中间相
介孔二氧化硅
纳米颗粒
介孔材料
成核
水解
材料科学
化学工程
醇盐
肺表面活性物质
水溶液
阳离子聚合
疏水二氧化硅
冷凝
介孔有机硅
无机化学
纳米技术
化学
有机化学
高分子化学
催化作用
物理
工程类
热力学
相(物质)
作者
Zhen‐An Qiao,Ling Zhang,Mingyi Guo,Yunling Liu,Qisheng Huo
摘要
The cooperative self-assembly of silica species and cationic surfactant cetyltrimethylammonium chloride (CTA+Cl− or CTAC) and the formation of mesoporous silica nanoparticles occur following the hydrolysis and condensation of silica precursor TEOS in the solution. The particle size can be controlled from ∼25 nm to ∼200 nm by adding suitable additive agents (e.g., inorganic bases, alcohols) which affect the hydrolysis and condensation of silica species. The in situ pH measurement of synthesis system is introduced to investigate the formation process of mesoporous silica nanoparticles. Our results show that a certain acid−base buffer capacity of the reaction mixture in a range of pH 6−10 is essential for the formation of mesoporous silica nanoparticles in the TEOS−CTA+ system. The nucleation and growth process of the nanoparticles can be extended into the self-assembly system of inorganic−surfactant and the formation of mesophase in aqueous media.
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