Chumbimuni-Torres Karin Y, Calvo-Marzal Percy, Wang Joseph, Bakker Eric
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Anal Chem. 2008 Aug 1;80(15):6114-8. doi: 10.1021/ac800595p. Epub 2008 Jun 21.
Potentiometric sensors are today sufficiently well understood and optimized to reach ultratrace level (subnanomolar) detection limits for numerous ions. In many cases of practical relevance, however, a high electrolyte background hampers the attainable detection limits. A particularly difficult sample matrix for potentiometric detection is seawater, where the high saline concentration forms a major interfering background and reduces the activity of most trace metals by complexation. This paper describes for the first time a hyphenated system for the online electrochemically modulated preconcentration and matrix elimination of trace metals, combined with a downstream potentiometric detection with solid contact polymeric membrane ion-selective microelectrodes. Following the preconcentration at the bismuth-coated electrode, the deposited metals are oxidized and released to a medium favorable to potentiometric detection, in this case calcium nitrate. Matrix interferences arising from the saline sample medium are thus circumvented. This concept is successfully evaluated with cadmium as a model trace element and offers potentiometric detection down to low parts per billion levels in samples containing 0.5 M NaCl background electrolyte.
如今,电位传感器已得到充分理解和优化,能够实现对多种离子的超痕量水平(亚纳摩尔)检测限。然而,在许多具有实际意义的情况下,高电解质背景会阻碍可达到的检测限。对于电位检测而言,特别困难的样品基质是海水,其中高盐浓度形成主要干扰背景,并通过络合作用降低大多数痕量金属的活性。本文首次描述了一种联用系统,用于痕量金属的在线电化学调制预富集和基质消除,并结合使用固体接触聚合物膜离子选择性微电极进行下游电位检测。在铋涂层电极上进行预富集后,沉积的金属被氧化并释放到有利于电位检测的介质中,在这种情况下是硝酸钙。因此,避免了来自含盐样品介质的基质干扰。以镉作为模型痕量元素对该概念进行了成功评估,在含有0.5 M NaCl背景电解质的样品中,实现了低至十亿分之几水平的电位检测。