Search Results (2,215)

The liquid spreading on structured packings plays an essential role in affecting gas–liquid mass transfer in separation columns, yet the synergistic mechanism of surface wettability and textured geometries remains insufficiently understood. This study integrates experimental and computational methods to systematically investigate the liquid spreading characteristics on textured surfaces. The synergistic combination of hydrophilic modification and surface textures markedly enhances liquid spreading performance. Compared with the hydrophilic plane surface, the spherical cap texture increases the interface area and wetted area by 25.2% and 49.6%, respectively, while the pyramid-shaped texture leads to improvements of 24.5% and 48.9%, respectively. Based on Weber number analysis, it is identified that the competition between inertial force and surface tension governs the evolution of liquid spreading regimes. In addition, the results suggest that variations in liquid viscosity and density may further influence spreading behavior by modifying the balance among inertial, viscous, and surface tension forces. The geometric parameters of spherical cap textures are systematically examined, and it is revealed that a spherical cap with a non-uniform staggered configuration (Mode III) enables the efficient liquid spreading. A new non-uniform spherical cap texture is designed to enhance liquid spreading, which enhances spreading performance compared with the original plate, increasing the interface area by 27.3% and the wetted area by 47.4%. Although the liquid film thickness increases slightly, the wetted area ratio is significantly improved, indicating enhanced effective surface coverage. Both simulations and experiments confirm that the new textured structure further enhances liquid spreading performance on the textured surface. This research unveils a strategy to improve liquid spreading through tailored surface textures, opening up new possibilities for the design of efficient packings. Full article

Gallium-based liquid metals have garnered significant attention due to their distinct combination of metallic and liquid behavior at room temperature. This review systematically examines the fundamental properties and advanced multifunctional applications of this class of materials. Key characteristics such as low melting point, excellent fluidity, high electrical and thermal conductivity, and biocompatibility are first highlighted. Subsequently, progress in four major application areas is discussed. In sensing, these materials enable the fabrication of highly compliant and responsive devices capable of monitoring strain, temperature, and electromagnetic fields. Within biomedical engineering, their inherent low toxicity and biocompatibility underpin advances in biosensing platforms, precision drug delivery, and engineered tissue scaffolds. For energy-related applications, they are utilized in batteries and high-efficiency thermoelectric systems for converting heat into electricity. In catalysis, their dynamic and tunable interfaces facilitate efficient carbon dioxide conversion and selective thermocatalytic reactions. This review summarizes current advances in the application of gallium-based liquid metals and provides critical perspectives on future developments and opportunities in this technology. Full article

Oxidative stress generates oxidized phospholipids (OxPLs) that alter membrane structure and inflammatory lipid signaling, yet the underlying biophysical mechanisms remain poorly understood. Here, we examine how two structurally distinct truncated oxidized phosphatidylcholines (OxPCs), 1-palmitoyl-2-(5′-oxo-valeroyl)-sn-glycero-3-phosphocholine (POVPC) and 1-palmitoyl-2-glutaryl-sn-glycero-3-phosphocholine (PGPC), remodel membrane lateral organization and regulate secretory phospholipase A₂ (sPLA₂) activity. Large unilamellar vesicles composed of sphingomyelin, cholesterol, and either monounsaturated 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) or polyunsaturated 1-palmitoyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine (PDPC) were used to reconstitute the liquid-ordered/liquid-disordered (L_o/L_d) phase coexistence characteristic of eukaryotic plasma membranes. Fluorescence spectroscopy revealed that OxPLs modulate lipid packing and nanodomain organization in a structure- and composition-dependent manner. POVPC promoted pronounced membrane ordering and L_o domain stabilization compared with PGPC, particularly in monounsaturated membranes with low cholesterol content. In contrast, PDPC-containing membranes, especially at elevated cholesterol, exhibited enhanced structural resilience to OxPL-induced perturbations. These biophysical changes were associated with distinct functional outcomes. Notably, the relationship between membrane structural parameters and sPLA₂ activity was not linear, indicating a decoupling between bulk membrane properties and enzymatic response. sPLA₂ activity was linked to membrane lateral organization: the size of L_o domains modulate hydrolysis by influencing the physicochemical properties of L_o/L_d interfaces, which may represent preferential sites for enzyme activation. Consistent with this, POVPC reduced sPLA₂ activity through stabilization of ordered domains at both low and high cholesterol, while PGPC enhanced hydrolysis at high cholesterol. Importantly, PDPC-containing membranes attenuated sPLA₂ activity and exhibited a protective effect against OxPC-induced enzymatic activation. Together, these findings identify membrane lateral organization as a key regulator of sPLA₂ function and provide mechanistic insight into how oxidative stress can differentially modulate inflammatory lipid signaling depending on membrane composition. This work highlights membrane organization as an active determinant of enzyme activity and a potential target in pathologies associated with oxidative stress, including atherosclerosis, neuroinflammation, and metabolic disease. Full article

