Search Results (11,382)

Calcium aluminate cement (CAC) offers rapid strength development, chemical durability in harsh environments, and high-temperature resistance, but its long-term performance may be compromised by the conversion of metastable hexagonal hydrates into stable cubic phases. Concurrently, recycling spent fluorescent lamp glass (SFLG) is limited because of its residual mercury content. This study investigates the use of manually (MAN) and mechanically (MEC) processed SFLG as partial CAC replacements (up to 50 wt.%). Both SFLG types had irregular morphologies with mean particle sizes of ~20 µm and mercury concentrations of 3140 ± 61 ppb (MAN) and 2133 ± 119 ppb (MEC). Moreover, the addition of SFLG reduced the initial and final setting times, whilst MEC waste notably extended the plastic state duration from 20 min (reference) to 69 min (50 wt.% MEC). Furthermore, strength development was accelerated, with SFLG/CAC mortars reaching peak strengths at 7–10 days versus 28 days as in the CAC reference. CAC and 15 wt.% SFLG mortars showed strength loss over time by reason of their phase conversion, whereas mortars with 25–50 wt.% SFLG experienced significant long-term strength gains, reaching ~60 MPa (25 wt.%) and ~45 MPa (35 wt.%), respectively, after 365 days, with strength activity indexes (SAI) near 90% and 70%, respectively. These improvements are attributed to the formation of strätlingite (C₂ASH₈), which stabilized hexagonal CAH₁₀ and mitigated conversion to cubic katoite (C₃AH₆). Mercury leaching remained below 0.01 mg/kg dry matter for all mixes and curing ages, classifying the mortars as non-hazardous and inert under Spanish Royal Decree 646/2020. The results suggest that SFLG can be safely reused as a sustainable admixture in CAC systems, enhancing long-term mechanical performance while minimizing environmental impact. Full article

The integration of emulsion gels in 3D food printing has emerged as a promising strategy to enhance both the structural fidelity and functional performance of printed foods. Emulsion gels, composed of proteins, polysaccharides, lipids, and their complexes, can provide tunable rheological and mechanical properties suitable for extrusion and shape retention. This review explores the formulation strategies, including phase behavior (O/W, W/O, and double emulsions); stabilization methods; and post-printing treatments, such as enzymatic, ionic, and thermal crosslinking. Advanced techniques, including ultrasound and high-pressure homogenization, are highlighted for improving gel network formation and retention of active compounds. Functional applications are addressed, with a focus on meat analogs, bioactive delivery systems, and personalized nutrition. Furthermore, the role of the oil content, interfacial engineering, and protein–polysaccharide interactions in improving print precision and post-processing performance is emphasized. Despite notable advances, challenges remain in scalability, regulatory compliance, and optimization of print parameters. The integration of artificial intelligence can also provide promising advances for smart design, predictive modeling, and automation of the 3D food printing workflow. Full article

Tight oil is an important resource replacement in the petroleum industry, with the reserves of Type-II energy accounting for over 40%. However, these reservoirs have small pore throats and complex structures, and their wettability directly affects the EOR by affecting the occurrence of crude oil and multiphase flow mechanisms. In response to an unclear understanding of the evolution mechanism of wettability after energy replenishment in tight reservoirs with different reservoir formation conditions, the evolution law of wettability in different energy replenishment media for tight type-II reservoirs is evaluated by performing wettability experiments and nuclear magnetic resonance experiments, and the mechanism of differential changes in wettability after energy replenishment in different media is elucidated. The results show that the block with well-developed pores and good connectivity (Block: Z401) had the smallest in situ wetting angle, ranging from 27.1° to 30.4°, and that the interface effect had a small impact, resulting in a small change in the wetting angle after energy replenishment. The wetting angle of the developmental intersection block (Block: G93) is the highest, ranging from 36.6° to 46.4°. The connected pore and throats fully interact with the medium at the interface, resulting in a significant change in the wetting angle. In addition, after natural gas energy supplementation, the principle of similar solubility causes a significant change in the wetting angle of the pore throat interface after adsorption, with a maximum angle of 19.6°. The change in the wetting angle change of the CO₂ mixed-phase principle is in the middle, at about 13.6°, while the change in the wetting angle is minimal after N₂ replenishment, around 10°. The research results improve our understanding of the basic theory of tight oil supplementary energy development and have important practical significance. Full article

