Faculty Publications

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    Combined effect of marine environment and pH on the impedance of reinforced concrete studied by electrochemical impedance spectroscopy
    (Springer, 2019) Goudar, S.K.; Das, B.B.; Arya, S.
    In the present investigation, behavior of OPC and fly ash based concretes were assessed by electrochemical impedance spectroscopy (EIS) technique after exposing the samples to the marine environment in combination with five pH levels (1, 4, 7, 10, and 13). Three different dosages of fly ash (15, 25, and 35%) were used to produce fly ash based concretes. After 90 days of exposure to the aggressive environment, the OPC and fly ash based concretes were tested for impedance analysis and corrosion resistance by electrochemical studies. For the equivalent electrical circuit in EIS study, a total of four electrical circuits were tried for the possible best fit of obtained Nyquist plots. The equivalent electrical circuits proposed by previous researchers failed to provide the best fit for the obtained Nyquist plots. A new equivalent electrical circuit is being proposed in this study which will provide the possible best fit of Nyquist plots when the concrete is being exposed to acidic and alkaline marine environment. It is observed that the pH of the marine environment has a decisive influence on the impedance of reinforced concrete. As the acidity of marine environment reduces to pH 1, the impedance of OPC and fly ash based concrete reduced significantly due to the severe deterioration of concrete composites especially because of acid attack and Cl− ions migration. However, in the case of alkaline nature of the marine environment (pH 13), there was comparably less deterioration of concrete composites which reflected in higher impedance values. The higher dosage of fly ash addition has led to substantial improvement in concrete impedance and also lower corrosion rate. © Springer Nature Singapore Pte Ltd. 2019.
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    Role of porosity on electrochemical corrosion behavior of porous Ti-20Nb-5Ag alloy in simulated body fluid
    (Elsevier Ltd, 2020) Shivaram, M.J.; Arya, S.B.; Nayak, J.; Panigrahi, B.B.
    Porous titanium alloys are presently well-considered materials for orthopedic applications owing to their superior mechanical properties, excellent biocompatibility and high resistance to corrosion. Also, porous alloys are potentially minimizing the risk of stress-shielding effect as compared to bulk implant materials. In this present work focused to examine electrochemical corrosion behavior of porous Ti-20Nb-5Ag alloy (wt%) with different porosity levels. This designed alloy composition of elemental powders was mixed through mechanically alloying. The mechanically alloyed powder blended with four different amounts of NH4HCO3 (wt%), use to prepare the porous Ti-20Nb-5Ag alloy with porosity ranging from 22% to 68%. After the successful development of porous samples, we investigated the effect of porosity levels on electrochemical corrosion behavior of porous Ti-20Nb-5Ag alloys by means of potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) in simulated body fluid (SBF) at 37 °C. The results show that an increasing the trend of porosity level causes a reduction of corrosion resistance. With increasing porosity, the corrosion current density increased and decreases the electrochemical polarization resistance in the SBF solution. © 2019 Elsevier Ltd. All rights reserved.
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    Trifluoromethyl-quinolin-yl-thio-propanohydrazide as an effective inhibitor of mild steel corrosion in HCl solution
    (2006) Ramesh Saliyan, V.; Vasudeva Adhikari, A.V.
    3-{[8-(trifluoromethyl)quinolin-4-yl]thio}propanohydrazide(TFQTPH) was synthesized, characterized and tested as a corrosion inhibitor for mild steel in 1 M HCl and 2 M HCl solution using different techniques: potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results showed that TFQTPH is an excellent inhibitor for mild steel in acid medium. The inhibition was assumed to occur via adsorption of the inhibitor molecule on the metal surface. In the temperature range 20° to 60° C, the TFQTPH adsorption follows Langmuir isotherm model. The protection efficiency increased with increasing inhibitor concentration (10 to 500 ppm), even at higher temperature also, it recorded good inhibition efficiency. © 2006 SAEST.
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    Corrosion behavior of composition modulated multilayer Zn-Co electrodeposits produced using a single-bath technique
    (2009) Thangaraj, V.; Eliaz, N.; Hegde, A.
