Search Results (1,703)

Electrospinning is a versatile technique for producing polymer nanofibers with high ratios of surface area to volume and tunable porosity. Conventional approach to the optimization of processing parameters such as voltage and flow rate frequently encounters limitations in reproducibility and scalability. This review proposes a comprehensive framework that integrates macromolecular design principles with established electrohydrodynamic theories. We analyze how intrinsic molecular traits, specifically chain entanglement density, molecular weight distribution (MWD), topological architecture, and polymer–solvent thermodynamic interactions, define the boundaries of jet stability and solidification. Key findings highlight that while molecular weight establishes a baseline for spinnability, the MWD dictates the dynamic response under extreme deformation. Notably, high-molecular-weight fractions act as elastic load-bearers that suppress capillary breakup. Furthermore, we discuss here how molecular architecture and solvent-mediated segmental mobility determine whether molecular orientation is kinetically trapped or relaxed during the nanosecond timescales of jet flight. By establishing a hierarchical design logic prioritizing molecular and formulation variables over processing parameters, this framework provides a robust strategy to overcome challenges in scalability and reproducibility, positioning electrospinning as a sensitive probe for macromolecular dynamics under extreme elongation. Full article

As a result of the high safety, low cost, and environmental benignity, aqueous zinc-ion batteries are regarded as one of the most promising candidates for next-generation large-scale energy storage systems. However, their further development is constrained by performance bottlenecks in existing cathode materials, including capacity, cycle life, and reaction kinetics. In this study, a high-entropy design strategy is employed to synthesize the metal oxide (FeNiMnMgCuCo)₃O₄ with a cubic spinel structure, and its electrochemical performance as a cathode for zinc-ion batteries is systematically evaluated. The prepared (FeNiMnMgCuCo)₃O₄ high-entropy cathode exhibits high reversible capacity (341.3 mA h g⁻¹ at 0.1 A g⁻¹) and remarkable long-term cycling stability (76.1% retention after 1000 cycles at 3 A g⁻¹). This work not only demonstrates a high-entropy cathode material with practical potential but also provides new research insights for optimizing zinc-ion storage performance through composition design and entropy regulation. Full article

Anaerobic digesters operating under neotropical conditions face significant technological constraints. High humidity, intense solar radiation, and pronounced diurnal temperature variations increase conductive, convective, and radiative heat losses. These factors reduce internal thermal stability and directly affect methane production rates and overall energy efficiency. As a result, thermal instability becomes a recurrent operational bottleneck in biogas plants without active temperature control. This review examines the thermal and dynamic behavior of anaerobic reactors from a process-engineering perspective. It integrates energy balances, heat-transfer mechanisms, and computational fluid dynamics (CFD) modeling. The combined effects of temperature gradients, hydrodynamic mixing patterns, and structural material properties are analyzed to determine their influence on thermal homogeneity, microbial stability, and methane yield consistency under mesophilic conditions. Technological strategies to mitigate thermal losses are evaluated. These include passive insulation using low-conductivity materials, geometry optimization supported by numerical modeling, and thermal recirculation schemes, as these factors govern temperature distribution and process resilience. Current limitations are also discussed, particularly the frequent decoupling between ADM1-based kinetic models and transient heat-transfer analysis. This separation restricts predictive capability under real-scale diurnal temperature oscillations. The development and validation of coupled hydrodynamic–thermal–biokinetic models under fluctuating neotropical boundary conditions are proposed as critical steps. Such integrated approaches can enhance operational stability, ensure consistent methane production, and improve energy self-sufficiency in organic waste valorization systems. Full article

