Search Results (209)

High regeneration energy demand remains a critical barrier to the large-scale deployment of ethanolamine-based (MEA-based) CO₂ capture. This study adopts an Al₂O₃ ceramic-membrane heat exchanger (CMHE) to recover both sensible and latent heat from the stripped gas. Experiments confirm that heat and mass transfer within the CMHE follow a coupled mechanism in which capillary condensation governs trans-membrane water transport, while heat conduction through the ceramic membrane dominates heat transfer, which accounts for more than 80%. Guided by this mechanism, systematic structural optimization was conducted. Alumina was identified as the optimal heat exchanger material due to its combined porosity, thermal conductivity, and corrosion resistance. Among the tested pore sizes, CMHE-4 produces the strongest capillary-condensation enhancement, yielding a heat recovery flux (q value) of up to 38.8 MJ/(m² h), which is 4.3% and 304% higher than those of the stainless steel heat exchanger and plastic heat exchanger, respectively. In addition, Length-dependent analyses reveal an inherent trade-off: shorter modules achieved higher q (e.g., 14–42% greater for 200-mm vs. 300-mm CMHE-4), whereas longer modules provide greater total recovered heat (Q). Scale-up experiments demonstrated pronounced non-linear performance amplification, with a 4 times area increase boosting q by only 1.26 times under constant pressure. The techno-economic assessment indicates a simple payback period of ~2.5 months and a significant reduction in net capture cost. Overall, this work establishes key design parameters, validates the governing transport mechanism, and provides a practical, economically grounded framework for implementing high-efficiency CMHEs in MEA-based CO₂ capture. Full article

This study is based on in situ structural test sections and systematically explains the construction processes and key control points of different waterproofing methods by optimizing the self-waterproofing of structural concrete, controlling the installation process of external waterproofing membranes, and managing quality throughout the construction process. For various materials such as polymer-coated waterstops, steel-edged rubber waterstops, and composite grouting pipes with water-swelling strips, the waterproofing performance under the corresponding processes was analyzed through a combination of experiments and numerical simulations. The research focuses on investigating the influence of material selection and construction techniques on waterproofing effectiveness, clarifying the applicable conditions and performance differences among various materials and techniques. The results indicate that polymer-coated waterstops perform significantly better than other materials; self-compacting concrete causes minimal disturbance to waterstops, which is beneficial for waterproofing, but it exhibits deficiencies in early-age crack resistance; refined control of construction techniques plays a decisive role in the overall performance of the waterproofing system. Consequently, detailed construction quality control specifications for the main structure and its components were developed. Full article

Continuous-flow separation of magnetically labeled cells according to surface-marker expression levels is increasingly needed to study phenotypic heterogeneity and support downstream assays. Here, we present a microfluidic platform that uses spatially engineered soft magnetic strips (SMS) to sculpt lateral magnetic deflection fields for quantitative, label-guided cell fractionation. Under a uniform bias field, the SMS generates controllable magnetic gradients within the microchannel, producing distinct lateral velocities among EpCAM-labeled tumor cells that carry different Dynabead loads, which indirectly report membrane protein expression. Multi-outlet collection converts these “race-based” trajectory differences into discrete expression-level-resolved fractions. A COMSOL–MATLAB framework and a force-equivalent metric |(H·∇)H| are used to optimize key structural parameters of the magnetic interface, including strip thickness, width, and vertical spacing from the flow channel. Three journey nodes at 1.5, 3, and 9 mm along the flow path define a three-stage cascade that partitions MDA-MB-231, Caco-2, and A549 cells into four EpCAM-related magnetic subgroups: high (H), medium (M), low (L), and near-negative (N). Experiments show that the sorted fractions follow the expected expression trends reported in the literature, while maintaining high cell recovery (>90%) and viability retention of 98.2 ± 1.3%, indicating compatibility with downstream whole-blood assays and culture. Rather than introducing a new biomarker, this work establishes a quantitative magnetic-field design strategy for continuous microfluidic sorting, in which the spatial configuration of soft magnetic elements is exploited to implement expression-level-dependent fractionation in next-generation magneto-fluidic separation systems. Full article

