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Determination of Gold in Various Environment Samples by Flame Atomic Absorption Spectrometry Using Dispersive Liquid–Liquid Microextraction Sampling

机译:分散液-液微萃取火焰原子吸收光谱法测定各种环境样品中的金。

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摘要

A new dispersive liquid–liquid microextraction separation/preconcentration procedure as a rapid sample-preparation technique is proposed for detection of ultra trace amounts of Au(III) in various media by flame atomic absorption spectrometry using 1,5-diphenyl-1,3,5-pentanetrione as chelating agent. Carbon tetrachloride and methanol were used as extraction and dispersive solvents, respectively. Various parameters that affect the extraction efficiency such as pH, centrifugation rate and time, chelating agent concentration and sampling volume on the recovery of Au(III) were investigated. Under optimum conditions, the enhancement factor of 750, relative standard deviation of 2.7 % and calibration graphs obtained in the concentration range of 0.04–5.6 μg L−1 for gold were obtained. The limit of detection was 1.1 ng L−1. The accuracy of the method was performed by analysis of the certified reference material (CDN-PGMS-10). The developed method was applied successfully to the determination of gold in the catalytic converter, anode slime, ore and seawater samples. The results show that dispersive liquid–liquid microextraction procedure is sensitive, rapid, simple and safe for the separation/preconcentration of gold from complex sample media.
机译:提出了一种新的分散液-液微萃取分离/预浓缩方法,作为一种快速的样品制备技术,该方法通过使用1,5-二苯基-1,3的火焰原子吸收光谱法检测各种介质中的痕量Au(III), 5-戊三酮作为螯合剂。四氯化碳和甲醇分别用作萃取溶剂和分散溶剂。研究了影响萃取效率的各种参数,例如pH,离心率和时间,螯合剂浓度和取样量对金(III)回收率的影响。在最佳条件下,获得了750的增强因子,2.7%的相对标准偏差以及在0.04-5.6μgL-1的浓度范围内获得的金的校正图。检测限为1.1 ng L-1。该方法的准确性是通过分析认证的参考物质(CDN-PGMS-10)来进行的。该方法成功地用于催化转化器,阳极泥,矿石和海水样品中金的测定。结果表明,液-液分散微萃取程序灵敏,快速,简单且安全,可从复杂样品介质中分离/富集金。

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