2644 research outputs found

    Influence of rare earth content on electrode kinetics in Misch metal-based AB5 MH alloys – Cyclic voltammetric investigations

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    The influence of lanthanum/cerium ratio (0.42–14.14) in Misch metal (Mm)-based AB5-type hydrogen storage alloys has been investigated. The samples were subjected to X-ray florescence (XRF) and cyclic voltammetry (CV) studies. The metal hydride electrodes were assembled, and their discharge capacity was determined. These alloys delivered discharge capacity between 118 and 266 mAh/g. CV investigations threw light on charge-transfer reactions at the electrode/electrolyte interface and hydrogen surface coverage capacity. The CV parameters in general indicate that the battery activity increases with lanthanum/ cerium ratio. At low lanthanum/cerium values, the discharge reactions proceed at potentials that are more negative. Furthermore, electrochemical reversibility of the hydrogen absorption–desorption on the alloy surface is enhanced at optimum lanthanum/cerium ratio as revealed by decreasing values of peak separation. The slopes of graphical plots of Ipeak (anodic) vs. n1/2 for the fully charged samples reverse direction at very high lanthanum/cerium values. The results suggest that the discharge plateau is optimum at lanthanum/cerium ratio around 12

    Synthesis and characterization of ZnCo2O4 nanomaterial for symmetric supercapacitor applications

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    ZnCo2O4 nanomaterial was prepared by coprecipitation method and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), cyclic voltammetry (CV), and galvanostatic charge–discharge tests at various current densities. It is shown that the crystal structure and surface morphology play an important role in the enhancement of the specific capacitance. The TEM results clearly indicate that the prepared material shows aggregated particles. The particle size powder was about 50 nm, and SEM pictures indicate a porous morphology. The electrochemical behavior of ZnCo2 O4 was characterized by mixing equal proportion of carbon nanofoam (CNF). From CV, it is concluded that the combination of redox and pseudocapacitance increases the specific capacitance up to 77 F g−1 at 5 mV s−1 scan rate. The ZnCo2O4-based supercapacitor cell has good cyclic stability and high coulombic efficiency

    Effect of mixed cations in synergizing the performance characteristics of PVA-based polymer electrolytes for novel category Zn/AgO polymer batteries—a preliminary study

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    Thin films of polymer electrolytes comprising of PVA and KOH (A) with and without the addition of zinc salts, viz., zinc acetate (B) and zinc triflate (C) as mixed cations were prepared via. solution casting method. The thermal stability and ionic conductivity of PVA–KOH solid polymer electrolyte (A) were improved by the partial substitution of KOH with zinc salts. Among the two salts, zinc triflate was found to improve both the physical as well as electrochemical properties of the PVA–KOH films more significantly than zinc acetate. An attempt to optimize the ratio of various components of polymer electrolytes, viz., polymer: KOH: zinc salt was also made, based on the dimensional stability and ionic conductivity values. Finally, the select category polymer film containing PVA–KOH– zinc triflate (C) in an optimum ratio of 40:35:25 was deployed in coin cell fabrication and subjected to charge– discharge studies with a view to demonstrate the possible electrochemical reversibility characteristics. Based on the encouraging results obtained from the cycling study, C type films [PVA–KOH–zinc triflate] qualify themselves as potential polymer electrolytes for use in rechargeable Zn/ AgO polymer batteries

    Miscibility of Polymethylmethacrylate and Polyethyleneglycol Blends in Tetrahydrofuran

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    The miscibility of polymethylmethacrylate (PMMA) and polyethyleneglycol (PEG) blends in tetrahydrofuran (THF) has been investigated by viscosity, density, refractive index, and ultrasonic velocity studies. Various interaction parameters such as polymer–solvent and blend– solvent interaction parameters and heat of mixing have been calculated using the viscosity, density, and ultrasonic velocity data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible in THF in the entire composition range. The study also revealed that variation in the temperature does not affect the miscibility of PMMA and PEG blends in THF significantly. The presence of hydrogen bonding in the blends in the solid state has also been indicated by FTIR studie

    Waste Minimization in Electroplating Industries: A Review

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    Wastewater, spent solvent, spent process solutions, and sludge are the major waste streams generated in large volumes daily in electroplating industries. These waste streams can be significantly minimized through process modification and operational improvement.Waste minimization methods have been implemented in some of the electroplating industries. Suggestions such as practicing source reduction approaches, reduction in drag out and waste, process modification and environmental benefits, have also been adopted. In this endeavor, extensive knowledge covering various disciplines has been studied, which makes problem solving extremely easy. Moreover, available process data pertaining to waste minimization (WM) is usually imprecise, incomplete, and uncertain due to the lack of sensors, the difficulty of measurement, and process variations. In this article waste minimization techniques and its advantages on the improvement of working atmosphere and reduction in operating cost have been discussed

