Search Results (2,183)

Hydroxyapatite (HAp) is a key bioceramic for biomedical applications, but conventional pressureless sintering (PS) requires high temperatures that can promote phase degradation. Here, we compare PS (1100 °C/180 min) and cold sintering process (CSP) (150 °C/450 MPa/30 min) for pure HAp and an HAp composite containing 4 wt.% niobium–phosphate bioglass (BG), using a 2 M H₃PO₄ transient liquid (10 wt.%). CSP increased relative density from 73.10% to 79.92% for HAp and from 68.43% to 83.54% for HAp/BG, representing up to a 22.1% gain compared with PS. One-way ANOVA confirmed a significant effect of processing route/composition on relative density (F(3,24) = 919.69, p < 0.05), and Tukey HSD indicated that all groups differed statistically. SEM revealed a markedly more consolidated and homogeneous microstructure for CSP, particularly for HAp/BG, consistent with enhanced dissolution–reprecipitation and pore filling. XRD showed that PS at 1100 °C led to partial HAp degradation with β-TCP formation, whereas CSP preserved the HAp phase with broader peaks, smaller crystallite size, and higher specific surface area. These results demonstrate CSP as an efficient low-temperature alternative for densifying HAp-based bioceramics, with BG addition further improving consolidation. Full article

In ultra-high-temperature and high-pressure gas well drilling, the use of high-density drilling fluid inevitably invades the reservoir, and perforation operations require penetrating this invasion zone to further connect the reservoir. This paper first conducts core drilling fluid invasion experiments, introducing two parameters—filter cake loss and core slice permeability—to derive the long-term invasion depth pattern of drilling fluid. Then, through three types of perforation target experiments (steel target, cement ring target, and sandstone target), the penetration performance of this type of perforating charge is evaluated. The results indicate that the total volume of drilling fluid invasion depends on the pore permeability characteristics of the core, with a fitted final invasion depth of 7.24 cm after 30 days of actual operation. The edge effect of the perforating gun causes significant differences in penetration depth and hole diameter at different phases, where the near-edge penetration depth and hole diameter are 1.86 times and 1.75 times larger than the far-edge, respectively. When the temperature resistance exceeds 200 °C/100 h, penetration depth and hole diameter decrease significantly with increasing temperature and time, and under 250 °C/170 h conditions, the firing rate markedly decreases. Using sandstone targets with identical strength and pore permeability conditions as a South China Sea ultra-high-temperature and high-pressure well block, the average penetration depth is 197 mm, far exceeding the thickness of the drilling fluid invasion zone. These experimental results provide theoretical support for perforation operations in a South China Sea ultra-high-temperature and high-pressure well block. Full article

This study examines the carbonation behavior and CO₂ storage potential of a Ca-rich alkali-activated binder produced entirely from industrial residues-ladle furnace slag (LFS), coal ash (CA), and cement kiln dust (CKD). The system was designed as a one-part alkali-activated material (AAM), with CKD acting as an internal activator, and subjected to ambient curing, water curing, and accelerated CO₂ curing at ambient pressure. Phase evolution, microstructural development, and pore-structure characteristics were investigated using X-ray diffraction, FTIR spectroscopy, DSC–TG analysis, scanning electron microscopy, and X-ray micro-computed tomography, together with measurements of density, water absorption, and compressive strength. Loss-on-ignition measurements combined with chemical analysis were further used to quantify CO₂ uptake and evaluate the degree of carbonation of the binder system. CO₂ curing fundamentally altered the reaction pathway of the binder, shifting it from hydration-dominated to carbonation-controlled phase evolution, leading to the decomposition of calcium-bearing hydrates and complete carbonation of non-hydraulic γ-belite with the formation of vaterite, aragonite, and calcite. These transformations induced pronounced microstructural densification, reflected in a near-doubling of compressive strength (>48 MPa), increased apparent density, reduced water absorption, and simplified pore-network topology. A preliminary carbon footprint assessment indicates that the production of 1 m³ of the developed LFS–CA–CKD concrete generates about 14.36 kg CO₂-eq, while the carbonation process enables significant CO₂ sequestration, resulting in a net negative carbon balance. The results demonstrate that controlled carbonation is an effective post-treatment strategy for waste-derived alkali-activated binders, enabling simultaneous performance enhancement and permanent CO₂ sequestration. Full article

