Switched recognition and release ability of temperature responsive molecularly imprinted polymers based on magnetic halloysite nanotubes

被引:54
|
作者
Pan, Jianming [1 ,2 ]
Hang, Hui [1 ]
Dai, Xiaohui [1 ]
Dai, Jiangdong [1 ]
Huo, Pengwei [1 ]
Yan, Yongsheng [1 ,2 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
SELECTIVE REMOVAL; NANOPARTICLES; POLYMERIZATION; MICROSPHERES; COMPOSITES; ADSORPTION;
D O I
10.1039/c2jm32821f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CoFe2O4/halloysite nanotube magnetic composites (MHNTs) were firstly achieved via a wet impregnation technique, and then a thermal polymerization under (NH4)(2)S2O8 chain initiation in water was employed to obtain methacrylic acid-functionalized MHNTs (MAA-MHNTs). By decorating the MAA-MHNTs with the temperature responsive monomer N-isopropylacrylamide (NIPAM), a novel temperature responsive molecularly imprinted material based on the obtained NIPAM-MHNTs (TMMIPs) was synthesized by a surface imprinting technique. The results of characterization indicated that the TMMIPs exhibited magnetic sensitivity (M-s = 1.758 emu g(-1)), magnetic stability (in the pH range of 2.0-8.0), thermal stability (especially below 200 degrees C) and contained a temperature responsive imprinted layer (the lower critical solution temperature was 33.96 degrees C). Then the TMMIPs were applied to switched recognition and release of 2,4,5-trichlorophenol molecules (5-TCP) by changing the medium temperature. TMMIPs showed outstanding recognition ability towards the imprinted species under high temperature conditions (such as 60 degrees C), due to the loss of hydration and a collapsed state of inter-poly(N-isopropylacrylamide), which resulted in the formation of a specific structure between 5-TCP and the polymer network. In contrast, at relatively low temperatures (such as 20 degrees C), the captured 5-TCP was released from the swelled TMMIPs, which resulted from increasing the distance between 5-TCP and the polymer network. The selective analysis demonstrated the high affinity and selectivity of TMMIPs towards 5-TCP over competitive phenolic compounds, and the specific recognition of binding sites may be based on the distinct size, structure and functional groups of the template molecules.
引用
收藏
页码:17167 / 17175
页数:9
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