浊点萃取富集和测定水样中银的方法

IF 1.1 Q4 CHEMISTRY, ANALYTICAL
E. Azooz, Ghusoon Shabaa, E. Al-Mulla
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引用次数: 6

摘要

为了选择性提取银,开发了浊点提取(CPE)程序。通过银离子与2,4-二甲基戊烷-3-酮(2,4-DMP)的反应合成溶剂化物种后,在35°C下加入盐析剂(0.4 mol L-1 NaNO3),10分钟后,使用Triton X-114从水溶液中分离银离子。盐析剂的种类和数量、银离子、温度、加热时间和表面活性剂的体积都是决定CPE的重要因素。在最佳条件下,0.1-100μ。检测限(LOD)、定量限(LOQ)和富集因子(E)分别为0.05µg L-1、0.15µg L-1和200。相对于1、40和80μg L-1 Ag,相对标准偏差(RSD)估计为0.2-3.9%(n=5)。使用火焰原子吸收光谱法和双硫腙分光光度法评估CPE的准确性。然后将所提出的方法应用于河水、雨水和沙子样本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methodology for Preconcentration and Determination of Silver in Aqueous Samples using Cloud Point Extraction
For the selective extraction of silver, a cloud point extraction (CPE) procedure was developed. After synthesizing the solvation species through the reaction of silver ions with 2, 4-dimethyl pentane-3-one (2,4 DMP), the salting-out agent (0.4 mol L-1 NaNO3) was added at 35 °C and, after 10 min, Triton X-114 was used to separate silver ions from aqueous solution. The type and quantity of salting-out agent, silver ion, temperature, heating time, and surfactant volume were all examined as important factors determining the CPE. The analytical curve in the 0.1-100 μg L-1 Ag range was straight at optimal conditions. The detection limit (LOD), quantification limit (LOQ), and enrichment factor (E) were 0.05 µg L-1, 0.15 µg L-1, and 200, respectively. The relative standard deviation (RSD) was estimated as 0.2-3.9% (n = 5) in relation to 1, 40, and 80 μg L-1 Ag. Flame atomic absorption spectrometry and spectrophotometry exploiting dithizone were used to assess the CPE accuracy. The proposed approach was then applied to river water, rain water and sand samples.
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来源期刊
CiteScore
1.60
自引率
14.30%
发文量
46
期刊介绍: BrJAC is dedicated to the diffusion of significant and original knowledge in all branches of Analytical Chemistry, and is addressed to professionals involved in science, technology and innovation projects at universities, research centers and in industry.
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