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用于牙科纳米复合材料制备的二氧化硅纳米颗粒的尺寸控制及其表面处理

Size control of silica nanoparticles and their surface treatment for fabrication of dental nanocomposites.

作者信息

Kim J W, Kim L U, Kim C K

机构信息

School of Chemical Engineering and Materials Science, Chung-Ang University, 221 Huksuk-dong, Dongjak-gu, Seoul, 156-756, Korea.

出版信息

Biomacromolecules. 2007 Jan;8(1):215-22. doi: 10.1021/bm060560b.

Abstract

Nearly monodispersed silica nanoparticles having a controlled size from 5 to 450 nm were synthesized via a sol-gel process, and then the optimum conditions for the surface treatment of the synthesized silica nanoparticles with a silane coupling agent (i.e., 3-methacryloxypropyltrimethoxysilane (gamma-MPS)) were explored to produce dental composites exhibiting enhanced adhesion and dispersion of silica nanoparticles in the resin matrix. The particle size was increased by increasing amounts of the catalyst (NH4OH) and silica precursor (tetraethylorthosilicate, TEOS) and by decreasing the amount of water in the reaction mixtures regardless of solvents used for the synthesis. The particle size prepared by using ethanol as a solvent was significantly larger than that prepared by using methanol as a solvent when the composition of the reaction mixture was fixed. The nanosized particles in the 5-25 nm range were aggregated. The amount of grafted gamma-MPS on the surface of the synthesized silica nanoparticles was dependent on the composition of the reaction mixture when an excess amount of gamma-MPS was used. When surface treatment was performed at optimum conditions found here, the amount of the grafted gamma-MPS per unit surface area of the silica nanoparticles was nearly the same regardless of the particle size. Dispersion of the silica particles in the resin matrix and interfacial adhesion between silica particles and resin matrix were enhanced when surface treated silica nanoparticles were used for preparing dental nanocomposites.

摘要

通过溶胶 - 凝胶法合成了尺寸可控在5至450nm的近单分散二氧化硅纳米颗粒,然后探索了用硅烷偶联剂(即3 - 甲基丙烯酰氧基丙基三甲氧基硅烷(γ - MPS))对合成的二氧化硅纳米颗粒进行表面处理的最佳条件,以制备在树脂基体中二氧化硅纳米颗粒具有增强的附着力和分散性的牙科复合材料。无论合成中使用何种溶剂,通过增加催化剂(NH4OH)和二氧化硅前驱体(正硅酸四乙酯,TEOS)的用量以及减少反应混合物中的水量,粒径都会增大。当反应混合物的组成固定时,以乙醇为溶剂制备的粒径明显大于以甲醇为溶剂制备的粒径。5 - 25nm范围内的纳米颗粒发生了团聚。当使用过量的γ - MPS时,合成的二氧化硅纳米颗粒表面接枝的γ - MPS的量取决于反应混合物的组成。当在此处发现的最佳条件下进行表面处理时,无论粒径大小,二氧化硅纳米颗粒每单位表面积接枝的γ - MPS的量几乎相同。当使用表面处理的二氧化硅纳米颗粒制备牙科纳米复合材料时,二氧化硅颗粒在树脂基体中的分散性以及二氧化硅颗粒与树脂基体之间的界面附着力得到了增强。

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