Determination of cobalt in water samples by atomic absorption spectrometry after pre-concentration with a simple ionic liquid-based dispersive liquid-liquid micro-extraction methodology

被引:33
作者
Abdolmohammad-Zadeh, Hossein [1 ]
Ebrahimzadeh, Elnaz [1 ]
机构
[1] Azarbaijan Univ Tarbiat Moallem, Fac Sci, Dept Chem, Tabriz, Iran
来源
CENTRAL EUROPEAN JOURNAL OF CHEMISTRY | 2010年 / 8卷 / 03期
关键词
Cobalt; Ionic liquid; Dispersive liquid-liquid micro-extraction; Pre-concentration; Water samples; CLOUD POINT EXTRACTION; SOLID-PHASE EXTRACTION; EMISSION-SPECTROMETRY; TRACE AMOUNTS; SPECTROPHOTOMETRIC DETERMINATION; ONLINE PRECONCENTRATION; MICROEXTRACTION; NICKEL; HEXAFLUOROPHOSPHATE; SEPARATION;
D O I
10.2478/s11532-010-0030-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A rapid dispersive liquid-liquid micro-extraction (DLLME) methodology based on the application of 1-hexylpyridinium hexafluorophosphate [C(6)py][PF6] ionic liquid (IL) as an extractant solvent was applied for the pre-concentration of trace levels of cobalt prior to determination by flame atomic absorption spectrometry (FAAS). 1-Phenyl-3-methyl-4-benzoyl-5-pyrazolone (PMBP) was employed as a chelator forming a Co-PMBP complex to extract cobalt ions from aqueous solution into the fine droplets of [C6py][PF6]. Some effective factors that influence the micro-extraction efficiency include the pH, the PMBP concentration, the amount of ionic liquid, the ionic strength, the temperature and the centrifugation time which were investigated and optimized. In the optimum experimental conditions, the limit of detection (3s) and the enrichment factor were 0.70 mu g L-1 and 60, respectively. The relative standard deviation (RSD) for six replicate determinations of 50 mu g L-1 Co was 2.36%. The calibration graph using the pre-concentration system was linear at levels 2-166 mu g L-1 with a correlation coefficient of 0.9982. The applicability of the proposed method was evaluated by the determination of trace amounts of cobalt in several water samples.
引用
收藏
页码:617 / 625
页数:9
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