Polymers

Fog water collectors (FWCs) present a sustainable solution for arid regions where fog is a primary water source. To improve their efficiency, we developed a durable and high-performance mesh composed of electrospun hydrophobic thermoplastic polyurethane (TPU) fibers combined with hydrophilic cellulose acetate (CA) microbeads. This hybrid design represents a novel biomimetic strategy, mimicking natural fog-harvesting mechanisms by optimizing wetting and drainage. Despite the significant reduction in average fiber diameter, the TPU-CA mesh maintained mechanical strength close to 1 MPa, comparable to pristine TPU. The introduction of hydrophilic domains into a hydrophobic fibrous network is a unique architectural approach that enhanced fog collection performance, achieving a high water harvesting rate of 127 ± 12 mg·cm⁻²·h⁻¹. Remarkably, although the mesh remained predominantly hydrophobic, droplets shed completely from its vertical surface, exhibiting near-zero contact angle hysteresis. This synergistic wetting concept enables performance unattainable with conventional single-wettability meshes. Compared to single-material meshes, the TPU-CA hybrid showed nearly double the water collection efficiency. The innovative interplay between surface chemistry, microscale heterogeneity, and mechanical robustness is key to maximizing water capture and transport, offering a promising path for scalable, efficient FWCs in poor water-stressed regions.

This study investigated the properties of red algae (RA) biocomposite films reinforced with natural sisal fibers and plasticized with glycerol. The polymer was extracted from locally sourced red seaweed and combined sisal fibers at varying fiber loadings (0–45 wt%) using the doctor blading technique. Composite films were analyzed using a variety of methods to evaluate the chemical composition, thermal behavior and mechanical performance. Infrared spectroscopy confirmed the presence of kappa-carrageenan as the dominant polysaccharide in the RA matrix, whereas elemental analysis verified the dilution of sulfur content and enrichment of carbon with increasing fiber incorporation. Thermal stability increased with fiber loading, peaking at 30 wt% sisal fiber before decreasing slightly at 45 wt% due to poor fiber dispersion. Mechanical testing demonstrated an optimal balance between strength and flexibility at 30 wt% sisal fiber, with a 37% increase in strength compared to the pure RA film. Overall, the findings demonstrate that sisal fiber reinforcement enhances the structural integrity and stability of RA-based films, supporting their potential as biodegradable alternatives to petroleum-based plastics.

This study aims to optimize the physical, mechanical, and thermal properties of 100% Ground Granulated Blast Furnace Slag (GGBFS) based geopolymer wood-composite panels. Pine fibers were utilized as the primary reinforcement matrix, while glass and hemp fibers were introduced as secondary reinforcements at varying proportions (3%, 6%, 9% by weight). The research investigated the effects of fiber pretreatments (hot water vs. 1% NaOH) and reinforcement hybridization. Results indicate that GGBFS successfully geopolymerized, forming a hybrid N-A-S-H and C-A-S-H gel network. Quantitative analysis revealed that 9% glass fiber reinforcement yielded the highest mechanical performance, achieving a Modulus of Rupture (MOR) of 10.05 N/mm² and Internal Bond (IB) strength of 1.32 N/mm², alongside superior water resistance (1.0% Thickness Swelling). Conversely, while hemp fiber inclusion reduced mechanical strength (MOR: 5.77 N/mm² at 9%), it significantly enhanced thermal insulation, reducing thermal conductivity to 0.10 W/m·K. It was observed that aggressive NaOH pretreatment caused alkali-induced degradation of pine fibers, negatively impacting the composite’s integrity compared to hot water treatment. This study demonstrates the feasibility of tailoring 100% slag-based geopolymer composites for either structural (glass-reinforced) or insulating (hemp-reinforced) applications using industrial by-products.