Search Results (811)

Large-scale reuse of copper tailings can mitigate environmental hazards and recover strategic elements; this work investigates the feasibility of producing foam glass-ceramics with high copper-tailing content (>70 wt%) by tuning the CaO/SiO₂ ratio to couple melt viscosity and crystallisation. The comprehensive utilisation of these tailings helps mitigate environmental pollution and enhance resource efficiency. In this study, foam glass-ceramics with varying CaO/SiO₂ ratios were synthesised through melt quenching followed by foaming heat treatment. The effects of different CaO/SiO₂ ratios on the foaming behaviour, crystallisation, and microstructure were investigated using DSC, FTIR, viscosity, XRD, SEM, and CT. The results indicate that increasing the CaO/SiO₂ ratio disrupts the three-dimensional network structure of the glass, which lowers the glass viscosity and influences the bubble size and distribution in the foam glass-ceramics. Additionally, the increased CaO content promotes crystal precipitation and enhances the compressive strength of the foam glass-ceramics. At a CaO/SiO₂ mass ratio of 0.22, the foam glass-ceramics exhibited the lower bulk density (240 kg/m³) and thermal conductivity (0.07 W/m·K). The materials also demonstrated good water absorption and compressive strength. This study highlights the potential of using copper tailings in foam glass-ceramics to improve their overall performance, offering promising energy-saving and environmentally friendly solutions. Full article

This study investigates ice crystal sedimentation calculation errors arising from three-moment bulk cloud scheme. Both offline tests and one-dimensional cloud model simulations indicate that sedimentation calculation errors are most pronounced at both the cloud bottom and cloud top. At the cloud bottom, the error stems from how the bulk method treats ice crystal sedimentation. Specifically, the method uses three weighted fall velocities (corresponding to the three moments) to represent instantaneous fluxes through a fixed altitude, which inherently assumes that falling ice crystals can only affect the adjacent model layer below. This assumption artificially constrains the falling distance of larger ice crystals. At the cloud top, the differences among these three weighted fall velocities can give rise to physical inconsistencies. This issue is handled by artificial adjustment, which leads to a spurious narrow size distribution shape of ice crystals, especially under model configurations with coarse temporal resolution (large dT) and fine vertical resolution (small dH). If only the sedimentation process is considered, the above calculation errors can be effectively minimized by lowering the dT/dH ratio. Full article

Cobalt disulfide (CoS₂) features highly active catalytic sites and is regarded as a promising candidate for electrocatalytic hydrogen evolution. In this study, molybdenum-doped cobalt disulfide (CoS₂:Mo) was synthesized via a facile hydrothermal approach. XRD analysis confirms that the obtained samples crystallize in a cubic pyrite structure, with diffraction peaks consistently shifting towards lower angles. SEM characterization reveals that the samples exhibit microrod-like morphologies with an average size of approximately 1 μm. Integrated analyses from XRD, XPS, and EDS mapping demonstrate that Mo is uniformly distributed across the surface and successfully doped into the CoS₂ lattice. Electrochemical measurements indicate that the CoS₂:Mo sample delivers a low overpotential of 122 mV and a Tafel slope of 128 mV dec⁻¹ at a current density of 10 mA cm⁻² in alkaline media, significantly surpassing the performance of pure CoS₂ and MoS₂. Moreover, the CoS₂:Mo exhibits an enhanced double-layer capacitance, with a C_dl value of 2.72 mF cm⁻², superior to that of pure CoS₂ (1.63 mF cm⁻²) and MoS₂ (0.31 mF cm⁻²). Mo doping enhances conductivity and active sites, thereby boosting electrocatalysis. This work presents an effective strategy for the development of cost-efficient and high-performance non-precious metal electrocatalysts. Full article

