首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >High-capacity hollow porous dummy molecular imprinted polymers using ionic liquid as functional monomer for selective recognition of salicylic acid
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High-capacity hollow porous dummy molecular imprinted polymers using ionic liquid as functional monomer for selective recognition of salicylic acid

机译:使用离子液体作为功能性单体的高容量中空多孔伪分子印迹聚合物,用于选择性识别水杨酸

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摘要

The existence of strong intramolecular hydrogen bond in salicylic acid (SA) weakens its intermolecular hydrogen bonding with functional monomer, then it is a challenge work to fabricate molecularly imprinted polymers (MIPs) for SA recognition with high capacity and good selectivity. Here, hollow porous dummy MIPs (HPDMIPs) were prepared using benzoic acid (BA) as dummy template, ionic liquid (i.e. 1-vinyl-3-methylimidazolium chloride) as functional monomer, and MCM-48 as sacrificial support. Factors that affected adsorption, such as type of template and porogen, mole ratio of template-functional monomer-cross-linker and type of binding solvent, were optimized in detail. Multiple strong interactions between SA and ionic liquid in HPDMIPs deduced higher binding capacity (29.75 mg/g), imprinting factor (5.61) and selectivity than any previously reported MIPs by traditional or surface imprinting technology. The large surface area (543.9 m(2)/g) with hollow porous structure resulted in faster kinetic binding (25 min). The equilibrium data fitted well to Freundlich equation and the adsorption process could be described by pseudo-second order model. Finally, HPDMIPs were successfully applied to selectively extract and enrich SA from Actinidia chinensis with a relatively high recovery (84.6-94.5%). (C) 2016 Elsevier B.V. All rights reserved.
机译:在水杨酸(SA)中强的分子内氢键的存在削弱了其与功能性单体的分子间氢键,然后是制造分子印迹聚合物(MIPS)的攻击作用,以具有高容量和良好的选择性。这里,使用苯甲酸(BA)作为虚设模板,离子液体(即1-乙烯基-3-甲基咪唑鎓氯化物)作为功能性单体,以及MCM-48作为牺牲载体的制备中空多孔虚设MIPS(HPDMIPS)。详细地,优化了影响吸附的因素,例如模板和致孔剂,模板官能单体 - 交联剂和粘合溶剂的型摩尔比。 HPDMIPS中SA和离子液体之间的多重相互作用推导出较高的结合能力(29.75mg / g),印迹因子(5.61)和比通过传统或表面积印刷技术的任何先前报道的MIPS的选择性。具有中空多孔结构的大表面积(543.9μm(2)/ g)导致速度更快的动力学结合(25分钟)。可以通过伪二次阶模型描述对Freundlich方程的平衡数据和吸附过程。最后,成功地应用HPDMIPS以选择性地提取和富含猕猴桃中的CHES,恢复相对较高(84.6-94.5%)。 (c)2016 Elsevier B.v.保留所有权利。

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