Arbab-Zavar Mohammad Hossein, Chamsaz Mahmoud, Heidari Tahereh
Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran.
Anal Sci. 2010 Jan;26(1):107-10. doi: 10.2116/analsci.26.107.
A simple method was developed for speciation and spectrophotometric determination of inorganic As(III) and As(V) using an electrochemical hydride generation technique. For speciation of As(III) and As(V), a graphite rod was used as cathode to reduce As(III) to AsH(3), the rod was then replaced with a tin-lead alloy wire for reducing As(V) to AsH(3). The spectrophotometric determination was based on the reaction of AsH(3) with silver diethyldithiocarbamate to give an absorbing complex at 510 nm. Under the optimized conditions, the calibration curves were linear over the ranges of 0.1-5 microg ml(-1) for As(III) and 0.5-4.0 microg ml(-1) for As(V). The concentration detection limits of 0.02 and 0.06 microg ml(-1) were achieved for As(III) and As(V), respectively. The relative standard deviations for five replicate speciation and determination of 3.0 microg ml(-1) As(III) and As(V) were 0.8 and 7.2%, respectively. The accuracy and recovery of the method were evaluated by analyzing tap water spiked with As(III) and As(V).
开发了一种简单的方法,用于使用电化学氢化物发生技术对无机As(III)和As(V)进行形态分析和分光光度测定。对于As(III)和As(V)的形态分析,使用石墨棒作为阴极将As(III)还原为AsH(3),然后用锡铅合金丝代替该棒将As(V)还原为AsH(3)。分光光度测定基于AsH(3)与二乙基二硫代氨基甲酸银的反应,在510nm处产生吸收络合物。在优化条件下,As(III)的校准曲线在0.1 - 5μg ml(-1)范围内呈线性,As(V)的校准曲线在0.5 - 4.0μg ml(-1)范围内呈线性。As(III)和As(V)的浓度检测限分别为0.02和0.06μg ml(-1)。对3.0μg ml(-1) As(III)和As(V)进行五次重复形态分析和测定的相对标准偏差分别为0.8%和7.2%。通过分析添加了As(III)和As(V)的自来水来评估该方法 的准确性和回收率。