Piech Robert, Baś Bogusław, Kubiak Władysław W
Faculty of Materials Science and Ceramics, AGH University of Science and Technology, 30-059 Kraków, al. Mickiewicza 30, Poland.
Talanta. 2008 Jul 15;76(2):295-300. doi: 10.1016/j.talanta.2008.02.038. Epub 2008 Mar 4.
The new cyclic renewable mercury film silver based electrode (Hg(Ag)FE), applied for the determination of molybdenum(VI) traces using differential pulse adsorptive cathodic stripping voltammetry (DP AdSV) is presented. The Hg(Ag)FE electrode is characterized by very good surface reproducibility (<or=2%) and long-term stability (more than 2 thousand measurement cycles). The preparation of the Hg(Ag)FE is very simple and its operation may be controlled automatically. The effects of various factors such as: preconcentration potential and time, pulse height, step potential and supporting electrolyte composition are optimized. The calibration graph is linear from 2 nM (192 ng L(-1)) to 200 nM (19 microg L(-1)) for an accumulation time of 15s, with correlation coefficient of 0.9995. For a Hg(Ag)FE with a surface area of 3.5mm(2) the detection limit for an accumulation time of 60s is as low as 8 ng L(-1). The repeatability of the method at a concentration level of the analyte as low as 2.4 microg L(-1), expressed as R.S.D. is 1.3% (n=7). The proposed method was successfully applied and validated by studying the certified reference material TMRAIN-95 and simultaneous recovering of Mo(VI) from spiked water and sediment samples.
介绍了一种新型的基于循环可再生汞膜银的电极(Hg(Ag)FE),该电极采用差分脉冲吸附阴极溶出伏安法(DP AdSV)用于测定痕量钼(VI)。Hg(Ag)FE电极具有非常好的表面重现性(≤2%)和长期稳定性(超过2000次测量循环)。Hg(Ag)FE的制备非常简单,其操作可自动控制。优化了各种因素的影响,如:预富集电位和时间、脉冲高度、步长电位和支持电解质组成。对于15s的积累时间,校准曲线在2 nM(192 ng L⁻¹)至200 nM(19 μg L⁻¹)范围内呈线性,相关系数为0.9995。对于表面积为3.5mm²的Hg(Ag)FE,60s积累时间的检测限低至8 ng L⁻¹。该方法在低至2.4 μg L⁻¹的分析物浓度水平下的重复性,以相对标准偏差(R.S.D.)表示为1.3%(n = 7)。通过研究有证标准物质TMRAIN - 95以及从加标水样和沉积物样品中同时回收Mo(VI),成功应用并验证了所提出的方法。