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Cloud Point Extraction for the Determination of Trace Amounts of Cobalt in Water and Food Samples by Flame Atomic Absorption Spectrometry

机译:浊点萃取-火焰原子吸收光谱法测定水和食品中痕量钴。

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A cloud point extraction (CPE) procedure which was developed for the separation and preconcentration of trace amounts of cobalt is combined with flame atomic absorption spectrometry (FAAS) to determine trace amounts of cobalt in water and food samples. The procedure is based on the formation of the hydrophobic complex between Co(II) and 4-methoxy-2-sulfo-benzenediazoaminoazo-benzene (MOSDAA) followed by its extraction into a Triton X-114 surfactant-rich phase. The parameters such as pH of sample, concentrations of MOSDAA and Triton X-114, equilibrium temperature, and equilibrium time, which affect both complexation and extraction, are optimized. Under the selected optimum conditions, the preconcentration of 10.0 mL, 0.1 μg mL−1Co(II) solution results in a limit of detection of 0.47 ng mL−1(3σ) and an enrichment factor of 19. A relative standard deviation of 2.78% (n=6,c=0.1 μg mL−1) for the determination of Co(II) is obtained. The proposed method was applied for the determination of trace amounts of cobalt in river water and millet samples with satisfactory results.
机译:为分离和富集痕量钴而开发的浊点萃取(CPE)程序与火焰原子吸收光谱法(FAAS)结合使用,以确定水和食品样品中的痕量钴。该步骤基于在Co(II)和4-甲氧基-2-磺基苯重氮氨基偶氮苯(MOSDAA)之间形成疏水配合物,然后将其萃取到富含Triton X-114表面活性剂的相中。优化了诸如pH值,MOSDAA和Triton X-114的浓度,平衡温度和平衡时间等参数,这些参数会影响络合和萃取。在选定的最佳条件下,预浓缩10.0μmL,0.1μggmL-1Co(II)溶液的检出限为0.47μgmLmL-1(3σ),富集系数为19。相对标准偏差为2.78%获得了用于测定Co(II)的(n = 6,c = 0.1μgmL-1)。该方法用于河水和小米中痕量钴的测定,结果令人满意。

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