Obata H, van den Berg C M
Oceanography Laboratories, University of Liverpool, UK.
Anal Chem. 2001 Jun 1;73(11):2522-8. doi: 10.1021/ac001495d.
A new procedure for the direct determination of picomolar levels of iron in seawater is presented. Cathodic stripping voltammetry (CSV) is preceded by adsorptive accumulation of the iron(III)-2,3-dihydroxynaphthalene (DHN) complex from seawater, containing 20 microM DHN at pH 8.0, onto a static mercury drop electrode, followed by reduction of the adsorbed species. The reduction current is catalytically enhanced by the presence of 20 mM bromate. Optimized conditions include a 60-s adsorption period at -0.1 V and a voltammetric scan using sampled dc modulation at 10 Hz. In these conditions, a detection limit of 13 pM iron in seawater was achieved which can be lowered further by extending the adsorption time to 300 s. The new catalytic CSV method is approximately 5 times more sensitive than existing CSV methods and was tested on samples from the Atlantic Ocean.
本文介绍了一种直接测定海水中皮摩尔级铁含量的新方法。采用阴极溶出伏安法(CSV),先将海水中的铁(III)-2,3-二羟基萘(DHN)络合物在pH 8.0、含有20 μM DHN的条件下吸附富集到静态汞滴电极上,然后将吸附的物质还原。20 mM溴酸盐的存在可催化增强还原电流。优化条件包括在-0.1 V下吸附60 s以及使用10 Hz的采样直流调制进行伏安扫描。在这些条件下,海水中铁的检测限达到13 pM,通过将吸附时间延长至300 s可进一步降低检测限。新的催化CSV方法比现有的CSV方法灵敏度高约5倍,并在大西洋采集的样品上进行了测试。