Ga-based liquid metals (GLMs) have been considered as promising thermal and electrical interface materials for advanced power electronics, combining high thermal conductivity (some types even >30 W/m·K) with fluidity at room temperature. This review systematically evaluates the dual roles of GLMs in power electronics packaging. Their function in thermal management as both thermal interface materials and active cooling media is first examined, followed by an analysis of their capabilities in forming electrical interconnections via low-temperature bonding in fluidic and solid states. However, reliable integration remains challenging due to interfacial reactions and instability with metal substrates. We discuss interfacial mechanisms with Cu and common metallizations, along with emerging regulation strategies such as surface coatings and process acceleration techniques. By examining these interfacial interactions, this work aims to guide the selection and design of surface modification strategies to either promote or inhibit reactions as needed, supporting the development of robust power electronic packaging. Full article

The enzymatic saccharification of cellulose remains a key step in biomass conversion processes, often influenced by enzyme stability, distribution, and accessibility at solid–liquid interfaces. Immobilization of cellulolytic enzymes on nanostructured supports has been proposed as a strategy to modulate catalytic behavior; however, the relationship between enzyme loading and catalytic response remains insufficiently understood. In this study, CuO-based nanobiocatalysts were prepared through controlled cellulase immobilization and systematically evaluated under defined experimental conditions. Structural and physicochemical characterization was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and integrated thermal analysis (TGA–DTG–DSC), enabling a comparative assessment of the analyzed systems. SEM analysis showed that the average particle diameter increased from 39.5 ± 14.8 nm (CuO nanoparticles) to 95.6 ± 21.8 nm (NPI10), 106.6 ± 27.7 nm (NPI15), and 113.5 ± 23.1 nm (NPI20), indicating progressive variations in particle organization with increasing enzyme loading. Catalytic performance was evaluated through enzymatic hydrolysis of cellulose filter paper as a model substrate, with products quantified by HPLC at a representative reaction time. The system prepared at lower enzyme loading (NPI10) exhibited product formation comparable to that of the free enzyme, with apparent average glucose formation values of 1.054 and 1.047 mg·mL⁻¹·h⁻¹, respectively. In contrast, higher immobilization levels were associated with reduced catalytic output. Across all systems, glucose was the predominant product, with negligible accumulation of intermediate oligomers under the evaluated conditions. These results indicate that increasing enzyme loading does not correspond to proportional increases in product formation and highlight the influence of enzyme distribution and accessibility within the system. The combined structural and catalytic observations provide a controlled framework for evaluating how immobilization conditions influence system behavior in nanobiocatalytic systems. Full article

This review summarizes innovative co-formulation strategies for non-marketed dry powder inhalers (DPIs), enabling the simultaneous pulmonary delivery of multiple active pharmaceutical ingredients (APIs). Key approaches include co-amorphous systems (COAMS) and co-crystals, which combine two APIs into a single particle, improving aerodynamic properties, solubility, dissolution, and patient compliance while reducing manufacturing complexity. Core–shell microparticles, produced via spray drying, allow spatial separation and controlled release of APIs, minimizing drug–drug interactions and enabling tailored pharmacokinetics. Co-spray drying of dual APIs can yield particles with superior aerosolization and stability, though examples remain limited. Nanoparticle-based systems offer enhanced lung deposition and cellular uptake but face challenges in device compatibility, scalability, and regulatory approval. Each technology presents unique advantages and limitations regarding manufacturability, dose flexibility, and clinical translation. This review also highlights advances in in vitro toxicity testing, including air–liquid interface cultures, organoids, lung-on-chip models, and precision-cut lung slices, which are increasingly important as alternatives to animal studies. The importance of using an aerosol exposure system for the testing is highlighted. Ultimately, the choice of co-formulation platform should balance scientific innovation with practical considerations of manufacturing and regulatory requirements to maximize therapeutic benefit and commercial viability for future DPI combination products. Full article

