Search Results (1,998)

As avionics advance, heat dissipation becomes more challenging. Microencapsulated phase change material slurry (MPCMS), with its latent heat transfer properties, offers a potential solution. However, the low thermal conductivity of microencapsulated phase change material (MPCM) limits heat transfer rates, and most studies focus on improving conductivity, with little attention given to convective enhancement. This study prepared MPCMS with an MPCM mass fraction (W_m) of 10% and 20%, investigating melting heat transfer under mechanical stirring at 0–800 RPM and heat fluxes of 8.5–17.0 kW/m². Stirring significantly alters MPCMS heat transfer behavior. As rotational speed increases, both wall-to-slurry and internal temperature differences decrease. Stirring extends the time at which the heating wall temperature (T_w) stays below a threshold. For example, at W_m = 10% MPCM and 8.50 kW/m², increasing speed from 0 to 800 RPM raises the holding time below 70 °C by 169.6%. The effect of MPCM mass fraction on heat transfer under stirring is complex: at 0 RPM, 0% > 10% > 20%; at 400 RPM, 10% > 0% > 20%; and at 800 RPM, 10% > 20% > 0%. This is because as W_m increases, the latent heat and volume expansion coefficients of MPCMS rise, promoting heat transfer, while viscosity and thermal conductivity decrease, hindering it. At 0 RPM, the net effect is negative even at W_m = 10%. Stirring enhances internal convection and significantly improves heat transfer. At 400 RPM, heat transfer is positive at W_m = 10% but still negative at W_m = 20%. At 800 RPM, both W_m levels show positive effects, with slightly better performance at W_m = 10%. In addition, at the same heat flux, higher speeds maintain T_w below a threshold longer. Overall, stirring improves MPCMS cooling performance, offering an effective means of convective enhancement for avionics thermal management. Full article

Peach gum polysaccharide (PGP), a natural biopolymer extracted from the resin of the peach tree, holds significant potential for applications in food, cosmetics, and pharmaceutical industries. However, detailed analysis and exploration of its physical and chemical properties remain limited. This study investigates the physicochemical properties, rheological behavior and emulsion stability of PGPs extracted using thermal (TPGP) and enzymatic (EPGP) methods. The results indicate that both polysaccharide fractions exhibit similar arabinogalactan (AG) structures, with high contents of arabinose and xylose, as evidenced by FTIR spectra and monosaccharide composition. However, high-performance size-exclusion chromatography (HPSEC) revealed differences in molecular weights and chain conformations, leading to distinct rheological behaviors. PGP solutions exhibited pseudoplastic flow behavior, with TPGP demonstrating higher viscosity due to its larger molecular weight (1.295 × 10⁷ g mol⁻¹). As the PGP concentration increased, gel strength and emulsion stability improved significantly. This study provides more insight into the rheological and emulsifying characteristics of PGPs extracted by varied methods, facilitating their potential applications in food industries. Full article

Candida infections pose a significant health threat, and conventional antifungal drugs like nystatin are limited due to poor solubility, skin permeability, and frequent dosage requirements. Nystatin effectively targets Candida species by disrupting cell membranes, but formulation issues hinder clinical use. Lipid-based vesicular carriers, or novasomes, provide controlled, prolonged drug release and enhanced skin penetration. This study focuses on developing nystatin-loaded novasomal gels as an advanced drug delivery system to enhance therapeutic efficacy, bioavailability, and patient compliance. The formulation was prepared using a modified ethanol injection technique, combining stearic acid, oleic acid, Span 60, cholesterol, and Carbopol to produce a stable transdermal gel. Comprehensive in vitro characterization using FTIR, SEM, XRD, and thermal analysis confirmed the chemical compatibility, morphological uniformity, and physical stability of the nystatin-loaded novasomal gel. Entrapment efficiency differed significantly among the formulations (p < 0.05), with F7 achieving the highest value (80%). All formulations maintained pH levels within the skin-friendly range of 5.5 to 7.0. Viscosity measurements, ranging from 3900 ± 110 to 4510 ± 105 cP, confirmed their appropriate consistency for dermal use. Rheological analysis showed a dominant elastic response, as indicated by storage modulus values consistently higher than the loss modulus. Particle size ranged from 4143 to 9570 nm, while PDI values remained below 0.3, reflecting uniform particle distribution. Zeta potential values were strongly negative, supporting physical stability. XRD studies indicated reduced crystallinity of nystatin within the formulations, while FTIR confirmed drug-excipient compatibility. SEM images showed spherical particles within the micrometer range. In vitro release studies demonstrated sustained drug release over 12 h, with F6 releasing the highest amount. The novasomal gel formulations-maintained stability for 30 days, with no notable alterations in pH, viscosity, or entrapment efficiency. Antifungal evaluation showed a larger inhibition zone (23 ± 2 mm) compared with the plain drug solution (15 ± 1.6 mm), while the MIC value was reduced (4.57 µg/mL), indicating greater potency. Skin irritation assessment in rats revealed only minor, temporary erythema, and the calculated Primary Irritation Index (0.22) confirmed a non-irritant profile. These findings suggest that the developed novasomal gel offers a promising approach for enhancing the treatment of fungal infections by enabling prolonged drug release, minimizing dosing frequency, and improving patient compliance. Full article

