Dufour and Soret influence on MHD boundary layer flow of a Maxwell fluid over a stretching sheet with nanoparticles

An analysis has been carried out to examine the heat and mass transfer properties of a two-dimensional incompressible electrically conducting Maxwell fluid over a stretching sheet in the existence of Soret, Dufour, and nanoparticles. In many practical scenarios, such as the polymer extrusion process, the problem presented here is crucial. The flow is examined in terms of the impacts of magnetohydrodynamics and elasticity. Brownian motion and thermophoresis are incorporated into the transport equations. Using adequate similarity variables, the governing partial differential equations and related boundary conditions are non-dimensionalized. The fourth–fifth-order Runge–Kutta–Fehlberg procedure is utilized to solve the consequent transformed ordinary differential equations. The effects of various embedded thermo-physical parameters on the fluid velocity, temperature, concentration, Nusselt number, and Sherwood number have been determined and discussed quantitatively. A comparison of a special case of our results with the one previously reported in the literature shows a very good agreement. An increase in the values of Du and Sr leads to an increase in the temperature and concentration distribution. Nusselt number estimates decrease as Nb estimations increase. Furthermore, this study leads to the study of different flows of electrically conducting fluid over a stretching sheet problem that includes the two-dimensional nonlinear boundary equations.     

A high-throughput chaotic advection microreactor for preparation of uniform and aggregated barium sulfate nanoparticles

A high-throughput (105.5 g/h) passive four-stage asymmetric oscillating feedback microreactor using chaotic mixing mechanism was developed to prepare aggregated Barium sulfate (BaSO₄) particles of high primary nanoparticle size uniformity. Three-dimensional unsteady simulations showed that chaotic mixing could be induced by three unique secondary flows (i.e., vortex, recirculation, and oscillation), and the fluid oscillation mechanism was examined in detail. Simulations and Villermaux–Dushman experiments indicate that almost complete mixing down to molecular level can be achieved and the prepared BaSO₄ nanoparticles were with narrow primary particle size distribution (PSD) having geometric standard deviation, σ_g, less than 1.43 when the total volumetric flow rate Q_total was larger than 10 ml/min. By selecting Q_total and reactant concentrations, average primary particle size can be controlled from 23 to 109 nm as determined by microscopy. An average size of 26 nm with narrow primary PSD (σ_g = 1.22) could be achieved at Q_total of 160 ml/min.     

Cycling stability and adsorption mechanism at room temperature of the upscaled Ni-doped hierarchical carbon scaffold

Hydrogen adsorption performance and mechanism upon cycling of the upscaled Ni-doped hierarchical carbon scaffold (HCS) are investigated. Upon 22 hydrogen ad/desorption cycles (T = 25–50 °C and p (H₂) = 1–50 bar), the upscaled Ni-doped HCS shows excellent cycling stability with gravimetric capacity of up to 1.51 wt % H₂. This is due to mechanical stability of HCS and good distribution of Ni nanoparticles. Hydrogen adsorption mechanism of Ni-doped HCS upon cycling is experimentally and theoretically characterized. Besides dissociative adsorption onto the surface, hydrogen diffusion into the lattice structure of Ni is observed. The latter enhances with the number of ad/desorption cycles and alters the electron sharing mechanisms between Ni and H during adsorption.     

Inducing lattice defects in calcium ferrite anode materials for improved electrochemical performance in lithium-ion batteries

Enhancing the electrical conductivity of electrode materials via a cationic substitution strategy was recognized as an effective way of improving the electrochemical performance of Li-ion batteries. Thus, Li_xCa_1-xFe₂O₄ nanoparticles were synthesized via a facile inexpensive process at low temperature. XRD peaks refer to the formation of an orthorhombic structure with the Pnma space group. HR-TEM investigations reveal orthorhombic-like shape for pure CaFe₂O₄, nanoplatelet-like morphology for Li_0.05Ca_0.95Fe₂O₄ and irregular distorted crystals for Li_0.1Ca_0.9Fe₂O₄. Voids and pores in Li-doped CaFe₂O₄ were confirmed by FESEM and BET measurements. XPS spectra of O1s prove that Li-doped CaFe₂O₄ have higher conductivity due to the created lattice defects and oxygen species. Li-doped CaFe₂O₄ anodes exhibit great improvement in their initial discharge capacities ～1219 and 1606 mAhg^?1 upon substitution of Ca with 5% and 10% Li, respectively. Furthermore, 10% Li-doped CaFe₂O₄ anode displays the highest Li-ions diffusion coefficient and exchange current density due to the enhanced Li⁺ ions mobility. Moreover, the DC activation energies for the Li_xCa_1-xFe₂O₄ nanoparticles decreased with increasing Li content.     

