Search Results (753)

Diabetes mellitus is a serious public health problem, mainly due to the difficulty in healing chronic wounds, which present an inflammatory response for long periods of time and are more vulnerable to infections. Hydrogels are a promising therapeutic solution due to their biocompatibility, biodegradability, and ability to allow controlled release of therapeutic agents. The addition of bioactive glasses doped with therapeutic ions to hydrogels can also provide specific biological responses to the system and thus improve tissue regeneration. In this study, a hydrogel based on carboxymethylcellulose and polyethylene glycol with different degrees of crosslinking and enriched with 10% by weight of CeO₂-doped Bioglass 45S5 was developed. Structural, morphological, mechanical, and biological characterizations were performed on bioactive glass, hydrogels, and hydrogels enriched with bioactive glass. Structural analyses confirmed the preservation of the typical amorphous structure of Bioglass 45S5, even after the incorporation of 5% molar CeO₂, as well as the effectiveness of the polymer matrix crosslinking process. Structural analyses demonstrated the preservation of the typical amorphous structure of Bioglass 45S5, even after the incorporation of 5 mol% CeO₂, as well as the effectiveness of the polymer matrix cross-linking process. The hydrogels exhibited distinct behaviours in terms of water absorption and degradation, showing that the sample with the lowest concentration of crosslinkers and bioactive glass allowed for a higher expansion rate and a higher degradation rate. The hydrogel with 10 wt% BG did not compromise cell viability and showed structural integrity after being subjected to cyclic flexible deformations, indicating its safety and suitability for use in tissue engineering. Full article

Background/Objectives: The long-term clinical success of dental luting cements largely depends on their mechanical performance. This study systematically compared six commonly used definitive dental cements by assessing key mechanical characteristics such as compressive strength and fatigue resistance. Methods: The tested materials included Adhesor Zinc Phosphate (AphC), Harvard Zinc Phosphate (HphC), polycarboxylate cement (CaC), glass ionomer cement (GIC), resin-modified glass ionomer cement (RMGIC), and resin cement (ReC). Both static and dynamic compressive load tests were performed using an Instron ElectroPuls E3000 dynamic testing instrument. During static testing, 77 samples were subjected to an increasing load up to 1500 N. Dynamic tests on 78 samples involved cyclic loading over seven phases from 50 N to 1600 N, with 1500 cycles per phase at 10 Hz. Results: Static load results indicated that GIC, CaC, and phosphate cements exhibited similar performance and were significantly weaker compared to RMGIC and ReC. In the dynamic fatigue tests, most ReC and RMGIC samples maintained integrity throughout the entire protocol, demonstrating markedly superior mechanical reliability. Finite element analysis (FEA) further confirmed the experimental observations, revealing more homogenous stress distribution and lower peak stresses in ReC and RMGIC compared with the conventional cements. Conclusions: Overall, the resin-based and resin-modified glass ionomer cements showed the highest compressive strength and fatigue resistance, indicating superior long-term mechanical stability compared to the conventional cements. These findings support the clinical use of resin-based cements as reliable luting agents for definitive fixation in high-load prosthodontic applications. Full article

The growing energy demand in the residential sector, driven by the extensive use of air conditioning systems, poses serious environmental and economic challenges. A sustainable alternative is the use of efficient insulating materials derived from waste resources. This study presents the synthesis of glass–ceramic foams produced from recycled glass (90 wt%), pumice (5 wt%), and limestone (5 wt%), sintered at 800 °C for 10 min. The resulting foams exhibited a low apparent density of 684 kg/${\mathrm{m}}^3$ and thermal conductivity of 0.09 W/m·K. These were incorporated into composite insulating panels composed of 70 wt% ceramic pellets and 30 wt% Portland cement, achieving a thermal conductivity of 0.18 W/m·K. The panels were evaluated in a 64.8 ${\mathrm{m}}^2$ social housing model located in Chihuahua, Mexico, using TRNSYS v.17 to simulate annual energy performance. Results showed that applying a 1.5-inch ceramic foam panel reduced the annual energy demand by 16.9% and the total energy cost by 14.7%, while increasing the panel thickness to 2 in improved savings to 18.4%. Compared with expanded polystyrene (EPS), which achieved 24.9% savings, the proposed ceramic panels offer advantages in fire resistance, durability, local availability, and environmental sustainability. This work demonstrates an effective, low-cost, and circular-economy-based solution for improving thermal comfort and energy efficiency in social housing. Full article