Microbial fuel cells (MFCs) are an emerging technology that converts the chemical energy stored in organic substrates into electrical energy using microorganisms as catalysts. However, their performance is often limited by the anode design and architecture. To address this, conductive anodes with well-defined pore sizes were manufactured via 3D printing and evaluated for electrical energy generation and wastewater treatment in microbial fuel cells. The maximum power density, coulombic efficiency, and accumulated biomass observed were 14.94 mW/m², 4.87 ± 0.56%, and 0.186 ± 0.025 g, respectively, for the anode with a 2.3 mm pore size. The maximum chemical oxygen demand (COD) removal efficiency was 86.98 ± 1.89% for the anode with a pore size of 1.6 mm. However, this difference was minimal and not significant compared to the anode with a 2.3 mm pore size, which achieved 85.77 ± 2.31%. Additionally, the lowest internal resistance observed was 1246.44 Ω, corresponding to the MFC equipped with the anode with a pore size of 2.3 mm. Taken together, these results indicate that, when using 3D-printed anodes with controlled architectures, an intermediate pore size, neither too large nor too small, provides an adequate balance between electrochemical performance and efficient wastewater treatment in microbial fuel cells. Full article

Lithium–sulfur (Li-S) batteries hold great promise for next-generation energy storage, offering high theoretical energy density and cost-effectiveness. However, challenges like sulfur’s low conductivity, polysulfide dissolution, and significant volume changes limit their practical application. This study addresses these issues by investigating porosity-engineered carbon hosts, specifically potassium hydroxide (KOH)-activated Black Pearl carbons (BP2000, BP1300, and BP800). Varying KOH-to-carbon ratios allowed precise tailoring of micro- and mesoporous structures, optimizing sulfur loading, electrolyte infiltration, and ion transport. Composites were characterized by TGA, NLDFT, SEM, XRD, and FTIR and electrochemically (cycling, CV, EIS). The KOH-modified BP2000 1:1 cathode, exhibiting the highest mesopore volume increase, demonstrated superior electrochemical performance, including enhanced cycling stability, rate capability, and reduced charge-transfer resistance. These findings emphasize the importance of optimizing pore distribution in carbon hosts for high-performance Li-S batteries and provide valuable insights for advanced energy storage material design. Full article

Soil pore architecture and hydraulic functioning strongly regulate water flow and retention. However, despite the growing application of X-ray computed tomography (X-ray CT) in soil science, its application in characterizing the pore system and hydraulic functioning of native forest soils converted to sugarcane production systems in northeast Brazil is still poorly known. This study therefore quantified the soil structure, pore system, and hydraulic functioning of a native forest (NF) and an adjacent sugarcane field receiving vinasse and managed without intercropping (sole sugarcane (SG)) and with Brachiaria ruziziensis intercropping (SG + Bra intercrop) in northeastern Brazil, using conventional soil physical measurements and X-ray CT, in three soil layers (0–10, 10–20, and 20–40 cm). Soil physical and hydraulic properties, as well as soil water retention, were quantified. The native forest soil exhibited a uniformly sandy texture across all depths, whereas sugarcane systems ranged from loam to sandy textures in surface layers due to long-term management. Soil organic matter and total nitrogen in the 0–10 cm layer were approximately 75 and 65% higher, respectively, in sole Sole SG and SG + Bra intercrop than in NF. Soil bulk density increased with depth under sugarcane, reaching values about 10%–13% higher than NF in the 20–40 cm layer. Saturated hydraulic conductivity in the surface layer was higher in the NF, approximately five to nine times greater than in sole SG and SG + Bra intercrop, respectively. Conventional water retention analysis showed that sole SG and SG + Bra intercrop had greater total porosity (0.49–0.55 m³ m⁻³), microporosity (0.26–0.36 m³ m⁻³), field capacity (0.19–0.33 m³ m⁻³), and plant available water (0.09–0.15 m³ m⁻³) in the upper 20 cm compared with the NF (≤0.10 m³ m⁻³ available water). In contrast, X-ray CT revealed higher macroporosity (0.20–0.23 mm³ mm⁻³) and pore connectivity in the NF across all depths, with predominantly complex, inclined to near-horizontal pores and low anisotropy. Intercropping sugarcane with Brachiaria did not significantly alter (p > 0.05) bulk density, hydraulic conductivity, or CT-derived pore connectivity relative to sole sugarcane. The degree of anisotropy and fractal dimension derived from X-ray CT were significantly correlated (p < 0.05) with conventionally measured hydraulic properties. The X-ray computed tomography proved effective in linking pore-scale architecture to soil hydraulic functioning, providing insights beyond conventional measurements. The short-term inclusion of Brachiaria as a cover crop at 10 kg seed ha⁻¹ did not result in significant improvements in soil pore structure, indicating that longer-term adoption and/or higher planting densities may be required to induce measurable changes in pore system architecture and soil hydraulic functioning. Full article

