In this study, rice-husk fiber (RHF) extracted via alkali hydrolysis was used as a reinforcing material (0–10 wt%) in a pectin-sodium alginate (PE/SA) matrix to develop biofilms by the casting method. These biofilms were characterized by using FTIR, XRD, TGA, and DSC. The thickness, moisture content, water solubility, swelling behavior, water-contact angle, water-vapor permeability, optical transparency, and mechanical properties of biofilms were investigated. It was observed that the PE/SA/RHF film loaded with 5% RHF had better visual attributes, and a further increase in reinforcement was not found to be as favorable. The addition of 10 wt% RHF significantly enhanced the thickness from 0.094 to 0.127 mm, water solubility from 49.25 to 56.13%, water-contact angle from 48.4 to 62.6°, and tensile strength from 4.17 to 10.23 MPa. However, decreases in water-vapor permeability from 1.94 × 10−9 to 1.32 × 10−9 g·m−1·Pa−1·s−1 and in elongation at break from 19.24 to 2.87% were observed in the biofilms. Structurally, FTIR confirmed intermolecular hydrogen bonding between components. XRD revealed that the films remained predominantly amorphous, without significant crystalline alterations. Furthermore, thermal stability improved with the addition of RHF. Finally, these PE/SA/RHF composite films may be potential eco-friendly biodegradable packaging candidates for food industry applications.

Composites based on rPE and OPEFB waste are considered sustainable materials. However, their performance is limited by hydrophobic–hydrophilic incompatibility, which weakens interfacial adhesion. This study investigated the atmospheric-pressure air plasma treatment of rPE to enhance its compatibility with OPEFB fibers and evaluated its role as a compatibilizer. Atmospheric plasma treatment for 120 s introduced oxygen-containing groups onto the rPE surface, as evidenced by C-O and OH peaks in the FTIR spectra and the higher O/C ratio in the XPS analysis. Consequently, the water contact angle decreased, reducing the difference in surface tension between rPE and OPEFB from 45.61% to 7.80%. Composites containing 20 wt.% OPEFB were fabricated by varying the proportion of untreated rPE with p-rPE. All p-rPE-based composites exhibited fewer interfacial voids than untreated rPE composites, indicating improved fiber–matrix adhesion. The tensile strength and elastic modulus increased with the p-rPE content, whereas the elongation at break remained higher than that of the untreated composite. Therefore, p-rPE shows potential as a compatibilizer, enabling agricultural and plastic waste value enhancement.

This study presents an efficient, environmentally benign approach for synthesizing chitosan-entrapped titanium dioxide (TiO2) nanocomposites utilizing aqueous orange peel extract playing its role in reduction and stabilization of the nanoparticles and exploring its anticancer activity in vitro. TiO2 nanoparticles were initially synthesized via a modified sol-gel method incorporating the orange peel extract. Subsequently, these nanoparticles were entrapped within a chitosan matrix. The orange peel extract was thoroughly characterized using analysis of phytochemicals present, and Gas Chromatography–Mass Spectrometry (GC–MS) analysis of a reconstructed methanolic extract to identify potential biomolecules responsible for the reduction and capping processes. The synthesized chitosan-entrapped TiO2 nanoparticles were subjected to comprehensive characterization using various analytical techniques, like UV–visible spectroscopy, Dynamic Light Scattering (DLS) and Zeta Potential analysis, X-ray Diffraction (XRD), FTIR, High-Resolution Scanning Electron Microscopy (HR-SEM) and Energy-Dispersive X-ray Spectroscopy (EDAX). An absorption peak was observed at 296 nm, a hydrodynamic diameter of 400 nm, a+ 35.88 mV zeta potential, and an SEM image showing a diameter in the range of 300–645 nm, indicating polymer entrapment with enhanced size. Brine shrimp assay, MTT assay using normal fibroblasts, 3T3-L1, and zebrafish embryo assay were done to observe the biocompatibility of the synthesized nanostructure. The concentration of 50 μg/mL was found to be inert in both in vitro and in vivo. Furthermore, cervical cancer cells, SiHa, were treated with the nanoparticles to exhibit their cancer-killing capability with an IC50 value of 30.74 μg/mL. The results demonstrate the effectiveness of orange peel extract as a sustainable agent for TiO2 nanoparticle synthesis and the successful formation of a stable chitosan-entrapped nanocomposite. This approach offers a promising pathway for producing functional metal oxide nanomaterials with reduced environmental impact and enhanced properties for diverse biomedical applications. Future studies using other types of cancer cells and animal models for cancerous tumors need to be explored.