This study investigates the interfaces of ultra-high-performance fibre-reinforced concrete (UHPFRC). The interfaces of UHPFRC-to-UHPFRC were studied using two techniques: (i) slant shear test and (ii) shear key test. Moreover, the glass fibre-reinforced polymer (GFRP) rebars were also used in the shear plane to optimise durability. Six UHPFRC push-off specimens with different GFRP reinforcement ratios and changing shear plane angles were investigated and compared to existing models and codes. The results showed that the slant shear and shear test performed better without adding the epoxy agents due to the presence of steel fibres, which provided the excellent benefit of bridging the cracks and increasing the friction resistance. Furthermore, the shear strength increased substantially with inclined shear planes, rising from 607 kN in the vertical case to 1837 kN at a 60° inclination. However, the existing equations for predicting the shear strength overpredict the shear strength with a vertical shear plane and underpredict the shear strength of the angled shear plane. The test results also confirm that steel fibres enhance shear transfer through crack bridging, while epoxy weakens the interface by limiting mechanical interlock. The linear elastic behaviour of GFRP rebars also influences the shear transfer mechanism by contributing dowel action without yielding. Full article

Wind turbine blades (WTBs) have always been considered one of the greatest engineering achievements. They primarily use glass fiber-reinforced polymers (GFRPs) because of their lightweight nature, impressive strength-to-weight ratio, and durability. Until now, typical disposal methods of End-of-Life (EoL) WTBs are landfill or incineration. However, such practices are neither environmentally sustainable nor compliant with current regulations. This study investigates a low-temperature solvolysis process using a poly(ethylene glycol)/NaOH system under ambient pressure for efficient decomposition of the polyester matrix, promoting the potential of chemical recycling as an alternative to landfilling and incineration by offering a viable method for recovering glass fibers from WTB waste. A parametric study evaluated the influence of reaction time (4–5.5 h) and catalyst-to-resin ratio (0.1–2.0 g NaOH per g resin) on solvolysis efficiency. Optimal conditions (200 g PEG200, 12.5 g NaOH, 10 g GFRP, 5.5 h) achieved an ~80% decomposition efficiency and fibers exhibiting minimal surface degradation. SEM and EDX analyses confirmed limited morphological damage, while excessive NaOH (>15 g) caused notable etching of the glass fibers. ICP-OES of liquid residues detected high Na (780 mg/L) and Si (139 mg/L) concentrations, verifying partial dissolution of the fiber structure under strongly alkaline conditions. After applying a commercial sizing agent (Hydrosize HP2-06), TGA confirmed ~1.2% sizing mass, and nanoindentation analysis showed the interfacial modulus and hardness of re-sized fibers improved by over 70% compared to unsized recycled fibers, approaching the performance of virgin fibers. Full article

Background: Alveolar bone resorption remains a major challenge in implant and prosthetic rehabilitation. While autologous bone grafts are still considered the gold standard, their biological and surgical limitations have promoted the use of synthetic biomaterials such as biphasic calcium phosphate (BCP), β-tricalcium phosphate (β-TCP), nanocrystalline hydroxyapatite, and bioactive glass. Methods: This systematic review, conducted in accordance with PRISMA guidelines, was based on a comprehensive search performed in March 2025 across PubMed, MEDLINE, Embase, and Google Scholar. A total of 11 clinical studies—including both randomized and non-randomized comparative trials—were identified. Due to the marked heterogeneity of study designs and outcome measures, meta-analysis was not feasible. Reported outcomes focused on bone volume preservation, residual biomaterial, implant stability, histological integration, and postoperative complications. Results: Overall, synthetic biomaterials achieved satisfactory bone regeneration and implant stability, with mean bone preservation ranging between 85% and 95%, often comparable to xenografts and other grafting materials. Among the materials analyzed, β-TCP and BCP generally demonstrated superior resorption control and dimensional stability, while bioactive glass showed favorable integration and remodeling rates. The addition of bioactive agents such as rhBMP-2, rhPDGF-BB, or platelet-rich plasma further enhanced new bone formation. Conclusions: Within the limits of current evidence, synthetic biomaterials show clinical performance comparable to xenografts, particularly in socket preservation and ridge augmentation procedures. Their predictable handling, absence of donor-site morbidity, and potential for bioactive enhancement make them valuable tools for routine clinical use. Larger, standardized trials with long-term follow-up are needed to validate these findings and refine material selection in alveolar bone regeneration. Full article

