We have discovered that water-insoluble proteins (IM) isolated from whole soy meal (WM) have the capacity to improve the thermal stability of polypropylene (PP) wood composites without negatively impacting mechanical properties. We compared an undiluted composite to composites diluted with 5% by weight of a 3/1 w/w mixture of stearic acid and paraffin wax (SA/wax), 5% by weight IM, 5% by weight WM, 5% by weight of a 50/50 w/w mixture of IM in combination with SA/wax, and 5% by weight WM in combination with SA/wax. Water contact angle (CA) measurements and Fourier transform infrared spectroscopy (FTIR) revealed a synergy between IM and SA/wax, resulting in enhanced surface hydro - phobicity. Thermogravimetric analysis (TGA) showed lower weight loss in composites made with IM up to the onset of the degradation of PP, and reduced rates of lignin degradation, independently of the presence of SA/wax. Dynamic mechanical analysis (DMA) revealed higher modulus and lower viscoelastic loss resulting from the removal of water-soluble soy components from WM. Total reflectance ultraviolet spectroscopy (UV) showed that IM absorbs UV radiation strongly in the UV-B and UV-C regions. Collectively, these findings suggest that IM has the potential to become a multi-purpose additive for use in PP wood composites.

This article is devoted to the study of the degradation of two widely used biodegradable polymers, polylactic acid (PLA) and poly(butylene adipate-co-terephthalate) (PBAT), which are in demand in packaging, medicine, and agriculture. The effect of ultraviolet radiation (UV) at elevated temperatures on polymer ageing was investigated for 24, 120, and 240 h using a specially designed setup. Scanning electron microscopy, Fourier transform infrared spectroscopy, and tensile testing were employed to provide a comprehensive assessment of changes. PLA showed rapid degradation: after 120 h, its surface developed cracks and voids, and at 240 h, it became heavily damaged with cavities. PBAT degraded more gradually: at 240 h, large cracks and cavities were observed. For PLA, early ageing led to a shift and broadening of the carbonyl band, reflecting disorder and ester scission. For PBAT, a decrease in the intensity of the carbonyl shoulder and a slight shift of the main peak at elevated temperature indicated phase redistribution and the formation of new functional groups. Mechanically, PLA exhibited a sharp loss of strength and ductility in the first day of ageing, while PBAT showed greater stability, with slower reductions in stiffness and strength but a strong temperature-dependent decline in elongation. These findings are important for guiding the design of biodegradable polymers with improved durability.

This research presents an eco-friendly approach for extracting chitosan from shrimp shell waste through ultrasound-assisted extraction (UAE) to prepare biocompatible aerogel scaffolds for biomedical applications. The study investigates the influence of various ultrasonic treatment times (10, 20, 30, 40 min) on the yield and structural and physicochemical properties of the extracted chitosan via characterization using Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Among the tested conditions, the 30 min UAE-treated chitosan aerogels showed optimal porosity and structural integrity. Biocompatibility of the aerogels was evaluated, and the results confirmed their non-cytotoxic nature. The bioactivity of the chitosan aerogels was evaluated in terms of their in vitro wound closure ability and antibacterial properties. The aerogels demonstrated a wound closure rate of around 51% after 72 h, significantly higher than the untreated control (37%). In addition, they exhibited clear antibacterial activity against Escherichia coli and Staphylococcus aureus. This sustainable extraction and fabrication method not only adds value to marine waste but also produces functional biomaterials with potential applications in wound healing, tissue engineering, and regenerative medicine, supporting global efforts toward sustainability and circular bioeconomy.

In this work, we have developed a novel absorbent material using chitosan (CS), and further it was structurally modified via reaction with thiocarbaldehyde, forming a Schiff base intermediate. Simultaneously, graphene oxide was functionalized at the C-6 position of CS through an effective esterification process and composited with the incorporation of molybdenum disulfide (MoS₂) nanoparticles to synthesize a hybrid adsorbent material. The resulting material was characterized using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The synthesized adsorbent was subjected to the adsorptive removal of Cu(II) and Cr(VI) ions from dilute solutions. The maximum uptake of 66.66 mg/g for Cu(II) and 76.92 mg/g for Cr(VI) were recorded during the adsorption process, further following pseudo-second-order kinetics adsorptive nature and fitted well with the Langmuir isotherm model. Desorption studies indicated the material’s reusability, and the thermodynamic studies indicated a spontaneity with an endothermic adsorptive nature. These studies highlight the material’s potential as an effective adsorbent as a sustainable approach for efficient environmental remediation.

The growing need for sustainable materials has stimulated research into eco-friendly composites, with biochar emerging as an important reinforcement in polymer matrices. Biochar is a carbon-rich material produced by pyrolyzing organic biomass, offering various benefits over traditional fillers, including sustainability, waste reduction, and carbon sequestration. This study explores the effects of bamboo biochar as a hybrid reinforcement on the properties of polylactic acid (PLA)-rice husk composites. The present hybrid composites are prepared by varying the bamboo biochar from 5–25% and have better mechanical properties than PLA and its composite reinforced with a rice husk filler. The tensile, flexural, and compressive strengths of 51.5, 166.0, and 77.5 MPa are measured for the biochar percentage of 10%, representing increases of 73.1, 150.0, and 58.2% compared to PLA, and 158.2, 98.6, and 31% compared to the PLA composite with rice husk. Higher tensile and flexural moduli of 1.46 and 7.34 GPa are observed for 10 and 15%, respectively. However, the impact strength decreases with higher biochar content due to increased rigidity. The material’s hardness increases at higher biochar content due to enhanced stiffness. Thermal transition and degradation points rise due to increased crystallinity from the biochar reinforcement’s nucleation effect. Additionally, the hydrophobic biochar reinforcement reduces water absorption of PLA composite from 3.2 to 1.6%.