This study investigates the influence of RE elements on the room- and high-temperature properties of magnesium alloys. The effects of RE type, addition level, and multi-element alloying strategies were systematically analyzed to clarify the underlying strengthening mechanisms and processing pathways for optimizing Mg–RE alloys. RE elements enhance the mechanical and thermal properties of Mg alloys through crystal structure modification, formation of thermally stable dispersed phases, precipitation strengthening, and solid-solution strengthening. Compared with conventional alloying elements, RE additions offer distinct advantages in strengthening efficiency and overall performance. To fully exploit these benefits, new research paradigms that integrate machine learning and other advanced techniques are required, enabling the intelligent design of multicomponent alloy systems tailored to specific application requirements. Full article

This study investigates the presence of naturally occurring asbestos (NOA) in the Bajgora region of Mitrovica, Republic of Kosovo. Rock samples were collected and analyzed using X-ray powder diffraction (XRPD) and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM/EDX). The analyses confirmed the presence of the chrysotile mineral, which is part of the asbestos mineral family, while the minerals of the serpentine group, lizardite and antigorite, were identified. Also, in the last sample, in the flyschite sandstone formations, quartz was identified. XRPD enabled the identification of mineral phases, while SEM/EDX provided detailed morphological and chemical characterization, essential for confirming asbestos structures. The detection of asbestos near residential areas raises serious public health concerns, as airborne fibers may be inhaled during routine daily activities. Exposure to these fibers is linked to severe diseases, including asbestosis and mesothelioma. These findings highlight the need for continued monitoring and comprehensive assessment of asbestos contamination in the Bajgora region. The findings point to the need for continuous monitoring and comprehensive assessment of the Bajgora region for asbestos contamination. Furthermore, the ecological risks to human health resulting from the dispersion of asbestos mineral fibers in the soil, where their presence may be found in surface waters and in the air, these fibers represent a significant environmental risk that requires urgent attention by establishing a monitoring system for the benefit of public health. Full article

Reppe’s ethynylation of formaldehyde uses coal-based acetylene to produce commercially valuable 1,4-butynediol with a silica-supported copper oxide-bismuth oxide catalyst. Cuprous acetylide (Cu₂C₂) is generally accepted to be the catalytically active phase, which is formed in situ from the CuO-Bi₂O₃/SiO₂ pre-catalyst under ethynylation conditions. The catalytic performance and stability of this sensitive Cu₂C₂ phase are evaluated by long-term experiments (up to 240 h) and by catalyst recycling (10 cycles of 22 h). Powder X-ray diffraction and Raman spectroscopy are found to be the best and the only applicable analytical tools for qualitative evaluation of Cu₂C₂’s crystallinity, purity, and morphology during in situ formation and for phase transformations during the ethynylation. They were continuously correlated with the catalytic performance (1,4-butynediol yield determined by gas chromatography). No catalyst deactivation was observed, indicating outstanding catalyst stability. Observed structural changes within the active Cu₂C₂ phase have obviously limited influence on the catalytic cycle and performance. Full article