This study examines the effect of cationic bio-based adhesion promoters (APs) derived from rapeseed oil (RO) on the performance of bitumen and asphalt mixtures. Several synthesized APs with varying polyamine content were evaluated and compared with commercial additives (Wetfix^® BE, Nouryon, Netherlands and Carbazole AK-M, SPETSKONTRAKT, Kyiv, Ukraine). Modification of bitumen with bio-based APs improved adhesion to glass and crushed stone while keeping penetration, softening point, and ductility within standard limits. Among the tested formulations, AP20 demonstrated the most balanced performance, achieving high adhesion values even at low dosages (0.2–0.4 wt. %). Asphalt concrete mixes prepared with AP20 exhibited enhanced water resistance and higher indirect tensile strength ratio (ITSR), indicating improved durability under moisture exposure. These findings highlight the potential of rapeseed oil-based adhesion promoters as effective and sustainable alternatives to conventional anti-stripping agents in road construction. Full article

Polymer-dispersed liquid crystal (PDLC), as an electrically controlled dimming material, has broad application prospects in various fields, including smart glass, display technology, and optical devices. However, traditional PDLC materials still face some challenges in practical applications, such as a high driving voltage and insufficient optical contrast, which limit their further application in high-performance optoelectronic devices. In this study, PDLC composite films exhibiting low-voltage operation (23 V), high contrast ratios (135), and rapid response times (T_R ~1.28 ms, T_D ~48 ms) were developed. This was achieved by modifying the chain length of the crosslinking agent and polymer monomer as well as by incorporating molybdenum disulfide (MoS₂) nanosheets. It shows a good regulation ability in the sunlight range (ΔT_sol = 63.92%, ΔT_lum = 73.97%). Simultaneously, the various chemical bonds inside the film and its special network structure enable it to exhibit a good radiative cooling effect. The indoor sunlight simulation tests showed that the indoor temperature decreased by 5 °C. This study provides valuable ideas for the development and preparation of smart windows with high efficiency and energy savings. Full article

This study applies circular and sustainable principles to the formulation of biopolymer-based materials using naturally occurring additives. To improve the affinity between the host matrix and additives such as metal oxides, the work involves adding stearic acid-modified zinc oxide (f-ZnO) and sonicated titanium dioxide (s-TiO₂) to a polylactic acid and bio-derived polyamide 11 (PLA/PA11 = 70/30 w/w biopolymer blend via melt mixing. To evaluate the impact of the functionalization and sonication on metal oxides (i.e., f-ZnO and s-TiO₂) introduced into the PLA/PA11 blend, composites containing unmodified ZnO and TiO₂ prepared under the same processing conditions were compared with the modified ones. All of the composites were characterised in terms of their solid-state properties, morphology, melt behaviour, and photo-oxidation resistance. The addition of both f-ZnO and s-TiO₂ appears to exert a plasticising effect on the rheological behaviour, in contrast to unmodified ZnO and TiO₂. The presence of stearic acid tails on ZnO has been estimated at approximately 4%, whereas sonication reduces the diameter of TiO₂ particles by half. In the solid state, both unmodified and modified particles can reinforce the biopolymer matrix, enhancing the Young′s (elastic) modulus. Calorimetry analysis suggests that unmodified and modified metal oxide particles do not influence the glass transition of the PLA phase but affect the melt temperatures of both biopolymeric phases by reducing macromolecular mobility. Morphology analysis shows that the presence of both f-ZnO and s-TiO₂ particles does not reduce the size of the PA11 droplets. The f-ZnO particles, which have long stearic tails and are more compatible with the less-polar phase (PLA), are probably located at the interface between the two biopolymeric phases or in the PLA phase. Furthermore, s-TiO₂ particles, like TiO₂, do not reduce the dimensions of PA11 droplets, suggesting that there is no preferential location of the particles. Due to the presence of both f-ZnO and s-TiO₂, an increase in the hydrophobicity of the PLA/PA11 blend has been detected, suggesting enhanced water resistance. The photo-oxidation resistance of the PLA/PA11 blend is significantly reduced by the presence of unmodified metal oxides and even more so by the presence of modified metal oxides. This suggests that metal oxides could be considered photo-sensitive degradant agents for biopolymer blends. Full article