In the design of cellular structures using unit cell-based modeling, idealized structures with infinite dimensions and negligible boundary conditions are often assumed in order to simplify the analysis. However, such treatments also result in significant errors for the performance predictions of actual cellular components with finite dimensions. In this study, the pattern size effects resulting from finite-sized cellular designs were investigated systematically for various cellular designs. Two types of size effects, namely, lateral and along-stress size effects, were defined and investigated using simulation-based studies. It was found that different cellular designs exhibit significantly different size effects, which are also dependent on factors including Poisson’s ratio, structural symmetry, and the unit cell dimensional aspect ratio. The coupling effect between the two size effects was also discussed. This study provides a more systematic understanding of the size effects of cellular structures that can be used to guide future designs.

This review work highlights the eco-friendly synthesis and application of biomass-derived silica gel (SG)-supported metallic nanoparticles (MNPs), primarily focusing on their potential for sustainable drinking water disinfection and utilizing abundant biomass waste, such as agricultural residues, to extract silica through processes like pyrolysis, chemical treatment, or hydrothermal methods, creating a versatile support with high surface area, porosity, and biocompatibility. MNPs, notably silver, copper, zinc, etc., are immobilized onto these silica frameworks via green synthesis techniques, including plant extract-mediated methods, chemical reduction, and sol–gel processes, resulting in nanocomposites with controlled size, distribution, and enhanced stability. These MNPs are known for their potent antimicrobial activity, capable of inactivating a broad spectrum of pathogens like Staphylococcus aureus and Escherichia coli. Silica gel supports mitigating issues such as nanoparticle aggregation and leaching, thus improving reusability and environmental safety. The synthesis parameters of nanoparticle size, concentration, surface chemistry, and contact time directly influence disinfection efficacy, while biomass-based supports offer advantages including cost-effectiveness, environmentally benign production, and minimal pollution. Incorporating biomass-derived silica gel-supported AgNPs into water treatment systems presents a promising, sustainable alternative to conventional chemical methods like chlorination and ultraviolet (UV) irradiation, which can generate hazardous byproducts. These nanocomposites demonstrate significant potential in resource-limited settings due to their high surface area, porosity, and reusability, although concerns such as nanoparticle leaching, toxicity, scalability, and environmental impact warrant further investigation. Overall, biomass-supported MNPs represent an innovative frontier in water purification technology, aligning with principles of green chemistry and sustainability. Emphasizing the importance of optimizing synthesis protocols and assessing long-term safety, this review underscores their capacity to advance eco-friendly water disinfection strategies that can improve public health and promote sustainable water management practices worldwide.

This study presents a novel modified polylactic acid (PLA) composite material engineered to simultaneously achieve enhanced mechanical performance, crystallinity, degradability, and antibacterial activity through the incorporation of multi-arm Zn/CFR-PLA modifiers, derived from ZnO-loaded phenolic resin microspheres. The modifiers were synthesized via ring-opening polymerization (ROP) of lactide, initiated by phenolic resin microspheres with multiple surface hydroxyl groups, where multi-arm architecture was tailored to improve compatibility and interfacial bonding with PLA matrices. Mechanical characterization revealed significant reinforcement and toughening effects: the (Zn/CFR2-PLLA)2/PLLA composite exhibited an elongation at break of 102.7% (≈13-fold higher than pristine PLA) and a tensile strength of 19.6 MPa, alongside markedly improved impact strength. Notably, the Zn/CFR2-PDLA/PLLA composite, leveraging stereocomplex formation between PDLA and PLLA, achieved a higher tensile strength of 27.2 MPa with an elongation at break of 47.3%. Furthermore, the release of zinc ions from the modifiers endowed the composites with exceptional antibacterial activity, achieving more than 98% inhibition against Escherichia coli and Staphylococcus aureus. The composites also demonstrated degradability and processability, as melt-spun PLA fibers derived from them exhibited enhanced modulus (up to 4.51 GPa) and moisture-wicking capability. The composites can serve as potential candidates for biodegradable packaging films, antibacterial textiles for medical or hygienic uses, and sustainable materials for consumer products.

The lightning strike protection (LSP) performance of nickel-coated carbon fiber nonwoven veils (NiCVs) with varying areal densities, integrated onto the surface of CFRP laminates, was evaluated through simulated lightning strike tests. Post-strike damage was evaluated through visual inspection, non-destructive ultrasonic testing, residual strength measurements, and microstructural examinations. Results indicated that the protection effectiveness improved with increasing NiCV areal density. The laminate with a 68 g/m2 NiCV layer showed substantially reduced damage—its damage volume, damage area, and maximum damage depth decreased to 18%, 40%, and 51% of those of the control laminate—and it retained 95% of the reference compression strength, demonstrating the strong post-strike protection capability of this lightweight veil. A detailed analysis suggested that the NiCV LSP performance may arise from a mechanism involving high electrical conductivity, a thermally stable coated-fiber skeleton, as well as a distributed nonwoven network architecture. These results highlight NiCV as a promising functional approach for enhancing the lightning strike protection of CFRP aerostructures.

