Abstract

The silica aerogels were synthesized by sol–gel method via ambient pressure drying. Tetraethyl orthosilicate (TEOS) was used as a main silica source, methyltriethoxysilane (MTES) as a co-precursor silica source and (3-Glycidoxypropyl)trimethoxysilane (GPTMS) as a silane coupling agent. The silica aerogels obtained were further undergoing cross-linking epoxy from GPTMS with amine from diethylenetriamine (DETA) which played a dual role of base catalyst and reagent. The cumulative volumes for open pores of the cross-linked aerogels were evaluated to be 1.4cm3/g. The Young's modulus and maximum compression strength were 25.4MPa and 6.17MPa, respectively. The addition of MTES accelerated the solvent exchange of alcohol within the pores with n-hexane and reduced the shrinkage of aerogels network during the ambient pressure drying. The formation of organic network enhanced the strength of the cross-linked aerogels to prevent the crack generation and the subsequent failure of the monolith during the ambient drying, therefore, protected the nanoporous structure of aerogels.

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