Search Results (423)

Bamboo-derived biochar (BC) is promising for high-salinity wastewater treatment through photothermal evaporation. This study systematically evaluated BCs synthesized at 400–800 °C with residence times of 40 or 70 min. Pyrolysis temperature proved dominant, with 600 °C representing a critical threshold. Below this temperature, BCs maintained high carbon content and polar functional groups but exhibited limited porosity. Above it, structural reorganization enhanced pore development and aromaticity while reducing polar surface groups. Residence time primarily influenced volatile retention, and prolonged pyrolysis led to pore collapse. The optimal BC—produced at 800 °C for 40 min—combined hierarchical porosity with balanced surface chemistry, achieving an evaporation rate of 1.21 kg/m²·h and a photothermal efficiency of 70.45% under high-salinity conditions. Mechanistic analysis indicates that short, high-temperature pyrolysis preserves structural integrity and interfacial activity with minimal energy input. These results establish a thermal processing approach that reconciles carbon stability with surface functionality, offering practical guidance for scaling efficient and sustainable biochar-based wastewater treatment systems. Full article

Metal–organic frameworks (MOFs) typically exist in the form of powders or dispersed crystals, which limits their direct application in practical engineering scenarios that require monolithic structures and processability. To address this issue, the present study successfully anchored MOF (zeolitic imidazolate framework-8, ZIF-8) nanocrystals within a porous silicon carbide (p-SiC) substrate via a facile in situ growth strategy, achieving both stable macroscopic loading and intimate microscopic interfacial bonding. The resulting ZIF-8/p-SiC composite exhibits a hierarchical porous structure, with a specific surface area approximately 183 times higher than that of the raw p-SiC, alongside a substantially enhanced CO₂ adsorption capacity. By utilizing a low-cost p-SiC support and mild ZIF-8 synthesis conditions, this work demonstrates excellent reproducibility and scalability, providing a facile and effective pathway for fabricating MOF/porous media composite systems that possess both superior mechanical properties and tailored pore structures. Additionally, the developed MOF/p-SiC composites can serve as controllable rock-analog porous media, offering new perspectives for investigating MOF-rock interfacial interactions and CO₂ geological sequestration mechanisms, thereby establishing an organic link between fundamental materials science and geological engineering applications. Full article

In this study, a novel Bi₂O₃/BiOBr_0.9I_0.1 (BO0.9−BBI0.1) composite photocatalyst was successfully synthesized via a single-pot solvothermal method for the efficient degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) under visible light. The structure, morphology, and optical properties of the photocatalyst were characterized through X-ray diffraction (XRD), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectra (DRS), Steady-state photoluminescence (PL), and Electrochemical Impedance Spectroscopy (EIS). The composite exhibits a 3D hierarchical morphology with increased specific surface area and optimized pore structure, enhancing pollutant adsorption and providing more active sites. Under visible light irradiation, BO0.9−BBI0.1 achieved a 92.4% removal rate of 2,4-D within 2 h, with a reaction rate constant 5.3 and 4.6 times higher than that of pure BiOBr and BiOI, respectively. Mechanism studies confirm that photogenerated holes (h⁺) and superoxide radicals (·O₂⁻) are the primary active species, and the Z-scheme charge transfer pathway significantly promotes the separation of electron-hole pairs while maintaining strong redox capacity. The catalyst also demonstrated good stability over multiple cycles. This work provides a feasible dual-modification strategy for designing efficient bismuth-based photocatalysts for pesticide wastewater treatment. Full article

