首页> 外文期刊>Journal of the Iranian Chemical Society >Magnetic solid-phase extraction with copper ferrite nanoparticles for the separation and preconcentration of ultra-trace amounts of tellurium (IV) ion in aqueous samples
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Magnetic solid-phase extraction with copper ferrite nanoparticles for the separation and preconcentration of ultra-trace amounts of tellurium (IV) ion in aqueous samples

机译:用铜铁氧体纳米粒子萃取磁性相萃取用于在水上样品中的超痕量碲(IV)离子的分离和前浓度

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摘要

A selective, simple and rapid magnetic solid-phase extraction was developed using copper ferrite (CuFe2O4) as an efficient sorbent for the separation and preconcentration of tellurium (IV) ion prior to its determination by electrothermal atomic absorption spectrometry. In this method, only 5mg of the sorbent was needed to obtain a satisfactory extraction recovery. The CuFe2O4 was synthesized by means of a simple coprecipitation method and subsequently characterized by X-ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy. The factors affecting the separation and preconcentration of tellurium (IV) ions including, the type of desorption solvent, desorption solvent concentration and volume, desorption temperature and time, pH, amount of sorbent, extraction temperature and time were investigated and optimized. The effects of interfering ions on the extraction of Te (IV) ions were also investigated. Under the optimized conditions, the method exhibited a linear dynamic range of 0.04-0.5 mu gL(-1) with good linearity (r(2)=0.9982). The limit of detection and sorption capacity were found to be 0.012 mu gL(-1) and 89.0mgg(-1), respectively. Enrichment factor was 223. The intraday, interday, and batch-to-batch relative standard deviations were found to be 3.1, 4.4, and 6.0% for 0.25 mu gL(-1) concentration. Finally, the proposed analytical procedure was successfully applied to monitor tellurium (IV) ions in some aqueous samples, with relative recoveries of 96%.
机译:使用铜铁素体(CuFe2O4)开发一种选择性,简单,快速的磁性相萃取,作为通过电热原子吸收光谱法测定碲(IV)离子的分离和前浓缩的有效吸附剂。在该方法中,仅需要5mg的吸附剂来获得令人满意的提取恢复。通过简单的共沉淀方法合成CuFe 2 O 4,随后通过X射线衍射,傅里叶变换红外光谱和扫描电子显微镜来表征。影响碲(IV)离子分离和前浓缩的因素,包括解吸溶剂,解吸溶剂浓度和体积,解吸温度和时间,pH,吸附剂量,吸附剂,提取温度和时间,并优化。还研究了干扰离子对TE(IV)离子提取的影响。在优化条件下,该方法具有0.04-0.5μg(-1)的线性动态范围,具有良好的线性度(R(2)= 0.9982)。发现检测和吸附能力的极限分别为0.012μg(-1)和89.0mgg(-1)。富集因子为223.,盘中,间隔和分批相对标准偏差为3.1,4.4和6.0%,浓度为3.1,4.4和6.0%。最后,所提出的分析程序成功地应用于在一些含水样品中监测碲(IV)离子,相对回收的> 96%。

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