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424 result(s) for "Bellucci, Stefano"
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Carbon/Inorganic Hybrid Multifunctional Composites: Interface Engineering, Coupled Functions and Application-Ready Design
Carbon/inorganic hybrid composites have evolved from filler-reinforced materials into design platforms for coupled electromagnetic, thermal, sensing, environmental, protective and energy-related functions. Their distinctive value lies in the possibility of combining a conductive, polarizable or porous carbon phase with an inorganic phase that contributes dielectric, magnetic, catalytic, ionic, thermally conductive or barrier behavior. This review examines carbon/inorganic hybrid multifunctional composites from the viewpoint of structure–property relationships, with emphasis on interfacial design, percolation, anisotropy, hierarchical architecture, processing and metrology. Selected graphitic composite studies are discussed as case studies for broadband dielectric spectroscopy, microwave shielding, high-frequency contact metrology, thermal diffusivity analysis and impedance-monitored graphene filters; these case studies are integrated with the broader international literature on CNT and graphene polymer composites, MXene films and foams, graphene/metal oxide photocatalysts, boron nitride/carbon thermal networks, biochar–graphene adsorbents, smart coatings, sensors, supercapacitors and water remediation systems. The central argument is that credible multifunctionality requires more than measuring several properties on the same material. It requires simultaneous or service-relevant co-optimization under constraints of thickness, density, processability, aging, humidity, corrosive media, regeneration, toxicity, economic feasibility and scalable fabrication. The review concludes with design rules and reporting recommendations intended to help move the field from impressive property demonstrations toward application-ready hybrid material systems.
Biocompatible Carbon Nanotube-Based Drug Delivery System for Neurodegenerative and Regenerative Biomedical Applications
Carbon nanotubes (CNTs) represent promising nanoplatforms for drug delivery due to their high surface area, tunable surface chemistry, and unique physicochemical properties. This study investigated the effect of chemical functionalization on the dispersion, drug loading, release behavior, aerosolization, and preliminary in vitro cytotoxicity of CNT-based drug delivery systems, with a view toward potential intranasal applications. Pristine CNTs and CNTs functionalized with hydroxyl (–OH) and carboxyl (–COOH) groups were loaded with methylene blue as a model therapeutic compound. The nanosystems were characterized using Raman spectroscopy, UV–Vis analysis, aerosol deposition measurements, electrical mapping by conductive atomic force microscopy (C-AFM), and MTT cytotoxicity assays. Functionalization significantly enhanced CNT dispersion stability and drug release control, with COOH–CNTs exhibiting the most sustained release profile and improved cytocompatibility, maintaining cell viability above XX% at concentrations up to YY µg/mL. Aerosolization tests demonstrated stable droplet formation compatible with nasal delivery devices. Overall, this work provides a proof-of-concept physicochemical and technological assessment of functionalized CNTs as potential carriers for intranasal drug delivery, laying the groundwork for future in vivo validation.
Carbon Materials in 2025: From Lightweight Structures to Sustainable and Multifunctional Platforms
Carbon materials continue to occupy a singular place in materials science because they can be engineered across multiple length scales while retaining a rare combination of low density, high specific performance, chemical tunability, electrical functionality, and processing flexibility [...]
Advanced SPR-Based Biosensors for Potential Use in Cancer Detection: A Theoretical Approach
This study presents a numerical investigation of surface plasmon resonance (SPR) sensors based on multilayer configurations incorporating BK7, silver, silicon nitride (Si3N4), and black phosphorus (BP). Using the transfer matrix method, the optical performance of four architectures was evaluated under refractive index perturbations consistent with values reported in prior theoretical and experimental studies. The sensor response was characterized through metrics such as angular sensitivity, resonance shift, full width at half maximum, attenuation, and derived figures including detection accuracy and limit of detection. Parametric optimization was performed for the thickness of each functional layer to enhance sensing performance. Among all configurations, those incorporating both Si3N4 and BP demonstrated the highest angular sensitivity, reaching up to 394.46°/RIU. These enhancements were accompanied by increased attenuation and spectral broadening, revealing trade-offs in sensor design. The results, based entirely on numerical modeling, provide a comparative framework for guiding SPR sensor optimization under idealized optical conditions.
Effect of Fe Doping on Photocatalytic Dye-Degradation and Antibacterial Activity of SnO2 Nanoparticles
A simple hydrothermal method is utilized to synthesize iron-doped tin oxide nanoparticles (Fe-SnO2 NPs) at various doping concentrations. The structural characterization using XRD, Raman, and FTIR measurements confirmed the incorporation of Fe ions into the SnO2 lattice without any deviation in the tetragonal crystal system of SnO2 nanoparticles. SEM and HRTEM images show the spherical-shaped nanoparticles with agglomeration. The values of interplanar spacing (d-value) calculated from the HRTEM lattice are consistent with the XRD results. Further, optical analysis revealed a red shift in the optical absorption band and a decrease in the band gap energy with an increase in Fe-dopant concentration. The decrease of PL emission peak intensity with Fe doping revealed the generation of singly charged oxygen vacancies. The H2O2-assisted photocatalytic degradation efficiency of Fe-SnO2 NPs investigated against crystal violet dye indicated an efficiency of 98% for 0.05 M Fe-SnO2 NPs within 30 minutes under visible light illumination. In addition, the effects of pH, scavengers, and reusability of the catalyst are tested. The antibacterial behavior of Fe-SnO2 NPs against Escherichia coli is examined by using the colony count method, and the inhibition rate was found to be 49, 65, 70, and 78% for pure, 0.01, 0.03, and 0.05 M Fe-SnO2 NPs, respectively.
