Search Results (583)

The valorization of agricultural residues and post-consumer plastics is critical for achieving a circular economy. This study presents a sustainable pathway to fabricate eco-friendly acoustic panels by melt-blending recycled high-density polyethylene (rHDPE) with 10–50 wt% rice straw waste-derived nanofillers. Multi-stage chemical refinement (10% NaOH mercerization and H₂O₂ bleaching) before ball milling isolated nanofibrils under 50 nm. XRD analysis showed a crystallinity index increase from 37.0% (untreated) to 67.2% (bleached), confirming amorphous phase removal. FTIR and SEM verified successful delignification and excellent interfacial wetting. Consequently, the 50 wt% bleached cellulose composite exhibited the highest reinforcement, increasing flexural strength by 126% and flexural modulus by 132.6% over neat rHDPE. The hydrophilic framework enhanced environmental biodegradability, yielding a 15.18% maximum weight loss after a 90-day soil burial test, providing a viable end-of-life alternative to persistent synthetics. To optimize acoustic utility, a 1.76% geometric micro-perforation ratio was engineered into the panels. Backed by a 6 cm air cavity, the 50 wt% untreated composite achieved an outstanding peak sound absorption coefficient of 0.98 at a low frequency of 400 Hz. These findings establish these high-filler bio-nanocomposites as high-performance, low-carbon alternatives for noise control in construction and automotive infrastructure. Full article

The food packaging sector widely relies on polymeric materials, and as sustainability concerns grow, commodity polymers need to be replaced with innovative and more sustainable materials. Thermoplastic polyurethane (TPU) is a versatile elastomeric polymer characterized by flexibility, strength, chemical and abrasion resistance, and biocompatibility. However, it presents some limitations, notably in terms of functional properties (i.e., barrier properties). The use of nano-sized renewable fillers, such as cellulose nanocrystals (CNCs), may improve these properties, extending the applicability range of TPU. In this work, bio-based TPU nanocomposites were obtained by adding commercial silane-modified cellulose nanocrystals (Si−O−CNC) at different contents (1–5 wt.%). The nanocomposites were produced via melt mixing followed by compression molding and were characterized in terms of chemical (FTIR), morphological, thermal, mechanical, rheological, wettability, and barrier properties (i.e., water vapor permeability, WVP and oxygen transmission rate, OTR). The presence of Si−O−CNC promoted hydrogen bonding interactions with the TPU matrix, affecting the microphase separation and organization of the hard segments. These microstructural changes improved thermal stability, reduced WVP and OTR, and increased tensile properties at lower nanofiller contents (1–3 wt.%). At higher contents, partial nanofiller aggregation was observed, leading to a reduction in mechanical performance. Overall, these results suggest that TPU/Si−O−CNC nanocomposites have promising potential as sustainable food packaging materials. Full article

The Lantana genus, especially L. camara, has emerged as a potential yet underutilized lignocellulosic feedstock for various catalytic thermochemical conversion products and advanced carbon materials. This study reviews recent developments in the valorization of Lantana biomass to generate biofuels, bio-oil, syngas, and engineered biochar materials through pyrolysis, gasification, hydrothermal processing, and integrated biorefinery processes, in a critical manner. Particular focus will be on nanocomposite-modified, metal-doped biochar with catalytic elements such as ZSM-5, Fe₃O₄, TiO₂, and Ni-, Co-, and Zn-based oxides to enhance deoxygenation, catalytic cracking, tar reforming, pollutant remediation, and energy storage. Recent developments in catalyst synthesis techniques, such as impregnation, hydrothermal deposition, and in situ functionalization, are reviewed, along with characterization methods including BET, XRD, SEM/TEM, Raman spectroscopy, and XPS. The review further examines the impact of pore structure, surface chemistry, the presence of redox-active centers, and catalyst stability on product selectivity, syngas quality, and upgrading bio-oil performance. The effects of biochar on microbial immobilization, anaerobic digestion, and integrated biochemical conversion are discussed in detail, excluding thermochemical effects. The challenges of catalyst deactivation, biomass heterogeneities, scalability, techno-economic viability, and decentralized biomass logistics are also discussed. In summary, the development and implementation of catalytic reaction engineering, the design of nanocomposite biochar, and circular bioeconomy strategies have great potential to facilitate the conversion of invasive Lantana biomass into renewable fuels, multifunctional carbon materials, and environmentally friendly bioeconomy products. Full article

