Polymer composites are widely used in indoor and outdoor applications owing to their high strength-to-weight ratio, corrosion resistance, and design flexibility. However, exposure to environmental factors such as ultraviolet (UV) radiation, humidity, temperature fluctuations, and biological agents significantly affect their long-term durability and performance. In this review, we comprehensively examine the degradation mechanisms of polymer composites under both natural and accelerated weathering, with particular emphasis on degradation mechanisms, characterization techniques, and durability assessment. We critically discuss the fundamental degradation mechanisms, including photo-oxidation, hydrolysis, polymer chain scission, crosslinking and interfacial debonding. We also evaluated accelerated weathering techniques, conducted under standardized testing conditions, for their ability to simulate long-term outdoor exposure within significantly shorter timeframes, by controlling key environmental parameters such as UV radiation, humidity, and temperature. We also examine the influence of reinforcements, including natural fibres, synthetic fibres, and nanofillers, on the weathering resistance of polymer composites. Attention is given to natural fibre–reinforced composites because their inherent hydrophilicity promotes moisture absorption, accelerating degradation and weakening the fibre–matrix interface. Furthermore, we critically evaluate the effects of weathering on the mechanical properties, crystalline structure and barrier performance of polymer composite films, and discuss recent advances in enhancing weather resistance through hybridization, surface modification, and the incorporation of stabilizing additives. Finally, the review highlights the key challenges and future research directions for the development of durable, high-performance, and sustainable polymer composite systems for long-term outdoor applications.

This is an editorial article. It has no abstract.

This is an editorial article. It has no abstract.

This study investigates the structure–property relationships of multi-functional urethane acrylate resins designed as photoreactive binders for UV-curable nail coatings. Four systems were examined: a commercial resin urethane dimethacrylate (UDMA), a bio-based acrylated epoxidized soybean oil (AESO), and two newly synthesized bio-based urethane acrylates derived from 1,3-propanediol (PDO–UA) and eugenol (EUG–UA). Photopolymerization kinetics were analyzed by realtime FTIR, while the properties of the cured coatings were also determined. The mechanical and thermal behavior of selfsupporting polymer films was evaluated by tensile testing and DSC analysis. The UDMA network exhibited the highest crosslink density, reflected in its high modulus (≈0.5 GPa), tensile strength (≈15 MPa), and Tg (≈60°C), making it suitable for use as a top coat. AESO showed moderate stiffness and flexibility, whereas PDO–UA and EUG–UA formed soft, low-Tg (–12 and –17°C) and highly deformable networks typical of elastomeric materials. The combined mechanical and thermal results confirmed that crosslink density strongly governs coating performance and applicability. This study demonstrates that blending UDMA with bio-based oligomers enables the design of sustainable, UV-curable nail lacquers with an optimal balance of hardness, flexibility, and adhesion to the natural nail plate.

We report a green route to Ag–TiO₂ nanocomposites using an Allium tuberosum extract, rich in organosulfur and polyphenolic constituents, as a dual-function biogenic reducer and stabilizer, enabling efficient Ag⁺→Ag⁰ conversion and capping of Ag–TiO₂ without the use of harsh reagents. The nanocomposites are formulated into chitosan-based inks for direct ink writing (DIW) of porous, mechanically robust, reusable membranes (optimal formulation T@5Ag–5ATE–CS) with a homogeneous Ag dispersion. Multiscale characterization (SEM/TEM, XRD, FTIR, UV–vis DRS, EDS mapping) confirms metallic Ag⁰ uniformly decorating TiO₂ and an extended visible-light response attributable to strong localized surface plasmon resonance. Under near-UV/visible irradiation, the membranes decolorize Remazol Midnight Black RGB dye with pseudo-first-order kinetics, yielding k_app up to 5.99·10^–3 min^–1 with R² ≈ 0.99 and outperforming pristine TiO₂. Response surface methodology identifies an optimum at pH 5.67, 28.87 mg·L^–1 dye, and 0.0257 g catalyst, delivering a predicted 96.41% versus experimental 95.07% removal (validation error 1.39%) with excellent model statistics (R² ≈ 0.995). The combined effects of Allium-tuberosum-assisted Ag plasmonics, TiO₂ photocatalysis, and chitosan-enhanced adsorption underpin the high photocatalytic activity and reusability, highlighting a scalable, eco-friendly pathway to printable photocatalytic/antimicrobial membranes for wastewater treatment.