Search Results (5,370)

This study evaluates the intrinsic osteogenic potential of β-tricalcium phosphate (β-TCP)-containing composite scaffolds (PLCL–TCP, PLGA–TCP, and ZnO–TCP) on chorion-derived mesenchymal stem cells (CMSCs) under non-osteogenic in vitro conditions. CMSCs were cultured on the three biomaterials for 35 days without osteogenic supplements to isolate the material-driven cellular response. Cell viability was assessed via MTT assay, while osteogenesis-associated markers (alkaline phosphatase, type I collagen, and osteocalcin) were quantified using ELISA. Scaffold surface morphology and elemental composition were characterized before and after cultivation utilizing SEM and EDX. All investigated scaffolds supported long-term CMSC viability and induced measurable osteogenic responses. PLCL–TCP demonstrated a consistently strong biological response, characterized by sustained metabolic activity, elevated ALP and COL I production, and increased osteocalcin levels at later stages of cultivation. ZnO–TCP also exhibited favorable osteogenesis-associated responses, particularly with respect to late-stage osteocalcin production, while maintaining high structural stability. In conclusion, β-TCP composites can intrinsically modulate CMSC behavior without biochemical supplements. Osteogenic outcomes depend on a complex interplay of surface chemistry, scaffold architecture, and degradation profiles, with PLCL–TCP demonstrating favorable overall performance among the investigated biomaterials. Full article

Sponge spicules have emerged as promising biomaterial scaffolds due to their biocompatibility and unique structural properties; however, achieving stable and bioactive functionalization remains a key challenge. The tripeptide GHK is known to promote collagen synthesis and wound repair, yet its therapeutic efficacy is often limited by rapid diffusion and instability. Here, we report ALTUM, a thiol-functionalized sponge spicule composite in which GHK is covalently conjugated via disulfide linkage to enable controlled and redox-responsive peptide delivery. ALTUM exhibited sustained GHK retention under physiological and storage conditions, while exposure to reduced glutathione (GSH) selectively accelerated peptide release through disulfide bond cleavage. This dual release behavior—long-term stability combined with reduction-triggered activation—distinguishes ALTUM from conventional delivery systems. The composite also demonstrated structural stability under thermal, cyclic, and photostability conditions. In an artificial human skin model, ALTUM enhanced dermal penetration of GHK and significantly increased collagen deposition in the dermal layer, demonstrating its capacity to promote collagen production within deeper skin tissue, compared to simple spicule–peptide mixtures. ALTUM was fabricated at an optimized spicule-to-peptide ratio of 3% (w/w), preserving the needle-shaped spicule morphology after surface modification. In vitro, ALTUM exhibited a sustained release profile, with GHK release markedly accelerated in the presence of 10 mM glutathione (GSH) compared with non-reductive conditions, reaching approximately 60% cumulative release over 35 days. In the bioprinted artificial human skin model, ALTUM delivered 9.72 ng/cm² of GHK, more than five-fold higher than the physical mixture of spicules and free GHK (1.9 ng/cm²), and significantly increased type I collagen expression in human dermal fibroblasts. Mechanistically, ALTUM-mediated delivery was associated with increased TGF-β expression and engagement of the SMAD signaling pathway, as indicated by increased phosphorylation of SMAD2/3, consistent with involvement of the TGF-β–SMAD axis in the observed collagen induction. Collectively, these findings establish ALTUM as a structurally stable, redox-responsive dermal delivery platform that enhances collagen synthesis and skin regeneration. Full article

