Chen Zuliang, Naidu Ravendra
CSIRO Land and Water, Adelaide Laboratory, Glen Osmond, SA, Australia.
J Chromatogr A. 2002 Aug 9;966(1-2):245-51. doi: 10.1016/s0021-9673(02)00741-0.
On-column complexation of metal ions with 2,6-pyridinedicarboxylate (2,6-PDC) to form anionic complexes enabled their separation by capillary zone electrophoresis with direct UV detection at 214 nm. Nine metal ions, Cu2+, Zn2+, Ni2+, Cd2+ Mn2+, Pb2+, Fe3+, Al3+ and Ca2+, were determined in less than 7 min using 10 mM 2.6-PDC solution containing 0.75 mM tetradecyltrimethylammonium bromide at pH 4.0. Satisfactory working ranges (20-300 microM), detection limits (3-10 microM) and good repeatability of the peak areas (RSD 2.1-4.2%, n=5) were obtained using hydrodynamic injection (30 s). The proposed method was used successfully for the determination of Mn2+, Fe3+, Al3+ and Ca2+ in groundwaters.
金属离子与2,6 - 吡啶二甲酸(2,6 - PDC)在柱上形成阴离子配合物,使得它们能够通过毛细管区带电泳在214 nm处直接紫外检测进行分离。使用含有0.75 mM溴化十四烷基三甲基铵的10 mM 2,6 - PDC溶液在pH 4.0条件下,在不到7分钟内测定了9种金属离子,即Cu2 +、Zn2 +、Ni2 +、Cd2 +、Mn2 +、Pb2 +、Fe3 +、Al3 +和Ca2 +。采用流体动力学进样(30 s)获得了令人满意的工作范围(20 - 300 μM)、检测限(3 - 10 μM)以及良好的峰面积重复性(RSD 2.1 - 4.2%,n = 5)。所提出的方法成功用于测定地下水中的Mn2 +、Fe3 +、Al3 +和Ca2 +。