Search Results (6,040)

The reconstruction of detrital flux, paleoclimate, paleosalinity, paleo-primary productivity, paleohydrodynamic conditions, and paleo-water depth enhances understanding of sedimentary processes and their drivers during deep-time greenhouse-icehouse transitions, such as the Eocene–Oligocene transition. This study uses detailed geochemical analyses of major oxides and trace elements in sediment samples collected from the Beni Suef Formation (Bartonian–Priabonian) and the Maadi Formation (Priabonian) in the southern Tethys shelf (Egypt, northeastern Desert). Detrital proxies, including Si/Al, Ti/Al, and Zr/Al, indicate an enhanced influx of terrigenous sediments in the middle portion of the Qurn Member of the Beni Suef Formation, as further supported by noticeable facies variations, particularly the transition from shale to coarser silt- and sand-sized fractions. Paleoclimate indicators (Sr/Ba, Rb/Sr, K₂O/Al₂O₃, and Sr/Cu) point to a climatic shift from humid to arid conditions, consistent with the regional Late Eocene aridification across the Tethyan realm. Paleosalinity proxies (Sr/Ba, Ca/Al, and Mg/Al×100) suggest episodic intensification of open-marine influence and a reduction in freshwater input, with an upsection increase in Sr/Ba ratios, reflecting phases of enhanced marine water settings or decreased terrestrial runoff. Primary productivity was evaluated using multiple geochemical proxies, including P, Ni/Al, Cu/Al, P/Al, P/Ti, and Babio ratios. These collectively indicate generally low primary productivity interrupted by intervals of enhanced paleoproductivity or increased organic matter export to the sediments. This interpretation is further supported by the low total organic carbon (TOC) values. These results highlight the sensitivity of the southern Tethys shelf to Middle–Late Eocene climatic variability and the key role of prevailing paleoenvironmental conditions in controlling sediment supply, water chemistry, and biological productivity. Full article

Zirconia-based hybrid blends at various molecular or nanometer scales have attracted significant interest from a technological perspective. In particular, several inorganic-organic hybrids are being applied in the biomedical field. In this context, inorganic ZrO₂ and hybrids composed of ZrO₂, and polyethylene glycol (PEG) have been synthesized through the sol–gel process and characterized from both morphological and spectroscopic viewpoints to explore their potential as hybrid biomaterials. Atomic Force Microscopy (AFM) has enabled a quantitative assessment of the surface roughness of bioactive sol–gel-based materials. The findings indicated an increase in material porosity in relation to the amount of PEG present in the systems, underscoring the important role of PEG in influencing the morphological characteristics of zirconia-based blends. AFM images display the typical globular structure of PEG spread across the surface of all systems. All hybrid systems seem to be uniform, and no phase separation is evident, thereby validating that the produced materials are hybrid nanostructured ones. The simultaneous presence of both inorganic and organic phases was verified using Fourier-transform infrared spectroscopy (FT-IR). FT-IR deconvolution in 850–550 cm⁻¹ region showed that PEG progressively perturbs the Zr–O–Zr network, increasing disorder and establishing more flexible inorganic domains at high PEG content. Increasing polymer amount enhanced cell viability against NIH-3T3 cell line, while antibacterial activity decreased, with pure ZrO₂ showing the strongest inhibition against Escherichia coli (E. coli). Full article

The continuous demand for advanced composite materials with superior mechanical and electrical properties has driven the exploration of copper matrix composites for high-performance applications. The Cu–2Zr–0.6B (wt.%) powder mixtures were mechanically alloyed (MA) using two different ball-to-powder weight ratios (BPR: 10:1 and 15:1) to investigate the influence of milling conditions on the final composite material’s properties. MA powders milled with BPR 15:1 exhibited the highest values of dislocation densities, which induce higher hardness of Cu–ZrB₂ bulk materials. The MA powders were consolidated using three different methods: conventional cold pressing followed by sintering (CPS), hot pressing (HP), and spark plasma sintering (SPS). The in situ forming of ZrB₂ (3.5 vol.%) reinforcements during consolidation processes in Cu matrix proved to have a major impact on enhancing the hardness and structural stability, while the use of SPS and HP offered superior control over grain growth and porosity reduction compared to CPS. Main findings related to electrical and mechanical properties showed similar values for SPS (~38% IACS, ~173 HV1) and HP compacts (~39% IACS, ~155 HV1) but proved to be much higher compared to values of CPS compacts (~21% IACS, ~80 HV1). Full article

