Search Results (4,071)

The separation of rare earth elements (REEs) with similar chemical properties remains a relevant challenge today, most often addressed using liquid–liquid and solid-phase extraction with various chelating agents. Excellent complexing agents for REEs are 1,3-diketones and their analogs. We have for the first time proposed a method for preparing a material consisting of a covalently immobilized 3-acyl-4-hydroxycoumarin ligand on silica. For its synthesis, we employed a strategy based on the “click” reaction of 3-azidopropyl silica with a propargyl-containing coumarin–chalcone conjugate—this approach is the most tolerant and does not affect the coordinationally active fragment of the ligand. The material was characterized by thermal analysis, IR spectroscopy, and ¹³C NMR. The potential of the synthesized material for REE preconcentration was demonstrated at pH 5–5.5: high extraction efficiency for Gd(III), Dy(III), Er(III), Eu(III), Sm(III), and Yb(III) was observed, with fast adsorption kinetics (30 min) and extraction degrees of ~98%. Under unified conditions of static and dynamic extraction for Gd(III), Dy(III), Er(III), Eu(III), Sm(III), and Yb(III), affinity series toward the surface were obtained as a function of the distribution coefficient. It was shown that 10-fold molar excesses of Fe(III), Al(III), Cu(II), Ni(II), and Co(II) allow retention of more than 95% extraction for Dy(III) and Er(III). After adsorption of Dy(III) and Er(III), shifts in the carbonyl group absorption bands are visible in the IR spectra of the material, indicating a chelating mechanism of sorption. Additional studies are required for implementation in analytical and preparative REE separation schemes; however, preliminary data show that the material is a highly active adsorbent. Full article

Infectious pathogens pose serious threats to public health, necessitating the development of more antimicrobials. In this study, oligohydroxybutyrates were obtained through the catalyzed polymerization of β-butyrolactone using N, N-dimethyl-4-aminopyridine (DMAP) and aluminum isopropoxide [Al(OiPr)₃] and applied as sustainable antimicrobial agents. The poly3-hydroxybutyrate (PHB) oligomers exhibited broad-spectrum antibacterial activities against both Gram-negative (E. coli) and Gram-positive (S. aureus) model bacteria. Additionally, PHB oligomers displayed robust (inhibiting rate: >95%) and rapid (action time: <20 min) antiviral activity against three notorious single-stranded RNA viruses, that is, influenza A virus (H1N1 and H3N2) and coronavirus (SARS-CoV-2). In particular, a comprehensive set of advanced experimental characterizations, including FT-IR, ¹H- and ¹³C-NMR, and H-ESI-MS/MS, was applied to analyze their chemical structures. The results confirmed the loss of terminal hydroxyl groups in the PHB intermediate and end products associated with theoretical calculations. These findings will also help provide deep insight into the major chain growth mechanism during the synthesis of PHB. The structural variations, which were treated as unwanted side reactions, were identified as a pivotal factor by deactivating the terminal hydroxy during chain growth. Their effective sterilization properties and degradability endowed the as-prepared PHB oligomers with a promising biomedical potential, including for use as disinfectants, sanitizers, and antiseptics. Full article