In this study, the structural and electrochemical performance of Nb₂CT_x MXene-based composite electrodes modified with activated carbon (AC) derived from food waste was systematically investigated for supercapacitor applications. Three composites with Nb₂CT_x:AC mass ratios of 90:10 (MXAC1), 80:20 (MXAC2), and 70:30 (MXAC3) were prepared and comparatively evaluated. SEM/EDS, XRD, HR-TEM, XPS, and BET analyses revealed that, in the MXAC2 composite, activated carbon was homogeneously distributed between the MXene layers, effectively suppressing restacking and promoting the formation of a hierarchical micro/mesoporous structure. XPS results confirmed the preservation of the Nb–C framework and the enrichment of surface functional groups (–O, –OH, and –F). BET analysis demonstrated that MXAC2 possesses an optimized pore architecture that facilitates efficient ion diffusion. Electrochemical measurements revealed that the MXAC2 electrode exhibited the highest specific capacitance at all scan rates and current densities. At 5 mV·s⁻¹, MXAC2 achieved a specific capacitance of 651.84 F·g⁻¹ and maintained a substantial capacitance even at a high current density of 4 A·g⁻¹. EIS analysis confirmed the very low charge transfer resistance (0.023 Ω) and enhanced capacitive behavior for MXAC2. Additionally, MXAC2 has high cycle stability, demonstrating 82.15% capacitive retention and 92.45% coulombic efficiency after 10000 cycles. These results indicate that food waste-derived AC-optimized Nb₂CT_x MXene composite materials are a strong candidate for sustainable and high-performance supercapacitor electrodes. Full article

Linear alkylbenzene (LAB) is the main raw material used to make biodegradable detergents, and its production process is based on aromatic alkylation. HY zeolites that have undergone controlled dealumination and desilication have led industrial standards amongst solid acid catalysts because of their controllable acidity and hierarchical pore structure. Coke formation in such systems can assume a dual role, which is dependent on its condition. Though the over-deposition is known to cause deactivation by blocking the micropores, Bronsted acid-site masking, and diffusion collapse, the low-level deposition could also be done to increase the monoalkylate selectivity by the pore mouth catalysis, steric modulation, and selective suppression of secondary alkylation pathways. The critical review is done on the structural-kinetic interaction that determines the coke evolution in HY-based catalysts. In order to moderate the acid-site density and enhance hydrothermal stability, dealumination (Si/Al optimization of about 2.5 to 30–100) occurs, but to reduce deep-pore coke formation, desilication (interconnected mesopores) is created. The bimodal porosity and regulated acidity are found to be synergistic, as hierarchical HY zeolites produced through successive cycles of steam and alkaline treatments not only show LAB selectivity in excess of 90% but also exhibit much longer catalyst lifetimes. Quantitative research on the beneficial coke regime revealed that it was composed of about 36 wt% hydrogen-rich species, which were localized at the pore mouths, hence enhancing monoalkylation selectivity by 15–40%. Beyond a critical transition window (e.g., 8–12 wt.%), coke formation to condensed polyaromatic and graphitic products leads to fast deactivated coke formation, which is due to percolation limits and transport-controlled kinetics. More advanced techniques of characterization of the coke, e.g., temperature-programmed oxidation (TPO), ²⁷Al MAAS NMR, and UV-Raman spectroscopy, indicate how the coke is changed to highly structured graphitic deposits of high oxidation activation energy. Activity recovery of 85–98% is obtained in regeneration processes, including controlled oxidative calcination, microwave-based and plasma-based processes, and thermal management protocols, and it would be determined by the chemistry of the coke, its spatial distribution, and the regeneration protocols. This paper has developed a mechanistic coke control system by cross-tuning the acidity and development of an effective pore network, which led to a sustainable aromatic alkylation reaction with minimal activity loss, high selectivity, and long life. Full article

