Magnetomotive room temperature dicationic ionic liquid: A new concept toward centrifuge-less dispersive liquid-liquid microextraction

被引:36
作者
Beiraghi, Asadollah [1 ]
Shokri, Masood [1 ]
Seidi, Shahram [2 ]
Godajdar, Bijan Mombani [3 ]
机构
[1] Kharazmi Univ, Fac Chem, Tehran, Iran
[2] KN Toosi Univ Technol, Fac Chem, Dept Analyt Chem, Tehran, Iran
[3] Islamic Azad Univ, Omidiyeh Branch, Dept Chem, Omidiyeh, Iran
关键词
Dicationic ionic liquid; Magnetomotive; Dispersive liquid-liquid microextraction; Gold; Silver; Ore sample; SOLID-PHASE EXTRACTION; POLYCYCLIC AROMATIC-HYDROCARBONS; ATOMIC-ABSORPTION-SPECTROMETRY; ENVIRONMENTAL-SAMPLES PRIOR; SPECTROPHOTOMETRIC DETERMINATION; WATER SAMPLES; TRACE SILVER; GOLD; PRECONCENTRATION; SOLVENT;
D O I
10.1016/j.chroma.2014.12.004
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A new centrifuge-less dispersive liquid-liquid microextraction technique based on application of magnetomotive room temperature dicationic ionic liquid followed by electrothermal atomic absorption spectrometry (ETAAS) was developed for preconcentration and determination of trace amount of gold and silver in water and ore samples, for the first time. Magnetic ionic liquids not only have the excellent properties of ionic liquids but also exhibit strong response to an external magnetic field. These properties provide more advantages and potential application prospects for magnetic ionic liquids than conventional ones in the fields of extraction processes. In this work, thio-Michler's ketone (TMK) was used as chelating agent to form Ag/Au-TMK complexes. Several important factors affecting extraction efficiency including extraction time, rate of vortex agitator, pH of sample solution, concentration of the chelating agent, volume of ionic liquid as well as effects of interfering species were investigated and optimized. Under the optimal conditions, the limits of detection CLOD) were 3.2 and 7.3 ng L-1 with the preconcentration factors of 245 and 240 for Au and Ag, respectively. The precision values (RSD%, n=7) were 5.3% and 5.8% at the concentration level of 0.05 mu g L-1 for Au and Ag, respectively. The relative recoveries for the spiked samples were in the acceptable range of 96-104.5%. The results demonstrated that except Hg2+, no remarkable interferences are created by other various ions in the determination of Au and Ag, so that the tolerance limits (W-Ion/W-Au or Ag) of major cations and anions were in the range of 250-1000. The validated method was successfully applied for the analysis of Au and Ag in some water and ore samples. (C) 2014 Elsevier B.V. All rights
引用
收藏
页码:1 / 8
页数:8
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