Search Results (314)

The present study targets key limitation ‘separation after the process’ that is responsible for the loss of the photocatalyst in water treatment during heterogeneous photocatalysis. Therefore, eco-friendly nanostructured ZnO coatings were engineered by the doctor blade technique through the immobilization of green ZnO nanomaterials onto alumina substrate. ZnO/BPE 30 and ZnO/BPE 60 coatings were obtained from banana peel extract-based ZnO powder (ZnO/BPE). Likewise, ZnO/GTE 30 and ZnO/GTE 60 were prepared using green tea extract-based ZnO powder (ZnO/GTE). XRD characterization verified hexagonal wurtzite ZnO phase, while HRSEM analysis revealed that the flat surface of ZnO/BPE had rod-like nanostructures below 120 nm, and ZnO/GTE had spherical, porous nanoparticle networks with less than 70 nm. According to UV–vis spectrometry, all four coatings have bandgaps of ~5 eV. The highest efficiency for the solar-driven photocatalytic degradation of emerging organic pollutants was for ciprofloxacin (among pesticides clomazone and tembotrione; pharmaceuticals ciprofloxacin and 17α-ethinylestradiol; and mycotoxin zearalenone) in ultrapure water with the presence of all studied ZnO-based coatings, after 60 min of simulated solar irradiation. Its highest removal (89.1%) was achieved with ZnO/GTE 30, also having good reusability across three consecutive cycles in river water, thus supporting the application of eco-friendly, immobilized ZnO nanomaterials for wastewater treatment and environmental remediation. Full article

This paper investigates the flow of a second-grade hybrid nanofluid through a Darcy–Forchheimer porous medium under Cattaneo–Christov heat and mass flux models. The hybrid nanofluid, composed of alumina and copper nanoparticles in water, enhances thermal and mass transport, while the second-grade model captures viscoelastic effects, and the Darcy–Forchheimer medium accounts for both linear and nonlinear drag. Using similarity transformations and the spectral quasilinearisation method, the nonlinear governing equations are solved numerically and validated against benchmark results. The results show that hybrid nanoparticles significantly boost heat and mass transfer, while Cattaneo–Christov fluxes delay thermal and concentration responses, reducing the near-wall temperature and concentration. The distributions of velocity, temperature, concentration, and microorganism density are markedly affected by porosity, the Forchheimer number, the bio-convection Peclet number, and relaxation times. The results illustrate that hybrid nanoparticles significantly increase heat and mass transfer, whereas thermal and concentration relaxation factors delay energy and species diffusion, thickening the associated boundary layers. Viscoelasticity, porous medium resistance, Forchheimer drag, and bio-convection all have an influence on flow velocity and transfer rates, highlighting the subtle link between these mechanisms. These breakthroughs may be beneficial in establishing and enhancing bioreactors, microbial fuel cells, geothermal systems, and other applications that need hybrid nanofluids and non-Fourier/non-Fickian transport. Full article

Alumina nanoparticles have broad applications in catalysis, electronics, and the construction sector, and are widely incorporated as additives in coating formulations to enhance mechanical durability and functional performance. This work focuses on the green synthesis of aluminum oxide (Al₂O₃) nanoparticles using lemongrass (Cymbopogon citratus) extract. Aluminum nitrate [Al(NO₃)₃] and aluminum chloride (AlCl₃) were used with extract. The reaction was carried out at 70 °C for 1 h at 250 rpm and then thermal treatments at 700 °C and 900 °C were applied. The results showed that nanoparticles synthesized from the AlCl₃ and calcined at 700 °C exhibited a smaller particle size (36 ± 14 nm) as compared with those synthesized from the [Al(NO₃)₃] and calcined at 700 °C (49 ± 25 nm). Despite both precursors yielding nanoparticles, the peaks related to the γ-Al₂O₃ crystal phase were observed in the AlCl₃ at 700 °C calcination. Conversely, the nanoparticles synthesized from the [Al(NO₃)₃] required a high temperature treatment at 900 °C to display this stable crystal phase. This study reports an easy and cost-effective green chemistry route to obtain γ-Al₂O₃ nanoparticles, highlighting the importance of the selection of precursors as a critical step to achieve a sustainable and low-energy process, suggesting the potential applications in paints with multifunctional properties. Full article