TC4/Al₃Ti metal–intermetallic laminated (MIL) composites were fabricated by the vacuum hot-pressing process at 650 °C. The microstructure characteristics, i.e., grain boundary distribution, crystallographic orientation and Kernel Average Misorientation (KAM) map, were analyzed using EBSD. Meanwhile, the distribution of local strain and the fracture behavior of TC4/Al₃Ti MIL composites during tensile process were determined by Digital Image Correlation (DIC) and in situ tensile experiments, respectively. Results show that the TC4/Al₃Ti interfaces are well bonded and exhibit a distinct wavy morphology. The obvious Kirkendall pores and centerline are observed within the central region of the Al₃Ti layer. The texture components of (10-10) <0001> and (11-20) <10-10> are predominant in the TC4 layers; (100) <001> and (110) <001> are observed in the Al₃Ti layer. Additionally, the average geometrically necessary dislocation (GNDs) density is 2.53 × 10¹⁴ m⁻² in the TC4 layer, whereas it is 1.74 × 10¹⁴ m⁻² in the Al₃Ti layer. In the tensile test, the fracture resistance of TC4/Al₃Ti MIL composites is significantly improved by the plastic deformation of the TC4 layers and the suppression of crack-tip instability. It is found that the extrinsic toughening mechanisms contain crack deflection, crack blunting, crack bridging, multiple cracking modes, and the plastic deformation of ductile TC4 layers in TC4/Al₃Ti MIL composites. The real-time observation technique may provide more complete insights into the relationship between fracture behavior and enhanced toughness. Full article

This study presents the development of a three-dimensional (3D) filament assembly model for predicting the air permeability of woven fabrics composed of spun yarns. To address the limitations of conventional single-line yarn models, the proposed framework incorporates fiber-level geometric representations using non-uniform rational B-splines (NURBS) and simulates multiple weave patterns—including plain, basket, twill, and rib—under various set density configurations. Each yarn was modeled with accurate filament distribution and cross-sectional layering, enabling the construction of realistic unit-cell-based CAD geometries. Computational fluid dynamics (CFD) simulations were performed using the k-ε turbulence model in SolidWorks Flow Simulation and validated against experimental measurements conducted under ISO 9237:1995 conditions. The filament assembly model achieved high predictive accuracy, exhibiting a lower of percentage prediction errors than the single-line yarn path model, thereby more effectively capturing airflow behavior through inter-yarn and intra-yarn pores. These findings highlight the capability of integrated CAD/CFD methodologies for virtual prototyping of breathable textiles and provide a robust foundation for high-precision performance prediction in functional and technical fabric design. Full article

Poly(vinyl alcohol) (PVA)/montmorillonite (MMT)/Ti₃C₂T_x (MXene) nanocomposite membranes (PVA/MMT/MXene) were developed and evaluated in terms of their mechanical properties, mesoporosity, and adsorption performance toward Pb²⁺ ions and methylene blue (MB). The incorporation of MMT and MXene resulted in a strong synergistic reinforcement, increasing the ultimate tensile strength from 10 to 20 MPa, the Young’s modulus from 14.7 to 29.5 MPa, and reducing the swelling ratio from 2.0 to 1.1 g·g⁻¹. BJH porosimetry revealed a refined and interconnected mesoporous structure, with the cumulative pore volume increasing from 0.134 to 0.448 cm³·g⁻¹. In adsorption experiments (mono-solute systems, 25 °C), the ternary membrane achieved high uptake capacities of 55 mg·g⁻¹ for Pb²⁺ and 80 mg·g⁻¹ for MB, outperforming binary PVA/MMT and neat PVA. Statistical–physics modeling provided microscopic descriptors consistent with the experimental isotherms: Pb²⁺ adsorption follows a monolayer regime (n ≈ 1), whereas MB exhibits multilayer behavior (n > 1) with a higher site density (Nm ≈ 1.6 mmol·g⁻¹). These results demonstrate that the hybrid 2D–2D architecture of MMT and MXene significantly enhances the structural robustness, pore accessibility, and adsorption efficiency of PVA-based membranes, highlighting their potential for efficient removal of metal ions and dyes from aqueous media. Full article

The separation of xenon (Xe) and krypton (Kr) is very important for industrial applications and environmental protection. However, the lack of permanent dipoles, low polarizabilities arising from their spherical nature, and similar kinetic diameters make their efficient separation by porous adsorbents exceptionally challenging. This study explored the effects of pore geometry and surface polarity of a series of aluminum-based metal–organic frameworks (CAU-10-H, MIL-160, KMF-1, CAU-23) on Xe/Kr separation performance using a heteroatom engineering strategy. These MOFs are composed of AlO₆ clusters and bent dicarboxylic acid linkers, enabling us to systematically investigate the effects of pore size and heteroatom types on Xe/Kr separation performance. Among them, MIL-160 has a polar linker based on furan, showing the best balance performance. At 298 K and 1.0 bar, the uptake of Xe is 4.12 mmol g⁻¹ and the IAST selectivity is 7.63 for a Xe/Kr (20/80) mixture. The practical performance was verified by dynamic breakthrough experiments, which yielded a long Xe breakthrough time of 42.9 min g⁻¹. Grand Canonical Monte Carlo (GCMC) simulations and first-principles density functional theory (DFT) calculations revealed that the enhanced performance originates from cooperative confinement and polarization effects, with the furanyl oxygen atoms providing optimal Xe-binding sites. This work clarifies the structure–property relationships governing Xe/Kr separation in aluminum-based MOFs (Al-MOFs), highlighting the potential of heteroatom engineering for designing efficient noble gas adsorbents. Full article

