Faculty Publications

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    Modelling, analysis and optimization of adsorption parameters for H3PO4 activated rubber wood sawdust using response surface methodology (RSM)
    (2009) Helen Kalavathy, M.H.; Iyyaswami, I.; Ganesapillai, M.G.; Miranda, L.R.
    Adsorption capacity of Cu2+ from aqueous solution onto H3PO4 activated carbon using rubber wood sawdust (RSAC) was investigated in a batch system. Kinetic and isotherm studies were carried out, the thermodynamic parameters like standard Gibb's free energy (?G°), enthalpy (?H°) and entropy (?S°) were evaluated. The pseudo-second-order model was found to explain the kinetics of Cu2+ adsorption most effectively. The process optimization was performed through Central Composite Rotary Design using response surface methodology (RSM) by Design Expert Version 5.0.7 (STAT-EASE Inc., Minneapolis, USA). An initial concentration of 35 mg L-1, temperature of 26 °C, carbon loading of 0.45 g (100 mL)-1, adsorption time 208 min and pH of 6.5 was found to be the optimum conditions for the maximum uptake of copper ions of 5.6 mg g-1 in batch mode. © 2009 Elsevier B.V. All rights reserved.
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    Catalytic oxidation of alcohols by nickel(II) Schiff base complexes containing triphenylphosphine in ionic liquid: An attempt towards green oxidation process
    (2010) Ramakrishna, D.; Badekai Ramachandra, B.; Karvembu, R.
    A series of square planar nickel(II) complexes containing N,O donor Schiff base ligand, i.e. N-(2-pyridyl)-N?-(5-substituted-salicylidene)hydrazine and triphenylphosphine, have been synthesized and characterized by analytical and spectral methods. Catalytic activities of all the complexes have been studied for the oxidation of alcohols in ionic liquid media using NaOCl as oxidant. © 2009 Elsevier B.V. All rights reserved.
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    Colorimetric receptors for naked eye detection of inorganic fluoride ion in aqueous media using ICT mechanism
    (Royal Society of Chemistry, 2012) Kigga, M.; Nityananda Shetty, A.N.; Trivedi, D.R.
    A new series of receptors were designed and synthesized based on benzohydrazide for the colorimetric detection of fluoride ion. The receptors L1 and L2 are highly selective towards fluoride ion over other anions. These receptors are able to detect inorganic fluoride such as NaF in aqueous solutions. The presence of two carbonyl groups in the receptor molecule makes the -NH proton highly acidic and hence these receptors are capable of competing with water molecules to bind fluoride ion. The receptors L1 and L2 showed a significant colour change from colourless to yellow in aqueous solutions of NaF with a ??max of 149 nm and 147 nm respectively. The mechanism involved in the colour change was deprotonation, formation of imidic acid intermediate followed by stabilization of complex through Intramolecular Charge Transfer (ICT). This was further confirmed by 1H NMR titrations where the formation of imidic acid was observed. The receptor L1 proved itself to be potentially useful for real-life applications by detecting fluoride ion quantitatively in sea water and commercially available mouth wash. © 2012 The Royal Society of Chemistry.
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    Reactive distillation using an ion-exchange catalyst: Experimental and simulation studies for the production of methyl acetate
    (2013) Sandesh, K.; JagadeeshBabu, P.E.; Math, S.; Saidutta, M.B.
    In this study, the performance of a packed-bed reactive distillation (RD) column for the production of methyl acetate (MeOAc) using an ion-exchange catalyst and simulation of the same using CHEMCAD were analyzed. An ion-exchange catalyst, Indion 190, was used in this study. The performance of the RD column was evaluated based on the MeOAc concentration in the top product. Both steady- and unsteady-state behavior of the column was simulated using CHEMCAD, and the results were experimentally validated. The process parameters, viz., reboiler temperature, enriching temperature, reactor temperature, catalyst loading, molar ratio of the reactant, and flow rate of reactants, were studied, and the optimal values were found to be 73 C, 56 C, 72 C, 100 g, 1:2, and 15 mL/min, respectively. Feed locations of acid and alcohol to the reactor that gave maximum MeOAc concentration in the top product were determined. A mathematical model based on the rigorous calculation using SCDS (used to calculate the nonideal K value) was used to simulate the RD in CHEMCAD. The simulated values were found to deviate from the experimental values within ±5-10%. © 2013 American Chemical Society.