The long-term success of composite restorations largely depends on the performance of dental adhesives at the adhesive–tooth interface. Despite ongoing improvements, secondary caries remains the leading cause of restoration failure, primarily due to the adhesive layer’s susceptibility to hydrolytic degradation, bacterial invasion, and limited biological functionality. This review provides a comprehensive overview of recent advances in bioactive dental adhesives for preventing recurrent caries, focusing on their mechanisms of action, material performance, therapeutic functions, and clinical potential. Bioactive adhesives combine durable bonding with biofunctional benefits, including remineralization, antimicrobial activity, enzymatic inhibition, and support for tissue regeneration. By integrating these properties, they enhance both the durability of the adhesive interface and oral health. Recent strategies include the incorporation of ion-releasing fillers such as calcium phosphate and bioactive glass, antimicrobial monomers such as MDPB and quaternary ammonium methacrylates, enzymatic inhibitors, and hydrolytically stable resin matrices. Together, these components strengthen the adhesive interface and provide biologically active effects to prevent recurrent caries. Although in vitro findings are promising, challenges remain, including limited long-term clinical data, the absence of standardized evaluation protocols, and barriers to clinical translation. Addressing these gaps is essential to ensure predictable clinical outcomes. Bioactive dental adhesives represent a paradigm shift in restorative dentistry, evolving from passive bonding agents to multifunctional therapeutic materials. By combining structural durability with biological protection, they hold significant potential to prevent recurrent caries and improve the long-term success of composite restorations. Full article

The aim of this study was the valorization of brewer’s yeast waste as a low-cost, biodegradable filler for polylactide (PLA) and the evaluation of the effect of yeast biomass on the processing, mechanical, thermal properties, and biodegradation of the resulting composites. The materials were prepared using extrusion and injection molding techniques, with the addition of brewer’s yeast (Saccharomyces cerevisiae) in amounts ranging from 5 to 30 wt%. Fourier-transform infrared spectroscopy (FTIR) analysis revealed the absence of strong interfacial chemical interactions, indicating physical dispersion of the filler within the matrix. The addition of biomass significantly modified the properties of PLA. The results demonstrated increased melt flowability (melt flow rate increased from 18.8 to 39.8 g/10 min) and stiffness (a 13% increase in Young’s modulus for 20 wt%), accompanied by a considerable reduction in tensile strength (from 63.2 to 20.2 MPa) and impact strength (from 22.8 to 6.2 kJ/m²). Thermal analyses showed a systematic decrease in the glass transition temperature by approximately 5 °C and a dual effect of the filler on crystallization behavior. At low concentrations, the waste acted as a nucleating agent, while at higher loadings it limited crystallinity, leading to an amorphous structure. Thermal stability decreased with increasing biomass content (from 329.3 °C to 266.8 °C). Industrial composting tests indicated that at a 30 wt% yeast content, the mass loss (27.5%) was higher than that of neat PLA (25.5%), suggesting accelerated biodegradation. Despite the deterioration of mechanical performance, the developed biocomposites represent a promising material for single-use applications, combining low cost, easy processability, and an environmentally favorable profile consistent with the principles of the circular economy. Full article

The local segmental mobility of polymer chains in polydimethylsiloxane (PDMS) plays a critical role in determining the material’s behaviour. Incorporation of zeolite particles can modify these local dynamics, which is crucial as they affect the overall performance of the resulting composite material with potential for various industrial applications. The aim of this study was to investigate the influence of zeolite addition on the local dynamic behaviour of PDMS chain segments in PDMS–zeolite composites. To investigate the effect of zeolite morphology and loading on the segmental dynamics and phase behaviour of PDMS, Zeolite A (with cubic and spherical morphologies) and Zeolite X were incorporated into the PDMS matrix at 20, 30, and 40 wt%. The electron spin resonance (ESR)-spin probe method was used to study molecular dynamics, while the thermal behaviour was analysed using differential scanning calorimetry (DSC). ESR results revealed that the presence of zeolites increases the isothermal crystallisation rate affecting segmental mobility in the amorphous phase below the crystallisation temperature. This effect was found to depend more strongly on zeolite morphology than on filler content. DSC measurements showed no change in glass transition temperature with the addition of zeolite; however, shifts in cold crystallisation and melting behaviour were observed, indicating changes in crystal structure and its degree of perfection. These findings suggest that zeolites act as heterogeneous nucleation agents, with their structural properties playing a critical role in the crystallisation behaviour of PDMS. Full article

