Search Results (201)

Guided bone regeneration (GBR) heavily relies on barrier membranes, with collagen being the clinical standard material. Human amniotic epithelial cells (hAECs) represent a promising, non-controversial stem cell source with substantial osteogenic and immunomodulatory potential. This study aimed to comparatively evaluate the structural characteristics of three commercial collagen membranes (Biocollagen^®, Derma^®, and VantyColl^®) and their influence on the biological behavior, viability, and osteogenic differentiation of hAECs and hFOB 1.19 human fetal osteoblasts. The microarchitecture was assessed via scanning electron microscopy (SEM). Biological response was evaluated over 14 days, using MTT assays, calcium and phosphorus quantification, alkaline phosphatase (ALP) activity, and quantitative real-time PCR (qRT-PCR) for osteogenic markers (Runx2, Osterix, ALP, and OPN). SEM revealed a dense lamellar structure for Biocollagen^®, a fibrillar and oriented architecture for Derma^®, and a highly porous network for VantyColl^®. Both cell types adhered to and proliferated on all membranes. Derma^® provided the best long-term proliferative support for both lineages. Conversely, VantyColl^® induced robust early osteoblastic differentiation, marked by exceptional upregulation of Osterix (24.93-fold) and Runx2 (2.64-fold), though it exhibited diminished long-term hAEC viability. Ultimately, collagen membrane microarchitecture dictates cell fate; dense fibrillar networks (Derma^®) favor sustained growth and late matrix maturation (OPN), whereas high-porosity scaffolds (VantyColl^®) amplify early osteoinductive cascades. Full article

In this study, porous polyvinylidene fluoride (PVDF) hollow fiber (HF) membranes for membrane distillation applications were successfully prepared using TamiSolve^® NxG, an innovative lower-hazard solvent, through the non-solvent induced phase inversion technique. The influence of the bore fluid composition and bore fluid flow rate on membrane morphology and performance was systematically investigated while maintaining a fixed polymer dope formulation. The prepared hollow fibers were thoroughly characterized in terms of morphology, membrane thickness, porosity, contact angle, mechanical resistance, pore size, and pure water permeability. In addition, their performance was investigated through Direct Contact Membrane Distillation (DCMD) tests in order to evaluate their applicability in desalination processes. The developed PVDF HF membranes exhibited pore sizes comparable to those of commercial polypropylene (PP) membranes and achieved high permeate flux together with excellent salt rejection, demonstrating their promising potential for sustainable membrane distillation and desalination applications. Full article

The fading of painted relics is a widespread deterioration phenomenon in ancient painted cultural relics, yet its underlying mechanism has long been attributed solely to pigment oxidation. Directed at colored drawings with complex surface microstructures, such as pottery paintings, wall murals and architectural paintings, here we challenge this view by demonstrating that light scattering induced by sub-micron pores within the paint layer plays a dominant role, especially Mie scattering when pore sizes approach visible light wavelengths (400–700 nm). In order to minimize the damage to the genuine painted relics, a large number of simulated experiments were conducted first. Using porous polyacrylamide (PAM) membranes and nylon 6 filter membranes as model systems, we show that pore-induced scattering reduces the optical path length for light absorption, leading to a significant decrease in color saturation and brightness. By filling the pores with non-volatile colorless ionic liquids ([BMIM]PF₆) (n = 1.41) or glycerol (n = 1.47)—both possessing refractive indices close to those of the pigments—the scattering is effectively suppressed, and the original color is restored. The filling treatment reduces the color difference (ΔE*ab) by 30%–50% and the surface reflectivity by 20%–40%. Mercury intrusion porosimetry and fluorescence spectroscopy confirm that pore elimination and optical path lengthening are responsible for the color recovery. The proposed mechanism and restoration strategy were successfully validated on authentic painted brick fragments from the Western Qing Tombs (Hebei, China), where severely faded green and red patterns reappeared after ionic liquid treatment. This study provides a new interface-regulation paradigm for the conservation of painted cultural heritage, shifting the focus from irreversible chemical remediation to reversible physical restoration and offers a generalizable platform for controlling light scattering in porous optical materials. Full article

