Chemistry Department, Shahid Bahonar University of Kerman, Kerman, Iran.
Talanta. 2012 Jan 15;88:759-64. doi: 10.1016/j.talanta.2011.11.078. Epub 2011 Dec 4.
In the present study, a new, simple and efficient method for the preconcentration of ultra trace amounts of Te (IV) is developed using ultrasound-assisted emulsification solidified floating organic drops microextraction (USAE-SFODME) before graphite furnace atomic absorption spectrometry determination. In this method, tellurium is extracted into the fine droplets of 1-undecanol after chelate formation with the water soluble ligand, ammonium pyrrolidinedithiocarbamate (APDC). Several factors such as pH, chelating agent amount, type and volume of the extracting solvent, sonication and centrifuging time that influence the extraction and complex formation are optimized. Under the optimum conditions, the calibration graph is linear in the range of 0.01-0.24ngmL(-1) of tellurium in the original solution, with limit of detection of 0.003ngmL(-1). The relative standard deviation (RSD) for seven replicated determinations of tellurium ion at 0.08ngmL(-1) concentration level is calculated as 3.4%. The proposed method was successfully applied to the determination of Te (IV) in a standard soil and several water samples.
在本研究中,开发了一种新的、简单且高效的方法,用于在石墨炉原子吸收光谱法测定前,通过超声辅助乳化固-液萃取(USAE-SFODME)预浓缩痕量 Te(IV)。在该方法中,Te(IV)与水溶性配体氨丙基二硫代氨基甲酸铵(APDC)形成螯合物后,被萃取到 1-十一醇的细小液滴中。优化了影响萃取和络合形成的几个因素,如 pH 值、螯合剂用量、萃取溶剂的类型和体积、超声和离心时间等。在最佳条件下,原溶液中 Te 的浓度在 0.01-0.24ngmL(-1) 范围内呈线性,检出限为 0.003ngmL(-1)。在 0.08ngmL(-1)浓度水平下,Te 离子的 7 次重复测定的相对标准偏差(RSD)计算为 3.4%。该方法成功应用于标准土壤和几种水样中 Te(IV)的测定。