Search Results (200)

Zirconia, also known as zirconium dioxide ZrO₂, is well known for its good mechanical properties, like its inertness, good wear resistance, high temperature resistance and good strength. To enhance the mechanical properties of many materials, a technique known as transformation toughening is widely used today. This research focuses on achieving an optimized composition of zirconia and alumina Al₂O₃ to achieve zirconia-toughened alumina ZTA with a maximum density and other mechanical properties using a cost-effective and time-efficient approach. Doing so will make it possible to make more and more use of this valuable ceramic. The curing of zirconia and alumina samples with 3d—printing resins in silicone dies was performed so that we could obtain the optimum ratio of the resin and ZTA powder that would produce the most desirable results and properties. For 3d printing, ZTA samples with 19% zirconia ZrO₂ were used with alumina at two different temperatures (i.e., Sample 1, consisting of three pellets weighing 5–6 g, was sintered at 1500 °C, and Sample 2, also containing three pellets weighing 5 g (approx.), was sintered at 1600 °C). The green-state preparation of these samples (Sample 1 and Sample 2) was performed using milling media of WC balls/ethanol and a milling ratio of 1:3, and a milling time of 4 h 100 rpm was used while drying at 80 °C for 5.5 h. The relative density (70%) and Vickers hardness (14–17 GPa) were obtained for Al₂O₃/ZrO₂/MgO samples. Mechanical properties like hardness and strength strongly depend on the holding time, the rate of the temperature increase while sintering and the sintering temperature itself. Full article

Alkali resistance is a critical factor for the long-term performance of glass fibers in cementitious composites. While zirconium oxide doping has proven effective in enhancing the durability of basalt fibers, its high cost and limited solubility motivate the search for viable alternatives. This study presents the first systematic investigation of titanium dioxide (TiO₂) doping in basalt-based glasses across a wide compositional range (0–8 mol%). X-ray fluorescence and diffraction analyses confirm complete dissolution of TiO₂ within the amorphous silicate network, with no phase segregation. At low concentrations (≤3 mol%), Ti⁴⁺ acts as a network modifier in octahedral coordination ([TiO₆]), reducing melt viscosity and lowering processing temperatures. As TiO₂ content increases, titanium in-corporates into tetrahedral sites ([TiO₄]), competing with Fe³⁺ for network-forming positions and displacing it into octahedral coordination, as revealed by Mössbauer spectroscopy. This structural redistribution promotes phase separation and triggers the crystallization of pseudobrukite (Fe₂TiO₅) at elevated temperatures. The formation of a protective Ti(OH)₄ surface layer upon alkali exposure enhances chemical resistance, with optimal performance observed at 4.6 mol% TiO₂—reducing mass loss in NaOH and seawater by 13.3% and 25%, respectively, and improving residual tensile strength. However, higher TiO₂ concentrations (≥5 mol%) lead to pseudobrukite crystallization and a narrowed fiber-forming temperature window, rendering continuous fiber drawing unfeasible. The results demonstrate that TiO₂ is a promising, cost-effective dopant for basalt fibers, but its benefits are constrained by a critical solubility threshold and structural trade-offs between durability and processability. Full article

This work presents a theoretical investigation of ionic conductivity in cubic zirconia (c-ZrO₂) doped with magnesium, using density functional theory (DFT) with the hybrid B3LYP functional as implemented in the CRYSTAL23 software package. It was found that the spatial arrangement of magnesium atoms and oxygen vacancies significantly affects the energy barriers for oxygen ion migration. Configurations with magnesium located along and outside the migration path were analyzed. The results show that when Mg²⁺ is positioned along the migration trajectory and near an oxygen vacancy, stable defect complexes are formed with minimal migration barriers ranging from 0.96 to 1.32 eV. An increased number of Mg atoms can lead to a further reduction in the barrier, although in certain configurations the barriers increase up to 3.0–4.6 eV. When doping occurs outside the migration path, the energy profile remains symmetric and moderate (0.9–1.1 eV), indicating only a weak background influence. These findings highlight the critical role of coordinated distribution of Mg atoms and oxygen vacancies along the migration pathway in forming efficient ion-conducting channels. This insight offers potential for designing high-performance zirconia-based electrolytes for solid oxide fuel cells and sensor applications. Full article