The use of aeolian sand as a fine aggregate in concrete production provides a sustainable pathway to valorize abundant aeolian resources while alleviating the global shortage of natural construction aggregates. However, the high ultrafine particle content of aeolian sand results in the formation of highly porous interfacial transition zones (ITZ) between sand particles and cement paste, which is the primary cause of the inherent brittleness and inferior mechanical performance of aeolian sand concrete. To overcome this critical limitation, an alkali-activated surface layer (ASL) was constructed on aeolian sand via 4 mol/L KOH activation. This process induced the surface micro-dissolution of minerals to create high-density active ion sites (specifically Ca²⁺, K⁺, Na⁺, and Fe³⁺). These sites facilitated the precise anchoring of carbon nanotubes (CNTs) through the chemical coordination of single-stranded deoxyribonucleic acid (ssDNA). The influence of the ASL and the ssDNA/CNTs nanocomposite on the ITZ was elucidated through macro-mechanical testing and multi-scale microstructural characterization. Experimental results demonstrated that compressive strength, flexural strength, and compressive energy dissipation increased by 48%, 67%, and 42%, respectively. Microstructurally, the modification promoted a pore refinement mechanism, reducing the proportion of harmful (pores > 0.1 μm) from 51% to 20% and narrowing the ITZ width from 20–40 μm to 10–15 μm (a 67% reduction). The observed performance enhancement is attributed to the synergistic effect of the ASL and ssDNA/CNTs, which transforms the inherently weak ITZ into a chemically reinforced interfacial phase via molecular-scale coordination bonding and optimized stacking of cement hydration products. Full article

Aiming at the contradiction between forming quality and efficiency in the existing research on thick-layer laser powder bed fusion (LPBF) manufacturing of Ti6Al4V, this study focused on the influence of near-circular keyhole defects caused by scanning speed on the short-term mechanical properties of Ti6Al4V alloy manufactured by high-efficiency LPBF with a 100 μm layer thickness, the build rate of which reached 14 mm³/s. When the scanning speed decreased to 800 mm/s, the relative density decreased from 99.87% to 99.27%, and the maximum pore size increased from 19.6 μm to 87.2 μm. Under the conditions of high relative density (above 99.8%) and maximum pore size less than 20 μm, the annealed Ti6Al4V samples could achieve a tensile strength of 1009.7 MPa, a yield strength of 914.0 MPa, an elongation of 15.2%, and an impact toughness of 41.71 J/cm². With the increase in porosity and a maximum pore size exceeding 50 μm, the tensile strength became more unstable and exhibited a declining trend, while the impact toughness decreased by more than 5%. This is mainly attributed to the stress concentration around large-sized pores, leading to the easy generation of long and deep cracks at the edges and reducing the material’s ability to resist crack initiation and propagation. Full article

A nano-TiO₂-modified silicone-based reflective thermal insulation coating is successfully synthesized. The influence of the nano-TiO₂ content on the microstructure, adhesion strength as well as near-infrared reflectivity (NIR) of the coatings before and after heat treatment is investigated. The results demonstrate that the coating is an organic/inorganic composite coating composed of muscovite, rutile-phase titanium dioxide and an organosilicon binder before heat treatment. The addition of an appropriate amount of nano-TiO₂ helps fill the pores in the coating, resulting in a dense coating and improved adhesion. Meanwhile, due to the reduced average size of the pigment, the reflectance of the coating is maintained or enhanced. When the addition amount is 5.0 wt.%, the coating achieves the highest bonding strength of Grade 1 with a reflectivity of 0.830. After heat treatment at 1000 °C for an hour, the coating transforms into an inorganic coating composed of partially melted muscovite and rutile-phase TiO₂. The nano-TiO₂ promotes the formation of a molten phase, which further increases the coating density and makes the surface smoother. Consequently, the coating’s bonding strength and reflectance are further improved, reaching Grade 0 and 0.945 respectively. Full article