Search Results (725)

The structural origin of the germanate anomaly in glasses, which involves complex Ge–O coordination environments, is frequently studied using crystalline analogs. This study aims to provide reliable spectroscopic fingerprints by performing a detailed structural and thermal analysis of crystalline A₄Ge₉O₂₀ model systems with A = Li, Na, K. The compounds were synthesized via melt crystallization and characterized using powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), and Raman spectroscopy techniques. The results demonstrate clear cation-dependent crystallization pathways. The Li-containing system predominantly forms Li₂Ge₇O₁₅ in mixture with Li₄Ge₉O₂₀, indicating a preference for thermodynamically stable phases. The Na-system successfully yields the target Na₄Ge₉O₂₀ compound. In contrast, the K-system primarily produces the likely metastable K₂Ge₄O₉ phase with a significant amorphous fraction, highlighting the role of kinetic limitations. This comparative study demonstrates that the size of the alkali cation is a critical factor for controlling phase formation under identical stoichiometric and thermal conditions. Full article

Cryotherapy and radiofrequency (RF) treatments modulate tissue temperature to induce therapeutic effects; however, improper application can result in thermal injury. Traditional temperature-based monitoring methods rely on multiple thermal sensors whose accuracy strongly depends on their number and spatial positioning, often failing to detect early tissue crystallization. This study introduces a fractional order bioimpedance modelling framework for the early detection of tissue freezing during cryogenic and thermal medical treatments, with the feasibility and effectiveness of this approach having been reported in our prior publications. While bioimpedance spectroscopy itself is a well-est. The corresponablished technique in biomedical engineering, its novel application to predict and identify premature freezing events provides a new pathway for safe and efficient energy-based therapies. Fractional-order models derived from the Cole family accurately reproduce the complex electrical behavior of biological tissues using fewer parameters than classical integer-order models, thus reducing both hardware requirements and computational cost. Experimental impedance data from human abdominal, gluteal, and femoral regions were modelled to extract fractional parameters that serve as sensitive indicators of phase-transition onset. The results demonstrate that the proposed approach enables real-time identification of freezing-induced electrical transitions, offering a physiologically grounded alternative to conventional temperature-based monitoring. Furthermore, the fractional order bioimpedance method exhibits high reproducibility and selectivity, and its analytical figures of merit, including the limits of detection and quantification, support its use for reliable real-time tissue monitoring and early injury detection. Overall, the proposed fractional order bioimpedance framework enhances both safety and control precision in cryogenic and thermal medical applications. Full article

With the rapid depletion of natural graphite, the synthesis of artificial graphite from high-carbon precursors has garnered growing interest. However, conventional artificial graphitization typically requires extremely high temperatures. This study demonstrates that natural halloysite mineral can serve as an effective catalyst to lower the graphitization temperature threshold of anthracite. The results show that halloysite exerts a pronounced catalytic effect within the temperature range of 1400–2300 °C. The enhancement in graphitization is primarily attributed to the formation and subsequent decomposition of intermediate phases between halloysite and the carbon matrix. From 1400 to 1700 °C, the interlayer spacing decreases significantly with halloysite as a catalyst due to the nucleation of highly ordered “multilayer graphene” structures surrounding intermediates. However, these graphene layers exhibit a confined and curved morphology that spatially restricts crystallite growth, resulting in relatively small in-plane (L_a) and stacking (L_c) crystallite dimensions. Moreover, multilayer graphene originating from intermediate crystal corners tends to generate numerous dislocation defects. From 1700 to 2300 °C, significant increases in both L_a and L_c are observed, accompanied by a marked improvement in structural order. This evolution is driven by the progressive inward decomposition of intermediate phases, which causes the “circular-shaped” graphene domains to collapse at the dislocation defects and subsequent straightening of the curved graphene layers. These findings provide new microstructural insights into mineral-catalyzed graphitization mechanisms in anthracite and present a promising pathway toward energy-efficient production of synthetic graphite. Full article

