Search Results (604)

Europium (Eu) is a rare-earth element with unique optoelectronic properties that underpin its applications in displays and lighting, X-ray imaging, anti-counterfeiting, and biomedicine. Conventional methods typically involve the synthesis of europium-based luminescent materials in powder or crystalline form via high-temperature solid-state reactions or solution processes, followed by secondary processing such as spin coating or evaporation to fabricate films or devices. In this work, we report a direct approach to prepare trivalent europium-based luminescent materials using divalent europium bromide (EuBr₂) as the precursor via a gas-phase vacuum evaporation approach (GPVEA). This “deposition-as-synthesis” method enables the fabrication of the hybrid nanoscale films with various blending ratios, which exhibit changes in the fine structure of the emission peaks. The luminescence spectra remain nearly identical across the temperature range from 80 K to 320 K. The photoluminescence emission intensity is stronger in air than in a vacuum. The films show a maximum photoluminescence quantum yield (PLQY) of 8.27% and good photostability, with an emission decay of 3.44% over 50 min under continuous 300 nm excitation. Through patterned design, we demonstrate their value for anti-counterfeiting applications. This work thus provides guidance for the preparation of europium-based luminescent nanomaterials via GPVEA and their application in anti-counterfeiting. Full article

To address heat accumulation, localized hot spots, and non-uniform temperature distribution in large-capacity lithium iron phosphate energy storage battery modules under high ambient temperature and high-rate charge/discharge conditions, this study proposes a fin-enhanced phase change material (PCM)-air hybrid thermal management structure for a 100 Ah prismatic lithium iron phosphate battery and a 2P18S energy storage battery module. First, the battery thermal model is validated using single-cell experimental data reported in the literature. Subsequently, a three-dimensional transient fluid–solid coupled heat transfer model is established by considering transient battery heat generation, PCM solid–liquid phase change, air-side flow and heat transfer, and temperature-dependent thermophysical properties. User-defined functions are employed to implement the transient heat source and temperature-dependent material properties. Under identical boundary conditions, the thermal management performances of three configurations, namely Fin-Air, PCM-Air, and Fin-PCM-Air, are compared. The effects of ambient temperature (20 °C, 25 °C, and 30 °C) and inlet air velocity (1 m/s, 2 m/s, and 3 m/s) on the maximum module temperature, temperature uniformity, PCM liquid fraction evolution, and flow field distribution are quantitatively analyzed. The results show that, compared with the Fin–Air system without PCM and the PCM-Air system without fins, the Fin-PCM-Air configuration reduces the maximum module temperature by 1.57% and 0.25%, respectively, at an ambient temperature of 30 °C and an inlet air velocity of 3 m/s. After four charge–discharge cycles, the peak maximum temperature of the module is approximately 38.56 °C, and the peak maximum temperature difference remains below 3.6 K, indicating good temperature uniformity and latent heat buffering capability. In addition, the air velocity trade-off analysis indicates that increasing the inlet air velocity can improve cooling performance but also increases the air-channel pressure drop and fan power consumption. Therefore, the Fin-PCM-Air structure is more suitable for high-thermal-load conditions, and its practical application should comprehensively consider cooling benefits, additional mass, manufacturing cost, and long-term reliability. This study provides a reference for the design and engineering application of hybrid thermal management structures for large-capacity energy storage battery modules. Full article

It is well-known that high-performance thermal protective clothing is crucial for personnel working in high-temperature environments, such as firefighters. Thermal protective clothing design usually integrates textile materials’ type, thickness, physical and chemical properties (such as thermal conductivity), ergonomics, and environmental adaptability. In this study, the heat transfer process and the optimal thickness are mainly discussed for providing some references on the design of this clothing. The thickness design of thermal protective clothing fabrics is carried out via numerical heat transfer simulations based on experimental data obtained from manikin tests. Firstly, one heat transfer model for thermal protective clothing, including three textile materials’ layers and one air layer, is constructed according to Fourier’s law of heat conduction, Newton’s law of cooling, and the Stefan–Boltzmann law, with appropriate boundary conditions assigned. Secondly, the finite volume element method, which has the important advantage of preserving conservation properties for physical quantities, is employed to discretize the heat transfer model. Thirdly, the convective heat transfer coefficient, which characterizes heat exchange between fluid and solid surfaces, is determined approximately by the least-squares method based on the given data, while the heat transfer process is simultaneously simulated. Fourthly, the thicknesses of the second and fourth layers are critical to the performance of thermal protective clothing. Two optimization algorithms are proposed to determine the optimal thickness configuration that effectively balances thermal insulation and wearing comfort. From the above results, it is recommended to use multilayer textile composite materials incorporating aerogel insulation layers and phase-change material interlayers. Full article