In this study, we examine an ex-service, Ni-base single-crystal blade made of alloy PWA1483, which was in service for 6000 h. Using light optical, scanning, and transmission electron microscopy, we analyzed the microstructure at the blade’s tip, middle, and root. Key focus areas included surface features, dendrite spacings, γ’-particle sizes, and dislocation densities. The findings reveal that the bulk microstructure hardly evolved. Dendrite spacings exhibited a consistent microstructure across all locations and there were no significant differences between the local alloy chemistries of dendritic and interdendritic regions, indicating high-quality processing. A bimodal γ’-particle distribution was observed. Variations in γ’-sizes and γ-channel widths were noted, with the tip showing rounded γ’-particles. Small spherical particles occurred only in the root and middle of the blade. The middle location exhibited the highest hardness. Dislocation densities were low and uniform, with the highest density correlating with the highest hardness. Full article

To address the capacity decay of NCM811 caused by microcracks and cation disorder during cycling, La, Al, and F tri-doped micron-sized single-crystal NCM811 material with a LiNbO₃ coating was synthesized via a facile co-solvent method. Using a mixed glucose–urea thermal solution as the reaction medium, metal salts were incorporated, followed by step-wise sintering, ball-milling, heat treatment, and wet-chemical coating. This approach enables atomic-level precursor mixing and ensures homogeneous element distribution. La³⁺ enlarges the lithium layer spacing to enhance ion diffusion and Al³⁺ suppresses Ni³⁺ reduction to Ni²⁺, mitigating cation mixing and improving conductivity, while F⁻ stabilizes the crystal structure via its strong electronegativity. The LiNbO₃ coating protects the interface from electrolyte attack, and the single-crystal morphology effectively suppresses microcracking. Compared to unmodified single-crystal NCM811 prepared identically, the modified material exhibits reduced cation disorder, improved crystallinity, and superior thermal stability. Electrochemical tests in half-cells with 1 M LiPF₆/(EC/EMC/DMC) electrolyte (2.8–4.3 V) show an initial discharge capacity of 208.32 mAh/g at 0.1 C and 194.05 mAh/g at 1 C. After 200 cycles at 1 C, the capacity retention remains at 92.21%, exceeding the market average. Rate performance is also notably enhanced, with the 5 C discharge capacity increasing from 141.12 mAh/g (unmodified) to 166.81 mAh/g, demonstrating improved kinetics and structural stability. Full article

In this study, the growth of high-quality graphite single crystals from a molten metal flux at atmospheric pressure was optimized. The crystals were precipitated from a saturated iron–carbon solution by slowly cooling (4 °C/h) from a maximum temperature to reduce the carbon solubility. The graphite flakes were >25 square millimeters in area and >10 microns thick, with individual crystal grains as large as 1.2 mm². The crystals were (0002) oriented, as determined by X-ray diffraction. The high structural quality of the graphite crystals was verified by Raman spectroscopy. For graphite with the natural distribution of carbon isotopes, the G-peak at 1580 cm⁻¹ was narrow (~12 cm⁻¹) and the defect peak (D-peak) was absent. To demonstrate the process versatility, graphite crystals enriched in the ¹³C isotope were grown at 5 degrees of enrichment. The Raman G-peak linearly shifted from 1580 cm⁻¹ to 1520 cm⁻¹ for graphite crystals enriched from 1 to 99% ¹³C. The etch pit densities from defect-sensitive etching ranged from 0 to 1.6 × 10⁸ per cm². The process was refined by examining the grain size and quality as functions of the carbon concentration in the starting sources, the carrier gas composition, and maximum temperature. The simplicity of this process suggests it can be scaled to produce very large graphite crystals that would be suitable for a wide range of technologies. Full article

