Faculty Publications
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Item Membrane technology—a promising approach for metal ion extraction(Elsevier, 2024) Antony, N.; Vijesh, A.M.; Isloor, A.M.Metal ion extraction using ion exchange membranes (IEM) receives much attention as it can find a solution to environmental problems to reduce emissions of heavy metals from wastewater contaminated with industrial effluents. Among the various IEM available, cation exchange membranes are widely used by researchers due to its enhanced ability to hold the metal ion and retain them in the organic phase. This review book chapter emphasizes the extraction of metal ions, specifically about the studies carried out in the field of iron, zinc, and copper metal ions using IEM. © 2024 Elsevier Inc. All rights reserved.Item 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.Item Studies on the effect of pH, temperature and metal ions on the production of pectinase from tamarind kernel powder by submerged fermentation using Aspergillus foetidus (NCIM 505)(2010) JagadeeshBabu, P.E.; Viswanathan, R.Filamentous fungi Aspergillus foetidus NCIM 505 was studied for its capacity to produce exo-pectinase in submerged fermentation (SMF) from a new substrate of tamarind kernel powder (TKP). The process was further studied to optimize the initial operating variables like pH, time and temperature. Maximum pectinolytic activity was reached at 72 h of growth and the best fungal strain was found to be A. foetidus NCIM 505. Further, to increase the production rate of pectinase, the effects of metal ions were studied. Metal ions like Cu ++, Mg++, Fe++, Co++ and Zn ++ at different concentrations were used. © 2009 Curtin University of Technology and John Wiley & Sons, Ltd.Item Spectrophotometric determination of platinum(IV) in alloys, complexes, environmental, and pharmaceutical samples using 4-[N,N-(diethyl)amino] benzaldehyde thiosemicarbazone(2010) Naik, P.P.; Karthikeyan, J.; Nityananda Shetty, A.N.4-[N,N-(Diethyl)amino] benzaldehyde thiosemicarbazone (DEABT) is proposed as an analytical reagent for the spectrophotometric determination of platinum(IV). The DEABT forms 1:2 yellow complex with Pt(IV), which is sparingly soluble in water and completely soluble in water-ethanol-DMF medium. The Pt(IV)-DEABT complex shows maximum absorbance at 405 nm. Beer's law is valid up to 7.80 ?g cm-3, and optimum concentration range for the determination of platinum(IV) is 0.48-7.02 ?g cm-3. The molar absorptivity and Sandell's sensitivity of the method are found to be 1.755 × 104 dm3 mol-1 cm-1 and 0.0012 ?g cm-2, respectively. The relative error and coefficient of variation (n=6) for the method does not exceed ±0.43% and 0.35%, respectively. Since the method tolerates a number of metal ions commonly associated with platinum, it can be employed for the determination of platinum in environmental samples, pharmaceutical samples, alloys, catalysts, and complexes. The method is rapid as the Pt(IV)-DEABT complex is soluble in water-ethanol-DMF medium and not requiring any time consuming extraction method for the complex. © 2010 Springer Science+Business Media B.V.Item Molecular dynamics investigation of dipeptide - Transition metal salts in aqueous solutions(American Chemical Society service@acs.org, 2010) Santosh, M.S.; Lyubartsev, A.; Mirzoev, A.; Bhat, D.K.Molecular dynamics (MD) simulations of glycylglycine dipeptide with transition metal ions (Mn2+, Fe2+, Co2+, Ni2+, Cu2+, and Zn2+) in aqueous solutions have been carried out to get an insight into the solvation structure, intermolecular interactions, and salt effects in these systems. The solvation structure and hydrogen bonding were described in terms of radial distribution function (RDF) and spatial distribution function (SDF). The dynamical properties of the solvation structure were also analyzed in terms of diffusion and residence times. The simulation results show the presence of a well-defined first hydration shell around the dipeptide, with water molecules forming hydrogen bonds to the polar groups of the dipeptide. This shell is, however, affected by the strong electric field of divalent metal ions, which at higher ion concentrations lead to the shift in the dipeptide-water RDFs. Higher salt concentrations lead also to increased residence times and slower diffusion rates. In general, smaller ions (Cu2+, Zn2+) demonstrate stronger binding to dipeptide than the larger ones (Fe2+, Mn 2+). Simulations do not show any stronger association of peptide molecules indicating their dissolution in water. The above results may be of potential interest to future researchers on these molecular interactions. © 2010 American Chemical Society.Item Composition modulated multilayer Zn-Fe alloy coatings on mild steel for better corrosion resistance(2011) Venkatakrishna, K.; Hegde, A.C.Composition modulated alloy (CMA) of Zn-Fe coatings were developed on mild steel galvanostatically from chloride bath containing sulphanilic acid (SA) and ascorbic acid (AA) through single bath technique (SBT). The properties of CMA coatings were found to depend on the thickness of individual layers and switching cathode current densities (SCCDs). The CMA (Zn-Fe) coating, having 120 layers, deposited at 20 and 50mAcm-2, were found to show the least corrosion rate (1.545 × 10-2mmy-1) compared to monolithic alloy (32.5 × 10-2mmy-1) of the same thickness. The improved corrosion resistance of multilayered coatings was due to the fact that the defects and failures occurring in a single layer in the deposition process is covered by the successively deposited coating layers, and hence the corrosive agent path is extended or blocked. Further, the high corrosion resistance of CMA Zn-Fe coatings was attributed to the "dielectric barrier" of the coatings, evidenced by dielectric spectroscopy and Mott-Schottky's plot. The corrosion rate was found to increase at high