Topaz is one of the most economically important fluorine-rich nesosilicates, which are predominantly colorless in natural crystals. Hence, the trade relies almost entirely on irradiated blue topaz with an unstable color center, which has been shown to fade over time. The cobalt (Co) diffusion treatment is a stable alternative process for converting colorless topaz to blue by a solid-state diffusion mechanism. To investigate the potential role of Co²⁺ substitution in the formation of the blue layer and the coupled behavior of F/OH dehydroxylation in facilitating this process, systematic diffusion treatments have been successfully conducted and compared. In this study, gem-quality topazes were annealed in air at 1000 °C for 20–40 h (hr) along with CoO, Fe₂O₃, Cr₂O₃, and CuO powders. The diffused products were characterized using Scanning Electron Microscope (SEM), Ultraviolet-Visible absorption spectroscopy (UV-Vis), Near-Mid Infrared spectroscopy (NMIR), and X-ray photoelectron spectroscopy (XPS). Parallel runs with CuO, Fe₂O₃, or Cr₂O₃ alone confirmed that none of these oxides produces a stable blue layer, underscoring the unique role of Co. The Co-diffused sample displays an intense blue layer characterized by a Co²⁺ octahedral isomorphism triplet at 540, 580, and 630 nm, which are absent from both untreated and heat-only controls. XPS analysis reveals the emergence of Co²⁺ (binding energy: 780.63 eV) and a concomitant depletion in F⁻, along with the disappearance of the OH overtone absorption at 7123 cm⁻¹. These observations confirm that defluorination generates octahedral vacancies accommodated by the coupled substitution: CoF₂ (solid reactant) + (AlO₂)⁻ (fragment of topaz structure) → AlOF (solid product) + (CoOF)⁻ (fragment of topaz structure). Prolonged annealing leads to decreased relative atomic percentages of K⁺ and F⁻ ions, consistent with volatilization losses during the high-temperature process, thereby directly correlating color intensity with cobalt valence state, which transfers from Co²⁺ to Co³⁺. These findings establish a Co-incorporation chronometer for F–rich aluminosilicate systems, with an optimal annealing time of approximately 20 hr at 1000 °C. Furthermore, the above results demonstrate that the color mechanism in nesosilicate gems is simultaneously governed by volatile release and cation availability. Full article

Hard anodic oxide coatings on aluminium have long been used to enhance surface functionality. However, increasing industrial demands are driving the need for coatings with superior hardness, wear resistance, corrosion resistance and self-lubricating properties. Due to their porous structure, anodic oxide coatings can be modified by incorporating various nanoparticles. The properties of the modified coatings depend on both the type of nanoparticles used and the method employed to incorporate them. In this study, anodic oxide coatings were produced using direct and duplex methods on a semi-industrial scale to enable process control and potential industrial implementation. The coatings were modified with hard (Al₂O₃) and soft (CaCO₃, PTFE) nanoparticles in order to customise their functional properties. Their microstructure and chemical composition were characterised by SEM and TEM. Their microhardness, abrasion resistance and electrochemical behaviour were also evaluated. Among the tested production methods and methods for modifying nanoparticles, the duplex process incorporating Al₂O₃ particles proved to be the most promising. Its optimisation resulted in coatings with a microhardness of 430 HV0.05 and a mass loss of 9.4 mg after the Taber abrasion test, demonstrating the potential of this approach for industrial applications. Full article

Conversion of carbon dioxide (CO₂) to methanol in a traditional reactor (TR) with catalytic packed bed faces the challenge of lower reactant conversion due to thermodynamic limitations. On the contrary, membrane reactors selectively remove reaction products, enhancing the conversion, but it is still limited, and existing designs face challenges of structural integrity and scale-up complications. Therefore, for the first time, a ceramic membrane microchannel reactor (CMMR) system was developed with 500 µm deep microchannels, incorporated with catalytic membrane for CO₂ conversion to methanol. Computational fluid dynamic (CFD) simulations confirmed the uniform flow distribution among the microchannels. A catalytic LTA zeolite membrane was synthesized with thin layer (~45 µm) of Cu-ZnO-Al₂O₃ catalyst coating and tested at a temperature of 220 °C and 3.0 MPa pressure. The results showed a significantly higher CO₂ conversion of 82%, which is approximately 10 times higher than TR and 3 times higher than equilibrium conversion while 1.5 times higher than conventional tubular membrane reactor. Additionally, methanol selectivity and yield were achieved as 51.6% and 42.3%, respectively. The research outputs showed potential of replacing the current industrial process of methanol synthesis, addressing the Sustainable Development Goals of SDG-7, 9, and 13 for clean energy, industry innovation, and climate action, respectively. Full article