Proton binding (i.e., charging) isotherms of halloysite nanotubes (HNT) were determined from cycled acid-base potentiometric titrations in KCl solution at constant ionic strengths (0.01, 0.10, 1.00 mol dm⁻³). The isotherms measured in the pH cycle from 3 to 11 and back exhibit a pronounced hysteresis with respect to the direction of pH change, which is accurately reproducible when the cycle is repeated. The hysteresis is absent if the cycled titration is performed within a narrow pH range between 5 and 9. These results align with the dissolution rates of alumina and silica, which form the two surfaces of the rolled kaolinite sheet in HNT, and clearly point to reversible partial dissolution-deposition processes in the HNT interior during a titration cycle, outside the above pH range (alumina dissolution below pH ≈ 5 and silica dissolution above pH ≈ 8.5). In the studied titration experiments, these processes produce partially dissolved surface-bound, rather than completely dissolved species (reversible surface etching). Under the applied conditions, reversible surface etching is less pronounced in the acidic part of the titration cycle. Charging isotherms recorded in the decreasing pH titrations at varied ionic strength exhibit a common intersection point very close to zero charge (point of zero charge) around pH ≈ 8.1, characteristic for an amphoteric solid surface. These isotherms were reasonably well fitted by applying the surface protonation model in the HNT interior, which invokes the Stern model of the electric double layer (EDL), by summing the surface charges calculated for alumina and silica as separate components (surfaces). The model surface charge isotherms for alumina surface in the HNT interior exhibit a point of zero charge at pH = 9.0, while the silica surface has a negative charge above pH > 8.5, which is in very good agreement with the values reported in the literature: as for these two surfaces, thus for kaolinite nanoparticles. The best-fit protonation site density for both surfaces is equal to 8.0 nm⁻², while the best-fit intrinsic pK_a for alumina and silica surfaces of HNT are equal to 9.0 and 8.5, respectively. The pH-dependence of electrophoretic mobility, measured by means of electrophoretic light scattering, reveals a more acidic behavior of the outermost silica surface than within the inner HNT phase, which is consistent with the literature result reported for kaolinite. The results reported herein confirm that the inner and outer surfaces of the HNT are oppositely charged below pH < 8.0 and negatively charged above that value, and importantly, they reveal new details about the protonation affinities and EDL parameters at active surfaces of HNT, important for the colloidal stability of HNT suspensions and the functionalization of HNT through the electrostatic binding of active molecules. Full article

Textile dyeing effluents are characterized by recalcitrant organics and high salinity, requiring robust pretreatments prior to biological polishing. The heterogeneous Fenton-type (HFT) oxidation over Prussian Blue nanoparticles supported on γ-alumina (PBNP/γ-Al₂O₃) was investigated in a liquid batch-recycle packed-bed reactor treating a synthetic textile wastewater (STW) reproducing an industrial dye bath with the Reactive Black 5 (RB5) dye, together with simplified RB5 and RB5 + NaCl matrices. Hydrogen peroxide decay followed pseudo-first-order kinetics. Using fixed initial doses (11, 20, 35 mmol L⁻¹), the catalyst exhibited an early adaptation phase and then reproducible operation: from the fourth reuse onward, both the H₂O₂ decomposition rate constant and DOC removal varied by <10% under identical conditions. Among matrices, STW exhibited the highest oxidant efficiency. With an initial H₂O₂ dose of 11 mmol L⁻¹, the treatment enabled complete discoloration and produced effluents with negligible toxicity. Increasing the initial dose to 20 or 35 mmol L⁻¹ did not improve treatment and led to a decrease in the hydrogen peroxide decomposition rate with reuses and loss of PB ν(C≡N) Raman bands, indicating surface transformation. Overall, PBNP/γ-Al₂O₃ demonstrated reproducible activity and structural resilience in saline, dyeing-relevant matrices at H₂O₂ doses that preserve catalytic integrity, confirming its feasibility as a stable and reusable pretreatment catalyst for saline dyeing effluents, and supporting its integration into hybrid AOP–biological treatment schemes for dyeing wastewater. Full article