    Composition modulated alloy (CMA) electrodeposits of Zn-Co were produced from acid chloride baths by the single-bath technique. Their corrosion behavior was evaluated as a function of the switched cathode current densities and the number of layers. The process was optimized with respect to the highest corrosion resistance. Enhanced corrosion resistance was obtained when the outer layer was slightly richer with cobalt. At the optimum switched current densities 40/55 mA cm-2, a coating with 600 layers showed ~6 times higher corrosion resistance than monolithic Zn-Co electrodeposit having the same thickness. The CMA coating exhibited red rust only after 1,130 h in a salt-spray test. The increased corrosion resistance of the multilayer alloys was related to their inherent barrier properties, as revealed by Electrochemical Impedance Spectroscopy. The corrosion resistance was explained in terms of n-type semiconductor films at the interface as supported by Mott-Schottky plots. © 2008 Springer Science+Business Media B.V.
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    N?-[4-(diethylamino)benzylidine]-3-{[8-(trifluoromethyl) quinolin-4-yl]thio}propano hydrazide) as an effective inhibitor of mild steel corrosion in acid media
    (2009) Ramesh, S.V.; Vasudeva Adhikari, A.V.
    N?-[4-(diethylamino)benzylidine]-3-{[8-(trifluoromethyl)quinolin-4-yl]thio}propano hydrazide (DEQTPH) was newly synthesized, characterized and tested as a corrosion inhibitor for mild steel in HCl (1 M, 2 M) and H2SO4 (0.5 M, 1 M) solutions using weight loss method, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization method. The corrosion inhibition efficiencies measured by all the above three techniques were in good agreement with each other. The mild steel samples were also analyzed by scanning electron microscopy (SEM). The results showed that DEQTPH is an excellent inhibitor for mild steel in acid media. The inhibition efficiency in different acid media was found to be in the order, 0.5 M H2SO4 > 1.0 M HCl > 2.0 M HCl > 1.0 M H2SO4. The inhibition was assumed to occur via adsorption of the inhibitor molecule on the metal surface. It acts as an anodic inhibitor. In the 30-60 °C temperature range, the DEQTPH adsorption follows Langmuir isotherm model. The protection efficiency increased with increasing inhibitor concentration in the range 0.2 × 10-4 to 10.5 × 10-4 M and slightly increased with increasing temperature. Thermodynamic characteristics were discussed. Chemisorption mechanism is proposed. © 2009 Elsevier B.V. All rights reserved.
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    Electrical and magnetic properties of chitosan-magnetite nanocomposites
    (2010) Bhatt, A.S.; Bhat, D.K.; Santosh, M.S.
    Magnetite powders in nanometer size have been synthesized by the hydrothermal process. Various magnetic films of chitosan and the synthesized magnetite nanopowders containing different concentrations of the latter were prepared by ultrasonication route. The X-ray diffraction (XRD) studies and the transmission electron microscopy (TEM) images showed that the synthesized magnetite particles had 80 nm dimensions. The band gap of the composites was evaluated using the UV-visible Spectroscopy. The influence of magnetite content on the magnetic properties of the composite showed a decrease in the saturation magnetization with the decrease in the magnetic content. The effect of magnetite content on the dielectric properties of the polymer film at different frequencies from 0.01 to 105 Hz was studied using an electrochemical impedance spectroscopy. The possible mechanism for the observed electrical properties of the composite films was discussed. © 2010 Elsevier B.V. All rights reserved.
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    Nano ZnO-activated carbon composite electrodes for supercapacitors
    (2010) Muthu, M.S.; Bhat, D.K.; Aggarwal, A.; Prahladh Iyer, S.; Sravani, G.
    A symmetrical (p/p) supercapacitor has been fabricated by making use of nanostructured zinc oxide (ZnO)-activated carbon (AC) composite electrodes for the first time. The composites have been characterized by field emission scanning electron microscopy (FESEM) and X-ray diffraction analysis (XRD). Electrochemical properties of the prepared nanocomposite electrodes and the supercapacitor have been studied using cyclic voltammetry (CV) and AC impedance spectroscopy in 0.1 M Na2SO4 as electrolyte. The ZnO-AC nanocomposite electrode showed a specific capacitance of 160 F/g for 1:1 composition. The specific capacitance of the electrodes decreased with increase in zinc oxide content. Galvanostatic charge-discharge measurements have been done at various current densities, namely 2, 4, 6 and 7 mA/cm2. It has been found that the cells have excellent electrochemical reversibility and capacitive characteristics in 0.1 M Na2SO4 electrolyte. It has also been observed that the specific capacitance is constant up to 500 cycles at all current densities. © 2010 Elsevier B.V. All rights reserved.
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    Electrolytic preparation of cyclic multilayer Zn-Ni alloy coating using switching cathode current densities
    (2010) Venkatakrishna, K.; Hegde, A.C.
