Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran.
Talanta. 2012 Sep 15;99:335-41. doi: 10.1016/j.talanta.2012.05.061. Epub 2012 Jun 4.
A new method has been proposed based on hollow fiber-based liquid three-phase micro extraction and in-situ differential pulse anodic stripping voltammetry (DPASV) for the micro extraction and quantification of mercury(II) ions. Different factors affecting the liquid-three phases micro extraction, including organic solvent, pH of the donor and acceptor phases, concentration of the complexing agent, extraction time, and stirring rate were investigated and the optimal extraction conditions were established. Three microelectrodes designed and constructed for this study were inserted into the two ends of a hollow fiber inside the acceptor solution, and then voltammetric analysis was performed in-situ during the extraction time. After 1600 s, final stable signal was used for the analytical applications. Under the optimized conditions, an enrichment factor of 277 was achieved and the relative standard deviation (R.S.D.) of the method was 6.2% (n=5). The calibration curve was obtained in the range of 0.2-30.0 nmol L(-1) Hg(II) with a reasonable linearity (R(2)>0.9880) and a limit of detection of 0.06 nmol L(-1). Finally, the applicability of the proposed method was evaluated by extraction and determination of mercury in real samples such as fish and rice.
一种基于中空纤维液相三相微萃取和原位示差脉冲阳极溶出伏安法(DPASV)的新方法已被提出,用于汞(II)离子的微萃取和定量分析。考察了影响液-三相微萃取的不同因素,包括有机溶剂、供体和受体相的 pH 值、络合剂浓度、萃取时间和搅拌速度,并确定了最佳萃取条件。本研究设计和构建了三个微电极,插入到受体溶液中的中空纤维的两端,然后在萃取过程中进行原位伏安分析。经过 1600 秒后,使用最终稳定的信号进行分析应用。在优化条件下,实现了 277 的富集因子,方法的相对标准偏差(RSD)为 6.2%(n=5)。在 0.2-30.0 nmol L(-1) Hg(II)范围内获得了合理线性(R(2)>0.9880)的校准曲线,检测限为 0.06 nmol L(-1)。最后,通过对鱼和米饭等实际样品进行萃取和测定,评估了所提出方法的适用性。