This study investigates pristine and doped ZnO thin films fabricated via the sol-gel technique, aiming to address efficiency challenges when used as transparent conductive oxide (TCO) layers in thin-film solar cells. ZnO was first doped with aluminum (Al), and subsequently with both Al and reduced graphene oxide (rGO), to evaluate the individual and combined effects of these dopants. The optimal pH value for the ZnO structure was initially determined, with the film produced at pH 9 exhibiting the most favorable characteristics. Al doping was then optimized at a ratio of Al/(Al + Zn) = 0.2, followed by optimization of the graphene content at 1.5 wt%. In this context, the structural, optical, and electrical properties of pristine ZnO, Al-doped ZnO (AZO), and Al and graphene co-doped ZnO (Gr:AZO) thin films were systematically investigated. These films were integrated as TCO layers into Cu₂SnS₃ (CTS)-based thin-film solar cells fabricated via physical vapor deposition (PVD). The cell architecture employed an 80 nm pristine ZnO window layer, while the doped ZnO films (300 nm) served as TCO layers. To assess the influence of the chemically deposited top layers, device performance was compared against a reference cell in which all layers were fabricated entirely using PVD. As expected, the reference cell exhibited superior performance compared to the cell whose AZO layer deposited chemically; however, the incorporation of both Al and graphene significantly enhanced the efficiency of the chemically modified cell, outperforming devices using only pristine or singly doped ZnO films. These results demonstrate the promising potential of co-doped solution-processed ZnO films as an alternative TCO layer in improving the performance of thin-film solar cell technologies. Full article

In order to meet the ever-growing demand in modern power electronics, the advanced soft magnetic materials (SMMs) are required to exhibit both excellent soft magnetic performance and mechanical properties. In this work, the effects of an annealing treatment on the soft magnetic properties, mechanical properties and microstructure of the Fe_24.94Co_24.94Ni_24.94Al_24.94Si_0.24 high-entropy alloy (HEA) are investigated. The as-cast HEA consists of a body-centered cubic (BCC) matrix phase and spherical B2 nanoprecipitates with a diameter of approximately 5 nm, where a coherent relationship is established between the B2 phase and the BCC matrix. After annealing at 873 K, the alloy retains both the BCC and B2 phases, with their coherent relationship preserved; besides the spherical B2 nanoprecipitates, rod-shaped B2 nanoprecipitates are also observed. After the annealing treatment, the saturation magnetization (M_s) of the alloy varies slightly within the range of 103–113 Am²/kg, which may be induced by the precipitation of this rod-shaped nanoprecipitate phase in the alloy. The increase in the coercivity (H_c) of annealed HEA is due to the inhomogeneous grain distribution, increased lattice misfit and high dislocation density induced by the annealing. The nanoindentation result reveals that the hardness after annealing at 873 K exhibits a 25% improvement compared with the hardness of as-cast HEA, which is mainly due to dislocation strengthening and precipitation strengthening. This research finding can provide guidance for the development of novel ferromagnetic HEAs, so as to meet the demands for materials with excellent soft magnetic properties and superior mechanical properties in the field of sustainable electrical energy. Full article

Neurodegenerative diseases (NDDs), including Alzheimer’s disease (AD), Parkinson’s disease (PD), amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), are becoming more prevalent and still lack effective disease-modifying therapies (DMTs). However, translational efficiency remains critically low. For example, a ClinicalTrials.gov analysis of AD programs (2002–2012) estimated ~99.6% attrition, while PD programs (1999–2019) achieved an overall success rate of ~14.9%. In vitro platforms are assessed, ranging from immortalized neuronal lines and primary cultures to human-induced pluripotent stem cell (iPSC)-derived neurons/glia, neuron–glia co-cultures (including neuroinflammation paradigms), 3D spheroids, organoids, and blood–brain barrier (BBB)-on-chip systems. Complementary in vivo toxin, pharmacological, and genetic models are discussed for systems-level validation and central nervous system (CNS) exposure realism. The therapeutic synthesis focuses on AD, covering symptomatic drugs, anti-amyloid immunotherapies, tau-directed approaches, and repurposed drug classes that target metabolism, neuroinflammation, and network dysfunction. This review links experimental models to translational decision-making, focusing primarily on AD and providing a brief comparative context from other NDDs. It also covers emerging targeted protein degradation (PROTACs). Key priorities include neuroimmune/neurovascular human models, biomarker-anchored adaptive trials, mechanism-guided combination DMTs, and CNS PK/PD-driven development for brain-directed degraders. Full article

