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用于水样中二苯甲酮微萃取和测定的磁性氧化石墨烯复合材料

Magnetic Graphene Oxide Composite for the Microextraction and Determination of Benzophenones in Water Samples.

作者信息

Medina Alejandro, Casado-Carmona Francisco Antonio, López-Lorente Ángela I, Cárdenas Soledad

机构信息

Departamento de Química Analítica, Instituto Universitario de Investigación en Química Fina y Nanoquímica IUNAN, Universidad de Córdoba, Campus de Rabanales, Edificio Marie Curie, E-14071 Córdoba, Spain.

出版信息

Nanomaterials (Basel). 2020 Jan 18;10(1):168. doi: 10.3390/nano10010168.

DOI:10.3390/nano10010168
PMID:31963652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7022302/
Abstract

Magnetite nanoparticles (FeO) functionalized with graphene oxide (GO) have been synthesized through a silanization process of the magnetic nanoparticles with tetraethyl orthosilicate and (3-aminopropyl)triethoxysilane and further coupling of GO. The synthesized nanomaterials have been characterized by several techniques, such as transmission electron microscopy (TEM), and infrared and Raman spectroscopy, which enabled the evaluation of the different steps of the functionalization process. The hybrid nanomaterial has been employed for the extraction of five benzophenones (benzophenone-1, benzophenone-3, 4-hydroxybenzophenone, benzophenone-6 and benzophenone-8) in aqueous samples by dispersive micro-solid phase extraction, combining the magnetic properties of magnetite nanoparticles with the excellent sorption capacity of graphene oxide via hydrophobic interactions with the analytes. The subsequent separation and quantification of the analytes was performed by liquid chromatography with tandem mass spectrometric detection, achieving limits of detection (LODs) in the range 2.5 to 8.2 μg·L, with relative standard deviations ranging from 1.3-9.8% and relative recovering in the range 86 to 105%. Positive swimming pool water samples analysed following the developed method revealed the presence of benzophenones in from 14.3 to 39 μg·L.

摘要

通过用正硅酸四乙酯和(3-氨丙基)三乙氧基硅烷对磁性纳米颗粒进行硅烷化处理,以及进一步使氧化石墨烯(GO)偶联,合成了用氧化石墨烯功能化的磁铁矿纳米颗粒(FeO)。已通过多种技术对合成的纳米材料进行了表征,如透射电子显微镜(TEM)、红外光谱和拉曼光谱,这些技术能够评估功能化过程的不同步骤。通过分散微固相萃取,将磁铁矿纳米颗粒的磁性与氧化石墨烯通过与分析物的疏水相互作用而具有的出色吸附能力相结合,该杂化纳米材料已用于萃取水性样品中的五种二苯甲酮(二苯甲酮-1、二苯甲酮-3、4-羟基二苯甲酮、二苯甲酮-6和二苯甲酮-8)。随后通过液相色谱-串联质谱检测对分析物进行分离和定量,检测限(LOD)在2.5至8.2 μg·L范围内,相对标准偏差在1.3 - 9.8%之间,相对回收率在86至105%之间。按照所开发的方法分析的阳性游泳池水样显示,二苯甲酮的含量在14.3至39 μg·L之间。

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