Analytical study of nuclear-coupled density-wave instability in a natural circulation pressure tube type boiling water reactor

An analytical model has been developed to study the nuclear-coupled density-wave instability in the Indian advanced heavy water reactor (AHWR) which is a natural circulation pressure tube type boiling water reactor. The model considers a point kinetics model for the neutron dynamics and a lumped parameter model for the fuel thermal dynamics along with the conservation equations of mass, momentum and energy and equation of state for the coolant. In addition, to study the effect of neutron interactions between different parts of the core, the model considers a coupled multipoint kinetics equation in place of simple point kinetics equation. Linear stability theory was applied to reveal the instability of in-phase and out-of-phase modes in the boiling channels of the AHWR. The results indicate that the stability behavior of the reactor is greatly influenced by the void reactivity coefficient, fuel time constant, radial power distribution and channel inlet orificing. The delayed neutrons were found to have a strong influence on the Type I and Type II instabilities observed at low and high channel powers, respectively. Also, it was found that the coupled multipoint kinetics model and the modal point kinetics model predict the same threshold power for out-of-phase instability if the coupling coefficient in the former model is half the eigen value separation between the fundamental and the first harmonic mode in the latter model. Decay ratio maps were predicted considering various operating parameters of the reactor, which are useful for its design.     

Phase behaviour modelling of Athabasca bitumen for in situ combustion applications

Phase behaviour modelling of reservoir fluid is a fundamental step for reservoir simulation. Furthermore, as the complexity of the recovery process increases, the fluid model plays a more important role in the reliability of the simulation outputs. Although the in situ combustion enhanced oil recovery method (ISC) is one of the most complex recovery techniques available in the petroleum engineering literature, for most of the simulation jobs related to this elaborate process only simple and rudimentary fluid characterization layouts are considered. In this work, the principal fluid properties of Athabasca bitumen with regard to the ISC process are recognized, extracted from the literature, validated for consistency, and used for the development of an inclusive and accurate fluid model. Then the fluid model is fully developed while considering the ISC reaction kinetics so that the model has both accuracy, indispensable for phase behaviour modelling, and consistency, essential for the reactions definitions.     

Solid Yttria-Stabilized Zirconia Films by Pulsed Chemical Vapor Deposition from Metal-organic Precursors

A pulsed chemical vapor deposition from metal-organic precursors (MOCVD) system was used to produce solid zirconia, and yttria-stabilized zirconia (YSZ) films. A total of six candidate metal-organic precursors for zirconia and three for yttria were investigated. Three precursor solutions for YSZ proved suitable for pulsed-MOCVD processing. Layers were deposited on metal, alumina, and porous nickel cermet substrates. Under optimal deposition conditions, precursor conversion efficiency of 90% was achieved using a solution of 3.74 vol% zirconium 2-methyl-2-butoxide + 0.42% yttium methoxyethoxide in toluene. The film growth rate was 7.5 μm·h⁻¹ at 525°C deposition temperature. Two alkoxide precursors produced YSZ layers with material costs under $0.50/(μm·cm²).     

A green and facile one-pot synthesis of Ag–ZnO/RGO nanocomposite with effective photocatalytic activity for removal of organic pollutants

In this study, Ag–ZnO/reduced graphene oxide (Ag–ZnO/RGO) composite was synthesized by a green and facile one-step hydrothermal process. Aqueous suspension containing Ag and ZnO precursors with graphene oxide (GO) sheets was heated at 140 °C for 2 h. The morphology and structure of as-synthesized particles were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, and Photoluminescence (PL) spectroscopy which revealed the formation of composite of metal, metal oxide and RGO. It was observed that the presence of Ag precursor and GO sheets in the hydrothermal solution could sufficiently decrease the size of ZnO flowers. The hybrid nanostructure, with unique morphology, obtained from this convenient method (low temperature, less time, and less number of reagents) was found to have good photocatalytic and antibacterial activity. The perfect recovery of catalyst after reaction and its unchanged efficiency for cyclic use showed that it will be an economically and environmentally friendly photocatalyst.     

Dynamic mechanical analysis and broadband electromagnetic interference shielding characteristics of poly (vinyl alcohol)-poly (4-styrenesulfonic acid)-titanium dioxide nanoparticles based tertiary nanocomposites

ABSTRACT

Novel tertiary nanocomposite films comprising of poly (vinyl alcohol) (PVA), poly (4-styrenesulfonic acid) (PSSA) and titanium dioxide (TiO₂) nanoparticles (NP_S) were prepared using simple solvent casting method. The structural, thermal, morphological, thermo-mechanical and electromagnetic interference (EMI) shielding properties of PVA/PSSA/TiO₂ nanocomposite films were investigated. The EMI shielding effectiveness (SE) of PVA/PSSA/TiO₂ nanocomposite films in the X and Ku band was found to be 12 dB and 13 dB respectively at 25 wt% TiO₂ NPs loading. These results demonstrate the possible applications of PVA/PSSA/TiO₂ nanocomposite films as low cost, lightweight and flexible material for EMI shielding.     

