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Cathodic Stripping Voltammetry of Selenium(Ⅳ) at a Silver Disk Electrode

机译:银圆盘电极上硒(Ⅳ)的阴极溶出伏安法

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摘要

A new, simple, and reproducible method is described for the determination of selenium(Ⅳ) based on differential pulse cathodic stripping voltammetry. The optimized experimental conditions are as follows: selenium(Ⅳ) ions In an acidic medium (0.06 M HCl-0.07 M HNO_3) are electrodeposited on a rotating silver disk electrode as silver selenide at -0.4 V vs SCE for 30 min; the deposit is then cathodically stripped in another solution (2 M NaOH) at a scan rate of 50mV s~(-1) to -1.2Vvs SCE. The cathodic stripping results in only a single well-defined peak at about -0.95 V vs SCE. The calibration (peak height vs selenium concentration) graph is linear up to at least 40 ng mL~(-1) of selenium(Ⅳ) and passes through the origin, with a relative standard deviation of 2.7% for 20 ng mL~(-1) (n = 5). The detection limit (3σ) is 0.20 ng mL~(-1). The possible interferences have been evaluated. Dissolved oxygen does not affect the peak height of selenium. The electrode can be used repeatedly at least 20 times with excellent reproducibility without further polishing. The proposed method is an improvement over the existing cathodic stripping techniques.
机译:介绍了一种基于差分脉冲阴极溶出伏安法测定硒(Ⅳ)的新方法,该方法简便,可重复。优化的实验条件如下:硒(Ⅳ)离子在酸性介质(0.06 M HCl-0.07 M HNO_3)中作为硒化银在-0.4 V vs SCE下电沉积在旋转的银盘电极上30分钟;然后将沉积物在另一溶液(2 M NaOH)中以50mV s〜(-1)至-1.2Vvs SCE的扫描速率进行阴极剥离。相对于SCE,阴极剥离仅在-0.95 V处产生一个明确定义的峰。硒(Ⅳ)至少达到40 ng mL〜(-1)时,校准曲线(峰高与硒浓度)呈线性关系,并且通过原点,相对于20 ng mL〜(-的相对标准偏差为2.7%) 1)(n = 5)。检出限(3σ)为0.20 ng mL〜(-1)。已经评估了可能的干扰。溶解氧不影响硒的峰高。该电极可重复使用至少20次,重复性极佳,无需进一步抛光。所提出的方法是对现有阴极剥离技术的改进。

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