Water scarcity in semi-arid regions threatens seed germination and early crop establishment, driving the development of biodegradable Nature-based Solutions to replace synthetic plastic mulches. Porous cellulose membranes were fabricated from rice husk (RH), banana pseudostem (BP), and sugarcane bagasse (SB) by thermo-chemical extraction and high-shear homogenization (n = 5 replicates per membrane type). Membranes were characterized by ATR-FTIR and scanning electron microscopy, confirming removal of non-cellulosic components and biogenic silica preservation in RH, and revealing biomass-dependent porous architectures linked to mechanical and transport behavior. RH produced the most compact fibrillar matrix (compressive strength: 8.16 ± 0.24 MPa; WVT: 170 ± 60 g m⁻² day⁻¹), BP an open interconnected network with superior deformability (9.83 ± 0.25% elongation) and moisture transport (WVT: 400 ± 100 g m⁻² day⁻¹), and SB the highest moisture-retention capacity (215.7 ± 15.8%). Germination assays with Brassica oleracea var. botrytis under water stress showed SB achieved the highest germination rate (90.5 ± 0.99%), confirming that sustained moisture availability governs germination more decisively than transport rate alone. Soil burial tests confirmed biodegradable behavior across all membranes (R² ≥ 0.995; k = 0.043–0.046 day⁻¹). These findings establish a hydrogen-bond-mediated structure–property–function framework for designing biomass-specific cellulose membranes as biodegradable solutions for water-limited agricultural systems. Full article

This study reports the fabrication of porous anodic aluminum oxide (AAO) on a 6xxx series aluminum alloy by a two-step anodization route and systematically examines how anodization parameters govern the resulting morphology and wetting behavior. AAO samples were prepared in two groups: in Group 1, the anodization voltage was varied between 20 and 60 V at a fixed time of 60 min; in Group 2, the anodization time was varied between 30 and 120 min at a fixed voltage of 30 V. All anodizations were carried out in 0.3 M oxalic acid at room temperature. The AAO structures were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and contact angle measurements. The pore diameters and interpore distances were found to be 13.3–40.6 nm and 45.3–86.7 nm, respectively, in Group 1, and 19.1–23.6 nm and 41.0–44.4 nm in Group 2. Analysis of SEM images reveals that increasing the anodization voltage results in larger pore diameters, interpore spacings, and porosity, but a reduced pore density. In contrast, changes in anodization time at a fixed voltage have a more modest effect on pore geometry. The anodized surfaces exhibit a marked change in wettability, with the water contact angle increasing from ~45° for the non-anodized alloy to ~123° for the best-performing AAO surface, without any additional chemical modification. These results demonstrate that, even under simple room-temperature conditions, AAO morphology and hydrophobic behavior can be tuned in a predictable manner by appropriate choice of anodization parameters, which is relevant for the design of membranes, sensors, and functional surface coatings. Full article

Through-plane electronic transport in porous membrane electrode assembly (MEA) electrodes is governed by the three-dimensional (3D) connectivity of the conducting phase. Here, we quantify the role of the spanning-cluster fraction $P_{\infty }$, defined as the fraction of conducting-phase voxels that belong to the $z$-spanning connected component in a finite reconstructed volume, on effective conductivity using scanning electron microscopy (SEM)-informed 3D reconstructions of four archetypal morphologies: a granular catalyst layer (CL), labeled CL1; a fibrous gas diffusion layer (GDL), labeled GDL1; an open-cell foam (OCF); and a micro-fibrous non-woven (MFM), labeled MFM1. Each morphology is reconstructed on a $150\times 150\times 150$ voxel grid, and $z$-spanning connectivity is identified with a 26-neighbor flood-fill algorithm. Steady-state conduction is solved by a finite-volume method (FVM) with an imposed potential difference between the z-faces and no-flux lateral boundaries. Although all samples exhibit through-thickness connectivity, the normalized conductivity ${\sigma }_{\mathrm{e}\mathrm{f}\mathrm{f}}/{\sigma }_{\mathrm{b}\mathrm{u}\mathrm{l}\mathrm{k}}$ varies widely, from $\approx 0.134$ (MFM1) to $\approx 0.706$ (OCF). The corresponding ${(P}_{\infty },{\sigma }_{eff}/{\sigma }_{bulk})$ pairs are $\left(0.996,\approx 0.306\right)$ for CL1, $\left(0.999,\approx 0.303\right)$ for GDL1, $\left(0.997,\approx 0.706\right)$ for OCF, and $\left(0.901,\approx 0.134\right)$ for MFM1. OCF exhibits the highest response due to vertically coherent channels, whereas MFM1 underperforms due to laminated constrictions; CL1 and GDL1 lie in an intermediate regime with nearly isotropic skeletons. Overall, the results show that while a $z$-spanning connected component is required for measurable conduction, the magnitude of ${\sigma }_{\mathrm{e}\mathrm{f}\mathrm{f}}$ is dictated by percolating-skeleton quality (bottlenecks, cross-sectional constrictions, and pathway alignment) rather than phase amount alone. The proposed descriptors therefore enable percolation-aware screening metrics for designing and comparing MEA-relevant GDL and CL microstructures. Full article

