Search Results (822)

To address the issues of high wastewater treatment costs and the lack of recycling associated with conventional precipitants such as oxalic acid and ammonium bicarbonate in rare earth precipitation processes, this study proposes a novel gradient alkali conversion–carbonation method based on a green process coupling “rare earth chloride alkali conversion-carbonation with sodium chloride electrolysis.” The primary scientific objective is to elucidate the crystallization mechanism and to achieve controlled preparation of high-quality lanthanum carbonate. By gradient-controlling the addition sequence and rate of alkali liquor and CO₂, lanthanum carbonate tetrahydrate was successfully synthesized. Characterization by XRD, SEM, ICP, and laser particle size analysis indicates that the product prepared by the gradient alkali conversion–carbonation method exhibits a single phase with high crystallinity, as evidenced by sharp and clear XRD diffraction peaks. Furthermore, the median particle size of the product obtained via this method is relatively large, reaching approximately 10 μm, while the particle size distribution Span value remains around 1.0. Mechanistic studies suggest that this method effectively regulates the crystallization process by precisely controlling the introduction and slow dissolution of the La(OH)₃ precursor, thereby reducing the supersaturation of the system during carbonation and facilitating the dissolution–reprecipitation of La³⁺. This work provides a theoretical basis for the preparation of high-quality rare earth carbonates and a process reference for the green recycling route. Full article

Background/Objectives: This study addresses the need for scalable and predictive strategies linking mixing conditions to nanocarrier properties by developing and analyzing a coaxial jet antisolvent process for the continuous production of pharmaceutical nanocarriers. Methods: A single experimental platform was used to generate both curcumin-based nanoparticles and nanoliposomes, enabling direct comparison of how mixing regime and formulation variables influence product characteristics. Results: Fluid-dynamic behavior was first characterized using tracer and micromixing experiments, revealing a strong dependence of mixing time on flow conditions, with characteristic mixing times decreasing from >1000 ms under laminar conditions to approximately 10–30 ms in turbulent regimes. Nanoparticles and liposomes obtained under optimized conditions exhibited mean sizes in the range of 120–250 nm, with polydispersity indices typically below 0.2 under optimized turbulent conditions. To rationalize these observations, a computational framework was implemented, combining Reynolds-averaged computational fluid dynamics with a population balance formulation solved by the method of moments. The model provided spatially resolved insight into solvent exchange, supersaturation development, and nucleation–growth dynamics, showing good agreement with experimental trends and capturing the effect of mixing conditions on particle size across different regimes. Conclusions: Although simplified, the modeling approach establishes the basis for future extensions toward full population-balance distribution simulations capable of predicting complete particle size distributions, highlighting the ability of the coaxial jet mixer to control supersaturation and particle formation through tunable hydrodynamic conditions. This capability makes the system particularly attractive compared to conventional batch or less controllable mixing technologies, enabling a more rational and scalable design of pharmaceutical nanocarriers, with good encapsulation performance as discussed in the main text. Full article

Nephrocalcinosis, defined as the deposition of calcium salts within the renal parenchyma, represents a radiologic and pathologic endpoint shared by a broad spectrum of metabolic and monogenic disorders. Advances in genomic medicine have identified more than 30 genes involved in tubular transport, mineral and acid–base homeostasis, oxalate metabolism, mitochondrial function, ciliary signaling, and nephron development, reframing nephrocalcinosis as a heterogeneous manifestation of discrete molecular defects rather than a single disease entity. Despite this diversity, these conditions converge on common physicochemical pathways of tubular supersaturation, crystal nucleation, growth, and intrarenal retention. These processes are amplified by the intrinsic vulnerability of the renal medulla—characterized by hyperosmolality, hypoxia, and slow tubular flow—and by epithelial injury, loss of crystallization inhibitors, and impaired ciliary signaling. Distinct genotype–phenotype signatures, including age at onset, biochemical profiles, and extrarenal manifestations, provide important diagnostic clues and help differentiate major monogenic entities. The increasing availability of targeted gene panels, whole-exome sequencing, and whole-genome sequencing has substantially improved diagnostic yield, particularly in pediatric populations. Molecular diagnosis now directly informs therapeutic decision-making and long-term management, enabling a shift toward precision nephrology. This narrative review integrates genetic, mechanistic, and clinical perspectives to illustrate how molecular diagnosis reshapes the evaluation, prognosis, and treatment of nephrocalcinosis. Full article

