Mixed convection flows of tangent hyperbolic fluid past an isothermal wedge with entropy: A mathematical study

The nonlinear, steady, and mixed convective boundary layer flow and heat transfer of an incompressible tangent hyperbolic non-Newtonian fluid over an isothermal wedge in the presence of magnetic field are analyzed numerically using the implicit Keller-Box finite-difference technique. The entropy analysis due to MHD flow of a tangent hyperbolic fluid past an isothermal wedge and viscous dissipation is also included. The numerical code is validated with previous Newtonian studies available in the literature. Graphical and tabulated results are analyzed to study the behavior of the fluid velocity, temperature, concentration, shear stress, heat transfer rate, entropy generation number, and Bejan number for various emerging thermophysical parameters, namely Weissenberg number (We), power-law index (n), mixed convection parameter (λ), pressure gradient parameter (m), Prandtl number (Pr), Biot number (γ), Hartmann number (Ha), Brinkmann number (Br), Reynolds number (Re), and temperature gradient (Π). It is observed that velocity, entropy, Bejan number, and surface heat transfer rate are reduced with the increase in the Weissenberg number, but temperature and local skin friction are increased. An increase in pressure gradient enhances velocity, entropy, local skin friction, and surface heat transfer rate, but reduces temperature and Bejan number. An increase in an isothermal power-law index (n) is observed to increase velocity, Bejan number, and surface heat transfer rate, but it decreases temperature, entropy, and local skin friction. An increase in the magnetic parameter (Ha) is found to decrease temperature, entropy, surface heat transfer rate, and local skin friction, and it increases velocity and Bejan number. The research is applicable for coating materials in chemical engineering, for instance, robust paints, production of aerosol deposition, and water-soluble solution thermal treatment.     

Evaluation of Nano Zinc (ZnO) for Surface Enhancement of ATR–FTIR Spectra of Butter and Spread

The effect of nano zinc (ZnO) particles in surface enhancement of attenuated total reflection–Fourier transform mid-infrared spectroscopy (ATR–FTIR) has been studied in butter and spread. Due to the health implications associated with consumption of trans fats, the studies also included the determination of band corresponding to trans fats of butter/spread in the nano-zinc-treated samples. The FTIR spectra of nano-zinc-treated butter showed enhancement of bands related to (―C―O, ―CH₂―) at wave number 1,238 cm⁻¹ and (O―C―C) band of esters at wave number 1,100 cm⁻¹. Shifting in wave number to 1,150 cm⁻¹ and reduction in its peak intensity was observed with the band corresponding to 1,162 cm⁻¹ (―C―O stretch). Reduction in peak intensity of the bands at about 2,915 and 2,850 cm⁻¹ (C―H groups) was also observed. In the case of spread, nano zinc reduced the peak intensities of FTIR bands at 2,915 cm⁻¹, 2,850 cm⁻¹ (―C―H― (CH₂) stretches), 1,746 cm⁻¹ (―C═O ester), 1,465 cm⁻¹ (―C―H (CH₂, CH₃)), 1,375 cm⁻¹ (―C―H (CH₃)) and 1,156 cm⁻¹ (C―O, ―CH₂). Trans fats band corresponding to ═C―H stretch (trans bonds, 966 cm⁻¹), was observed in pure butter and spread. Trans fatty acids in butter and spread were quantified with the aid of calibration/validation standards using trielaidin and triolein and by using partial least squares regression analysis. However, the band at 966 cm⁻¹ was hindered in Zn-treated butter and reduced in Zn-treated spread.     

Effects of dietary consumption of cranberry powder on metabolic parameters in growing rats fed high fructose diets

The effect of dietary consumption of a cranberry powder (CP) containing increased amounts of procyanidins and other phytochemicals on metabolic parameters associated with metabolic syndrome was investigated in growing rats fed a high fructose diet. Dietary treatments were control (starch based), high fructose (HF), and HF containing either 3.3, 6.6, or 33 g CP/kg diet. Fasting plasma glucose and triglycerides tended to be higher with HF feeding and were reduced by feeding CP. The area under curve following an oral glucose tolerance test was 35-50% higher in animals fed HF diet vs. control and was decreased to control levels by the low or medium but not high CP diet. Feeding CP tended to lower fasting plasma insulin. Homeostatic models of insulin resistance (HOMA-IR) and β-cell function (HOMA-BCF) were lowest in animals fed low or medium CP diets (p < 0.05). Rats fed the control starch diet had slightly higher food intake, final body weight, and abdominal fat compared to animals fed other diets. Kidney weight was higher in HF group and feeding CP decreased kidney weight to normal levels. In the fed state, plasma triglyceride was increased with HF diet, whereas insulin was lower in animals fed HF diet. Overall, inclusion of CP in the diet was effective in modulating some aspects of metabolic parameters associated with metabolic syndrome and the medium level of CP in the diet produced a better response than the lower and higher CP levels.     

