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基于多巴胺辅助的金属有机方法的高性能纳米复合印迹膜的仿生合成。

Bioinspired synthesis of high-performance nanocomposite imprinted membrane by a polydopamine-assisted metal-organic method.

机构信息

School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, China.

School of Energy and Power Engineering, Jiangsu University, Zhenjiang 212013, China.

出版信息

J Hazard Mater. 2017 Feb 5;323(Pt B):663-673. doi: 10.1016/j.jhazmat.2016.10.030. Epub 2016 Oct 15.

Abstract

Significant efforts have been focused on the functionalization and simplification of membrane-associated molecularly imprinted materials, which can rapidly recognize and separate specific compound. However, issues such as low permselectivity and unstable composite structures are restricting it from developing stage to a higher level. In this work, with the bioinspired design of polydopamine (pDA)-assisted inorganic film, we present a novel molecular imprinting strategy to integrate multilevel nanocomposites (Ag/pDA) into the porous membrane structure. The molecularly imprinted nanocomposite membranes were then obtained through an in situ photoinitiated ATRP method by using tetracycline (TC) as the template molecule. Importantly, attributing to the formation of the Ag/pDA-based TC-imprinted layers, largely enhance TC-rebinding capacity (35.41mg/g), adsorption selectivity and structural stability (still maintained 92.1% of the maximum adsorption capacity after 10 cycling operations) could been easily achieved. Moreover, largely enhanced permselectivity performance toward template molecule (the permeability factor β values were also more than 5.95) was also obtained. Finally, all synthesis methods were conducted in aqueous solution at ambient temperature, which was environmental friendly for scaling up without causing pollution.

摘要

人们已经做出了巨大努力来对膜相关的分子印迹材料进行功能化和简化,使其能够快速识别和分离特定的化合物。然而,低选择性和不稳定的复合结构等问题限制了它从发展阶段到更高的水平。在这项工作中,我们受多巴胺(pDA)辅助的无机膜的仿生设计启发,提出了一种新的分子印迹策略,将多级纳米复合材料(Ag/pDA)整合到多孔膜结构中。然后,通过原位光引发原子转移自由基聚合(ATRP)方法,以四环素(TC)为模板分子,获得了分子印迹纳米复合膜。重要的是,由于形成了基于 Ag/pDA 的 TC 印迹层,很容易实现 TC 再结合能力(35.41mg/g)、吸附选择性和结构稳定性(经过 10 次循环操作后仍保持最大吸附容量的 92.1%)的提高。此外,还获得了对模板分子的大大增强的选择性渗透性能(渗透率因子β值也超过 5.95)。最后,所有的合成方法都是在环境友好的温和条件下,在水溶液中进行的,无需进行污染性的放大操作。

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