Under the conditions of laser power of 1500 W, scanning speed of 5 mm/s, spot diameter of 3.5 mm, and powder feeding rate of 10 r/min, this study systematically investigated the influence of different tempering temperatures (200 °C and 600 °C) on the microstructure, friction and wear properties, and corrosion resistance of laser cladding Ni25 coatings, as well as the underlying mechanisms. The phase composition, microstructure, chemical composition, wear resistance, and corrosion resistance of the coatings were characterized and analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), pin-on-disk friction and wear tests, and electrochemical workstations. The results showed that the as-clad coating was composed of γ-Ni supersaturated solid solution and various metastable borides/carbides (such as Cr₃B₄), presenting fine-grained and non-equilibrium features. Tempering at 200 °C mainly achieved stress relaxation, enhancing and shifting the diffraction peaks to the left without changing the phase composition, while tempering at 600 °C drove significant diffusion-type phase transformation, leading to the decomposition of metastable Cr₃B₄ and the precipitation of stable phases such as Ni₂Si, accompanied by grain growth and microstructure coarsening. Friction tests indicated that the coating tempered at 600 °C exhibited the lowest average friction coefficient (0.679) and wear volume (0.0582 mm³) due to stable microstructure and hard phase strengthening, demonstrating the best wear resistance. However, electrochemical tests revealed a “trade-off” effect: the fine-grained microstructure of the as-clad coating, with its uniform composition, had the lowest corrosion current density (8.10 × 10⁻⁵ A/cm²) in 3.5% NaCl solution, showing the best resistance to uniform corrosion, while tempering, especially at 600 °C, caused grain growth, coarsening of the second phase, and micro-galvanic effects, slightly reducing the anodic dissolution resistance and increasing the corrosion current. This study clarified that heat treatment can significantly enhance the mechanical and tribological properties of Ni25 coatings by regulating their transformation from metastable to stable states, but at the potential cost of some corrosion resistance, providing a theoretical basis for optimizing post-treatment processes for different service conditions (wear resistance or corrosion resistance). Full article

The microstructure of a high-manganese low-activation austenitic steel after aging for 500 and 1000 h at 700 °C was investigated using transmission and scanning electron microscopy. Two structural states were examined: cold rolling (CR) and high-temperature thermomechanical treatment (HTMT). After CR, aging leads to the precipitation of dispersed M₂₃C₆ carbides (M = Cr, W), primarily along grain and deformation twin boundaries. After HTMT, these particles are mainly localized at grain and low-angle boundaries. With increasing aging time, both the size and volume fraction of the particles increase. In both states, the microtwin and substructure are partially retained after aging. Local regions corresponding to the early stages of recrystallization were identified after both treatments. These regions were associated with intense decomposition of the supersaturated solid solution and the coarsening of carbide particles. The mechanical properties were evaluated by tensile testing at 20, 650, and 700 °C. Aging reduced average ductility after both treatments and at all test temperatures, with this trend persisting with increasing aging time. After CR and aging, a significant scatter in elongation to failure was observed, with minimum values of ≈2–3%. This behavior is attributed to the high density of plate-like M₂₃C₆ carbides at grain and microtwin boundaries. Microcrack formation and intercrystalline fracture features were observed, directly linked to the high density of boundary carbides. These effects were less pronounced in the HTMT condition after aging. In this paper, strategies for suppressing carbide precipitation in high-manganese low-activation austenitic steels via chemical composition and thermomechanical processing optimization are discussed. Full article

