Search Results (13,508)

This study investigates the synthesis of silver nanoparticles (AgNPs) using Crassula ovata (Jade plant) leaf extract and their subsequent incorporation into chitosan-based nanocomposite films for enhanced antimicrobial activity against four pathogenic microorganisms: Escherichia coli, Pseudomonas aeruginosa, Staphylococcus epidermidis, and Methicillin-resistant Staphylococcus aureus. Jade AgNPs were chosen for their ease of synthesis, stability, and potent antimicrobial activity. Chitosan encapsulation improved the stability of AgNPs and enhanced their interaction with bacterial cells, leading to improved bactericidal performance. The addition of gentamicin to the nanocomposite further amplified antibacterial activity, reducing the MBC values from 10 to 4 µg/mL for E. coli, 12.5 to 6 µg/mL for P. aeruginosa, 10 to 6 µg/mL for S. epidermidis, and 15 to 8 µg/mL for MRSA, compared to AgNPs alone. Mechanical characterization using dynamic mechanical analysis revealed improved robustness, with storage modulus increasing from approximately 24 MPa for chitosan-AgNPs films to 36 MPa for gentamicin-loaded nanocomposite films, while maintaining elasticity. Overall, these multifunctional nanocomposite films demonstrate strong antimicrobial activity and improved mechanical performance, supporting further evaluation as candidate materials for wound-related antimicrobial applications and localized infection control strategies. Such localized antimicrobial platforms may also contribute to strategies aimed at mitigating antibiotic resistance. Full article

Self-healing polymer nanocomposites are increasingly investigated as damage-tolerant materials for structural and functional applications; however, their engineering translation remains limited by the difficulty of achieving high mechanical reinforcement while retaining sufficient polymer mobility for effective repair. Previous reviews have largely summarized healing chemistries or nanofiller classes but have rarely established quantitative structure–property–healing relationships or resolved contradictory trends reported across studies. In this review, we develop an integrated framework that links polymer network architecture, nanofiller geometry/percolation behavior, and interfacial dynamics to healing kinetics, and we compile quantitative design windows for nanofiller loading, percolation thresholds, activation conditions, and durability metrics. The synthesis reveals that healing performance is maximized within intermediate filler contents near the percolation regime, whereas excessive nanofiller loading commonly suppresses healing by nanoscale confinement and interphase immobilization despite improving modulus and conductivity. Finally, we propose application-oriented design rules and benchmarking priorities, emphasizing standardized fracture/fatigue-based evaluation, multi-cycle healing retention, and scalable interphase engineering as the key pathways for translating self-healing nanocomposites from laboratory demonstrations to validated engineering systems. Full article

A flexible piezoresistive material based on vulcanized natural rubber (VNR) and multiwalled carbon nanotubes (MWCNTs) was developed and systematically investigated for strain sensing applications. The nanocomposites were prepared by melting and vulcanizing MWCNT, while keeping the rubber composition constant to isolate the effect of the conductive nanofiller. By scanning electron microscopy, morphological analyses indicated that MWCNTs were dispersed throughout the rubber matrix, with localized agglomerations becoming more evident at higher loadings. In mechanical tests, MWCNT incorporation increases the tensile strength of VNR, increasing the stress at break from 8.84 MPa for neat VNR to approximately 10.5 MPa at low MWCNT loadings. According to the electrical characterization, VNR-MWCNT nanocomposite exhibits a strong insulator–conductor transition, with the electrical percolation threshold occurring between 2 and 4 phr. The dc electrical conductivity increased sharply from values on the order of 10⁻¹⁴ S·m⁻¹ for neat VNR to approximately 10⁻³ S·m⁻¹ for nanocomposites containing 7 phr of MWCNT. Impedance spectroscopy revealed frequency-independent conductivity plateaus above the percolation threshold, indicating continuous conductive pathways, while dielectric analysis revealed strong interfacial polarization effects at the MWCNT–VNR interfaces. The piezoresistive response of samples containing MWCNT exhibited a stable, reversible, and nearly linear response under cyclic tensile deformation (10% strain). VNR/MWCNT nanocomposites demonstrate mechanical compliance and tunable electrical sensitivity, making them promising candidates for flexible and low-cost piezoresistive sensors. Full article

In recent years, significant advancements have been made in the exploitation, combustion, ignition, and application of innovative nano-metric energetic materials (nEMs), including solid fuels, energetic combustion catalysts, metal particles, thermites, energetic composites, and more, thanks to new technological developments in the field of nano-scale science and technology [...] Full article