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

Multilayer liquid crystal devices can offer enhanced optical functionalities for augmented reality and photonic applications, but fabrication remains severely limited by solvent incompatibility between photoalignment materials and underlying polymerized layers. Conventional photoalignment agents use aggressive solvents like N,N-dimethylformamide that damage polymerized substrates, necessitating protective interlayers. This study demonstrates a water-soluble photoalignment approach using AbA-2522 that eliminates these fabrication barriers. The water-soluble alignment material enables direct multilayer processing without layer damage while maintaining alignment quality equivalent to conventional materials. We successfully fabricate compact transmissive devices integrating liquid crystal polarization gratings with quarter-wave plates, achieving a first-order diffraction efficiency of 65.4% for 9 μm period gratings for linearly polarized incident light (λ = 457 nm). The multilayer structure exhibits highly selective polarization-dependent diffraction with efficiency ratios exceeding 10:1 between preferred and suppressed orders, eliminating external polarization control elements. Polarized optical microscopy confirms excellent alignment uniformity, while the fabrication process offers environmental benefits and reduced complexity. This approach establishes a practical pathway for advanced multilayer photonic devices critical for next-generation augmented reality systems and photonic integration, addressing fundamental challenges that have limited multilayer liquid crystal device development. Full article

To address the challenge of treating refractory organic dyes in textile wastewater, this study synthesized a novel copper-based composite material (designated MEL-Cu-6HNA) via a supramolecular self-assembly–pyrolysis pathway. Its core component consists of CuO/Cu₂O(SO₄), which was applied to efficiently degrade the Reactive Red 3BS dye within a sodium bicarbonate-activated hydrogen peroxide (BAP) system. This material was applied to degrade the Reactive Red 3BS dye using a sodium bicarbonate-activated hydrogen peroxide system. The morphology, crystal structure, and surface chemistry of the material were systematically characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Electron paramagnetic resonance (EPR) was employed to identify reactive species generated during the reaction. The effects of dye concentration, H₂O₂ concentration, MEL-Cu-6HNA dosage, and coexisting substances in water on degradation efficiency were systematically investigated, with active species identified via EPR. This study marks the first application of the supramolecular self-assembled CuO/Cu₂O(SO₄)₂ composite material MEL-Cu-6HNA, prepared via pyrolysis, in a sodium bicarbonate-activated hydrogen peroxide system. It achieved rapid and efficient decolorization of the recalcitrant Reactive Red 3BS dye. The three-dimensional sulfate framework and dual Cu²⁺ sites of the material significantly enhanced the degradation efficiency. MEL-Cu-6HNA achieved rapid and efficient decolorization of the recalcitrant Reactive Red 3BS in a sodium bicarbonate-activated hydrogen peroxide system. The material’s three-dimensional sulfate framework and dual Cu²⁺ sites significantly enhanced interfacial electron transfer and Cu²⁺/Cu⁺ cycling activation capacity. ·OH served as the primary reactive oxygen species (ROS), with SO₄²⁻, ¹O₂, and ·O₂⁻ contributing to sustained radical generation. This system achieved 95% decolorization within 30 min, demonstrating outstanding green treatment potential and providing a reliable theoretical basis and practical pathway for efficient, low-energy treatment of dyeing wastewater. Full article

