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用于环境和食品样品中氯酚的移液器吸头固相萃取的沸石咪唑酯骨架-8/氟化石墨烯包覆SiO复合材料

Zeolitic imidazolate framework-8/ fluorinated graphene coated SiO composites for pipette tip solid-phase extraction of chlorophenols in environmental and food samples.

作者信息

Zhang Juan, Yu Chen, Chen Zhipeng, Luo Xiaogang, Zhao Haiyan, Wu Fengshou

机构信息

Schoolof Chemistry and Environmental Engineering, Key Laboratory for Green Chemical Process of Ministry of Education, Wuhan Institute of Technology, Wuhan, 430205, China.

Schoolof Chemistry and Environmental Engineering, Key Laboratory for Green Chemical Process of Ministry of Education, Wuhan Institute of Technology, Wuhan, 430205, China.

出版信息

Talanta. 2021 Jun 1;228:122229. doi: 10.1016/j.talanta.2021.122229. Epub 2021 Feb 18.

DOI:10.1016/j.talanta.2021.122229
PMID:33773733
Abstract

In this work, a novel composite adsorbent was successfully prepared by zeolite imidazolate framework-8/fluorinated graphene layer-by-layer covalently bonded on SiO microspheres, and followed to be packed into micro pipette tip for extraction of trace chlorophenols prior to their detection by high performance liquid chromatography (HPLC). The morphology and structure of adsorbent material was characterized by field emission scanning electron microscopy with energy dispersive spectrometer, X-ray diffraction, and N adsorption. The parameters including the amount of adsorbent, sampling volume, sampling rate, sample pH, and desorption solvent affected the extraction performance was systematically investigated by pipette tip solid-phase extraction (PT-SPE) coupled with HPLC analysis. Under the optimized condition, the linearity of this method ranged from 20 to 2000 ng mL for chlorophenols (CPs) with determination coefficient higher than 0.99. The limit of detection (at a signal-to-noise ratio of 3) were in the range 2-20 ng mL for tap water and black tea drinks, 0.2-2 μg g for honey. The relative recoveries of the CPs from spiked samples ranged from 71.8% to 104.7%, with relative standard deviations less than 6.2%. The filled extraction tube exhibited good stability and reproducibility. The proposed method has been successfully used to detect CPs in water and drinks with satisfactory recoveries.

摘要

在本工作中,通过将沸石咪唑酯骨架-8/氟化石墨烯逐层共价键合在SiO微球上,成功制备了一种新型复合吸附剂,随后将其填充到微量移液器吸头中,用于在通过高效液相色谱(HPLC)检测之前萃取痕量氯酚。采用场发射扫描电子显微镜结合能谱仪、X射线衍射和N吸附对吸附剂材料的形貌和结构进行了表征。通过移液器吸头固相萃取(PT-SPE)结合HPLC分析,系统研究了吸附剂用量、进样体积、进样速率、样品pH值和解吸溶剂等参数对萃取性能的影响。在优化条件下,该方法对氯酚(CPs)的线性范围为20至2000 ng mL,测定系数高于0.99。自来水和红茶饮料的检测限(信噪比为3)在2至20 ng mL范围内,蜂蜜的检测限在0.2至2 μg g范围内。加标样品中CPs的相对回收率在71.8%至104.7%之间,相对标准偏差小于6.2%。填充的萃取管表现出良好的稳定性和重现性。所提出的方法已成功用于检测水和饮料中的CPs,回收率令人满意。

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