The high-temperature corrosion behavior of A1, T22, and T91 steels was investigated in molten nitrate salts at 400, 500, and 600 °C during 100 h of exposure. The combined influence of temperature and chromium content on corrosion kinetics and oxide-scale stability was evaluated using open-circuit potential (OCP), linear polarization resistance (Rp), electrochemical impedance spectroscopy (EIS), scanning electron microscopy, X-ray diffraction, and cross-sectional elemental mapping. OCP measurements showed a progressive shift toward more negative potential with increasing temperature, indicating enhanced oxidation tendency. Electrochemical measurements revealed a systematic decrease in Rp and impedance magnitude as temperature increased, confirming accelerated corrosion kinetics and reduced interfacial resistance. EIS spectra exhibited two characteristic time constants associated with the outer corrosion products and the inner metal/oxide interface. Significant differences in scale growth were observed depending on alloy composition. At 600 °C, oxide thickness reached approximately 700–800 μm for A1, ~100 μm for T22, and ~10 μm for T91. Chromium-containing steels promoted the formation of a compact Cr-rich inner oxide layer that improved scale adhesion and suppressed the exfoliation phenomena observed in A1 steel. Overall, temperature controls corrosion kinetics, whereas chromium content governs oxide-scale compactness and long-term stability in molten nitrate environments. Full article

To address the inherent low voltage and poor energy density of LiFePO₄, LiFe_0.6Mn_0.4PO₄ (LFMP) has emerged as a promising cathode for next-generation lithium-ion batteries. However, its practical application is severely hindered by intrinsic limitations such as low electronic conductivity and sluggish Li⁺ diffusion. To address these challenges, this study investigates the effects of silver (Ag) doping on the structural and electrochemical performance of LFMP. Through a facile high-temperature solid-state approach, Ag⁺ ions are successfully incorporated into the LFMP matrix, and the resulting material (LFMP-Ag) is systematically characterized. The results reveal that partial Ag is doped into the LFMP lattice while an Ag-rich secondary phase within LFMP particles is detected, significantly enhancing the charge transfer kinetics. The Ag-doped LFMP cathodes exhibit superior discharge capacity of 142.1 mAh g⁻¹ at 0.1 C, enhanced rate capability, better cyclic stability (92.3% retention after 300 cycles) and enhanced thermal stability, surpassing the undoped LFMP counterparts. These findings demonstrate that Ag doping is an effective strategy for optimizing the electrochemical performance of LFMP cathodes, offering a viable pathway toward advanced battery technologies. Full article

P2/O3-type Ni/Mn-based layered oxides are regarded as promising cathode materials for sodium-ion batteries (SIBs) because of their high energy density. However, their practical application is limited by low initial Coulombic efficiency, sluggish Na⁺ kinetics, transition-metal dissolution/migration and irreversible phase transitions during cycling. Herein, a controlled P2 phase was achieved through elemental ratio regulation, enabling systematic synthesis of a series of Na_xNi_0.4Co_0.1Mn_0.5O₂(x-NCMO) materials with tailored P2/O3 ratios. The optimized composition (x = 0.8), containing 16.6% P2 and 83.4% O3 phases, achieves an optimal phase equilibrium, thereby maximizing the synergistic coupling between the two layered polymorphs. This biphasic architecture demonstrates significantly enhanced Na⁺ transport kinetics and exceptional electrochemical performance, high initial capacity of 168.65 mAh g⁻¹ and excellent rate performance, maintaining 84.88 mAh g⁻¹ at 10 C, outperforming most reported P2/O3 biphasic cathodes. Structural analysis and electrochemical analysis reveal that elemental ratio regulation modulates the TM–O electronic structure, promotes electronic transport, and accelerates Na⁺ migration. These effects collectively reduce polarization, stabilize the structure, and thereby improve rate capability and long-term cycling capacity retention. This work provides an effective design strategy for designing high-performance layered oxide cathodes with improved structural and interfacial stability. Full article

