Modeling of transient natural convection heat transfer in electric ovens

Prediction of transient natural convection heat transfer in vented enclosures has multiple applications such as understanding of cooking environment in ovens and heat sink performance in electronic packaging industry. The thermal field within an oven has significant impact on quality of cooked food and reliable predictions are important for robust design and performance evaluation of an oven. The CFD modeling of electric oven involves three-dimensional, unsteady, natural convective flow-thermal field coupled with radiative heat transfer. However, numerical solution of natural convection in enclosures with openings at top and bottom (ovens) can often lead to non-physical solutions such as reverse flow at the top vent, partly a function of initialization and sometimes dependent on boundary conditions. In this paper, development of a physics based robust CFD methodology is discussed. This model has been developed with rigorous experimental support and transient validation of this model with experiments show less than 3% discrepancy for a bake cycle. There is greater challenge in simulating a broil cycle, where the fluid inside the cavity is stably stratified and is also highlighted. A comparative analyses of bake and broil cycle thermal fields inside the oven are also presented.     

CO2 absorption kinetics and equilibrium solubility measurements in potassium salts of renewable amino acids from plant- and animal-protein

Aqueous solutions containing alkaline salts of natural amino acids, such as those from protein in plant seeds or high protein animal-based waste, are green CO₂-separation solvents. In the present work, potassium salts of nine such amino acids were chosen for an in-depth study: alanine, arginine, aspartic acid, glutamic acid, glycine, leucine, proline, serine, and valine. The kinetics of CO₂ absorption in aqueous solutions of these salts was studied using a stirred cell. From the measurements of the absorption rate at different salt concentrations (molarity 0.1 and higher), CO₂ partial pressures (5–25 kPa), and temperatures (298–308 K), values of the reaction order, rate constant, and activation energy were determined. Additionally, the liquid-side mass transfer coefficient (0.005 cm/s) was also found. Potassium salts of proline, glycine, and arginine were most reactive and, hence, were chosen for equilibrium study. The loading capacity of these salts was measured at 308 K in a vapour–liquid equilibrium setup at near-ambient pressure. On the contrary, the other chosen acids were comparatively less reactive with CO₂.     

Experimental investigation on the effect of MgO and TiO2 nanoparticles in stepped solar still

This work aims at augmenting the amount of potable water using MgO and TiO₂ in stepped solar still. Experiments were carried out for the climatic conditions of Chennai, India, with two different concentrations of nanofluids inside a stepped basin under three different cases. Results show that there is an improvement in yield of fresh water from stepped solar still by 33.18% and 41.05% using 0.1% and 0.2% volume concentration of TiO₂ nanofluid, respectively, whereas the freshwater yield from stepped still with MgO nanofluids improved by 51.7% and 61.89%. Furthermore, the economic analysis revealed that the cost of potable water from the modified solar still reduced from 0.029 to 0.016 $/kg. Similarly, the useful annual energy, yearly cost per kilogram, and annual cost per kilowatt hour are significantly profitable with the use of MgO nanofluid in the stepped basin and found as 512.46 kWh, 0.025 $/kg, and 0.026 $/kWh, respectively. It is also found that the cost of potable water from the modified still significantly increases as the amount of fresh water produced is decreased with increased fabrication cost of the solar still.     

A first-principle investigation into effect of B- and BN-doped $$\hbox {C}_{60}$$ in lowering dehydrogenation of $$\hbox {MXH}_{4}$$MXH4 (where M $$=$$= Na,Li and X $$=$$= Al,B)

The present paper reports the effect of B- and BN-doped \(\hbox {C}_{60}\) as catalysts for lowering the dehydrogenation energy in \(\hbox {MXH}_{4}\) clusters (M = Na and Li, X = Al and B) using density functional calculations. \(\hbox {MXH}_{4}\) interacts strongly with B-doped \(\hbox {C}_{60}\) and weakly with BN-doped \(\hbox {C}_{60}\) in comparison with pure \(\hbox {C}_{60}\) with binding energy 0.56–0.80 and 0.05–0.34 eV, respectively. The hydrogen release energy \((E_{\mathrm{HRE}})\) of \(\hbox {MXH}_{4}\) decreases sharply in the range of 38–49% when adsorbed on B-doped \(\hbox {C}_{60}\); however, with BN-doped \(\hbox {C}_{60}\) the decrease in the \(E_{\mathrm{HRE}}\) varies in the range of 6–20% as compared with pure \(\hbox {MXH}_{4}\) clusters. The hydrogen release energy of second hydrogen atom in \(\hbox {MXH}_{4}\) decreases sharply in the range of 1.7–41% for BN-doped \(\hbox {C}_{60}\) and decreases in the range of 0.2–11.3% for B-doped \(\hbox {C}_{60}\) as compared with pure \(\hbox {MXH}_{4}\) clusters. The results can be explained on the basis of charge transfer within \(\hbox {MXH}_{4}\) cluster and with the doped \(\hbox {C}_{60}\).     

4D Biofabrication: 3D Cell Patterning Using Shape‐Changing Films

A novel approach for fabrication of 3D cellular structures using new thermosensitive shape‐changing polymer films with photolithographically patterned surface—4D biofabrication is reported. The surface of shape‐changing polymer films is patterned to selectively adsorb cells in specific regions. The 2D cell pattern is converted to the 3D cell structure after temperature‐induced folding of the polymer films. This approach has a great potential in the field of tissue engineering and bioscaffolds fabrication.     