Herbs offer people not just sustenance and housing but also serve as a key supplier of pharmaceuticals. This research is designed to assess the antioxidant and antidiabetic properties of green-produced zirconium dioxide and magnesium oxide nanoparticles (ZrO₂ and MgO NPs) utilizing extracts from unripe Solanum trilobatum fruit. ZrO₂ and MgO NPs have garnered considerable interest owing to their superior bioavailability, lower toxicity, and many uses across the healthcare and commercial industries. Scientific approaches, such as diverse spectroscopic and microscopic approaches, validated the creation of agglomerated spherical ZrO₂ and MgO NPs, measuring between 15 and 30 and 60 and 80 nm, with a mixed-phase composition consisting of monoclinic and tetragonal phases for ZrO₂ and a face-centered cubic structure for MgO NPs. UV–vis studies revealed a distinct peak at 378 and 290 nm for ZrO₂ and MgO NPs, suggesting efficient settling through the phytonutrients in S. trilobatum. The antioxidant capacity of ZrO₂ and MgO NPs was evaluated utilizing DPPH and FRAP reducing power assays. The diabetic effectiveness of ZrO₂ and MgO NPs was examined by alpha-amylase and alpha-glucosidase assays. The optimum doses of 500 and 1000 μg/mL were shown to be efficient in reducing radical species. Green-produced ZrO₂ and MgO NPs exhibited a dose-dependent reaction, with greater amounts of ZrO₂ and MgO NPs exerting a more pronounced inhibitory effect on the catalytic sites of enzymes. This work suggests that ZrO₂ and MgO NPs may attach to charge-carrying entities and function as rival inhibitors, therefore decelerating the enzyme–substrate reaction and inhibiting enzymatic degradation. Molecular docking analysis of ZrO₂ and MgO NPs with three proteins (2F6D, 2QV4, and 3MNG) implicated in antidiabetic and antioxidant studies demonstrated the interaction of ZrO₂ and MgO NPs with the target proteins. The results indicated the in vitro effectiveness of phytosynthesized ZrO₂ and MgO NPs as antidiabetic antioxidant agents, which may be used in the formulation of alternative treatment strategies against diabetes and oxidative stress. In summary, the green production of ZrO₂ and MgO NPs with Solanum trilobatum unripe fruit extract is an efficient, environmentally sustainable process that yields nanomaterials with significant antioxidant and antidiabetic characteristics, underscoring their prospective uses in biomedical research. Full article

RMB₆-TMB₂ (RM = rare earth elements, TM = transition metal elements) composites retain superior field emission properties of RMB₆ while addressing its inherent mechanical limitations by constructing a eutectic structure with TMB₂. Herein, an in situ route for synthesizing RMB₆-TMB₂ composite nanopowders with homogeneous phase distribution using reduction reactions was proposed. The LaB₆-ZrB₂ composite nanopowders were synthesized in situ for the first time using sodium borohydride (NaBH₄) as both a reducing agent and boron source, with lanthanum oxide (La₂O₃) and zirconium dioxide (ZrO₂) serving as metal sources. The effects of the synthesis temperature on phase compositions and microstructure of the composites were systematically investigated. The LaB₆-ZrB₂ system with a eutectic weight ratio exhibited an accelerated reaction rate, achieving a complete reaction at 1000 °C, 300 °C lower than that of single-phase ZrB₂ synthesis. The composite phases were uniformly distributed even at nanoscale. The composite powder displayed an average particle size of ~170 nm when synthesized at 1300 °C. With the benefit of the in situ synthesis method, LaB₆-TiB₂, CeB₆-ZrB₂, and CeB₆-TiB₂ composite powders were successfully synthesized. This process effectively addresses phase separation and contamination issues typically associated with traditional mixing methods, providing a scalable precursor for high-performance RMB₆-TMB₂ composites. Full article

