2644 research outputs found

    Characteristics of slurry coated lead selenide films

    No full text
    Thin lead selenide films were deposited by the slurry coating technique using the powder chemically synthesized in the laboratory. The as prepared powder exhibited cubic structure. This powder was slurry coated onto alumina substrates. The films exhibited cubic structure with peaks corresponding to single phase PbSe. The films exhibited a carrier density of 3 ×1018 cm-3 and mobility value of 50 cm2V-1s-1. XPS studies indicated peaks corresponding to Pb4f5/2 and Se3d. Laser Raman studies exhibited a peak at 135 cm- 1

    Studies on the Removal of Iron from Drinking Water by Electrocoagulation – A Clean Process

    No full text
    The present study describes an electrocoagulation process for the removal of iron from drinking water using magnesium as the anode and galvanized iron as the cathode. Experiments were carried out as a function of pH, temperature and current density. The adsorption capacity was evaluated using both the Langmuir and the Freundlich isotherm models. The results show that the maximum removal efficiency of 98.4% was achieved at a current density of 0.06 A dm– 2, at a pH of 6.0. The adsorption of iron was better explained by fitting the Langmuir adsorption isotherm, which suggests a monolayer coverage of adsorbed molecules. The adsorption process followed a second-order kinetics model. Temperature studies showed that adsorption was endothermic and spontaneous in nature

    Feasibility studies on newly identified LiCrP2O7 compound for lithium insertion behavior

    No full text
    A new category of lithium intercalating cathode candidates, namely LiCrP2O7, was synthesized at 800°C using a citric acid assisted modified (CAM) sol–gel method and examined for possible lithium insertion behavior. The formation of a phase pure and monoclinic LiCrP2O7 compound with finer crystallite size was confirmed from the Xray diffraction patterns. The presence of nano-sized particles as observed from a transmittance electron microscope image of LiCrP2O7 and the presence of a preferred local cation environment, evidenced from Fourier transform infra-red and 7Li nuclear magnetic resonance studies, are the added advantages of the present study. Further, cyclic voltametry study performed on 2016 coin cells consisting of the synthesized LiCrP2O7 cathode revealed an excellent cycling reversibility and structural stability. Hence, CAM sol–gel synthesized LiCrP2O7 is found to possess desirable physical as well as electrochemical properties, leading one to consider the same as a possible lithium intercalating cathode material

    Determination of migration efficiency of amino alcohol based migrating corrosion inhibitor through concrete

    No full text
    The migration efficiency of an amino alcohol based migrating corrosion inhibitor (MCI) through hardened concrete of two different strengths (20 and 30 MPa) with two different thicknesses (25 and 40 mm) has been studied using diffusion test cell arrangement. The corrosion current Icorr was measured using Tafel extrapolation technique. There is a 20 times reduction in Icorr of steel in presence of MCI compared to that of bare steel. The migration efficiency decreases with an increase in thickness as well as strength of concrete. The density of concrete influences the diffusion rate of MCI. The diffusion rate is two times higher in 20 MPa concrete than that of 30 MPa concrete. The studies have indicated that the passive layer formed on the rebar surface is not stable in presence of 1% of chloride in 20 MPa concrete. Because of higher chloride threshold level the MCI has performed better in 30 MPa concrete. The results conclude that if higher protection efficiency is needed where structure is exposed to high chloride environments, it is more appropriate that the MCI shall be added at the rate of 2?45 kg m23 along with concrete/ repair mortar than applied on the concrete surface

    Studies on the effect of titanium addition on LiCoO2

    No full text
    The lithiated transition metal oxide has been used as the cathode materials for lithium ion rechargeable batteries. Among the various cathode materials, LiCoO2 has been widely used. There are lot of reports on the substituted LiCoO2 replacing small amount of Cobalt with other transition and nontransitional metals. Here, we focus on to a tetravalent transition metal atom such as titanium, as an addition in LiCoO2 and studied its performance. The titled cathode material was synthesized by solid-state reaction method. Thermogravimetric/differential thermal analysis, X-ray diffraction, X-ray fluorescence, scanning electron microscopy, and particle size analysis were carried out to assess the effect of addition of titanium on LiCoO2. Electrochemical studies were carried out by cyclic voltammetry and life cycle analyzer

    Electrochemical Synthesis and Studies of Polypyrroles Doped by Renewable Dopant Cardanol Azophenylsulfonic Acid Derived from Cashew Nutshells

    No full text
    The raw material cardanol, a renewable resource, is industrial waste and a pollutant from the cashew nut industry. Cardanol is a useful starting material for synthesizing a new amphiphilic molecule, cardanol azophenylsulfonic acid (CAPSA). In this study, polypyrroles were electrochemically synthesized with the renewable dopant CAPSA. The polymers were characterized with ultraviolet–visible, Fourier transform infrared, conductivity, impedance, charge–discharge, and cyclic voltammetry analyses. The conductivity of the films doped by CAPSA was in the range of 1.23–3.98 � 10�5 S/cm, and they exhibited moderate specific capacitance values