Biaxially stretched polytetrafluoroethylene (PTFE) membranes are promising media for high-efficiency air filtration because of their stable node–fiber microstructure and environmental durability. To clarify how resin properties and microstructure govern filtration behavior, ten PTFE resins with different average molecular weights (Mn) and particle size characteristics were processed into membranes under essentially identical biaxial stretching and sintering conditions. Resin particle size, fiber diameter and pore size distributions were quantified, and coefficients of variation (CVs), together with Spearman rank correlations, were used to analyze material–structure–performance links. Filtration efficiency, pressure drop and quality factor (QF) were measured according to ISO 29463-3 using 0.1–0.3 μm aerosols. Higher Mn combined with lower particle-size dispersion favored finer fibers and narrower pores, yielding efficiencies close to 100%, but increased pressure drop and slightly reduced QF, indicating a trade-off between efficiency and flow resistance. The sample with the lowest Mn in its group and a high machine-direction draw ratio (12×), showed pronounced fibril breakage, node coalescence, broadened pore-size distribution and degraded QF, illustrating the sensitivity of structure and performance to resin-process mismatch. Overall, the study establishes a hierarchical material–fiber–pore–performance relationship that can guide resin selection, structural tuning and process optimization of biaxially stretched PTFE membranes. Full article

The selective hydrocracking of polycyclic aromatic hydrocarbons to BTX requires precise control over catalyst porosity and metal–acid balance. Hierarchical porosity, integrating microporous and mesoporous networks, is pivotal for enhancing mass transport and regulating reaction pathways. USY zeolites were engineered to create distinct hierarchical architectures via HCl, urea, and NaOH–surfactant treatments. HCl treatment constructed a gradient pore acidity system, urea treatment enhanced acidity while preserving microporosity, and NaOH–surfactant fabricated ordered mesopores with reduced acidity. The catalyst with the HCl-engineered gradient pore (NiMo/YH-1) achieved a 91% BTX yield at 425 °C in naphthalene hydrocracking, outperforming others. This performance is attributed to its gradient structure that enforces an optimal “hydrogenation-then-cracking” pathway, highlighting the critical role of tailored hierarchical porosity. Full article

Atmospheric water harvesting (AWH) offers a decentralized and renewable solution to global freshwater scarcity. Bio-derived and hybrid aerogels, characterized by ultra-high porosity and hierarchical pore structures, show significant potential for high water uptake and energy-efficient, low-temperature regeneration. This PRISMA-guided systematic review synthesizes evidence on silica, carbon, MOF-integrated, and bio-polymer aerogels, emphasizing green synthesis and circular design. Our analysis shows that reported water uptake reaches up to 0.32 g·g⁻¹ at 25% relative humidity (RH) and 3.5 g·g⁻¹ at 90% RH under static laboratory conditions. Testing protocols vary significantly across studies, and dynamic testing typically reduces these values by 20–30%. Ambient-pressure drying and solar-photothermal integration enhance sustainability, but performance remains highly dependent on device architecture and thermal management. Techno-economic models estimate water costs from USD 0.05 to 0.40 per liter based on heterogeneous assumptions and system boundaries. However, long-term durability and real-world environmental stressor data are severely underreported. Bridging these gaps is essential to move from lab-scale promise to scalable, commercially viable deployment. We propose a strategic roadmap toward 2035, highlighting the need for improved material stability, standardized testing protocols, and comprehensive life cycle assessments to ensure the global viability of green aerogel technologies. Full article

The increasing generation of biomass-derived waste has accelerated the development of sustainable strategies for its valorization into functional materials. Activated carbon (AC), due to its high surface area, tunable porosity, and chemical versatility, has emerged as a key product for applications in adsorption, catalysis, energy storage, and biosensing, among others. Recent studies have highlighted the importance of symmetry and asymmetry in determining the structural and functional performance of AC. Symmetric architectures, typically generated via templating methods, yield ordered pore networks, whereas asymmetric structures, commonly produced through direct chemical activation or heteroatom doping, exhibit hierarchical porosity and heterogeneous surface functionalities. This work critically examines the fundamentals of symmetry and asymmetry in AC materials, as well as their influence on design and use. It discusses synthesis strategies, characterization techniques, and recent approaches that enable the rational engineering of carbon structures. Application-specific case studies are presented, along with current challenges related to feedstock variability, scalability, and regulatory integration. By highlighting the interplay between structural order and functional diversity, this work provides a conceptual framework for guiding future research in the development on symmetrical and asymmetrical carbonaceous materials for sustainable waste valorization. Full article