Clay mineral authigenesis and transformation are key diagenetic processes that influence the evolution of sandstone reservoir quality. Although smectite formation and its transformation to illite have been widely studied in clay-rich and feldspathic systems, their development in highly quartz-rich sands remains less well constrained. This study investigates the experimental formation of authigenic smectite and its subsequent illitization in a quartz-dominated sand under controlled hydrothermal experiments. Quartz-rich glass sand from the Middle Jurassic Mariedal Formation (Skåne, Sweden) was reacted with natural Red Sea water in sealed reactors at 80, 150, 200, and 250 °C for 14 days to simulate progressive burial diagenesis. Mineralogical, textural, and geochemical changes were evaluated using thin-section petrography, SEM-EDS, WD-XRF, XRD, and ICP-OES. The starting material is composed predominantly of quartz (91.3%), with minor K-feldspar (6.2%) and muscovite (1.4%), providing limited but sufficient reactive components for clay mineral formation. Dissolution of K-feldspar and muscovite began at 80 °C and continued throughout the experiments. Authigenic smectite was first detected at 150 °C as discontinuous grain-coating phases, indicating nucleation through dissolution–precipitation reactions linked to feldspar alteration and uptake of Mg from the reacting fluid. At 200 °C, the smectite coating became thicker and more extensive, with the onset of transformation to illite through mixed layer stages. By 250 °C, illite becomes the dominant clay mineral, recording progressive smectite illitization with increasing temperature. Fluid chemistry shows systematic variations with temperature, including decreasing Mg and evolving K concentrations, reflecting progressive mass transfer between solid and fluid phases. These results demonstrate that even highly quartz-rich sands can generate authigenic clay minerals when minor reactive phases and suitable fluid chemistry are present. The experiments provide a process-based analogue for clay mineral evolution in quartz-rich sandstone reservoirs and highlight the importance of coupled mineral–fluid reactions during burial diagenesis. Full article

This study investigates the effect of mineral additives of different natures, namely blast-furnace slag, fly ash, and bentonite, on structure formation, phase composition, microstructure, and physicomechanical properties of cement matrices. The analysis included measurements of mass change and linear shrinkage during hardening, determination of density and microhardness, X-ray phase analysis, and microstructural examination by scanning electron microscopy. It was found that the introduction of mineral additives reduced linear shrinkage from 6.06 mm for the control composition to 0.25 mm for the composition with blast-furnace slag, 2.31 mm for the composition with fly ash, and 1.01 mm for the composition with bentonite. The maximum density and microhardness values were obtained for the matrix with blast-furnace slag and amounted to 1.99 ± 0.03 g/cm³ and 39.95 ± 1.12 HV1, respectively, whereas the overall range of values for the investigated compositions was 1.52–1.99 g/cm³ and 30.2–39.95 HV1. X-ray phase analysis showed that the amorphous component varied from 61 to 78%, reaching its maximum value in the composition with blast-furnace slag, which is associated with the formation of poorly crystalline C–S–H and aluminosilicate phases. According to the SEM data, the average size of visible pore-like defects was 2.4 μm for the control composition, 1.4 μm for the composition with blast-furnace slag, 1.3 μm for the composition with fly ash, and 1.7 μm for the composition with bentonite. The most favorable combination of high density, microhardness, developed amorphous component, and homogeneous microstructure was established for the composition with blast-furnace slag. The obtained results can be used as a materials-science basis for the development of cement matrices intended for further studies on the immobilization of solid radioactive waste. Full article