Controlling radical selectivity within nanoreactors remains a formidable challenge due to the inherent high reactivity and short half-lives of reactive species. Herein, we report a novel size-matched nanoconfinement strategy using a cobalt-nickel-layered double hydroxide (CoNi-LDH) nanoreactor for the highly selective generation and stabilization of sulfate radicals (SO₄^∙−) via piezoelectric activation of peroxymonosulfate (PMS). By precisely tailoring the LDH interlayer spacing to 5.27 Å to match the kinetic diameter of SO₄^∙−, the nanoreactor effectively suppresses non-selective side reactions and radical quenching. Consequently, the CoNi-LDH achieves an unprecedented reaction rate (k_obs = 0.40 min⁻¹) and superior defluorination efficiency (78.9%) for fluoroquinolone antibiotics, significantly outperforming non-size-confined counterparts. Mechanistic insights reveal a synergistic pathway where piezo-generated hot electrons, mediated by Ni sites, accelerate the Co²⁺/Co³⁺ redox cycle to ensure long-term catalytic stability. The robustness of this nanoconfined system is further demonstrated by its exceptional tolerance to complex water matrices and its practical operability in a continuous-flow reactor. This study provides a pioneering approach for spatial radical control at the nanoscale to achieve efficient and targeted environmental remediation. Full article

An important challenge for materials researchers in the modern era is the fabrication of high-performance electrodes with novel designs and structures to enhance electrochemical sensing and energy storage performance. Recently, perovskite-structured bimetallic hydroxide materials, owing to their high conductivity, decent surface area, abundant redox activity, and good stability, have emerged as promising candidates for bifunctional electrochemical applications. In this study, we designed perovskite-type CuSn(OH)₆ microspheres via a facile coprecipitation method for nifedipine (NFD) sensing and supercapacitors (SCs). Various characterization techniques were employed to confirm the successful synthesis of CuSn(OH)₆. The uniform formation and distribution of CuSn(OH)₆ within the sphere structure provide rich reactive sites and enhance structural stability, thereby improving electrochemical activity. This architecture also induces a synergistic effect between Cu and Sn, which increases conductivity and accelerates redox kinetics. Consequently, the electrode modified with CuSn(OH)₆/GCE exhibited a wide linear concentration range of 0.4–303.3 µM and a low detection limit of 0.44 µM for NFD detection. This sensor further demonstrated superior analytical reliability, with selectivity of <5%, cycling stability of 84.79%, reproducibility of 3.3%, and recovery rates of 99.2–99.8% in the serum sample. Concurrently, the CuSn(OH)₆/NF showcased a high specific capacitance of 514 F g⁻¹ at 1 A g⁻¹, good longevity of 83.05% retention after 5000 cycles, and low charge transfer resistance of 6.56 Ω and solution resistance of 1.04 Ω, validating fast ion–electron transport. These results underscore that perovskite-based CuSn(OH)₆ is an efficient dual-functional electrocatalyst for sensitive electrochemical detection and high-performance SCs. Full article

Sodium alginate (SA)-modified shellac nanoparticles were developed as pH-responsive carriers for cinnamon essential oil (CEO) encapsulation in aquatic product preservation. Three polyelectrolytes (SA, chitosan (CS), gelatin (Gel)) were evaluated at concentrations of 0.025–0.3% (w/v). Under pH conditions simulating spoilage (6.0–7.5), SA-SNPs exhibited superior stability with minimal changes in particle size, PDI, and zeta potential, while CS and Gel systems aggregated near their pKa values. At 0.1% SA, CEO-loaded nanoparticles (SA-SCNPs) showed excellent properties: small size (160 nm), high encapsulation efficiency (90%), and pH-triggered release (77.76% at pH 7.0 via Ritger–Peppas kinetics, n = 0.58). FT-IR confirmed ionic and hydrogen bonding between the SA and shellac. SA-SCNPs enhanced antibacterial efficacy against Shewanella putrefaciens and Pseudomonas fluorescens and maintained stability under ionic strength (300 mmol/L NaCl) and temperature variations (−18 °C to 25 °C), attributed to SA’s cryo-resistance and steric effects. This system offers a smart delivery platform for aquatic preservation. Full article