The combination of gold nanoparticles (AuNPs) with hydrogels has drawn significant interest in the design of smart materials as advanced platforms for biomedical applications. These systems endow light-responsiveness enabled by the AuNPs localized surface plasmon resonance (LSPR) phenomenon. In this study, we propose a nanocomposite hydrogel in which gold nanorods (AuNRs) are included in an agarose–carbomer–hyaluronic acid (AC-HA)-based hydrogel matrix to study the correlation between light irradiation, local temperature increase, and drug release for potential light-assisted drug delivery applications. The gel is obtained through a facile microwave-assisted polycondensation reaction, and its properties are investigated as a function of both the hyaluronic acid molecular weight and ratio. Afterwards, AuNRs are incorporated in the AC-HA formulation, before the sol–gel transition, to impart light-responsiveness and optical properties to the otherwise inert polymeric matrix. Particular attention is given to the evaluation of AuNRs/AC-HA light-induced heat generation and drug delivery performances under near-infrared (NIR) laser irradiation in vitro. Spatiotemporal thermal profiles and high-resolution thermal maps are registered using fiber Bragg grating (FBG) sensor arrays, enabling accurate probing of maximum internal temperature variations within the composite matrix. Lastly, using a high-steric-hindrance protein (BSA) as a drug mimetic, we demonstrate that moderate localized heating under short-time repeated NIR exposure enhances the release from the nanocomposite hydrogel. Full article

Thorium carbide (ThC${}_{2\pm x}$) nano-structured thin disc-like pellets were produced from thoria nanoparticles (ThO${}_2$-NP) and multi-walled carbon nanotubes (MWCNT). These composites are to be studied as a target material candidate for radioactive ion beam (RIB) production via nuclear reactions upon impact with high-energy proton beams on a stack of solid pellets. The ThO${}_2$-NP precursor was produced via precipitation of thorium oxalate from a thorium nitrate solution with oxalic acid and subsequent hydrothermal oxidation of the oxalate, creating the thoria nanoparticles. The ThO${}_2$-NP were then mixed with MWCNT in isopropyl alcohol and sonicated by two different methods to create a nanoparticle dispersion. This dispersion was then heated under medium vacuum to evaporate the solvent; the resulting powder was pressed into pellets and taken to an inert-atmosphere oven, where it was heated to 1650 ${}^{\circ }$C and carbothermally reduced to ThC${}_{2\pm x}$. The resulting pellets were characterized via XRD, SEM-EDS, and Raman spectroscopy. The resulting thorium pellets exhibited, at most, trace levels of the oxide precursor. Furthermore, the nanotube structures were still present in the final product and are expected to contribute positively towards faster radioisotope release times by lowering isotope diffusion times, which is required for the efficient extraction of the shortest-lived (<1 s half-life) radioisotopes. Full article

Introduction: Magnetic nanoparticles are widely investigated as multifunctional platforms for drug delivery and theranostic applications, yet their biomedical implementation is hindered by aggregation, limited colloidal stability, and insufficient biocompatibility. Hybrid biopolymer coatings can mitigate these issues while supporting drug incorporation. Aim: This study aimed to develop casein–pullulan-coated Fe₃O₄ nanocomposites loaded with xanthohumol, enhancing stability and enabling controlled release for potential theranostic use. Methods: Fe₃O₄ nanoparticles were synthesized through co-precipitation and incorporated into a casein–pullulan matrix formed via polymer complexation and glutaraldehyde crosslinking. A 3² full factorial design evaluated the influence of casein:pullulan ratio and crosslinker concentration on physicochemical performance. Nanocomposites were characterized for size, zeta potential, morphology, composition, and stability, while drug loading, encapsulation efficiency, and release profiles were determined spectrophotometrically. Molecular docking was performed to examine casein–pullulan interactions. Results: Uncoated Fe₃O₄ nanoparticles aggregated extensively, displaying mean sizes of ~292 nm, zeta potential of +80.95 mV and high polydispersity (PDI above 0.2). Incorporation into the biopolymer matrix improved colloidal stability, yielding particles of ~185 nm with zeta potentials near –35 mV. TEM and SEM confirmed spherical morphology and uniform magnetic core incorporation. The optimal formulation, consisting of a 1:1 casein:pullulan ratio with 1% glutaraldehyde, achieved 5.7% drug loading, 68% encapsulation efficiency, and sustained release of xanthohumol up to 84% over 120 h, fitting Fickian diffusion (Korsmeyer–Peppas R² = 0.9877, n = 0.43). Conclusions: Casein–pullulan hybrid coatings significantly enhance Fe₃O₄ nanoparticle stability and enable controlled release of xanthohumol, presenting a promising platform for future targeted drug delivery and theranostic applications. Full article

