Search Results (5,904)

The Cu-Cr-Zr alloy is regarded as an optimal material for high-end electronic information industries owing to its high electrical strength, high conductivity, and outstanding softening resistance. Nevertheless, the impacts of Cr content and microstructure evolution on performance enhancement during the processing stage remain unclear. In this research, Cu-xCr-0.1Zr alloys with varying Cr contents were fabricated via the thermo-mechanical approach. The microstructure evolution, as well as the mechanical and electrical properties before and after aging were investigated. It was discovered that Cr can mitigate the grain deformation degree of the copper alloy during cold rolling, notably augment the proportion of large-angle grain boundaries, and diminish the dislocation density induced by plastic deformation. As the Cr content increases, the conductivity of the sample declines from 86% IACS (0Cr) to 34.1% IACS (1.8Cr), and the tensile strength rises from 435 MPa (0Cr) to 542 MPa (1.8Cr) after cold rolling; the conductivity decreases from 89.4% IACS (0Cr) to 77.3% IACS (1.8Cr), and the tensile strength increases from 278 MPa to 607 MPa (1.0Cr). Based on the comprehensive outcomes, the aged 1.0Cr sample, with a tensile strength of 607 MPa and a conductivity of 80.9% IACS, satisfies the performance requirements of high-strength and high-conductivity copper alloys. Full article

This research examines the feasibility of recovering and recycling condensate water, a waste byproduct generated by Atlas Copco ZR315 FF industrial air compressors utilizing oil-free rotary screw technology with integrated dryers. Given the growing severity of global water scarcity, finding alternative water sources is essential for sustainable industrial practices. This study specifically evaluates the potential of capturing and treating compressed air condensate as a viable method for water recovery. The investigation analyzes both the quantity and quality of condensate water produced by the ZR315 FF unit. It contrasts this recovery approach with traditional water production methods, such as desalination and atmospheric water generation (AWG) via dehumidification. The findings demonstrate that recovering condensate water from industrial air compressors is a cost-effective and energy-efficient substitute for conventional water production, especially in water-stressed areas like Morocco. The results show a significant opportunity to reduce industrial water usage and provide a sustainable source of process water. This research therefore supports the application of circular economy principles in industrial water management and offers practical solutions for overcoming water scarcity challenges within manufacturing environments. Full article

Due to the Von Neumann bottleneck of traditional CMOS computing, there is an urgent need to develop in-memory logic devices with low power consumption. In this work, we demonstrate ferroelectric diode devices based on the TiN/Hf_0.5Zr_0.5O₂/HfO₂/TiN structure, implementing 16 Boolean logic operations through single-step or multi-step (2–3 steps) cascade and achieving attojoule-level one-bit full-adder computation. The TiN/Hf_0.5Zr_0.5O₂/HfO₂/TiN ferroelectric diode exhibits non-destructive readout and bidirectional rectification characteristics, with the conduction mechanism following Schottky emission behavior in the on-state. Based on its bidirectional rectification characteristics, we designed and simulated the circuit scheme of 16 Boolean logic and one-bit full-adder through cascaded operations. Both the input and output logic values are represented in the form of resistance, without the need for additional form conversion circuits. The state writing is performed by pulse-controlled polarization flipping, and the state reading is non-destructive. The logic circuits in this work demonstrate superior performance with ultralow computing power consumption in simulation. This breakthrough establishes a foundation for developing energy-efficient and scalable in-memory computing systems. Full article