Traditional chemical-based sanitizers pose risks to health and the environment, highlighting the need for safer natural alternatives. We developed biocompatible hydrogels from carbohydrate-based biopolymers, chitosan (1.5% and 2.5%), and carboxymethylcellulose (CMC, 3% and 5%), each incorporating one of four antimicrobials: microcin J25, nisin Z, pediocin PA-1, or reuterin. Hydrogels were prepared by dissolving the polymers in aqueous solution and incorporating antimicrobials before gelation. The formulations were characterized using viscosity measurements, antimicrobial assays, and stability testing over 28 days of storage at room temperature (23–25 °C). Chitosan hydrogels with microcin J25 maintained strong activity against Salmonella enterica ATCC 6962, while nisin Z retained activity in gel and solution forms, though with some decline during storage. Pediocin PA-1 remained active in 1.5% and 2.5% chitosan hydrogels against Listeria monocytogenes ATCC 19115, but activity was lost in 3% and 5% CMC hydrogels. Reuterin preserved activity in CMC-based hydrogels throughout storage. In solution, microcin J25 and nisin Z consistently achieved ~7-log reductions, whereas pediocin PA-1 and reuterin reached up to ~5-log reductions. In gels, efficacy decreased at lower concentrations and shorter contact times, likely due to diffusion barriers. Overall, the hydrogels remained stable during storage, and CMC- and chitosan-based matrices with selected antimicrobials show promise as alternatives to chemical sanitizers. Their application should be tailored to specific needs, with formulations requiring longer contact times best suited for surfaces that allow prolonged exposure. Full article

To address issues of traditional coalbed methane (CBM) fracturing fluids (high displacement, weak sand-carrying, poor stability, severe coal seam damage), this study synthesized CO₂-responsive erucamide propyl dimethylamine surfactant (C₂₂ZEA, yield 99%), with molecular structure verified by ¹H NMR (400 MHz, CDCl₃) matching the target. Molecular simulation showed CO₂ protonates C₂₂ZEA into EA⁺: 1 wt% forms a simple micelle network, while 3 wt% enhances entanglement into a dense 3D network. Experiments indicated: 3 wt% solution reaches 160 mPa·s viscosity in 200 s under CO₂ (0.2 L·min⁻¹); 1.5–4.5 wt% solutions are pseudoplastic (n = 0.14–0.18), with G′ > G″ when concentration > 2 wt%; viscosity recovery rate > 95% after alternating shear (170 s⁻¹/10 s⁻¹); viscosity remains > 160 mPa·s after 1 h shear (170 s⁻¹) at 70 °C; gel breaks to 0.01–0.02 Pa·s in 15 min with N₂ at 45 °C; 1.0–3.0 wt% solutions meet non-toxic standards via EC₅₀/96 h LC₅₀. This study supports high-efficiency low-damage smart fracturing fluids, boosting CBM extraction efficiency. Full article

Although extensive studies have been conducted on the component ratios and performance of fire extinguishing foams, most research has not explored the coupling relationship between foam wettability and adhesion. Therefore, this study aims to develop an efficient foam extinguishing agent for solid fires by focusing on both wettability and adhesion. First, the influence of chemical functional groups on foam wettability and adhesion was elucidated, and the contributions of individual components to foam properties were experimentally investigated. Second, adhesion and wettability tests revealed a negative correlation between these two properties, consistent with variations in foam solution viscosity and wetting time. Third, a novel adhesion evaluation method was proposed, defined as the time required for foam to flow a fixed distance on inclined wooden surfaces; longer flow times indicated stronger adhesion. Fourth, foaming and fire suppression experiments confirmed the practical performance of the optimized formulations. A composition containing 8 wt% Polyoxyethylene ether and 5 wt% Sulfobetaine yielded a wetting-type foam suitable for rapid cooling, whereas 8 wt% Polyoxyethylene ether combined with 9 wt% Sulfobetaine produced an adhesive-type foam capable of persistent attachment to combustibles. Microscopic observations further demonstrated that foams with superior extinguishing performance developed dense lamellae. Full article