This paper explores ferroelectric–dielectric heterostructures comprising a ferroelectric oxide (Lead Zirconium Titanate $\left(\mathrm{P}\mathrm{b}\mathrm{Z}{\mathrm{r}}_{1-\mathrm{x}}\mathrm{T}{\mathrm{i}}_{\mathrm{x}}{\mathrm{O}}_3\right)$) with a varying mole fraction and a fixed dielectric oxide (Silicon dioxide $\left(\mathrm{S}\mathrm{i}{\mathrm{O}}_2\right)$). The study aims to enhance capacitance, optimize voltage amplification, and achieve stable negative capacitance. An isolated ferroelectric capacitor is examined by varying mole fractions of ferroelectric oxide. The negative capacitance in isolated ferroelectric capacitor is highly unstable in nature. The instability problem is fixed and the overall capacitance of the heterostructure is raised while the negative capacitance is stabilized by connecting a dielectric oxide in series with the ferroelectric capacitor. $\mathrm{P}\mathrm{b}\mathrm{Z}{\mathrm{r}}_{1-\mathrm{x}}\mathrm{T}{\mathrm{i}}_{\mathrm{x}}{\mathrm{O}}_3$ is utilized as the ferroelectric oxide, with mole fractions $x=0,0.2,0.4,0.6,0.8,1.0$. Among the investigated mole fractions, ferroelectric oxide with $x=0.6$ offers the maximum voltage amplification and improved capacitance because its capacitance closely matches the dielectric capacitance. Also, dynamic response and temperature analysis of heterostructure are studied further. Full article

This narrative review explores the role of additive manufacturing (AM) technologies in the production of dental implants, focusing on materials and key AM methods. The study discusses several materials used in implant fabrication, including porous titanium, trabecular tantalum, zirconium dioxide, polymers, and composite materials. These materials are evaluated for their mechanical properties, biocompatibility, and suitability for AM processes. Additionally, the review examines the main AM technologies used in dental implant production, such as selective laser melting (SLM), electron beam melting (EBM), stereolithography (SLA), selective laser sintering (SLS), and direct metal laser sintering (DMLS). These technologies are compared based on their accuracy, material limitations, customization potential, and applicability in dental practice. The final section presents a data source analysis of the Web of Science and Scopus databases, based on keyword searches. The analysis evaluates the research trends using three criteria: publication category, document type, and year of publication. This provides an insight into the evolution and current trends in the field of additive manufacturing for dental implants. The findings highlight the growing importance of AM technologies in producing customized and efficient dental implants. Full article

This article deals with the effect of Kr¹⁵⁺ ion irradiation on the structure and properties of partially stabilized zirconium dioxide (ZrO₂ + 3 mol. % Y₂O₃) ceramics. Ion irradiation is used to simulate radiation damage typical of operating conditions in nuclear reactors and space technology. It is shown that with an increase in the irradiation fluence, point defects are formed, dislocations accumulate, and the crystal lattice parameters change. At high fluences (>10¹³ ions/cm²), a phase transition of the monoclinic (m-ZrO₂) phase to the tetragonal (t-ZrO₂) and cubic (c-ZrO₂) modifications is observed, which is accompanied by a decrease in the crystallite size and an increase in internal stresses. Changes in the mechanical properties of the material were also observed: at moderate irradiation fluences, strengthening is observed due to the formation of dislocation structures, whereas at high fluences (>10¹⁴ ions/cm²), a decrease in strength and a potential amorphization of the structure begins. The change in the phase composition was confirmed by X-ray phase analysis and Raman spectroscopy. The results obtained allow a deeper understanding of the mechanisms of radiation-induced phase transformations in stabilized ZrO₂ and can be used in the development of ceramic materials with increased radiation resistance. Full article

This paper presents the results of a comprehensive study of the structure, phase composition, thermal corrosion, and tribological properties of multilayer gradient coatings based on YSZ/NiCrAlY obtained using detonation spraying. X-ray phase analysis showed that the coatings consist entirely of metastable tetragonal zirconium dioxide (t’-ZrO₂) phase stabilized by high temperature and rapid cooling during spraying. SEM analysis confirmed the multilayer gradient phase distribution and high density of the structure. Wear resistance, optical profilometry, wear quantification, and coefficient of friction measurements were used to evaluate the operational stability. The results confirm that the structural parameters of the coating, such as porosity and phase gradient, play a key role in improving its resistance to thermal corrosion and CMAS melt, which makes such coatings promising for use in high-temperature applications. It is shown that a dense and thick coating effectively prevents the penetration of aggressive media, providing a high barrier effect and minimal structural damage. Tribological tests in the temperature range from 21 °C to 650 °C revealed that the best characteristics are observed at 550 °C: minimum coefficient of friction (0.63) and high stability in the stage of stable wear. At room temperature and at 650 °C, there is an increase in wear due to the absence or destabilization of the protective layer. Full article

