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Modification of mesoporous silica with molecular imprinting technology: A facile strategy for achieving rapid and specific adsorption

机译:用分子印迹技术改性介孔二氧化硅:实现快速和特异性吸附的简便策略

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摘要

In order to improve the diffusion kinetics of molecularly imprinted materials (MIMs), applying imprinting technology to mesoporous materials is a promising strategy. In the present study, an imprinting approach based on the combination of mesoporous silica materials and molecular imprinting technology is reported. Molecularly imprinted material (MIM) for 2,4-dichlorophenoxyacetic acid (2,4-D) was prepared by using 2,4-D as the template molecule, alkyne-modified beta-cyclodextrin and propargyl amine as the combinatorial functional monomers and SBA-15 as the supporter. The functional monomers were anchored to the azide-modified SBA-15 by azide-alkyne Click reaction. The synthesized MIM was characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), elemental analysis (EA), thermal gravimetric analysis (TGA), low-angle X-ray diffraction (XRD) and N-2 adsorption-desorption analysis. The interactions between template and functional monomers were studied by proton NMR analysis and UV-vis experiments. The results of the equilibrium binding experiments and selective tests showed that the prepared MIM has binding affinity and specificity for a group of analytes which have similar size and shape to those of template. Binding kinetic experiments demonstrated that the present imprinting approach can effectively enhance the mass transfer rate. The solid phase extraction of 2,4-D using MIM as the adsorbent was investigated. The extraction conditions for the processes of loading, washing and eluting were optimized. The recoveries of the molecularly imprinted solid phase extraction (MISPE) column for 2,4-D were 76.3-88.9% with relative standard deviations (RSD) of 3.48-7.64%.
机译:为了改善分子印迹材料(MIM)的扩散动力学,将印迹技术应用于中孔材料是一种有前途的策略。在本研究中,报道了基于介孔二氧化硅材料和分子印迹技术相结合的印迹方法。以2,4-D为模板分子,炔烃修饰的β-环糊精和炔丙基胺为组合功能单体,通过SBA制备2,4-二氯苯氧基乙酸(2,4-D)的分子印迹材料(MIM)。 -15为支持者。通过叠氮化物-炔的Click反应将功能单体锚定到叠氮化物改性的SBA-15上。通过透射电子显微镜(TEM),傅立叶变换红外光谱(FT-IR),元素分析(EA),热重分析(TGA),低角度X射线衍射(XRD)和N-2对合成的MIM进行了表征吸附-解吸分析。通过质子核磁共振分析和紫外可见实验研究了模板与功能单体之间的相互作用。平衡结合实验和选择性测试的结果表明,制备的MIM对一组大小和形状与模板相似的分析物具有结合亲和力和特异性。结合动力学实验表明,目前的印迹方法可以有效地提高传质速率。研究了以MIM为吸附剂的2,4-D固相萃取。优化了上样,洗涤和洗脱过程的提取条件。分子印迹固相萃取(MISPE)色谱柱对2,4-D的回收率为76.3-88.9%,相对标准偏差(RSD)为3.48-7.64%。

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