Natural lacquer, a bio-based polymer derived from Toxicodendron vernicifluum, has attracted renewed scientific interest as a sustainable coating material with exceptional mechanical durability, chemical resistance, and aesthetic qualities. This review synthesizes current knowledge on the chemical composition, enzymatic curing mechanisms, and structure–property relationships of lacquer-based polymer systems, with particular focus on recent advances in functional modification and processing technology. Key findings indicate that laccase-catalyzed oxidative polymerization, operating optimally at pH 6.0–7.5 and 20–30 °C, governs the formation of a highly cross-linked urushiol network whose properties are fundamentally determined by side-chain unsaturation and emulsion stability. Mechanistic analysis reveals that polyurethane hybridization improves weathering resistance by introducing flexible aliphatic segments and additional hydrogen-bonding cross-links, while graphene oxide incorporation enhances anticorrosion performance through a physical barrier mechanism that prolongs ionic diffusion pathways. UV-curable LPEA derivatives achieve an 83% reduction in curing time relative to ambient-cured lacquer, enabling integration with industrial spray-coating lines. Despite these advances, several critical limitations remain inadequately resolved. Allergen reduction strategies have not yet achieved sufficient quantitative efficiency for large-scale commercial deployment, and the long-term stability of nanocomposite lacquer films under sustained UV exposure and hydrothermal conditions is not well established. Furthermore, most high-performance modification systems reported in the literature are demonstrated only on laboratory scale, with scalability, substrate compatibility, and lifecycle performance remaining largely unvalidated. The review identifies the absence of standardized performance evaluation protocols and the fragmentation of structure–property data across studies as key barriers to systematic progress, and proposes that future work prioritize the development of integrated processing–modification–performance frameworks to guide the rational design of next-generation lacquer-based functional materials. Full article

Raw lacquer, a natural polymer derived from the bast of lacquer trees (Toxicodendron vernicifluum), is renowned as the “King of Coatings” due to its exceptional film-forming properties, abrasion resistance, corrosion resistance, and biocompatibility. However, its inherent limitations—including stringent drying conditions, slow curing rates, deep coloration, and difficult application—have severely restricted its modernization and widespread adoption. This review systematically summarizes recent research advances in the modification and application of raw lacquer, focusing on four major modification strategies: (1) Nanocomposite modification—incorporating functional nanofillers such as Al₂O₃, cellulose nanofibrils (CNF), polydopamine (PDA) melanin-like nanoparticles, and SiO₂ to significantly enhance film hardness, compactness, UV-aging resistance, and drying kinetics. (2) Chemical structure modification—employing molecular design strategies including aminoanthraquinone grafting, tung oil blending, water-based emulsification, and terpene/allyl group functionalization to improve hydrophobicity, flexibility, fast-drying properties, and achieve dual photo/oxygen curing. (3) Biomass synergistic composites—utilizing natural polymers such as chitosan and lignin, along with bio-inspired adhesion mechanisms (e.g., PDA), to confer advanced functionalities including antibacterial and antifouling properties. (4) Curing behavior regulation—precisely controlling drying kinetics through inorganic salt ion microenvironment engineering, nonionic surfactants, and salicylaldehyde Schiff base-based driers. Building upon these foundations, this review further expands on the emerging high-value applications of modified lacquer in preventive conservation of cultural heritage, advanced functional coatings (anti-corrosion, super-hydrophobicity, flame retardancy), biomedical materials (hemostasis, antibacterial activity, drug-controlled release, water treatment adsorption), and intelligent responsive flexible electronics. Finally, addressing challenges including weak fundamental research, bottlenecks in green industrialization, and lack of standardization, future development directions are proposed encompassing interdisciplinary innovation, sustainable modification strategies, integration of multifunctional intelligent systems, and big data-driven research paradigms, aiming to provide theoretical guidance and technical references for the high-value utilization and modernization of lacquer resources. Full article