Heteroatom functionalization of graphene is an effective strategy for designing more sustainable lithium-ion battery electrodes, as it can tune both interfacial adhesion and the electronic features of the carbon lattice. In this work, we investigated the interfacial compatibility between three graphene sheets—pristine graphene, graphene doped with one nitrogen atom (Graphene–N), and graphene doped with one sulfur atom (Graphene–S)—and three lignocellulosic binders (carboxymethylcellulose (CMC); coniferyl alcohol (LcnA); and sinapyl alcohol (LsiA)) using density functional theory (DFT). Geometries were optimized using CAM-B3LYP and M06-2X in combination with the LANL2DZ basis set, while ωB97X-D/LANL2DZ was employed for dispersion-consistent single-point refinements. The computed adsorption energies indicate that all binder–surface combinations are thermodynamically favorable within the present finite-model framework (ΔEint ≈ −22.6 to −31.1 kcal·mol−1), with LSiA consistently showing the strongest stabilization across surfaces. Nitrogen doping produces a modest but systematic strengthening of adsorption relative to pristine graphene for all binders and is accompanied by electronic signatures consistent with localized donor/basic sites while preserving the delocalized π framework. In contrast, sulfur doping yields a more binder-dependent response: it maintains strong stabilization for LSiA but weakens LCnA relative to pristine/N-doped sheets, consistent with an S-induced local distortion/polarizability pattern that can alter optimal π–π registry depending on the adsorption geometry. A combined interpretation of adsorption energies, electronic descriptors (including ΔEgap as a model-dependent HOMO–LUMO separation), and topological analyses (AIM, ELF, LOL, and MEP) supports that Graphene–N provides the best overall balance between electronic continuity and chemically active interfacial sites, whereas Graphene–S can enhance localized anchoring but introduces more heterogeneous, lone-pair–dominated domains that may partially perturb electronic connectivity.

Conductive polymers (CPs), such as polypyrrole (PPy), have shown promising properties for use as electro-responsive bioactive scaffolds for tissue regeneration. PPy can be synthesized by chemical electrosynthesis and doped with biomolecules such as hyaluronic acid (HA). Taking advantage of the electrochemical synthesis versatility, nanofibers for surface-modified indium tin oxide (ITO) electrodes can be used as templates to produce tridimensional HA-doped PPy scaffolds. In this study, polyvinyl alcohol/chitosan (PVA/CTS) electrospun nanofibers deposited on ITO electrodes were used as a 3D template for the in situ electrosynthesis of HA-doped PPy to produce a bioactive scaffold for tissue engineering. The final material gathers the advantages of each biopolymer, the porous morphology of the nanofiber, and the conductivity of the electrosynthetized polymer. Furthermore, the biological activity of the NF-PVA/CTS@PPy:HA composite was evaluated in NIH-3T3 fibroblasts by MTT, resulting in a cell viability of 146 ± 40% and wound-healing capacity of 97 ± 1.9% at 24 h of culture.

The mechanical behavior of carbon-fiber-reinforced polymer (CFRP) laminates manufactured using plasma-assisted solvolysis recycled fibers was evaluated experimentally through a comprehensive mechanical testing campaign. The plasma-assisted solvolysis parameters were selected based on an earlier sensitivity analysis. Prepregs made from both virgin and recycled carbon fibers were fabricated via a hand lay-up process and manually stacked to produce unidirectional laminates. Longitudinal tension tests, longitudinal compression tests, and interlaminar shear strength (ILSS) tests were performed to assess the fundamental mechanical response of the recycled laminates and quantify the retention of mechanical properties relative to the virgin-reference material. Prior to mechanical testing, all laminates underwent ultrasonic C-scan inspection to assess manufacturing quality. While both laminate types exhibited generally satisfactory quality, the recycled-fiber laminates showed a higher density of defects. The recycled laminates preserved around 80% of their original tensile strength and maintained an essentially unchanged elastic modulus. Compressive strength was more susceptible to imperfections introduced during remanufacturing, with the recycled laminates exhibiting roughly a 14% decrease compared with the virgin material. On the contrary, the compressive modulus was largely retained. The most substantial reduction occurred in ILSS, which dropped by 58%. Overall, the results demonstrate that plasma-assisted solvolysis enables the recovery of carbon fibers suitable for remanufacturing CFRP laminates, while the observed reduction in mechanical properties of recycled CFRPs is mainly attributed to defects in manufacturing quality rather than to intrinsic degradation of the recycled carbon fibers.