This study investigates the effect of controlled acid demineralization of coal shale from Shubarkol Komir JSC using HCl solutions with concentrations of 9–37% by mass on its structural characteristics, the kinetics of thermal decomposition, and the ability to concentrate rare and dispersed trace elements in the solid residue from the hydrodemetallization of the heavy fraction of coal tar. Analysis of IR spectroscopy, TG/DTG and isoconversional kinetics showed that acid treatment leads to the removal of carbonate and partially iron-containing phases while maintaining the aluminosilicate framework, increasing the structural uniformity of the matrix and moving to a more ordered thermal decomposition mechanism. The activation energy in the range of α = 0.1–0.7 is 83–87 kJ/mol for all modified samples, increasing to 96.20 kJ/mol at α = 0.9 for CS100. It has been established that the ability of coal shale to concentrate rare and dispersed trace elements in the solid residue of hydrodemetallization changes non-monotonically: the total content of trace elements reaches a maximum of 1452.19 g/t with moderate acid treatment (CS50) and sharply decreases to 137.85 g/t with deep demineralization (CS100). It has been shown that the degree of acid treatment acts as a controlled parameter that allows for purposefully regulating the ability of coal shale to concentrate rare and dispersed trace elements in the process of hydrodemetallization of heavy hydrocarbon raw materials. Full article

Oil sands tailings from tailings solvent recovery units (TSRU) contain elevated sulfide minerals and can generate acid mine drainage (AMD) upon atmospheric exposure. This study investigated how prior weathering influences acidity and solute release under controlled laboratory conditions. A six-month column leaching experiment was conducted using TSRU tailings with distinct exposure histories: weathered and semi-weathered tailings from a previous greenhouse-scale reclamation capping experiment, along with weakly weathered tailings stored in sealed barrels. Columns were subjected to repeated wet–dry cycles, analyzing the geochemistry of the leachate and solid-phase changes using X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). All treatments produced highly acidic leachates (pH < 2), indicating that TSRU tailings retain the capacity to generate acidity regardless of prior exposure. However, the dominant geochemical mechanisms differed by weathering history. Weakly weathered tailings generated progressive increases in acidity and solute release, consistent with active sulfide oxidation. Semi-weathered tailings had more stable responses, suggesting partial sulfide depletion and secondary phase formation. Weathered tailings produced leachates showing evidence of rapid flushing with limited new solute generation. After leaching, residual pyrite remained in all materials, with shifts in surface sulfur speciation providing evidence of progressive surface sulfur oxidation, transformation, and the redistribution of sulfate phases. These results demonstrate the mechanisms involved in AMD generation in TSRU tailings, highlighting the importance of the weathering history and the need for field-scale validation. Full article

High-entropy alloys (HEAs) have emerged as an important class of materials for solid-state hydrogen storage because their compositional complexity provides access to diverse phase constitutions, local lattice environments, and hydrogen-related responses. However, hydrogen-storage behavior in these alloys cannot be understood from composition alone. What ultimately governs performance is the microstructural state generated during preparation. This perspective examines HEAs from that standpoint, focusing on how different preparation routes produce distinct structural states and how those states determine hydrogen accommodation, diffusion, phase transformation, and reversibility. Arc melting and subsequent homogenization typically generate bulk refractory alloys with comparatively simple average phase constitution, whereas mechanical alloying and reactive ball milling produce defect-rich, fine-scale, and metastable non-equilibrium structures. Representative systems are discussed to show that even alloys with similar nominal compositions may follow different hydriding pathways once their structurally realized state changes. The article further evaluates the structural descriptors most often invoked in the field, including phase constitution, local lattice environment, grain size, defect density, interface density, chemical homogeneity, and processing history. It is argued that future progress will depend less on continued composition screening alone than on establishing more transferable microstructure–hydrogen-storage relationships across route-defined structural states. Full article

To enhance the energy efficiency of data center cooling systems, this study introduces Micro-encapsulated Phase Change Material Suspension (MPCMS) into a naturally stratified cold storage system. Leveraging its superior properties, including high latent heat, high specific heat, and excellent fluidity, a three-dimensional transient numerical model was developed to investigate the thermal stratification characteristics during the discharging process. The analysis focuses on the impacts of operational conditions (flow rate and mass fraction) alongside key tank structural parameters (height-to-diameter ratio, uniform flow plate perforation rate, installation position, and aperture). The results indicate that the thermal stratification performance of MPCMS is significantly superior to that of water. Specifically, during the middle discharge stage (t* = 0.4) at a high flow rate of 12.56 m³/h, the thermocline thickness of MPCMS-10 wt% is restricted to only 245 mm, representing a 93.82% reduction compared to 3964 mm for water. Furthermore, at the initial discharge stage (t* = 0.05), the thermocline thickness decreases significantly with increasing MPCMS mass fraction; as the mass fraction rises from 10 wt% to 30 wt%, the thickness sharply drops from 421 mm to 120 mm (a 71.44% reduction), and the stratification number (Str) reaches an optimal 1.00. In terms of macroscopic structural optimization, a height-to-diameter (H/D) ratio between 2 and 4 provides the best balance of stratification stability and cold storage efficiency. Mechanistically, integrating a uniform flow plate effectively suppresses thermal jet disturbances. During the initial discharge stage, a plate with a 10% perforation ratio reduces the thermocline thickness by 69.12% (from 421 mm to 130 mm) relative to the no-plate baseline. The optimal flow plate configuration was identified as a 10% perforation rate, a 20 mm aperture, and an installation spacing of 1.25% of the tank height. Ultimately, this study validates the substantial potential of MPCMS through robust quantitative data, providing a solid theoretical foundation and precise design guidelines for high-efficiency cold storage systems. Full article