    Modeling electrowinning process in an expanded bed electrode

    No full text
    A theoretical model has been developed to describe the flow behavior of conducting particles in a fluidized bed electrode for electro winning of metal ions present in the dilute solution. Model equations have been developed for potential and current distributions and mass transfer rates. The influence of operating parameters on particle growth has been critically examined. It has been observed from the present investigation that the particle size increased with electrolysis time. The present model simulations have been compared with the experimental data reported in the literature and observed that the model predictions satisfactorily match with the reported experimental findings

    Influence of foreign Fe ions on wet chemical synthesis of Pt nanoparticle thin films at ambient temperature: in situ versus direct addition

    No full text
    Novel Pt nanoparticle thin films have been successfully synthesized on glass surfaces via a wet chemical method that comprised reduction of aqueous hexachloroplatinic acid solution by ascorbic acid in the presence of hematite (a-Fe2O3) at room temperature. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (XRD), atomic absorption spectroscopy, X-ray photoelectron spectroscopy (XPS), UV-Vis absorption spectroscopy and a scratch testing method have been used to characterize the final and intermediate products of Pt films. It was found that there existed competition between precipitation of nanoparticles and formation of Pt nanoparticle thin films, which is controlled by the source of foreign Fe ions i.e. in situ or direct addition of foreign ions. Besides, the negatively charged glass surface and positively charged hematite surface under the synthesis condition of pH 3 assisted heterogeneous nucleation of Pt on glass surfaces. The measured adhesive strength of the film on glass substrate is 106 Mpa and the density of states overlaps the Fermi energy (Ef ¼ 0), indicating the conducting films are strongly bonded on the glass surface. The synthetic protocol outlined here shows a new synthetic route to integrate metal nanoparticles directly on glass substrates

    High efficiency quasi-solid-state dye-sensitized solar cell based on polyvinyidene fluoride-co-hexafluoro propylene containing propylene carbonate and acetonitrile as plasticizers

    No full text
    Quasi-solid-state dye-sensitized solar cells (DSSCs) with differentweight ratios of polyvinyidene fluorideco- hexafluoro propylene (PVDF-HFP) containing two different plasticizers such as propylene carbonate (PC) and acetonitrile (AN) were fabricated and the effects of TiO2 morphology, light intensities as well as different organic iodides on the solar cell performance were studied. Two TiO2 photoelectrodes were designedby the coating of low(P1) and high molecularweight poly(ethylene glycol) (P2) incorporatedinto the TiO2 suspension. The DSSCs fabricated with the P2 TiO2 electrode showbetter performance in terms of short-circuit current densities (JSC) and conversion efficiencies than the P1 for all the weight percentages of PVDF-HFP containing both plasticizers. Further, the maximum current density (JSC) and conversion efficiency of PVDF-HFP containing different organic iodides follow the order: TBAI > TPAI >NH4I irrespective of the solvents and light intensity. A good conversion efficiency of 6.74% with JSC of 16.04mA/cm2, an open-circuit voltage (VOC) of 0.657V and a fill factor of 0.64 under illumination of 100mW/cm2 was obtained for the DSSC with 10% of PVDF-HFP containing 0.4M of TBAI and 0.04M of I2 in PVDF-HFP/AN system

    Thermal analysis of LixCoO2 cathode material of lithium ion battery

    No full text
    Thermal behavior of LixCoO2 cathode material from cells charged to different voltages has been analyzed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The mass loss appearing between 60 and 125 ◦C in TGA and the exothermic peaks with 4.9 and 7.0 J g−1 in DSC around 75 and 85 ◦C for the LixCoO2 cathodes of 4.20 and 4.35V cells has been explained based on solid electrolyte interface (SEI) film-break down. The SEI film-break down for the highly charged cathode at low temperature region has been attributed to the conversion of lithium fluoride into hydrofluoric acid in concomitant with the reaction, Li2CO3 + 2HF→2LiF + CO2 +H2O. Presence of ionic carbonate in the positive electrode has been identified by ion chromatography (IC). The thermal peaks appearing in different temperature regions have been explained based on decomposition reaction of LixCoO2 cathodes and the SEI film

    1,182

    full texts

    2,644

    metadata records
    Updated in last 30 days.
    IR@CECRI
    Access Repository Dashboard
    Do you manage Open Research Online? Become a CORE Member to access insider analytics, issue reports and manage access to outputs from your repository in the CORE Repository Dashboard! 👇