吸附
膜
化学工程
材料科学
苯酚
选择性吸附
X射线光电子能谱
分子印迹聚合物
分子印迹
化学
傅里叶变换红外光谱
接触角
复合数
色谱法
选择性
有机化学
复合材料
催化作用
工程类
生物化学
作者
Yun Qu,Lei Qin,Mingcong Guo,Xuguang Liu,Yongzhen Yang
标识
DOI:10.1016/j.seppur.2021.119915
摘要
Abstract Molecularly imprinted composite membrane (MIM) for selective separation of specific compound has broad applications for wastewater treatments. Herein, a multilayered molecularly imprinted composite membrane (m-MIM) with porous carbon nanospheres/polydopamine (pDA) cooperative structure was proposed to improve phenol selective adsorption efficiency. pDA layer was previously synthesized on the basal membrane to augment interfacial adhesion. Subsequently, carbon nanospheres were uniformly and firmly loaded on the double sides of pDA-modified membrane, whose active surface provided more distribution sites for imprinted cavities. The abundant hydroxyl and amino groups on pDA can enhance the hydrophilicity and imprinting activity of m-MIM, which promote mass transfer and adsorption. The characterizations including SEM, FTIR, XPS, and AFM confirmed the formation of cooperative structure on the basal membrane. The BET result show that the specific surface area of m-MIM was about 2.72 times that of basal membrane, and in term of hydrophilicity, water contact angle decreased from 46° (basal membrane) to 29°. Attributed to the abundant imprinted cavities, m-MIM acquired excellent adsorption capacity (51.40 mg g−1) and high permselectivity coefficients (more than 7.6). m-MIM remained stable adsorption capacity after nine cycles, which provides potential for water treatment and selective separation of specific substances. Mechanism of selective separation was unveiled by molecular simulation.
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