This study experimentally investigates single-phase forced convection heat transfer and flow characteristics of Al₂O₃-water nanofluids under rotating hypergravity conditions ranging from 1 g to 5.1 g. While nanofluids offer enhanced thermal properties for advanced cooling applications in aerospace and rotating machinery, their performance under hypergravity remains poorly understood. Experiments employed a custom centrifugal test rig with a horizontal test section (D = 2 mm, L = 200 mm) operating at constant heat flux. Alumina nanoparticles (20–30 nm) were dispersed in deionized water at mass fractions of 0.02–0.5 wt%, with stability validated through transmittance measurements over 72 h. Heat transfer coefficients (HTC), Nusselt numbers (Nu), friction factors (f), and pressure drops were measured across Reynolds numbers from 500 to 30,000. Results demonstrate that hypergravity significantly enhances heat transfer, with HTC increasing by up to 40% at 5.1 g compared to 1 g, most pronounced at the transition from 1 g to 1.41 g. This enhancement is attributed to intensified buoyancy-driven secondary flows quantified by increased Grashof numbers and modified particle distribution. Friction factors increased moderately (15–25%) due to Coriolis effects and enhanced viscous dissipation. Optimal performance occurred at 0.5 wt% concentration, effectively balancing thermal enhancement against pumping penalties. Random forest (RF) and eXtreme gradient boosting (XGBoost) achieved R² = 0.9486 and 0.9625 in predicting HTC, respectively, outperforming traditional correlations (Gnielinski: R² = 0.9124). These findings provide crucial design guidelines for thermal management systems in hypergravity environments, particularly for aerospace propulsion and centrifugal heat exchangers, where gravitational variations significantly impact cooling performance. Full article

Titanium alloys are widely employed in structural and electrochemical applications owing to their excellent mechanical properties and inherent corrosion resistance. However, their stability in harsh acidic environments, such as those encountered in energy storage systems, remains a critical issue. In this study, composite ceramic coatings were synthesized on a Ti6Al4V alloy using plasma electrolytic oxidation (PEO) in silicate-, phosphate-, and sulfate-based electrolytes, with and without the addition of α-alumina nanoparticles. The resulting coatings were comprehensively characterized to assess their surface morphology, chemical and phase compositions, and corrosion performance. Thus, the corrosion current density decreased from 9.7 × 10⁴ for bare Ti6Al4V to 143 nA/cm² for the coating fabricated in phosphate electrolyte with alumina nanoparticles, while the corrosion potential shifted anodically from –0.68 to +0.49 V vs. silver chloride electrode in 5 M H₂SO₄. Among the tested electrolytes, coatings produced in the phosphate-based electrolyte with Al₂O₃ showed the highest polarization resistance (113 kΩ·cm²), outperforming those fabricated in silicate- (71.6 kΩ·cm²) and sulfate-based (89.0 kΩ·cm²) systems. The composite coatings exhibited a multiphase structure with reduced surface porosity and the incorporation of crystalline oxide phases. Notably, titania–alumina nanoparticle composites demonstrated significantly enhanced corrosion resistance. These findings confirm that PEO-derived composite coatings provide an effective surface engineering strategy for enhancing the stability of the Ti6Al4V alloy in aggressive acidic environments relevant to advanced electrochemical systems. Full article

In this study, we report, for the first time, the tribo-catalytic degradation of methyl orange (MO) using Cu/Al₂O₃ nanoparticles under mechanical stirring conditions. The hybrid catalyst was synthesized via a wet impregnation method and characterized through different techniques, confirming structural integrity and compositional uniformity. When subjected to friction generated by a PTFE-coated magnetic stir bar, Cu/Al₂O₃ nanoparticles exhibited high tribo-catalytic activity, achieving up to 95% MO degradation within 10 h under dark conditions. The observed activity surpasses that of alumina alone and is attributed to the synergistic effects between copper and alumina, facilitating charge separation and enhancing reactive oxygen species (ROS) formation. Tribo-catalytic efficiency was further influenced by stirring speed and contact area, confirming the key role of mechanical friction. Reusability tests demonstrated stable performance over five cycles, highlighting the material’s durability and potential for practical environmental remediation applications. Full article

This research investigates the multi-objective optimization of micro-milling processes for the titanium alloy Ti-3Al-2.5V (grade 9) through the application of grey relational analysis. The incorporation of nanometer-sized particles in hybrid machining lubricants plays a crucial role in improving heat transfer during machining. The approach aims to increase the efficiency and effectiveness of micro-milling by addressing various performance metrics simultaneously, leading to better machining results for this titanium alloy. Additionally, the integration of nanoparticles into the machining lubricant significantly improves the lubrication properties, reducing friction during the machining process. The study analyzed four machining parameters: machining speed, rate of feed, axial depth of cut, and the weight percentage concentration of hybrid machining lubricants Multi-wall Carbon Nano Tube and Alumina Oxide (MWCNT and Al₂O₃). The machining nanolubricant was formulated by adding 1% and 2% volume concentrations of MWCNT and Al₂O₃ nanoparticles to the industrial machining fluid. In this machining context, the friction between the machining tool and the Ti-3Al-2.5V work piece is a vital factor influencing the output quality. The results demonstrate that the chosen machining parameters and machining lubricants have a direct impact on the coefficient of friction and surface roughness. The study concludes that utilizing machining nanolubrication for machining Ti-3Al-2.5V (grade 9) significantly enhances the quality compared with traditional machining lubricants. Full article