Unraveling specific role of carbon matrix over Pd/quasi-Ce-MOF facilitating toluene enhanced degradation

Metal organic frameworks (MOFs) derivatives represented by quasi-MOFs have excellent physical and chemical properties and can be applied for the catalytic combustion of volatile organic compounds (VOCs). In this work, Pd/quasi-Ce-BTC synthesized by simple one-step N₂ pyrolysis was applied to the oxidation of toluene, showing excellent toluene catalytic activity (T₉₀ = 175 °C, 30000 mL/(g·h)). Microscopic analyses indicate the formation and interaction of a carbon matrix composite quasi-MOF structure interface. The results show that the amorphous carbon matrix formed during the partial pyrolysis of Ce-BTC significantly improves the adsorption and activation capacity of toluene in the reaction, and constructs a reductive system to maintain high concentrations of Ce³⁺ and Pd⁰, which can facilitate the activation and utilization of oxygen in reaction. Quasi in-situ XPS proves that carbon matrix is indirectly involved in the activation and storage of oxygen, and Pd⁰ is the crucial active site for the activation of oxygen. Stability and water resistance tests display good stability of Pd/quasi-Ce-BTC. This work provides a potential method for designing quasi-MOF catalysts towards VOCs effective abatement.     

Upconversion nanoparticles: Recent strategies and mechanism based applications

Upconversion nanoparticles (UCNPs) doped with lanthanides can convert near-infrared excitation into UV and visible emissions. Because of their relatively high emission efficiency, UCNPs are appealing materials for use in a variety of sectors. UCNPs are known for low auto-fluorescence, excellent chemical and thermal photo-stability, deep tissue penetration, exceptional biocompatibility, low toxicity, color purity, and ease of surface functionalization. In this review, we explain a few recent strategies to boost the efficiency and luminescence of upconversion nanoparticles and minimize quenching by fabricating them as core/shell, nanofibers, or heavily doped lanthanides. Applications of UCNPs in drug delivery, Photodynamic therapy (PDT), biosensors, bioimaging, and optogenetics are also discussed along with their mechanism of action. Our motivation for this review is to understand the working mechanism of UCNPs and their applications in various fields.     

Fe3O4-carbon spheres core–shell supported palladium nanoparticles: A robust and recyclable catalyst for suzuki coupling reaction

Suzuki-Miyaura (S-M) is regarded the most powerful way for synthesis biaryls, triaryls, or incorporating of substituted aryl moieties in organic preparation by the cross-coupling of aryl boronic acid with aryl halides using the Pd catalyst. This work reports the combining of the hydrothermal and microwave-assisted protocol to convert the glucose to magnetic carbon spheres (Fe₃O₄-CSPs) decorated with Pd nanoparticles (NPs) as the catalyst for Suzuki-Miyaura cross-coupling reactions. The physicochemical properties in the produced composite were examined using FESEM, HRTEM, nitrogen isotherms, Raman spectroscopy, FTIR, XPS, and XRD. The as-fabricated composite Pd/Fe₃O₄-CSPs is mostly spherical with a core–shell structure and possesses a great surface area of 253.2 m²·g^-1. Its catalytic performance demonstrates that the composite has excellent stability and high tolerance Suzuki-Miyaura cross-coupling reactions in 30 min at 80 ℃. Both activated and deactivated aryl halides provided excellent yield. The as-fabricated catalyst was recycled for up to four catalytic cycles without a substantial decline in performance. Moreover, this research offers a facile roadmap for synthesizing Pd/Fe₃O₄-CSPs composites and promoting the practical implementation of Pd/Fe₃O₄-CSPs catalysts for organic transformation processes.     