Steady-shear rheology and surface activity of surfactant–polymer solutions were investigated experimentally. Four different polymers were studied as follows: cationic hydroxyethyl cellulose, nonionic hydroxyethyl cellulose, nonionic guar gum, and anionic xanthan gum. The influence of the following four surfactants on each of the polymers was determined: nonionic alcohol ethoxylate, anionic sodium lauryl sulfate, cationic hexadecyltrimethylammonium bromide, and zwitterionic cetyl betaine. The interaction between cationic hydroxyethyl cellulose and anionic sodium lauryl sulfate was extraordinarily strong, resulting in dramatic changes in rheological and surface-active properties. The consistency increased initially, reached a maximum value, and then fell off with the further addition of surfactant. The surface tension of surfactant–polymer solution dropped substantially and exhibited a minimum value. Thus, the surfactant–polymer solutions were much more surface-active compared with pure surfactant solutions. The interaction between anionic xanthan gum and cationic hexadecyltrimethylammonium bromide was also strong, resulting in a substantial decrease in consistency. The surfactant–polymer solution became less surface-active compared with pure surfactant solution due to the migration of surfactant from solution to polymer. The interactions between other polymers and surfactants were weak to moderate, resulting in small to modest changes in rheological and surface-active properties. Surface activity of surfactant–polymer solutions often increased due to the formation of complexes more surface-active than pure surfactant molecules. Full article

We report calculations for electron–radon scattering using a complex relativistic optical potential method. The energy range of this study is 0–1000 eV, with results for the elastic (total, momentum-transfer and viscosity-transfer) cross section, summed discrete electronic-state integral excitation cross sections and electron-impact ionization cross sections presented. Here, we obtain our cross sections from a single theoretical relativistic calculation. Since radon is a heavy element, a relativistic treatment is very desirable. The electron transport coefficients are subsequently calculated for reduced electric fields ranging from 0.01 to 1000 Td, using a multi-term solution of Boltzmann’s equation. Full article

Carbon dioxide (CO₂) capture using alkanolamines remains the most mature technology, yet faces challenges including solvent loss, high regeneration energy and equipment corrosion. Ionic liquids (ILs) are proposed as alternatives, but their high viscosity and production costs hinder industrial use. Thus, blending ILs with amines offers a promising approach. This work presents new experimental data for aqueous blends of 1-butyl-3-methylimidazolium hydrogen sulfate, $\left[\mathrm{B}\mathrm{m}\mathrm{i}{\mathrm{m}}^{+}\right]\left[\mathrm{H}\mathrm{S}{\mathrm{O}}_4^{-}\right],$ with 2-amino-2-methyl-1-propanol (AMP) and 3-(methylamino)propylamine (MAPA) and for choline glycine, $\left[\mathrm{C}{\mathrm{h}}^{+}\right]\left[\mathrm{G}\mathrm{l}{\mathrm{y}}^{-}\right]$, with AMP, modeled using the modified Kent–Eisenberg approach. It was shown that substituting a portion of the amine with $\left[\mathrm{B}\mathrm{m}\mathrm{i}{\mathrm{m}}^{+}\right]\left[\mathrm{H}\mathrm{S}{\mathrm{O}}_4^{-}\right]$ reduces CO₂ uptake per mole of amine due to the lower solution’s basicity, despite the added sites for physical absorption. In contrast, the replacement of an amine portion with $\left[\mathrm{C}{\mathrm{h}}^{+}\right]\left[\mathrm{G}\mathrm{l}{\mathrm{y}}^{-}\right]$ enhances both physical and chemical interactions, leading to increased CO₂ solubility per mole of amine. Finally, replacing a small portion of water with $\left[\mathrm{C}{\mathrm{h}}^{+}\right]\left[\mathrm{G}\mathrm{l}{\mathrm{y}}^{-}\right]$ does not significantly alter the bulk CO₂ solubility (moles of CO₂ per kg of solvent) but lowers the solvent’s vapor pressure. Given the non-toxic nature of $\left[\mathrm{C}{\mathrm{h}}^{+}\right]\left[\mathrm{G}\mathrm{l}{\mathrm{y}}^{-}\right]$, the resulting solvent poses no added environmental risk. Model predictions agree well with experimental data (deviations of 2.0–11.6%) and indicate low unreacted amine content at CO₂ partial pressures of 1–10 kPa for carbamate-forming amines, i.e., $\left[\mathrm{G}\mathrm{l}{\mathrm{y}}^{-}\right]$, and MAPA. Consequently, at higher CO₂ partial pressures, the solubility increases due to carbamate hydrolysis and molecular CO₂ dissolution. Full article

