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Highly Sensitive Detection of Arsenite Based on Its Affinity toward Ruthenium Nanoparticles Decorated on Glassy Carbon Electrode

机译:基于砷修饰玻碳电极上的钌纳米粒子的高灵敏度检测

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Metallic ruthenium nanoparticles (Ru NPs) are formed on the glassy carbon electrode (GC) at electrodeposition potential of-0.75 V, as observed from X-ray photoelectron spectroscopy. Thus formed Ru NPs have the arsenite selective surface and conducting core that is ideally suited for designing a highly sensitive and reproducible response generating matrix for the arsenite detection at an ultratrace concentration in aqueous matrices. Contrary to this, arsenate ions sorb via chemical interactions on the ruthenium oxide (RuO2 and RuO3) NPs formed at-0.25 V, but not on the Ru NPs. For exploring a possibility of the quantification of arsenite in the ultratrace concentration range, the Ru NPs have been deposited on the GC by a potentiostatic pulse method of electrodeposition at optimized-0.75 V for 1000 s. Arsenite preconcentrates onto the Ru surface just by dipping the RuNPs/GC into the arsenite solution as it interacts chemically with Ru NPs. Electrochemical impedance spectroscopy of As(III) loaded RuNPs/GC shows a linear increase in the charge transfer resistance with an increase in As(III) conc. Using a differential pulse voltammetric technique, arsenite is oxidized to arsenate leading to its quantitative determination without any interference of Cu2+ ions that are normally encountered in the water systems. Thus, the use of RuNPs/GC eliminates the need for a preconcentration step in stripping voltammetry, which requires optimization of the parameters like preconcentration potential, time, stirring, inferences, and so on. The RuNPs/GC based differential pulse voltammetric (DPV) technique can determine the concentration of arsenite in a few min with a detection limit of 0.1 ppb and 5.4% reproducibility. The sensitivity of 2.38 nA ppb(-1) obtained in the present work for As(III) quantification is considerably better than that reported in the literature, with a similar detection limit and mild conditions (pH = 2). The RuNPs/GC based DPV has been evaluated for its analytical performance using the lake water, ground water, and seawater samples spiked with known amounts of As(III).
机译:从X射线光电子能谱观察到,金属钌纳米颗粒(Ru NPs)形成在玻碳电极(GC)上的电沉积电位为-0.75V。如此形成的Ru NP具有亚砷酸盐选择性表面和导电核,非常适合设计用于在水溶液基质中超痕量浓度下检测亚砷酸盐的高灵敏度和可重现的反应生成基质。与此相反,砷酸根离子通过化学相互作用吸附在-0.25 V形成的氧化钌(RuO2和RuO3)NP上,而不吸附在Ru NP上。为了探索在超痕量浓度范围内量化亚砷酸盐的可能性,通过电沉积的恒电位脉冲方法在优化的0.75 V电压下1000 s沉积了Ru NPs。只需将RuNPs / GC浸入砷溶液中,砷与Ru NPs发生化学相互作用即可将其预浓缩到Ru表面。负载有As(III)的RuNPs / GC的电化学阻抗谱显示,随着As(III)浓度的增加,电荷转移电阻呈线性增加。使用差分脉冲伏安法,亚砷酸盐被氧化成砷酸盐,从而定量测定了水系统中通常不会遇到的Cu2 +离子的任何干扰。因此,RuNPs / GC的使用消除了溶出伏安法中的预浓缩步骤,该步骤需要优化诸如预浓缩电位,时间,搅拌,推论等参数。基于RuNPs / GC的差分脉冲伏安法(DPV)技术可以在几分钟内确定亚砷酸盐的浓度,检出限为0.1 ppb,重复性为5.4%。本研究中获得的2.38 nA ppb(-1)对As(III)定量的灵敏度明显优于文献报道,具有相似的检测限和温和条件(pH = 2)。基于RuNPs / GC的DPV已使用加有已知量的As(III)的湖水,地下水和海水样品进行了分析性能评估。

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