Papers by Author: Juan Primera

Abstract: This study introduces a method for a computational calculus of the Elasticity Modulus (E) of simulated porous media using the Monte Carlo technique. The porous media of known geometry is simulated as an elastic network of central forces, to which a known deformation is applied. The minimum strain energy is calculated applying the Monte Carlo technique. The Elasticity Modulus is obtained from the theoretical relations between the elastic energy of a system and its deformation. The computational method is validated by applying it in systems of known analytic solution and over porous media generated through aggregation algorithm in two dimensions i.e. Random Sequential Aggregation and Diffusion Limited Cluster-Cluster Aggregation (RSA and DLCA respectively). The latter used to simulate the structure of silica aerogels. As for the range of concentrations studied for the DLCA and RSA systems, it was found that the elasticity modulus E decreases as the porosity of the system increases, being the E value higher for the DLCA system with respect to RSA. The method used is able to differentiate the elastic properties for two different aggregation models. Being E values different for equal porosities, the coordination number (Z) was the geometric parameter that best explains the behavior of the Elasticity Modulus.

Abstract: Silica aerogels have been studied with the objective of understanding the mechanical behavior of these extremely porous (pore volume higher than 85%) glassy materials. Elastic and plastic behaviors are investigated using Hg porosimetry. Because of the peculiar structure of these materials, Hg liquid cannot enter their porous network and consequently induces an isostatic pressure. Due to the high compliance of the solid network, under isostatic pressure aerogels display an irreversible shrinkage caused by plastic deformation. The magnitude of the plastic shrinkage and the increase of the associated mechanical properties depend on the different parameters (porosity, elastic properties and structural features). The structural features are followed by X Rays scattering. The irreversible compaction can be explained by siloxane bond formation between clusters constituting the porous materials, retaining the strained structure. The pore collapse mechanism is favored by the large pores structure and loose cluster structure (low fractal dimension). This densification process could offer a new way to synthesize porous glasses at room temperature.

Abstract: Different sets of silica aerogels (classical aerogels, partially dense aerogels, composite aerogels) have been studied in the objective to understand the mechanical behaviour of these extremely porous solids. The mechanical behaviour of xerogels and aerogels is generally described in terms of brittle and elastic materials, like glasses or ceramics. The main difference compared to silica glass is the order of magnitude of the elastic and rupture modulus which are 104 times lower. However, if this analogy is pertinent when gels are under a tension stress (bending test) they exhibit a more complicated response when the structure is submitted to a compressive stress. The network is linearly elastic under small strains, then exhibits yield followed by densification and plastic hardening. As a consequence of the plastic shrinkage it is possible to compact and stiffen the gel at room temperature. These opposite behaviours (brittle and plastic) are surprisingly related to the same kinds of gel features: pore volume silanol content and the pore size. Both elastic modulus and plastic shrinkage depend strongly on the volume fraction of pores and on the condensation reaction between silanols. On the mechanical point of view (rupture modulus and toughness), it is shown that pores size plays likely an important role. Pores can be considered as flaws in the terms of fracture mechanics and the flaw size, calculated from rupture strength and toughness is related to the pore size distribution.