Silicomanganese slag (SiMnS), a Mn-bearing by-product from silicomanganese alloy production, is often stockpiled in large quantities and may pose environmental concerns due to potential metal leaching. This study develops an OPC-rich hybrid SiMnS–steel slag–fly ash–OPC-activated composite binder, referred to as SMSAB, in which OPC accounts for 55% of the solid precursor mass. Different alkali contents and sodium silicate moduli were investigated, and the optimised paste was characterised in terms of mechanical strength, reaction products, pore structure, carbon-footprint and heavy-metal leaching. The best performance was obtained at an alkali content of 4% and a sodium silicate modulus of 1.0, giving 28-day compressive and flexural strengths of 65.13 MPa and 3.37 MPa, respectively. XRD, SEM-EDS, FTIR and MIP results showed that the main reaction products were C-(A)-S-H, N-A-S-H and C-N-A-S-H gels, which refined the pore structure and produced a dense matrix. The reduction in Mn leaching may be associated with physical encapsulation, possible charge-balancing interactions within gel structures, changes in Mn-related bonding environments and the presence of Mn-bearing phases. Leaching concentrations of Zn, Mn, Cr, Cu and Ni satisfied the Grade III groundwater limits used in China. The calculated carbon intensity of SMSAB was 3.97 kg·(m³·MPa)⁻¹, indicating a favourable strength-to-emission balance compared with the reference systems considered. It should be noted that the present work examines paste specimens only; aggregate skeleton, traffic loading, freeze–thaw cycling and wet–dry/moisture cycling were not included. Therefore, the results demonstrate binder-level potential rather than direct qualification of SMSAB as a pavement base or subbase material. Full article

Three crosslinked polyurethane copolymers were successfully synthesized as polymeric solid–solid phase change materials (SSPCMs) for thermal energy storage. These materials were fabricated utilizing trihydroxy compounds (glycerol, triethanolamine, and trimethylolethane) as chain extenders and polyethylene glycol (PEG) as the phase change functional segment. A comprehensive suite of characterization techniques was employed to investigate the chemical structures, thermal properties, and crystalline behaviors of the resulting SSPCMs. Fourier transform infrared (FTIR) spectroscopy confirmed the successful synthesis of the crosslinked polyurethane network. Polarizing optical microscopy (POM) and wide-angle X-ray diffraction (WAXD) analyses revealed that all three SSPCMs exhibit regular spherulitic morphologies with sharp diffraction peaks resembling those of pure PEG, although variations in spherulite size and diffraction intensity were observed among the samples. Differential scanning calorimetry (DSC) demonstrated the reversible latent heat storage and release capabilities of the synthesized SSPCMs, with a maximum endothermic enthalpy (ΔH_endo) of 115.7 J/g. Furthermore, thermal cycling tests and thermogravimetric (TG) analysis verified their exhibit excellent reusability, thermal reliability, and high thermal stability. Full article