This paper presents two capacitors fabricated using the metallic nanowire membrane (MnM) interposer technology operating at mmWaves. Standard 2D interdigital capacitors (IDCs) are designed to operate up to 70 GHz, which presents a straightforward and non-complex fabrication. In comparison, this work also proposes an improved device that is more compact and exhibits large capacitance density, as high-performance vias enable the realization of high-depth capacitors. The fabrication process of 3D devices presents advanced maturity and innovation as it takes advantage of the porous nature of the interposer material to overcome the device complexity, and is also described in detail. Both capacitor types are modeled by a numerical lumped-element model that also considers parasitics. The 3D capacitors were successfully fabricated and characterized up to 70 GHz, displaying capacitance values between 30 fF and 160 fF and self-resonant frequencies in good agreement with mmWave applications. The quality factor of these devices, measured at 40 GHz, lies between 16 and 4, and the superficial capacitance density is between 4 pF/mm² and 8 pF/mm², showing that these devices are indeed promising for mmWave applications. These devices present considerably larger capacitance density compared to 2D traditional capacitors fabricated on the high-performance substrate, highlighting the advantage of 3D fabrication using nanowire growth. In addition, thin-film resistances are simulated and fabricated, projecting their functions as an RF-choke in a bias tee configuration using Ti thin film sputtering deposition step that is also part of the capacitors fabrication. Full article

This article delineates the electrical characteristics and usefulness of a plasticized polymer electrolyte (PPE) manufactured from PVDF/PEO blends, using varying weight percentages of the plasticizer ethylene carbonate (EC) in conjunction with a liquid electrolyte. Micro-porous solid-state polymer electrolyte membranes were fabricated using the non-solvent-induced phase separation (NIPS) method. The polymer composite membranes modified by the incorporation of a plasticizer (40 weight percent of EC) exhibited enhanced porosity and absorbed a significant quantity of liquid electrolyte (313.3%). A N₂ adsorption isotherm study indicates an increase in pore volume and pore size resulting from the incorporation of EC in PPE. This resulted in a satisfactory level of ionic conductivity (2.08 mS/cm) at 25 °C, attributable to the inclusion of 40 wt.% EC-based PPE, which has a high dielectric constant and a rapid relaxation time. The AC/40 wt.% EC-based PPE/LTO hybrid supercapacitor exhibits a superior specific capacitance, reduced internal resistance, and enhanced retention values after 10,000 cycles in comparison to the AC/10 wt.% EC-based PPE/LTO hybrid supercapacitor. Full article

Electrochemical carbon dioxide reduction reaction (CO₂RR) offers a promising route to mitigate climate change while simultaneously enabling renewable energy storage and the sustainable production of value-added chemicals. A wide variety of CO₂RR reactor designs have been developed, including both liquid-phase cells and gas-phase configurations. Among these, gas-phase systems, particularly flow-cell and membrane electrode assembly (MEA) designs, have become the primary focus of recent research due to their ability to overcome mass transport limitations and operate at high currents. While catalyst development has received considerable attention in advancing CO₂RR performance, the role of membranes in these gas-phase electrolyzers has been less systematically reviewed. This article addresses that gap by critically examining the functions, advantages, and limitations of the major membrane classes used in CO₂ electrolysis: anion exchange membranes, cation exchange membranes, bipolar membranes, and non-ion-exchange porous membranes within flow-cell and MEA configurations. We highlight how membrane properties influence local pH regulation, water management, crossover behavior, and overall reactor performance, while emphasizing that product identity is primarily catalyst-determined. By analyzing recent progress and remaining challenges, this review provides design insights for membrane selection and development toward efficient, stable, and scalable CO₂ electrolysis systems. Full article