Dimethyl sulfoxide (DMSO) is widely utilized in the vitrification of oocytes, but DMSO exhibits concentration-dependent toxicity, which can compromise oocyte developmental potential by disrupting key cellular processes. This study reports the first successful use of cold shock protein B (CspB protein) as a substitute for DMSO in vitrification solutions for oocyte vitrification. Combining dynamics simulations and experimental validation, we demonstrated CspB’s ability to inhibit ice crystallization and recrystallization by stabilizing its position at the ice–water interface and reducing ice formation rates. Recombinant CspB was successfully expressed and shown to bind to the oolemma. In vitrification solutions, CspB (1–2 mg/mL) effectively reduced ice crystal size and enabled a significant reduction or complete replacement of DMSO. This strategy markedly improved the post-thaw survival rates of both mouse and bovine metaphase II (MII) oocytes. Furthermore, oocytes vitrified with an optimized formulation (15% ethylene glycol + 2 mg/mL CspB) exhibited developmental competence (cleavage and blastocyst rates), oxidative stress markers (ROS, GSH), mitochondrial function (membrane potential and content), and apoptosis levels (Caspase-3/9) comparable to those treated with a standard DMSO-containing system. Transcriptomic analysis revealed that CspB’s cryoprotection involves the modulation of the mTOR signaling pathway. This role was functionally confirmed, as activation of mTOR abolished CspB’s beneficial effects, reinstating oxidative damage, mitochondrial dysfunction, and apoptosis. Thus, the CspB protein replaces DMSO with direct ice crystal formation suppression and mTOR-mediated oxidative stress regulation. This study offers a protein-based alternative to conventional permeable cryoprotectants. This approach holds promise for improving reproductive biotechnologies across species. Full article

Catalytic dry reforming of ethanol offers a sustainable pathway for syngas and hydrogen production through CO₂ utilization, though its efficiency depends heavily on the strategic synthesis of catalysts and the optimization of reaction parameters. This study employs Box–Behnken Design (BBD) and Response Surface Methodology (RSM) to optimize hydrogen yield from CO₂ reforming of ethanol over a Yttrium-promoted Ni-Co/MCM-41 catalyst. The catalyst was synthesized using sequential wet impregnation method and characterized for its physicochemical properties. The catalyst was tested in fixed-bed reactor using experimental data obtained from BBD considering the effects of temperature (550–700 °C), ethanol flowrate (0.5–1 mL/min) and CO₂ flowrate (15–30 mL/min) on the hydrogen yield. The experimental conditions were optimized using RSM quadratic model. The characterization revealed that the ordered mesoporous nature of the MCM-41 is maintained providing a high surface area of 597.75 m²/g for the catalyst. The addition of Yttrium as a promoter facilitates the formation of well crystallized nanoparticles. Maximum hydrogen yield of 85.09% was obtained at 700 °C, 20.393 mL/min and 0.877 mL/min for temperature, CO₂ and ethanol flowrate, respectively. The predicted hydrogen yield obtained is strongly correlated with the actual values as indicated by R² of 0.9570. Full article

Bacterial urinary tract infections (UTIs) are common in dogs and cats. This study examined the correlations between routine urinalysis and culture-confirmed infections and described the etiologic agents and antimicrobial susceptibility to support stewardship. In 2023, 1787 urine samples (854 dogs, 933 cats) underwent urinalysis, aerobic culture with species identification, and disk-diffusion testing per Clinical and Laboratory Standards Institute standards; non-parametric statistics with effect sizes were applied. Pyuria was the strongest correlate of infection in both species. Low urine specific gravity was associated with infection and crystal detection, and urine pH correlated weakly with growth in dogs. Nitrite positivity was strongly associated with infection in dogs but showed no diagnostic value in cats. Hematuria showed a weak inverse association in dogs and no association in cats. Females and older animals were more frequently infected, and infections were slightly more common in summer. Most episodes were monomicrobial (85%), predominantly caused by Escherichia coli (48.4% of dogs; 51.5% of cats). E. coli remained broadly susceptible to nitrofurantoin and aminoglycosides. Fluoroquinolone activity was variable. Pseudomonas spp. showed the highest susceptibility to ceftazidime, cefepime, and aminoglycosides. These findings support culture when pyuria, dilute urine, or nitrite positivity is detected and favour short, targeted empiric therapy pending results, guided by a stepwise clinical decision pathway. Full article

