Poly(lactic acid) (PLA) has attracted much attention and shows promising applications in numerous fields. In this study, PLA was plasticized using bio-based castor oil derivatives - hydrogenated castor oil (HCO) and castor oil glycidyl ether (COGE). These eco-blends were measured using a Fourier transform infrared spectrometer, a scanning electron microscope, a contact angle test, rheology, a differential scanning calorimeter, thermogravimetry, polarized optical microscopy, and a tensile test, respectively. The findings show that a core-shell morphology of COGE-HCO encapsulation is formed in PLA matrix, and the hydrogen bonding interaction and ring-opening chemical reaction among functional groups of the components greatly improve the compatibility, ductility, cold crystallization ability, and thermostability of the eco-blends, but the melt crystallization ability is hindered. The incorporation of HCO improves the hydrophobicity and oleophobicity of the eco-blends. Due to the combined effect of HCO and COGE, the melt viscosity reduces, and the Newtonian behavior enhances; the nucleation density and spherulitic growth of PLA increase. The strain at break of the PLA/HCO/COGE (90/7.5/2.5) blend reached 221%, which is 22.6 times higher than that of the neat PLA. These eco-blends present appropriate rheological, thermal, and mechanical properties, showing application scenarios in biodegradable packaging and disposable appliances.

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.

The growing focus on sustainability, eco-friendly technologies, decarbonization, and reducing carbon footprints shapes current industry challenges. This article reviews the potential of cinnamon as a bio-additive for polymer stabilization in packaging. Samples were prepared from ethylene-norbornene copolymer (Topas), a cyclic olefin copolymer known for purity, transparency, and low gas permeability, and poly(lactic acid) (PLA), a bio-based alternative to petroleum plastics. Cinnamon powder was added in 0.5, 1.0, and 1.5 wt%. After solar and thermo-oxidative aging, hydrophobicity, chemical composition, mechanical, and color properties were analyzed. Results showed higher hydrophobicity and resistance to hydrolytic degradation due to reduced water penetration. PLA, normally brittle, became more flexible, with 0.5 wt% cinnamon showing optimal performance after 100 h of solar aging, similar to Topas composites. Overall, PLA and cyclic olefin copolymer (COC) films with cinnamon improved durability, extended food shelf life, and acted as natural color indicators of material aging.

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.

Bacterial cellulose (BC) is an eco-friendly biopolymer with outstanding structural and functional properties, offering promising applications in sustainable packaging and bio-based materials. In this study, we demonstrate the feasibility of producing BC via spontaneous fermentation, using grape pomace supplemented with sucrose as the sole carbon source, nutrient substrate, and microbial inoculum, without the addition of commercial strains or nitrogen supplements. Fermentation was conducted under static conditions, yielding biofilms with stable structural characteristics and BC production of up to 14.1 g/L, thereby confirming the efficiency of this low-cost, residue-based process. The films obtained exhibited well-organized polymeric networks, with thermal stability in the range of T_g ≈ 159–266 °C and mechanical resistance comparable to or higher than conventional biopolymers. Characterization confirmed reproducible chemical profiles, thermal stability, and measurable variation in mechanical performance, with a tensile strength ranging from 0.0001 to 105 MPa and an elongation at break of 15±5%. The process highlights a resource-efficient and sustainable pathway, adaptable to rural contexts and aligned with circular economic principles. While minor variations among replicates reflected the intrinsic variability of biological systems, mean values and standard deviations demonstrated reproducible physicochemical and mechanical properties. These findings demonstrate that BC derived from agro-industrial residues can be produced under simple, low-input conditions, opening opportunities for scalable valorization in functional and sustainable materials.