In this study, commercial Ospray-2507 super-duplex stainless steel powder was investigated for the first time as a potential metal support material for solid oxide cells. Initially, metal supports were fabricated and processed in air using various sintering profiles, followed by comprehensive mechanical, structural and electrochemical characterization. The optimal sintering condition was identified as 900 °C for 5 h. Subsequently, sintering under a H₂ atmosphere was explored, and its effects on the microstructural and functional properties of the metal supports were systematically to assessed to evaluate the influence of the sintering atmosphere on material performance. Although X-ray diffraction patterns showed no phase changes between the two sintering atmospheres, notable improvements were observed in mechanical, electrochemical, and microstructural properties under H₂ sintering. XPS spectra reveal that both air- and hydrogen-treated surfaces remain rich in chromium (Cr) and Manganese (Mn), which together dominate the surface and consequently attenuate the signal from the underlying iron. The thickness of the Cr- and Mn-based oxide layer decreases when sintering MS in H₂ atmosphere. Specifically, mechanical strength, as measured by three-point bending tests, increased by a factor of 12.5, and hardness rose from 500.3 to 523.5 HV. Furthermore, electrical conductivity also improved significantly, exhibiting an approximately 2.3–2.4 fold increase under H₂-sintered conditions. Full article

Metastructures, waveguides composed of multiple unit cells (meta-atoms), have gained significant attention for controlling wave propagation in engineering applications, especially in the context of elastic and acoustic waves. However, existing metastructures often lack sufficient tunable functionality to dynamically control both elastic vibration and acoustic wave transmission using a single external parameter. This study introduces a phase-change material (PCM)-embedded meta-atom, where a core mass is connected to an outer shell by Archimedean spiral bridges. The solid–liquid phase transition of PCM induces a notable change in the effective shear modulus, enabling dynamic wave control. The mechanism for bandgap formation transitions from Bragg scattering in the solid PCM state to local resonance in the liquid state. Core rotation, driven by the phase transition, is key to generating flat bands and low-frequency locally resonant bandgaps at high temperatures. Temperature-dependent, mode-selective transmission behavior is observed, with transverse vibrations and acoustic waves exhibiting opposite blocking and transmission characteristics at the same frequency. This design provides a promising approach for decoupling sound and vibration management, using temperature control driven by the PCM phase transition. The work contributes to multifunctional metastructures with applications in adaptive noise control, structural health monitoring, and tunable vibration isolation systems. Full article

Epoxy materials are an important class of thermosets whose properties strongly depend on the used formula, the curing parameters, and many available hardeners. Achieving desired properties such as enhanced thermal stability, extended lifetime, or self-regeneration requires selecting suitable precursors and carefully tuning curing conditions. In this work, a selected biphenyl epoxy precursor was used as a model compound to assess whether using different hardeners could be an effective factor in tailoring the elasticity of cured epoxy networks. We employed two chemically distinct hardeners—4,4′ diaminodiphenylmethane (DDM) and suberic acid—to generate materials with markedly different final properties. For instance, the glass transition temperature T_g varied within a range of over 35 °C. Two complementary experimental techniques were used in this paper to establish the optimal curing parameters: differential scanning calorimetry (DSC) and broadband dielectric spectroscopy (BDS). Both techniques supported tracking of changes in the mixture while curing and enabled determination of T_g in the obtained products. Dielectric relaxation spectroscopy revealed various molecular motions (α, β, and γ-processes) occurring in different phases, especially in glass-forming solids. BDS is therefore a good tool for testing new organic materials. The analytic route used in this work, based on a combination of calorimetric and electrical approaches, enables precise adjustment of the curing parameters to a specific hardener and helps verify the effects of using different hardeners on the elastic properties of the product. This allows the creation and modification of epoxy matrices towards modern materials, such as composites with self-healing properties or enhanced thermal stability. Full article

To overcome the low thermal conductivity and flow channel clogging inherent in traditional phase change materials (PCMs) for immersion cooling, this study develops a novel oil-based phase change emulsion (PCE) integrating high thermal transport with adaptive rheological behavior. A liquid thermal conductivity enhancer was synthesized by modifying epoxidized soybean oil with LiTFSI and blending it with a synthetic ester to form a dielectric base fluid. A mid-to-low-temperature PCM (Span65) was then incorporated via surfactant-free ultrasonic emulsification. The resulting PCE exhibits a tunable phase-change window (25~40 °C) driven by interfacial confinement effects and a multiscale lamellar network. It achieves significantly enhanced thermal conductivity (15% increase over base oil) while maintaining excellent electrical insulation (<10⁻⁹ S/cm). Rheologically, the emulsion transitions from shear-thinning in the solid state to near-Newtonian in the liquid state, optimizing both suspension stability and pumping efficiency. This work establishes a strategy for designing high-performance, safe, and energy-efficient dielectric coolants, offering a robust solution for next-generation electronic and battery thermal management systems. Full article