An infrared heat reflecting multilayer thin film filter comprising alternate layers of ZrO2 and SiO2 has been modeled and prepared on a BK7 glass substrate using RF-magnetron sputtering. Initially, the individual films of the used materials have been characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) for structural and surface quality prior to the deposition of multilayer structure. Spectral analysis showed that the filter has an average transmission of greater than 90% in 450 to 700 nm range and less than 2% in 700-1100 nm band fulfilling the design requirements. The XRD study of multilayer structure showed few peaks of ZrO2 along with a solitary peak for SiO2 indicating some crystallinity for ZrO2 layers in the structure. Hardness analysis showed that the initial phase of the indentation is predominantly ductile with gradual transition in behaviour from ductile to brittle with increased penetration. Interface analysis of multilayered structure was carried out by Rutherford back scattering using Tandem 5 MeV ion accelerator, showed that interfaces formed in the multilayer structure are sharp and no substantial evidence of interlayer diffusion or mixing at the interfaces.

Thin films of zinc cadmium sulphide - a ternary compound intended to be used in solar cells - are prepared by co-evaporation. The films are prepared at room temperature, in a vacuum better than 10^-5 Torr. The composition of these films is varied from x = 0 to x = 1 in the compound ZnxCd1-xS. The structural, optical and electrical properties have been investigated as a function of x. The direct band gap varies from 2.415 eV to 3.41 eV for x = 0 to x = 1 respectively. The crystal structure is found to be hexagonal (Wurtzite) for 0<=x<=0.8 and cubic zinc-blende for x > 0.8. The lattice constants decrease and the optical bandgap increases with the increase in the value of x. The resistivity of the ZnxCd1-xS films is found to decrease from 3.6 x 10^4 ohmcm for x = 0 to 69.5 ohmcm for x = 0.3 and again increases beyond this range to a value of 6.3 x 10^3 ohmcm for x = 1.0.

The aim of the present study was to extend the use of flurbiprofen in clinical settings by avoiding its harmful gastric effects. For this purpose, we designed the controlled release solid lipid flurbiprofen microspheres (SLFM) by emulsion congealing technique. Drug was entrapped into gastro resistant biodegradable beeswax microspheres which were prepared at different drug/beeswax ratios 1:1, 1:2 and 1:3 using gelatin and tween 20 as emulsifying agents. The effect of emulsifiers and the effect drug/beeswax ratios were studied on hydration rate, encapsulating efficiency, micromeritic properties, scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), X-ray diffraction (X-RD) analysis and in vitro drug release at pH 1.2 for 2 h and at pH 6.8 for 10 h. SEM revealed that microspheres made with tween 20 were smooth while microspheres made with gelatin showed porous morphology, however, they were all spherical in nature. The practical yield (recovery)showed a dependence on drug-beeswax ratio and it was variable from 53 to 84%. High loading encapsulating efficiency of flurbiprofen from 8 to 94% was achieved. FTIR and DSC analysis confirmed the absence of any drug polymer interaction indicating drug stability during microencapsulation. XRD of pure flurbiprofen shows sharp peaks, which decreases on encapsulation, indicating decrease in the crystallinity of drug in microspheres. The micromeritic studies confirmed the presence of excellent and good flow properties of microspheres. Entrapment efficiency, morphology, practical yield, hydration rate, flow properties demonstrated their dependence on the HLB value of emulsifiers and emulsifiers with higher HLB were found more appropriate for effective microencapsulation of flurbiprofen. The release kinetics followed zero order mechanism of drug release at pH 6.8. Release pattern depends on the morphology of flurbiprofen microspheres and amount of beeswax used in the microspheres preparation. The microspheres prepared with high HLB values i.e., tween 20 showed effective control of drug release from microspheres. The absence of drug release at pH 1.2 proved the suitability of beeswax for its use as a gastro resistant material.

In the present work crosslinked hydrogels based on chitosan (CS) and acrylic acid (AA) were prepared by free radical polymerization with various feed compositions using N,N methylenebisacrylamide (MBA) as crosslinking agent. Benzoyl peroxide was used as catalyst. Fourier transform infrared spectra (FTIR) confirmed the formation of the crosslinked hydrogels. This hydrogel is formed due to electrostatic interaction between cationic groups in CS and anionic groups in AA. Prepared hydrogels were used for dynamic and equilibrium swelling studies. For swelling behavior, effect of pH, polymeric and monomeric compositions and degree of crosslinking were investigated. Swelling studies were performed in USP phosphate buffer solutions of varying pH 1.2, 5.5, 6.5 and 7.5. Results showed that swelling increased by increasing AA contents in structure of hydrogels in solutions of higher pH values. This is due to the presence of more carboxylic groups available for ionization. On the other hand by increasing the chitosan content swelling increased in a solution of acidic pH, but this swelling was not significant and it is due to ionization of amine groups present in the structure of hydrogel. Swelling decreased with increase in crosslinking ratio owing to tighter hydrogel structure. Porosity and sol-gel fraction were also measured. With increase in CS and AA contents porosity and gel fraction increased, whereas by increasing MBA content porosity decreased and gel fraction increased. Furthermore, diffusion coefficient (D) and the network parameters i.e., the average molecular weight between crosslinks (Mc), polymer volume fraction in swollen state (V2s), number of repeating units between crosslinks (Mr) and crosslinking density (q) were calculated using Flory-Rehner theory. Selected samples were loaded with a model drug verapamil. Release of verapamil depends on the ratios of CS/AA, degree of crosslinking and pH of the medium. The release mechanisms were studied by fitting experimental data to model equations and calculating the corresponding parameters. The result showed that the kinetics of drug release from the hydrogels in both pH 1.2 and 7.5 buffer solutions was mainly non-Fickian diffusion.