The emerging threat of antibiotic-resistant pathogens and the limitations that conventional cancer chemotherapies display have created an urgent need for the development of innovative therapeutic strategies. Combining the pleiotropic biological roles of antimicrobial peptides (AMPs) and nanomaterials through their conjugation presents a promising possibility of targeting both microbial membranes and malignant cells. In the present study, we engineered a novel bioactive material by immobilizing the insect-derived AMP Papiliocin onto multi-walled—decorated with polyethylene–glycol—carbon nanotubes (PEG-MWCNTs) to prevent proteolytic degradation of the peptide and enhance its cellular delivery. Recombinant Papiliocin was cloned, heterologously expressed, purified and conjugated onto the PEG-MWCNT carrier. Successful expression and conjugation were validated via immunoblotting and Fourier transform infrared (FT-IR) spectroscopy, respectively. Further physicochemical characterization of the bionanocomposites was conducted using Dynamic Light Scattering (DLS) and Zeta potential measurements. Biologically, the biofunctionalized material exhibited potent, broad-spectrum antimicrobial activity both on Staphylococcus aureus and Escherichia coli, inhibiting almost 90% of the latter’s growth, highlighting the bioconjugate’s specific interactions with the Gram-negative pathogens’ membranes. Furthermore, it significantly reduced biofilm formation in Candida albicans, as indicated by the TCP assay. In parallel with its antimicrobial effects, CNTs-PEG–Papiliocin significantly reduced cancer cell viability and induced apoptosis via the extrinsic apoptosis pathway in HeLa cells, a response assisted by efficient intracellular delivery. Notably, cytotoxicity assays demonstrated lesser cytotoxic effect against non-tumorigenic HaCaT cells relative to the cancerous cell line. Collectively, these findings indicate the Papiliocin–biofunctionalized CNTs as a versatile, dual-action therapeutic agent with potential for antimicrobial activity and anticancer mode of action. Full article

The growing demand for sustainable water treatment technologies requires photocatalysts that combine low environmental impact, energy efficiency, and mechanistic robustness. In this work, $Ag/Zn$ nanocomposites were green-synthesized using Chlorella vulgaris polar extract as a bio-mediated reducing and stabilizing agent, eliminating hazardous reagents and high-energy processing steps. Structural characterization (XRD, FTIR, SEM, UV–Vis) confirmed the coexistence of crystalline wurtzite $ZnO$ with metallic $Ag$ and ${Ag}_{2}O$ phases. Photocatalytic activity was evaluated through Congo Red degradation under a sequential dark–light protocol, enabling clear separation of adsorption and photoactivated pathways. During the $60 \mathrm{m}\mathrm{i}\mathrm{n}$ dark stage, removal remained limited ($~9–11\%$), consistent with adsorption–desorption equilibration. Upon UV irradiation, a distinct kinetic transition occurred, leading to final removal efficiencies of $44–49\%$ after $180 \mathrm{m}\mathrm{i}\mathrm{n}$. Notably, performance remained stable across the investigated photon flux range, indicating operation beyond a strictly photon-limited regime and highlighting an intrinsically energy-resilient catalytic response. A mechanistic kinetic model integrating reversible adsorption with light-dependent degradation accurately reproduced all experimental profiles ($NRMSE=3.14\%$) and successfully predicted an independent dark-control experiment without additional fitting. By coupling green synthesis with quantitative kinetic validation, this study proposes a sustainability-oriented framework for designing photocatalysts that align low-impact fabrication with energy-conscious water remediation. Full article