The demand for sustainable, high-performance biomaterials has driven intense research towards natural polysaccharide hydrogels. Accordingly, this study aimed to synthesize novel starch-based hydrogel materials, considering their inherent hydrogel-forming capabilities together with diverse potential applications (e.g., pharmaceuticals, medicine, and the cleaning application for the artifacts). To obtain hydrogels with enhanced mechanical and physico-chemical properties, starch was combined with other polymeric species (i.e., alginate, polyvinyl alcohol, and polyvinylpyrrolidone), and a gelling process was induced by using calcium cations or borate anions. Two distinct hydrogels (named S-Ca and S-SB, respectively) were prepared and characterized by a range of instrumental and experimental techniques. The assessed properties included water and solvent resistance, equilibrium water content, water-releasing capacity, morphology and microstructural features with their composition by SEM-EDS analysis, and mechanical properties (tensile strength, elasticity, Young’s modulus, and hardness). The results indicated that the investigated hydrogels exhibited suitable properties for a variety of applications, including surface cleaning processes in the field of cultural heritage conservation. For instance, they showed equilibrium water content (between 80 and 90%) comparable with other hydrogels commonly used as cleaning tools (e.g., agar and p(HEMA)/PVP) and quite low water-releasing capacity (between 10 and 17 mgcm⁻²). Moreover, the S-SB hydrogel displayed distinctly better tensile strength and elongation at break than hydrogel prepared in the presence of Ca²⁺ (S-Ca). Notably, S-SB experienced considerable elasticity improvement after freezing–thawing cycles, as indicated by a decrease in tensile strength (from 275 to 102 kPa) and an increase in elongation at break (from 121 to 275%). However, it should be noted that the hydrogel selection depends on the requirements of the target application, as different processes demand materials with distinct characteristics. Hence, both S-Ca and S-SB hydrogels were tested as cleaning tools for the removal of artificially aged acrylic coating (i.e., Paraloid B-72) from the surface of marble and wood specimens, respectively. The tests provided positive results, as aged coating was satisfactorily removed by applying the hydrogels loaded with a nanostructured emulsion (NSE). These novel starch-based hydrogels demonstrate significant potential as high-performance alternatives to conventional hydrogel systems currently used in conservation science as well as in other industrial applications. Full article

This study reports the preparation of a nanocomposite using a black cumin surface as a carbon framework on which zinc oxide-doped manganese ferrite nanoparticles were deposited and grown. A simple precipitation method was used to prepare the nanocomposite. The resulting composite was characterized using various characterization analyses such as FTIR, XRD, EDX, SEM, TEM, and TGA. The composite surface was highly conformed with functional groups, and the nanocomposite was formed due to electrostatic and non-electrostatic interactions between the carbon framework and the nanoparticles. X-ray analysis revealed a crystalline structure with crystal sizes up to 45 nm. Microscopic images revealed the surface morphology, confirming the irregular distribution of particles within the composite. The resulting composite material was used for adsorption application. The composite material was tested for the removal of Congo red dye from water. It was found that under optimal conditions, a dose of 2 g per liter of absorbent removed nearly 100% of dye from a 10 mL volume of 10 mg per liter Congo red solution within 90 min and 7 pH. A monolayer adsorption was confirmed by the isotherm analysis. The monolayer adsorption capacity for the present study was ~13.0 mg per gram. The adsorption kinetics suggested the fitting of pseudo-second order. Based on the findings, it was concluded that the chemical mechanism was responsible for the present adsorption process. The regeneration study demonstrates the stability of current adsorbent up to two cycles only. This nanocomposite is the first of its kind which promotes the creation of nanocomposites in the future by using natural materials and reduces the dependency on activated carbon. Full article

Titanium-doped diamond-like carbon (DLC:Ti) films were deposited by magnetron sputtering. The effects of Ti concentration on the microstructure, phase composition and piezoresistive properties of the films were systematically investigated. The surface morphology, crystal structure and chemical bonding states of the samples were characterized using SEM, XRD and XPS. The piezoresistive properties were then assessed by monitoring the resistance change in the thin films using a precision resistance meter under controlled external stimulation. The results demonstrate that the sp²/sp³ ratio of the DLC:Ti films increases with rising Ti concentration, and both Ti–C and Ti–Ti chemical bonds are formed within the films. An excessive β-Ti phase forms when the Ti concentration exceeds 39.7 at.%. The electrical resistance of DLC:Ti films decreases linearly as the applied normal stress increases from 0 to 35 MPa, with a maximum piezoresistive coefficient of −9.0 × 10⁻² GPa⁻¹ achieved for the film with a Ti doping concentration of 12.9 at.%. One hundred cyclic loading–unloading tests induce the structural transition from sp³ to sp², resulting in the graphitization of DLC:Ti films. In addition, external stress facilitates the fracture of Ti–C bonds and the relaxation of residual stress in the DLC:Ti films; the β- to α-Ti phase transformation induced by external loading is also observed in the films. Cyclic piezoresistive tests reveal that the piezoresistive stability of the DLC:Ti films is enhanced with increasing Ti concentration, which is attributed to the increased formation of Ti–C bonds in the films. Full article