Background/Objectives: Nanotherapies are a strategy to combat Candida resistance. This study analyzed the impacts of iron oxide nanoparticles (IONPs) functionalized with a chitosan (CS) layer acting as carriers of chlorhexidine (CHX) on an oral candidiasis microcosm biofilm. Methods: Saliva samples from three healthy donors were used to form biofilms, to which Candida species were added to reproduce an oral candidiasis microcosm. Biofilms were cultivated for 72 h on glass coverslips using an active adhesion model. Biofilms without Candida served as a control model. The nanocarrier loaded with CHX at 78 (IONPs-CS-CHX78) or 156 µg/mL (IONPs-CS-CHX156) was co-incubated with the biofilms for 24 h. Controls included isolated IONPs, CS, and CHX, in addition to an untreated group (NC). Assays for biomass production, metabolism, microbial load, and lactic acid production were conducted to assess antibiofilm effects. Biofilm structure, viability, and thickness were also examined by confocal microscopy. Statistical analysis was performed using one-way ANOVA or Kruskal–Wallis, subsequently accompanied by the Student–Newman–Keuls post hoc test (p < 0.05). Results: CHX and IONPs-CS-CHX156 were the most effective agents against all tested biofilm models, significantly reducing metabolism, microbial load (bacterial and fungal), and viability. For the oral candidiasis biofilm, the nanocarrier did not affect biomass or biofilm thickness but led to a significant increase in lactic acid levels compared to NC. Conclusions: It is concluded that the nanocarrier of CHX exhibits a significant reducing effect on oral candidiasis microcosm biofilms at half the concentration required for non-carried CHX. This nanostructure can be explored in the development of antiseptic or disinfectant solutions for managing oral candidiasis. Full article

Currently, resin polymer anchoring agents are widely used for bolting support in coal mine roadways to anchor the bolts to the surrounding rock mass. However, due to the relatively low strength of the resin anchoring agent itself, the required anchoring length tends to be excessively long. Based on this, this paper proposes the use of resin concrete as a replacement for resin. Compared to resin anchoring agents, resin concrete offers greater mechanical interlocking force with anchor rods, which can reduce the theoretical anchoring length. To systematically investigate the influence of factors such as the diameter and anchorage length of Glass Fiber-Reinforced Polymer (GFRP) bolt on the bond behavior between GFRP bolts and resin concrete, 33 standard pull-out tests were designed and conducted in accordance with the CSA S807-19 standard. Taking the 18 mm-diameter bolt as an example, when the bond lengths were 2D, 3D, 4D, and 5D, the average bond strengths were 41.32 MPa, 39.18 MPa, 38.84 MPa, and 37.44 MPa, respectively. This represents a decrease of 5.18%, 6.00%, and 9.39% for each subsequent increase in bond length. The results indicate that the bond strength between GFRP anchors and resin decreases as the anchorage length increases. Due to the shear lag effect, the average bond strength also decreases with increasing anchor diameter. Taking a 5D (where D is the anchor diameter) anchorage length as a reference, the average bond strengths for anchor diameters of 18 mm, 20 mm, 22 mm, and 24 mm were 37.44 MPa, 33.97 MPa, 32.18 MPa, and 31.50 MPa, respectively. The corresponding reductions compared to the 18 mm diameter case were 9.27%, 14.05%, and 15.87%. Based on the experimental results, this paper proposes a bond–slip constitutive model between the bolt and resin concrete, which consists of a rising branch, a descending branch, and a residual branch. A differential equation relating shear stress to displacement was established, and the functions describing the variation in displacement, normal stress, and shear stress along the position were solved for the ascending branch. Although an analytical solution for the differential equation of the descending branch was not obtained, it will not affect the subsequent derivation of the theoretical anchorage length for the GFRP bolt–resin concrete system, as structural components in practical engineering are not permitted to undergo excessive bond-slip. Full article

Ultrasonication offers a safer, lower-temperature method for synthesizing zinc oxide nanoparticles (ZnO-NPs). This study details the development of a pectin-glycerol bionanocomposite film reinforced with ZnO-NPs produced using the top-down ultrasonication method. ZnO-NPs were fabricated with varying ultrasonication durations (0, 30, and 60 min) and the addition of pectin as a capping agent. Extended ultrasonication duration resulted in smaller particle size and more defined morphology. Bionanocomposite films were prepared using the solvent casting method by incorporating ZnO-NPs (0, 0.5, 1, 2.5% w/w) and glycerol (0, 10, 20% w/w) as a plasticizer to a pectin base. The inclusion of ZnO-NPs and glycerol did not affect the shear-thinning behavior of the film-forming solution. FTIR analysis indicated interactions between ZnO-NPs, glycerol, and pectin. The addition of ZnO-NPs and glycerol reduced tensile strength but increased flexibility. ZnO-NPs improved barrier and thermal properties by reducing water vapor permeability and increasing melting point, whereas glycerol lowered glass transition temperature, thus enhancing film flexibility. The best film performance was observed with a combination of 0.5% ZnO and 20% glycerol. These results highlight the effectiveness of the top-down ultrasonication method as a sustainable approach for ZnO-NPs fabrication, supporting the development of pectin/ZnO-NPs/glycerol films as a promising material for eco-friendly packaging. Full article