Materials Science and Engineering, University of Arizona, Tucson, Arizona 85721-0012, USA.
ACS Appl Mater Interfaces. 2009 Jul;1(7):1364-9. doi: 10.1021/am900240h.
Strong polymer-silica aerogel composites were prepared by chemical vapor deposition of cyanoacrylate monomers onto amine-modified aerogels. Amine-modified silica aerogels were prepared by copolymerizing small amounts of (aminopropyl)triethoxysilane with tetraethoxysilane. After silation of the aminated gels with hexamethyldisilazane, they were dried as aerogels using supercritical carbon dioxide processing. The resulting aerogels had only the amine groups as initiators for the cyanoacrylate polymerizations, resulting in cyanoacrylate macromolecules that were higher in molecular weight than those observed with unmodified silica and that were covalently attached to the silica surface. Starting with aminated silica aerogels that were 0.075 g/cm(3) density, composite aerogels were made with densities up to 0.220 g/cm(3) and up to 31 times stronger (flexural strength) than the precursor aerogel and about 2.3 times stronger than an unmodified silica aerogel of the same density.
通过将氰基丙烯酸酯单体化学气相沉积到胺改性气凝胶上,制备了强聚合物-硅气凝胶复合材料。胺改性硅气凝胶是通过少量(氨丙基)三乙氧基硅烷与四乙氧基硅烷共聚制备的。在用六甲基二硅氮烷硅烷化胺化凝胶后,它们使用超临界二氧化碳处理作为气凝胶干燥。所得气凝胶仅具有胺基团作为氰基丙烯酸酯聚合的引发剂,导致氰基丙烯酸酯大分子的分子量高于用未改性的硅观察到的分子量,并且共价连接到硅表面。从密度为 0.075 g/cm(3)的胺化硅气凝胶开始,制备了密度高达 0.220 g/cm(3)的复合气凝胶,其弯曲强度比前体气凝胶高 31 倍(弯曲强度),比相同密度的未改性硅气凝胶强约 2.3 倍。