2644 research outputs found

    Investigations on the Structural, Morphological, Electrical, and Magnetic Properties of CuFe2O4-NiO Nanocomposites

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    CuFe2O4-xNiO (x ) 1, 5, 10, and 20 wt %) nanocomposites have been successfully prepared by a simple combustion method using urea-nitrate precursors. The samples were sintered at different temperatures, namely 600, 800, 1000, and 1100 °C, for 5 h to enhance the compound formation and phase purity, studied by means of XRD patterns. Then the 1100 °C sintered sample was further characterized for its structural (EXAFS, XANES, FT-IR, UV–vis), morphological (SEM, TEM, HRTEM, SAED), electrical (ac conductivity, dielectric constant, dielectric loss tangent), and magnetic (Mössbauer) properties. The EXAFS and XANES studies reveal the formation of NiFe2O4 and CuO, in addition to the existence of CuFe2O4 and NiO phases. A partial substitution of metal cations by nickel ions could also be evidenced. The stretching and bending vibration of the tetrahedral and octahedral complexes have been established from FT-IR spectra. The UV–vis spectra elucidate that the prepared materials are semiconductors and also show the quantum size confinement effect. The well-defined grain and grain boundary structure was identified from the SEM studies. The nanosize of the synthesized materials has been identified by TEM investigations. The HRTEM and SAED images reveal the crystallinity and polycrystalline behavior of the as-synthesized materials. The electrical studies show the normal ferrimagnetic behavior of the materials. The inverse spinel nature of the materials has been enumerated from Mössbauer spectra, which also illustrates the phase transition behavior

    A complex parameter boundary element method for modeling AC impedances of electrochemical systems by analytic continuation— Application to a slit geometry

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    A complex parameter boundary element method is advanced to compute the AC impedances of electrochemical systems by solving the Laplace equation with complex boundary conditions. This method, which is based on analytic continuation from the corresponding secondary current distribution, is applied to a slit geometry, besides two illustrative cases: plane-parallel electrodes and concentric cylinder electrodes. The AC impedance responses for the slit geometry are computed for several electrode and slit dimensions for (1) purely capacitive working electrode and (2) a working electrode represented by a Voigt element. Interesting effects of the electrode and the slit dimensions on the AC response are noted. Applications of this method in viscoelastic systems, rheology and electronic/electrical devices are discussed. User-friendly implementations of the method in the BEASY group of softwares are also suggested

    Molecular interactions of polyvinylpyrrolidone and cellulose acetate butyrate solutions in dimethylformamide

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    The ultrasonic velocity, density, and ViScosIties of polyvinylpYITolidone (PVP) and cellulose acetate butyrate (CAB) solutions in dimethyllonnamide (DMF) have been measured in the temperature range, 303K-323 K. Using these data, free energy of mixing, solvation number and different polymer-solvent interaction parameters for the solution systems have been calculated to know the presence of molecular interactions in the system. The trends in the variation of the solution property parameters indicate the existence of positive molecular interactions between tile polymer and the solvent in solutions. The results also show the presence of higher degree of interaction between I'VP and DMF in solution compared to CAB and DMF

    Study of CuFe2O4–SnO2 nanocomposites by Mössbauer spectroscopy with high velocity resolution

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    High velocity resolution Mössbauer spectroscopy was used to study of (CuFe2O4)1−x(SnO2)x nanocomposites (x = 0, 1, 5, 10, 20 wt.%). Mössbauer spectra were measured at room temperature with registration in 4,096 channels and further presentation in 1,024 channels. Mössbauer spectra of CuFe2O4 and (CuFe2O4)0.99 + (SnO2)0.01 were better fitted using three sextets while spectra of (CuFe2O4)0.95 + (SnO2)0.05 and (CuFe2O4)0.80 + (SnO2)0.20 were better fitted using four sextets and one doublet. In contrast, spectrum of (CuFe2O4)0.80 + (SnO2)0.20 was better fitted using five sextets and one doublet. Mössbauer hyperfine parameters were related to octahedral and tetrahedral sites in copper ferrites. The presence of two different tetrahedral sites in studied ferrites and two different octahedral sites in (CuFe2O4)0.80 + (SnO2)0.20 was supposed

    Studies on the Fluidized Bed Electrode

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    The present investigation attempts to study the hydrodynamic characteristics of the fluidized bed electrode. A core-annular flow model with a transfer of particles between core-annular layers has been proposed to describe the flow behavior of conducting particles in the fluidized bed electrode. The effect of individual parameters on the rate of the particle transfer across the layer and thickness of the core-annular has been critically examined and the model simulation has been verified with the data reported in the literature

