Recently, the goal of space exploration has shifted from the incognito of the solar system to the Moon. Concepts like human permanence on the Moon and thermal protective structures made with ISRU (in situ resource utilization) of raw materials have started to be implemented. By limiting the need to launch supplies from the Earth, the paradigm of spaceflight is changed, privileging the vanguard of the utilisation of resources in situ. Still, the main challenges of surviving the radiation dose and the cryogenic temperatures of the lunar night remain. Recent studies have demonstrated how innovative composite materials can help reduce the temperature stress on exploration vehicles. This research presents the material properties of aerogel insulating materials combined with LHS (lunar highlands simulant) regolith obtained by freeze frying. Organic-based aerogels with different percentages of LHS have been analysed in terms of material, morphology, and thermal properties.

The prediction of heat transport in aerogel composite materials remains a challenge due to the complex interplay between filler morphology, connectivity, and dispersion. In this work, the Percolation Effective-Medium Approximation (P-EMA) is employed as a unifying framework to describe thermal transport across a wide range of filler geometries. By introducing a scaling factor, P-EMA successfully captures the transition between effective medium behaviour and percolation-dominated regimes. Fibre-like fillers are characterized by scaling factors well below unity, reflecting their tendency to form conductive networks at low concentrations, while spherical fillers exhibit values slightly above unity, in line with the well-known effective medium approximations. This approach demonstrates the ability of P-EMA to integrate percolating behaviour with effective medium predictions in cases of weak filler connectivity and relatively homogeneous dispersions.

Hydrogels with protein–polysaccharide combinations are widely used in the field of tissue engineering, as they can mimic the in vivo environments of native tissues, specifically the extracellular matrix (ECM). However, achieving stability and mechanical properties comparable to those of tissues by employing natural polymers remains a challenge due to their weak structural characteristics. In this work, we optimized the fabrication strategy of a hydrogel composite, comprising gelatin and sodium alginate (Gel-SA), by varying reaction parameters. Magnetite (Fe₃O₄) nanoparticles were incorporated to enhance the mechanical stability and structural integrity of the scaffold. The changes in hydrogel stiffness and viscoelastic properties due to variations in polymer mixing ratio, crosslinking time, and heating cycle, both before and after nanoparticle incorporation, were compared. FTIR spectra of crosslinked hydrogels confirmed physical interactions of Gel-SA, metal coordination bonds of alginate with Ca²⁺, and magnetite nanoparticles. Tensile and rheology tests confirmed that even at low magnetite concentration, the Gel-SA-Fe₃O₄ hydrogel exhibits mechanical properties comparable to soft tissues. This work has demonstrated enhanced resilience of magnetite-incorporated Gel-SA hydrogels during the heating cycle, compared to Gel-SA gel, as thermal stability is a significant concern for hydrogels containing gelatin. The interactions of thermoreversible gelatin, anionic alginate, and nanoparticles result in dynamic hydrogels, facilitating their use as viscoelastic acellular matrices.