The rational design and regulation of interfacial microenvironments represents an effective strategy for enhancing reaction performance. Previous studies have demonstrated that constructing air–liquid–solid triphase interfaces can substantially enhance catalytic reactions involving gaseous reactants. However, research on regulating the triphasic interfacial microenvironment remains limited and challenging. Herein, we fabricated a triphase photocatalytic system by depositing hydrophobic materials onto ordered TiO₂ porous (OTP), achieving significantly enhanced performance in visible-light-driven dye-sensitized photooxidation. Further, we regulated the triphasic microenvironment by systematically adjusting the chain length of hydrophobic molecules. It was found that the chain length greatly affects the interfacial properties, including O₂ concentration, the organic molecule adsorption and the interfacial electron transfer efficiency, thereby influencing photocatalytic reaction kinetics and pathways. We demonstrated a high-performance triphase photocatalytic system using 1H,1H,2H,2H-perfluorooctyl triethoxysilane as the hydrophobic material, which optimized multiple interfacial properties through synergistic effects, leading to optimal photocatalytic performance. Full article

Mitochondrial dysfunction drives persistent inflammation in severe asthma, yet its upstream metabolic regulation remains unclear. Induced sputum from patients with severe asthma was analyzed and integrated with transcriptomic datasets from independent cohorts. Two mouse models (C57BL/6J) were used for in vivo validation with multi-omics profiling, and mechanistic studies were performed in air–liquid interface-cultured primary human airway epithelial cells. Glutathione reduced form (GSHr) was markedly depleted in sputum and associated with poor disease control and mixed granulocytic inflammation in patients with severe asthma. Multi-omics analyses revealed coordinated disruption of glutathione (GSH) metabolism, including oxidized GSH accumulation, reduced synthesis and glutathione-S-transferase activity, and impaired mitochondrial GSH transport. GSH supplementation alleviated airway inflammation, oxidative stress, and mitochondrial dysfunction, whereas pharmacological inhibition of GST exacerbated these effects. Mitochondrial analyses identified suppressed SLC25A39 expression as a key mediator of defective GSH transport and redox imbalance. Transcriptomic profiling of airway biopsies showed upregulation of Neuropilin-1 (Nrp1), closely associated with altered glutathione pathways. Targeting the Nrp1 b1 domain restored mitochondrial GSH metabolism and attenuated airway inflammation. These findings identify an Nrp-centered metabolic pathway that disrupts mitochondrial homeostasis and drives inflammatory amplification, highlighting mitochondria-targeted therapeutic strategies for severe asthma. Full article

Nickel-based superalloy GH3625 is widely used in extreme environments due to its exceptional high-temperature strength and corrosion resistance; however, optimizing its comprehensive performance through precise microstructural control remains a critical challenge. In this study, the effect of withdrawal rate (10–200 μm/s) on the microstructural evolution, mechanical properties, and corrosion resistance of GH3625 alloy was investigated using a liquid-metal-cooled directional solidification system. The microstructural characteristics, elemental segregation, and phase distributions were systematically analyzed via OM, SEM, and EDS, followed by uniaxial tensile and electrochemical polarization tests. The results show that with increasing withdrawal rate, the solid–liquid interface morphology evolves from cellular to cellular-dendritic and finally to fully dendritic. Correspondingly, the primary dendrite arm spacing decreases from 270.4 μm to 100.2 μm, and the secondary dendrite arm spacing decreases from 66.5 μm to 12.3 μm. The area fraction of the detrimental Laves phase first decreases and then increases, reaching a minimum at 100 μm/s. Correspondingly, the yield strength increases from 282 MPa to 409 MPa, and the corrosion resistance is optimized at 100 μm/s. The microstructure–property relationships are discussed based on second-phase strengthening theory and microstructural refinement. This study provides a theoretical basis and practical process windows for optimizing directional solidification parameters to achieve enhanced mechanical and corrosion performance in GH3625 alloy. Full article