Recycling water offers a powerful way to lower the environmental water impact of mining activities. Pressure-retarded osmosis (PRO) represents a promising pathway for simultaneous water reuse and clean energy generation from salinity gradients. In this study, the performance of a thin-film nanocomposite (TFN) membrane containing functionalized multi-walled carbon nanotubes (fMWCNTs) within a polyacrylonitrile (PAN) support layer, followed by polydopamine (PDA) surface modification, was investigated under a PRO operation using pretreated gold mining wastewater as the feed solution. Unlike most previous studies that rely on synthetic feeds, this work evaluates the membrane performance under a PRO operation using a real mining wastewater stream. The membrane with fMWCNTs and PDA exhibited a maximum power density of 25.22 W/m² at 12 bar, representing performance improvements of 23% and 68% compared with the pristine thin-film composite (TFC) and commercial cellulose triacetate (CTA) membranes, respectively. A high water flux of 75.6 L·m⁻²·h⁻¹ was also obtained, attributed to enhanced membrane hydrophilicity and reduced internal concentration polarization. The optimized membrane, containing 0.3 wt% fMWCNTs in the support layer and a PDA coating on the active layer, produced a synergistic enhancement in the PRO performance, resulting in a lower reverse salt flux and an improved flux–selectivity trade-off. Furthermore, the ultrafiltration (UF) and nanofiltration (NF) pretreatment effectively reduced the hardness and ionic content, enabling a stable PRO operation with real mining wastewater over a longer period of time. Overall, this study demonstrates the feasibility of achieving both reusable water and enhanced osmotic power generation using modified TFN membranes under realistic mining wastewater conditions. Full article

Atherosclerosis remains a leading cause of cardiovascular mortality despite advances in pharmacological and interventional therapies. Current treatment approaches face limitations including systemic side effects, inadequate local drug delivery, and restenosis following vascular interventions. Gel-based technologies offer unique advantages through tunable mechanical properties, controlled degradation kinetics, high drug-loading capacity, and potential for stimuli-responsive therapeutic release. This review examines gel platforms across multiple scales and applications in atherosclerosis research and intervention. First, gel-based in vitro models are discussed. These include hydrogel matrices simulating plaque microenvironments, three-dimensional cellular culture platforms, and microfluidic organ-on-chip devices. These devices incorporate physiological flow to investigate disease mechanisms under controlled conditions. Second, therapeutic strategies are addressed through macroscopic gels for localized treatment. These encompass natural polymer-based, synthetic polymer-based, and composite formulations. Applications include stent coatings, adventitial injections, and catheter-delivered depots. Natural polymers often possess intrinsic biological activities including anti-inflammatory and immunomodulatory properties that may contribute to therapeutic effects. Third, nano- and microgels for systemic delivery are examined. These include polymer-based nanogels with stimuli-responsive drug release responding to oxidative stress, pH changes, and enzymatic activity characteristic of atherosclerotic lesions. Inorganic–organic composite nanogels incorporating paramagnetic contrast agents enable theranostic applications by combining therapy with imaging-guided treatment monitoring. Current challenges include manufacturing consistency, mechanical stability under physiological flow, long-term safety assessment, and regulatory pathway definition. Future opportunities are discussed in multi-functional integration, artificial intelligence-guided design, personalized formulations, and biomimetic approaches. Gel technologies demonstrate substantial potential to advance atherosclerosis management through improved spatial and temporal control over therapeutic interventions. Full article