Dermal drug delivery is a promising alternate route of drug administration, offering localized therapeutic effects, reduced systemic effects, and improved patient compliance. However, the skin’s intricate configuration, especially the stratum corneum (SC), presents formidable barriers, restricting drug permeation. This review summarizes biological, synthetic, and methodological models employed to study dermal absorption and permeability. Ex vivo human skin is a reference point, but limited availability and ethical constraints necessitate reliance on animal models, including porcine, rodent, rabbit, monkey, and even snake skin, each with unique advantages and drawbacks. Synthetic substitutes, e.g., reconstructed human epidermis and Strat-M^® membranes, provide reproducibility and economic practicality, though none fully mimic the barrier functions of human skin. Innovative analytical methods, including diffusion cells, skin-PAMPA, tape stripping, and advanced imaging techniques, enable quantitative, semi-quantitative, and qualitative insights into drug transport. Collectively, these tools support formulation optimization and aid regulatory bioequivalence assessments. However, challenges remain in correlating in vitro, ex vivo, and in vivo outcomes and in replicating the skin’s dynamic physiology. This review highlights current opportunities and limitations, emphasizing the need for more physiologically relevant models to advance safe, effective, and innovative dermal drug delivery systems. Full article

The long-term conservation of Prunus persica (peach), a crop of significant agronomic and genetic value, remains challenging due to its recalcitrance to conventional cryopreservation methods. Low tolerance to dehydration and cryoprotectant toxicity often results in poor survival and regrowth, thereby limiting the reliability of germplasm storage. This study evaluated whether combining an alginate hydrogel matrix with Pluronic F-68 improves vitrification efficiency and post-thaw regeneration of peach shoot tips by enhancing dehydration dynamics and reducing cryo-injury. Shoot tips were immobilized in thin sodium alginate layers on aluminum foil strips, with the hydrogel providing mechanical stabilization and moderating water loss during exposure to PVS3 and subsequent liquid nitrogen immersion. To further mitigate cryoinjury, Pluronic F-68, a non-ionic surfactant with membrane-stabilizing properties, was incorporated into the system. Differential scanning calorimetry revealed that the hydrogel reached complete vitrification after 120 min in PVS3, whereas encapsulated shoot tips required 150 min for full suppression of crystallization. The optimized system achieved 71% post-cryopreservation survival and 40% regrowth, compared with 25% and 9% in non-encapsulated controls. PF-68 accelerated vitrification kinetics, lowered crystallization enthalpies, and improved post-thaw viability. These findings demonstrate that engineered hydrogel–surfactant matrices can stabilize the microenvironment during vitrification and offer a promising approach for the long-term cryopreservation of peach germplasm. Full article

A novel fluorescent probe (PYB) for selective and sensitive detection of Cu²⁺ ions was rationally designed and synthesized via a multi-step organic reaction using pyrene as the fluorophore and salicylaldehyde-diethylenetriamine Schiff base as the recognition moiety. The structural characterization of PYB was confirmed by ¹H NMR, ¹³C NMR, and high-resolution mass spectrometry (HRMS). Photophysical properties investigation revealed that the probe exhibited strong fluorescence emission at 362 nm in DMF/HEPES-NaOH buffer solution (v:v = 1:1, pH 7.4), which underwent a significant fluorescence quenching response (quenching efficiency up to 77%) upon the addition of Cu²⁺, attributed to the formation of a 1:1 PYB-Cu²⁺ complex (binding constant K = 799.65 M⁻¹). The probe showed excellent selectivity for Cu²⁺ over other common metal ions (Ba²⁺, Na⁺, Mg²⁺, Zn²⁺, Cd²⁺, Ca²⁺, Mn²⁺, Pb²⁺, Hg²⁺, Fe³⁺, Co²⁺), with a low detection limit of 8.35 × 10⁻⁷ M, which is well below the maximum allowable concentration of Cu²⁺ in drinking water specified by the World Health Organization (WHO). Furthermore, a portable fluorescent test strip based on PYB was successfully fabricated, enabling rapid and visual detection of Cu²⁺ under UV light. Fluorescence imaging experiments in living HepG2 cells demonstrated that PYB could penetrate cell membranes efficiently and realize the intracellular detection of exogenous Cu²⁺. These results collectively indicate that PYB holds great potential as a practical tool for Cu²⁺ detection in environmental monitoring, food safety, and biological systems. Full article

