Search

As naturally derived material, cellulose aerogels have excellent thermal insulation properties due to their unique high porosity and three-dimensional mesoporous structure. However, its hydrophilic properties limit its application in the field of building insulation. Here, we propose a method to prepare high hydrophobicity by adopting the sol-gel method and chemical vapor reaction strategy using cellulose acetate type II as raw material and 2,4-toluene diisocyanate as the cross-linking agent. Thermal properties of cellulose acetate aerogels (CAAs) were measured, where pyridine was the catalyst, acetone was the solvent, and perfluorodecyltriethoxysilane (PFDS), hexamethyldisilazane (HMDS), and methyltriethoxysilane (MTES) were used as hydrophobic agents (by process hydrophobic test). Compared with MTES-modified cellulose acetate aerogels (M-CAAs) and HMDS (H-CAAs)-modified cellulose acetate aerogels, PFDS-modified (P-CAAs) cellulose acetate aerogels are the most hydrophobic. By implementing hydrophobic modification of PFDS both inside and outside the structure of cellulose acetate aerogels, the water contact angle can reach up to 136°, strongly demonstrating the potential of PFDS as a hydrophobic agent. The results show that the thermal conductivity and compressive strength of cellulose acetate aerogel with the best hydrophobic properties are 0.035 W m−1 K−1 at normal pressure and 0.39 MPa at 3% strain, respectively. This work shows that the highly hydrophobic cellulose acetate aerogel has potential as a waterproof material in the field of building thermal-insulation materials. [ABSTRACT FROM AUTHOR]

• A boric acid-regulated sol–gel transition strategy is used to achieve modulation of the morphology. • Ethanol is employed as a green solvent for the preparation of boron-doped polybenzoxazine (BPBz) aerogels. • The introduction of boric acid provides multifunctional properties to BPBz aerogels. • The BPBz aerogels exhibit intrinsic and alterable wettability that correlates with their morphologies. Polybenzoxazine aerogels have gained widespread attention in recent years, but the prevalent use of hazardous solvents in the preparation process has severely impeded their further development and promotion for practical applications. Herein, using ethanol as a solvent, a strategy of boric acid-induced microstructure regulation is proposed to construct boron-doped polybenzoxazine (BPBz) aerogels, which provides a feasible approach to overcome the above situation. The introduction of boric acid enhances the backbone strength by forming intermolecular bridged structures between PBz chains and allows the use of ambient pressure drying. The resulting BPBz aerogel demonstrates high stiffness (specific modulus up to 255.97 kN·m·kg−1), low bulk density (0.203 g·cm−3), and low thermal conductivity (0.043 W·m−1·K−1), exhibiting excellent fire resistance when exposed to a 1200 °C flame (the self-extinguishing interval less than 1 s). More interestingly, the aerogel demonstrates intrinsic and tunable wettability that correlates with the morphology. Combining the environmentally friendly preparation strategy and these advantages, BPBz aerogels hold promise for thermal management and fire protection applications in energy-saving construction and other harsh conditions. [ABSTRACT FROM AUTHOR]

Polybenzoxazine (PBO) aerogels with low densities and low thermal conductivities are prepared from Bisphenol A (BPA) benzoxazine monomers by ring‐opened polymerisation using HCl as a catalyser at 10 °C. The obtained PBO aerogels have cross‐linked and 3D network structures with the densities ranging from 0.084 to 0.526 g cm−3. The thermal conductivities under different pressures (3–105 Pa, air) and different atmospheres (N2, Ar, and CO2, 105 Pa) are investigated. The thermal conductivities are in the range of 0.0335–0.0652 W m K−1 under ambient pressure and 0.0098–0.0571 W m K−1 at 3 Pa. The thermal transfer mechanism under different gas pressures is analyzed with increasing pressure. Under different atmospheres, the thermal conductivities decrease as the molecular weight of the gas increases. Compared with the traditional organic foam insulating materials of phenolic foam, polyurethane and polystyrene, which have similar apparent densities, PBO aerogels exhibit lower thermal conductivity of 0.0335 W m K−1 than that of traditional organic foam at room temperature. [ABSTRACT FROM AUTHOR]

Silica aerogels with different particle size were prepared by monodispersed silica sol for the first time. The properties of the silica aerogels under normal and high temperature were systematically studied. Among the four different particle size aerogels, the SA-2 sample consisted of 20.31 ± 1.21 nm particles with narrow size distribution had high temperature resistance and low thermal conductivity. Compared with the traditional acid-base two-step prepared silica aerogels, the monodisperse silica aerogels can significantly increase the temperature resistance while maintaining a low thermal conductivity (0.02723 W·m−1·K−1). The sturdy skeleton structure formed by the interconnection of large particles can effectively inhibit the viscous flow between aerogel particles and avoid pore collapse caused by skeleton failure which can maintain a stable structure until 900 °C and retain a relatively complete structure at 1000 °C with only about 35% volume shrinkage after 2 h heat treatment. At 1100 °C, the viscous flow between aerogel particles and pore collapse cannot be effectively suppressed, and the pure silica aerogels can only be used during a short period at 1100 °C. The results will be meaningful for the design of super thermal insulation materials with high temperature resistance and low thermal conductivity. Unlabelled Image • SiO 2 aerogels with high temperature resistance are prepared by controllable particle size monodispersed silica sol. • Thermal conductivity of SiO 2 aerogels is as low as 0.02723 W·m−1·K−1 despite forming large particle structure. • The aerogel large particle skeleton structure can inhibit the viscous flow between aerogel particles. • Pore collapse caused by skeleton failure can be obviously inhibited depending on formed sturdy skeletons. [ABSTRACT FROM AUTHOR]