分子印迹聚合物
甲基丙烯酸
吸附
傅里叶变换红外光谱
没食子酸
分子印迹
聚合物
聚合
化学
核化学
共价键
高分子化学
化学工程
选择性
有机化学
催化作用
工程类
抗氧化剂
作者
Li‐Ping Zhang,Fu‐Hua Zhu,Yu Guo,Hui Yang,Lan Wang,Yifan He,Shu‐Jing Li,Tian Li
摘要
Abstract The molecularly imprinted polymer (MIP) for gallic acid (GA) was prepared based on the cooperative imprinting of boronate affinity interactions and hydrogen bond. The fabricated MIP were designed by the polymerization of template with co‐functional monomer, 3‐acrylamidophenylboronic acid (AAPBA) and methacrylic acid (MAA). The characteristics of the resulting polymer (AAPBA‐ co ‐MAA MIP) were tested by scanning electron microscope (SEM), Fourier transform infrared spectra (FTIR) and nitrogen adsorption–desorption. Bonding performance demonstrated that the AAPBA‐ co ‐MAA MIP possessed the excellent recognition ability in the incubation solution with pH 7.4 and presented higher adsorption capacity, faster adsorption rate and satisfactory selectivity for GA. Additionally, the AAPBA‐ co ‐MAA MIP revealed the good applications in the separation and enrichment of GA from Puer tea, and the amount of GA enriched by them was determined to be 2.75 mg g −1 . This work suggested that the integration of cooperative imprinting strategy between covalent and non‐covalent would be an effective way to improve the specific recognition performance of the MIP.
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