Driven by advances in multifunctional materials design, silver halides—both natural (AgCl, AgBr, AgI, and mixed phases such as embolite) and synthetic—have emerged as versatile functional materials characterized by tunable crystallography, phase stability, and compositional variability. This study investigates global research trends, interdisciplinary development, and emerging application areas of silver halides through a bibliometric analysis of 23,841 publications indexed in the Web of Science (1975–2025). CDPI, TELM, VOSviewer, and Excel were employed to evaluate publication growth, disciplinary integration, and thematic evolution. Research output increased markedly after 2005, reaching approximately 700–1000 publications annually during 2020–2025. China (18.3%) and the United States (17.5%) were the leading contributors, while the Chinese Academy of Sciences, Russian Academy of Sciences, and CNRS showed the highest scientific impact. Materials Science Multidisciplinary (CDPI = 0.72), Chemistry Multidisciplinary (0.70), and Physical Chemistry (0.67) exhibited the strongest interdisciplinary integration, whereas Nanoscience and Nanotechnology demonstrated the fastest growth. Keyword co-occurrence analysis identified six major research domains focused on functional materials engineering, including environmental remediation, catalysis, crystal growth, antibacterial materials, interfacial processes, and electroanalytical systems. Recent studies increasingly emphasize structure–property relationships and synthetic control of crystal size, morphology, and surface characteristics to enhance performance in photocatalysis, sensing, antimicrobial coatings, and advanced optical applications. Overall, the results highlight the growing importance of silver halides as strategic functional materials and provide a quantitative framework for future research and technological development. A limitation of this study is its exclusive reliance on the Web of Science database, which may underrepresent relevant publications indexed elsewhere. Full article

The development of sustainable electrocatalysts for clean energy by modifying biomass-derived activated carbon with nitrogen and transition metals is presented. Activated carbon (AWC) material was obtained using alder wood char as a precursor, while nitrogen and cobalt or copper nanoparticles were incorporated with the aim of creating efficient materials for hydrazine oxidation (HzOR) and direct hydrazine–hydrogen peroxide fuel cells (DHHPFC, N₂H₄–H₂O₂). The composition, structure, and surface morphology of the created materials were examined using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The activity of the AWC, AWC–Co–N, and AWC–Cu–N catalysts for HzOR was investigated using cyclic voltammetry (CV) and linear sweep voltammetry (LSV). N₂H₄–H₂O₂ fuel-cell tests were performed by applying the catalysts as both the anode and cathode. It was found that all materials retained a hierarchical porous carbon framework, while metal incorporation altered surface compactness. Cobalt doping produced well-dispersed Co nanoparticles and abundant Co–N–C coordination sites, whereas Cu introduction resulted in moderately compact structures with uniformly distributed Cu-based nanoparticles. Electrochemical measurements demonstrated that both metal dopants enhanced HzOR activity, with the catalytic performance following the order of AWC–Co–N > AWC–Cu–N > AWC. Fuel-cell testing further confirmed this trend: AWC–Co–N achieved the highest maximum power density (30.4 mW cm⁻²), outperforming AWC–Cu–N (17.7 mW cm⁻²). These results identify AWC–Co–N as a highly effective bifunctional electrocatalyst for DHHPFCs. Full article

Nanoemulsions are thermodynamically unstable but kinetically stable colloidal dispersion systems with droplet sizes ranging from 20 to 500 nm. With their high specific surface area, excellent optical properties, tunable rheology, and remarkable penetration ability, these systems demonstrate enormous potential in enhanced oil recovery (EOR). This paper systematically reviews the significant advances in nanoemulsion characterization techniques and oil displacement mechanisms. The nanoemulsion characterization techniques are examined, covering a comprehensive multi-scale characterization system from particle size and distribution analysis (e.g., dynamic light scattering, laser diffraction), micro-morphology and structure visualization (e.g., transmission electron microscopy, atomic force microscopy), and interface and surface property characterization (e.g., interfacial tension measurement, zeta potential analysis) to stability and rheology assessment, as well as chemical composition and structure analysis. Furthermore, core mechanisms of nanoemulsions in oil displacement processes are briefly summarized, revealing multiple synergistic enhancement mechanisms including ultra-low interfacial tension and oil film stripping, rock wettability alteration, emulsification and viscosity reduction, improved fluid flow and injection pressure reduction. Finally, prospects for the potential application of nanoemulsion oil displacement technology in the development of low-permeability, tight, and heavy oil reservoirs are described by analyzing the current challenges such as unclear structure–activity relationships, full-chain stability (including storage, transport, injection, and reservoir aging), and environmental safety, and future research directions are pointed out, including clarifying structure–activity relationships, smart responsive system development, artificial intelligence-assisted design, and pilot-scale validation. Clarifying the link between nanoemulsion characterization techniques and oil displacement mechanisms is of significant academic and engineering value for promoting the transition from empirical application to rational design of related technologies. Full article