Cold-mercury gilding uses mercury as an adhesive to bond gold foil onto the surface of copper and silver artifacts. This technique and mercury gilding (fire gilding) both belong to the Au-Hg system and are closely related in technology. Clarifying the technical differences between them is of great significance for revealing the developmental sequence of ancient gilding technologies. On the basis of reconstructing traditional fire gilding, simulated cold-mercury-gilded samples were successfully prepared using experimental archeological methods, and multi-scale characterization was performed using SEM-EDS, XRD, and XPS. The results show that the surface of cold-mercury-gilded samples displays a micromorphology of folded and overlapped gold foil accompanied by locally dense particle aggregation. The cross-section of the gold layer exhibits a multilayer stacked structure, in which mercury is enriched at the gold layer/substrate interface and forms an AuHgCu/Ag diffusion layer. Room-temperature-stable Au-Hg and Ag-Hg phases such as Au₂Hg and AgHg are present in the gold layer, reflecting complex phase transformation behavior of the Au-Hg/Ag-Hg system at room temperature. During cold-mercury gilding, liquid mercury first adheres to the gold foil, and then interdiffusion and phase reactions occur between mercury, gold, and copper/silver atoms at room temperature. Intermetallic compounds and diffusion layers formed at the interface achieve firm bonding between the gold layer and the substrate. Both cold-mercury gilding and mercury gilding achieve metallurgical bonding through atomic interdiffusion. However, affected by differences in the initial state of mercury and operating temperature, the phase transformation and atomic diffusion behaviors of the system differ significantly, which are ultimately reflected in the cross-sectional structure of the gold layer, the composition of the interfacial diffusion layer, and the types of phases. Therefore, mercury-gilded artifacts show superior gold layer durability and bonding strength with the substrate compared with cold-mercury-gilded artifacts. Both techniques pioneered the application of mercury in metallic gilding and represent important innovations in ancient surface decoration technology. Full article

Raman spectroscopy is capable of determining the composition of mixtures quantitatively and qualitatively. However, this technology reaches its limits when used to examine liquid dispersed mixtures of substances. In these emulsions, light scattering occurs at the interfaces of the particles and/or droplets, leading to signal losses that make the results impossible to evaluate. Our previous publications have shown, however, that it is possible to quantify the signal losses using a scattered light probe. In an investigation of the water–toluene–acetone emulsion, the acetone concentration could be determined with a root mean squared error of prediction (RMSEP) of up to 1.5 wt%. Based on this method, further analyses are now being carried out to demonstrate that the correction also makes it possible to determine the acetone concentration in each individual liquid phase. First, a ternary diagram is analytically created by establishing stable conditions and separating the phases for individual measurement. In a second step, the samples are measured as a dispersed mixture with the droplets as interfering factors, demonstrating that the same concentration differences can be measured between both phases. Full article

A thin-film surface plasmon resonance (SPR) sensor is presented using a prism-coupled Kretschmann configuration and an optimized multilayer architecture incorporating black phosphorus (BP) as an ultrathin overlayer. The response is modeled at 633 nm under TM polarization using the transfer-matrix method. Low-concentration sensing conditions in the 1–5 ng/mL range are represented through small effective-refractive-index perturbations of the aqueous sensing medium, providing a preliminary optical framework for evaluating refractive-index response in biosensing-related scenarios. The coupling prism, Au film thickness, and Si₃N₄ spacer thickness are optimized to control resonance depth, linewidth, and angular shift. The optimized CaF₂/Au/Si₃N₄/BP configuration exhibits systematic condition-dependent displacement of the SPR minimum and an evanescent-field distribution that remains strongly localized at the sensing interface while extending into the sensing medium, enabling refractive-index interrogation. High angular sensitivity is obtained at low levels, reaching 517.62°/RIU at 2 ng/mL and 482.82°/RIU at 1 ng/mL, with quality factors above 120 RIU⁻¹ in the same regime. Composite indicators (figure of merit and contrast signal factor) peak at intermediate levels, whereas resonance broadening at higher levels reduces the quality factor and increases the inferred limit of detection, evidencing a sensitivity–resolution trade-off. Benchmarking against reported SPR platforms indicates that BP-assisted interface engineering provides a competitive low-level operating window within a preliminary refractive-index-sensing framework that is relevant to future biosensor design. These results motivate further experimental validation, including BP stabilization, surface biofunctionalization, and practical implementation under liquid-phase sensing conditions. Full article