This study characterizes the hydrochemistry and geochemical signature of the Upper Cretaceous geothermal aquifer in the Zharkunak zone (Eastern Ili Depression, SE Kazakhstan) using certified analytical datasets from five deep wells (5539, 1-RT, 3-T, 1-TP, and 2-TP). The waters are hyperthermal (89–103 °C), alkaline (pH 8.1–9.0), and weakly mineralized (TDS 0.3–1.0 g/L), with sodium-dominated facies ranging from Na–HCO₃–SO₄ to Na–SO₄–Cl. Hydrochemical analysis indicates that water–rock interaction and cation exchange are the primary controls on fluid evolution, with limited influence from evaporation or external salinity sources. Elevated fluoride (up to ~10 mg/L) and dissolved silica (H₂SiO₃, often >50 mg/L) reflect prolonged high-temperature interaction with silicate-rich lithologies under low Ca²⁺ conditions. Trace elements and radon activity (up to 0.32 nCi/L) further support deep, fault-controlled circulation pathways. PHREEQC modeling indicates near-equilibrium to slight supersaturation with respect to silica phases, suggesting a potential risk of silica scaling during cooling, while carbonate scaling remains limited. Although the dataset is based on discharge conditions from a limited number of wells, the results demonstrate that the Zharkunak system has strong geothermal utilization potential, with management considerations related to fluoride, radon, and silica scaling. Future work should focus on integrating isotopic analyses and reactive transport modeling to better constrain subsurface processes and long-term system behavior. Full article

Gypsum (CaSO₄·2H₂O) crystallization is highly sensitive to the supersaturation pathway, which governs the balance between nucleation and crystal growth and ultimately controls growth morphology. In this study, gypsum was synthesized via two contrasting routes—diffusion-controlled crystallization and rapid precipitation—using identical reactant systems to enable a direct comparison of distinct kinetic regimes. A polycarboxylate-based superplasticizer was incorporated to investigate pathway-dependent additive effects. Time-resolved observations reveal that rapid precipitation is characterized by high nucleation density under steep supersaturation, whereas diffusion-controlled crystallization proceeds under gradually increasing supersaturation with restricted nucleation and sustained anisotropic growth. Powder X-ray diffraction confirms the formation of phase-pure gypsum under all conditions. Scanning electron microscopy shows that the presence of the superplasticizer reduces crystal number density and modifies crystal habit in both pathways, although the extent and manifestation of these effects depend strongly on the governing kinetic regime. Under diffusion-controlled conditions, the increasing superplasticizer dosage promotes the transition from elongated to more tabular morphologies, while rapid precipitation results in dense, intergrown aggregates under high supersaturation. Overall, the results demonstrate that the effectiveness of the superplasticizer is not intrinsic but depends on the crystallization pathway. These findings provide new insight into how supersaturation profiles mediate the interplay between additive interactions and growth processes, enabling improved control over gypsum crystal morphology. Full article

Nanofiltration (NF) is increasingly applied for advanced drinking water treatment, but achieving stable operation at high recovery rates remains challenging for surface waters with high scaling potential. This pilot study investigated the performance and optimization of a three-stage NF270 system (4:2:1 tapered array) for treating coagulated surface water in northern Jiangsu, China, aiming to identify sustainable operating conditions for high-recovery applications. The NF system was operated at recoveries of 80–90% with a feed flux of 20–23 LMH, and the effects of forward flushing frequency, acid dosing location, and concentrate recirculation on fouling behavior were evaluated. The NF270 membrane achieved consistent removal of organic matter (effluent chemical oxygen demand (COD_Mn) < 0.5 mg/L), hardness (40–60% rejection), and alkalinity (~20% rejection), meeting Jiangsu Province drinking water standards. However, operation at 90% recovery resulted in rapid third-stage fouling, with permeate flow declining by >60% within 2.5 h. Osmotic pressure analysis (local concentrate osmotic pressure: 3.8–4.2 bar; net driving pressure: 0.8–2.2 bar) confirmed physical scaling rather than hydraulic limitation as the dominant mechanism. Stage-wise concentration factor calculations (CF₁ = 1.6, CF₂ = 2.9, CF₃ = 4.4) revealed local Langelier Saturation Index (LSI) values of 1.8–2.2 in the third stage, identifying CaCO₃ supersaturation as the primary scaling cause. Reducing recovery to 85% and flux to 20 LMH with 2 h forward flushing extended stable operation. Acid addition effectively mitigated scaling, but dosing location was critical: first-stage addition (pH 8.1 → 7.6) reduced third-stage LSI to 0.7–0.9 and stabilized performance, whereas third-stage addition (pH 8.0 → 7.3) inadvertently promoted Al(OH)₃ precipitation from residual coagulant (feed Al: 0.07–0.11 mg/L). Concentrate recirculation (90% ratio) did not alleviate fouling. These findings demonstrate that for aluminum-rich coagulated surface waters, optimizing recovery, flushing frequency, and acid dosing location is essential for sustainable NF operation, and provide engineering guidance for full-scale applications. Full article

