Gupta Ruma, Gamare Jayashree S, Pandey Ashok K, Tyagi Deepak, Kamat Jayshree V
Fuel Chemistry Division, ‡Radiochemistry Division, and §Chemistry Division, Bhabha Atomic Research Centre , Trombay, Mumbai-400085, India.
Anal Chem. 2016 Feb 16;88(4):2459-65. doi: 10.1021/acs.analchem.5b04625. Epub 2016 Jan 29.
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 Cu(2+) 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).
从X射线光电子能谱观察到,在-0.75V的电沉积电位下,金属钌纳米颗粒(Ru NPs)在玻碳电极(GC)上形成。如此形成的Ru NPs具有亚砷酸盐选择性表面和导电核心,非常适合设计用于在水性基质中检测超痕量浓度亚砷酸盐的高灵敏度和可重现响应生成基质。与此相反,砷酸根离子通过化学相互作用吸附在-0.25V下形成的氧化钌(RuO2和RuO3)NPs上,而不是Ru NPs上。为了探索在超痕量浓度范围内定量亚砷酸盐的可能性,通过在优化的-0.75V下进行1000s的恒电位脉冲电沉积方法,将Ru NPs沉积在GC上。通过将RuNPs/GC浸入亚砷酸盐溶液中,亚砷酸盐由于与Ru NPs发生化学相互作用而预富集到Ru表面。负载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。使用差分脉冲伏安技术,亚砷酸盐被氧化为砷酸盐,从而实现其定量测定,而不会受到水系统中通常存在的Cu(2+)离子的干扰。因此,使用RuNPs/GC消除了溶出伏安法中预富集步骤的需要,该步骤需要优化诸如预富集电位、时间、搅拌、干扰等参数。基于RuNPs/GC的差分脉冲伏安(DPV)技术可以在几分钟内测定亚砷酸盐的浓度,检测限为0.1 ppb,重现性为5.4%。在本工作中获得的用于As(III)定量的2.38 nA ppb(-1)的灵敏度明显优于文献报道的灵敏度,具有相似的检测限和温和的条件(pH = 2)。基于RuNPs/GC的DPV已使用添加了已知量As(III)的湖水、地下水和海水样品评估了其分析性能。