Metastable β titanium alloys with low elastic modulus and excellent plasticity represent highly attractive materials for biomedical stent application. Our work shows that Zr plays a crucial role in regulating β stability to significantly reduce the modulus and enhance plasticity. A series of Ti-25Nb-2Mo-xZr (x = 0, 3, 9, 12 wt%) alloys were designed based on the d-electron theory, and the influence of Zr content on the microstructure, mechanical properties, and deformation mechanism were systematically investigated. The results demonstrated that as the Zr content increases, the β phase stability was significantly enhanced. This leads to, first, the suppressed formation of the high modulus α″ phase and ω phase, which results in the decrease in apparent overall elastic modulus. Second, the dominant mode of deformation shifts from martensite dislocation slip (0Zr) to martensitic variant reorientation (3Zr), then to stress-induced martensite transform (SIMT, 9Zr), and finally to a combination of SIMT and deformation twinning (12Zr). Such shifting effectively increases the alloy’s tensile plasticity. Among the series, the Ti-25Nb-2Mo-12Zr alloy exhibited the lowest elastic modulus of 56.3 GPa, together with the highest elongation to failure of 48.2%, demonstrating that the alloy possesses considerable potential for biomedical applications. Full article

The efficient recovery of rare earth elements (REEs) from low-concentration mine tailwater is crucial for resource sustainability. In this study, a novel composite adsorbent, sesame stalk biochar-supported zirconium phosphate (sBC/ZrP), was synthesized for the selective adsorption and recovery of La³⁺ as a representative REE. The material was characterized using SEM-EDS, BET, XRD, FTIR, and XPS. Batch adsorption experiments were conducted to evaluate the effects of pH, coexisting ions, and the adsorption kinetics and thermodynamics. The results showed that sBC/ZrP exhibited a high adsorption capacity (up to 185.83 mg/g at 35 °C for 4 h) and strong selectivity for La³⁺, particularly in the presence of common competing cations, although Al³⁺ demonstrated significant interference. The adsorption process followed pseudo-second-order kinetics and the Langmuir isotherm model, indicating monolayer chemisorption, and was determined to be spontaneous and endothermic. The material maintained over 90% adsorption efficiency after five consecutive adsorption–desorption cycles. The mechanism primarily involved complexation of La³⁺ with the P-OH and Zr-O groups on the composite. This work demonstrates that sBC/ZrP is a highly efficient, stable, and reusable adsorbent with significant potential for the recovery of REEs from mining tailwater. Full article

In recent years, the incidence of breast cancer has increased significantly; therefore, much attention is being paid to research on natural plant-based raw materials in the treatment and prevention of cancer as well as in the treatment of antibiotic-resistant infections. Therefore, Chlorella vulgaris algae extract and indole-3-acetic acid (IAA)—a plant hormone with potential anticancer and antimicrobial properties—were selected for the study. The main objective was to evaluate the effect of algae extract and IAA on the proliferation of cells from three different breast cancer lines: MCF-7, ZR-75-1, and MDA-MB-231. In addition, an analysis of apoptosis and oxidative stress parameters in cancer cells was performed, as well as an assessment of IAA toxicity towards E. coli, S. aureus, and C. albicans. The results obtained allow us to conclude that the extract is effective against estrogen-dependent cells, while the effect of IAA alone varies depending on the microorganism studied, the cell line analyzed, and the concentration used. The extract in selected concentrations induces apoptosis and activates oxidative stress mechanisms, while IAA exhibits cytotoxicity at higher concentrations and stimulates proliferation at lower concentrations. This indicates the need to investigate the mechanisms of action of both Chlorella vulgaris algae extract and IAA in cancer and bacterial cells. Full article

