Mahmoodmalmberg7650

The structure and corrosion resistance of Grade 2 titanium subjected to the hydroextrusion processes were examined. The microstructure was characterized using optical microscopy and transmission electron microscopy. The corrosion resistance was determined using the impedance and potentiodynamic methods, in 0.1 M H2SO4 solutions and an acidified 0.1 M NaCl solution with a pH of 4.2, at ambient temperature. Nanohardness tests were performed under a load of 100 mN. It has been demonstrated that the hydroextrusion method makes it possible to obtain relatively homogeneous nanocrystalline titanium Grade 2 with an increased hardness, the elastic modulus almost unchanged with respect to that of the initial structure and a lower corrosion resistance.Poloxamer finds excellent clinical and therapeutic uses for curing of various ailments. The Zin- giber officinale (Z. officinale) is one of the well-known medicinal plants. The poloxamer188 and the rhizome extract of Z. officinale have been used to synthesize the gold nanoparticles (AuNPs) by a green approach. The Z. officinale extract has been used as a reducing agent while the polox- amerl88 has been used as a stabilizing agent. The effect of addition of poloxamer on the controlling the shape and size of the AuNPs has been investigated by transmission electron microscopy (TEM) and dynamic light scattering techniques. The formation of AuNPs has also been confirmed by UV-Visible spectral, energy dispersive X-ray (EDX) and powder X-ray diffraction (XRD) analyses. The anti-bacterial activity of the green synthesized AuNPs has been investigated on the three human pathogens Staphylococcus aureus, Escherichia coli, and Klebsiella pneumonia. The poloxamer188 protected AuNPs inhibit the bacterial growth more effectively than the pure Z. officinale extract and the standard tetracycline (TA).In the present work, a multifunctional nanomaterial, methylene blue-incorporated folate-functionalized Fe3O4/mesoporous silica core/shell magnetic nanoparticles, has been developed. Firstly, highly biocompatible monodisperse superparamagnetic Fe3O4@mSiO2 core/shell nanoparticles with mesoporous silica shells were synthesized. Then these particles were coated with the covalently bonded biocompatible polymer poly(ethylene glycol) (PEG) and modified with the cancer targeting ligand folic acid (FA). Finally, the water-soluble photosensitizer methylene blue (MB) was loaded into the mesoporous silica shell. selleck compound Systematic experiments were performed to carefully evaluate the physical and chemical properties, cytotoxicity and cellular uptake of the multifunctional nanomaterial.This paper reports the temperature-dependant electrical characteristics of n-ZnO hexagonal nanorods/p-Si heterojunction diodes. The n-ZnO hexagonal nanorods were grown on p-Si substrate by a simple thermal evaporation process using metallic zinc powder in the presence of oxygen. The spectroscopic characterization revealed well-crystalline nanorods, quasi-aligned to the substrate and possessing hexagonal shape. The as-grown nanorods exhibited a strong near-band-edge emis- sion with very weak deep-level emission in the room-temperature photoluminescence spectrum, confirming good optical properties. Furthermore, the electrical properties of as-grown ZnO nanorods were examined by fabricating n-ZnO/p-Si heterojunction assembly and the I-V characteristics of the fabricated heterojunction assembly were investigated at different temperatures. The fabricated n-ZnO/p-Si heterojunction diodes exhibited a turn-on voltage of ~5 V at different temperatures with a mean built-in-potential barrier of 1.12 eV. Moreover, the high values of quality factor obtained from I-V analysis suggested a non-ideal behavior of Schottky junction.The polyaniline-coated ordered mesoporous carbon (PCOMC) material was prepared by chemical polymerization of aniline monomers on the ordered mesoporous carbon (OMC). The synthesized PCOMC materials were characterized by scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption isotherms and Fourier infrared spectroscopy. It was demonstrated that the polyaniline was successfully incorporated and well deposited on the external surface and inner pores of the OMC material. Furthermore, the electrochemical performance of the original OMC and PCOMC materials are compared by using cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge-discharge tests. The results showed that the electrochemical performance of the OMC material was enhanced after the incorporation of polyaniline. The specific capacitance of PCOMC electrode (813.4 F/g) measured by cyclic voltammetry at the scan rate of 2 mV/s was much higher than that of the OMC electrode (200.9 F/g). The discharge specific capacitance of the PCOMC supercapacitor could be kept at 119.4 F/g when the current density was 5 A/g, indicating its good rate performance even at high charge/discharge current density. Moreover, the PCOMC supercapacitor exhibited long cycling stability with the capacitance retention remained 77% after 3500 cycles.Ni-doped ZnFe2O4 (Ni(X)Zn1-x,Fe2O4; x = 0.0 to 0.5) nanoparticles were synthesized by simple microwave combustion method. The X-ray diffraction (XRD) confirms that all compositions crystallize with cubic spinel ZnFe2O4. The lattice parameter decreases with increase in Ni content resulting in the reduction of lattice strain. High resolution scanning electron microscope (HR-SEM) and transmission electron microscope (HR-TEM) images revealed that the as-prepared samples are crystalline with particle size distribution in 42-50 nm range. Optical properties were determined by UV-Visible diffuse reflectance (DRS) and photoluminescence (PL) spectroscopy respectively. The