首页> 外文期刊>Journal of the Iranian Chemical Society >Development of a new method for extraction and preconcentration of cadmium and zinc ions in edible oils based on heat-induced homogeneous liquid-liquid microextraction
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Development of a new method for extraction and preconcentration of cadmium and zinc ions in edible oils based on heat-induced homogeneous liquid-liquid microextraction

机译:基于热诱导的均匀液 - 液微萃取的食用油中镉和锌离子萃取和锌离子的新方法的研制

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摘要

A new sample preparation method, cyclohexylamine-based heat-induced homogeneous liquid-liquid microextraction, has been developed for the extraction and preconcentration of Cd(II) and Zn(II) ions in edible oils followed by flame atomic absorption spectrometry determination. First, the analytes are extracted into an acidic solution (a balanced mixture of HNO3 and HCl). Second, they are preconcentrated via the microextraction method. Accordingly, cyclohexylamine (as a complexing agent and an extraction solvent) is added at mu L-level into the obtained solution containing the analytes to form a homogeneous solution followed by the addition of sodium chloride. After manual shaking, the obtained solution is placed in a water bath thermostated at 60 degrees C. A cloudy solution because of the decrease in cyclohexylamine solubility in water at high temperature is formed. After centrifuging fine droplets of cyclohexylamine containing Cd(II) and Zn(II)cyclohexylamine complexes are collected on the top of the aqueous phase. The preconcentrated analytes in the upper phase by use of flame atomic absorption spectrometry are analyzed and determined. Several variables possibly affecting the extraction efficiency were investigated and optimized. Under the optimum conditions, the calibration curves were linear in the ranges of 10-300 and 2.5-200 mu g kg(-1) for Cd(II) and Zn(II), respectively. Repeatability of the proposed method, expressed as relative standard deviation, was obtained 2.4 and 1.7% for Cd (II) and Zn(II), respectively. Moreover, the detection limits of the selected analytes were obtained 3.8 and 0.6 mu g kg(-1) for Cd(II) and Zn(II), respectively.
机译:已经开发了一种新的样品制备方法,基于环己酰胺基热诱导的均匀液 - 液体微萃取,用于在食用油中的CD(II)和Zn(II)离子中的萃取和前浓缩,其次是火焰原子吸收光谱法测定。首先,将分析物萃取到酸性溶液中(HNO 3和HCl的平衡混合物)。其次,它们通过微萃取方法预先浓缩。因此,将环己胺(作为络合剂和萃取溶剂)加入μl水平中,进入含有分析物的所得溶液中以形成均匀溶液,然后加入氯化钠。手动摇动后,将所得溶液置于60℃下恒温的水浴中。由于在高温下的水中的环己胺溶解度降低,浑浊的溶液。离心含有Cd(II)和Zn(II)的环己酰胺的细液滴后,在水相顶部收集环己酰胺复合物。通过使用火焰原子吸收光谱法进行上阶段的前浓度分析物进行分析和测定。研究和优化了几种可能影响提取效率的变量。在最佳条件下,校准曲线分别为CD(II)和Zn(II)的10-300和2.5-200μmGkg(-1)的线性。所提出的方法的可重复性分别表示为相对标准偏差,分别获得2.4和1.7%的CD(II)和Zn(II)。此外,对于CD(II)和Zn(II),分别获得3.8和0.6μg(-1)的选定分析物的检测限。

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