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首页> 外文期刊>Journal of the Iranian Chemical Society >Simultaneous spectrophotometric determination of uranium and zirconium using cloud point extraction and multivariate methods
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Simultaneous spectrophotometric determination of uranium and zirconium using cloud point extraction and multivariate methods

机译:浊点萃取-多元法同时分光光度法测定铀和锆

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摘要

A cloud point extraction (CPE) process using the nonionic surfactant Triton X-114 to simultaneous extraction and spectrophotometric determination of uranium and zirconium from aqueous solution using partial least squares (PLS) regression is investigated. The method is based on the complexation reaction of these cations with Alizarin Red S (ARS) and subsequent micelle-mediated extraction of products. The chemical parameters affecting the separation phase and detection process were studied and optimized. Under the optimum experimental conditions (i.e. pH 5.2, Triton X-114 = 0.20%, equilibrium time 10 min and cloud point 45℃), calibration graphs were linear in the range of 0.01-3 mg L~(-1) with detection limits of 2.0 and 0.80 μg L~(-1) for U and Zr, respectively. The experimental calibration set was composed of 16 sample solutions using an orthogonal design for two component mixtures. The root mean square error of predictions (RMSEPs) for U and Zr were 0.0907 and 0.1117, respectively. The interference effect of some anions and cations was also tested. The method was applied to the simultaneous determination of U and Zr in water samples.
机译:研究了使用非离子表面活性剂Triton X-114的浊点萃取(CPE)工艺,同时使用偏最小二乘(PLS)回归从水溶液中同时萃取和分光光度法测定铀和锆。该方法基于这些阳离子与茜素红S(ARS)的络合反应以及随后的胶束介导的产物提取。研究和优化了影响分离阶段和检测过程的化学参数。在最佳实验条件下(pH 5.2,Triton X-114 = 0.20%,平衡时间10 min,浊点45℃),校正曲线在0.01-3 mg L〜(-1)范围内呈线性,且有检测限U和Zr分别为2.0和0.80μgL〜(-1)。实验校准集由16种样品溶液组成,采用正交设计设计,用于两种组分的混合物。 U和Zr的预测均方根误差(RMSEPs)分别为0.0907和0.1117。还测试了一些阴离子和阳离子的干扰作用。该方法用于水样中铀和锆的同时测定。

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