High-temperature proton exchange membrane systems (HT-PEM) based on polybenzimidazole (PBI) membranes are a promising technology offering significant advantages over their low-temperature counterparts. A key challenge limiting its long-term durability is the leaching of phosphoric acid (PA) from the membrane during operation. This work introduces, for the first time, the strategy of modifying polybenzimidazole (PBI) membranes with amino-functionalized porous aromatic frameworks (PAF-20-NH₂) to fundamentally enhance their PA retention and operational stability, a critical challenge for high-temperature PEM technologies. We propose that the synergistic combination of the framework’s nanoscale porosity and the specific interaction of its amino groups create an unprecedented network for acid immobilization via reinforced hydrogen bonding. A comprehensive study of the membranes’ physicochemical and structural properties reveals that PAF-20-NH₂ modification results in a significant and quantitatively demonstrated improvement in acid retention capacity, directly translating into a notable increase in proton conductivity compared to both pristine PBI and membranes modified with the non-functionalized PAF-20. These findings establish a new, highly effective pathway for the rational design of next-generation high-performance PBI-based membranes. Full article

Islet encapsulation has the potential to enable transplantation without requirement for life-long immunosuppression. The period between implantation and revascularisation is most harmful for encapsulated islets as they receive nutrients and oxygen exclusively via diffusion. This critical time gap must be bridged with a temporary oxygen supply to prevent inflammation and apoptosis. Hence, we compared the efficiency of individual components of an oxygen-delivering matrix (hyaluronic acid (HA); HA + perfluorodecalin nanoemulsion; HA + perfluorodecalin nanoemulsion + oxygen) to provide a substitute for the extracellular matrix and to facilitate human islet survival. The islets were loaded into silicone-based macroencapsulation devices with multi-scale porous membranes designed to optimise revascularisation. Four to five days of normoxic culture revealed that non-oxygen-charged nanoemulsion prevented islet disintegration but did not reduce necrosis or apoptosis. Oxygen supply decreased the generation of reactive oxygen species and chemokines, thereby increasing islet yield. Stimulated insulin secretion of encapsulated islets was marginal and severely delayed. Islets incubated in oxygen-precharged nanoemulsion were characterised by the highest stimulation index. These data suggest that islet survival in macroencapsulation devices can be optimised with a multi-functional matrix providing mechanical support and temporary oxygen supply to reduce the production of pro-inflammatory mediators. Suitable oxygen delivery systems with an extended life span must identified before in vivo experiments can be undertaken. Full article

New approaches to the characterization of porous materials must satisfy principles of green analytical chemistry; in addition, they should be reproducible, versatile, and capable of providing relevant information for specific applications. Membrane characterization techniques often fail to meet some of these requirements. Specifically, hydrodynamic porous-based model methods (HPMMs) enable the simulation and evaluation of membrane properties, as well as the monitoring of changes in the response to controlled and uncontrolled modifications. Nevertheless, HPMMs are limited by the multifactorial relationships between their variables and by the generation of only single-value responses. Here, a semi-empirical approach to the characterization of membrane pore structure is proposed and evaluated using simple experimental measurements from pristine and modified membranes. The model enables the determination of the effective pore radius based on two size descriptors related to porosity and permeability, the construction of pore size distributions, and the estimation of structural parameters, such as the number of pores, pore size, and surface porosity. Furthermore, it allows for the simulation of Darcy-type flow behavior in both linear and nonlinear regimes. The model was evaluated on pristine and poly(vinyl alcohol)-modified poly(ethersulfone) ultrafiltration membranes (60–120 mmolL⁻¹) by diafiltration (100–400 kPa). Results demonstrate the usefulness of the model in characterizing membrane pore structure by using simple, fast, and non-destructive methods, thereby enabling advances in analytical diafiltration for membrane characterization. Full article