The present study investigates the effect of low-temperature ion plasma nitriding on the phase composition, microstructure, tribological behavior, and corrosion resistance of 30Cr13 martensitic stainless steel. Plasma nitriding was carried out at temperatures of 400, 450, and 480 °C in a dissociated ammonia atmosphere using a pulsed DC glow discharge. The phase composition and structural evolution of the surface layer were analyzed by X-ray diffraction, while the morphology and thickness of the modified zone were examined using scanning electron microscopy. The tribological properties were evaluated under dry sliding conditions using a ball-on-disk configuration, and corrosion resistance was assessed by potentiodynamic polarization in a 3.5 wt.% NaCl solution. It was established that low-temperature ion plasma nitriding leads to the formation of nitrogen supersaturated martensite (α′N) and the nitride phase ε-(Fe_2–3)N, with their relative fraction governed by the treatment temperature. An increase in the nitriding temperature resulted in a rise in the surface’s microhardness up to 1100–1150 HV and a change in the thickness of the modified layer, reflecting nitrogen redistribution between the solid solution and nitride constituents. The predominance of the α′N phase at 400–450 °C ensured the most stable tribological behavior and reduced corrosion rate, whereas an increased fraction of ε-(Fe_2–3)N at 480 °C led to a higher microhardness and a greater abrasive wear component while maintaining satisfactory corrosion resistance. The obtained results confirm the decisive role of phase composition in the nitrided layer in determining the tribological and corrosion performance of 30Cr13 steel, and may be used for optimizing the surface hardening parameters of components operating under combined friction and corrosive environments. Full article

Gallbladder diseases spanning cholelithiasis, cholecystitis, and gallbladder cancer represent a clinically heterogeneous continuum in which type 2 diabetes mellitus (T2DM) acts as a key metabolic modifier. Conventional models centered on bile supersaturation alone do not sufficiently account for the persistent inflammation and inter-individual variability frequently observed in practice. Here, we synthesize emerging evidence implicating the gut microbiota–bile acid (BA) axis as an integrative mechanism linking metabolic dysregulation, barrier dysfunction, and biliary pathobiology in the diabetic host. Hyperglycemia and insulin resistance, together with impaired mucosal resilience, are associated with shifts in microbial community structure and BA-transforming functions (e.g., bile salt hydrolase and 7α-dehydroxylation), favoring a more hydrophobic BA pool. These changes may disrupt BA receptor signaling, including FXR–FGF15/19 and TGR5-related pathways, thereby amplifying metabolic inflammation, promoting lithogenic bile formation, and impairing gallbladder motility. In parallel, barrier vulnerability may facilitate microbial translocation and LPS-driven immune activation, reinforcing a feed-forward loop that supports the gallstone–inflammation–carcinogenesis trajectory. Translationally, microbiome- and BA-oriented strategies (dietary patterns, bile acid therapeutics, and targeted microbiome modulation) are promising adjuncts, yet precision management should explicitly consider medication- and weight loss–related confounding—particularly with incretin-based therapies—to optimize biliary outcomes across disease stages. Full article