In this study, high-yield biopolymer/ceramic hollow fibers were fabricated via a facile, modified polyol process in a spinneret setup, enabling the controlled adsorption of Cu²⁺ ions. Post sintering transformed these into catalytic copper-decorated carbon/ceramic (alumina) composite hollow fibers, with alginate serving as both a metal ion binder and a copper nanoparticle stabilizer. The resulting hollow fibers featured porous walls with a high surface area and were densely decorated with copper nanoparticles. Their structural and morphological characteristics were analyzed, and their NO reduction performance was assessed in a continuous flow configuration, where the gas stream passed through both the shell and lumen sides of a fiber bundle in a tangential flow mode. This study also examined the stability, longevity and regeneration potential of the catalytic fibers, including the mechanisms of deactivation and reactivation. Carbon content was found to be decisive for catalytic performance. High-carbon fibers exhibited a light-off temperature of 250 °C, maintained about 90% N₂ selectivity and sustained a consistently high NO reduction efficiency for over 300 h, even without reducing gases like CO. In contrast, low-carbon fibers displayed a higher light-off temperature of 350 °C and a reduced catalytic efficiency. The results indicate that carbon enhances both activity and selectivity, counterbalancing deactivation effects. Owing to their scalability, durability and effectiveness, these catalytic fibers and their corresponding bundle-type reactor configuration represent a promising technology for advanced NO abatement. Full article

Pyridine is a recalcitrant organic compound present in industrial wastewater that causes severe effects on the environment and the health of living beings, as it is considered a toxic, mutagenic, teratogenic, and carcinogenic agent. Therefore, this research explored the efficacy of a zinc oxide catalyst, doped with platinum nanoparticles and supported alumina through the precipitation method, for the photocatalytic degradation of pyridine using a fluidized bed reactor. A Box–Behnken experimental design was used to analyze the effect of the pH (4–10), the pyridine concentration (20–300 ppm), and the amount of catalyst (20–100 g). The X-ray diffraction (XRD) characterization results confirmed the hexagonal structure of the zinc oxide and the successful incorporation of platinum. Scanning electron microscopy (SEM) revealed a nano-bar morphology upon catalyst doping, favoring the photocatalytic activity. Pyridine removal of 57.7% was achieved under the following conditions: a pH of 4, 160 ppm of pyridine, and 100 g of catalyst. The process followed a pseudo-first-order model, obtaining the reaction constant k₁ = 1.943 × 10⁻³ min⁻¹ and the adsorption constant k₂ = 1.527 × 10⁻³ L/mg. The results showed high efficiency and stability of the catalyst in the fluidized bed reactor for pyridine degradation, especially under acidic conditions, representing a promising technological alternative for treating industrial wastewater contaminated with N-heterocycles such as pyridine. Full article

The development of mineral, biodegradable sunscreens that can offer both high photoprotection and long-term colloidal stability, while limiting synthetic additives, presents a significant challenge. A linseed oil nanoemulsion co-stabilised by ZnO nanoparticles and the eco-friendly surfactant Appyclean 6552 was formulated, and the effect of incorporating fumed silica/alumina (Aerosil COK 84) was evaluated. A central composite response surface design was used to ascertain the oil/ZnO ratio that maximised the in vitro sun protection factor at sub-300 nm droplet size. The incorporation of Aerosil at concentrations ranging from 0 to 2 wt.% resulted in a transformation of the dispersion from a nearly Newtonian state to a weak-gel behaviour. This alteration was accompanied by a reduction in the Turbiscan Stability Index. Microscopic analysis has revealed a hierarchical particle architecture, in which ZnO forms Pickering shells around each droplet, while Aerosil aggregates bridge neighboring interfaces, creating a percolated silica scaffold that immobilises droplets and amplifies multiple UV scattering. The findings demonstrate that coupling interfacial Pickering armour with a continuous silica network yields a greener, physically robust mineral sunscreen and offers a transferable strategy for stabilising plant-oil emulsions containing inorganic actives. Full article