Reactivity of Hydroxamate Ions in Cationic Vesicular Media for the Cleavage of Carboxylate Esters

The hydrolysis of carboxylate esters viz. p‐nitrophenyl acetate (PNPA), p‐nitrophenyl butyrate (PNPB) and p‐nitrophenyl octanoate (PNPO) in the presence of cationic vesicles of the surfactant dioctadecyldimethylammonium bromide (DODAC) by different hydroxamate ions i.e. acetohydroxamate (AHA^?), benzohydroxamate (BHA^?) and salicylhydroxamate (SHA^?) were studied. The kinetic data was supported by spectrophotometric measurements. The effects of vesicular size on the reaction have been discussed. The differential reactivity under endo‐ and exovesicular conditions has also been evaluated. Critical vesicle concentrations (CVC) of cationic vesicular surfactants were determined from conductometric and fluorimetric measurements at 300 K. Fluorescence probe pyrene and pyrene‐1‐carboxaldehyde have been used for determination of CVC. Further, thermodynamic parameters viz. Standard Gibb's energy (?G°), enthalpy (?H°), and entropy (?S°) of vesicles has also been evaluated within a temperature range of 303.15–328.15 K.     

In Vivo Delivery and Activation of Masked Fluorogenic Hydrolase Substrates by Endogenous Hydrolases in C. elegans

Protein expression and localization are often studied in vivo by tagging molecules with green fluorescent protein (GFP), yet subtle changes in protein levels are not easily detected. To develop a sensitive in vivo method to amplify fluorescence signals and allow cell‐specific quantification of protein abundance changes, we sought to apply an enzyme‐activated cellular fluorescence system in vivo by delivering ester‐masked fluorophores to Caenorhabditis elegans neurons expressing porcine liver esterase (PLE). To aid uptake into sensory neuron membranes, we synthesized two novel fluorogenic hydrolase substrates with long hydrocarbon tails. Recombinant PLE activated these fluorophores in vitro. In vivo activation occurred in sensory neurons, along with potent activation in intestinal lysosomes quantifiable by imaging and microplate and partially attributable to gut esterase 1 (GES‐1) activity. These data demonstrate the promise of biorthogonal hydrolases and their fluorogenic substrates as in vivo neuronal imaging tools and for characterizing endogenous C. elegans hydrolase substrate specificities.     

Performance analysis of evacuated tubes coupled solar still with double basin solar still and solid fins

ABSTRACT

Experimental set up of double basin solar still with evacuated tubes has been fabricated by locally available materials and then carry out research work by use of solid fins. Here 2.5?cm constant depth of water maintained and 3?cm depth mild steel fins are used. Experimental results have been obtained during month of March and April 2018 during clear sky days. Month of March 2018 is chosen for experiments on double basin solar still with evacuated tubes only and April 2018 is chosen for experiments on double basin solar still with evacuated tubes and fins. After series of experiments, it has been found that, the fins increase 25% distillate output compared with alone double basin solar still with evacuated tubes. It also increases distillate output during sunshine hours as well as off-sunshine hours.     

Effect of Silicon Nitride Ball on Adhesive Wear of Martensitic Stainless Steel Pyrowear 675 and AISI M-50 Races with Type II Ester Oil

Advanced bearing materials for future military and commercial gas turbines are required to operate at high speeds, high temperature, and higher thrust loads. At elevated operating conditions, the bearing and gear materials must be able to operate with ultrathin oil films without suffering detrimental effects of adhesive wear. The development of materials with rolling-element fatigue and corrosion resistance properties without deterioration in adhesive wear attributes is a significant challenge. To meet those performance requirements, the forerunner, martensitic stainless steel Pyrowear 675 (AMS 5930), has been in development for aerospace bearing and gear applications. This article addresses the adhesive wear performance of three variants of Pyrowear 675 with silicon nitride ball material simulating a hybrid bearing evaluated using a WAM8 machine. Baseline testing was conducted using conventional bearing steel AISI M-50. Adhesive wear testing was conducted at a temperature of 200°C and at different contact slips (15, 30, 50, and 70%) and entraining velocities (1.3 to 10.2 m/s). Posttest specimens were analyzed by scanning electron microscopy (SEM) and auger electron spectroscopy (AES). All the hybrid material pairs demonstrated very good adhesive wear performance compared to the baseline AISI M-50–AISI M-50 pair.     

Validation of a reduced combustion mechanism for light hydrocarbons

Due to the tremendous costs and difficulties associated with flare measurements, computational fluid dynamics (CFD) simulation could be a viable approach to predict the combustion efficiency as well as VOC/NO _x emissions from industrial flaring activities. However, consisting of a large number of reactions and species, most of the detailed kinetic mechanisms for the speciation study of flaring events are too complicated to use in the CFD simulation of industrial-scale flares. A reduced combustion mechanism will lead to improved computational efficiency; however, its fidelity must be validated. This study uses 2D CFD simulations and 1D Chemkin simulations to validate a reduced mechanism developed for the combustion of light hydrocarbons up to C₁–C₃. This mechanism, consisting of 50 species and 337 reactions, is applicable to C₁–C₃ hydrocarbons and can be used to predict the combustion efficiency and fate of pollutants released from industrial flares composed of C₁–C₃ waste gases. In this article, experimental data reported in the literatures have been used to validate the reduced mechanism. The key performance indicators used for comparison are laminar burner-stabilized flames, laminar flame speeds, adiabatic flame temperatures, ignition delay tests, and temperature and concentration profiles of the critical species. The software package CHEMKIN 4.1.1 was used to verify the computational results of laminar flame speeds, adiabatic flame temperatures, and ignition delays. The axial profiles of various critical species are simulated using the commercial CFD software package FLUENT. It is demonstrated that simulation results using this reduced mechanism are in good agreement with reported experimental results.