Background: Persistent intraradicular infection and biofilm survival remain major challenges in endodontic treatment, particularly because residual microorganisms may remain within dentinal tubules despite chemomechanical preparation. The antimicrobial efficacy of sealers may be insufficient against resistant bacteria. This study evaluated the effect of incorporating red and black iron oxide nanoparticles into BioRoot RCS on its antimicrobial activity and cytocompatibility. Methods: BioRoot RCS was modified with red or black iron oxide nanoparticles at 0.5 wt% and 2.0 wt%, generating 5 groups: unmodified sealer, 0.5% red, 2.0% red, 0.5% black, and 2.0% black. Surface morphology was analyzed using scanning electron microscopy, while elemental composition was determined by energy-dispersive X-ray spectroscopy. Antibacterial activity against Enterococcus faecalis and Fusobacterium nucleatum was assessed using a direct contact test, antibiofilm activity by colony-forming unit reduction on infected dentin discs, and cytocompatibility using human gingival fibroblasts and the AlamarBlue assay. Results: Iron was detected in the modified formulations, and elemental mapping showed homogenous distribution of calcium and iron. The 2.0% formulations showed significantly higher antibacterial and antibiofilm effects than the corresponding 0.5% groups (p < 0.05), with 2.0% black showing the lowest bacterial counts. Cytocompatibility differed at 1 and 3 days but not at 7 days, and all groups remained close to the control level with no significant difference (p > 0.05). Conclusions: Within the limitations of this in vitro study, experimental modification of BioRoot RCS with iron oxide nanoparticles, particularly at 2.0 wt%, improved the antimicrobial and antibiofilm efficacy of BioRoot RCS while maintaining acceptable cytocompatibility. However, physicochemical and handling properties must be evaluated before the clinical relevance of this modification can be determined. Full article

The development of low-cost and highly sensitive electrochemical sensing platforms for pesticide monitoring has attracted significant attention in recent years. In this study, coke-derived carbon (CDC) was successfully synthesized from petroleum coke through high-temperature carbonization under a nitrogen atmosphere. Subsequently, a CDC@CuO-NP nanocomposite was fabricated by depositing copper oxide nanoparticles onto the CDC matrix. The morphology, structure, and elemental composition of the synthesized materials were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and elemental mapping analyses, confirming the successful formation of the composite and the uniform distribution of CuO nanostructures on the carbon surface. Electrochemical characterization demonstrated that the incorporation of CuO significantly enhanced the electrochemical performance of CDC by increasing the electroactive surface area and facilitating electron transfer. The CDC@CuO-NP-modified glassy carbon electrode was applied for the electrochemical detection of dichlorvos (DDVP) using electrochemical impedance spectroscopy (EIS). The sensor exhibited a concentration-dependent increase in charge-transfer resistance and showed a linear response in the concentration range of 247–3770 nM, with the regression equation y = 47.1458C + 111.8162 and a correlation coefficient of R² = 0.9832. The developed sensor achieved a low limit of detection (LOD) of 2.3 nM, demonstrating high sensitivity toward DDVP. These results indicate that the CDC@CuO-NP nanocomposite is a promising, low-cost, and efficient electrode material for the sensitive determination of organophosphorus pesticides and has considerable potential for environmental monitoring and food safety applications. Full article

Biomass-derived carbons are promising sustainable anode materials for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) because biomass is renewable, abundant, low-cost, and naturally diverse in composition and morphology. Lignocellulosic frameworks, intrinsic heteroatoms, and biomass-derived inorganic species can be converted through carbonization, activation, graphitization, and doping into carbon architectures with tunable porosity, carbon ordering, and surface chemistry. This review first summarizes the compositional and structural features of biomass precursors and explains how processing conditions convert them into carbon frameworks. Recent advances in biomass-derived carbon anodes are then discussed by comparing the distinct design requirements for LIBs and SIBs. For LIBs, accessible surface area, hierarchical porosity, heteroatom-derived active sites, and improved electronic conductivity are generally beneficial for enhancing Li⁺ storage and rate capability. In contrast, SIB hard carbons require controlled surface exposure, expanded turbostratic spacing, and closed or latent pores to improve Na⁺ storage reversibility and initial Coulombic efficiency. These comparisons emphasize that biomass-derived carbon anodes should be designed according to system-specific storage mechanisms rather than a universal carbon design strategy. Full article