Background/Objectives: The increasing prevalence of multidrug-resistant bacteria presents a major global health challenge, prompting a search for innovative antimicrobial strategies. This study aimed to develop and evaluate a novel nanobiostructure combining alumina nanoparticles (NPs) with the antimicrobial peptide lunatin-1 (Lun-1), forming peptide-functionalized nanofilaments. The main objective was to investigate how the site of peptide functionalization (C-terminal vs. N-terminal) affects membrane interactions and antibacterial activity. Methods: NP–peptide conjugates were synthesized via covalent bonding between lun-1 and alumina NP and characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), zeta potential analysis, dynamic light scattering (DLS), Fourier-transform infrared (FTIR), and solid-state ¹³C NMR. Antibacterial activities were assessed against different Gram-positive and Gram-negative strains. Biophysical analyses, including circular dichroism (CD), isothermal titration calorimetry (ITC), differential scanning calorimetry (DSC), and solid-state ²H NMR, were employed to evaluate peptide–membrane interactions in the presence of membrane-mimetic vesicles composed of POPC:POPG (3:1) and DMPC:DMPG (3:1). Results: Characterization confirmed the successful formation of NP–peptide nanofilaments. Functionalization at the N-terminal significantly influenced both antibacterial activity and peptide conformation compared to C-terminal attachment. Biophysical data demonstrated stronger membrane interaction and greater membrane disruption when lun-1 was conjugated at the N-terminal. Conclusions: The site of peptide conjugation plays a crucial role in modulating the biological and biophysical properties of NP–lunatin-1 conjugates. C-terminal attachment of lunatin-1 retains both membrane interaction and antibacterial efficacy, making it a promising strategy for the design of peptide-based nanotherapeutics targeting resistant pathogens. Full article

The synthesis of oxide nanopowders through ultrasonic spray pyrolysis (USP) represents a sustainable method for producing high-purity, spherical particles tailored for advanced material applications. Recent developments in USP synthesis leverage the continuous transport of aerosols from an ultrasonic generator to a high-temperature furnace, with nanopowders collected efficiently using an electrostatic precipitator. This study explored the use of USP for titanium oxysulfate and aluminum nitrate solutions derived from the aluminum industry, focusing on resource recovery and waste reduction. Titanium oxysulfate was synthesized by leaching slag, generated during the reduction of red mud, with sulfuric acid under oxidizing, high-pressure conditions. After purification, the titanium oxysulfate solution was processed using USP in a hydrogen reduction atmosphere to yield spherical titanium dioxide (TiO₂) nanopowders. The hydrogen atmosphere enabled precise control over the nanoparticles’ morphology and crystallinity, enhancing their suitability for use in applications such as photocatalysis, pigments, and advanced coatings. In parallel, both synthetic and laboratory solutions of aluminum nitrate [Al(NO₃)₃] were prepared. The laboratory solution was prepared by leaching aluminum hydroxide oxide (AlOOH) with hydrochloric acid to form aluminum chloride (AlCl₃), followed by a conversion to aluminum nitrate through the addition of nitric acid. The resulting aluminum nitrate solution was subjected to USP, producing highly uniform, spherical alumina (Al₂O₃) nanopowders with a narrow size distribution. The resulting nanopowders, characterized by their controlled properties and potential applicability, represent an advancement in oxide powder synthesis and resource-efficient manufacturing techniques. Full article

Nanofluids—engineered suspensions of nanometer-sized particles—have attracted significant attention due to their reportedly enhanced thermal properties, making them promising candidates for advanced heat transfer applications. However, despite extensive studies, uncertainties remain regarding the magnitude and origin of these effects, limiting their practical implementation. To address this, we present a comprehensive study on nanofluid formulations based on the commercial refrigerant HFE-7500, incorporating surfactant-stabilized dispersions of several metal oxide and nitride nanoparticles. We measured key physicochemical properties, including zeta potential, particle size, viscosity, and thermal conductivity. Our results show that while the nanofluids exhibited high stability, their particle sizes in suspension were significantly larger than the primary nanoparticle sizes measured by TEM. Notably, alumina-based suspensions demonstrated the greatest enhancement, exhibiting approximately 10–15% increases in thermal conductivity as a function of volume percentage. These surpassed the 5–10% improvements observed with other metal oxides, an effect that may be linked to their comparatively larger particle sizes. However, the observed enhancements were lower than some previously reported values that claimed anomalously high thermal conductivity increases. Furthermore, steady shear viscosity increased with particle concentration, showing enhancements of 10–20%, which suggests a potential trade-off for practical implementation. Our findings refine the understanding of nanofluid behavior in refrigerants and establish a foundation for optimizing their performance in thermal management applications. However, viscosity increases must be carefully considered when designing next-generation nanofluids for real-world use. Full article