Department of Chemistry, Faculty of Sciences, Payame Noor University, PO Box 19395-3697, Tehran, Iran.
Young Researchers Club and Elites, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
J Adv Res. 2014 Nov;5(6):685-93. doi: 10.1016/j.jare.2013.11.003. Epub 2013 Nov 20.
A new procedure is presented for the determination of low concentrations of lead and cadmium in water samples. Ligand assisted pseudo-stir bar hollow fiber solid/liquid phase microextraction using sol-gel sorbent reinforced with carbon nanotubes was combined with differential pulse anodic stripping voltammetry for simultaneous determination of cadmium and lead in tap water, and Darongar river water samples. In the present work, differential pulse anodic stripping voltammetry (DPASV) using a hanging mercury drop electrode (HMDE) was used in order to determine the ultra trace level of lead and cadmium ions in real samples. This method is based on accumulation of lead and cadmium ions on the electrode using different ligands; Quinolin-8-ol, 5,7-diiodo quinoline-8-ol, 4,5-diphenyl-1H-imidazole-2(3H)-one and 2-{[2-(2-Hydroxy-ethylamino)-ethylamino]-methyl}-phenol as the complexing agent. The optimized conditions were obtained. The relationship between the peak current versus concentration was linear over the range of 0.05-500 ng mL(-1) for Cd (II) and Pb (II). The limits of detection for lead and cadmium were 0.015 ng mL(-1) and 0.012 ng mL(-1), respectively. Under the optimized conditions, the pre-concentration factors are 2440 and 3710 for Cd (II) and Pb (II) in 5 mL of water sample, respectively.
一种新的程序被提出,用于测定水样中的低浓度铅和镉。采用溶胶-凝胶固载碳纳米管修饰的配体辅助伪搅拌棒中空纤维固/液微萃取与差分脉冲阳极溶出伏安法联用,用于同时测定自来水中的镉和铅,以及达隆格河水样中的镉和铅。在本工作中,采用悬汞电极(HMDE)的差分脉冲阳极溶出伏安法(DPASV)用于测定实际样品中超痕量水平的铅和镉离子。该方法基于使用不同的配体在电极上累积铅和镉离子;8-羟基喹啉、5,7-二碘-8-羟基喹啉、4,5-二苯基-1H-咪唑-2(3H)-酮和 2-[[2-(2-羟乙基氨基)乙基氨基]甲基]苯酚作为络合剂。优化了条件。在 0.05-500ngmL(-1)范围内,Cd(II)和 Pb(II)的峰电流与浓度之间呈线性关系。铅和镉的检出限分别为 0.015ngmL(-1)和 0.012ngmL(-1)。在优化条件下,Cd(II)和 Pb(II)在 5mL 水样中的预浓缩因子分别为 2440 和 3710。