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UiO-66-OH锆基金属有机框架的合成及其在分光光度法选择性萃取和痕量测定水样中钍的应用。

Synthesis of UiO-66-OH zirconium metal-organic framework and its application for selective extraction and trace determination of thorium in water samples by spectrophotometry.

作者信息

Moghaddam Zahra Safaei, Kaykhaii Massoud, Khajeh Mostafa, Oveisi Ali Reza

机构信息

Department of Chemistry, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan 98135-674, Iran.

Department of Chemistry, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan 98135-674, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2018 Apr 5;194:76-82. doi: 10.1016/j.saa.2018.01.010. Epub 2018 Jan 5.

Abstract

In this study, a zirconium-based metal-organic framework (Zr-MOF), named UiO-66-OH, was synthesized by the solvo-thermal method and characterized by Fourier transform-infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), and scanning electron microscopy (SEM). This Zr-MOF was then employed as a sorbent for selective extraction and preconcentration of thorium ions after their complexation with 2‑(2,4‑dihydroxyphenyl)‑3,5,7‑trihydroxychromen‑4‑one (morin) from environmental water samples prior to its spectrophotometrical determination. The experimental parameters affecting extraction, such as pH of sample solution, amount of Zr-MOF, type and volume of eluting solvent, adsorption and desorption time, and concentration of complexing agent were evaluated and optimized. Under the optimized conditions, an enrichment factor of 250 was achieved. The limit of detection was calculated to be 0.35μg·L with a linear range between 10 and 2000μg·Lof thorium. The maximum sorption capacity of MOF toward thorium was found to be 47.5mg·g. The proposed procedure was successfully applied to the analysis of real water samples.

摘要

在本研究中,通过溶剂热法合成了一种名为UiO-66-OH的锆基金属有机框架材料(Zr-MOF),并通过傅里叶变换红外光谱(FTIR)、粉末X射线衍射(PXRD)和扫描电子显微镜(SEM)对其进行了表征。然后,将这种Zr-MOF用作吸附剂,用于在对环境水样中的钍离子与2-(2,4-二羟基苯基)-3,5,7-三羟基色原酮(桑色素)络合后进行选择性萃取和预富集,随后进行分光光度测定。评估并优化了影响萃取的实验参数,如样品溶液的pH值、Zr-MOF的用量、洗脱溶剂的类型和体积、吸附和解吸时间以及络合剂的浓度。在优化条件下,实现了250的富集因子。计算得出检测限为0.35μg·L,钍的线性范围在10至2000μg·L之间。发现MOF对钍的最大吸附容量为47.5mg·g。所提出的方法成功应用于实际水样的分析。

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