This article investigates a mathematical model with the Caputo derivative for the transient unidirectional flow of an incompressible viscous fluid with pressure-dependent viscosity. The fluid flows in the spatial domain bounded by two parallel plates extended to infinity. The plates translate in their planes with time-dependent velocities, and the fluid adheres to the solid boundaries. The generalization of the model consists of formulating a fractional constitutive equation to introduce the memory effect into the mathematical model. In addition, the fluid’s viscosity is assumed to be pressure-dependent. More precisely, in this article, the viscosity is considered a power function of the vertical coordinate of the channel. Analytic solutions of the dimensionless initial and boundary value problems have been determined using the Laplace transform and Bessel equations. The inversion of Laplace transforms is conducted using both the methods of complex analysis and the Stehfest numerical algorithm. In addition, we discuss the explicit solution in some meaningful particular cases. Using numerical simulations and graphical representations, the results of the ordinary model $(\alpha =1)$ are compared with those of the fractional model $(0<\alpha <1)$, highlighting the influence of the memory parameter on fluid behavior. Full article

Crosslinked hyaluronic acid dermal fillers are widely used for non-permanent aesthetic enhancement, offering safe and effective solutions for facial volume restoration. Specific formulations are designed for targeted facial regions, with highly crosslinked hydrogels often recommended for volumizing areas such as the jawline, chin, and cheeks due to their structural properties. While elasticity and viscosity are commonly evaluated, broader comparative analyses remain limited. In this study, we assess five commercially available HA-based fillers with similar HA concentrations, all optimised for volume enhancement. Alongside widely used reference products, we evaluate BtHCROSS 2%^®, a novel formulation not previously compared to established fillers. We examined the degree of chemical modification, mechanical viscoelastic behaviour, susceptibility to enzymatic degradation by hyaluronidase, and injection force. While all tested fillers are suitable for volume restoration, BtHCROSS 2%^® demonstrates a distinctive combination of mechanical adaptability, structural support, enzymatic resistance, and low injection force, making it a versatile option for practitioners. Full article

Soil CO₂ emissions, driven primarily by microbial respiration, represent a major component of terrestrial carbon flux and play a crucial role in global climate change. Although several soil physicochemical factors regulating microbial activity are well known, the role of soil solution viscosity remains largely unexplored. This study evaluated how polyethylene glycol (PEG6000)-induced increases in soil solution viscosity affect microbial activity-derived CO₂ emissions in a Rhodic Ferralsol (eutric). Three concentrations of PEG6000 (50, 75, and 100 g L⁻¹), corresponding to viscosities of 1.93, 2.76, and 3.88 cP, respectively, were compared to a water-based control (1.11 cP). Soil CO₂ emissions, soil O₂ capture, temperature, and water content were measured over a 60-day period using standard methods. Results showed significant reductions in cumulative CO₂ emissions of 20%, 25%, and 12% for PEG6000 treatments, respectively, compared to the control. Decreased O₂ capture at viscosities of 1.93 and 2.76 cP (50 and 75 g L⁻¹, respectively) indicated reduced microbial activity. These findings reveal a previously underappreciated biophysical mechanism regulating soil carbon emissions. Understanding and managing soil solution viscosity could offer a novel strategy to mitigate CO₂ emissions in tropical soils, thus contributing to climate change mitigation and sustainable soil management, particularly in highly weathered tropical ecosystems. Full article