Biodegradable materials offer promising alternatives to petroleum-based polymers. This study investigates poly(ε-caprolactone) (PCL) and poly(lactic acid) (PLA) nanocomposites reinforced with 1, 3 and 5 wt.% cellulose nanocrystals (CNCs) extracted from sugarcane bagasse via melt blending. The thermal, structural, morphological and biodegradation properties were evaluated using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X-ray scattering (WAXS/SAXS), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and biodegradation tests. SEM results revealed uniform dispersion of CNCs at low concentrations, whereas agglomeration occurred at higher concentrations for both PCL and PLA. At 1 wt.% CNCs, there was minimal impact on the biodegradation rates of both polymers, despite achieving uniform dispersion. However, significant acceleration in biodegradation was observed at 5 wt.% CNCs, attributed to the enhanced hydrophilic nature of the nanocomposites. CNCs acted as nucleating agents in PCL crystallization, while reducing the crystallization rate of PLA. This led to a mass loss of 36.4% for PCL and 82.2% for PLA, correlating with increased and decreased crystallinities, respectively. The study concludes that the hydrophilic–hydrophobic balance has a more significant influence on biodegradation rates than crystallinity or CNC dispersion. Full article

Accurate thermal characterization of building insulation materials is essential for reliable energy performance assessment, regulatory compliance, and the development of high-performance envelopes. On one hand, the growing adoption of innovative insulating products, such as nanoporous materials, aerogel-based composites, bio-based panels, and thin insulating coatings, helps to enhance buildings’ energy efficiency by means of sustainable raw materials. On the other hand, conventional measurement techniques encounter significant challenges, due to their heterogeneity, reduced thickness, and unconventional geometries. In this study, an intra-laboratory comparison of three widely used methods for thermal conductivity determination is presented: the Transient Plane Source (TPS, Hot Disk) method, the Guarded Hot Plate (GHP) method, and the Heat Flow Meter (HFM) method. A total of twelve insulating materials, spanning super-insulating cores, insulating renders, bio-based panels, and nanocomposite coatings, were experimentally characterized under controlled laboratory conditions. A view on the analyzed insulating materials’ cradle-to-grave environmental impact is also given, to enhance the users’ awareness for the highly informed choice. The results highlight systematic differences between transient and steady-state approaches, with TPS measurements generally exhibiting larger deviations for materials characterized by surface roughness, limited thickness, or strong internal heterogeneity. In contrast, GHP and HFM methods show closer agreement when specimen geometry and stabilization requirements are satisfied. The influence of contact resistance, probing depth, specimen preparation, and uncertainty propagation is critically analyzed for each technique. The study provides practical insights into the applicability limits of commonly used thermal characterization methods and emphasizes the importance of selecting measurement techniques in relation to material morphology and testing constraints. These findings support more reliable thermal property assessment of emerging insulation materials and contribute to improved consistency between laboratory measurements and energy performance evaluations for buildings. Full article

Two hemostatic bionanocomposite dressings were developed using natural, semi-natural (or semi-synthetic) and synthetic polymers. The first system consisted of chitosan (CS), polyvinyl alcohol (PVA), and carboxymethyl cellulose (CMC) (CS/PVA/CMC), while the second was based on CS, PVA, and starch (SR) (CS/PVA/SR). Zinc oxide (ZnO) nanoparticles and bicyclic monoterpene camphor (CP) ketone were incorporated as bioactive agents in order to enhance antimicrobial and hemostatic performance. FTIR spectroscopy confirmed the successful solvent casting synthesis of the dressings and the interactions between the biopolymers and additives. XRD analysis indicated a predominantly amorphous structure, while SEM images and EDS analysis revealed uniform dispersion of ZnO particles within the polymer matrices without aggregation. Furthermore, the CS/PVA/CMC-1ZnO/CP sample exhibited a water sorption of 12,666 ± 126%, while CS/PVA/SR-1ZnO/CP reached 7013 ± 215%. ZnO incorporation also improved mechanical performance, with CS/PVA/SR-2ZnO/CP displaying the highest tensile strength (39.18 ± 0.2 MPa) and elongation at break (9.54 ± 1.04%). ZnO incorporation also led to a concentration-dependent increase in antibacterial activity, with SR-based dressings achieving near-complete bacterial reduction at higher ZnO loadings. All the dressings demonstrated good biocompatibility, while CS/PVA/SR-1ZnOCP showed the fastest clotting time (420 s ± 40), highlighting its potential for hemostatic applications. Full article