Corrosion in harsh environments causes global economic losses exceeding 3 trillion US dollars annually. Traditional silicone epoxy (SE) coatings are prone to failure due to insufficient physical barrier properties and lack of active protection. In this study, cerium dioxide (CeO₂) was in situ grown on the surface of hexagonal boron nitride (h-BN) mediated by polydopamine (PDA) to prepare BN-PDA-CeO₂ ternary nanocomposites, which were then incorporated into SE coatings to construct a multi-scale synergistic corrosion protection system. Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and transmission electron microscopy (TEM) confirmed the successful preparation of the composites, where PDA inhibited the agglomeration of h-BN and CeO₂ was uniformly loaded. Electrochemical tests showed that the corrosion inhibition efficiency of the extract of this composite for 2024 aluminum alloy reached 99.96%. After immersing the composite coating in 3.5 wt% NaCl solution for 120 days, the coating resistance (Rc) and charge transfer resistance (Rct) reached 8.5 × 10⁹ Ω·cm² and 1.2 × 10¹⁰ Ω·cm², respectively, which were much higher than those of pure SE coatings and coatings filled with single/binary fillers. Density functional theory (DFT) calculations revealed the synergistic mechanisms: PDA enhanced interfacial dispersion (adsorption energy of −0.58 eV), CeO₂ captured Cl⁻ (adsorption energy of −4.22 eV), and Ce³⁺ formed a passive film. This study provides key technical and theoretical support for the design of long-term corrosion protection coatings in harsh environments such as marine and petrochemical industries. Full article

A sustainable circular pathway was developed for poly(ethylene terephthalate) (PET) nanocomposites through a catalyst-driven polymerization and depolymerization process. In this study, calcium dodecylbenzene sulfonate with n-butyl alcohol modified ZnAl layered double hydroxides (LDHs) were utilized as bifunctional catalysts to synthesize highly exfoliated PET/LDH nanocomposites via in situ polycondensation of bis(2-hydroxyethyl) terephthalate (BHET). The organic modification of LDHs expanded interlayer spacing, improved interfacial compatibility, and promoted uniform dispersion, leading to enhanced mechanical, thermal, and barrier properties. In the second stage, the pristine LDH catalyst efficiently depolymerized the prepared PET/LDH nanocomposites back into BHET through glycolysis, completing a closed-loop BHET-to-BHET cycle. This integrated strategy demonstrates the reversible catalytic functionality of LDHs in both polymerization and depolymerization, reducing metal contamination and energy demand. The proposed approach represents a sustainable route for designing recyclable high-performance PET nanocomposites aligned with the principles of green chemistry and circular material systems. Full article

Poly(lactic acid) (PLA)-based nanocomposites containing a mixture of graphene nanoplatelets (GNP) and carbon nanotube (CNT) as hybrid fillers were prepared using a solution-assisted sonication process followed by melt processing. The effects of the filler dispersion on dielectric properties and microwave absorbing (MWA) performance were systematically investigated. Two ionic liquids (ILs), trihexyl-(tetra-decyl)phosphonium bis (trifluoromethanesulfonyl)imide (IL1) and 11-carboxyundecyl-triphenylphosphonium bromide (IL2), were employed as dispersing agents for the carbonaceous fillers. Incorporation of IL-treated fillers resulted in enhanced dielectric permittivity and improved MWA performance of the PLA composites. The MWA properties were evaluated in X- band and Ku-band. A minimum reflection loss (RL) of −34 dB and an effective absorption bandwidth (EAB) of 2.1 GHz were achieved for the composite containing GNP/CNT/IL2 (HB3) at a weight ratio of 2.5:0.5:0.5 wt% with one 3 mm thick layer. The superior performance of IL2 is attributed to π-π and π-cation interactions between its phenyl-containing cation and the carbonaceous fillers, as well as improved compatibility with the PLA matrix due to carboxyl groups. Additionally, three-layered composite structures, combining PLA/GNP as the outer layer with IL-assisted hybrid fillers in the core and PLA/CNT at the bottom layer, achieved an extended EAB of 4.5 GHz for GNP/HB2/CNT arrangement and 4.35 GHz for the GNP/HB3/CNT arrangement, driven by enhanced scattering and internal reflection of microwaves. These results demonstrate the potential of IL-assisted hybrid filler dispersion in PLA for developing biodegradable materials with multifunctional applications as charge storage capacitors and microwave absorbing materials for sustainable electronics. Full article

