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Development of cloud-point extraction method for preconcentration of trace quantities of cobalt and nickel in water and food samples

机译:水和食品样品中痕量钴和镍的前浓度云点提取方法的研制

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摘要

A new, efficient, and sensitive cloud point methodology was developed for preconcentration of trace quantities of cobalt and nickel in water and food samples prior to their determination by flame atomic absorption spectrometry (FAAS). The metals react with 2-(benzothiazolylazo)-4-nitrophenol (BTANP) at pH 7.0 and micelle-mediated extraction using the nonionic surfactant Triton X-114 medium. The surfactant-rich phase was diluted with acidified methanol and the cobalt and nickel content was determined by FAAS. The optimum conditions (e.g. pH, reagent and surfactant concentrations, temperature and centrifugation times) were evaluated and optimized. The proposed CPE method showed linear calibration within the ranges 5.0-100 and 5.0-150 ng mL(-1) of cobalt and nickel, respectively, and the limits of detection of the method was 1.4 and 1.0 ng mL (1) of cobalt and nickel, respectively. The interference effect of some cations and anions was also studied. The method was applied to the determination of both metals in water and food samples with a recovery from the spiked water samples in the range of 95-102%. The validation of the procedure was carried out by analysis of a certified reference material.
机译:一种新的,有效的和灵敏的浊点的方法是为水和食物样品中的钴和镍的痕量的富集其判定通过火焰原子吸收光谱法(FAAS)之前开发的。金属与2-(苯并噻唑偶氮)-4-硝基苯酚(BTANP)在pH 7.0和胶束介导的提取反应使用的非离子表面活性剂Triton X-114平台。的富含表面活性剂相,用酸化的甲醇稀释,钴和镍的含量通过FAAS测定。的最佳条件(例如pH值,试剂和表面活性剂浓度,温度和离心次)进行了评价和优化。所提出的方法,CPE显示线性校准分别钴和镍,的范围5.0-100和5.0-150纳克毫升(-1)内,并检测该方法的极限为1.4和1.0纳克钴的溶液(1)和镍,分别。一些阳离子和阴离子的干扰影响进行了研究。该方法适用于这两种金属的测定水和食物样品中与来自加标水样中的95-102%范围内的恢复。该过程的验证是由标准物质的分析来进行。

著录项

  • 来源
    《RSC Advances》 |2016年第96期|共10页
  • 作者单位

    Zagazig Univ Fac Sci Dept Chem Zagazig Egypt;

    Umm Al Qura Univ Fac Sci Appl Dept Chem Mecca Saudi Arabia;

    Umm Al Qura Univ Deanship Sci Res Mecca Saudi Arabia;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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