Ti₂AlC, an important member of the MAX phase family, exhibits combined metallic and ceramic characteristics, showing potential for applications in conductive composites and high-temperature structural components. However, this phase possesses a narrow thermodynamic stability window, making high-purity synthesis challenging. Conventional solid-state synthesis requires temperatures exceeding 1300 °C, where aluminum volatilization and kinetic limitations of carbon diffusion lead to impurity phases such as TiC and Ti₃AlC₂. Based on the ionic transport characteristics of molten salt media, this study employed the eutectic NaCl-KCl molten salt method to synthesize Ti₂AlC using Ti, Al, and TiC powders within the temperature range of 1000–1150 °C. Systematic investigations revealed that an optimized raw powder composition (Ti:Al:TiC = 1:1.10:0.95) at 1100 °C yielded Ti₂AlC powders with 96.1% phase purity, high crystallinity, and typical laminated structure with stable stoichiometry (Ti/Al ≈ 2:1). Furthermore, Ag/Ti₂AlC composites demonstrated excellent electrical conductivity (resistivity of 5.72 μΩ·cm) and favorable mechanical properties, validating the applicability of this synthetic route for conductive composite materials. Full article

Drip irrigation system performance is largely governed by emitter hydraulic characteristics. This study systematically compares the hydraulic performance of a novel cylindrical asteroid-shaped channel emitter against a conventional toothed labyrinth design. Standardized specimens were produced using precision molds and integrated into drip tapes at 300 mm spacing. To comprehensively analyze flow behavior, pressure–discharge relationships, flow indices, and internal flow fields, a combination of physical experiments and CFD simulations was employed. Experimental results showed that across 20–200 kPa, the cylindrical asteroid-shaped emitter delivered flow rates 24–28% higher than the labyrinth type while maintaining a lower flow index, demonstrating enhanced hydraulic stability. Flow field analysis at 100 kPa revealed that the divergent asteroid geometry generates more intense and sustained turbulent kinetic energy throughout the channel units, resulting in superior energy dissipation. The cylindrical asteroid-shaped unit achieved a pressure drop of 17.5 kPa, exceeding the 15.3 kPa observed in the labyrinth channel, with outlet velocities of 1.6 m/s versus 1.76 m/s. Additionally, the flow pattern promotes comprehensive wall scouring through large-scale vortices, indicating improved resistance to clogging. These findings validate the design superiority of the cylindrical asteroid-shaped emitter and offer a theoretical reference for developing high-uniformity, water-saving irrigation devices. Full article

Carbon dioxide (CO₂) hydrate slurries have emerged as promising candidates for cold thermal energy storage (CTES) and refrigeration systems due to their high latent heat, controllable flow behavior, and environmentally friendly nature. These slurries are formed by dispersing solid CO₂ hydrate particles in a liquid phase, forming a multiphase system with tunable thermophysical and rheological properties. The performance of these slurries is dependent on nucleation kinetics, particle sizes and their distribution, solid content, and thermal transport characteristics under flow conditions. This review paper gives an assessment of CO₂ hydrate slurries from a thermofluid’ perspective by focusing on key aspects such as hydrate nucleation mechanisms, viscosity behavior, shear response, thermal conductivity, convective heat transfer, and slurry stability. Particular attention is given to the role of surfactants and nanoparticle additives that enhance hydrate formation and improve slurry performance. The addition of nanofluids is discussed both in terms of their effect on thermal properties as well as in flow stability. Full article