A nanoliter-scale fabrication method was applied to construct a colorimetric lateral flow strip for urea detection (Urea-CLFS). The device involves two main papers: a nitrocellulose membrane (NC-Mb) for urease enzyme immobilization and chromatography paper (CH-PP) containing a phenol red indicator. Urea-CLFS is a tool for detecting urea that is based on enzyme catalysis and the change in color of phenol red when urea is present. The Urea-CLFS fabrication was made possible by the minimal amount of nanoliters used in reagent consumption. The use of small arrays of phenol red dots provides a higher response result compared to single dots applied on CH-PP. To find the most effective design, it analyzed how urease was aligned on NC-Mb horizontally and vertically. According to our findings, the vertical alignment of the urease enzyme on NC-Mb leads to a prolonged reaction time, which leads to higher product production. The optimization process included optimizing various parameters, including the layer number of phenol red on CH-PP, phenol red concentration, urease concentration, reaction time, and sample volume. Under optimal conditions, the Urea-CLFS provided a linear range of 0.25–8.0 mmol L⁻¹ with an LOD of 0.34 mmol L⁻¹, which is sufficient for human health diagnostics. The accuracy of the Urea-CLFS was demonstrated by the recovery of the human urine sample between 95 ± 3% and 103 ± 3% (n = 3). Full article

Membrane technology plays a vital role in environmental protection, chemical industry, and pharmaceuticals, where understanding the “structure-property” relationship of composite membranes through transmission electron microscopy (TEM) is crucial. Conventional ultramicrotomy methods for preparing ultra-thin sections of polymer composite membranes often result in significant damage and non-uniform thickness due to interference from non-woven substrates. In this study, we developed an innovative substrate stripping and double-orientation embedding technique that overcomes these limitations. A special embedding device was designed to facilitate the preparation of polymeric membrane cross-sections for TEM analysis. The device incorporates dual functionality, enabling both non-woven substrate detachment and bidirectional alignment of functional membrane layers. TEM characterization showed that the ultra-thin sections of membrane cross-sections prepared using the improved method were damage-free (0% damage rate), had uniform thickness, and showed distinct structural clarity. This method addressed three major challenges: (i) substrate-induced section damage, (ii) orientation deviation, and (iii) interlayer separation. This advancement provides researchers with a reliable tool for accurate cross-sectional analysis of composite membranes, facilitating deeper insights into membrane microstructure-performance relationships. Full article

Hospitals often use diatrizioic acid (DTZA), an iodinated radiocontrast agent, which is poorly biodegradable and persistent in aqueous media. Therefore, the objective of this work is to remove DTZA from water using an advanced separation process, namely liquid surfactant membrane (LSM) or emulsion liquid membrane. The LSM system is composed of Aliquat 336 as extractant, Span 80 as emulsifier, kerosene as diluent, and KCl as internal stripping phase. The impacts of experimental parameters impacting the extraction of DTZA from water by LSM, namely surfactant concentration, initial pH of the contaminated solution, extractant dosage, nature of base in the contaminated solution, concentration of the internal stripping phase, nature of stripping solution, emulsion/external solution volume ratio, internal solution/organic phase volume ratio, mixing rate, nature of diluent, emulsification time, emulsification rate, and initial DTZA concentration, were investigated. A highly stable emulsion with a good degree of removal of 90.8% of DTZA in water was obtained for an emulsifier dosage of 3% (w/w), an extractant dosage of 1.0% (w/w), a pH of the contaminated solution of 10 using NH₄OH, a concentration of the inner phase of 0.3 N KCl, an internal solution/organic phase volume ratio of 1/1, an emulsion/external solution volume ratio of 20/250, a mixing speed of 250 rpm, an emulsification time of 4 min, and an emulsification speed of 20,000 rpm. Additionally, the extraction of DTZA from various natural water matrices (natural mineral water, tap water and seawater) was examined. The developed LSM method offers a fascinating enhanced separation method for the elimination of DTZA in waters with low chloride ion concentrations. Full article

