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氨基丙基功能化硅胶溶胶的制备、纯化和表征。

Preparation, purification, and characterization of aminopropyl-functionalized silica sol.

机构信息

Department of Biological Nanochemistry, Institute of Molecular Pharmacology, Research Centre for Natural Sciences, Hungarian Academy of Sciences (IMP RCNS HAS), Budapest, Hungary.

出版信息

J Colloid Interface Sci. 2013 Jan 15;390(1):34-40. doi: 10.1016/j.jcis.2012.09.025. Epub 2012 Sep 26.

Abstract

A new, simple, and "green" method was developed for the surface modification of 20 nm diameter Stöber silica particles with 3-aminopropyl(diethoxy)methylsilane in ethanol. The bulk polycondensation of the reagent was inhibited and the stability of the sol preserved by adding a small amount of glacial acetic acid after appropriate reaction time. Centrifugation, ultrafiltration, and dialysis were compared in order to choose a convenient purification technique that allows the separation of unreacted silylating agent from the nanoparticles without destabilizing the sol. The exchange of the solvent to acidic water during the purification yielded a stable colloid, as well. Structural and morphological analysis of the obtained aminopropyl silica was performed using transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential measurements, Fourier-transform infrared (FTIR), (13)C and (29)Si MAS nuclear magnetic resonance (NMR) spectroscopies, as well as small angle X-ray scattering (SAXS). Our investigations revealed that the silica nanoparticle surfaces were partially covered with aminopropyl groups, and multilayer adsorption followed by polycondensation of the silylating reagent was successfully avoided. The resulting stable aminopropyl silica sol (ethanolic or aqueous) is suitable for biomedical uses due to its purity.

摘要

一种新的、简单的“绿色”方法被开发用于在乙醇中用 3-氨丙基(二乙氧基)甲基硅烷对 20nm 直径的斯托伯二氧化硅颗粒进行表面改性。通过在适当的反应时间后添加少量冰醋酸,可以抑制试剂的本体缩聚并保持溶胶的稳定性。为了选择一种方便的纯化技术,可以在不破坏溶胶稳定性的情况下将未反应的硅烷化剂与纳米颗粒分离,比较了离心、超滤和透析。纯化过程中将溶剂交换为酸性水也得到了稳定的胶体。使用透射电子显微镜 (TEM)、动态光散射 (DLS) 和zeta 电位测量、傅里叶变换红外 (FTIR)、(13)C 和 (29)Si MAS 核磁共振 (NMR) 光谱以及小角 X 射线散射 (SAXS) 对获得的氨丙基硅进行了结构和形态分析。我们的研究表明,二氧化硅纳米颗粒表面部分被氨丙基基团覆盖,并且成功地避免了多层吸附和硅烷化试剂的缩聚。由于其纯度,所得的稳定氨丙基硅溶胶(乙醇或水)适用于生物医学用途。

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