Ruas de Souza Ana P, Foster Christopher W, Kolliopoulos Athanasios V, Bertotti Mauro, Banks Craig E
Faculty of Science and Engineering, School of Chemistry and the Environment, Division of Chemistry and Environmental Science, Manchester Metropolitan University, Chester Street, Manchester M15 GD, UK.
Analyst. 2015 Jun 21;140(12):4130-6. doi: 10.1039/c5an00381d. Epub 2015 Apr 23.
Screen-printed back-to-back microband electroanalytical sensors are applied to the quantification of lead(II) ions for the first time. In this configuration the electrodes are positioned back-to-back with a common electrical connection to the two working electrodes with the counter and reference electrodes for each connected in the same manner as a normal "traditional" screen-printed sensor. Proof-of-concept is demonstrated for the electroanalytical sensing of lead(II) ions utilising square-wave anodic stripping voltammetry where an increase in the electroanalytical sensitivity is observed by a factor of 5 with the back-to-back microband configuration at a fixed lead(II) ion concentration of 5 μg L(-1) utilising a deposition potential and time of -1.2 V and 30 seconds respectively, compared to a conventional (single) microband electrode. The back-to-back microband configuration allows for the sensing of lead(II) ions with a linear range from 5 to 110 μg L(-1) with a limit of detection (based on 3σ) corresponding to 3.7 μg L(-1). The back-to-back microband configuration is demonstrated to quantify the levels of lead(II) ions within drinking water corresponding to a level of 2.8 (±0.3) μg L(-1). Independent validation was performed using ICP-OES with the levels of lead(II) ions found to correspond to 2.5 (±0.1) μg L(-1); the excellent agreement between the two methods validates the electroanalytical procedure for the quantification of lead(II) ions in drinking water. This back-to-back configuration exhibits an excellent validated analytical performance for the determination of lead(II) ions within drinking water at World Health Organisation levels (limited to 10 μg L(-1) within drinking water).
首次将丝网印刷背靠背微带电分析传感器应用于铅(II)离子的定量分析。在这种配置中,电极背靠背放置,两个工作电极共用一个电连接,每个电极的对电极和参比电极的连接方式与普通的“传统”丝网印刷传感器相同。利用方波阳极溶出伏安法对铅(II)离子进行电分析传感的概念验证得以实现,在固定铅(II)离子浓度为5 μg L⁻¹的情况下,与传统(单个)微带电极相比,背靠背微带配置的电分析灵敏度提高了5倍,沉积电位和时间分别为 -1.2 V和30秒。背靠背微带配置能够检测浓度范围为5至110 μg L⁻¹的铅(II)离子,检测限(基于3σ)为3.7 μg L⁻¹。背靠背微带配置被证明可对饮用水中浓度为2.8(±0.3)μg L⁻¹的铅(II)离子进行定量。使用电感耦合等离子体发射光谱法(ICP - OES)进行了独立验证,发现铅(II)离子的浓度为2.5(±0.1)μg L⁻¹;两种方法之间的良好一致性验证了饮用水中铅(II)离子定量分析的电分析程序。这种背靠背配置在测定世界卫生组织规定水平(饮用水中限量为10 μg L⁻¹)的饮用水中的铅(II)离子时,展现出经过验证的出色分析性能。