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Cloud point extraction for preconcentration of trace beryllium and chromium in water samples prior to electrothermal atomic absorption spectrometry

机译:浊点萃取用于电热原子吸收光谱法前富集水中样品中的痕量铍和铬

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In the present work, a simple, sensitive method was developed for the determination of beryllium and chromium by electrothermal atomic absorption spectrometry (ETAAS) after simultaneous pre-concentration by cloud point extraction (CPE). The procedure was based on the formation of the hydrophobic chelates of Be and Cr(III) and/or Cr(VI) with cupferron, followed by their quantitative extraction into the surfactant-rich phase by the Triton X-114. The effects of the main parameters affecting the extraction recovery of CPE, such as pH of the sample solution, concentration of the chelating agent and surfactant, equilibration temperature and incubation time, were investigated and optimised. Under the optimal experimental conditions, the limits of detection and limits of quantification for Be were 0.33 and 1.11 pg and for Cr(VI) were 0.98 and 3.28 pg, respectively. The pre-concentration factor for Be and Cr(VI) was found to be 20 for 10 mL of the water sample. The accuracy of the method was confirmed by analysis of certified reference materials of waters (a€?Trace Metals in Drinking Watera€? and SRM 1643e a€?Trace Elements in Watera€?) with satisfactory results. The method developed was successfully applied to the pre-concentration and determination of trace quantities of beryllium and chromium(VI) in different natural waters.
机译:在目前的工作中,开发了一种简单,灵敏的方法,通过浊点萃取(CPE)同时预浓缩后,通过电热原子吸收光谱法(ETAAS)测定铍和铬。该程序基于用铜铁形成Be和Cr(III)和/或Cr(VI)的疏水螯合物,然后通过Triton X-114将其定量萃取到富含表面活性剂的相中。研究并优化了影响CPE萃取回收率的主要参数,如样品溶液的pH,螯合剂和表面活性剂的浓度,平衡温度和孵育时间。在最佳实验条件下,Be的检出限和定量限分别为0.33和1.11 pg,Cr(VI)的检出限为0.98和3.28 pg。对于10 mL水样品,Be和Cr(VI)的预浓缩系数为20。通过对水的认证参考材料(饮用水中的微量金属和饮用水中的微量元素SRM 1643e)的分析,证实了该方法的准确性,结果令人满意。所开发的方法已成功应用于不同天然水中痕量的铍和铬(VI)的富集和测定。

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