Selective determination of inorganic cobalt in nutritional supplements by ultrasound-assisted temperature-controlled ionic liquid dispersive liquid phase microextraction and electrothermal atomic absorption spectrometry

2012 ◽  
Vol 713 ◽  
pp. 56-62 ◽  
Author(s):  
Paula Berton ◽  
Estefanía M. Martinis ◽  
Luis D. Martinez ◽  
Rodolfo G. Wuilloud
2017 ◽  
Vol 41 (15) ◽  
pp. 7038-7044 ◽  
Author(s):  
Leila Alavi ◽  
Shahram Seidi ◽  
Ali Jabbari ◽  
Tahmineh Baheri

In the present work, for the first time, a new carrier-mediated hollow fiber liquid phase microextraction (CM-HFLPME) technique was applied for the determination of lead in whole blood samples by means of ETAAS.


2012 ◽  
Vol 95 (5) ◽  
pp. 1534-1540 ◽  
Author(s):  
Qingxiang Zhou ◽  
Yuantuan Gao ◽  
Junping Xiao ◽  
Guohong Xie

Abstract This paper reports a new method for the determination of aromatic amines with temperature-controlled ionic liquid dispersive liquid-phase microextraction in combination with HPLC and results of investigation of the influence of anions in ionic liquids on the extraction performance. In these experiments, 1-octyl-3-methylimidazolium hexafluorophosphate ([C8MIM][PF6]), 1-octyl-3-methylimidazolium bis (trifluoromethanesulfonyl) imide ([C8MIM][NTf2]), and 1-octyl-3-methylimidazolium tetrafluoroborate ([C8MIM][BF4]) were used as the extraction solvents for the investigation of the effect of anions in ionic liquids. Other parameters affecting the microextraction performance were also investigated. Under the optimal conditions, the proposed method had good linearity over the concentration ranges of 1.0–100 μg/L for 2, 4-dimethylaniline, 2-chloroanline, and N,N-dimethylaniline, and 1.5–150 μg/L for N,N-dimethylaniline and alpha-naphthylamine, with excellent correlation coefficients (R2 ≥ 0.999), excellent detection sensitivity with LODs (S/N = 3) in the range of 0.39–0.63 μg/L, and precision in the range of 3.2–5.4% RSD (n = 6). Real water samples were analyzed with the established method, and good spike recoveries in the range of 86.3 to 98.9% were obtained. These results indicated that this method would be useful in the routine analysis of such pollutants.


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