Alginate aerogels are attractive candidates for biomedical scaffolds because they combine high mesoporosity with biocompatibility and can be processed into open, interconnected macroporous networks suitable for tissue engineering. Here, we systematically investigate how CO₂-induced foaming parameters govern the hierarchical pore structure of alginate aerogels produced by subsequent supercritical CO₂ drying. Sodium alginate–CaCO₃ suspensions are foamed in a CO₂ atmosphere at 50 or 100 bar, depressurization rates of 50 or 0.05 bar·s⁻¹, temperatures of 5 or 25 °C, and, optionally, under pulsed pressure or with Pluronic F-68 as a surfactant. The resulting gels are dried using supercritical CO₂ and characterized by micro-computed tomography and N₂ sorption. High pressure combined with slow depressurization (100 bar, 0.05 bar·s⁻¹) yields a homogeneous macroporous network with pores predominantly in the 200–500 µm range and a mesoporous texture with 15–35 nm pores, whereas fast depressurization promotes bubble coalescence and the appearance of large (>2100 µm) macropores and a broader mesopore distribution. Lowering the temperature, applying pulsed pressure, and adding surfactant enable further tuning of macropore size and connectivity with a limited impact on mesoporosity. Interpretation in terms of Peclet and Deborah numbers links processing conditions to non-equilibrium mass transfer and gel viscoelasticity, providing a physically grounded map for designing hierarchically porous alginate aerogel scaffolds for biomedical applications. Full article

Member 2 of the Xujiahe Formation in the Anyue area of the Sichuan Basin exhibits significant resource potential for tight sandstone gas. However, its characteristic of “extensive gas presence with localized enrichment” leads to substantial variations in single-well productivity, challenges in target zone optimization, and unclear enrichment mechanisms, which hinder efficient exploration and development. This study proposes a hierarchical classification scheme of “two-level, six-type” source–reservoir structures based on the developmental characteristics of fault–fracture systems and vertical source–reservoir configurations. The gas-bearing heterogeneity is quantitatively characterized using parameters such as effective gas layer thickness, charge intensity, and effective gas layer probability, thereby revealing the differential enrichment mechanisms of tight sandstone gas controlled by source–reservoir structures. Our key findings include the following: (1) Member 2 of the Xujiahe Formation develops six subtypes of source–reservoir structures grouped into two levels, with gas-bearing capacities ranked as follows: source–reservoir separation type > source–reservoir adjacent type I > source–reservoir adjacent type II. Among these, the source–reservoir separation type (Level I) and fault–fracture conduit type (Level II) represent the most favorable structures for gas enrichment. (2) Tight sandstone gas enrichment is governed by a tripartite synergistic mechanism: hydrocarbon supply from source rocks, vertical cross-layer migration dominated by fault–fracture systems, and reservoir storage capacity determined by fracture density and reservoir thickness. (3) Three enrichment models are established: (i) a strong enrichment model characterized by “multi-layer source rocks beneath the reservoir, cross-layer migration, and thick fractured reservoirs”; (ii) a moderate enrichment model defined by “single-layer source rocks, localized migration, and medium-thick fractured reservoirs”; and (iii) a weak enrichment model featuring “single-layer hydrocarbon supply, pore-throat migration, and thin tight reservoirs.” This research provides a theoretical basis for optimizing exploration targets in Member 2 of the Xujiahe Formation in the Anyue area and offers insights applicable to analogous continental tight gas reservoirs. Full article

