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首页> 外文期刊>Analytical methods >Ion pair based dispersive liquid–liquid microextraction for the preconcentration of ultra-trace levels of bismuth(III) and its determination by electrothermal atomic absorption spectroscopy
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Ion pair based dispersive liquid–liquid microextraction for the preconcentration of ultra-trace levels of bismuth(III) and its determination by electrothermal atomic absorption spectroscopy

机译:基于离子对的分散液-液微萃取用于痕量铋(III)的预浓缩及其电热原子吸收光谱法的测定

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摘要

A simple, selective and efficient ion pair based dispersive liquida€“liquid microextraction method was used for the preconcentration of ultra-trace levels of Bi(III) prior to its determination by electrothermal atomic absorption spectrometry. This method is based on the complexation of Bi(III) with thiocyanate anion to form the anionic complexes, Bi(SCN)63a?’ and Bi(SCN)4a?’. A cationic surfactant, cetylpyridinium chloride (CPC), was used as a counter ion. The resulting ion pair complexes were extracted into fine droplets of carbon tetrachloride by rapid injection of a mixture of acetone (as the disperser solvent) and carbon tetrachloride (as the extraction solvent) into the sample solution. Important parameters affecting the extraction efficiency, including sample pH, thiocyanate and CPC concentrations, and type and volume of the extraction and disperser solvents, were examined and optimized. Under the optimum conditions, the calibration graph was linear in the range of 0.3a€“8 ??g La?’1 Bi (III) with a correlation coefficient of 0.9979. The relative standard deviation (RSD, %) based on eight replicate analyses of 2 ??g La?’1 Bi(III) was 4.8%, and the detection limit (DL) of Bi(III) was 0.07 ??g La?’1. The proposed method was validated by the analysis of a certified reference material and the spike method. The obtained results were in very good agreement with the certified values. The proposed method was successfully applied for the determination of ultra-trace levels of Bi(III) in different water and human serum samples.
机译:一种简单,选择性和有效的基于离子对的分散液/液体微萃取方法用于在电热原子吸收光谱法测定前痕量的Bi(III)超痕量水平的预浓缩。该方法基于Bi(III)与硫氰酸根阴离子的络合形成阴离子络合物Bi(SCN)63a?和Bi(SCN)4a?。阳离子表面活性剂氯化十六烷基吡啶鎓(CPC)被用作抗衡离子。通过将丙酮(作为分散溶剂)和四氯化碳(作为萃取溶剂)的混合物快速注入样品溶液中,将所得的离子对络合物萃取成四氯化碳的细小液滴。检查并优化了影响萃取效率的重要参数,包括样品的pH值,硫氰酸盐和CPC浓度以及萃取和分散剂溶剂的类型和体积。在最佳条件下,校正曲线在0.3a×8 ?? g La?1 Bi(III)范围内呈线性,相关系数为0.9979。基于2 ?? g La?'1 Bi(III)的八次重复分析,相对标准偏差(RSD,%)为4.8%,Bi(III)的检出限(DL)为0.07 ?? g La?1。 '1。通过对认证参考材料和加标方法的分析验证了所提出的方法。获得的结果与认证值非常吻合。所提出的方法已成功用于测定不同水和人血清样品中痕量的Bi(III)。

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