The objective of this study was to examine the physicochemical properties of maltodextrins derived from starch isolated from red- and purple-fleshed potatoes, in comparison to those obtained from light-fleshed potatoes. The investigation focused on several parameters, including dextrose equivalent (DE), non-carbohydrate components, maltooligosaccharide profile, particle size, surface morphology, water-binding capacity, solubility, rheological properties, structural composition as determined by Fourier transform infrared spectroscopy (FT-IR), and molecular weights. Maltodextrins sourced from the starch of colored potato varieties exhibit superior functional properties, notably nearly 100% solubility and enhanced water absorption capacity. This is attributed to their fine microstructure, which promotes hydration and facilitates the diffusion of water into the interior of the particles, in contrast to maltodextrins derived from the starch of yellow potato varieties. This phenomenon is also influenced by the maltooligosaccharide profile, characterized by a high proportion of low-molecular-weight sugars, lower molecular weights, and polydispersity (Pd), as well as the low SPAN of these maltodextrins. Additionally, maltodextrins derived from the starch of yellow potato varieties (Tajfun and Lord) formed soft gels, whereas those from colored potatoes resulted in hard gels. Full article

Neutral salt spray tests were conducted on assemblies comprising H59 brass and either electrogalvanized or hot-dip galvanized bolts. The polarization curves, electrochemical impedance spectroscopy (EIS), corrosion morphology, elemental distribution, and corrosion product composition of the H59 brass were systematically characterized. The results demonstrated that upon coupling with galvanized bolts, the formation of a protective Cu₂O film on the H59 brass is significantly weakened, leading to accelerated corrosion. After coupling with electrogalvanized bolts, the i_corr reached a maximum value of 0.21 mA/cm². A corrosion layer predominantly composed of ZnO formed on the sample surface with a thickness of approximately 13 μm, and no penetration or enrichment of Cl was observed in the matrix. More seriously, when the brass was assembled with hot-dip galvanized bolts, the i_corr never dropped below 0.2 mA/cm². A porous and complex Zn-Cu-O-Cl mixed corrosion layer developed on its surface. This loose structure allows Cl⁻ to reach a depth of 55 μm into the matrix and continue causing corrosion. The mechanisms underlying the different corrosion behaviors of H59 brass caused by different galvanizing bolt processes require further investigation. Full article

To date, lithium–ion batteries (LIBs) are considered one of the most promising and market-leading energy storage systems due to their high theoretical capacity and energy density. However, poor thermal and cyclic stability, low electrolyte uptake, and the possibility for frequent short circuits of typical separators and evolution of several gases during long cycle operation pose several problems for LIBs. Metal-organic frameworks (MOFs) have attracted widespread interest as a promising material for improving the cycle stability and safety of rechargeable batteries due to their inherent surface and structural properties such as high specific surface area, high porosity, and ionic conductivity. In this work, the aim is to provide detailed descriptions of the synthesis routes and parameters for obtaining various MOFs such as Zr-MOF-808 and Ni-MOF-74 nanoparticles and the fabrication of those MOF-integrated separators. To optimize the crystallinity, morphological and compositional characteristics, and several material characterizations such as XRD, SEM, and EDX have been applied. Afterwards, the synthesized MOF-integrated glass fiber (GF) separators have been developed for lithium–ion battery (LIB) applications. To investigate the electrochemical performance and the effect of MOF integration into the separators, electrochemical studies in the form of galvanostatic charge–discharge (GCD), electrochemical impedance spectroscopy (EIS) have been evaluated by preparing CR2032-type half-coin cells. This MOFs-integrated GF-separators and synthesized LiNi_0.6Mn_0.2Co_0.2O₂ (NMC622) cathode materials-based coin cell LIB exhibited higher cycle stability than bare GF-separator based LIB. This novel approach and extensive research suggest that development of MOF-integrated separators could significantly improve cycle stability by reducing the internal cell degradation for next generation energy storage devices. Full article

Rapid economic development has led to a growing reliance on private car commuting, making the mitigation of carbon dioxide (CO₂) pollution along road environments critical for the health of nearby residents. Road greening serves as an ecological barrier between traffic emissions and adjacent residential areas, and its effectiveness in reducing local CO₂ pollution has been widely studied. However, the influence of different spatial morphologies of road greening on the distribution of CO₂ around buildings remains underexplored. In this study, we developed a numerical simulation model to investigate CO₂ dispersion on building surfaces under various road greening spatial configurations. Simulation results indicate that a “tree–shrub–grass” composite configuration significantly reduces CO₂ concentrations around buildings. These findings provide practical guidance for optimizing vegetation spatial layouts in high-density road networks and contribute to the global pursuit of carbon peak and carbon neutrality goals. Full article