Manzoori Jamshid L, Amjadi Mohammad, Abulhassani Jafar
Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.
Talanta. 2009 Feb 15;77(4):1539-44. doi: 10.1016/j.talanta.2008.09.045. Epub 2008 Oct 5.
Room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate [C(4)MIM][PF(6)], was used as an alternative to volatile organic solvents in single drop microextraction-electrothermal atomic absorption spectrometry (SDME-ETAAS). Manganese was extracted from aqueous solution into a drop of the ionic liquid after complextaion with 1-(2-thiazolylazo)-2-naphthol (TAN) and the drop was directly injected into the graphite furnace. Several variables affecting microextraction efficiency and ETAAS signal, such as pyrolysis and atomization temperature, pH, TAN concentration, extraction time, drop volume and stirring rate were investigated and optimized. In the optimum experimental conditions, the limit of detection (3s) and the enhancement factor were 0.024 microg L(-1) and 30.3, respectively. The relative standard deviation (RSD) for five replicate determinations of 0.5 microg L(-1) Mn(II) was 5.5%. The developed method was validated by the analysis of a certified reference material (NIST SRM 1643e) and applied successfully to the determination of manganese in several natural water samples.
室温离子液体1-丁基-3-甲基咪唑六氟磷酸盐[C(4)MIM][PF(6)]被用作单滴微萃取-电热原子吸收光谱法(SDME-ETAAS)中挥发性有机溶剂的替代品。在与1-(2-噻唑基偶氮)-2-萘酚(TAN)络合后,将锰从水溶液中萃取到一滴离子液体中,然后将液滴直接注入石墨炉。研究并优化了影响微萃取效率和ETAAS信号的几个变量,如热解温度、原子化温度、pH值、TAN浓度、萃取时间、液滴体积和搅拌速率。在最佳实验条件下,检测限(3s)和增强因子分别为0.024 μg L(-1)和30.3。对0.5 μg L(-1) Mn(II)进行五次重复测定的相对标准偏差(RSD)为5.5%。通过分析有证标准物质(NIST SRM 1643e)对所建立的方法进行了验证,并成功应用于几种天然水样中锰的测定。