Thermo-responsive polymer tethered metal-organic framework core-shell magnetic microspheres for magnetic solid-phase extraction of alkylphenols from environmental water samples

被引:41
|
作者
Jia, Yuqian [1 ]
Su, Hao [1 ]
Wong, Y. -L. Elaine [2 ]
Chen, Xiangfeng [1 ,2 ]
Chan, T. -W. Dominic [2 ]
机构
[1] Shandong Acad Sci, Key Lab Appl Technol Sophisticated Analyt Instrum, Jinan, Shandong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetic solid-phase extraction; Alkylphenol; Thermo-responsive polymer; Metal-organic frameworks; Environmental water samples; ADSORBENT; GRAPHENE; SORBENT; SHEETS;
D O I
10.1016/j.chroma.2016.06.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, the thermo-responsive polymer PNIPAM tethered to Fe3O4@SiO2@MOF core-shell magnetic microspheres was first synthesized by a surface-selective post-synthetic strategy and underwent highly efficient magnetic solid-phase extraction (MSPE) of alkylphenols from aqueous samples. Alkylphenols, including 4-tert-octylphenol (OP) and 4-n-nonylphenol (NP), were selected as target compounds. The sample quantification was carried out using LC-MS/MS in multiple reaction monitor (MRM) mode. Under optimal working conditions, the developed method showed good linearity in the range of 5-1000 ng L-1, a low limit of detection (1.5 ng L-1), and good repeatability (relative standard deviation, <8%, n = 5) for NP and OP. Owning to the hydrophilic/hydrophobic switchable properties of the nanocomposite, high recoveries (78.7-104.3%) of alkylphenols were obtained under different extraction conditions. The levels of OP and NP in environmental samples collected from local river, lake and pond waters were analyzed using the developed method. It was believed that the synthesized material with the thermo-responsive coating, large surface areas and magnetic properties should have great potential in the extraction and removal of alkylphenols from environmental samples. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 48
页数:7
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