The optical and vibrational responses of Gd₃Ga₅O₁₂ (GGG) single crystals to 147 MeV Kr-ion irradiations were systematically investigated to clarify defect formation pathways and their influence on luminescence mechanisms. Absorption spectra measured at room temperature reveal a stepwise redshift of the fundamental edge and the progressive development of a broad sub-band-gap tail between 4.4 and 5.3 eV, indicating the accumulation of F- and F⁺-type oxygen-vacancy centers and increasing structural disorder. Raman spectroscopy shows that, despite substantial track overlap at fluences up to 10¹⁴ ions/cm², the crystal preserves its phonon frequencies and linewidths, while peak intensities decrease due to a growing disordered volume fraction. Low-temperature (13 K) photoluminescence demonstrates the persistence of a dominant broad band near 2.4 eV and the emergence of an additional irradiation-induced band at ~2.75 eV whose width increases with fluence, reflecting the formation of vacancy-related defect complexes. Excitation spectra transform from band-edge-dominated behavior in the pristine crystal to defect-tail-mediated excitation in heavily irradiated samples. These results provide a consistent spectroscopic picture of ion-track-induced disorder in GGG and identify the defect states governing its luminescence under extreme irradiation conditions. Full article

The ongoing expansion of industrial operations has resulted in the generation of a large amount of high-salinity wastewater with complex compositions. The direct discharge of this wastewater poses significant threats to ecosystems and leads to the loss of valuable salt resources, for example, triggering freshwater salinization syndrome and mobilizing heavy metals to form toxic “chemical cocktails”, leading to the loss of valuable salt resources. Desalination of high-salinity wastewater primarily involves two key processes: concentration and crystallization, whereby a concentrated brine is first obtained through membrane-based or thermal methods, followed by salt recovery via crystallization. This review begins by employing a bibliometric analysis to map the knowledge structure and trace the evolution of research trends, revealing that “membrane-thermal integration” has become a dominant research hotspot since 2020. It then provides a systematic examination of advanced treatment technologies, chronicling the progression from early biological methods to contemporary membrane-based and thermal desalination approaches. A specific analysis of the influence of salinity on membrane scaling is also included. Consequently, this paper critically assesses the prospects and challenges of several alternative desalination technologies and proposes that integrated processes, combining membrane-based and thermal desalination, represent a highly promising pathway for achieving zero liquid discharge (ZLD). Finally, we suggest that future research should prioritize the development of key functional materials, explore efficient hybrid physiochemical–biochemical processes, and advance emerging technologies, aimed at enhancing treatment efficiency and reducing operational costs. Full article

The reusability of enzymes is a fundamental aspect of sustainable biotechnology and the development of biosensors. This study presents one of the first quantitative evaluations of DNA polymerase reusability by utilizing integrated quartz crystal microbalance (QCM) kinetics and real-time monitoring of exonuclease activity. The results showed that immobilized T7 DNA polymerase retained approximately 50% of its initial activity after three 90-min cycles and around 20% after five cycles. Significantly lower activities were observed for shorter, 45-min cycles. This indicates an unexpected time-dependent enhancement in stability for longer reaction times. The findings suggest a promising trend in enzyme stability and reusability, establishing a quantitative relationship between reaction duration and enzyme performance. This relationship offers a scalable pathway for the regeneration of biosensors and for sustainable enzymatic catalysis. Additionally, the work provides a transferable framework that can be applied to other DNA-processing enzymes, which supports long-term biosensor performance and industrial biocatalysis. The demonstrated approach offers a transferable and scalable methodology for the development of reusable polymerase-based biosensors and sustainable biocatalytic systems. Full article

Lithium is an essential material for lightweight batteries. Traditional mining of soluble salts expanded to include the extraction of hard rocks, which requires their solubilization through roasting. Among hard lithium rocks, spodumene has recently received attention from the scientific community. Its metallurgical processing can be classified according to the type of reagents, as well as the operating temperature and pressure. The use of calcium carbonate as a natural alkali avoids aggressive chemicals such as sulfuric acid or caustic soda. In this article, 0.5 g of jewelry-grade spodumene was loaded into a ceramic crucible with 2.5 g of reducing agent in a tandem of roasting at 1050 °C-1 bar-30 min and leaching with neutral water at 90 °C-1 bar-20 min at a water/clinker mass ratio of 25. Measurements by XRD, ICP-OES, and SEM-EDX suggest a pathway of spodumene cracking because of poor contact with the reductant. Potassium present in the crucible acts as a flux and encapsulates spodumene crystals, causing lithium to end up bound to silica. While lithium metasilicate is barely soluble in water, leaching potassium aluminate hoards in the liquid. The empirical observations were supported with thermodynamic spontaneity studies, which required compiling the mineral properties based on open reference tabulations. Full article

