Temperature-controlled ionic liquid-based dispersive liquid-phase microextraction, preconcentration and quantification of nano-amounts of silver ion by using disulfiram as complexing agent

被引:22
作者
Absalan, Ghodratollah [1 ]
Akhond, Morteza [1 ]
Sheikhian, Leila [1 ]
Goltz, Douglas M. [2 ]
机构
[1] Shiraz Univ, Prof Massoumi Lab, Dept Chem, Coll Sci, Shiraz 71454, Iran
[2] Univ Winnipeg, Dept Chem, Winnipeg, MB R3B 2E9, Canada
关键词
ATOMIC-ABSORPTION-SPECTROMETRY; CLOUD POINT EXTRACTION; SOLVENT-EXTRACTION; WATER SAMPLES; SILICA-GEL; MEMBRANE; TRANSPORT; DERIVATIVES; ACID;
D O I
10.1039/c1ay05226h
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Microextraction and preconcentration of Ag+ by using temperature-controlled ionic liquid-based dispersive liquid-phase microextraction (TCIL-DLPME) method is reported. It was found that tetraethylthiuram disulfide (disulfiram) dissolved in 1-hexyl-3-methylimidazolium hexaflorophosphate, [C(6)mim][PF6] was useful as extracting media. Graphite furnace atomic absorption spectroscopy was used to quantify Ag+. To improve extraction efficiency, different experimental factors, such as volume of ionic liquid phase, pH and volume of aqueous solution, cooling and centrifugation periods, and dissolving temperature were investigated. The calibration curve was linear in the concentration range of 6.0-100.0 ng l(-1) of Ag+. Relative standard deviation (n = 7), detection limit, and preconcentration factor for determination of Ag+ were found to be 4.5%, 5.2 ng l(-1), and 120, respectively. The method was successfully applied for determination of Ag+ in drinking water and hair samples. Percent recoveries for solutions containing Ag+ indicated that chemical interferences by selected anions (NO3-, Cl-, I-, Br- and citrate) or cations (Ni2+, Cu2+, Mg2+, Zn2+, Pb2+, Ca2+, Co2+, Hg2+, Na+ and Mn2+) in solution were minimal or non-existent.
引用
收藏
页码:2354 / 2359
页数:6
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