This study presents the synthesis, characterization, and application of magnetic magnetite–zirconium dioxide (Fe₃O₄–ZrO₂) nanoparticles as an efficient nanoadsorbent for fluoride removal from water. The nanoparticles were synthesized using a wet chemical co-precipitation method with Fe/Zr molar ratios of 1:1, 1:2, and 1:4, and characterized using Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). FTIR analysis confirmed the presence of Fe₃O₄ and ZrO₂ functional groups, while XRD showed that increased Zr content led to a dominant amorphous phase. SEM and EDS analyses revealed quasi-spherical and elongated morphologies with uniform elemental distribution, maintaining the designed Fe/Zr ratios. Preliminary adsorption tests identified the Fe/Zr = 1:1 (M1) nanoadsorbent as the most effective due to its high surface homogeneity and optimal fluoride-binding characteristics. Adsorption experiments demonstrated that the material achieved a maximum fluoride adsorption capacity of 70.4 mg/g at pH 3, with the adsorption process best fitting the Temkin isotherm model (R² = 0.987), suggesting strong adsorbate–adsorbent interactions. pH-dependent studies confirmed that adsorption efficiency decreased at higher pH values due to electrostatic repulsion and competition with hydroxyl ions. Competitive ion experiments revealed that common anions such as nitrate, chloride, and sulfate had negligible effects on fluoride adsorption, whereas bicarbonate, carbonate, and phosphate reduced removal efficiency due to their strong interactions with active adsorption sites. The Fe₃O₄–ZrO₂ nanoadsorbent exhibited excellent magnetic properties, facilitating rapid and efficient separation using an external magnetic field, making it a promising candidate for practical water treatment applications. Full article

In this work, the development of Al-based metal matrix composites (MMCs) is achieved using hybrid SiC and ZrO₂ reinforcement particles for automotive applications. Powder metallurgy (PM) is employed with various combinations of important process parameters for the fabrication of MMCs. MMCs were characterized using scanning electron microscopy (SEM), X-ray diffractometry (XRD), and a microhardness study. All XRD graphs adequately exhibit Al, SiC, and ZrO₂ peaks, indicating that the hybrid MMC products were satisfactorily fabricated with appropriate mixing and sintering at all the considered fabrication conditions. Also, no impurity peaks were observed, confirming high composite purity. MMC products in all the XRD patterns, suitable for the desired applications. According to the SEM investigation, SiC and ZrO₂ reinforcement components are uniformly scattered throughout Al matrix in all produced MMC products. The occurrence of Al, Si, C, Zr, and O in EDS spectra demonstrates the effectiveness of composite ball milling and sintering under all manufacturing conditions. Moreover, an increase in interfacial bonding of fabricated composites at a higher sintering temperature indicated improved physical properties of the developed MMCs. The highest microhardness value is 86.6 HVN amid all the fabricated composites at 7% silica, 14% zirconium dioxide, 500° sintering temperature, 90 min sintering time, and 60 min milling time. An integrated Particle Swarm Optimization–Support Vector Machine (PSO-SVM) model was developed to predict microhardness based on the input parameters. The model demonstrated strong predictive performance, as evidenced by low values of various statistical metrics for both training and testing datasets, highlighting the PSO-SVM model’s robustness and generalization capability. Specifically, the model achieved a coefficient of determination of 0.995 and a root mean square error of 0.920 on the training set, while on the testing set, it attained a coefficient of determination of 0.982 and a root mean square error of 1.557. These results underscore the potential of the PSO-SVM framework, which can be effectively leveraged to optimize process parameters for achieving targeted microhardness levels for the developed Al-SiC-ZrO₂ Composites. Full article