We co-modified layered double hydroxide (LDH) in water using phosphocreatine (PC) and dodecylphosphoric acid (DPA) to obtain a highly dispersible LDH. Embedding this LDH in epoxy enabled V-0 at 7 wt% and lowered HRR, THR and TSP, attributed to a dense char and PC-DPA synergy. SEM, WAXS, and TGA characterised the structure and thermal behaviour of the functionalised LDHs. These modified LDHs were then loaded into the epoxy resin (EP) to develop flame-retardant nanocomposites. Compared to unmodified LDH (NO₃-LDH) and PC-modified LDH (PC-LDH), PC-DPA-LDH showed superior dispersion and compatibility within the epoxy matrix. As a result, PC-DPA-LDH/EP achieved a UL-94 V-0 rating at only 7 wt% loading, while NO₃-LDH/EP had no rating, and PC-LDH/EP reached only V-2. Moreover, PC-DPA-LDH/EP demonstrated significant decreases in peak heat release rate (46.4%), total heat release (34.5%), and total smoke production (59.7%) compared with neat EP. These improvements were attributed to the synergistic flame-retardant effects of PC and DPA, as well as to the formation of a compact char layer that effectively insulated the underlying material and suppressed volatile emissions. This work highlights the potential of bio-based, aqueous-synthesised nanohybrids for high-efficiency, eco-friendly flame-retardant epoxy systems. Full article

Conventional chemotherapies for cervical cancer, such as cisplatin (CDDP)-based treatments, are limited by high systemic toxicity and the development of cellular resistance. To address these drawbacks, this study reports the green synthesis of selenium nanoparticles (SeNPs) using Amphipterygium glaucum leaf extract (AGLE) and the development of a guar gum-based nanocomposite (SeNPs@GG) loaded with these NPs. The synthesized SeNPs showed a stable UV–Vis absorption band at 275 nm, a spherical morphology, and sizes ranging from 11 to 21 nm, as confirmed by TEM. FTIR and XPS analyses demonstrated interactions between Se and functional groups from the plant extract, indicating its dual role as a reducing and stabilizing agent. The guar gum nanocomposites (NCs) exhibited a porous structure with a homogeneous distribution of SeNPs, as evidenced by SEM and EDS. At the same time, XRD confirmed the crystalline nature of the SeNPs. In vitro cytotoxicity assays using HeLa cervical cancer cells revealed significant antiproliferative effects with a biphasic response related to Se’s dual biological role. The IC₅₀ values were 98.3 µg/mL for SeNPs, 93.7 µg/mL for SeNPs@GG1, and 93.5 µg/mL for SeNPs@GG2. Additional analyses confirmed apoptosis, DNA fragmentation, ROS production, mitochondrial dysfunction, and G2/M cell cycle arrest, supporting the potential of these systems as alternative chemotherapeutic strategies. Full article

