exchange conditions, with high efficiency separations of other ions including cadmium and lead being possible with short analysis times (approximately 5-15 min). Examples are given of separations obtained using 4-(2-pyridylazo)resorcinol or Arsenazo III as the post-column chromogenic reagents, demonstrating the potential versatility and utility of this stationary phase for heavy metal ion analysis.
描述了一种市售离子交换固定相(戴安公司的IonPac CS12A柱)在含有氯化钾和硝酸钾的硝酸洗脱液中对多种过渡金属离子和重金属离子的色谱行为。发现分离选择性源于同时发生的离子交换相互作用以及与连接的羧酸和膦酸基团的螯合作用。通过改变洗脱液的离子强度和pH值以及柱温来研究这些相互作用。在螯合离子交换条件下,低pH时观察到固定相对重金属离子,特别是铋离子和铀酰离子具有很强的亲和力,对于其他离子(包括镉和铅),在短分析时间(约5 - 15分钟)内即可实现高效分离。给出了使用4 - (2 - 吡啶偶氮)间苯二酚或偶氮胂III作为柱后显色试剂获得的分离示例,证明了该固定相在重金属离子分析方面具有潜在的多功能性和实用性。