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    A new colorimetric receptor for selective detection of maleate vs. fumarate and ratiometric detection of F- ions
    (Royal Society of Chemistry, 2014) Kigga, M.; Trivedi, D.R.
    Two new receptors, R1 and R2, were designed and synthesized for the isomeric discrimination of maleate ions over fumarate ions. Receptor R1 showed high selectivity with a significant color change from colorless to orange red with ??max of 104 nm. This was owing to the hydrogen bonded electrostatic interactions of maleate ions with receptor R1. The formation of hydrogen bond between receptor R1 and maleate ions was confirmed by 1H NMR titrations, where the signal at ? 12.25 corresponding to the benzohydrazide -NH proton showed a downfield shift upon binding with the anion. Receptor R3 did not show any binding with maleate ions or fumarate ions due to steric hindrance. Receptors R1 and R2 detected F- ions with color changes from colorless to orange and colorless to pale yellow, respectively. Upon incremental addition of F- ions, the color was further transformed from orange to blood red in receptor R1 and pale yellow to dark yellow in receptor R2. This result was due to the formation of initial hydrogen bonds followed by the deprotonation of receptors at higher concentrations of F- ions. © the Partner Organisations 2014.
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    Structural, optical and mechanical properties of ternary CaO-CaF2-P2O5 glasses
    (Tsinghua University, 2014) Venkateswara Rao, G.V.; Shashikala, H.D.
    The ternary phosphate glass series (50?x)CaO-xCaF2-50P2O5 (x = 0–20 mol%) were synthesized using melt quench technique. Structural, optical and mechanical properties were investigated with increase in CaF2 content. Using X-ray diffraction (XRD), synthesized glasses were confirmed to be amorphous in nature. Replacement of oxygen ions by fluorine ions increased the values of density. Decrease in refractive index due to the low polarizability of fluorine ions in the glass matrix was observed. In Fourier transform infrared (FTIR) spectra, the slight variation in ?as (PO2) band position and intensity could be attributed to replacement of fluorine ions for oxygen ions in phosphate glass structure. These data were well supported by Raman spectra. Optical band gap energy increased from 3.44 eV to 3.64 eV with increase in CaF2 content, and Urbach energy decreased suggesting that the fluorine ions reduced the tail energy states in the band gap compared to the oxygen ions. Mechanical parameters such as Vickers hardness, fracture toughness and brittleness were evaluated from the Vickers micro indentation measurements. Increase in Vickers hardness, decrease in fracture toughness and increase in brittleness were observed with increase in CaF2 content. © 2014, The Author(s).
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    Thermal and optical properties of BaO-CaF2-P2O5 glasses
    (Elsevier B.V., 2015) Narayanan, M.K.; Shashikala, H.D.
    Thermal and optical properties of ternary phosphate glasses prepared by conventional melt-quenching technique, belonging to the series (50 - X)BaO-XCaF2-50P2O5 (X = 0 to 10 mol%) were investigated with increase in CaF2 content. Thermal stability and glass forming ability studied using differential thermal analysis (DTA) were found to increase with the increase in CaF2 content. Powder X-ray diffraction (XRD) analysis of heat treated samples also revealed that CaF2 addition improves the thermal stability against crystallization. Increase in both glass transition temperature and onset crystallization temperature with the increase in CaF2 content can be attributed to the partial substitution of Ba2 + ion with Ca2 + ion, which is having larger field strength. The observed decrease in the melting temperature of glass batch with the increase in CaF2 content indicates that CaF2 acts as a flux and reduces the viscosity of the glass melt. The decrease in refractive index of the glasses with the increase in CaF2 content can be attributed to replacement of lower field strength Ba2 + by Ca2 + or the partial substitution of more polarizable oxygen ion by fluorine. Optical band gap energy slightly increased and Urbach energy marginally reduced with the increase in CaF2 content. Increase in optical band gap energy was further confirmed by calculating theoretical optical basicity of glasses. Average anion polarizability (?O/F) of (50 - X)BaO-XCaF2-50P2O5 glasses calculated from refractivity data using Lorentz-Lorentz relation was correlated with its theoretical optical basicity (?th) using the previously established correlation for oxyfluoro phosphate glasses. © 2015 Elsevier B.V. All rights reserved.