This study investigated the effect of supersolidus liquid-phase sintering conditions on the powder particle bonding and the AlN-phase formation of an AlSi10Mg alloy. Sintering was conducted at temperatures between 550 and 579 °C, with a holding duration of 2 h under a nitrogen atmosphere. The sintering cycles included four heating segments, performed at rates ranging from 0.2 to 5 °C/min for a total of between 5 and 15 h, and a cooling segment performed at two different cooling rates, 0.15 and 5 °C/min, resulting in durations of 12 and 70 h, respectively. Three powder batches exhibiting different particle size distributions were tested. An X-ray diffractometer, optical microscopy, and scanning electron microscopy were used to characterize phase formation and particle bonding. The results show that higher sintering temperatures and faster heating/cooling rates led to a lower fraction of AlN. In contrast, lower sintering temperatures or slow heating promoted the development of a thicker AlN shell around powder particles, inhibiting the bonding of the AlSi10Mg powder and preventing densification via the sintering process. These findings suggest that sintering at temperatures between 570 and 575 °C, with heating and cooling rates of at least 2 °C/min, constitutes a more favorable window for the densification of AlSi10Mg under a nitrogen atmosphere. Full article

This study investigates the optimal duration for forming a uniform oxide layer and evaluates its influence on water-splitting performance. We selected a Ti₅₀Cu₃₂Ni₁₅Sn₃ amorphous ribbon, which is known to simultaneously form anatase TiO₂ and Sn oxide via a single hydrothermal process. Hydrothermal treatments were conducted at 220 °C in 150 mL of distilled water for durations of 3 and 6 h. The process successfully formed nanoscale metal oxides on the alloy surface, with the uniformity of the oxide layer increasing over time. The amorphous phase of the alloy was retained under all conditions. X-ray photoelectron spectroscopy (XPS) analysis confirmed the formation of TiO₂ and SnO_x, while Cu and Ni remained in their metallic state. Furthermore, we verified the coexistence of these oxides with metallic Ti and Sn. Photoelectrochemical analysis showed that the sample treated for 6 h exhibited the best water-splitting performance, which correlated directly with the most uniform oxide coverage. This time-controlled hydrothermal oxidation method, using only water, presents a promising and efficient approach for developing functional surfaces for electronic and photoelectrochemical applications of metallic glasses (MGs). Full article

Among different formations, inorganic/inorganic assemblies can be considered “two in one” systems offering collective and/or new physical-chemical properties and substantial activity. Herein, a post-synthetic approach involving the assembly through Van der Waals forces and/or hydrogen bonding of the preformed ZnO@OAm NPs and Ca(OH)₂@OAm NPs of non-uniform sizes (9 nm and 27 nm, respectively), albeit coated with the same surfactant (oleylamine-OAm), is reported. The resulting semiconductor hetero-nanostructure (named CaZnO) has been physicochemically characterized. The X-ray diffraction (XRD) peaks correspond to both ZnO and Ca(OH)₂, confirming the successful formation of a dual-phase system. Field emission scanning electron microscopy coupled with energy-dispersive spectroscopy (FESEM-EDS) of CaZnO indicated the formation of Ca(OH)₂ NPs decorated with irregular-shaped ZnO NPs. The synthesized hetero-nanostructure was evaluated by assessing any negative effects on the photosynthetic function of tomato plants as well as for the generation of reactive oxygen species (ROS). The impact of the CaZnO hetero-nanostructure on photosystem II (PSII) photochemistry was evaluated under both the growth light intensity (GLI) and a high light intensity (HLI) at a short (90 min) and long (96 h) duration exposure. An enhancement of photosystem II (PSII) function of tomato plants by 15 mg L⁻¹ CaZnO hetero-nanostructure right after 90 min was evidenced, indicating its potential to be used as a photosynthetic biostimulant, improving photosynthetic efficiency and crop yield, but pending further testing across various plant species and cultivation conditions. Full article