Gold nanoparticles (AuNPs) were synthesized via two complementary routes, an inorganic surfactant-mediated method and a plant-extract-assisted biosynthesis, to elucidate how synthesis pathways influence nanoparticle physicochemical properties. In the inorganic route, hexadecyltrimethylammonium bromide (CTAB)-stabilized AuNPs were prepared using CTAB dissolution temperatures of 70–90 °C. UV–Vis spectroscopy showed localized surface plasmon resonance (LSPR) bands at 554–556 nm, while dynamic light scattering (DLS) indicated a decrease in hydrodynamic diameter from 110 to 97 nm with increasing dissolution temperature. Zeta potentials above +40 mV indicated strong electrostatic stabilization, and transmission electron microscopy (TEM) revealed ultrasmall Au cores with a narrow size distribution (2.4–3.0 nm) and a face-centered cubic crystal structure. In the biosynthetic route, AuNPs were obtained using aqueous Erythroxylum coca leaf extracts (1–4% w/v). The extracts exhibited a concentration-dependent red shift (~380 to ~420 nm), and biosynthesized AuNPs displayed LSPR bands in the 550–580 nm range. DLS yielded hydrodynamic diameters of 270–390 nm, with pronounced aggregation (3341 nm) at the lowest extract concentration. Under optimized conditions (HC5, n = 5), reproducible plasmonic and colloidal properties were obtained (maximum absorbance, localized surface plasmon resonance wavelength (λ_max) = 569.6 ± 1.7 nm; hydrodynamic diameter (D_H) = 237.6 ± 24.3 nm; absolute zeta potential (|ζ|)= 32.2 ± 2.6 mV). TEM analysis indicated predominantly quasi-spherical particles with a broader, log-normal size distribution, consistent with extract-mediated growth under heterogeneous organic capping environments. Full article

This work investigates the reactive crystallization of lithium carbonate (Li₂CO₃) by rapidly mixing concentrated aqueous solutions of LiCl (3.0–4.0 M) and Na₂CO₃ (1.5–2.0 M) at 65 °C, using focused beam reflectance measurement (FBRM) for online, in situ monitoring. The effect of low concentrations of poly(acrylic acid) (PAA), sodium hexametaphosphate (SHMP), and sodium tripolyphosphate (STPP) on nucleation and growth dynamics was systematically analyzed. The results show that the process is dominated by an intense initial supersaturation pulse, which governs early nucleation and subsequent population restructuring through growth and aggregation. Additives significantly modify the nucleation-growth coupling: PAA exhibits concentration- and time-dependent behavior, suppressing the detectable fines population and promoting consolidation into coarse fractions under high supersaturation; SHMP acts as a strong kinetic inhibitor, markedly reducing nucleation and, to a greater extent, growth; while STPP exhibits an intermediate, dose-dependent response, maintaining nucleation but limiting effective growth at high concentrations. Scanning electron microscopy observations confirm the formation of spherulitic Li₂CO₃ aggregates in all cases, with compactness and radial organization dependent on the additive. These results demonstrate that targeted additive selection allows for precise control of population dynamics and solid properties in reactive crystallization systems, within the investigated high-supersaturation concentration window, with useful mechanistic guidance for the design and control of Li₂CO₃ precipitation processes. Full article

This study focuses on the surface materials of rammed-earth walls of Fujian Tulou in Xiaoshu Village, exploring the microscopic characteristics of rammed earth in different orientations and the microclimate adaptation mechanism and degradation law of the walls. Specimens were collected from the inner and outer surface soil layers of the four directional walls of a representative Tulou. SEM, XRD, and XRF analyses were performed to characterize the materials’ microstructure, mineral composition, and elemental distribution, with the test results correlated to the microclimatic conditions of each wall orientation. The conclusion is as follows: (1) The microscopic particle size of rammed earth exhibits significant directional differences at dual scales of 300 nm and 2 μm. Solar radiation duration and wind speed are positively correlated with the coefficient of variation in particle size. (2) The southeast and north walls were the most severely damaged (soil loss, quartz enrichment: 79.9%), the west wall had minor cracks, the north wall showed slight salt crystallization (Halite = 0.3%), and the east wall exhibited moisture-related moss growth. (3) Traditional organic additives (bamboo strips, rice husks) mitigate deterioration and enhance structural integrity. (4) The diversity of soil color (related to hematite and iron oxide) can serve as a simple indicator of deterioration. This study has proposed differentiated protection schemes for the “microclimate-compounds” on walls facing different directions on the rammed-earth surface of the Tulou. The findings provide a theoretical basis for orientation-specific conservation of Tulou heritage and offer scientific references for the modification of modern rammed-earth materials. Full article

