气凝胶
环境压力
材料科学
比表面积
化学工程
溶剂
介孔材料
体积热力学
傅里叶变换红外光谱
聚合
溶胶凝胶
表面改性
催化作用
复合材料
有机化学
化学
纳米技术
聚合物
热力学
物理
工程类
量子力学
作者
Pradip B. Sarawade,Jong-Kil Kim,Ho-Kun Kim,Hee-Taek Kim
标识
DOI:10.1016/j.apsusc.2007.06.063
摘要
The experimental results on the synthesis of tetraethoxysilane (TEOS)-based silica aerogel with high specific surface area and large pore volume, via ambient pressure drying (APD) route, are reported. The silica aerogels were prepared by the acid–base sol–gel polymerization of TEOS precursor followed by the drying of the alcogels at an ambient pressure. The solvent present in the alcogel (i.e. ethanol) was replaced by a non-polar solvent such as hexane prior to the surface modification step. In order to minimize the drying shrinkage, the surface of the gels was modified using trimethylchlorosilane (TMCS) before the APD. The FTIR spectra of the surface modified aerogels showed Si–CH3 peaks at 2965 and 850 cm−1. The effect of the base catalyst (NH4OH) addition to the sol, at different time intervals (T), on the physical and textural properties of the resulting aerogels has been investigated. It has been observed that the surface area and the cumulative pore volume of the aerogels enhanced considerably from 819 to 1108 m2 g−1 and 2.65 to 4.7 cm3 g−1, respectively with an increase in the T value from 6 to 48 h. Silica aerogels with very low bulk density (0.06 g cm−3), extremely high specific surface area (1108 m2 g−1) and large cumulative pore volume (4.7 cm3 g−1) could be synthesized by drying the alcogels at the ambient pressure. The aerogels were mesoporous solids with the average pore size ranging from 12 to 17 nm. The results have been discussed by taking into consideration the hydrolysis and condensation reactions during the sol–gel polymerization of the TEOS precursor.
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