Poor aqueous solubility remains a major limitation for the oral delivery of many active pharmaceutical ingredients (APIs). Deep eutectic solvents (DESs) exhibit remarkable drug-solubilization capacity, yet rapid precipitation upon aqueous dilution can compromise their ability to sustain supersaturation. This study investigates polymer-embedded DES (PEDES) systems as liquid supersaturating drug delivery platforms in which hydration and polymer chemistry jointly govern thermodynamic solubilization and kinetic stabilization. A choline chloride/DL-malic acid DES was prepared with 5% or 15% (w/w) water and combined with polyvinylpyrrolidone (PVP) or polyacrylic acid (PAA). Griseofulvin (GRF) was used as a precipitation-prone model drug. Structural characterization (ATR-FTIR, ¹H-NMR), equilibrium solubility measurements, storage stability studies, and non-sink dissolution testing were conducted to elucidate formulation behavior. The DES systems enhanced GRF solubility by up to ~59-fold relative to phosphate buffer (PBS, pH 6.8). Polymer incorporation produced hydration- and concentration-dependent effects. These results suggest the presence of competitive or cooperative interaction regimes. At 5% water, PEDES formulations failed to prevent recrystallization and showed limited supersaturation maintenance. In contrast, PEDES systems containing 15% water exhibited improved stability, with the formulation containing 4% PAA sustaining elevated drug concentrations for 120 min under non-sink conditions. Low-frequency solution-state ¹H-NMR confirmed stronger GRF–PAA interactions relative to PVP, supporting the role of polymer–drug association in supersaturation stabilization. These findings demonstrate that PEDES performance emerges from a hydration-dependent balance between solvent structuring and drug–polymer interactions, highlighting hydration and polymer functionality as key parameters for the rational design of liquid supersaturating systems. Full article

Canine urolithiasis is a common and highly recurrent urinary tract disease, with struvite and calcium oxalate being the predominant stone types. Stone formation has traditionally been attributed to urinary physicochemical factors, including urine pH, mineral supersaturation, and urinary tract infection. However, these factors alone cannot fully explain the persistent growth and rapid progression of stones in affected dogs. In this study, we provide evidence that innate immune mechanisms, particularly neutrophil extracellular traps (NETs), are associated with canine urolith formation. We found that neutrophils, key cells of the innate immune system, release neutrophil extracellular traps composed of DNA and antimicrobial proteins, which are consistently present within urinary stones and their surrounding microenvironments. Common canine urinary pathogens were shown to trigger this response, and these immune-derived structures promoted crystal nucleation, aggregation, and stone growth in experimental systems. Importantly, enzymatic degradation of NETs by DNase I attenuated NET-associated stone growth under in vitro conditions. These findings suggest that canine urinary stones develop not only as a consequence of physicochemical factors, but also in association with inflammation-driven biomineralization processes involving NETs. Recognizing the contribution of innate immunity provides new insight into stone recurrence and may inform future preventive and therapeutic strategies. Full article

Mineral scale deposition remains a major flow-assurance constraint in oil and gas operations, especially in water-flooding and produced-water reinjection, where mixing between incompatible brines promotes super-saturation and precipitation of poorly soluble salts. This work introduces a novel extension of traditional methods used for modeling chemical inhibition and the predictive evaluation of oilfield scale-inhibitor molecules. A systematically optimized Two-Dimensional Quantitative Structure–Activity Relationship Model based on the k-Nearest Neighbors algorithm 2D-QSAR-KNN model was developed to quantitatively link molecular constitution of phosphonate inhibitors, brine chemistry, and operating factors with inhibition efficiency IE %. The optimized model achieved strong accuracy and generalization R²_train = 0.9182, R²_test = 0.9306, and R²_global = 0.9208 with low prediction errors RMSE_train = 4.7888%, RMSE_test = 4.5485%, and RMSE_global = 4.7421%. Median absolute errors remained minimal for the train set = 0.80%, and test set = 1.63%, and model stability was confirmed by high correlation with experimental IE % r = 0.94 and R²_train/R²_test ≈ 0.99, showing no sign of overfitting. Additionally, an inverse-2D-QSAR framework was applied to identify the optimal molecular descriptor profile expected to maximize inhibitory performance within normalized bounds, providing rational rules for next-generation inhibitor design. The findings highlight the practical value of QSAR-inspired AI modeling to accelerate molecule screening and dosage exploration prior to laboratory validation, supporting more cost-effective, interpretable, and environmentally aware sulfate-scale inhibition strategies under high-salinity reservoir conditions. Full article

