2644 research outputs found

    CAM sol–gel synthesized LiMPO4 (M=Co, Ni) cathodes for rechargeable lithium batteries

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    The emerging category cathode candidates such as LiCoPO4 and LiNiPO4 were synthesized at 800 �C using Citric acid assisted modified sol–gel (CAM sol–gel) method and examined for possible lithium intercalation behavior. Compound formation temperature is confirmed from thermogravimetry and differential thermal analysis (TG/DTA). Powder X-ray diffraction (PXRD) pattern evidenced the absence of undesirable peaks and confirmed the formation of phase pure LiMPO4 (M=Co, Ni) compounds with an orthorhombic structure and finer crystallite size. Presence of nanosized particles as observed from TEM image of LiCoPO4 and the presence of preferred local cation environment as understood from FT–IR studies are the added advantages of CAM sol–gel synthesis. Further, Cyclic voltametry (CV) and Impedance spectroscopy (EIS) studies performed on the synthesized LiCoPO4 and LiNiPO4 cathodes revealed excellent reversibility and structural stability of CAM sol–gel synthesized cathodes, especially upon storage as well as during cycling

    Generation of gold–PEDOT nanostructures at an interface between two immiscible solvents

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    Gold–poly(3,4-)ethylenedioxythiophene (Au–PEDOT) composite with variant morphology was synthesized through interfacial polymerization at room temperature in the absence of a template, phase transfer catalyst or surfactant. A systematic variation of the relative concentration of the reactants yields morphologies typical of nanorods of diameter approximately 20–30 nm and length of few 0.5–1 mm. Transmission electron microscopy reveals the structure of the nanowire to be the one in which the core is Au and the outer shell is made of PEDOT. Oligomer formation, speculated during the interfacial reaction was confirmed by the analysis of the organic phase using ultraviolet–visible (UV–vis) and nuclear magnetic resonance (NMR) spectroscopy techniques

    Predictive Modeling of Copper in Electro-deposition of Bronze Using Regression and Neural Networks

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    The aim of this research is to obtain electrodeposits of copper-tin over mild steel substrate. The plating parameters were studied and a model is developed using Artificial Neural Networks (ANN). The electrodeposition of copper-tin was carried out from an alkaline cyanide bath. Copper content of coatings in alloy deposition was determined by using X-ray fluorescence spectroscopy. The results were used to create a model for the plating characteristics and also for studies using ANN. The ANN model is compared with the conventional mathematical regression model for analysis

    Evaluation of EK system by DC and AC on removal of nitrate complex

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    DC (Direct current) is used in electrokinetic (EK) technology to extract hazardous materials from soils. Besides, AC (alternating current) electric field is also used to induce particle and fluid motion in electrokinetics. The influence of AC and DC on electrokinetic phenomena was studied for the removal of nitrate complex in soil environment. The experiments were performed by employing three systems – DC, AC, and AC overlapped DC. The removal of cations was higher at the anodic spot while applying DC. Involvement of AC on cation removal was very poor and nitrate removal was about 50%. AC and DC can be used for the removal of nitrate complex in agricultural soils

    Pulse plated CdSxTe1-x films and their properties

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    CdSxTe1-x films were deposited on titanium and conducting glass substrates at room temperature using 0.25 M cadmium sulphate, the concentration of sodium thiosulphate and TeO2 dissolved in sodium hydroxide was varied in the range of 0.01–0.05 M. The as deposited films exhibited hexagonal structure irrespective of the composition. The FWHM maximum of the x-ray diffraction peaks were found to decrease with increase of duty cycle. The optical energy gap values are in the range of 1.54–2.32 eV for films of different composition, it is observed that the band gap shifts towards CdS side as the concentration of CdS in the films increase. XPS studies indicated the formation of CdSTe solid solution. The grain size increases from 11.54 to 99.40 nm as the value of x increases from 0.2 to 0.8. The surface roughness is found to increase from 0.22 to 2.50 nm as the value of ‘x’ increases from 0.2 to 0.8. The resistivity is found to vary from 53 to 8 ohm cm as the ‘x’ value decreases from 1 to 0

    Synthesis of Boron Carbide by Calciothermic Reduction Process

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    Boron carbide (B4C) powders were synthesized by calciothermic reduction process from the mixtures of borax (or boron trioxide), petroleum coke, and calcium. The synthesized materials were characterized by XRD, SEM, and chemical analysis