The demand for high-energy-density and fast-charging solid-state lithium metal batteries (SSLMBs) often subjects practical devices to internal thermal loads, making high-temperature operation a common operational condition rather than an isolated scenario. To address the interfacial degradation and dendrite growth accelerated by such thermomechanical stresses, we developed a composite gel electrolyte (CGE) by incorporating an optimal concentration of active Li_6.4La₃Zr_1.4Ta_0.6O₁₂ (LLZTO) into a fluoropolymer network. The abundant Lewis acidic sites on the LLZTO surfaces promote competitive solvation decoupling by interacting with anions, thereby modulating the primary solvation sheath of Li⁺. This localized modulation lowers the lithium-ion migration activation energy to 0.248 eV and facilitates a dual-interfacial passivation mechanism. Specifically, a rigid, inorganic-rich solid electrolyte interphase (SEI) forms to suppress morphological instability at the lithium anode, while an organic-dominated cathode electrolyte interphase (CEI) enhances the oxidative stability up to 4.3 V. As a result, symmetric cells demonstrate stable electrodeposition for over 450 h at 80 °C and 0.5 mA cm⁻². Furthermore, NCM811/Li full cells utilizing this CGEs exhibit significantly improved thermal resilience and cycling stability. Full article

This work focuses on the study of tribo-mechanical and microstructural properties of TiCN/ZrCN multilayer coatings with a modulation period of 12 nm, obtained by a conventional cathodic arc technique. The coatings were deposited at a temperature of 320 °C using nitrogen and methane reactive gases (N₂/CH₄) mixture in three different proportions. Surface morphology, composition, hardness, adhesion, friction and wear behavior were studied using atomic force microscopy, scanning electron microscopy with energy dispersive spectroscopy, X-ray diffraction, Raman spectroscopy, nanoindentation, and scratch and wear tests. The analysis of the coating composition revealed a strict dependence of the carbon content on the CH₄ flow rate. It was found that the coatings with a carbon content of 14.6 at.% and 15.9 at.% consist of crystalline TiZr (C,N) with the presence of amorphous carbon. All the studied TiCN/ZrCN coatings showed improved tribo-mechanical properties compared to TiN/ZrN multilayers obtained under the same deposition conditions. The highest hardness of 40 GPa was obtained for the coating deposited at a N₂/CH₄ flow rate of 370/100 sccm. The lowest wear rate of 3.16 × 10⁻⁶ mm³/N·m under dry sliding conditions was observed in the multilayer coatings deposited at the N₂/CH₄ flow rates of 330/140 sccm. Full article

Titanium alloys, particularly β-type Ti-13Nb-13Zr, are promising biomedical materials due to their low elastic modulus and excellent biocompatibility. However, their bioactivity needs improvement for better bone integration. In this study, a calcium-phosphate (Ca/P) coating was prepared on a Ti-13Nb-13Zr alloy via micro-arc oxidation (MAO) in an electrolyte containing calcium acetate and dipotassium hydrogen phosphate. The effect of applied voltage (300 V, 400 V, and 500 V) on the phase composition, surface morphology, and in vitro bioactivity of the coatings was investigated. Surface characterization was performed using scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy-dispersive spectroscopy (EDS). The results show that increasing the voltage increased the surface roughness, average pore size, and rutile TiO₂ content in the coating. The Ca/P ratio in the coating approached 1.67 at 500 V, similar to that of natural bone. After immersion in simulated body fluid (SBF) for 20 days, the coating formed at 500 V induced the highest deposition of hydroxyapatite (HA), completely covering the microporous surface. These findings indicate that MAO treatment at 500 V significantly enhances the bioactivity of the Ti-13Nb-13Zr alloy, making it a promising candidate for orthopedic implants. Full article