The Permian Qixia dolostone in the Central Sichuan Basin is a significant hydrocarbon reservoir of hydrothermal origin, linked to the Emeishan Large Igneous Province and structurally controlled by E–W strike–slip faults. However, how this process controls reservoir quality remains poorly understood. To address this, we integrate core observation, thin-section petrography, XRD analysis, thickness mapping, MICP, and μ-CT to characterize the lithofacies and pore structures of the Qixia Formation in the study area. Six lithofacies are recognized, including mudstone (F1), wackestone (F2), packstone (F3), grainstone (F4), rudstone (F5), and dolostone (F6), and F6 is further divided into three subtypes (F6-1, F6-2, F6-3). Dolostones exhibit superior reservoir quality relative to limestones, and among the dolostone, reservoir quality improves progressively from F6-1 to F6-3 with increasing crystal size and dolomite content. Dolostone distribution is spatially tied to E–W strike–slip faults, and its formation age coincides with documented fault activity, implicating these faults as the primary fluid conduits. Quantitative pore structure analyses further indicates that dolomitization enhanced permeability by enlarging pore–throat radii and improving macropore connectivity, with associated dissolution contributing additional secondary porosity. Full article

Microbially Induced Carbonate Precipitation (MICP) is a biochemical process that promotes the precipitation of calcium carbonate, mainly in the mineral form of calcite, using urease-producing bacteria. This method has numerous applications, particularly in the field of geotechnical engineering when it is adopted for soil improvement or for the consolidation of porous or cracked construction materials such as stone and concrete. One microfluidic platform made of polymethylmethacrylate (PMMA) was designed with multiple channels, and the minerals precipitated were visualized using an optical microscope. The precipitated mineral observed in all channels analyzed formed spherical mineral structures with a core and multiple external rings. The same spherical mineral structures were observed in the biocement layer precipitated on plates of the same material as that of the microfluidic platform and on limestone, following the same treatment protocol. SEM images of pieces of these layers, complemented with EDS and mineral analysis by XRD, have confirmed the existence of multiple layers of minerals with spherical structures, mainly vaterite, precipitated around a nucleation point. Overlapping minerals in both the confined microfluidic channels and the unconstrained plates indicate that overlap results from repeated injections rather than physical confinement. From the tests with the microfluidic devices, these studies revealed that crystallization depends on different factors, namely the size of the channels and the number of Sporosarcina pasteurii cells. The number of injections appeared to affect the number of rings precipitated around the inner core. Substrate effects on spatial distribution or adhesion may still exist but were not detectable in this study and require further investigation. The observation of similar mineralogical structures in both the microfluidic devices and the plates, particularly the limestone, demonstrates that microfluidic systems are effective tools for small-scale visualization of geological processes. Full article

Previous research indicates that WC-12Co contents above 60 wt.% in feedstock powders for cermet coatings impair adhesion and wear resistance. This study characterizes NiCrFeSiAlBC coatings—unreinforced or reinforced with 65 wt.% or 85 wt.% WC-12Co—applied via high-velocity oxy-fuel (HVOF) spraying onto stainless steel substrates under controlled parameters. It quantifies the influence of high carbide volume fractions within the NiCrFeSiAlBC matrix on microstructure and tribomechanical performance. Microstructural analysis revealed uniformly distributed cermet layers featuring dissolved reinforcements and WC hard phase formation, with minimal W₂C crystallization. Elevated WC-12Co incorporation promoted densification and reduced porosity. Vickers microhardness tests (HV 0.3) demonstrated increased hardness upon WC-12Co addition, attributable to finer particle sizes, lower porosity, and the presence of WC phases alongside crystallographic refinements. Under dry reciprocating sliding conditions, friction coefficients and wear volumes decreased markedly. Consequently, the coating with 85 wt.% WC exhibited the best mechanical and tribological properties. Full article