High-entropy alloys (HEAs) exhibit superior properties for extreme environments, yet the effects of laser scanning speed on the microstructure and performance of laser-clad NiAlNbTiV HEA coatings remain unclear. This study systematically investigates NiAlNbTiV coatings on 316 stainless steel fabricated at scanning speeds of 800–1100 mm/min via laser cladding. Characterizations via XRD, SEM/EDS, microhardness testing, high-temperature wear testing, and electrochemical measurements reveal that increasing scanning speed enhances the cooling rate, promoting γ-(Ni, Fe) solid solution formation, intensifying TiV peaks, and reducing Fe-Nb intermetallics. Higher speeds refine grains and needle-like crystal distributions but introduce point defects and cracks at 1100 mm/min. Microhardness decreases from 606.2 HV (800 mm/min) to 522.4 HV (1100 mm/min). The 800 mm/min coating shows optimal wear resistance (wear volume: 0.0117 mm³) due to dense eutectic hard phases, while higher speeds degrade wear performance via increased defects. Corrosion resistance follows a non-linear trend, with the 900 mm/min coating achieving the lowest corrosion current density (1.656 μA·cm⁻²) due to fine grains and minimal defects. This work provides parametric optimization guidance for laser-clad HEA coatings in extreme-condition engineering applications. Full article

The solid-state reactions between Fe₂O₃ and molecular sulfur sources could produce FeS nanoparticles efficiently, while the functions of these molecules have been ignored except for the role as sulfur sources. In this work, thioacetamide and thiourea were employed as sulfur sources for the solid-state reactions with Fe₂O₃ to explore their effects on the microstructure and electrochemical performance of the produced FeS. Despite the slight difference in one functional group for two molecules (−CH₃ against −NH₂), thiourea leads to a more complex reaction pathway with FeS₂ as the intermediate phase, while no such an intermediate phase is observed in the reaction with thioacetamide. The former yields FeS of 2D nanoflakes as the final products, compared with the aggregated nanoparticles in reactions with thiourea. As a result, the nanoflakes exhibit a higher discharge capacity with enhanced stability (388.9 mAh∙g⁻¹ vs. 374.7 mAh∙g⁻¹ above 1 V). According to the reaction pathways, the formation of FeS nanoflakes and superior electrochemical performance were addressed, paving a route for the solid-state reactions with molecules to develop high-performance sulfide electrode materials. Full article

Compounds known as liquid organic hydrogen carriers (LOHCs) offer a promising pathway for storing hydrogen. Beyond the use of pure hydrocarbons, the incorporation of oxygen atoms offers a way to modify thermodynamic properties and potentially improve suitability for hydrogen storage. This study explores the effect of oxygen functionalization in aromatic ethers and lactones on the reaction equilibrium of reversible hydrogenation. To address this question, reaction enthalpies and entropies are calculated using both experimental and theoretically determined pure substance data. The equilibrium position shift in the hydrogenation of furan derivatives has been shown to follow a similar trend to that of their hydrocarbon counterparts upon the addition of aromatic rings. This shift is, however, more pronounced in the case of the furan-based systems. The effect is reflected in increasing Gibbs reaction energies during the dehydrogenation process. Both the formation of lactones and the addition of a second ring to the furan core leads to a further increase in the Gibbs reaction energy. The highest value is observed for dibenzofuran, with a Gibbs reaction energy of 36.6 kJ∙mol⁻¹ at 500 K. These findings indicate that, from a thermodynamic perspective, hydrogen release is feasible at temperatures below 500 K, which is an important feature for the potential application as a hydrogen storage system. Full article

This work aims to present tes-thermo, a Python library developed to solve thermodynamic equilibrium problems using the Gibbs energy minimization approach. The library is a variant of TeS v.3, a standalone executable developed for the same purpose. The tool formulates the chemical equilibrium problem of combined phases as a nonlinear programming problem, implemented using Pyomo (Python Optimization Modeling Objects) and solved with IPOPT (Interior Point OPTimizer). To validate the tool and demonstrate its robustness, the supercritical water gasification (SCWG) of methanol and ethanol was investigated. The Peng–Robinson equation of state was employed to account for non-idealities in the gas phase. Experimental and simulated data from the literature were used for validation, and, in both cases, the results were satisfactory, with root mean square errors consistently below 0.23. The SCWG processes studied revealed that hydrogen production is favored by increasing temperature and decreasing pressure. For both methanol and ethanol, increasing the carbonaceous substrate fraction in the feed promotes hydrogen formation; however, it also leads to reduced hydrogen relative yield due to the enhanced formation of methane and carbon monoxide under these conditions. Consequently, although hydrogen production increases, the hydrogen molar fraction in the dry gas stream tends to decrease with the higher substrate content. As expected, the SCWG of methanol produces more hydrogen and less carbon monoxide compared to ethanol under similar conditions. This behavior is consistent with the higher carbon content in ethanol, which favors reactions leading to carbon oxides. In summary, tes-thermo proves to be a robust and reliable tool for conducting research and studies on topics related to thermodynamic equilibrium. Full article