    Effect of swift heavy ion irradiation in Fe/W multilayer structures

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    Present study reports effect of swift heavy ion irradiation on structural and magnetic properties of sputtered Fe/W multilayer structures (MLS) having bilayer compositions of [Fe(20A˚ )/W(10A˚ )]5BL and [Fe(20A˚ )/W(30A˚ )]5BL. These MLS are irradiated by 120 MeV Au9+ ions up to fluence of 4 1013 ions/cm2. X-ray reflectivity (XRR), wide-angle X-ray diffraction (WAXD), cross-sectional transmission electron microscopy (X-TEM) and magneto optical Kerr effect (MOKE) techniques are used for structural and magnetic characterization of pristine and irradiated MLS. Analysis of XRR data using Parratt’s formalism shows a significant increase in W/Fe interface roughness. WAXD and X-TEM studies reveals that intralayer microstructure of Fe-layers in MLS becomes nano-crystalline on irradiation. MOKE study shows increase in coercivity at higher fluence, which may be due to increase in surface and interface roughness after recrystallization of Fe-layers

    Characteristics of brush plated ZnS films

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    Zinc sulphide(ZnS) thin films were deposited by the brush electrodeposition technique at 80°C and at different deposition current densities in the range of 80 – 200 mA cm-2.The films were polycrystalline with peaks corresponding to single phase cubic ZnS. Films with direct band gap in the range of 3.79–3.93 eV were obtained. The grain size increased from 20 – 70 nm as the deposition current density increased. The films exhibited resistivity in the range of 100 – 1000 ohm cm. The photooutput obtained with photoelectrochemical cells employing these films was higher than the previous report

    Experimental aspects of combined NOx and SO2 removal from flue-gas mixture in an integrated wet scrubber-electrochemical cell system

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    The objective of this work was to study the effect of some operating conditions on the simultaneous removal of NOx and SO2 from simulated NO–SO2–air flue-gas mixtures in a scrubber column. The gaseous components were absorbed into 6 M HNO3 electrolyte in the scrubber in a counter-current mode, and were oxidatively removed by the Ag(II) mediator oxidant electrochemically generated in an electrochemical cell set-up. The integration of the electrochemical cell with the scrubber set-up ensured continuous regeneration of the Ag(II) mediator and its repeated reuse for NOx and SO2 removal purpose, thereby avoiding: (1) the usage of chemicals continuously for oxidation and (2) the production of secondary waste. The influences of packing material (raschig glass rings, raschig poly(vinylidene) fluoride rings, Jaeger tri-pack perfluoroalkoxy spheres), feed concentrations of NO and SO2 (100–400 ppm NO and 100– 400 ppm SO2), superficial gas velocity (0.061–0.61 m s�1) and liquid velocity (0.012–0.048 m s�1) were investigated. The raschig glass rings with high surface area provided highest NO removal efficiency. NO and NOx showed decreasing abatement at higher feed concentrations. The removal of nitrogen components was faster and also greater, when SO2 co-existed in the feed. Whereas the gas flow rate decreased the removal efficiency, the liquid flow rate increased it for NO and NOx. The flow rate effects were analyzed in terms of gas/liquid residence time and superficial liquid velocity/superficial gas velocity ratio. SO2 removal was total under all conditions

    A new mixed-matrix membrane for DMFCs

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    A new mixed-matrix membrane based on stabilized phosphotungstic acid (PTA) incorporated to chitosan (CS)-hydroxy ethyl cellulose (HEC) for application in direct methanol fuel cells (DMFCs) is reported. Membranes are characterised using Fourier Transform Spectroscopy (FTIR), Thermo-Gravimetric Analysis (TGA), Scanning Electron Microscopy (SEM) and their mechanical properties are evaluated. The PTA content in the CS-HEC blend and its influence on proton conductivity, water/methanol sorption, and methanol cross-over in the DMFC is studied. The DMFC with 3 wt. % stabilized PTA-CS-HEC mixed-matrix membrane delivers peak power-density of 58 mW/cm2 at a load current-density of 210 mA/cm2 with a lower methanol cross-over than that observed for a DMFC operating with a Nafion membrane electrolyte

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