Rare earth elements (REEs) play a critical role in provenance tracing and the environmental reconstruction of the Earth. However, systematic investigations into the geochemical behavior and fractionation mechanisms of REEs during halite crystallization in brine–salt systems remain limited. This study reports new trace element and REE data for Late Cretaceous halites from the Thakhek Basin, Laos. Ratios of Sr/Ba, Sr/Cu, and V/Cr indicate a marine origin for the halites, which formed under hot climatic and oscillating oxidizing–anoxic redox conditions. Both primary and secondary halites display uniform Post-Archean Australian Shale (PAAS)-normalized REE distribution patterns, characterized by relative enrichment in medium rare earth elements (MREE) and depletion in light (LREE) and heavy rare earth elements (HREE). Similar REE patterns are also observed in halites from other modern and ancient, continental and marine salt basins worldwide. These observations suggest that the influences of parent brine composition and external provenance supplies on REE fractionation are negligible, given the consistent source, salinity, and redox conditions recorded in these halites. Accordingly, REE fractionation in halite was largely controlled by crystallographic effects, with aqueous MREE preferentially incorporated into halite crystals during deposition. In addition, the relatively lower Zr/Hf ratios in secondary halites compared to primary halites further validate the utility of the Zr/Hf ratio for distinguishing authigenic halite from salt modified by diagenesis, weathering, dissolution, or recrystallization. While our results establish a fundamental REE distribution pattern for halite, further research is needed to better constrain the underlying fractionation mechanisms of REEs in evaporite minerals within brine–salt systems. Full article

Metal–organic frameworks (MOFs) are unique microporous materials being explored for a wide range of applications. Their porosity and high surface areas can readily be exploited for guest–host interactions, separations, and photochemical catalysis, but many suffer from poor charge separation and fast electron–hole recombination. Introducing structural defects, such as missing linkers or metal nodes, can create unsaturated metal sites and alter band structure, conductivity, and light absorption, improving photocatalytic performance. UiO-66-NH₂ and MIL-125-NH₂ are water-stable, visible-light-absorbing MOFs well suited for photocatalytic degradation of organic dyes. In this work, the influence of defect engineering on photocatalytic properties of MOFs was investigated using formic and acetic acid modulators with UiO-66-NH₂ and variable temperature with MIL-125-NH₂ during synthesis. The resulting materials were characterized by XRD, FTIR and SEM/EDS. Defect states were tracked using N₂ adsorption/BET analysis and UV–Vis spectroscopy. Photocatalytic activity was evaluated by monitoring Rhodamine B (RhB) degradation in aqueous solution under simulated solar irradiation. It was found that increased temperature beyond 120 °C during synthesis promotes mesopore formation and decreases the bandgap in MIL-125-NH₂, resulting in a more photoactive material. Defective MIL-125-NH₂ synthesized at 150 °C showed the most defects and proved to be the best photocatalyst investigated in this study. Formic acid modulation in UiO-66-NH₂ generated smaller crystallites that slightly increased the bandgap; however, the surface area decreased proportionally with the amount of formic acid used. The decreased surface area and observed enhancement in photocatalytic degradation of RhB suggest that formic acid introduces defects into the UiO-66-NH₂ framework that enhance photocatalytic properties. UiO-66-NH₂ treated with acetic acid resulted in larger crystals, increased bandgaps, and increased surface areas, suggesting that acetic acid simply modulates growth rather than imparting defects to the framework. Full article