The green transformation of the shipping industry urgently requires zero-carbon power, and hydrogen-powered ships such as hydrogen fuel cell ships face bottlenecks in in situ hydrogen production and storage and transportation. Methanol steam reforming (MSR) online hydrogen production is suitable for ship scenarios, reducing costs and increasing efficiency while helping achieve zero carbon throughout the entire lifecycle, which has important practical significance. The key technology for MSR technology is the performance of the catalyst. A series of Cu_1−xMn_xAl₂O₄ catalysts were successfully synthesized and applied for hydrogen production in this study. The catalyst structure was characterized using physicochemical techniques including XRD, SEM, and EDS. Hydrogen production performance was evaluated in a fixed-bed reactor under the following conditions: a liquid hourly space velocity (LHSV) of 20 h⁻¹, a water-to-methanol molar ratio of 3:1, and a reaction temperature range of 275 °C–350 °C. The results demonstrate that A-site Mn substitution significantly enhanced the catalytic performance. In addition, XRD analysis revealed that Mn incorporation effectively suppressed the formation of segregated CuO phases. However, excessive substitution (x is 0.9) led to the generation of an MnAl₂O₄ impurity phase. Finally, the Cu_0.7Mn_0.3Al₂O₄ catalyst achieved a methanol conversion of 68.336% at 325 °C, with a hydrogen production rate of 5.611 mmol/min/g_cat, and maintained CO selectivity below 1%. The results demonstrate that the hydrogen production catalyst developed in this study is a promising material for meeting the requirements of online hydrogen sources for ships. Full article

Tea plants (Camellia sinensis) uniquely hyperaccumulate fluoride (F) and concurrently exhibit a preference for ammonium nitrogen (NH₄⁺-N) over nitrate nitrogen (NO₃⁻-N). However, the mechanistic basis for co-existence of NH₄⁺-N preference and F hyperaccumulation in C. sinensis remains unexplored. Here, we investigated F accumulation and translocation with varying N supplies (0 mM and 2.854 mM N with NH₄⁺-N:NO₃⁻-N ratios of 3:1, 4:0 and 0:4) and F concentrations (0, 8 and 16 mg·L⁻¹ NaF) to reveal the mechanism driving NH₄⁺-N preference and F hyperaccumulation in C. sinensis. Results show that NH₄⁺-N supply enhanced H⁺ efflux, mobilizing aluminum (Al) to form mobile Al-F complexes for translocation to shoots, thereby alleviating F toxicity in roots. This process was facilitated by transporters including CsCLCd, CsCLCe, CsCLCf2 and CsFEX. In contrast, NO₃⁻-N promoted root sequestration of F as immobile calcium (Ca)-F complexes, exacerbating damage. Under NO₃⁻-N supply, CsCLCb primarily mediated NO₃⁻ transport, while CsCLCc, CsCLCe, CsCLCf1, CsCLCf2 and CsFEX were involved in F transport. In leaves, CsCLCd, CsCLCe, CsCLCf1, CsCLCf2, CsCLCg and CsFEX mediated vacuolar sequestration under both N conditions. These findings elucidate that NH₄⁺-N preference is mechanistically linked to F hyperaccumulation through an Al-assisted translocation pathway, which confers tolerance by exporting F from roots. Full article