Macroporous silica thin films were synthesized via the sol–gel method to elucidate the relationship between pore structure and the degree of polarization of light (DoP). The films were characterized by scanning electron microscopy (SEM) to determine their mean pore size and surface porosity, while polarization-resolved speckle imaging was employed to evaluate the degree of polarization and its distribution on the Poincaré sphere. The results show that surface porosity is a key structural parameter governing the DoP, with increasing values leading to enhanced scattering and a progressive isotropization of the polarization-state distributions. Poincaré sphere mapping further reveals distinct scattering regimes and polarization-conversion pathways, providing insights that are not accessible with conventional optical measurements. Overall, these findings show that speckle imaging is a rapid, cost-effective, and non-destructive approach to probing structural and optical anisotropies in porous materials, with direct relevance to systems where pore accessibility dictates performance, including liquid-crystal devices, photochromic coatings, and other nanostructured photonic platforms. Full article

Nucleation remains one of the least understood steps during protein crystallization, although it strongly impacts product quality attributes, including total crystal numbers, final crystal size distributions, and thus downstream processing. In this work, the nucleation behavior of Lactobacillus brevis alcohol dehydrogenase (LbADH) wild type (WT) and five mutants (Q207D, Q126H, K32A, D54F, and T102E) is investigated in a stirred 7 mL crystallizer monitored by in situ multi-angle dynamic light scattering (MADLS). Nucleation was studied with highly pure homotetrameric LbADHs by establishing a crystallization, lyophilization, and re-solubilization protocol combined with size exclusion chromatography (SEC) and size exclusion high-performance liquid chromatography (SE-HPLC), yielding tetramer purities above 94% and removing low molecular weight impurities. During stirred batch crystallizations initiated by the addition of polyethyleneglycol 550 monomethyl ether (PEG 550 MME), SEC and SE-HPLC revealed decreasing tetramer peak areas but essentially constant peak apex positions, indicating that no long-lasting oligomeric intermediates accumulate at detectable levels. Time-resolved MADLS measurements using a custom-made flow-through cuvette in a bypass to the stirred crystallizer uncovered transient cluster populations. All protein variants exhibited an initial tetramer peak, followed by the formation of larger aggregates and a rapid rise in signal above a hydrodynamic diameter of 1000 nm, coinciding with the onset of macroscopic turbidity. A simple mesoscale nucleation model was formulated, yielding end-of-nucleation times, crystallized fractions, critical soluble concentrations, and apparent nucleation rate constants. The crystal contact mutations modulate both the timing and magnitude of the nucleation burst (rapid build-up of nuclei/cluster populations). The mutant Q207D showed strongly attenuated nucleation compared to the WT, whereas the other mutants (K32A, D54F, and particularly T102E) display markedly accelerated nucleation at nearly invariant critical concentrations. The combined workflow demonstrates how in situ MADLS, together with a tailored kinetic description, can provide mechanistic insight into protein nucleation in stirred batch crystallizers. Full article

Entangled-photon sources are indispensable components in free-space quantum key distribution (QKD) systems. Here, we present a compact, lightweight, and robust airborne entangled-photon source (AEPS) based on a Sagnac loop structure with single-mode fiber coupling. To meet the drone requirements for miniaturization, lightweight design, and high robustness, we developed a highly integrated entangled-photon source using customized miniature optical components and an adhesive bonding technique. The total volume and weight are only 38 × 40 × 24 mm³ and 58 g, respectively. Entangled-photon pairs at 810 nm are generated via Type-II spontaneous parametric down-conversion (SPDC) in a periodically poled KTiOPO₄ (PPKTP) crystal. We achieve a quantum state fidelity of F = 0.986 ± 0.0017, a photon-pair generation rate of 3.03 × 10⁶ pairs/s/mW, and a CHSH Bell parameter of S = 2.764 ± 0.082. Owing to its excellent size, weight, performance, and stability, the proposed entangled-photon source is particularly well suited for drone-based free-space mobile quantum communication. Full article