Despite their high porosity and wide applicability, silica xerogels face mechanical strength limitations for high-performance applications. This study presents an ambient-pressure sol-gel strategy utilizing calcium-glycerol synergy to produce robust xerogels with enhanced properties. Physicochemical analyses reveal that controlled Ca2+ incorporation (optimal at 6 wt.%) accelerates gelation kinetics while establishing a hybrid network through ionic complexation and hydrogen bonding. The resulting xerogels achieve exceptional compressive strength (30.8 MPa) while maintaining uniform mesoporosity (50–90 nm pore size). Remarkably, the as-prepared silica xerogels demonstrate outstanding thermal insulation, maintaining a 220 °C temperature differential in 300 °C environments. These results prove that the ambient-pressure sol-gel strategy utilizing calcium-glycerol synergy can enhance the mechanical performance and thermal insulation performance of silica xerogels with the dual actions of Ca2+-induced network reinforcement via silanol coordination and glycerol-mediated stress relief during ambient drying. Overall, this work can offer a scalable, energy-efficient approach to produce high-performance silica xerogels with huge potential in building envelopes and aerospace systems.
The interfacial incompatibility and insufficient mechanical performance of polylactic acid (PLA)/cellulose composites have severely restricted their practical applications. To address the critical issue of interfacial incompatibility in PLA/cellulose composites, this work developed a novel strategy employing rosin emulsion for blending modification of microcrystalline cellulose (MCC), followed by a one-step extrusion process to fabricate PLA composites. The corresponding analyses confirmed that the rosin has been successfully added to MCC surfaces, forming the hydrophobic interface while maintaining the cellulose I crystalline structure. Subsequently, rosin emulsion-modified MCC (MCC-R) reinforced PLA (PLA/MCC-R) composites were fabricated via twin-screw extrusion at varying MCC-R contents. The testing results illustrated that the introduction of 8 wt% MCC-R can enhance the mechanical properties of PLA/MCC-R composites with the flexural strength (125.5 MPa), tensile strength (30.8 MPa), Young’s modulus (1.19 GPa), and elongation at break (3.07%), which was attributed to enhanced filler dispersion and interfacial stress transfer. Overall, this work established a facile and sustainable strategy for developing multifunctional PLA composites with engineered interfaces and mechanical robustness, which is vital for practical application. The as-prepared PLA composites show promising application prospects in environmentally friendly packaging, biodegradable disposable products, and lightweight structural components.