saturation magnetization (Ms) shows the superparamagnetic nature of the sample for x = 0.0-0.2, whereas for x = 0.3-0.5, it shows ferromagnetic nature. The Ms value is 1.638 emu/g for pure ZnFe2O4 sample and it increases with increase in Ni content. Photoelectrochemical (PEC) measurements showed a significant increase of photocurrent density with increase in the Ni-dopant, and 0.5% Ni-doped ZnFe2O4 sample was found to show the better photoresponse than the other doping concentrations.In this present work, Multi-walled carbon nanotubes (MWNTs) with different content by weight (10%, 20%, 30%, 50% and 70%) are introduced into Polypyrrole nanoparticles (PPy NP) matrix and fabricated as Pt free counter electrodes (CEs) for dye-sensitized solar cell (DSSC). For comparison DSSCs using pristine PPy NP, MWNTs and Platinum (Pt) were also fabricated. The incorporation of MWNTs acts as conductive channel and co-catalyst to the PPy NP CEs in the reduction of li to I-. The electrochemical catalytic activities of different CEs were analysed by Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) and photovoltaic performance was studied under standard AM 1.5 sunlight illumination. It was observed that incorporation of MWNTs in the PPy NP CE greatly enhanced the catalytic activity for I3 reduction and significantly reduced the charge transfer resistance in the PPy NP/MWNTs composite CE finally improving short-circuit photocurrent density, fill factor, open circuit voltage and power conversion efficiency of DSSC. DSSC fabricated from PPy NP/MWNTs composite CE with 50% MWNTs content reached the highest photoconversion efficiency of 5.80% which is 91% that of Pt CE based DSSC (6.37%).Pure-phase (K, Na)NbO3 (KNN) powders with orthorhombic symmetry were successfully synthesized by solvothermal method using isopropanol as solvent, without the addition of water. The as-prepared powders were characterized by X-ray diffraction, scanning electron microscopy and energy dispersive spectrometry to show the variation of phase, morphology, size distribution and chemical composition under different synthetic conditions, such as fill factors (FF) of the solvothermal system and alkalinity of the starting solution. Compared with the traditional hydrothermal method and the so-called solvothermal method (water aided in fact), small grains with well crystallinity were obtained using 100% isopropanol as reaction medium. The results indicate that both fill factor and alkalinity have significant effects on the phase structure and size distribution of the as-obtained KNN powders. Pure orthorhombic perovskite-structured KNN powders with a grain size of 100 nm were synthesized at the following condition reaction time, 16 h; reaction temperature, 240 °C; fill factor, 70%; and alkalinity, 1 M. Small grains (~100 nm) tend to form mesocrystals (~10 µm) with tetrakaidecahedron structures, and the possible formation mechanism was proposed. The solvothermal method without the addition of water is a promising alternative to synthesize pure and refined powders under mild reaction conditions.Thin film microbatteries require electrode materials with high areal specific capacities and good cyclability. Use of vapor-deposited silicon thin films as anodes in Li-ion microbatteries offers the advantage of high capacity as well as compatibility with other processes used for microsystem fabrication. Unfortunately, monolithic silicon films greater than 200 nm in thickness pulverize during lithiation and delithiation. We have used metal-assisted-chemical-etching of sputter-deposited amorphous silicon films to make nanoporous silicon layers and arrays of silicon nanopillars as a means of achieving anodes with high areal capacity and good cyclability. We have compared the performance of these nanostructured layers with the performance of monolithic silicon films in Li half-cells. A reduced first cycle coulombic efficiency was observed in all cases and was attributed to the irreversible formation of Li2O due to the presence of oxygen in the sputter-deposited silicon films. This was controlled through modifications of the sputtering conditions. As expected, monolithic films thicker than 200 nm showed poor cycling performance due to pulverization of the film. Nanoporous silicon showed good initial cycling performance but the performance degraded due to porosity collapse and delamination. Arrays of silicon nanopillars made from 750 nm silicon films exhibited good cycling, rate performance and an areal capacity (0.20 mA h cm(-2)) 1.6 times higher than what could be obtained with monolithic Si films with similar cyclability.CeO2/nanographite (CeO2/nano-G) composite materials were got by chemical precipitation method with nanographite (nano-G) and cerous nitrate hexahydrate as raw materials. The microstructures of CeO2/nano-G composite materials were characterized by means of SEM, XRD, XPS and Raman. The cathodes were made by nano-G and CeO2/nano-G composite materials, respectively. The electrolysis phenol was conducted by the diaphragm cell prepared cathode and the Ti/RuO2 anode. The results indicated that the Cerium oxide is mainly in nanoscale spherical state, uniformly dispersed in the nanographite sheet surface, and there are two different oxidation states for elemental Ce, namely, Ce(III) and Ce(IV). In the diaphragm electrolysis system with the aeration conditions, the degradation rate of phenol reached 93.9% under 120 min's electrolysis. Ceria in the cathode materials might lead to an increase in the local oxygen concentration, which accelerated the two-electron reduction of O2 to hydrogen peroxide (H2O2). The removal efficiency of phenol by using the CeO2/nano-G composite cathode was better than that of the nano-G cathode.