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采用基于锆的氨基标记金属有机骨架纳米吸附剂分散固相萃取环境水样中的选定的硝基酚类化合物。

Dispersive solid-phase extraction of selected nitrophenols from environmental water samples using a zirconium-based amino-tagged metal-organic framework nanosorbent.

机构信息

Research Center for Environmental Health Technology, Iran University of Medical Sciences, Tehran, Iran.

Faculty of Engineering, Shohadaye Hoveizeh University of Technology, Dasht-e Azadegan, Susangerd, Iran.

出版信息

J Sep Sci. 2018 Nov;41(22):4159-4166. doi: 10.1002/jssc.201800764. Epub 2018 Oct 29.

DOI:10.1002/jssc.201800764
PMID:30221807
Abstract

This study has centered on the establishment of an efficient, simple and reliable dispersive solid-phase extraction method followed by an accurate trace determination of selected nitrophenols as a class of compounds with high toxicity and low degradability. To achieve the above goal, a zirconium-based amino-tagged metal-organic framework nanosorbent was synthesized, characterized and eventually employed for the extraction of two nitrophenols from various environmental water samples. Once the extraction of analytes had occurred, they were desorbed from the metal-organic framework sorbent using an appropriate mixed solvent followed by high-performance liquid chromatography with ultraviolet detection. Under the optimal extraction conditions, the calibration curves for the analytes were linear over the concentration range of 1-200 μg/L. The accuracy of the method was tested by the relative recovery experiments on the fortified real samples with the results falling within the range of 91 to 106%, while the corresponding precisions varied in the span of 4.6-9.0%. Based on a signal-to-noise ratio of 3, the method detection limits were determined to be 0.5 μg/L for both analytes.

摘要

本研究集中于建立一种高效、简单和可靠的分散固相萃取方法,随后对选定的硝基酚类化合物进行痕量准确测定,此类化合物具有高毒性和低降解性。为了实现上述目标,合成了一种基于锆的氨基标记金属-有机骨架纳米吸附剂,并对其进行了表征,最终用于从各种环境水样中萃取两种硝基酚类化合物。一旦分析物被萃取出来,它们就会从金属-有机骨架吸附剂上用合适的混合溶剂解吸,然后用高效液相色谱法结合紫外检测。在最佳萃取条件下,分析物的校准曲线在 1-200μg/L 的浓度范围内呈线性。方法的准确性通过对加标实际样品的相对回收率实验进行测试,结果在 91%至 106%之间,而相应的精密度在 4.6-9.0%之间变化。基于信噪比为 3,确定两种分析物的方法检测限均为 0.5μg/L。

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