    Cyclic multilayer alloy (CMA) coating of Zn-Ni was developed on mild steel using single bath technique, by proper manipulation of cathode current densities. The thickness and composition of the individual layers were altered precisely and conveniently by cyclic modulation of cathode current densities. Multilayer coatings, having sharp change in compositions were developed using square current pulses. Gelatin and sulphanilic acid (SA) acid were used as additives. Laminar deposits with different configurations were produced, and their corrosion behaviors were studied, in 5% NaCl solution by electrochemical methods. It was observed that the corrosion resistance of CMA coating increased progressively with number of layers (up to certain optimal numbers) and then decreased. Cyclic voltammetry study demonstrated the role of gelatin and SA in multilayer coating. The coating configuration has been optimized for the peak performance against corrosion. The substantial decrease of corrosion rate, in the case of multilayer coatings was attributed to the changed intrinsic electric properties, evidenced by Electrochemical Impedance Spectroscopy (EIS) study. The surface morphology and its roughness were examined by Atomic Force Microscopy (AFM). The surface and cross-sectional view of coatings were examined, using Scanning Electron Microscopy (SEM). X-ray photoelectron spectrum (XPS) study was carried out for surface analysis. The relative performance of pure Zn, monolithic and CMA coatings were compared and discussed. © 2010 Springer Science+Business Media B.V.
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    Electrodeposition of high performance multilayer coatings of Zn-Co using triangular current pulses
    (2010) Yogesha, S.; Hegde, A.C.
    Compositionally modulated alloy (CMA) coatings of Zn-Co were electrodeposited on to mild steel from an acid chloride bath containing thiamine hydrochloride, as an additive. Electroplating was carried out galvanostatically from a single bath containing Zn2+ and Co2+ ions. Gradual change in composition in each layer was effected by triangular current pulses, cycling between two cathode current densities. Compositionally modulated alloy coatings were developed under different conditions of cyclic cathode current density and number of layers, and their corrosion resistances were evaluated by potentiodynamic polarisation and electrochemical impedance spectroscopy. The formation of multilayer and corrosion mechanism was analysed using scanning electron microscopy. The corrosion resistances of CMA and monolithic alloy coatings were compared with that of the base metal. Compositionally modulated alloy coating at optimal configuration, represented as (Zn-Co) 2•0/4•0/300, was found to exhibit ?80 times better corrosion resistance compared with monolithic (Zn-Co)3•0 alloy, deposited for the same length of time from the same bath. Improved corrosion resistance was attributed to the formation of n-type semiconductor film at the interface, supported by Mott-Schottky plots. Decrease in corrosion resistance at high degree of layering was found, and is due to lower relaxation time for redistribution of solutes in the diffusion double layer, during plating. © 2010 Maney Publishing.
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    Electroplating and characterization of Zn-Ni, Zn-Co and Zn-Ni-Co alloys
    (2010) Eliaz, N.; Venkatakrishna, K.; Hegde, A.C.
    Zn-Ni, Zn-Co and Zn-Ni-Co coatings were electrodeposited on mild steel from an acidic chloride bath containing p-aminobenzenesulphonic acid (SA) and gelatin. These additives changed the phase content in the coatings, most likely as a result of their adsorption at the surface of the cathode. The effect of gelatin was more pronounced than that of SA. The Faradaic efficiency was higher than 90%. As the current density was increased or the bath temperature was decreased, the concentration of the nobler metal in the coating increased. Both concentrations of Ni and Co in the ternary alloy increased as the applied current density was increased. Nickel and cobalt were found to have a synergistic catalytic effect. The thickness of all coatings increased as the applied current density was increased. The hardness increased with current density to a peak value, and then decreased. The rate of Zn deposition was heavily influenced by mass-transport limitation at high applied current densities, while the rates of Ni and Co deposition were not. The anomalous codeposition was explained by the great difference between the exchange current densities of Zn and the iron-group metal. Potentiodynamic polarization scans and electrochemical impedance spectroscopy showed that the corrosion resistance of the ternary Zn-Ni-Co alloy coatings was approximately 10 times higher than that of Zn-Ni and 7 times higher than that of Zn-Co. The improved corrosion resistance of the ternary alloy was attributed to its surface chemistry, phase content, texture, and surface morphology. The ternary Zn-Ni-Co coating may thus replace the conventional Zn-Ni and Zn-Co coatings in a variety of applications. © 2010 Elsevier B.V.