    Electrochemical recovery of silver from waste aqueous Ag(I)/Ag(II) redox mediator solution used in mediated electro oxidation process

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    The paper presents a process for the electrochemical recovery of silver(Ag) by electro deposition on the electrode surface from the waste solutions of Ag(I)/Ag(II) redox system in nitric acid medium used for the mediated electrochemical process. Electrochemical recovery was carried out in an undivided cell with DSA-O2 electrodes at room temperature condition. At an optimized current density of 12 A/dm2, 99% of Ag recovery efficiency was achieved with high yield and low energy consumption. Experimental runs were made in order to observe the performance of the Ag recovery process. The operating conditions like current density, temperature and Ag(I) concentration of the electrolyte, the acid concentrations, agitation rate and inter-electrode distance were optimized

    Electrochemical characterization of supercapacitors based on carbons derived from coffee shells

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    Carbons derived by pyrolysis of coffee shells treated with ZnCl2 were used as electrode materials in symmetric electrochemical supercapacitors. Scanning electron microscopy showed that the carbon from the porogen-free shells showa flake-like structure, while those fromthe ZnCl2-treated coffee shells have a loose, disjointed structure with no definite shape. X-ray diffraction studies indicated the presence of small domains of coherent and parallel stacking of the graphene sheets. The average surface area of the carbon was 842m2 g−1, with an average micropore area of 400m2 g−1. Cyclic voltammetric studies suggested a specific capacitance of about 150 F g−1. Self-discharge studies on the devices showed a large retention time

    Electric field induced enhancement in the interfacial charge transfer kinetics of a solid polymer electrolyte

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    A novel electrostaticmethod for preparing modified solid polymer electrolytes (SPEs) is reported. Application of an electric field on an evaporating mixture of KYNAR, ethylene carbonate (EC), propylene carbonate (PC) and LiPF6 dissolved in tetra hydro furan (THF) resulted in a solid polymer electrolyte whose charge transfer resistance was at least an order of magnitude lower than that formed without the application of an electric field. We believe that the observed enhancement is probably due to an electric field induced orientation of dipoles in the polymer chai

    Anthraquinone catalysis in the glucose-driven reduction of indigo to leuco-indigo

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    Anthraquinone immobilised onto the surface of indigo microcrystals enhances the reductive dissolution of indigo to leuco-indigo. Indigo reduction is driven by glucose in aqueous NaOH and a vibrating gold disc electrode is employed to monitor the increasing leuco-indigo concentration with time. Anthraquinone introduces a strong catalytic effect which is explained by invoking a molecular ‘‘wedge effect’’ during co-intercalation of Na+ and anthraquinone into the layered indigo crystal structure. The glucose-driven indigo reduction, which is ineffective in 0.1 M NaOH at 65 1C, becomes facile and goes to completion in the presence of anthraquinone catalyst. Electron microscopy of indigo crystals before and after reductive dissolution confirms a delamination mechanism initiated at the edges of the plate-like indigo crystals. Catalysis occurs when the anthraquinone–indigo mixture reaches a molar ratio of 1 : 400 (at 65 1C; corresponding to 3 mM anthraquinone) with excess of anthraquinone having virtually no effect. A strong temperature effect (with a composite EA E 120 kJ mol�1) is observed for the reductive dissolution in the presence of anthraquinone. The molar ratio and temperature effects are both consistent with the heterogeneous nature of the anthraquinone catalysis in the aqueous reaction mixture

    Corrosion protective performance studies of coating systems in soda ash chemical industry

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    Organic coatings are widely used to protect steel structures. The performance of the coating system depends upon the atmospheric conditions prevailing in the chemical industry. Before selecting a protective system, the corrosivity of the atmosphere has to be determined. A study has been made for selecting a good protective system for a soda ash chemical industry where chemicals such as soda ash, sodium chloride and hydrochloric acid are produced by using sea water as a raw material. Under these conditions, after collecting the corrosivity rate at various places of industrial areas, coated steel panels with various paint combinations were exposed in different sites for a period of 2 years. The performance of the coatings was monitored by EIS studies besides visual inspection. The corrosion protection performance of the various coating systems of zinc rich primer with different types of under coats and top coats has been studied and the results are reported

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