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

Through the mechanical analysis of AlCoCrFeNi thin-walled high-entropy alloy materials fabricated by plasma arc additive manufacturing, this study examines the practical application prospects of plasma arc manufacturing technology for thin-walled high-entropy alloys and explores its future development directions. Using a plasma arc oscillation process, a 50-layer fine additive experiment was conducted on AlCoCrFeNi high-entropy alloy materials employing both reciprocating and layer-by-layer accumulation methods. The samples were analyzed for overall appearance, microstructure, hardness, and tensile properties. The results indicate that the proportions of columnar and intergranular dendrites in the thin-walled high-entropy alloy specimens are similar, and the columnar dendrites exhibit a uniformly sized cross shape. The variation in Vickers microhardness along the horizontal direction shows lower strength at the edge positions, gradually increasing with horizontal distance. A comparison of the alloy’s transverse and longitudinal tensile specimens revealed that samples parallel to the deposition direction exhibit more regular structural arrangements, while specimens perpendicular to the deposition direction show unavoidable stress concentration at the deposition sites during tensile testing. With the increase in the height of the longitudinal specimens, the FCC structures in the alloy are significantly refined, the organizational arrangement becomes more regular, and the elongation increases. This study elucidates the plasma arc preparation technique for thin-walled high-entropy alloy materials, which is expected to achieve precise control over material composition, accurate observation of grain refinement, and uniform distribution of Vickers hardness, thereby enhancing the mechanical properties and thermal stability of the materials, with promising applications in aerospace, energy, and industrial fields. Full article

Recent studies have shown that the use of non-Saccharomyces yeasts, either alone or in co-fermentation with Saccharomyces cerevisiae, can enhance the development of specialty beers with distinctive compositional characteristics. This study aimed to evaluate the main compositional and sensory differences between American Pale Ale (APA) beers produced using the commercial strain S. cerevisiae US-05 as a single starter (Test 1), and those produced through sequential inoculation with Metschnikowia pulcherrima 62 followed by S. cerevisiae US-05 (Test 2). Analyses focused on key chemical parameters and volatile compounds at the end of primary fermentation (F1) and after 20 days of refermentation at 20 °C (F2). After F1, Test 2 samples showed higher concentrations of glycerol and higher alcohols (isoamyl alcohol, benzeneethanol) and lower concentrations of esters (isoamyl acetate, ethyl hexanoate, ethyl octanoate) compared to Test 1. After F2, the differences in higher alcohol content became less significant, whereas ester concentrations, particularly ethyl acetate and ethyl octanoate, were significantly higher in Test 2. Sensory evaluation revealed that beers from Test 2 exhibited more pronounced floral and fruity notes and achieved higher overall scores in the panel assessment. These findings indicate that sequential inoculation with M. pulcherrima 62 followed by S. cerevisiae enhances both the chemical complexity and sensory appeal of APA beers, highlighting the strain’s potential as a valuable tool for developing specialty beers with unique aromatic profiles. Full article

In this paper, a series of Co-free FeCr_0.6Ni_0.6(AlSi)_x (x = 0, 0.1, 0.12, 0.14, 0.16) high-entropy alloys (HEAs) were designed and fabricated by suction casting, and the effects of equi-molar (Al, Si) co-addition in these Fe-rich Fe-Cr-Ni-based HEAs on microstructure, mechanical properties, and corrosion resistance were systematically investigated. It is found that equi-molar (Al, Si) co-addition could cause the phase formation from FCC to FCC + BCC, while the morphologies of the phases change from dendrite-type to sideplate-type. Moreover, trade-off between strength and plasticity occurs with the increase in (Al, Si) co-addition, and the production of ultimate tensile strength and plasticity reaches the highest value when x = 0.12, while there exists a narrow region for x values to realize excellent comprehensive mechanical properties. In addition, similar corrosion resistance in 3.5 wt.% NaCl solution higher than 316L stainless steel could be realized in the HEAs with x = 0.12 and 0.14, while the latter one is slightly lower in pitting corrosion and the width of passive region, which is possibly caused by the increase in the density of phase boundaries. This work provides a novel insight on designing high-performance cost-effective Fe-rich and (Al, Si)-containing (Fe-Cr-Ni)-based HEAs combining high mechanical properties and corrosion resistance. Full article