Transition metal (TM)-doped zinc oxide (ZnO) and zirconium dioxide (ZrO₂) nanocrystals exhibit complex correlations between crystal structure, defect chemistry, vibrational properties, and magnetic behavior that are strongly governed by synthesis route and dopant incorporation mechanisms. This review critically summarizes recent progress on Fe-, Mn-, and Co-doped ZnO and ZrO₂ nanocrystals synthesized by wet chemical, hydrothermal, and microwave-assisted hydrothermal methods, with emphasis on synthesis-driven phase evolution and apparent solubility limits. ZnO and ZrO₂ are treated as complementary host lattices: ZnO is a semiconducting, piezoelectric oxide with narrow solubility limits for most 3d dopants, while ZrO₂ is a dielectric, polymorphic oxide in which transition metal doping may stabilize tetragonal or cubic phases. Structural and microstructural studies using X-ray diffraction, electron microscopy, Raman spectroscopy, and Mössbauer spectroscopy demonstrate that at low dopant concentrations, TM ions may be partially incorporated into the host lattice, giving rise to diluted or defect-mediated magnetic behavior. When solubility limits are exceeded, nanoscopic secondary oxide phases emerge, leading to superparamagnetic, ferrimagnetic, or spin-glass-like responses. Magnetic measurements, including DC magnetization and AC susceptibility, reveal a continuous evolution from paramagnetism in lightly doped samples to dynamic magnetic states characteristic of nanoscale magnetic entities. Vibrational spectroscopy highlights phonon confinement, surface optical phonons, and disorder-activated modes that sensitively reflect nanocrystal size, lattice strain, and defect populations, and often correlate with magnetic dynamics. Rather than classifying these materials as diluted magnetic semiconductors, this review adopts a synthesis-driven and correlation-based framework that links dopant incorporation, local structural disorder, vibrational fingerprints, and magnetic response. By emphasizing multi-technique characterization strategies required to distinguish intrinsic from extrinsic magnetic contributions, this review provides practical guidelines for interpreting magnetism in TM-doped oxide nanocrystals and outlines implications for applications in photocatalysis, sensing, biomedicine, and electromagnetic interference (EMI) shielding. Full article

The electrochemical reduction of CO₂ to ethanol represents a sustainable alternative to recycle CO₂ into a value-added product, yet achieving high selectivity and efficiency remains a challenge. This work explores Cu-based catalysts supported on SiO₂ and ZrO₂, with and without ZnO doping, for ethanol production in a continuous flow-cell system. Gas diffusion electrodes are fabricated using commercial catalysts with varying Cu loadings (5–10%) and ZnO contents (2–3.5%). Comprehensive characterization by XPS confirms the presence of Cu²⁺ and Zn²⁺ species, while SEM reveals that ZnO incorporation improves surface uniformity and aggregate distribution compared to undoped samples. Electrochemical tests demonstrate that 10% Cu on SiO₂ achieves a Faradaic efficiency of 96% for ethanol at −3 mA cm⁻², outperforming both doped catalysts and previously reported materials. However, efficiency declines at higher current densities, indicating a trade-off between selectivity and productivity. ZnO doping enhances C₂⁺ product formation but does not surpass the undoped catalyst in ethanol selectivity. These results underline the importance of catalyst composition, support interactions, and operating conditions, and point to further optimization of electrode architecture and cell configuration to sustain high ethanol yields under industrially relevant conditions. Full article

Molecular dynamics simulations were conducted at a cooling rate of 1.0 × 10¹¹ K/s to investigate the solidification mechanism of zirconium (Zr) under high pressure. Three distinct pressure-dependent regimes are identified: crystallization into a body-centered cubic (BCC) phase below 27.5 GPa, vitrification between 27.5 and 65 GPa, and crystallization into an A15 phase above 65 GPa. The volume change during crystallization is found to reverse at critical pressures of 5 and 103 GPa, and anomalous behavior is observed at the phase boundaries: at 27.5 and 65 GPa, the volume varies continuously despite a sharp drop in potential energy, whereas at 65 GPa, the volume decreases abruptly while the energy changes smoothly. Structural analysis indicates that evolution in the low-pressure regime is governed by atomic configurations extending to the second-neighbor shell, while at high pressures, nearest-neighbor interactions become dominant. This work clarifies the microstructure–pressure relationship during metallic solidification, providing insights into controlling phase transitions under extreme conditions. Full article