The synergistic effect of using D2EHPA and TOPO together to enhance the extraction of samarium(III) from aqueous media via emulsion liquid membrane (ELM) technology was explored. D2EHPA in binary mixtures with TBP and in ternary mixtures with TOPO and TBP was also tested. Among the tested extractants, a binary mixture of 0.1% (w/w) D2EHPA and 0.025% (w/w) TOPO achieved 100% samarium(III) extraction at a low loading. This mixture outperformed D2EHPA-TBP and other systems because D2EHPA strongly binds to Sm(III) ions, while TOPO increases the solubility and transport efficiency of metal complexes. Additionally, process factors that optimize performance and minimize emulsion breakage were examined. Key insights for successfully implementing the process include the following: 5 min emulsification with 0.75% Span 80 in kerosene at pH 6.7 (natural), 250 rpm stirring, a 1:1 internal/membrane phase volume ratio, a 20:200 treatment ratio, and a 0.2 N HNO₃ stripping agent. These insights produced stable, fine droplets, enabling complete recovery and rapid carrier regeneration without emulsion breakdown. Extraction kinetics accelerate with temperature up to 35 °C but declined above this limit due to emulsion rupture. The activation energy was calculated to be 33.13 kJ/mol using pseudo-first-order rate constants. This suggests that the process is diffusion-controlled rather than chemically controlled. Performance decreases with Sm(III) feed concentrations greater than 200 mg/L and in high-salt matrices (Na₂SO₄ > NaCl > KNO₃). Integrating these parameters yields a scalable, low-loading ELM framework capable of achieving complete Sm(III) separation with minimal breakage. Full article

This study reports an investigation of the synergistic extraction of dysprosium (Dy(III)) from aqueous media using a low-concentration, binary carrier mixture of Cyanex 272 and D2EHPA within an emulsion liquid membrane (ELM). Within the tested formulations, the one containing 0.42% (w/w) Cyanex 272 and 0.28% (w/w) D2EHPA yielded the best results. The impact of process factors that maximize recovery efficiency and minimize emulsion breakdown was also examined. A Span 80 loading of 0.75% (w/w) achieved 97.5% extraction with minimal breakage (less than 2.1%). An external phase pH of 5.8 achieves an optimal balance of high-throughput Dy(III) recovery and membrane stability; 0.2 N HNO₃ as the stripping phase strikes the optimal balance, providing strong initial uptake with minimal emulsion degradation. As the initial Dy(III) loading increases, extraction efficiency decreases. Increasing the temperature from 15 to 45 °C accelerates mass transfer, achieving near-complete extraction in under 15 min. However, above 45 °C, emulsion breakage spikes, causing a collapse in efficiency. Similarly, increasing NaCl levels suppresses Dy(III) uptake and promotes coalescence. This reduces recovery from seawater to just over 70%. Nevertheless, the balanced mineral content of Zamzam water preserves emulsion integrity and enables 100% extraction. The activation energy was found to be 26.16 kJ/mol, suggesting that mass transfer, rather than the chemical reaction at the interface, controls the process. The results of this study highlight the synergistic efficiency advantage of the ELM system at lower carrier concentrations, even in complex water sources. Full article

Electrochemical sensors have been developed based on polyethylene terephthalate track-etched membranes (PET TeMs) modified by photograft copolymerization of N-vinylformamide (N-VFA) and trimethylolpropane trimethacrylate (TMPTMA). The modification, structure and properties of the modified PET TeMs were thoroughly characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM), thermogravimetric analysis (TGA), Fourier-transform infrared (FTIR) spectroscopy, gas permeability measurements and contact angle analysis. Optimal membrane modification was achieved using C = 10% (N-VFA), 60 min of UV irradiation and a UV lamp distance of 10 cm. Furthermore, the modified membranes were implemented in a two-electrode configuration for the determination of Eu³⁺, Gd³⁺, La³⁺ and Ce³⁺ ions via square-wave anodic stripping voltammetry (SW-ASV). The sensors exhibited a linear detection range from 10⁻⁷ M to 10⁻³ M, with limits of detection of 1.0 × 10⁻⁶ M (Eu³⁺), 6.0 × 10⁻⁶ M (Gd³⁺), 2.0 × 10⁻⁴ M (La³⁺) and 2.5 × 10⁻⁵ M (Ce³⁺). The results demonstrated a significant enhancement in electrochemical response due to the grafted PET TeMs-g-N-PVFA-TMPTMA structure, and the sensor showed practical applicability and consistent performance in detecting rare earth ions in tap water. Full article

