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Simultaneous application of cloud point and solid-phase extraction for determination of Fe(III) and Cu(II) ions by using SnO2 nanopowder in micellar medium

机译:SnO2纳米粉在胶束介质中同时应用浊点和固相萃取测定Fe(III)和Cu(II)离子

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摘要

A new approach was developed for sensitive determination of Fe(III) and Cu(II) ions using SnO2 nanopowder in the micellar medium on the contrary conventional cloud point extraction studies. The presented method contains a combination of solid-phase extraction and cloud point extraction. According to this procedure, the metal ions were firstly retained on modified SnO2 nanopowder and then passed to the surfactant-rich phase. The effect of experimental variables including pH, concentration of reagents, eluting solution, incubation time, equilibration temperature, sample volume, and effects of interfering ions have been investigated and optimized systematically. The calibration graphs were linear in the range of 0.23-100.00g L-1 and 0.30-110.00g L-1 for Fe(III) and Cu(II), respectively. Under optimized conditions, the limits of detections were 0.07 and 0.09g L-1 for Fe(III) and 0.09g L-1 for Cu(II). The proposed method offers satisfactory analytical features by means of combining two different and efficient preconcentration techniques. In addition, the method can be evaluated as an alternative and fast method according to only-surfactant-mediated extractions. The validation of method was carried out by recovery tests and certified reference material (CRM) analysis. The acceptable and compatible results were obtained in the analysis of CRM and real samples.
机译:与常规的浊点提取研究相反,开发了一种新方法用于使用胶束介质中的SnO2纳米粉敏感地测定Fe(III)和Cu(II)离子。提出的方法包含了固相萃取和浊点萃取的组合。根据该程序,金属离子首先保留在改性的SnO2纳米粉末上,然后进入富表面活性剂相。实验变量的影响包括pH,试剂浓度,洗脱液,温育时间,平衡温度,样品量以及干扰离子的影响已得到系统地研究和优化。对于Fe(III)和Cu(II),校准曲线分别在0.23-100.00g L-1和0.30-110.00g L-1范围内呈线性。在优化条件下,Fe(III)的检出限为0.07和0.09g L-1,Cu(II)的检出限为0.09g L-1。通过结合两种不同且有效的预浓缩技术,所提出的方法提供了令人满意的分析功能。此外,该方法可以根据表面活性剂介导的提取方法作为一种快速的替代方法进行评估。通过回收率测试和认证参考材料(CRM)分析进行方法的验证。在CRM和实际样品的分析中获得了可接受的兼容结果。

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