Magneto Binary Nanofluid Convection in Porous Medium

The effect of an externally impressed magnetic field on the stability of a binary nanofluid layer in porous medium is considered in this work. The conservation equations related to the system are solved using normal mode technique and Galerkin method to analyze the problem. The complex expressions are approximated to get useful results. Mode of heat transfer is stationary for top heavy distribution of nanoparticles in the fluid layer and top heavy nanofluids are very less stable than regular fluids. Oscillatory motions are possible for bottom heavy distribution of nanoparticles and they are not much influenced by properties of different nanoparticles. A comparative analysis of the instability of water based nanofluids with metallic (Cu, Ag) and semiconducting (TiO2, SiO2) nanoparticles under the influence of magnetic field is examined. Semiconducting nanofluids are found to be more stable than metallic nanofluids. Porosity destabilizes the layer while solute difference (at the boundaries of the layer) stabilizes it. Magnetic field stabilizes the fluid layer system significantly

Interfacial Tension of Some Newtonian and non-Newtonian Fluids by the Drop-Weight Method

Experimental data on interfacial tension of 42 binary liquid-liquid systems using water, aqueous glycerol, aqueous polymeric solutions of polyvinylpyrrolidone (PVP), poly(ethylene oxide) (PEO), carboxymethyl cellulose (CMC) and polyacrylamide (PAM) as continuous phase, and carbon tetrachloride, chlorobenzene, bromobenzene, nitrobenzene, nitrotoluene and ethyl chloroacetate as dispersed phase at 20 °C are reported. The interfacial tension has been measured using the drop-weight method at different compositions of continuous phases

Viscometric and Rheological Behaviour of Chitosan-Hydrophilic Polymer Blends

Blends of chitosan with hydrophilic polymers were investigated for miscibility. Chitosan/poly (vinyl alcohol) (CS/PVA), chitosan/poly vinylpyrollidone (CS/PVP) and chitosan/poly (ethylene oxide) (CS/PEO) blends were prepared in dilute aqueous acetic acid ( = 1 %) and found to be miscible over the entire composition range by dilute solution viscosity and rheological measurements. The miscibility of blends by viscosity measurements at 25 ± 0.1 C was estimated on the basis of experimental and ideal values of miscibility parameters bm, and μ. The rheological studies were performed on blends of mass fraction w = 2 % in dilute aqueous acetic acid ( = 1 %) at 25 ±0.1 C in controlled rate mode. The flow curves of blends and viscosities were found to lie between those of principal components of the blend over the entire compositional range. The flow behaviour index of blends was determined by the Power law model, indicating pseudoplastic behaviour with pseudoplasticity increasing with CS mass concentration. The rheological data of blends was best described by the Cross model. Results from Fourier transform infrared spectroscopy also indicate the blends to be miscible

Hydrogels of Poly(acrylamide-co-acrylic acid): In-vitro Study on Release of Gentamicin Sulfate

Poly(acrylamide-co-acrylic acid) hydrogels, poly(AAm-co-AAc), were synthesized by free radical polymerization in solution using N,N’-methylenebisacrylamide (MBAAm) as the crosslinker. The structural parameters and the swelling behavior of the synthesized hydrogels were investigated for varying nominal crosslinking ratio and composition of the hydrogels. The use of hydrogels for drug release was investigated with gentamicin sulfate (GS) as the model drug. The drug release from hydrogels was investigated as a function of hydrogel composition, nominal crosslinking ratio (X) and drug loading. The observed drug release data was fitted to a power law model and the power law exponent (n) suggested that the drug release mechanism from these hydrogels was sensitive to hydrogel composition and was swelling-controlled for low concentrations of AAc and showed Fickian diffusion for high concentrations of AAc in the hydrogels. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) studies were performed on control hydrogel samples and drug loaded hydrogels to understand the chemical interactions between the drug and the polymer. Specific drug interactions were observed in these hydrogels