The mechanical and durability performance of cementitious materials is fundamentally governed by the symmetry, anisotropy, and hierarchical organization of their microstructures. Conventional experimental characterization—based on imaging, spectroscopy, and physical testing—often struggles to capture these multiscale spatial patterns and their nonlinear correlations with macroscopic performance. Recent advances in machine learning (ML) provide unprecedented opportunities to interpret structural symmetry and anisotropy through data-driven analytics, computer vision, and physics-informed models. Furthermore, we summarize cases where symmetry-informed descriptors improve performance prediction accuracy in fiber- and nano-modified composites, demonstrating that ML-based symmetry analysis can substantially complement the limitations of conventional experimental-based characterization. We confirm that image-based models such as CNN and U-Net quantify the directionality and connectivity of pores and cracks, and that physically informative neural networks (PINNs) and heterogeneous data-based models enhance physical consistency and computational efficiency compared to conventional FEM and CFD. Finally, we present the conceptual and methodological foundation for developing AI-based microstructural symmetry analysis, aiming to go beyond simple prediction and establish a conceptual foundation for AI-driven cement design based on microstructure–performance causality. Full article

This study investigated the hierarchical structuring of *BEA zeolite using 0.2 M sodium hydroxide followed by 0.5 M hydrochloric acid (T-NaOH-HCl). Tungsten trioxide (WO₃) was then impregnated at different loadings (5, 10, 15, and 20 wt.%) onto the hierarchized materials (BEA-T). The modified zeolites were subsequently used as catalysts for the dehydration of ethanol (230 and 250 °C) and 1-propanol (230 °C). The hierarchization treatment increased the Si/Al ratio (from 13 to 39), decreased relative crystallinity by 15%, and reduced the average crystal-domain size (from 18 to 10 nm). After the NaOH–HCl treatment (BEA-T), the mesopore area increased by 7%, the mesopore volume by 19%, and the total pore volume by 12%. Conversely, the BET specific surface area and micropore volume decreased, indicating effective hierarchization of the *BEA zeolite. XRD, FT-IR and Raman confirmed the presence of monoclinic WO₃ on the BEA-T surface. MAS NMR analyses of ²⁷Al and ²⁹Si indicated that the T-NaOH-HCl treatment slightly increased the population of tetrahedral Al environments. The high conversion and selectivity from the dehydration of ethanol and 1-propanol can be attributed to a moderate reduction in the acidity of *BEA zeolite and tunned mesoporosity. Based on TON, catalysts with 10% and 20% WO₃ stood out in dehydration tests. Full article

The development of oil–water separation materials that combine high separation efficiency, robust mechanical properties, and environmental degradability remains a significant challenge. This study presents a novel degradable and superhydrophobic porous material fabricated via a multi-step process. A porous foam was first synthesized from degradable poly(ε-caprolactone-co-2-ethylhexyl acrylate) using a high internal phase emulsion templating technique. The foam was subsequently modified through in situ silica (SiO₂) deposition via a sol–gel process, followed by grafting with hydrophobic hexadecyltrimethoxysilane (HDTMS) to produce the final oil–water separation porous materials. Various characterization results showed that the optimized material featured a hierarchical pore structure in micro scales and the porosity of the foam remained ~90% even after the 2-step modification. Mechanical tests indicate that the modified material exhibited significantly enhanced compressive strength and the water contact angle measurements revealed a superhydrophobic surface with a value of approximately 156°. The prepared material demonstrated excellent oil/water separation performance with notable absorption capacities ranging from 4.11 to 4.90 g/g for oils with different viscosity. Additionally, the porous material exhibited exceptional cyclic stability, maintaining over 90% absorption capacity after 10 absorption-desorption cycles. Moreover, the prepared material achieved a mass loss of approximately 30% within the first 3 days under alkaline hydrolysis conditions (pH 12, 25 °C), which further escalated to ~70% degradation within four weeks. The current work establishes a feasible strategy for developing sustainable, high-performance oil–water separation materials through rational structural design and surface engineering. Full article