TiO₂ shows improved photocatalytic properties when combined with other oxides, such as ZrO₂. Unfortunately, this material does not exhibit a spectral response in the visible range, but this can be improved by adding WO₃. Here, the effect of the amount of WO₃ and the treatment temperature on TiO₂-ZrO₂-WO₃ materials applied in the solar photocatalytic oxidation of sildenafil was evaluated. The materials were synthesized using the sol–gel method and were characterized by N₂, XRD, UV-Vis RDS, SEM, PL, and XPS. Photocatalytic activity was determined by the degradation and mineralization of sildenafil. The most active photocatalysts were selected for stability testing and to determine the oxidizing species that dominate the reaction mechanism. The optimal amount of WO₃ that improves solar photocatalytic activity at both treatment temperatures was found to be 1% with a reaction mechanism based on OH· and h⁺. WO₃ reduces electron–hole pair recombination. At 500 °C, the crystallinity of the anatase phase is improved, while at 800 °C, the transformation to rutile is suppressed at low WO₃ concentrations. XPS observed the reduction in Ti⁴⁺ to Ti³⁺ and W⁶⁺ to W⁵⁺ in TiO₂–ZrO₂–WO₃ materials, which were found to be photoactive under sunlight with potential for use in industrial-scale reaction systems. Full article

Background/Objectives: NANOBODY^® molecules (VHHs) are attractive vectors for radiopharmaceuticals due to their small size and high target affinity, but rapid clearance and pronounced kidney retention limit their therapeutic applicability. Binding to serum albumin is a widely used strategy to prolong circulation, yet the respective contributions of albumin-binding affinity and molecular format remain insufficiently defined. This study aimed to systematically evaluate how affinity and valency modulate VHH pharmacokinetics. Methods: Four monovalent albumin-binding VHHs spanning nanomolar to micromolar affinities and two bivalent constructs were engineered, generated by fusing an albumin-binding VHH to an irrelevant non-binding VHH. All constructs incorporated a site-specific cysteine for DFO* conjugation, enabling uniform zirconium-89 labeling with high radiochemical purity. Pharmacokinetics were assessed in healthy mice using serial blood sampling and positron emission tomography. Blood and kidney exposure were quantified by non-compartmental analysis. Results: All albumin-binding constructs showed increased systemic exposure and reduced kidney uptake relative to a non-binding control. Nanomolar-affinity binders reached maximal exposure, and further affinity increases (K_D < ~100 nM) did not improve pharmacokinetics, suggesting a threshold. The micromolar binder showed intermediate exposure but still reduced renal retention compared with control. Valency effects were affinity-dependent. They were negligible at high affinity but pronounced at low affinity, where bivalency reduced systemic exposure and increased kidney uptake toward control levels. Conclusions: Albumin binding enables tuning of VHH pharmacokinetics in an affinity-dependent manner. Above an apparent affinity threshold, pharmacokinetics become format independent, whereas below this threshold, molecular format substantially influences systemic and renal disposition. Full article

Based on a novel semi-continuous casting mold with independent primary cooling regulation, a large-size Mg-9.4Gd-5.8Y-1Zn-0.5Zr alloy billet (Ø330 mm) was successfully fabricated via differential phase electromagnetic vibration casting. This process significantly improved microstructural homogeneity, with grain sizes ranging from 117 µm to 130 µm across the billet and elemental segregation of Gd and Y below 3%. Homogenization at 520 °C for 5 h effectively dissolved grain boundary eutectic phases; promoted diffusion of Gd, Y, and Zn into the α-Mg matrix; and stimulated the precipitation of fine LPSO lamellae. These microstructural improvements resulted in an excellent tensile strength of 208.4 MPa and elongation of 24.4%, demonstrating an optimal strength–ductility balance achieved through precise thermal processing. Full article