degree of layering, and is attributed to less relaxation time for redistribution of metal ions in diffusion layer, during plating. In other words, at higher layer thickness, the CMA coating tends to become a monolithic. CMA coatings were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). © Taylor & Francis Group, LLC.Item Development of nano-structured cyclic multilayer Zn-Ni alloy coatings using triangular current pulses(2011) Bhat, R.S.; Hegde, A.C.Cyclic multilayer alloy (CMA) deposits of Zn-Ni were developed on mild steel from sulphate bath having thiamine hydrochloride (THC) and citric acid (CA) as additives. CMA coatings were developed galvanostatically using triangular current pulses, under different conditions of cyclic cathode current density (CCCD's) and number of layers. The corrosion behaviors of the coatings were evaluated by potentiodynamic polarization and electrochemical impedance spectroscopy methods, and were compared with that of monolayer Zn-Ni alloy of same thickness. At optimal configuration, CMA coating represented as, (Zn-Ni)2.0/5.0/300 was found to exhibit ?40 times better corrosion resistance compared to monolayer alloy, (Zn-Ni)3.0. Cyclic voltammetry study demonstrated that THC and CA have improved the appearance of the deposit by complexation with metal ions. The corrosion protection efficacy of CMA coatings was attributed to the difference in phase structure of the alloy in successive layers, evidenced by XRD analysis. The formation of multilayer and corrosion mechanism was analyzed by Scanning Electron Microscopy (SEM) study. © 2011 Allerton Press, Inc.Item Corrosion stability of electrodeposited cyclic multilayer Zn-Ni alloy coatings(2011) Bhat, R.S.; Udupa, K.R.; Hegde, A.C.This paper reports on a study of electrodeposition and characterisation of cyclic multilayer coatings of Zn-Ni alloy from a sulphate bath. Cyclic multilayer alloy coatings were deposited on mild steel through the single bath technique by appropriate manipulation of cathode current densities. The thickness and composition of the individual layers of the CMA deposits were altered precisely and conveniently by cyclic modulation of the cathode current during electrodeposition. Multilayer deposits with sharp change in composition were developed using square current pulses, using thiamine hydrochloride and citric acid as additives. Laminar deposits with different configurations were produced and their corrosion behaviours were studied by AC and DC methods in 5%NaCl solution. It was observed that the corrosion resistance of the CMA coating increased progressively with the number of layers (up to certain optimal numbers) and then decreased. The decrease in corrosion resistance at high degree of layering was attributed to interlayer diffusion due to less relaxation time for redistribution of metal ions at cathode during deposition. The coating configurations have been optimised for peak performance of the coatings against corrosion. It was found that CMA coating developed at cyclic cathode current densities of 3.0/5.0 A dm-2 with 300 layers showed the lowest corrosion rate (0.112×10-2 mm/year) which is ?54 times better than that of monolithic Zn-Ni alloy, deposited from the same bath. The protection efficacy of CMA coatings is attributed to the difference in phase structure of the alloys in successive layers, deposited at different current densities, evidenced by X-ray diffraction analysis. The formation of multilayers and corrosion mechanism were examined by scanning electron microscopy. © 2011 Institute of Metal Finishing.Item Rhodamine-based Cu2+-selective fluorosensor: Synthesis, mechanism, and application in living cells(2013) Sikdar, A.; Roy, S.; Haldar, K.; Sarkar, S.; Panja, S.S.A rhodamine B-based fluorescence probe (1) for the sensitive and selective detection of Cu2+ ion has been designed and synthesized using pyridine moiety. The optical properties of this compound have been investigated in acetonitrile-water binary solution (7:3 v/v). Compound 1 is found to be an excellent sensor for a biologically/physiologically very important transition metal ion (Cu2+) using only the two very different modes of measurements (absorption and emission); one case displayed intensity enhancement whereas in other case showed intensity depletion (quenching). A mechanistic investigation has been performed to explore the static nature of quenching process. The sensor has been found to be very effective in sensing Cu 2+ ion inside living cells also. © 2013 Springer Science+Business Media New York.Item Production of layered coatings of Fe-Ni alloy for enhanced corrosion protection(2013) Pavithra, G.P.; Hegde, A.C.Layered Fe-Ni alloy coatings have been galvanostatically developed on copper using dual and triple square current pulse from acid sulfate bath. The cyclic cathode current density (CCCD) and number of layers have been optimized for enhanced performance of the coatings against corrosion. Corrosion behavior of the coatings is evaluated by potentiodynamic polarization and electrochemical impedance spectroscopy methods in 1 M HCl solution. The polarization study confirms that coatings developed using triple square pulses are more corrosion resistant than those deposited by dual square pulses. The improved corrosion behavior of layered coatings is due to the changed intrinsic electric properties evidenced by the electrochemical impedance spectroscopy. Under optimal conditions, the coatings developed using dual and triple square current pulse have been found to be by about 23 and 57 times, respectively, more corrosion resistant than the monolithic alloys. Surface morphology and layered coatings have been examined by scanning electron microscopy. Saturation of corrosion resistance at a high degree of layering was found, which is attributed to a shorter relaxation time for redistribution of metal ions during plating. © 2013 Allerton Press, Inc.