Bio-based, biodegradable, and renewable polymers offer a promising alternative to traditional synthetic polymers derived from petroleum or other non-renewable resources. However, their use is limited by suboptimal properties and high costs. Incorporating sustainable reinforcements into the polymer matrix significantly improves biopolymer performance while preserving key properties, sustainability, and cost-effectiveness. Bio-based polymeric composites have emerged as a crucial category of biopolymers, playing a key role in advancing a sustainable, circular economy. This review provides an updated overview of bio-based polymer composites and nanocomposites, focusing on reinforcement strategies using natural nanofillers and engineered nanoparticles. We summarize key synthesis and processing methods, discuss structure–property relationships, and highlight recent advances in applications such as food packaging, biomedical devices, energy systems, environmental remediation, 3D printing, and supercapacitors. Polymer nanocomposites are versatile, with their performance depending on the type, size, and interactions between the fillers and the polymer matrix. Progress in metallic, ceramic, carbon-based, natural, and hybrid fillers has improved their properties. Using bio-based polymers and renewable fillers supports sustainability. Natural nanofillers derived from renewable sources and industrial byproducts offer a sustainable approach to developing high-performance, biodegradable nanocomposites. Smart nanocomposites can react to external stimuli by integrating specialized fillers that enhance their mechanical and mobility properties. Shape memory nanocomposites can be remotely activated—using heat, electricity, magnets, or light—enabling advanced applications. Finally, we address major challenges and outline future directions for scalable, circular-material solutions, drawing on perspectives from the circular economy and life cycle assessment (LCA). Full article

This study investigates the valorisation of Salicornia ramosissima agro-industrial by-product by using cellulose nanofibers (CNFs) extracted from this halophyte to reinforce chitosan-based films. The physical, mechanical, and thermal properties of chitosan films containing 0% (control), 1%, and 2% (w/w) CNF were evaluated. Films were produced by solvent casting with glycerol as a plasticiser. At the 2% CNF concentration, films exhibited a reduced moisture content and increased solubility in aqueous solutions. The water vapour transmission rate (WVTR) decreased as CNF content increased under constant humidity but increased at higher temperature and humidity. Control films were more transparent, yet CNF-reinforced films had higher tensile strength and Young’s modulus, reflecting greater stiffness. Maximum elongation at break decreased markedly with the addition of CNFs. SEM revealed that reinforced films had more heterogeneous, rougher surfaces, particularly at 2% CNF. Thermogravimetric analysis showed that 2% CNF adversely affected the thermal stability of the chitosan film. ATR-FTIR spectra indicated that CNF reinforcement protected against UV-induced degradation. Degradability tests in soil and seawater confirmed that the chitosan–CNF mixture preserved degradability, especially at 1% CNF. These findings demonstrate that reinforcing chitosan-based films with CNFs from S. ramosissima can improve functional properties and suggest the potential of this approach for biomaterials development in food packaging applications. Full article

This study presents the post-synthetic functionalization of Ni-Co bimetallic nanoparticles (NPs) with a β-cyclodextrin (β-CD) framework using a green synthesis approach with Illicium verum (Star anise) extract. The synthesized nanocomposite was verified using physicochemical characterization techniques such as FTIR, XRD, Zeta potential, DLS, SEM, and TEM. This surface modification successfully yielded a stable core–shell architecture with a reduced crystallite size of 29.5 nm, compared to 41.2 nm for bare Ni-Co NPs. The β-CD coating shifted the Zeta potential from −33.07 mV to −27.65 mV, establishing an electro-steric stabilization mechanism. Sensing performance toward Cd²⁺ ions was evaluated via the QCM-D technique. The Ni-Co/β-CD nanocomposite demonstrated a superior sensitivity of 34.72 Hz/mM and a remarkably low limit of detection (LOD) of 17.3 µM, representing a 27-fold enhancement over the bare Ni-Co NPs (LOD: 472.2 µM). The mechanical signature, characterized by negative dissipation shifts and a high acoustic ratio (ΔD/Δf = 79.410 × 10⁻⁶), confirms an analyte-induced conformational rigidification driven by a host–guest interaction mechanism. These findings establish a robust method of producing bio-based, “smart” nanocomposites for high-precision environmental sensing. Full article