A reaction mechanism for gasoline surrogate fuels for large polycyclic aromatic hydrocarbons

This work aims to develop a reaction mechanism for gasoline surrogate fuels (n-heptane, iso-octane and toluene) with an emphasis on the formation of large polycyclic aromatic hydrocarbons (PAHs). Starting from an existing base mechanism for gasoline surrogate fuels with the largest chemical species being pyrene (C₁₆H₁₀), this new mechanism is generated by adding PAH sub-mechanisms to account for the formation and growth of PAHs up to coronene (C₂₄H₁₂). The density functional theory (DFT) and the transition state theory (TST) have been adopted to evaluate the rate constants for several PAH reactions. The mechanism is validated in the premixed laminar flames of n-heptane, iso-octane, benzene and ethylene. The characteristics of PAH formation in the counterflow diffusion flames of iso-octane/toluene and n-heptane/toluene mixtures have also been tested for both the soot formation and soot formation/oxidation flame conditions. The predictions of the concentrations of large PAHs in the premixed flames having available experimental data are significantly improved with the new mechanism as compared to the base mechanism. The major pathways for the formation of large PAHs are identified. The test of the counterflow diffusion flames successfully predicts the PAH behavior exhibiting a synergistic effect observed experimentally for the mixture fuels, irrespective of the type of flame (soot formation flame or soot formation/oxidation flame). The reactions that lead to this synergistic effect in PAH formation are identified through the rate-of-production analysis.     

Elucidating the Effects of Cu‐Nanoparticles in a Porous Medium vis‐à‐vis Heat Transfer Phenomena

In this paper, a numerical simulation technique is developed to investigate the qualitative and quantitative behaviour of Cu‐nanoparticles in a porous medium vis‐a‐vis the heat transfer enhancements—buoyancy driven flow in a two‐dimensional square cavity, with moving walls is presented. The model utilizes the finite volume approach to solve the Brinkman–Darcy equations for Cu‐nanoparticles in a porous media. Discretization is carried out for convective and diffusive fluxes using Quadratic Upwind Interpolation for Convective Kinematics (QUICK) and central difference schemes, respectively. Tri‐Diagonal Matrix Algorithm is invoked to solve the set of algebraic equations. The Darcy number (Da), Prandtl number (Pr), and volume fraction (χ) are varied from 10^?3 to 10^?1, 3 to 7, and 0% to 20%, respectively. Insight into the cause of variations in isotherms, streamlines, Nusselt number (Nu), and mid‐plane velocities is explicated. The present numerical results are compared with the existing literature and found to be in good agreement. Even though nanoparticles slightly hinder the activity of the fluid, they can augment the average Nu by 90% for Pr = 7, Da = 0.1, and χ = 20% as compared to the absence of nanoparticles. Their efficacy is more prominent for flows with higher Da and Pr. Quantitative values for Nu were obtained for various combinations of Pr, Da, and χ.     

rGO Sheets/ZnFe2O4 Nanocomposities as an Efficient Electro Catalyst Material for I3−/I− Reaction for High Performance DSSCs

In this paper, Reduced Graphene Oxide (rGO)/ZnFe₂O₄ (rZnF) nanocomposite is synthesized by a simple hydrothermal method and employed as a counter electrode (CE) material for tri-iodide redox reactions in Dye sensitized solar cells (DSSC) to replace the traditional high cost platinum (Pt) CE. X-ray diffraction analysis and High resolution Transmission electron microscopy, clearly indicated the formation of rZnF nanocomposite and also amorphous rGO sheets were smoothly distributed on the surface of ZnFe₂O₄ (ZnF) nanostructure. The rZnF-50 CE shows excellent electro catalytic activity toward I₃^? reduction, which has simultaneously been confirmed by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization measurements. A DSSC developed by rZnF-50 CE (η?=?8.71%) obtained quite higher than the Pt (η?=?8.53%) based CE under the same condition. The superior performances of rZnF-50 CE due to addition of graphene in to Spinel (ZnF) nanostructure results in creation of highly active electrochemical sites, fast electron transport linkage between CE and electrolyte. Thus it’s a promising low cost CE material for DSSCs.