Centre of Bioanalysis, National Institute of Research and Development for Biological Sciences, 296, Splaiul Independentei, Bucharest 060031, Romania.
Sensors (Basel). 2010;10(12):11340-51. doi: 10.3390/s101211340. Epub 2010 Dec 13.
A new modified glassy carbon electrode (GCE) based on a synthesized N-(2-aminoethyl)-4,4'-bipyridine (ABP) was developed for the determination of Ag(I) by differential pulse voltammetry (DPV). ABP was covalently immobilized on GC electrodes surface using 4-nitrobenzendiazonium (4-NBD) and glutaraldehyde (GA). The Ag(I) ions were preconcentrated by chemical interaction with bipyridine under a negative potential (-0.6 V); then the reduced ions were oxidized by differential pulse voltammetry and a peak was observed at 0.34 V. The calibration curve was linear in the concentration range from 0.05 μM to 1 μM Ag(I) with a detection limit of 0.025 μM and RSD=3.6%, for 0.4 μM Ag(I). The presence of several common ions in more than 125-fold excess had no effect on the determination of Ag(I). The developed sensor was applied to the determination of Ag(I) in water samples using a standard addition method.
一种新型的基于合成的 N-(2-氨乙基)-4,4'-联吡啶(ABP)的修饰玻碳电极(GCE)被开发出来,用于通过差分脉冲伏安法(DPV)测定 Ag(I)。ABP 通过 4-硝基苯重氮(4-NBD)和戊二醛(GA)共价固定在 GC 电极表面。Ag(I)离子通过与联吡啶的化学相互作用在负电位(-0.6 V)下预富集;然后通过差分脉冲伏安法氧化还原离子,并在 0.34 V 处观察到一个峰。在 0.05 μM 至 1 μM Ag(I)的浓度范围内,校准曲线呈线性关系,检测限为 0.025 μM,RSD=3.6%,对于 0.4 μM Ag(I)。超过 125 倍过量的几种常见离子的存在对 Ag(I)的测定没有影响。该传感器被用于使用标准加入法测定水样中的 Ag(I)。