This study investigated the radiation attenuation characteristics of commonly used dental implant materials across an energy spectrum relevant to dental radiology. Two titanium implants were examined, with densities of 4.428 g/cm³ and 4.51 g/cm³, respectively. The first consisted of 90.39% titanium, 5.40% aluminum, and 4.21% vanadium, while the second comprised 58% titanium, 33% oxygen, 7% iron, 1% carbon, and 1% nitrogen. The third material was a zirconia implant (5Y form) composed of 94.75% zirconium dioxide, 5.00% yttrium oxide, and 0.25% aluminum oxide, exhibiting a higher density of 6.05 g/cm³. Monte Carlo simulations (MCNP6) and XCOM data were utilized to estimate photon source parameters, geometric configuration, and interactions with biological materials to calculate the half-value layer, mean free path, and tenth-value layer at varying photon energies. The results indicated that titanium alloys are well suited for low-energy imaging modalities such as CBCT and panoramic radiography due to their reduced artifact production. While zirconia implants demonstrated superior attenuation at higher energies (e.g., CT), their higher density may induce beam-hardening artifacts in low-energy systems. Future research should validate these simulation results through in vitro and clinical imaging and further explore the correlation between material-specific attenuation and CBCT image artifacts. Full article

The aim of this work was the preparation of ceramic monolithic catalysts for the catalytic oxidation of gaseous mixture of benzene, toluene, ethylbenzene and o-xylene BTEX. The possibility of using zirconium dioxide (ZrO₂) as a filament for the fabrication of 3D-printed ceramic monolithic carriers was investigated using fused filament fabrication. A mixed manganese and iron oxide, MnFeO_x, was used as the catalytically active layer, which was applied to the monolithic substrate by wet impregnation. The approximate geometric surface area of the obtained carrier was determined to be 53.4 cm², while the mass of the applied catalytically active layer was 50.3 mg. The activity of the prepared monolithic catalysts for the oxidation of BTEX was tested at different temperatures and space times. The results obtained were compared with those obtained with commercial monolithic catalysts made of ceramic cordierite with different channel dimensions, and with monolithic catalysts prepared by stereolithography. In the last part of the work, a kinetic analysis and the modeling of the monolithic reactor were carried out, comparing the experimental results with the theoretical results obtained with the 1D pseudo-homogeneous and 1D heterogeneous models. Although both models could describe the investigated experimental system very well, the 1D heterogeneous model is preferable, as it takes into account the heterogeneity of the reaction system and therefore provides a more realistic description. Full article

Titanium has specific uses due to its cost, which is counterbalanced by its extraordinary chemical and physical properties. Submarine hulls and nuclear power plant pipes have been made of titanium since the last century due to its high corrosion resistance, and the aircraft industry has also exploited its remarkable properties, such as lightness and high melting point. Surface modifications by plasma electrolytic oxidation (PEO) may increase its corrosion resistance, roughness and wettability. Furthermore, greater corrosion resistance is a rather attractive property in nuclear power plant pipes, although the increased roughness and wettability are disadvantageous downsides as they favor the attachment of marine organisms. Nonetheless these new features are particularly interesting for biomedical applications. In this study, PEO films were produced on commercially pure titanium substrates using different electrolytes, one of which contains zirconium dioxide and the other consisting of tantalum pentoxide, in addition to a third one composed of a combination of the former two. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) analyses were performed in addition to contact angle and roughness measurements, and electrochemical tests were carried out to comparatively characterize the different film compositions. The results revealed that excellent corrosion resistance was achieved by mixing oxides in the electrolyte. Full article

The synthesis and characterization of MgO-ZrO₂ heterostructures are examined in this work. To promote the creation of nanowires, the Si substrate is first covered with a catalyst layer of various Au thicknesses. Sputtering is used to achieve this deposition. After that, chemical vapor deposition (CVD) with a Au catalyst layer is used to create MgO nanowire arrays on the silicon substrate. Second, MgO/ZrO₂ Core–shell Nanowire Arrays are created by applying ZrO₂ layers to the surface of MgO nanowires of different diameters using chemical vapor deposition (CVD) procedures. The presence of both magnesium oxide (MgO) and zirconium dioxide (ZrO₂) in their oxidized forms was shown by the detailed characterization of the MgO-ZrO₂ core–shell nanowire samples utilizing a variety of methods. Phase formation, mechanical homogeneity, optical characteristics, and topographical structure and roughness were all thoroughly examined at various stresses. MgO hardness values ranged from 1.4 to 3.2 GPa, whereas MgO-ZrO₂ ranged from 0.38 to 1.2 GPa. The I–V parameter study was a further step in the examination of the heterostructure’s electrical properties. The structural, morphological, optical, mechanical, and electrical properties of the MgO-ZrO₂ heterostructure were all thoroughly described using these techniques. Full article