Water contamination by synthetic dyes such as malachite green (MG) remains a significant environmental and public health challenge due to their high toxicity, chemical stability, and resistance to biodegradation. In this study, a CaO-CuFe₂O₄ composite was synthesized through a sustainable route using eggshells and orange peel as agro-industrial waste precursors. Comprehensive structural, spectroscopic and microscopic analyses confirmed the coexistence of a predominant CaO-based phase with spinel CuFe₂O₄, together with nanometric features, satisfactory elemental dispersion and practical magnetic recoverability. Under the experimental conditions employed, the composite exhibited high adsorption performance towards MG, reaching an equilibrium capacity of 2288.4 mg g⁻¹ and 99.98% decolorization within 60 min. The kinetics were better described by the pseudo-second-order model, while the equilibrium behavior was more satisfactorily fitted by the Langmuir isotherm than by the Freundlich model. Thermodynamic analysis indicated that the adsorption process was favorable over the temperature range studied and became more pronounced at higher temperature. The results suggest that the adsorption behavior arises from the combined influence of surface chemistry, calcium-derived basic sites, ferrite-associated metal centers and interfacial accessibility, rather than from surface area alone. In addition, the material could be readily separated from aqueous solution using an external magnetic field, highlighting its practical post-treatment recoverability. Overall, this work demonstrates a viable waste valorization strategy for the development of a magnetically recoverable CaO-CuFe₂O₄ adsorbent for cationic dye removal. Beyond the specific case of MG, the study underscores the potential of agro-waste-derived hybrid oxides as application-relevant materials for water remediation. Full article

Carbon dioxide (CO₂) capture is a cornerstone of global carbon neutrality, yet the high energy penalty associated with solvent regeneration—particularly for monoethanolamine (MEA) systems—remains a major barrier to its sustainable deployment. This study presents a sustainable and high-performance catalytic solution using micro-sized iron oxyhydroxide (β-FeOOH). Characterized by a high specific surface area ($287 m²/g) and a synergistic distribution of abundant Lewis and Brønsted acid sites, the β-FeOOH catalyst significantly enhances CO₂ desorption kinetics. Experimental results demonstrate that the incorporation of β-FeOOH into a 30 wt% MEA solution increases the CO₂ desorption rate by 10.9% while simultaneously lowering the regeneration temperature from the conventional 120 °C to 85 °C. Such a reduction in thermal requirements offers a pathway to utilize low-grade industrial waste heat, drastically improving the process’s energy efficiency. Furthermore, the catalyst exhibited remarkable cyclic stability over ten consecutive cycles, maintaining its structural integrity and catalytic activity. These findings highlight β-FeOOH as an eco-friendly, cost-effective, and robust catalyst that aligns with the principles of green chemical engineering, offering a scalable strategy to enhance the sustainability of carbon capture operations. Full article

Carbon-based bifunctional oxygen electrocatalysts with rationally designed architectures are essential for high-performance rechargeable zinc–air batteries (ZABs), yet the concurrent optimization of catalytic activity, durability, and mass transport remains challenging. Herein, hierarchical ZnCo carbon nanofibers/carbon nanotubes (CNFs@CNTs) are fabricated via single-nozzle electrospinning followed by melamine-assisted pyrolysis under a ZnCl₂-regulated atmosphere. During thermal treatment, Co species embedded within carbon nanofibers catalyze in situ carbon nanotube growth, while ZnCl₂ vapor modulates the carbonization process and surface chemistry, collectively generating a hierarchical CNFs@CNTs architecture with high surface area and abundant exposed active sites. As a result, ZnCo CNFs@CNTs exhibit outstanding bifunctional ORR/OER activity, surpassing Zn-free and Co-free counterparts. Combined structural and electrochemical analyses reveal that the synergistic interaction between Co active centers and Zn-assisted carbon structural regulation enhances reaction kinetics and long-term stability. When implemented as air electrodes in rechargeable ZABs, ZnCo CNFs@CNTs deliver high power density, reduced charge–discharge polarization, and excellent cycling durability, demonstrating strong practical applicability. This work presents an effective strategy for constructing hierarchical CNFs@CNTs composites via electrospinning and dual-component thermal regulation, offering new insights into the design of high-efficiency bifunctional air electrodes for advanced ZABs. Full article