    Influence of Sacrificial Cathodic Protection on the Chloride Profile in Concrete

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    The durability of reinforced concrete structures significantly depends on the condition of the steel embedded in them. Structures exposed to chloride containing environment have reduced durability due to corrosion of the reinforcement steel. Several diffusion models have been proposed for chloride penetration. They mainly aim at predicting the initiation of corrosion of the reinforcement. They are based on diffusion conditions influenced by parameters such as relative humidity, temperature, rains etc. This work presents the influence of sacrificial cathodic protection on the chloride profile in concrete. Cathodic protection to the embedded steel in concrete was established by plugging-in a sacrificial magnesium alloy anode at the center of the slab and providing an electrical link between them. The current flowing between the magnesium anode and the embedded steel was regularly measured. The water soluble chloride content at different distances from the anode and at different times was determined after implementation of cathodic protection. The chloride content decreased at different distances from the anode, with increase in time. The diffusion of chloride occurred at a more accelerated rate due to the flow of cathodic protection current

    Synthesis of Poly(p-phenylene diamine) and Its Corrosion Inhibition Effect on Iron in 1M HCl

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    Water-soluble poly(p-phenylene diamine) was chemically synthesized. Its corrosion inhibition performance was evaluated for iron corrosion in 1M HCl at various concentrations, and the results were compared with that of the monomer. The corrosion inhibition properties were evaluated by polarization techniques and electrochemical impedance spectroscopy. The results showed that poly(p-phenylene diamine) was a more efficient corrosion inhibitor than the monomer and gave an 85% inhibition efficiency at a concentration of 50 ppm, whereas the monomer gave an efficiency of 73% at 5000 ppm

    Characteristics of sol–gel dip coated Ceria films

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    Cerium oxide(CeO2) thin films were deposited by the sol–gel dip coating technique using cerium chloride, acrylamide and N,N bis methylene acrylamide. The as deposited films were heat-treated at different temperatures in air. X-ray diffraction studies indicated the films to be of single phase CeO2. Optical bandgap in the range of 3.53– 3.60 eV was obtained from optical studies. Laser Raman studies exhibited Raman bands around 457 cm�1

    Effect of varying poly(styrene sulfonic acid) content in poly(vinyl alcohol)–poly(styrene sulfonic acid) blend membrane and its ramification in hydrogen–oxygen polymer electrolyte fuel cells

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    Poly(styrene sulfonic acid) (PSSA) content in poly(vinyl alcohol) (PVA) and PSSA blend membrane is varied and its effect on proton conductivity is studied at varying relative humidity (RH) values. The maximum proton conductivity is observed for the PVA–PSSA membrane with about 35 wt. % PSSA at all humidity values. At 30% RH value, the conductivity of PVA–PSSA blend membrane is 1.20×10−3 S/cm, which is about two orders of magnitude higher than the conductivity value of 2.27×10−5 S/cm observed for pristine PVA membrane. Water self-diffusion coefficients and water release kinetics of these materials have been characterized by nuclear magnetic resonance (NMR) imaging technique, which validate the use of this membrane in polymer electrolyte fuel cells (PEFCs). A peak power density of 210mW/cm2 at a load current-density of 500mA/cm2 is achieved for the PEFC with the optimized PVA–PSSA membrane as electrolyte compared to a peak power density of only 38mW/cm2 observed at a load current-density of 80mA/cm2 for the PEFC with pristine PVA membrane as electrolyte while operating at 75 ◦C with H2 and O2 feeds to the fuel cell maintained at atmospheric pressure

    Polyvinylidene fluoride–hexafluoropropylene (PVdF–HFP)-based composite polymer electrolyte containing LiPF3(CF3CF2)3

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    This paper describes the preparation and characterization of lithium fluoroalkylphosphate-containing composite polymer electrolyte based on a polyvinylidene fluoride–hexafluoropropylene (PVdF–HFP) matrix. A mixture of ethylene carbonate and diethyl carbonate was used as a plasticizing agent and nanoscopic Al2O3 as a filler. The membranes were characterized by ac impedance, SEM, DSC, FTIR and fluorescence. An electrolyte with 2.5 wt% Al2O3 exhibited a conductivity of 9.8 104 S cm1 at ambient temperature. It was found that filler contents above 2.5 wt% rendered the membranes less conducting

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