The travertine formed through the precipitation of supersaturated calcium carbonate from geothermal or surface waters due to CO₂ degassing, evaporation, and biological activities not only exhibits remarkable landscape value but also holds significant scientific importance in geological research. Current conservation efforts face critical challenges including travertine degradation, increased algal biomass accumulation, and progressive marshification processes. The study focused on how Vallisneria natans (V. natans) and Ceratophyllum demersum (C. demersum) affected travertine deposition. Analyzing the physical and chemical parameters, phase structure, crystal morphology, and microbial community in the aquatic environment, it was observed that under conditions of low c (Ca²⁺) concentration in solution (≤100 mg L⁻¹), both species significantly increased the rate of travertine deposition. The effect of plant biomass was species-specific: V. natans showed the highest promotion at 70 g L⁻¹, while C. demersum performed effectively at moderate biomass levels (140 and 280 g L⁻¹). Specifically, C. demersum exhibited enhanced photosynthetic activity, elevated pH, increased dissolved oxygen (DO) content and more epibiotic microorganisms, with higher levels of Aeromonas compared to V. natans. Therefore, C. demersum demonstrated a greater capacity for travertine deposition. However, the culture environment with elevated c (Ca²⁺) ≥ 500 mg L⁻¹ or higher biomass levels (420 g L⁻¹) impeded the stable growth of submerged plants and exerted a stress effect on them, hindering travertine deposition. The morphology of travertine crystals promoted by the two submerged macrophytes was distinct. In the V. natans treatment, the crystals were square and elongated, whereas in the C. demersum treatment, they were spheraragonite, droplet-like, and petal-shaped. This study reveals the mechanisms by which submerged macrophytes promote travertine deposition and provides new insights for adopting nature-based ecological restoration strategies to sustainably maintain travertine landscapes. By leveraging the promoting effects of submerged macrophytes, travertine deposition and the aquatic environment were improved while reducing energy and chemical inputs. Such biological regulation approaches help synergistically achieve the dual objectives of geological heritage conservation and ecosystem health restoration. Full article

Background: Myricetin (MYR) is a natural flavonol with antioxidant, neuroprotective, anti-inflammatory, antidiabetic, and cardioprotective activities. Still, its pharmaceutical use is limited by very low aqueous solubility (~16.6 µg/mL) and poor oral bioavailability (<10%). This study aimed to enhance the solubility and potentially improve the bioavailability of MYR by developing an amorphous nanofibrous delivery system. Methods: Electrospinning was applied to fabricate MYR-loaded nanofibers using polyvinylpyrrolidone K30 (PVP30), and the influence of key processing parameters on MYR solubility was evaluated. Nanofibers produced under selected electrospinning conditions were characterized in terms of morphology, encapsulation efficiency, and physicochemical properties. Results: X-ray powder diffraction confirmed complete amorphization of MYR within the BB5 fiber structure (distance: 12 cm, voltage: 25 kV, flow rate: 1.5 mL/h). FTIR analysis indicated hydrogen-bonding interactions between MYR hydroxyl groups and PVP30 carbonyl groups, contributing to stabilization of the amorphous form. SEM images revealed homogeneous, defect-free fibers with diameters below 400 nm, although localized MYR agglomerates were observed. Solubility and release studies demonstrated a characteristic spring-and-parachute effect, enabling rapid MYR release and maintenance of a supersaturated state. Enhanced solubility resulted in significantly improved antioxidant activity in DPPH and CUPRAC assays compared with crystalline MYR. Conclusions: Electrospun PVP30 nanofibers represent a promising platform for improving the solubility, dissolution behavior, and functional activity of poorly soluble bioactive compounds such as myricetin, supporting their potential application in pharmaceutical formulations. Full article