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通过微乳液聚合制备的磁性聚合物纳米球的表面改性与表征

Surface modification and characterization of magnetic polymer nanospheres prepared by miniemulsion polymerization.

作者信息

Liu Xianqiao, Guan Yueping, Ma Zhiya, Liu Huizhou

机构信息

Laboratory of Separation Science and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, P.O. Box 353, Beijing 100080, People's Republic of China.

出版信息

Langmuir. 2004 Nov 9;20(23):10278-82. doi: 10.1021/la0491908.

Abstract

A novel and effective protocol for the surface modification and quantitative characterization of magnetic polymeric nanospheres prepared by miniemulsion polymerization is reported. Composite nanospheres consisting of polymer-coated iron oxide nanoparticles were prepared by the miniemulsion polymerization of methyl methacrylate and divinylbenzene in the presence of magnetic fluid. Surface modification reaction of the magnetic polymer with poly(ethylene glycol) (PEG) was employed to obtain a hydrophilic hydroxyl-group-functionalized magnetic nanospheres. An affinity dye, Cibacron blue F3G-A (CB), was then coupled covalently to prepare a magnetic nonporous affinity adsorbent. The morphology and magnetic property of the polymer nanospheres obtained were examined by transmission electron microscopy and a vibrating sample magnetometer. The contents of surface groups modified were quantitatively measured by using diffusive reflectance Fourier transform infrared spectroscopy on the basis of a linear relationship between the intensity ratio of IC-O-C/IC=O and the content of PEG. X-ray photoelectron spectroscopy (XPS) was used to examine the surface of magnetic nanospheres. It was confirmed by the comparison of XPS spectra of both dye-coated and uncoated magnetic nanospheres to which the CB ligand was coupled, and the surface of the PEG-modified nanospheres had an exact 3:7 atomic ratio of sulfur to nitrogen.

摘要

报道了一种用于通过微乳液聚合制备的磁性聚合物纳米球的表面改性和定量表征的新颖且有效的方案。在磁流体存在下,通过甲基丙烯酸甲酯和二乙烯基苯的微乳液聚合制备了由聚合物包覆的氧化铁纳米颗粒组成的复合纳米球。采用磁性聚合物与聚乙二醇(PEG)的表面改性反应来获得亲水性羟基官能化的磁性纳米球。然后将亲和染料汽巴克隆蓝F3G - A(CB)共价偶联以制备磁性无孔亲和吸附剂。通过透射电子显微镜和振动样品磁强计对所得聚合物纳米球的形态和磁性进行了研究。基于C - O - C / C = O的强度比与PEG含量之间的线性关系,使用漫反射傅里叶变换红外光谱法定量测量了改性表面基团的含量。采用X射线光电子能谱(XPS)对磁性纳米球的表面进行了检测。通过比较偶联了CB配体的染料包覆和未包覆磁性纳米球的XPS光谱证实,PEG改性纳米球的表面硫与氮的原子比恰好为3:7。

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