Diffusion-controlled processes exert an indispensable influence on the thermal processing and microstructural homogenization of β-titanium alloys containing multiple β-stabilizing elements. However, credible multicomponent diffusion kinetic data corresponding to the β-phase within the Ti–Zr–Ta ternary system remain inadequate. In this work, diffusion characteristics within the β single-phase domain of the Ti–Zr–Ta system were investigated using solid-state diffusion couples combined with a numerical inverse method. Twelve diffusion couples in total were synthesized and subjected to annealing treatments at 1373, 1423, and 1473 K, with the corresponding composition–distance distributions quantified by electron probe microanalysis (EPMA). The composition-dependent main interdiffusion coefficients were measured via the numerical inverse method embedded in the HitDIC computational platform, while the atomic mobility parameters corresponding to the β-phase were refined to replicate the experimental concentration distributions and diffusion trajectories across the studied temperature and composition intervals. The results reveal pronounced temperature and composition dependence of the main interdiffusion coefficients, and the diffusion rate of Zr is faster than that of Ta in the β phase. Full article

EGFR signaling, which requires ligand shedding by ADAM proteases, drives the progression of a variety of cancers, including breast, ovarian and lung. We previously reported the generation and characterization of a fully human, affinity-matured anti-ADAM17 monoclonal antibody, D8P1C1, which inhibits both the proliferation of an array of cancer cell lines in vitro as well as breast cancer growth in a mouse xenograft model. Here, we show that the mAb inhibits the shedding of EGFR ligands and EGFR phosphorylation in cancer cell lines, thus explaining its anti-tumor effects. In a xenograft model with a high-grade serous ovarian cancer (HGSOC) cell line, D8P1C1 showed only modest therapeutic effect, without any discernible toxicity. These results suggest that ovarian cancers are less susceptible than breast cancers to therapeutic targeting of ADAM17- or EGFR-dependent signaling. Radioimmuno PET imaging with ⁸⁹Zr-DFO-D8P1C1 confirmed tumoral accumulation of the mAb in high-grade and non-high-grade serous ovarian tumor xenografts. Furthermore, we report the generation and preliminary characterization of a bispecific T cell engager derivative of D8P1C1 with improved anti-tumor efficacy in vitro. Full article

Modern bioimplants increasingly depend on surface-engineered functionality to elicit adaptive biological responses. One promising strategy involves the electrodeposition of bioresponsive elements such as magnesium (Mg), which plays a critical role in osseointegration. In this study, we present a novel approach for modifying anodized zirconia nanotubes (ZrNTs) via Mg decoration using electrochemical deposition. A controlled pulsed cathodic linear sweep protocol was employed to control Mg deposition behaviour, enabling reduced clustering and improved spatial distribution. Notably, ultraviolet (UV) irradiation was found to influence Mg adsorption dynamics, revealing a distinct pattern of interaction. Comprehensive surface characterization was conducted to assess nanotube morphology, Mg adherence, and distribution. These modified surfaces were subsequently evaluated for their potential in further functionalization, targeting surface chemistries conducive to biomaterial viability. The biomineralization capacity of Mg-decorated ZrNTs was systematically investigated using electrochemical impedance spectroscopy (EIS) and Tafel analysis, demonstrating enhanced apatite formation and improved corrosion resistance. This work establishes Mg decoration of ZrNTs as a viable route for developing bioactive, corrosion-resistant implant surfaces. Full article

High-temperature particulate matter (PM) filtration remains a fundamental challenge, because most fiber filters not only face the challenge of high temperatures but also suffer from an inherent trade-off between capture efficiency, pressure drop, and service life. This paper reports a hierarchical layered zirconia (ZrO₂) ceramic fiber aerogel featuring a continuous multiscale gradient. The aerogel was prepared by gradient air-blown spinning, and the resulting structure has directional order, with the fiber diameter gradually decreasing from upstream to downstream, thus forming a pore size gradient and achieving hierarchical particle interception across multiple scales. This rational design simultaneously suppresses surface clogging and reduces flow resistance, resolving the longstanding trade-off between efficiency and permeability. Consequently, this aerogel achieves an ultra-high filtration efficiency of 99.96%, a low pressure drop of 156 Pa, and a high dust-holding capacity of 101 g m⁻². The material also exhibits outstanding mechanical toughness (80% compressive strain elasticity and 25.75% tensile fracture strain) and thermal stability up to 1000 °C. Moreover, it maintains over 99.95% filtration efficiency at high temperatures and can be fully regenerated through 800 °C heat treatment. This work establishes a structure-based design paradigm for high-temperature filtration media and provides a scalable pathway for next-generation industrial flue gas purification. Full article