The exceptional stability of C-F bonds renders PFAS highly persistent in aqueous environments, posing significant challenges for conventional treatment technologies. While plasma-based technologies show promise, their efficiency is often limited by poor gas–liquid mass transfer in bulk liquid. Here, an in-house constructed ultrasonic atomization–dielectric barrier discharge (UEN-DBD) system was developed to promote PFAS degradation under non-thermal plasma conditions. Ultrasonic atomization generated microdroplets, which promoted PFAS enrichment at the surface of microdroplets and facilitate interactions with plasma-generated reactive species. Using perfluorooctanoic acid (PFOA) and perfluorooctanesulfonate (PFOS) as model compounds, degradation behavior was evaluated over an initial concentration range of 0.01–1.0 ppm. At 0.01 ppm, degradation efficiencies of 96.06% for PFOA and 94.86% for PFOS were achieved within 5 min. Electron paramagnetic resonance (EPR) spectroscopy confirmed the formation of oxidative radicals (·OH) and suggested a mixed redox environment involving reactive species, potentially including superoxide (O₂·⁻) or hydrated electrons (e_aq⁻), in the discharge-treated system. High-resolution mass spectrometry results are consistent with a stepwise chain-shortening pathway dominated by successive –CF₂– scission, while fluoride-release measurements provided supporting evidence for partial defluorination. These findings advance the understanding of plasma-assisted PFAS degradation at the gas–liquid interface and provide a basis for the further development of plasma-assisted PFAS treatment strategies. Full article

To address the existing challenges in mold slag thickness measurement—such as the susceptibility of contact sensors to high-temperature degradation and the limitation of non-contact methods to detecting only the upper slag surface—this study proposes an integrated approach that fuses millimeter-wave radar and eddy current sensors for measuring mold slag thickness in a continuous casting mold. The method innovatively combines two sensing principles: the millimeter-wave radar employs an improved FFT-CZT² high-precision ranging algorithm to perform high-resolution scanning of the solid slag upper surface, reconstructing its topography (error: $\pm$1 mm), while Mel-frequency cepstral coefficients (MFCC) are applied to extract features from the radar intermediate-frequency signals, combined with an enhanced PSO-BP neural network algorithm to predict the thickness of the solid slag layer (error: $\pm$5 mm). Concurrently, an eddy current sensor monitors the liquid slag–molten steel interface position (error: $\pm$1 mm). Through dual-sensor data fusion, the upper surface topography data and solid slag thickness obtained from the radar are spatially registered in three dimensions with the molten steel level information derived from the eddy current sensor. This integration ultimately enables the non-contact synchronous measurement of three key parameters within the mold: solid slag layer thickness, liquid slag layer thickness inversion, and molten steel level. Furthermore, by reconstructing the upper slag surface morphology, the method successfully resolves practical issues such as uneven material distribution, local material deficiency, or excessive feeding. Preliminary experimental verification confirms that the proposed method maintains stable performance even under high-temperature and complex environmental conditions. It thus provides a real-time, accurate, and full-cross-section monitoring solution for mold slag in continuous casting, offering significant practical value for the development of smart steel plants. Full article

Amidst the high global reliance on petroleum, this study addresses energy inefficiency in beam-pumping units used for oil extraction. We developed a tubular solid–liquid triboelectric nanogenerator (TENG) based on fluorinated polydimethylsiloxane (PDMS) films. Self-assembled surface modification with fluorosilane molecular chains enhanced charge transfer, achieving a 2.7-fold increase with 13F-PDMS. The enclosed tubular design utilizes periodic liquid-electrode contact to generate a volumetric effect. Experiments investigated the influence of liquid composition and device configuration on performance. Using a 1.69 mol/L FeCl₃ solution with four series-connected units, the TENG reached 29 V and 263 nA, powering 150 LEDs. This demonstrates its potential for harvesting reciprocating mechanical energy from pumping units to reduce operational energy consumption. Full article