Hall current effects on MHD flow of chemically reacting fluid through a porous medium with heat source

We considered the magnetohydrodynamic (MHD) free convective flow of an incompressible electrically conducting viscous fluid past an infinite vertical permeable porous plate with a uniform transverse magnetic field, heat source and chemical reaction in a rotating frame taking Hall current effects into account. The momentum equations for the fluid flow during absorbent medium are controlled by the Brinkman model. Through the undisturbed state, both the plate and fluid are in a rigid body rotation by the uniform angular velocity perpendicular to an infinite vertical plate. The perpendicular surface is subject to the homogeneous invariable suction at a right angle to it and the heat on the surface varies about a non-zero unvarying average whereas the warmth of complimentary flow is invariable. The systematic solutions of the velocity, temperature, and concentration distributions are acquired systematically by utilizing the perturbation method. The velocity expressions consist of steady-state and fluctuating situations. It is revealed that the steady part of the velocity field has a three-layer characteristic while the oscillatory part of the fluid field exhibits a multi-layer characteristic. The influence of various governing flow parameters on the velocity, temperature, and concentration are analyzed graphically. We also discuss computational results for the skin friction, Nusselt number, and Sherwood number in the tabular forms.     

Carbon-based TiO2-x heterostructure nanocomposites for enhanced photocatalytic degradation of dye molecules

Application of brown titanium dioxide (TiO_2-x) and its modified composite forms in the photocatalytic decomposition of organic pollutants in the environment is a promising way to provide solutions for environmental redemption. Herein, we report the synthesis of effective and stable TiO_2-x nanoparticles with g-C₃N₄, RGO, and multiwalled carbon nanotubes (CNTs) using a simple hydrothermal method. Among all the as-synthesized samples, excellent photocatalytic degradation activity was observed for RGO-TiO_2-x nanocomposite with high rate constants of 0.075 min^?1_, 0.083 min^?1 and 0.093 min^?1 for methylene blue, rhodamine-B, and rosebengal dyes under UV–Visible light irradiation, respectively. The altered bandgap (1.8 eV) and the large surface area of RGO-TiO_2-x nanocomposite impacts on both absorption of visible light and efficiency of photogenerated charge electron (e^?)/hole (h⁺) pair separation. This resulted in enhanced photocatalytic property of carbon-based TiO_2-x nanocomposites. A systematic study on the influence of different carbon nanostructures on the photocatalytic activity of brown TiO_2-x is carried out.     

Effect of oxygen deficiency (δ) on transition temperature of yttrium cuprate superconductors

The nature of pairing mechanism as well as transition temperature of yttrium cuprates is discussed using the strong coupling theory. An interaction potential has been developed for the layered structure with two conducting CuO₂(a–b) layers in a unit cell. The interaction potential properly takes care of electron-electron, electron-phonon and electron-plasmon interactions. Furthermore, the electron-phonon coupling parameter (λ), the modified Coulomb repulsive parameter (μ*) and the 2D acoustic phonon (plasmon) energy as a function of oxygen deficiency is worked out. Finally, the superconducting transition temperature (T _c) is then evaluated by using these coupling parameters and obtainedT _c = 95(92)K for Y(Yb)Ba₂Cu₃O_7−δ superconductors withδ = 0·0. The model parameters estimated from the layered structure approach are consistent with the strong coupling theory. The result deduced on the variation ofT _c withδ are in fair agreement with the earlier reported data on yttrium cuprates. The analysis of the above results are discussed.     

Prediction of the maximum spoutable height in spout-fluid beds

The development of the semi-theoretical correlation in Hadzisdmajlovic et al. (1983) for predicting the maximum spoutable height in a spout-fluid bed, is observed to involve certain discrepancies. Based on their experimental data, a new correlation is proposed.     

Chemical control of superconducting properties of (Y,Ca)(Sr,Ba)2Cu2.7Ga0.3O7−δ

The partial substitution of Ga at the Cu(1) (chain) sites of the YBa₂Cu₃O₇ structure allows synthesis at ambient pressure of Ba-free analogs, e.g., YSr₂Cu_2.7Ga_0.3O_7?δ . Materials with this composition have been found to be nonsuperconducting, but superconductivity has been induced by one or more of the following methods: Ca substitutions at the Y site; Ba substitutions at the Sr site; annealing in high-pressure oxygen. The influence of these chemical manipulations onT _c has been monitored and all methods have been found to enhanceT _c . The electronic effects of Ba substitutions have been deduced indirectly using powder neutron diffraction, and such substitutions appear to result in a redistribution of hole density into the Cu(1) sites from the superconducting CuO₂ planes.     

Solution synthesis of crystallized AMO4 (A=Ba, Sr, Ca; M=W, Mo) film at room temperature

A well-crystallized AMO₄ (A=Ba, Ca, Sr; M=W, Mo) films have been prepared at room temperature through a simple solution reaction in respective alkaline solution at higher pH ranging from 12–14. Adopting the corrosion principle for oxidation of metal substrate, these double oxide films were carried out in presence of chemical driving force without any special apparatus or devices. Hydrogen peroxide was used to enhance the dissolution rate of metal substrates. The driving force for the film formation and growth were high concentration of A²⁺, MO₄²⁻ ions with high pH conditions. Average grain sizes of 8–10 μm with bipyramidal shaped particle were grown to the thickness of about 10–14 μm after 3–6 hours treatment. The crystallization of AMO₄ was characterized by three-dimensional nucleation. This work demonstrates the possibility of fabrication of functional ceramic films directly from the aqueous solution in a single step by solution reactions.