Nanocrystalline Cu0:5Zn0:5AlxFe2¡xO2 (x=0.0, 0.1, 0.2, 0.3, 0.4, and 0.5) ferrite materials were synthesized using standard solid state reaction technique. The effects of Al3+ contents on the structural, electrical, and magnetic properties were investigated. Single phase cubic spinel structure was revealed by X-ray diffraction analysis. The crystallite size was evaluated considering the most intense diffraction peak (311) using Scherrer formula. Lattice constant decreased, whereas porosity increased with the increase in Al3+ concentration. The value of saturation magnetization decreased with increasing aluminum contents. Temperature dependent value of direct current electrical resistivity has been determined. It is observed that the substitution of Al3+ has significant impact on the dielectric constant, tangent of dielectric loss angle and dielectric loss factor. The variation in dielectric properties was attributed to space charge polarization.

Mn doped ZnO nano-crystallites were synthesized by state of the art sol-gel derived auto- combustion technique. As-burnt powder was investigated with different characterization techniques to explore the properties of Mn doped ZnO dilute magnetic semiconductor. X-ray diffraction measurements indicate that Mn doped ZnO retain wurtzite type hexagonal crystal structure like ZnO. Compositional and morphological studies were carried out by energy dispersive X-ray analysis and scanning electron microscopy, respectively. Temperature dependent resistivity of the sample exhibited the semiconducting behavior of the DMS material. Room temperature magnetic properties determined by vibrating sample magnetometer, revealed the presence of ferromagnetic and diamagnetic contributions in Mn doped ZnO.

We employ the full-potential linearized augmented plane wave plus local orbital (FP-L/APW + lo) method based on spin-polarized density functional theory (DFT) in order to investigate the structural, electronic and magnetic properties of ordered dilute ferromagnetic semiconductors Zn1?xCrxS and Cd1?xCrxS (x = 0.25) in the zinc blende (B3) phase. For the exchange-correlation functional, the generalized gradient approximation GGA (Wu-Cohen 06) has been used. Results of calculated electronic band structures and density of states of these dilute magnetic semiconductors (DMSs) are discussed in terms of the contribution of Cr 3d5 4s1, Zn 3d10 4s2, Cd 4d10 5s2 and S 3s2 3p4 partial density of states. For Cr-based systems without n or p-type doping, the stability of the ferromagnetic spin state versus the antiferromagnetic state is predicted. Band structure and density of states studies show half-metallic ferromagnetic nature for both alloys, Zn1?xCrxS and Cd1?xCrxS. Calculations of the s–d exchange constant N0? and p–d exchange constant N0? clearly indicate the magnetic nature of these compounds. From the calculated total magnetic moments we observe that p–d hybridization reduces the local magnetic moment of Cr from its free space charge value and produces small local magnetic moments on the nonmagnetic Zn, Cd and S sites. The robustness of half-metallicity of Zn1?xCrxS and Cd1?xCrxS as a function of lattice constant is also discussed.

A hard/soft SmCo5/Fe nanocomposite magnetic bilayer system is fabricated on x-ray transparent 100–200 nm thin Si3N4 films by magnetron sputtering. The microscopic magnetic domain pattern and its behaviours during magnetization reversal in the hard and the soft magnetic phases are studied separately by element specific magnetic soft x-ray microscopy at a spatial resolution of better than 25 nm. We observe that the domain patterns for the soft and hard phases show coherent behaviours in varying magnetic fields. We derive local M(H) curves from the images of Fe and SmCo5 separately and find the switches for hard and soft phases to be the same.

Trilayers of Sm-Co/Mo/Fe were deposited by DC and RF magnetron sputtering on Si (100) substrate at 650 °C. Effect of very thin Mo interlayers on energy product of magnetic layers was studied. All the samples showed strong exchange coupling and single phase behavior. With increasing Mo interlayer thickness, we observed oscillating behavior of saturation magnetization and energy product. The rise in energy product was observed as 22% for 0.3 nm Mo interlayer as compared to sample without Mo interlayer.

Sm-Co/Fe, hard/soft magnetic bilayers have been fabricated on 70 nm Cr buffered Si (100) substrate by dc and rf magnetron sputtering and annealed at 525OC for 30min. Very thin Mo layers (0-0.7 nm) were introduced between Sm-Co and Fe layers. The samples were analyzed by X-Ray Diffraction (XRD) and Alternating Gradient Magnetometer (AGM). All of the samples showed strong exchange coupling between hard and soft magnetic phases. Magnetization, coercivity and energy product (BH)max suggest a sinusoidal behavior. The energy product was found increased to 45% for 0.3 nm Mo interlayer as compared to sample without Mo layer.