Study of Barium Adsorption from Aqueous Solutions Using Copper Ferrite and Copper Ferrite/rGO Magnetic Adsorbents
The development of advanced materials for the removal of heavy metal ions is a never-ending quest of environmental remediation. In this study, a facile and cost-effective approach was employed to synthesize copper ferrite (CF) and copper ferrite/reduced graphene oxide (CG) by microwave assisted combustion method for potential removal of barium ions from aqueous medium. The physiochemical characterizations indicated the formation of magnetic nanocomposite with an average crystallite size of CF and CG is 32.4 and 30.3 nm and with specific surface area of 0.66 and 5.74 m2/g. The magnetic results possess multidomain microstructures with saturation magnetization of 37.11 and 33.84 emu/g for CF and CG. The adsorption studies prove that upon addition of rGO on the spherical spinel ferrite, the adsorption performance was greatly improved for CG nanocomposite when compared with the bare CF nanoparticles. The proposed magnetic adsorbent demonstrated a relatively high Ba2+ adsorption capacity of 161.6 mg·g-1 for CG nanocomposite when compared to 86.6 mg·g-1 for CF nanoparticles under optimum conditions (pH=7;T=25°C). The pseudo-first-order (PFO), pseudo-second-order (PSO), and Elovich models were fitted to the kinetic data, the yielded R2 value of 0.9993 (PSO) for CF and 0.9994 (PSO) for CG which is greater than the other two models, which signify that the adsorption process is chemisorption. Thermodynamic studies show that barium adsorption using CF and CG adsorbents is endothermic. The as-fabricated CuFe2O4/rGO nanocomposite represents a propitious candidate for the removal of heavy metal ions from aqueous solutions.
Phosphorus Loading Drives Microalgal Community Changes and Enhances Nutrient Removal in Photobioreactors Treating Synthetic Wastewater
Phosphorus is a key nutrient regulating algal growth and eutrophication in aquatic systems, yet its isolated effect on microalgae-based wastewater treatment remains underexplored. This study evaluated how varying phosphorus loads drive microalgal community structure and purification performance in controlled photobioreactors fed synthetic wastewater. The synthetic wastewater was formulated with constant carbon and nitrogen but graded phosphorus at C/N/P ratios of 100/5/1, 100/5/10, and 100/5/20 under 6000 lux, a 14 h photoperiod, and 24 ± 2 °C with a 15-day hydraulic retention time. Monitoring of chlorophyll a, pH, total and volatile suspended solids, and algal composition showed that phosphorus enrichment significantly increased chlorophyll a (up to 43.9 µg/L at 20 mg P/L) and particulate biomass (TSS and VSS), while pH remained near neutral to slightly alkaline, with no significant differences among the three bioreactors. Although the same core taxa—Chlorella spp., Scenedesmus spp., Navicula spp., and filamentous algae were present across all bioreactors, their relative abundances shifted significantly with phosphorus concentration. A two-way ANOVA confirmed a highly significant interaction between bioreactor (P level) and genus (p < 0.001), demonstrating phosphorus-driven changes in the microalgal community. Notably, filamentous cyanobacteria (Anabaena spp.) were undetectable in the low- and medium-phosphorus treatments but emerged prominently only at the highest phosphorus level (20 mg/L). Nutrient removal efficiencies peaked in this high-phosphorus bioreactor (C), achieving 85% for bCOD, 78% for nitrogen, and >70% for phosphorus. These results show that phosphorus loading drives predictable shifts in microalgal community composition toward fast-growing algae and cyanobacteria and that these shifts likely contribute to enhanced nutrient removal. The findings support optimization of phosphorus supply and hydraulic residence time in low-cost, sunlight-driven systems to improve polishing performance for small settlements in arid regions.
Graphene Oxide (GO) Materials—Applications and Toxicity on Living Organisms and Environment
Graphene-based materials have attracted much attention due to their fascinating properties such as hydrophilicity, high dispersion in aqueous media, robust size, high biocompatibility, and surface functionalization ability due to the presence of functional groups and interactions with biomolecules such as proteins and nucleic acid. Modified methods were developed for safe, direct, inexpensive, and eco-friendly synthesis. However, toxicity to the environment and animal health has been reported, raising concerns about their utilization. This review focuses primarily on the synthesis methods of graphene-based materials already developed and the unique properties that make them so interesting for different applications. Different applications are presented and discussed with particular emphasis on biological fields. Furthermore, antimicrobial potential and the factors that affect this activity are reviewed. Finally, questions related to toxicity to the environment and living organisms are revised by highlighting factors that may interfere with it.
Overview of Physicochemical Properties of Nanoparticles as Drug Carriers for Targeted Cancer Therapy
The advent of nanotechnology has brought about revolutionary innovations in biological research techniques and medical practice. In recent years, various “smart” nanocarriers have been introduced to deliver therapeutic agents specifically to the tumor tissue in a controlled manner, thereby minimizing their side effects and reducing both dosage and dosage frequency. A large number of nanoparticles have demonstrated initial success in preclinical evaluation but modest therapeutic benefits in the clinical setting, partly due to insufficient delivery to the tumor site and penetration in tumor tissue. Therefore, a precise understanding of the relationships betweenthe physicochemical properties of nanoparticles and their interaction with the surrounding microenvironment in the body is extremely important for achieving higher concentrations and better functionality in tumor tissues. This knowledge would help to effectively combine multiple advantageous functions in one nanoparticle. The main focus of the discussion in this review, therefore, will relate to the main physicochemical properties of nanoparticles while interacting within the body and their tuning potential for increased performance.