Magnetoelectric (ME) materials that exhibit simultaneous coupling between electric polarization and magnetization have attracted significant attention due to their potential technological applications in the emerging generation of multifunctional devices. In this research, Ba_0.85Ca_0.15Ti_0.92Zr_0.08O₃-CoFe₂O₄:x (x = 0.1, 0.2, 0.3% mol) composites were synthesized using solid-state and sol–gel combustion chemical methods to elucidate their ME coupling at ultra-low concentrations of the magnetic phase. Rietveld refinement and Raman spectroscopy results confirm a shift in the morphotropic phase boundary (MPB), evidenced by an increase in the tetragonal phase relative to the orthorhombic structure. High stability of the P4mm and Amm2 symmetries is reached at 1300 °C without diffusion of Fe and Co into the octahedral site. At this temperature, the CoFe₂O₄ spinel structure remains stable without secondary phases. The orthorhombic phase fraction decreases from 55% to 37% as the magnetic phase fraction increases, driven by stress and constraint rather than ionic interactions alone. The Curie temperature decreases from 99 to 90 °C, attributed to the grain-size reduction effect rather than structural disorder. The dielectric permittivity (ε_r) reaches an absolute value of 5070 and progressively decreases with increasing magnetic saturation. An increase in compressive residual stress is observed, which ensures the mechanical stability of the electroceramics. Magnetoelectric (ME) coupling, evaluated through measurements of electric polarization as a function of the magnetic field, shows an increase from 3.8 to 4.9 μC/cm² under a magnetic field of 50 Oe. The composites with x = 0.2 and 0.3 mol% exhibit potential for applications in fast-switching magnetoelectric devices and magnetic field sensors. Full article

In the current paper, the nonlinear absorption characteristics and laser modulation performance of the ternary anisotropic semiconductor material ZrGeTe₄ were successfully explored. The recovery time of the ZrGeTe₄-PVA thin film was measured to be 5.74 ps by the pump–probe technology. By employing ZrGeTe₄ as a saturable absorber, a passive mode-locked Yb-doped fiber laser was demonstrated for the first time. In the 1 µm mode-locked operation, the central wavelength was 1031.29 nm, the pulse repetition rate was 24.85 MHz, and the pulse width was 786.3 ps. In an Er-doped fiber laser operating at a wavelength of 1561.10 nm, the pulse width was as short as 1.26 ps with a repetition rate of 4.38 MHz. The results show that ZrGeTe₄ has excellent broadband nonlinear optical characteristics. Full article

In this work, for the first time, we applied and determined the mechanical characteristics of protective coatings made of high-entropy alloy (TiZrVCrAl)N with different architectures onto the surface of Ti-6Al-4V alloy with the initial coarse-grained and ultrafine-grained structure using arc physical vapor deposition. We designed and prepared three coating architectures: a monolayer nitride coating (TiZrVCrAl)N, a multilayer coating consisting of nine alternating layers of TiZrVCrAl and (TiZrVCrAl)N, and a multilayer coating consisting of 720 alternating layers of (TiZrVCrAl)N and TiN, with a total thickness not exceeding 2 microns. We evaluated their protective performances by nanoindentation and scratch tests. Importantly, the effect of the substrate microstructure on the coatings’ performance is investigated by comparing their mechanical behavior on coarse-grained and ultrafine-grained Ti-6Al-4V. Our experimental results show that the coating performance improves with increasing number of layers in the coating, and this effect is even more pronounced for the multilayer coating deposited on the ultrafine-grained titanium alloy substrate. We also find that the (TiZrVCrAl)N/TiN (720 layers) multilayer coating deposited on the UFG Ti-6Al-4V alloy substrate exhibits the highest H/E- and H³/E²-values, indicating the coating’s high innovative potential for performance in extreme conditions. The origins of this phenomenon are analyzed and discussed. Full article