The Mianhuakeng deposit, located within the Zhuguangshan batholith in the Nanling area, is currently recognized as the largest granite-related uranium deposit in China. A portion of the uranium ore bodies is spatially associated with NE-trending mafic veins within the granite. In this study, the field investigation, zircon U-Pb dating, S and Pb isotope analysis, and whole-rock geochemical analysis were conducted on these mafic veins to explore their crystallization age, petrogenesis, tectonic setting, and relationships with uranium mineralization. The weighted mean result of zircon U-Pb is 189 ± 3 Ma, suggesting that the mafic dyke was crystallized during the Early Jurassic. The whole-rock geochemistry and isotopes exhibit characteristics of intraplate basalts, suggesting that the mafic dykes originate from an enriched mantle source consisting of garnet–spinel lherzolite, with an estimated partial melting of 1%–5%. Mafic magmas underwent low-degree contamination from the lower crust during upwelling, induced by the extension of the lithosphere during the Early Jurassic. The analyses of pyrite sulfur isotopes in mafic samples vary between −2.9‰ and 1.8‰, significantly different from that of pyrite (−14.4‰ to −7.8‰) formed during the uranium mineralization. Furthermore, the ages of the pitchblende of 127–54 Ma are much younger than the crystallization ages of mafic dykes, indicating that the mafic magmas did not contribute to the uranium mineralization of Mianhuakeng deposit during magmatism. However, the abundant reducing minerals (e.g., pyrite, hornblende, and Fe²⁺-bearing minerals) in the mafic dykes can act as a redox barrier, reducing mobile U⁶⁺ to immobile U⁴⁺ during fluid–rock interaction, thereby facilitating uranium precipitation from the hydrothermal ore-forming fluids. The secondary fractures created by the intrusion of mafic magma probably provided favorable pathways for the movement of hydrothermal fluids. Full article

Coordination polymers (CPs) are garnering attention in the field of medicine day by day. The goal is to develop a CP with biosafe and environment-friendly characteristics. Herein, we report two such novel 3D coordination polymers of zinc-inosine-5′-monophosphate (Zn-IMP) and bpe/azpy (as linkers) which were engineered as metal–organic frameworks that can be used as drug carriers for hydroxyurea (HU). We employed SCXRD, PXRD, solid-state CD, FTIR and TGA for crystal structure characterizations; the results achieved 3D coordination polymers which contain a P2₁ space group with chiral distorted tetrahedral geometry. Solution phase studies like UV–vis and CD were carried out to understand mechanistic pathways for interaction and chirality, respectively. We have also performed computational studies to evaluate the drug delivery capacity of both 3D CPs. Molecular docking and multi-pH molecular dynamics (MD) quantify that HU binds more strongly with CP−1 (ΔG =−10.87 ± 0.12) as compared to CP−2 (ΔG = −7.59 ± 0.26 kcal·mol⁻¹), at normal and basic pH. MD simulation analysis indicated that a more compact and rigid cavity is observed by CP−1 as compared to CP−2 at physiological pH. Across acidic pH, for CP−1 the ligand RMSD increases markedly and U becomes slightly less negative, which indicated partial loss of contacts, thus releasing drugs in a tumor-like environment more easily. These result showed that CP−1 offers stronger binding, higher structural stability and a more pronounced pH-responsive release profile than CP−2, making CP-1 more promising candidate for targeted HU drug delivery, while CP−2 may serve as a weaker-binding, faster-release complement. Full article