Geopolymers represent an innovative and environmentally sustainable alternative to traditional construction materials, offering significant potential for reducing anthropogenic CO₂ emissions. Among these, phosphoric acid-activated metakaolin-based systems have attracted increasing attention for their chemical and thermal resilience. In this study, we present a comprehensive structural and mechanical evaluation of metakaolin-based geopolymers synthesized across a wide range of Al/P molar ratios (0.8–4.0). Six formulations were systematically prepared and analyzed using X-ray powder diffraction (XRPD), small-angle X-ray scattering (SAXS), Fourier-transform infrared spectroscopy (FTIR), solid-state nuclear magnetic resonance (ssNMR), and complementary mechanical testing. The novelty of this work lies in the integrated mapping of composition–structure–property relationships across the broad Al/P spectrum under controlled synthesis, combined with the rare application of SAXS to reveal composition-dependent nanoscale domains (~18–50 nm). We identify a stoichiometric window at Al/P ≈ 1.5, where complete acid consumption leads to a structurally homogeneous AlVI–O–P network, yielding the highest compressive strength. In contrast, acid-rich systems exhibit divergent flexural and compressive behaviors, with enhanced flexural strength linked to hydrated silica domains arising from metakaolin dealumination, quantitatively tracked by ²⁹Si MAS NMR. XRPD further reveals the formation of uncommon Si–P crystalline phases (SiP₂O₇, Si₅P₆O₂₅) under low-temperature curing in acid-rich compositions. Together, these findings provide new insights into the nanoscale structuring, phase evolution, and stoichiometric control of silica–alumino–phosphate geopolymers, highlighting strategies for optimizing their performance in demanding thermal and chemical environments. Full article

Tight sandstone gas is currently one of the largest unconventional oil and gas resources being developed. In actual reservoir development, the complex pore structure affects the distribution of residual gas and water during the displacement process. However, there is still a lack of experimental research on the multi-scale visualization of pore structures in high-water-content tight gas reservoirs. Therefore, based on the porosity and permeability properties of reservoir cores and the micropore throat structural characteristics, this study designs and prepares three micro-physical models with different permeability ranges. Through micro-experiments and visualization techniques, the microscopic flow phenomena and gas–water distribution in the pore medium are observed. When the water–gas ratio exceeds 5, the produced water type is free water; when the water–gas ratio is between 2 and 5, the produced water type is weak capillary water; and when the water–gas ratio is less than 2, the produced water type is strong capillary water. The latter two types are collectively referred to as capillary water. In the Jin 30 well area, the main types of produced water are first free water, followed by capillary water, accounting for 58.5%. The experimental results of the micro-physical models with different permeability levels show that the production pattern of formation water varies due to differences in pore connectivity. In the low-permeability model, the high proportion of nano-pores and small pore throats requires a large pressure difference to mobilize capillary water, resulting in a higher proportion of residual water. Although the pores in the medium-permeability model are larger, the poor connectivity of nano-pores leads to local water phase retention. In the high-permeability model, micro-fractures and micropores are highly developed with good connectivity, allowing for rapid mobilization of multi-scale water phases under low pressure. The connectivity of nano-pores directly impacts the mobilization of formation water in micron-scale fractures, and poor pore connectivity significantly increases the difficulty of capillary water mobilization, thus changing the production mechanism of formation water at different scales. Full article