Hosseini Mohammad Saeid, Hashemi-Moghaddam Hamid, Kardan-Moghaddam Gholamreza
Department of Chemistry, Faculty of Science, Birjand University, Birjand, P.O. Box 79, Iran.
Ann Chim. 2007 Jan-Feb;97(1-2):17-23. doi: 10.1002/adic.200690082.
A simple method for separation/preconcentration and determination of Ag(I) in aqueous samples is described. The method is based on formation of an ion-associate between Ag(I)-iodide complex and ferroin, which can be floated at the interface of the aqueous/n-heptane phases. The flotation process was carried out using 500-ml aliquot of the aqueous solution and the floated layer was dissolved in 5 ml of 1 M HNO3 containing methanol (50% v/v) as the solvent. The Ag(I) content was then determined by flame atomic absorption spectrometry (FAAS). The method so could be considered as an enrichment process, was achieved to a quantitative feature, when the pH of the solution was adjusted to 4 and the concentrations of iodide and ferroin were about 3.2 x 10(-4) M and 6.25 x 10(-5) M, respectively. The LOD and RSD (n = 7) were obtained 1.0 x 10(-8) M and 2.4%, respectively. It was found that a large number of cations and anions even at high considerably foreign ion/Ag(I) ratios were not interfered. The method was applied satisfactorily to recovery of Ag(I) from different aqueous samples.
本文描述了一种用于分离/预富集和测定水样中Ag(I)的简单方法。该方法基于Ag(I)-碘化物络合物与邻二氮菲亚铁形成离子缔合物,该离子缔合物可在水/正庚烷相界面上浮。浮选过程使用500 ml水样进行,浮层溶解于5 ml含甲醇(50% v/v)的1 M HNO3中作为溶剂。然后用火焰原子吸收光谱法(FAAS)测定Ag(I)含量。该方法可视为一种富集过程,当溶液pH调至4且碘化物和邻二氮菲亚铁浓度分别约为3.2×10(-4) M和6.25×10(-5) M时,具有定量特性。检测限和相对标准偏差(n = 7)分别为1.0×10(-8) M和2.4%。结果发现,即使在大量阳离子和阴离子存在且外来离子/Ag(I)比例相当高的情况下也不产生干扰。该方法成功应用于从不同水样中回收Ag(I)。