To address the fluctuation and instability of renewable power generation and the steady-state demands of chemical processes, a single-channel, non-isothermal computational fluid dynamics 3D model was developed. This model explicitly incorporates the coupling effects of electrochemical reactions, two-phase flow, and heat transfer. Subsequently, the influence of key operating parameters on proton exchange membrane water electrolyzer (PEMWE) system performance was investigated. The model accurately predicts the current–voltage polarization curve and has been validated against experimental data. Furthermore, the CFD model was employed to investigate the coupled effects of several key parameters—including operating temperature, cathode pressure, membrane thickness, porosity of the porous transport layer, and water inlet rate—on the overall electrolysis performance. Based on the numerical simulation results, the evolution of the ohmic polarization curve under temperature gradient, the block effect of bubble transport under high pressure, and the influence mechanism of the microstructure of the multi-space transport layer on gas–liquid, two-phase flow distribution are mainly discussed. Operational strategy analysis indicates that the high-efficiency mode (4.3–4.5 kWh/Nm³) is suitable for renewable energy consumption scenarios, while the economy mode (4.7 kWh/Nm³) reduces compression energy consumption by 23% through pressure–temperature synergistic optimization, achieving energy consumption alignment with green ammonia synthesis processes. This provides theoretical support for the optimization design and dynamic regulation of proton exchange membrane water electrolyzers. Full article

Low-salinity water flooding is a commonly used method to enhance oil recovery. At the microscopic scale, changes in pore structure and the distribution of remaining oil are critical to the effectiveness of water flooding. However, current research on the relationship between pore structure and remaining oil distribution is relatively limited. Therefore, this study employed micro-CT technology to analyze changes in pore structure and the distribution characteristics of remaining oil in sandstone cores during the water flooding process. Micron CT technology provides non-destructive, high-resolution three-dimensional imaging, clearly revealing the dynamic changes in the oil-water interface and remaining oil. The experiments included water saturation, oil saturation, and multi-stage water displacement processes in sandstone cores with different permeability values. The results show that the oil saturation in the rock core decreases during water flooding, and the morphology of remaining oil changes with increasing water flooding volume: cluster-like remaining oil decreases rapidly, while porous and membrane-like remaining oil gradually transforms, and columnar and droplet-like remaining oil increases under specific conditions. The study results indicate that at 1 PV flooding volume, the crude oil recovery rate reaches 57.56%; at 5 PV, the recovery rate increases to 64.00%; and at 100 PV, the recovery rate reaches 75.53%. This indicates that water flooding significantly improves recovery rates by enhancing wettability and capillary forces. Meanwhile, pore connectivity decreases, and particle migration becomes prominent, especially for particles smaller than 20 μm. These changes have significant impacts on remaining oil distribution and recovery rates. This study provides microscopic evidence for optimizing reservoir development strategies and holds important implications for enhancing recovery rates in mature oilfields. Full article

Background: Articular cartilage has limited self-repair capacity. While thermoresponsive poly N-isopropyl acrylamide (pNIPAAm)-based Cell Sheet Engineering (CSE) is a promising scaffold-free strategy, its inherent material properties pose limitations. This study developed and validated a novel, non-thermoresponsive CSE platform for functional cartilage regeneration. Methods: A culture platform was fabricated by grafting the biocompatible polymer poly gamma-glutamic acid (γ-PGA) and a disulfide-containing amino acid onto porous PET membranes. This design enables intact cell sheet detachment with its native extracellular matrix (ECM) via specific cleavage of the disulfide bonds by a mild reducing agent. Results: The hydrated substrate exhibited a biomimetic stiffness (~16.2 MPa) that closely mimics native cartilage. The platform showed superior biocompatibility and supported the cultivation of multi-layered rabbit chondrocyte sheets rich in Collagen II and Glycosaminoglycans. Critically, in a rabbit full-thickness defect model, transplanted autologous cell sheets successfully regenerated integrated, hyaline-like cartilage at 12 weeks, as confirmed by MRI, CT, and histological analyses. Conclusions: This novel CSE platform, featuring highly biomimetic stiffness and a gentle, chemically specific detachment mechanism, represents a highly promising clinical strategy for repairing articular cartilage defects. Full article