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Contribution of migration current to the voltammetric deposition and stripping of lead with and without added supporting electrolyte at a mercury-free carbon fibre microdisc electrode

机译:在无汞碳纤维微盘电极上添加和不添加支持电解质的情况下,迁移电流对铅的伏安法沉积和剥离的贡献

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摘要

In order to assess the contribution and analytical significance of migration,electrochemical studies on the deposition and stripping of lead at a carbon fibre microelectrode (diameter of 10 mum) have been undertaken in aqueou solutions containing 1 mM lead ions with variable KNO_3 supporting electrolyte concentrations (10~(-1) to 10~(-5) M),as well as in the total absence of deliberately added supporting electrolyte.The methodology involved the application of cyclic voltammetry to characterise the Pb~(2+) (solution) +2e~- Pb(metal) process in both the reduction (Pb deposition) and stripping (Pb dissolution) directions.The use of a mercury-free carbon surfaces means that the lead stripping does not occur form the amalgam state,as is commonly the case in anodic stripping voltammetry.In the deposition step,the current rises sharply with potential in response to a lead nucleation-growth process and then reaches an almost potential independent limiting value.The stripping step,obtained on the reverse scan,exhibited oxidation peak currents resulting from the redissolution or stripping of the metal from the electrode surface.The influence of the electrolyte concentration and hence migration current at -0.8 V versus Ag/AgCl for the deposition process,as well on the redissolution peak current and the dependence of the voltammograms on scan rate (10-1000 mV) are discussed.Interestingly,neither deposition limiting nor stripping peak currents vary in a simple manner with added supporting electrolyte concentrations,with maximum values being observed at 10~(-5) M rather than zero concentration of added KNO_3.An important implication for the voltammetric determination of lead in low ionic strength media by the very sensitive technique for anodic stripping voltammetry is that use of the method of standard additions commonly employed to minimise unknown matrix problems,is prone to error when contributions to the process from migration current are important.
机译:为了评估迁移的贡献和分析意义,已在含有1 mM铅离子且KNO_3支持电解质浓度可变的水溶液中对碳纤维微电极(直径为10 mum)上铅的沉积和剥离进行了电化学研究( 10〜(-1)到10〜(-5)M)以及完全没有故意添加支持电解质的情况。该方法包括应用循环伏安法表征Pb〜(2+)(溶液)+ 2e〜-Pb(金属)工艺在还原(Pb沉积)和汽提(Pb溶解)方向上的使用。无汞碳表面的使用意味着从汞齐状态不会发生铅汽提,通常是在阳极溶出伏安法的情况下。在沉积步骤中,电流随着铅成核-生长过程而随着电位急剧上升,然后达到几乎为电位的独立极限值。反向扫描显示了由于再溶解或电极表面金属剥离而产生的氧化峰值电流。在沉积过程中,电解质浓度的影响以及因此在-0.8 V相对于Ag / AgCl的迁移电流对再溶解的影响讨论了峰值电流和伏安图对扫描速率(10-1000 mV)的依赖性。有趣的是,沉积极限和溶出峰电流都不会以简单的方式随添加的辅助电解质浓度而变化,在10〜(- 5)M而不是零浓度的添加的KNO_3。采用非常灵敏的阳极溶出伏安法技术对低离子强度介质中的铅进行伏安测定的重要意义在于,使用通常用于最小化未知基质问题的标准添加方法如果迁移电流对过程的贡献很重要,则容易出错。

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