Cellulose and chitin are the most abundant natural polymers, and their exploitation paves the way for sustainable materials and products. This work investigates the preparation of composites based on acetylated cellulose and partially deacetylated chitin, i.e., chitosan, using versatile and robust air-assisted solution spraying (AASS), a potential method for preparing materials both in situ and ex situ. These materials, in the form of films, despite being prepared from high-molecular-weight and rigid biopolymers, show high flexibility (Young’s moduli below 1 GPa), outstanding mechanical properties (tensile strengths above 19 MPa and strain at failure higher than 2%), and bioactivity towards E. coli. The unprecedented flexibility, obtained without the use of any plasticizer or by casting with humidity control, is a direct consequence of the specific film morphology, whereby films are constituted from merging droplets. Depending on the solution properties (viscosity, surface tension), various droplet sizes are obtained, thus influencing the roughness and indirectly the wettability. Wettability analysis towards water and oil revealed higher contact angles towards both fluids as the content of chitosan increases in the composite what directly impacts packaging applications by better protecting the food. Besides this, higher chitosan content in the composite (7.5% w/w) enabled bioactivity against E. coli, where colony development was inhibited on the film surface compared with the neat cellulose acetate. This study shows a very high potential for AASS for obtaining uniform thin flexible films for food packaging applications, allowing faster drying and lower energy consumption than other film-forming techniques. Full article

This study presents an integrated experimental and computational investigation into the thermal and hydraulic performance of three oxide-based nanofluids: aluminum oxide (Al₂O₃), titanium dioxide (TiO₂), and copper oxide (CuO) for advanced engine cooling applications. A custom-built test rig was used to assess nanofluid behavior under varying flow rates, nanoparticle volume fractions, and temperature gradients, replicating realistic engine conditions. According to the results, at ideal concentrations, CuO nanofluids continuously demonstrate better heat transfer properties, outperforming TiO₂ by up to 15% and AlO₃ by 7%. However, performance plateaus beyond 1.5% volume fraction due to increased viscosity and pressure drop. A multilayer feedforward artificial neural network (ANN) model was developed to predict convective heat transfer coefficients and friction factors based on experimental inputs, achieving a mean absolute percentage error below 5% and a coefficient of determination (R²) exceeding 0.98. The ANN demonstrated robust generalization across varying operating conditions and nanoparticle types, confirming its utility for surrogate modeling and optimization. This work is distinguished by its dual focus on thermal efficiency and hydraulic stability, as well as its use of data-driven modeling validated by empirical results. The findings provide actionable insights for thermal management system design in internal combustion, hybrid, and electric vehicles, where efficient, compact, and reliable cooling solutions are increasingly vital. The study advances the practical application of nanofluids by offering a comparative, ANN-validated framework that bridges the gap between lab-scale performance and real-world automotive cooling demands. Full article

To enhance the fire suppression performance of Class A foam, this study identifies sodium dodecyl sulfate (SDS) as the primary foaming agent and develops a high-efficiency foam system comprising primary and auxiliary foaming agents, wetting agents, and foam stabilizers. It interprets these macroscopic findings at the molecular level through molecular dynamics simulations. Sixteen formulations were designed using orthogonal experiments and evaluated in terms of surface tension, viscosity, wetting performance, and foam expansion ratio. The results demonstrated that the formulated systems exhibited superior foaming characteristics compared to conventional aqueous film-forming foam (AFFF), while other physicochemical properties were inferior. Two high-performing foam systems were further investigated using molecular dynamics simulations. Analysis of the spatial concentration distributions, diffusion coefficients, and the hydrogen-bonding networks of water molecules revealed 14.3% and 14.2% increases in the peak values of the radial distribution function (RDF) for the two systems modified with auxiliary foaming agents, respectively. The auxiliary foaming agents exhibited synergistic effects with SDS, enhancing its water activation capability. The incorporation of wetting agents reduced the water diffusion coefficients by 4.7% and 21.9%, indicating that sodium bis(2-ethylhexyl) succinate sulphonate (T) interferes less with the primary foaming agent than alcohol ethoxylate (AEO). The selected formulations also demonstrated 4.4% and 3.5% reductions in water hydrogen bonding compared to SDS-only solutions, indicating decreased molecular cohesion and improved water activation. By integrating physicochemical evaluation with molecular simulation, the optimized formulation was determined to be SDS (primary foaming agent), sodium fatty alcohol ether sulfate (auxiliary foaming agent), alcohol ethoxylate (wetting agent), lauryl hydroxysultaine (foam stabilizer), and ethylene glycol butyl ether (cosolvent). Full article