Using multifunctional dual-cure smart bioactive resin luting agents (DRLs) offers benefits in adhesive dentistry, but their optical stability remains a concern. Their pre-cured form is a shear-thinning structure with thixotropic gel-like behavior. The effect of their hydrophilicity and different thicknesses of nanoceramic hybrid on the final shade of milled esthetic restorations needs further investigation. This study examined how the optical function deterioration of dual-cure smart bioactive resin luting agents used to bond a CAD/CAM nano-ceramic hybrid composite would influence the restoration’s final shade at three different thicknesses. A nanoceramic hybrid composite (GD) was cut into blocks and grouped by thickness (0.8, 1.0, 1.5 mm). Ten blocks from each group were assigned to subgroups based on the DRL type: Panavia SA Universal (PN), Predicta Bioactive (PR), and ACTIVA BioACTIVE (AC). Color and whiteness changes after a 24 h/day (24 days) coffee immersion were analyzed using statistical methods (ANOVA and Tukey’s HSD for ΔE₀₀; Welch’s ANOVA and Games-Howell for ΔWI_D and ΔL*). DRL type significantly affected ΔE₀₀, ΔWI_D, and ΔL* (p < 0.001). All materials showed the least color change and optical function deterioration at a restoration thickness of 1.5 mm, which was below the acceptability threshold (AT). Despite PR’s bioactive functionality, it maintained its primary optical function with the least color change at GD thicknesses of 1.0 and 1.5 mm (p < 0.001). AC exhibited the greatest ΔE₀₀ above AT, especially at a thickness of 0.8 mm (p < 0.001). ΔL*, ΔE₀₀, and ΔWI_D varied significantly based on DRL type, GD thickness, and the interaction between DRL and thickness (p < 0.05). This suggests that although dual-cure smart DRLs containing bioactive glasses are advantageous, their optical function shifts may become more noticeable in thin, translucent restorations. Increasing the restoration thickness can help mitigate this by altering the optical pathway. Full article

Thermoplastic starch (TPS) nanocomposites with unprecedentedly high loadings of up to 15 wt.% of the nano-clays Laponite (LAP; a synthetic product capable of good dispersion in suitable media) or Montmorillonite (MMT; modified with dialkyldimethylammonium chloride) were prepared by means of our new, two-step TPS preparation protocol. In both the TPS/LAP and TPS/MMT composites, we achieved perfect dispersion and extensive exfoliation of the nano-clays, resulting in pronounced improvements in mechanical performance (modulus increased up to one order of magnitude) and in excellent gas-barrier properties (extremely small permeabilities for O₂, CO₂, and even H₂). MMT, owing to its larger platelet size and to the formation of partially exfoliated multi-layer structures, generated a percolating filler network that provided particularly strong reinforcement, especially at 15 wt.% loading. LAP, though more completely exfoliated, generated a somewhat smaller mechanical reinforcement, but it more strongly increased processing viscosity due to its high specific surface area, which generated highly stable physical crosslinking that persisted even at processing temperatures of T ≥ 120 °C. Efficient matrix–filler interactions were confirmed by thermogravimetric analysis, where the better-exfoliated LAP generated a higher stabilization. The combination of strong mechanical reinforcement with outstanding gas-barrier properties makes the TPS/MMT and TPS/LAP nanocomposites attractive for food-packaging applications, where their natural origin, non-toxicity, bio-degradability, and abundance of nanocomposite components are an additional bonus. Full article

Objectives: This study aims to evaluate the efficacy of hydroxyapatite-tricalcium phosphate (HAP-TCP) as a bone substitute in subantral augmentation for dental implants. Specifically, it investigates the effects of HAP-TCP on bone quality, density, and integration with implants over time. Methods: A prospective controlled longitudinal study was conducted on 22 patients (39–75 years of age) undergoing subantral augmentation and dental implantation. A total of 52 sites of augmented bone and 67 sites of native bone were analyzed using computed tomography (CT) to assess bone density in Hounsfield Units (HU), insertion torque measurements, and the Misch classification for bone quality. Augmented and native bone measurements were compared within each patient. Results: The augmented bone exhibited an average density of 1132.6 ± 334.9 HU, which is significantly higher (45.9%) than the average density of native bone at 519.3 ± 395.0 HU. Insertion torque values in the HAP-TCP augmented sites averaged 35 N·cm, showing a 71.4% increase compared to adjacent native bone sites (25 N·cm). The study found notable improvements in bone homogeneity and vascularization within the augmented zones. Conclusion: HAP-TCP demonstrates significant potential as a reliable and effective synthetic bone substitute for subantral augmentation in dental implants. It yields higher radiodensity and insertion torque than adjacent native bone, while mitigating complications associated with autogenous grafts. These observational findings support the potential clinical use of HAP-TCP for sinus augmentation. Full article