Department of Chemistry, University of California, Riverside, California 92521, USA.
Langmuir. 2011 Apr 5;27(7):3372-80. doi: 10.1021/la1048216. Epub 2011 Feb 28.
Mercapto-silica spheres with controllable size from ∼150 nm to ∼3.5 μm and narrow size distribution have been prepared in water using a one-pot synthesis, in which 3-mercaptopropyltrimethoxysilane (MPS) was used as the sole silica source and ammonia as the base catalyst. The hydrolysis of MPS at the early stage of the reaction produces amphiphilic silicate species which initiate the self-emulsification of the system and lead to the formation of oil-in-water emulsion droplets. Further hydrolysis and condensation promote the nucleation and growth of the mercapto-silica spheres inside the emulsion droplets. These mercapto-silica spheres are both structurally and functionally different from typical silica particles prepared from silicon alkoxides. Understanding the formation mechanism allows systematic tuning of the size of mercapto-silica spheres in a wide range by changing the amount of precursor, the concentration of ammonia, the amount of additional surfactants, and the reaction time. We find that Ostwald ripening may occur quickly if the spheres are kept in the reaction solution, resulting in significant broadening of the particle size distribution. In order to obtain uniform and stable samples, it is important to quench the growth of the mercapto-silica spheres by separating them from the original reaction mixture and then storing them in solvents that can prevent further ripening.
已经在水中使用一锅合成法制备了具有可控尺寸(约 150nm 至约 3.5μm)和窄尺寸分布的巯基-硅球,其中 3-巯丙基三甲氧基硅烷(MPS)用作唯一的硅源,氨用作碱催化剂。反应早期 MPS 的水解产生两亲性硅酸盐物种,引发体系的自乳化,并导致水包油乳液液滴的形成。进一步的水解和缩合促进了在乳液液滴内的巯基-硅球的成核和生长。这些巯基-硅球在结构和功能上与典型的硅烷醇盐制备的二氧化硅颗粒不同。了解形成机理可以通过改变前体的量、氨的浓度、额外表面活性剂的量和反应时间来系统地调节巯基-硅球的尺寸在很宽的范围内。我们发现,如果将球保留在反应溶液中,奥斯特瓦尔德熟化可能会很快发生,导致粒径分布显著变宽。为了获得均匀稳定的样品,通过将它们与原始反应混合物分离并用可以防止进一步熟化的溶剂储存来阻止巯基-硅球的生长是很重要的。