7xxx series aluminum alloys are critical structural materials in aerospace applications, but their susceptibility to hydrogen embrittlement (HE) poses significant challenges to service safety and durability. The effects of Si, Er, and Zr microalloying, combined with optimized heat treatments on the HE resistance of Al–Zn–Mg–Cu alloys, were systematically investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and mechanical testing. Three alloys—1# (AlZnMgCuZr), 2# (AlZnMgCuErZr), and 3# (AlZnMgCuSiErZr)—were subjected to single-stage or two-stage homogenization, followed by solution treatments at 470 °C/2 h and 540 °C/1 h, and peak aging at 125 °C. The hydrogen charging experiment was conducted by first applying a modified acrylic resin coating to protect the gripping sections of the specimen, followed by a tensile test. Results demonstrate that alloy 3# with Si addition exhibited the lowest RA_loss, followed by the 2# alloy, which effectively improved the alloys’ hydrogen embrittlement behavior. Compared with the solution in 470 °C/2 h, the 540 °C/1 h solution treatment enabled complete dissolution of Mg₂Si phases, promoting homogeneous precipitation and peak hardness comparable to alloy 2#. Two-stage homogenization significantly enhanced the number density and refinement of L₁₂-structured Al₃(Er,Zr) nanoprecipitates. Silicon further accelerated the precipitation kinetics, leading to more Al₃(Er,Zr) nanoprecipitates, finely dispersed T′/η′ phases, and lath-shaped GPB-II zones. The GPB-II zones effectively trapped hydrogen, thereby improving HE resistance. This work provides a viable strategy for enhancing the reliability of high-strength aluminum alloys in hydrogen-containing environments. Full article

Advanced ceramics are known for their lightweight, high-temperature resistance, corrosion resistance, and biocompatibility. They are crucial in energy conversion, environmental protection, and aerospace fields. This review highlights the recent advancements in ceramic matrix composites, high-entropy ceramics, and polymer-derived ceramics, alongside various fabrication techniques such as three-dimensional printing, advanced sintering, and electric-field-assisted joining. Beyond the fabrication process, we emphasize how different processing methods impact microstructure, transport properties, and performance metrics relevant to catalysis. Additive manufacturing routes, such as direct ink writing, digital light processing, and binder jetting, are discussed and normalized based on factors such as relative density, grain size, pore architecture, and shrinkage. Cold and flash sintering methods are also examined, focusing on grain-boundary chemistry, dopant compatibility, and scalability for catalyst supports. Additionally, polymer-derived ceramics (SiOC, SiCN, SiBCN) are reviewed in terms of their catalytic performance in hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, and CO₂ reduction reaction. CeO₂-ZrO₂ composites are particularly highlighted for their use in environmental catalysis and high-temperature gas sensing. Furthermore, insights on the future industrialization, cross-disciplinary integration, and performance improvements in catalytic applications are provided. Full article

Taking advantage of the ionic size and mass disorder as component design criteria, three novel high-entropy rare-earth zirconate ceramics, including (Sm_0.2Gd_0.2Dy_0.2Er_0.2Tm_0.2)₂Zr₂O₇, (Gd_0.2Dy_0.2Ho_0.2Er_0.2Tm_0.2)₂Zr₂O₇ and (Gd_0.2Dy_0.2Ho_0.2Er_0.2Yb_0.2)₂Zr₂O₇, with single-phase fluorite structure were successfully synthesized. All compositions exhibited enhanced mechanical properties, with Vickers hardness and fracture toughness increasing as the grain size decreased. (Gd_0.2Dy_0.2Ho_0.2Er_0.2Yb_0.2)₂Zr₂O₇ demonstrated superior mechanical performance, achieving values of 11.41 ± 0.40 GPa and 1.78 ± 0.12 MPa·m^1/2, respectively. The thermal expansion coefficients at 1000 °C ranged from 10.80 × 10⁻⁶ K⁻¹ to 11.39 × 10⁻⁶ K⁻¹, which is proportional to the average ionic bond length. Notably, (Sm_0.2Gd_0.2Dy_0.2Er_0.2Tm_0.2)₂Zr₂O₇ exhibited low room-temperature thermal conductivity (1.58 W·m⁻¹·K⁻¹) due to pronounced size and mass disorder, without compromising structural stiffness. These findings highlight the potential of high-entropy design for advanced thermal barrier coatings. Full article