Novel methyl cellulose‐grafted‐acrylamide/gelatin microspheres for controlled release of nifedipine

Naturally available carbohydrate polymers such as methylcellulose (MC) and gelatin (Ge) have been widely studied in the previous literature for controlled release (CR) applications. In this study, methyl cellulose‐g‐acrylamide/gelatin (MC‐g‐AAm/Ge) microspheres were prepared by water‐in‐oil (W/O) emulsion method and crosslinked with glutaraldehyde to encapsulate with nifedipine (NFD), an antihypertensive drug. The microspheres prepared were characterized by differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and laser particle size analyzer. DSC thermograms of NFD‐loaded AAm‐MC/Gel microspheres confirmed the molecular level distribution of NFD in the matrix. SEM indicated the formation of spherical particles. Swelling experiments supported the drug diffusion characteristics and release data of the matrices. Cumulative release data were analyzed using an empirical equation to understand the nature of transport of drug through the matrices. Controlled release characteristics of the matrices for NFD were investigated in pH 7.4 media. Drug was released in a controlled manner up to 12 h. Particle size and size distribution of the microspheres as studied by laser light diffraction particle size analyzer indicated their sizes to be around 120 μm. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Direct Observation of Capacitor Switching Using Planar Electrodes

Ferroelectric polarization switching in epitaxial (110) BiFeO₃ films is studied using piezoresponse force microscopy of a model in‐plane capacitor structure. The electrode orientation is chosen such that only two active domain variants exist. Studies of the kinetics of domain evolution allows clear visualization of nucleation sites, as well as forward and lateral growth stages of domain formation. It is found that the location of the reverse‐domain nucleation is correlated with the direction of switching in a way that the polarization in the domains nucleated at an electrode is always directed away from it. The role of interface charge injection and surface screening charge on switching mechanisms is explored, and the nucleation is shown to be controllable by the bias history of the sample. Finally, the manipulation of domain nucleation through domain structure engineering is illustrated. These studies pave the way for the engineering and design of the ferroelectric device structures through control of individual steps of the switching process.     

Nanotwinning and structural phase transition in CdS quantum dots

Nanotwin structures are observed in high-resolution transmission electron microscopy studies of cubic phase CdS quantum dots in powder form by chemical co-precipitation method. The deposition of thin films of nanocrystalline CdS is carried out on silicon, glass, and TEM grids keeping the substrates at room temperature (RT) and 200°C by pulsed laser ablation. These films are then subjected to thermal annealing at different temperatures. Glancing angle X-ray diffraction results confirm structural phase transitions after thermal annealing of films deposited at RT and 200°C. The variation of average particle size and ratio of intensities in Raman peaks I_2LO/I_1LO with annealing temperature are studied. It is found that electron-phonon interaction is a function of temperature and particle size and is independent of the structure. Besides Raman modes LO, 2LO and 3LO of CdS at approximately 302, 603, and 903 cm⁻¹ respectively, two extra Raman modes at approximately 390 and 690 cm⁻¹ are studied for the first time. The green and orange emissions observed in photoluminescence are correlated with phase transition.     

Discovery of N-arylalkyl-3-hydroxy-4-oxo-3,4-dihydroquinazolin-2-carboxamide derivatives as HCV NS5B polymerase inhibitors

The metal ion chelating β-N-hydroxy-γ-ketocarboxamide pharmacophore was integrated into a quinazolinone scaffold, leading to N-arylalkyl-3-hydroxy-4-oxo-3,4-dihydroquinazolin-2-carboxamide derivatives as hepatitis C virus (HCV) NS5B polymerase inhibitors. Lead optimization led to the identification of N-phenylpropyl carboxamide 9 k (IC(50) =8.8 μM). Compound 9 k possesses selectivity toward HCV1b replicon Ava.5 cells (EC(50) =17.5 μM) over parent Huh-7 cells (CC(50) =187.5 μM). Compound 9 k effects a mixed mode of NS5B inhibition, with NTP-competitive displacement properties. The interaction between 9 k and NS5B is stabilized by the presence of magnesium ions. Docking studies showed that the binding orientation of 9 k occupies the central portions of both magnesium-mediated and NTP-ribose-response binding sites within the active site region of NS5B. As a result, 3-hydroxy-4-oxo-3,4-dihydroquinazolin-2-carboxamide derivatives are disclosed herein as novel, mainly active site inhibitors of HCV NS5B polymerase.     

Measurement and analysis of surface roughness in turning of aerospace titanium alloy (gr5)

Titanium alloys are extensively used in aerospace, biomedical applications and they are used in corrosive environments. In this study, the effect of cutting parameters on the surface roughness in turning of titanium alloy has been investigated using response surface methodology. The experimental studies were conducted under varying cutting speeds, feed and depths of cut. The chip formation and SEM analysis are discussed to enhance the supportive surface quality achieved in turning. The work material used for the present investigation is commercial aerospace titanium alloy (gr5) and the tool used is RCMT 10T300 – MT TT3500 round insert. The equation developed using response surface methodology is used for predicting the surface roughness in machining of titanium alloy. The results revealed that the feed was the most influential factor which affect the surface roughness.     

Preparation and comparative characterization of keratin–chitosan and keratin–gelatin composite scaffolds for tissue engineering applications

We report fabrication of three dimensional scaffolds with well interconnected matrix of high porosity using keratin, chitosan and gelatin for tissue engineering and other biomedical applications. Scaffolds were fabricated using porous Keratin–Gelatin (KG), Keratin–Chitosan (KC) composites. The morphology of both KG and KC was investigated using SEM. The scaffolds showed high porosity with interconnected pores in the range of 20–100 μm. They were further tested by FTIR, DSC, CD, tensile strength measurement, water uptake and swelling behavior. In vitro cell adhesion and cell proliferation tests were carried out to study the biocompatibility behavior and their application as an artificial skin substitute. Both KG and KC composite scaffolds showed similar properties and patterns for cell proliferation. Due to rapid degradation of gelatin in KG, we found that it has limited application as compared to KC scaffold. We conclude that KC scaffold owing to its slow degradation and antibacterial properties would be a better substrate for tissue engineering and other biomedical application.