Structural,optical, cytotoxicity,and antimicrobial properties of MgO,ZnO and MgO/ZnO nanocomposite for biomedical applications

In this study, MgO nanoparticles were successfully fabricated and incubated inside ZnO NPs to form MgO/ZnO nanocomposite for biomedical applications. The x-ray diffraction analysis of MgO, ZnO, and MgO/ZnO has shown the single-phase x-ray diffraction patterns through X'pert High score. The crystallite sizes were calculated as 18 nm, 42 nm, and 53 nm, respectively. The average particle size of MgO, ZnO, and MgO/ZnO nanopowders depicted from secondary electron images of field emission electron microscopy were 56 nm, 400 nm, and 450 nm, respectively. The presence of MgO NPs inside ZnO NPs was confirmed by transmission electron microscopy. The elemental dispersive spectroscopy of MgO, given the peaks of oxygen and magnesium, also showed only zinc and oxygen peaks in ZnO, which confirms no other impurities in MgO and ZnO powders. The elemental analysis of MgO/ZnO nanocomposite showed the peaks of Zinc and Oxygen, along with a tiny peak of Mg. The photoluminescence and UV–vis spectroscopy revealed the absorbance fluorescence limit of the nanomaterials. Fourier transform infrared spectroscopy confirmed the several groups present in the nanocomposite. The biocompatibility of MgO, ZnO, and MgO/ZnO was observed with human peripheral blood mononuclear cells. The cytotoxicity studies were also performed against human cancer (liver and breast) cell lines. The MgO, ZnO, and MgO/ZnO exhibited the antimicrobial properties against Escherichia coli and Staphylococcus aureus.     

Virus-Based Nanoreactors with GALT Activity for Classic Galactosemia Therapy

Enzymatic nanoreactors were obtained by galactose-1-phosphate uridylyl-transferase (GALT) encapsulation into plant virus capsids by a molecular self-assembly strategy. The aim of this work was to produce virus-like nanoparticles containing GALT for an enzyme-replacement therapy for classic galactosemia. The encapsulation efficiency and the catalytic constants of bio-nanoreactors were determined by using different GALT and virus coat protein ratios. The substrate affinity of nanoreactors was slightly lower than that of the free enzyme; the activity rate was 16 % of the GALT free enzyme. The enzymatic nanoreactors without functionalization were internalized into different cell lines including fibroblast and kidney cells, but especially into hepatocytes. The enzymatic nanoreactors are an innovative enzyme preparation with potential use for the treatment of classic galactosemia.     

Effect of hexagonal structure nanoparticles on the morphological performance of the ceramic scaffold using analytical oscillation response

Porous bony scaffolds are utilized to manage the growth and migration of cells from adjacent tissues to a defective position. In the current investigation, the effect of titanium oxide (TiO₂) nanoparticles on mechanical and physical properties of porous bony implants made of polymeric polycaprolactone (PCL) is studied. The bio-nanocomposite scaffolds are prepared with composition of nanocrystalline hydroxyapatite (HA) and TiO₂ powder using the freeze-drying technique for different weight fractions of TiO₂ (0 wt%, 5 wt%, 10 wt%, and 15 wt%). In order to identify the microstructure and morphology of the fabricated porous bio-nanocomposites, the X-ray diffraction (XRD), atomic force microscope (AFM) and scanning electron microscopy (SEM) are employed. Also, the biocompatibility and biodegradability of the manufactured scaffolds are examined by placing them in a simulated body fluid (SBF) for 21 days, their weight and pH changes are measured. The rate of degradation of the PCL-HA scaffold can be controlled by varying the percentage of its constituent components. Due to an increasing growth and activity of bone cells and the apatite formation on the free surface of the fabricated bio-nanocomposite implants as well as their reasonable mechanical properties, they have the potential to be used as a bone substitute. Additionally, with the aid of the experimentally extracted mechanical properties of the scaffolds, the vibrational characteristics of a beam-type implant made of the proposed porous bio-nanocomposites are explored. The results obtained from SEM image indicate that the scaffolds produced by the employed method have high total porosity (70%–85%) and effective porosity. The pore size is obtained between 60 and 200 μm, which is desirable for the growth and propagation of bone cells. Also, it is revealed that the addition of TiO₂ nanoparticles leads to reduce the rate of dissolution of the fabricated bio-nanocomposite scaffolds.