Ultrafiltration strips water of bacteria. The common misconception is that the filtrate is thus free of bacteria. This only applies, however, in the case that the filtrate compartment is sterile. In real-world applications, the filtrate is rapidly re-colonized, followed by regrowth. In extreme cases of low water usage, the cell numbers in the filtrate can even exceed those in the feed water, probably due to a combination of the microbial enrichment of the bulk water from surfaces, regrowth in the water body itself, and nutrient enrichment on the filter membrane. Regrowth is made possible because dissolved nutrients can freely pass through the membranes. This explains why the initial decrease in cell numbers in drinking water installation systems with ultrafiltration is often followed by an increase in the periphery of the plumbing system. The extent of actual regrowth hereby depends mostly on water usage behaviours. A shorter frequency of membrane wash cycles is beneficial for reducing cell numbers. Neither frequent wash cycles nor cleaning in place (CIP) in filtration units, however, seem to modulate the maximal regrowth potential. Although the effect of ultrafiltration on cell numbers is not sustainable, it causes profound changes in the bacterial communities, with highly distinct populations in the feed water and the filtrate. The microbiological “reset” is demonstrated using examples both from the fields of drinking water and water reuse. Overall, our results suggest that ultrafiltration has a profound impact on the microbiome, but the cell numbers in filtrates depend mostly on the water usage and operational conditions. Full article

The development of anode-free sodium metal batteries (AFSMBs) offers a promising pathway to achieve ultrahigh energy density and cost efficiency inherent to conventional sodium ion/metal batteries. However, irreversible Na plating/stripping and dendritic growth remain critical barriers. Herein, we demonstrate that separator engineering is a pivotal strategy for stabilizing AFSMBs. Through systematic evaluation of four separators—2500 separator (PP), 2325 separator (PP/PE/PP), glass fiber (GF), and an Al₂O₃-coated PE membrane, we reveal that the Al₂O₃-coated separator uniquely enables exceptional interfacial kinetics and morphological control. Na||Na symmetric cells with Al₂O₃ coated separator exhibit ultralow polarization (4.5 mV) and the highest exchange current density (1.77 × 10⁻² mA cm⁻²), while the anode-free AlC-NFPP full cells retain 91.6% capacity after 150 cycles at 2C. Specifically, the Al₂O₃ coating homogenizes Na⁺ flux, promotes dense and planar Na deposition, and facilitates near-complete stripping with minimal “dead Na”. This work establishes ceramic-functionalized separators as essential enablers of practical high-energy AFSMBs. Full article

The Akabane virus (AKAV) is a significant member of the Orthobunyavirus genus, with its envelope glycoprotein Gc, focusing on its molecular structural features, immunoregulatory mechanisms, and application value in pathogen diagnosis and vaccine design. As a key structural protein of AKAV, Gc mediates virus adsorption and neutralizing antibody recognition through the N-terminal highly variable region (HVR), while the C-terminal conserved region (CR) dominates the membrane fusion process, and its glycosylation modification has a significant regulatory effect on protein function. In clinical diagnostics, serological assays based on Gc proteins (e.g., ELISA, immunochromatographic test strips) have been standardized; in vaccine development, the neutralizing epitope of Gc proteins has become a core target for subunit vaccine design. Follow-up studies were deeply needed to analyze the structure-function interaction mechanism of Gc proteins to provide theoretical support for the construction of a new type of AKAV prevention and control system. Full article