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Ion Pair-Dispersive Liquid-Liquid Microextraction Coupled to Microsample Injection System-Flame Atomic Absorption Spectrometry For Determination of Gold at Trace Level in Real Samples

机译:离子对分散液 - 液体微萃取耦合到微粒喷射系统 - 火焰原子吸收光谱法,用于测定真实样品中痕量水平的金

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摘要

A novel ion pair-dispersive liquid-liquid microextraction (IP-DLLME) of gold followed by its determination with microsample injection system-flame atomic absorption spectrometry (MIS-FAAS) detection was developed. The extraction method was based on the reaction of anionic tetrachloro gold(III) complex with the cationic form of Rhodamine B to give a violet ion pair complex, which is extracted from 1.0 mol L-1 HCl solution of 8.0 mL to fine droplets of chloroform of 500 µL. A Plackett-Burman experimental design of MINITAB statistical program was employed to optimize the influence of main parameters to be controlled in DLLME.  After optimizing the extraction conditions, gold was quantitatively recovered by preconcentration factor of 40, limit of detection (LOD) of 1.8 μg L-1 and relative standard deviation of less than 6.8%. The proposed method was successfully applied to the preconcentration and determination of gold in some samples such as tap water, waste water, copper electrolysis solution and copper wire coated nickel.
机译:发育了一种新型离子对分散液 - 液 - 液体微萃取(IP-DLLME),随后进行了微小喷射系统 - 火焰原子吸收光谱法(MIS-FAAS)检测的测定。提取方法基于阴离子四氯金(III)复合物与罗丹明B的阳离子形式的反应,得到紫色离子对复合物,其从1.0mol L-1 HCl溶液中提取为8.0ml至细滴的细滴500μl。 Minitab统计计划的Plackett-Burman实验设计是为了优化在DLLME中控制主要参数的影响。优化提取条件后,通过预浓度为40的前浓度,检测极限(LOD)为1.8μg1-1的极限度,相对标准偏差小于6.8%。所提出的方法成功地应用于预浓缩和测定的金色,如自来水,废水,铜电解溶液和铜线涂覆的镍。

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