ABSTRACTThe copolymerization between TEOS (tetraethoxysilane) and silane derivatives was promoted by the application of high power ultrasound to the precursor liquid mixtures in the same way as in the classical sol-gel method. The specific organic precursor was selected from the silanol-terminated polymer family with different molecular functionality and the inorganic precursor was from the silicon alkoxide family. Ultrasound, through the acoustic cavitation process, influences the formation of a very fine distribution of silica particles and avoids cyclidation of the polymer, thus favoring copolymerization with the inorganic particles and leading to the formation of a highly porous and rubber-like solid aerogel. Creep compliance curves, corresponding to the time-dependent depth response to a step load, are imprint site dependent, with pore, soft and stiff sites discerned. In all cases, an instantaneous elastic deformation is apparent. For longer test times, depending on the imprint sites, elastic deformation and newtonian flow produce the rise and fall of the creep curve. Linear parts of the curve on a log-log scale indicate potential growth with small exponents for the creep compliance level. Isochrones stress-strain diagrams show a superlinear trend and an increase with time, which reveals the nonlinear viscoelasticity of these hybrid aerogels. The elasto-plastic response to creep can be tuned by the molecular functionality of the different silane derivatives studied.