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    Insights into the electrooptical anion sensing properties of a new organic receptor: Solvent dependent chromogenic response and DFT studies
    (Royal Society of Chemistry, 2016) Pangannaya, P.; Tarafder, K.; Nityananda Shetty, A.N.; Trivedi, D.R.
    A highly selective hydrazine based electrooptical receptor featuring solvent based color transition properties in the presence of acetate ions has been developed. The AcO- ion mediated color transition properties of a new organic receptor in solvents of varying polarity highlights the influence of dipole moment in stabilizing the excited state. Selective detection of acetate ions by a new organic receptor in the presence of DMSO : Tris HCl buffer (9 : 1, v/v) has been the pivotal concept of the present work. 1H-NMR titration and DFT studies provide quantitative proof of the underlying detection mechanism. Solution and solid state sensing response of anions by the receptor reflects the practical utility in real time sample analysis. © 2016 The Royal Society of Chemistry.
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    Pharmaceutical salts of ethionamide with GRAS counter ion donors to enhance the solubility
    (Elsevier B.V., 2017) Nechipadappu, S.K.; Trivedi, D.R.
    Pharmaceutical salts of BCS class II second line anti-tuberculosis drug ethionamide (ETH) with various counter ions namely, 2-chloro-4-nitrobenzoic acid (CNB), 2,6-dihydroxybenzoic acid (2,6HBA), 2,3-dihydroxybenzoic acid (2,3HBA) and 2,4-dinitrobenzoic acid (DNB) were synthesized by crystal engineering approach. All the synthesized salts were characterized by various spectroscopic (NMR, FT-IR,), thermal (DSC & TGA) and PXRD techniques. The crystal structure of the synthesized salts was determined by single-crystal X-ray diffraction techniques. All the reported salts, except ETH-2,3HBA exhibited charge assisted acid pyridine heterosynthon. In ETH-2,3HBA hydoxyl pyridine heterosynthon is observed. In ETH-CNB salt, both ionic and neutral acid pyridine heterosynthon were observed in the asymmetric unit. ETH-DNB salt consists of both partial and complete proton transfer from DNB to ETH in the asymmetric unit. All the synthesized salts were found to be non-hygroscopic at accelerated humid condition (~ 75% RH). Solubility experiment has been performed in purified water and in 0.1 N HCl (pH = 1) solution and found that the solubility of ETH-CNB salt was about eight-fold higher soluble than ETH in purified water. The solubility of synthesized salts follows the order of ETH < ETH-2,3HBA < ETH-2,6HBA < ETH-CNB in purified water. © 2016 Elsevier B.V.
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    Electrochemical corrosion study of Mg-Al-Zn-Mn alloy in aqueous ethylene glycol containing chloride ions
    (Elsevier Editora Ltda, 2017) Medhashree, H.; Nityananda Shetty, A.N.
    Nowadays most of the automobiles use magnesium alloys in the components of the engine coolant systems. These engine coolants used are mainly composed of aqueous ethylene glycol along with some inhibitors. Generally the engine coolants are contaminated by environmental anions like chlorides, which would enhance the rate of corrosion of the alloys used in the coolant system. In the present study, the corrosion behavior of Mg-Al-Zn-Mn alloy in 30% (v/v) aqueous ethylene glycol containing chloride anions at neutral pH was investigated. Electrochemical techniques, such as potentiodynamic polarization method, cyclic polarization and electrochemical impedance spectroscopy (EIS) were used to study the corrosion behavior of Mg-Al-Zn-Mn alloy. The surface morphology, microstructure and surface composition of the alloy were studied by using the scanning electron microscopy (SEM), optical microscopy and energy dispersion X-ray (EDX) analysis, respectively. Electrochemical investigations show that the rate of corrosion increases with the increase in chloride ion concentration and also with the increase in medium temperature. © 2016 Brazilian Metallurgical, Materials and Mining Association.