Ionic liquids versus ionic liquid-based surfactants in dispersive liquid-liquid microextraction for determining copper in water by flame atomic absorption spectrometry

被引:27
|
作者
Ayala-Cabrera, Juan F. [1 ]
Trujillo-Rodriguez, Maria J. [1 ]
Pino, Veronica [1 ]
Hernandez-Torres, Oscar M. [1 ]
Afonso, Ana M. [1 ]
Sirieix-Plenet, Juliette [2 ]
机构
[1] Univ La Laguna, Dept Quim, Unidad Dept Quim Analit, E-38207 San Cristobal la Laguna, Tenerife, Spain
[2] Univ Paris 06, Sorbonne Univ, CNRS, Lab PHENIX, Paris, France
关键词
Dispersive liquid-liquid microextraction; metals; ionic liquids; ionic liquid-based surfactants; in situ microextraction; environmental analysis; CLOUD POINT EXTRACTION; OPTICAL-EMISSION-SPECTROMETRY; GREEN ANALYTICAL-CHEMISTRY; PHASE MICROEXTRACTION; SPECTROPHOTOMETRIC DETERMINATION; PRECONCENTRATION METHOD; SAMPLES; METALS; NICKEL; COBALT;
D O I
10.1080/03067319.2015.1128538
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work compares the performance of dispersive liquid-liquid method (DLLME) as a prior step for determining copper by flame atomic absorption spectrometry (FAAS), when using the ionic liquid (IL) 1-butyl-3-methylimidazolium hexafluorophosphate (C(4)MIm-PF6) or the IL-based surfactant 1-hexadecyl-3-butylimidazolium bromide (C(16)C(4)Im-Br) as extractant solvents. For the water-insoluble C(4)MIm-PF6, the most conventional DLLME mode using acetonitrile as dispersive solvent was employed. For the water-soluble C(16)C(4)Im-Br, the in situ DLLME mode with lithium bis[(trifluoromethane) sulfonyl] imide (Li-NTf2) as metathesis reagent was employed. In both approaches, some effective parameters such as volumes of extractant and dispersive solvents, concentration of complexing agent, pH of sample solution, salting-out effect and final diluting solvent to ensure compatibility with FAAS, were properly optimised. The optimum conditions for the IL-DLLME method using C(4)MIm-PF6 were: 100 mu L of neat C(4)MIm-PF6, 1 mL of acetonitrile, 10 mL of water, no control of pH for environmental waters, NaCl content of 23 g L-1, diethyl dithiocarbamate (DDTC) as complexing agent at 10 mg L-1 and final dilution of the micro-droplet with acetonitrile up to 70 mu L. The optimum conditions for the in situ IL-DLLME method using C(16)C(4)Im-Br were: 0.8 mL of acetonitrile, 10 mL of water containing C(16)C(4)Im-Br at 25.2 mmol L-1, final dilution step of the micro-droplet with 200 mu L of acetonitrile and remaining conditions as those of C(4)MIm-PF6. The analytical performance of both methods was similar, being slightly better for the IL-DLLME method using C(4)MIm-PF6, with limits of detection (LOD) of 3.3 mu g L-1 (versus 5.1 mu g L-1 when using C(16)C(4)Im-Br), precision values as intraday relative standard deviation (RSD in %) lower than 8.8% (being of 10% for the C(16)C(4)Im-Br method) and an enrichment factor of 54 (being 27 when using C(16)C(4)Im-Br). The DLLME-FAAS method with C(4)MIm-PF6 was used in the analysis of environmental waters with successful performance, with relative recoveries of 110% and 105%, and interday precision with RSD values of 21% and 7.4% for spiked levels of 60 and 160 mu g L-1, respectively. The results obtained when analysing an urban wastewater sample coming from an inter-laboratory exercise was comparable to those obtained for other 93 laboratories. The method was also valid for the determination of Cu2+ in presence of foreign ions commonly found in natural waters.
引用
收藏
页码:101 / 118
页数:18
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