Titanium (Ti) and its alloys are widely used in orthopedic applications, including total hip and knee replacements, bone plates, and dental implants, because of their superior biocompatibility, bioactivity, corrosion resistance, and mechanical robustness. These alloys effectively overcome several limitations of conventional metallic implants, such as 316L stainless steel and Co-Cr alloys, particularly with respect to corrosion, fatigue performance, and biological response. However, dense Ti alloys possess a relatively high elastic modulus, which can cause stress shielding in load-bearing applications. This challenge has motivated significant research toward engineered porous Ti structures that exhibit a reduced and bone-matched modulus while preserving adequate mechanical integrity. This review provides a comprehensive examination of powder metallurgy and additive manufacturing approaches used to fabricate porous Ti and Ti-alloy scaffolds, including additive manufacturing and different powder metallurgy techniques. Processing routes are compared in terms of achievable porosity, pore size distribution, microstructural evolution, mechanical properties, and biological outcomes, with emphasis on the relationship between processing parameters, pore architecture, and functional performance. The reported findings indicate that optimized powder-metallurgy techniques can generate interconnected pores in the 100–500 μm range suitable for osseointegration while maintaining compressive strengths of 50–300 MPa, whereas additive manufacturing enables the precise control of hierarchical architectures but requires careful post-processing to remove adhered powder, stabilize microstructures, and ensure corrosion and wear resistance. In addition, this review integrates fundamental aspects of bone biology and bone implant interaction to contextualize the functional requirements of porous Ti scaffolds. Full article

Listeria monocytogenes (LM) poses a serious threat to food safety and public health. Current detection methods suffer from drawbacks such as expensive equipment, complex procedures, and time-consuming processes, highlighting the urgent need for a simple, rapid, accurate, and cost-effective detection approach. The bacterial metabolite 3-hydroxy-2-butanone (3H2B), due to its high abundance, can serve as a reliable biomarker for detection. Herein, ordered mesoporous silica nanoparticles (MSNs) were synthesized via a one-pot method and subsequently functionalized with APTES. The NH₂-MSNs-2 exhibits extremely high sensitivity (768 Hz@50 ppm) and selectivity towards 3H2B due to its high specific surface area, abundant mesoporous structure, and weak chemical adsorption between amino groups and the 3H2B. The quartz crystal microbalance (QCM) sensor developed based on this material demonstrated outstanding performance in testing the contamination levels of LM in food. This study provides a solid foundation for further exploring the fundamental mechanisms of QCM sensors in the real-time, non-invasive detection of LM, while also demonstrating significant application potential in the field of food safety assurance. Full article

Activated carbons derived from coconut coir dust were synthesized via a two-step process combining carbonization and steam activation for application as electrode materials in supercapacitors. The influence of carbonization temperature (500–700 °C) on the morphological, structural, textural, and electrochemical properties of the resulting activated carbons was systematically investigated. Increasing the carbonization temperature led to a progressive collapse of the cellular structure and formation of a more compact and thermally stable carbon matrix, while the overall morphology remained largely unchanged after steam activation. The steam-activated carbon prepared from the carbonized sample at 700 °C (SA-CCD-7) exhibited the highest specific surface area (889 m² g⁻¹) and a well-developed hierarchical micro–mesoporous structure. Structural analyses confirmed the amorphous nature and an increase in structural disorder after activation, consistent with the enhanced pore development. Electrochemical measurements in 6 M KOH using a three-electrode system revealed that the SA-CCD-7 displayed a typical electric double-layer capacitor (EDLC) behavior, delivering the highest specific capacitance of 86 F g⁻¹ at 1 A g⁻¹ and retaining 81% of its initial capacitance at 20 A g⁻¹, demonstrating excellent rate capability. The symmetric coin-cell supercapacitor device assembled with SA-CCD-7 as the electrodes achieved an energy density of 0.9–1.2 Wh kg⁻¹ and a power density of 50–2500 W kg⁻¹, along with remarkable cycling stability over 10,000 cycles with negligible capacitance loss. These findings highlight steam activation of coconut coir dust as a simple, scalable, and eco-friendly approach for producing biomass-derived carbon electrodes for sustainable energy storage applications. Full article