Faculty Publications
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Item Ceria-based electrospun nanofibers and their widespread applications: A review(Academic Press, 2025) Prasad Dasari, H.P.; Patil, S.S.; Kamath, R.S.; Kisiela-Czajka, A.M.Electrospinning is a highly efficient technique for producing nanofibers, and it is noted for its cost-effectiveness, versatility, and user-friendly nature. The article evaluates the production of Ceria-based nanofibers primarily utilizing electrospinning technology and electrospinning parameters and explores their various potential applications. Ceria infused with lanthanoids and transition metals demonstrates significant potential as catalysts, optical sensors, and supercapacitors in various energy-related industrial applications. Their role as catalysts in water-gas and reverse water-gas shift reactions greatly enhances the water-splitting reaction in the Deacon process. Composite ceria nanofibers for wound therapy were developed by integrating polyurethane, cellulose acetate, and zein for biological applications. Soot-induced blockages in automobile filters pose challenges for the regeneration process of diesel particle filters, and the effectiveness of ceria-based nanofibers in soot and CO oxidation has been explored. Ce-based nanofibers produced via the electrospinning technique, with different operating parameters, exhibit notable variations in their morphology. Research indicates that, compared to traditional ceria, Ce-based nanofibers demonstrate greater surface area and porosity, a higher density of oxygen vacancies, and improved oxygen transfer efficiency, all essential for numerous redox and catalytic processes. The nanofibrous structure enhances electrical conductivity by expanding the surface area accessible for interaction with active components. The nanofibrous composite structure exhibits enhanced thermal and mechanical durability, making it appealing for numerous applications. © 2025 Elsevier LtdItem Methanol selective oxidation to formaldehyde over a modified Fe-Mo catalyst with two different stoichiometric (Mo/Fe atomic ratio = 1.5 and 3.0) was studied experimentally in a fixed bed reactor over a wide range of reaction conditions. The physicochemical characterization of the prepared catalysts provides evidence that Fe2(MoO4)3 is in fact the active phase of the catalyst. The experimental results of conversion of methanol and selectivity towards formaldehyde for various residence times were studied. The results showed that as the residence time increases the yield of formaldehyde decreases. Selectivity of formaldehyde decreases with increase in residence time. This result is attributable to subsequent oxidation of formaldehyde to carbon monoxide due to longer residence time.(Selective oxidation of methanol to formaldehyde using modified iron-molybdate catalysts) Kim, T.-H.; Badekai Ramachandra, B.; Choi, J.-S.; Saidutta, M.B.; Choo, K.-Y.; Song, S.-D.; Rhee, Y.-W.2004Item The direct conversion of benzene to phenol by hydroxylation with hydrogen peroxide was carried out over catalyst containing various transition metals impregnated on activated carbon. Iron and vanadium impregnated catalysts gave better yields of phenol compared to copper impregnated catalysts. The activity of transition metals supported on activated carbon catalyst in the production of phenol was V > Fe > Cu. In addition to the role of transition metals in catalyzing the hydroxylation reaction, the hydrophobic nature of the activated carbon surface and also the surface acidity and basicity seems to have enhanced the performance of these catalysts. © 2005 Springer Science + Business Media, Inc.(Transition metals supported on activated carbon as benzene hydroxylation catalysts) Choi, J.-S.; Kim, T.-H.; Choo, K.-Y.; Sung, J.-S.; Saidutta, M.B.; Song, S.-D.; Rhee, Y.-W.2005Item The direct conversion of benzene to phenol by hydroxylation with hydrogen peroxide was carried out over catalysts containing iron impregnated on activated carbon. Iron was impregnated on various surface modified activated carbons. The catalyst that was made by treating activated carbon with nitric acid, that was treated thermally in the presence of nitrogen at 600 °C and impregnated with 5 wt.% iron, gave a phenol yield of 20%. It was found that the synergistic interactions of surface groups and the impregnated iron have enhanced the performance of these catalysts. © 2005 Elsevier B.V. All rights reserved.(Direct synthesis of phenol from benzene on iron-impregnated activated carbon catalysts) Choi, J.-S.; Kim, T.-H.; Choo, K.-Y.; Sung, J.-S.; Saidutta, M.B.; Ryu, S.-O.; Song, S.-D.; Badekai Ramachandra, B.; Rhee, Y.-W.2005Item Molybdenum based mixed oxide containing Mo0.65V 0.25W0.10 was investigated for the partial oxidation of methanol. The structural property and catalytic activity of the mixed oxide catalyst was studied by surface area (BET), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infra-red spectroscopy (FTIR) and X-ray diffraction (XRD). The thermal activation of the catalyst resulted increase in the conversion of methanol and the selectivity to formaldehyde. The thermal activation of the MoVW mixed oxide in nitrogen atmospheres induces partial crystallization of a Mo5O14-type oxide at 813 K. The SEM images of the thermally activated catalyst show needle like particles. These particles were agglomerates of platelet-like crystallites of a few hundreds of nanometers in size. SEM and EDX techniques show that the mixed oxide is characterized by an inhomogeneous elemental distribution on the length scale of a few microns. XRD of the thermally activated catalyst showed a nanocrystalline material identified as a mixture of Mo5O 14, MoO3 and MoO2-type MoVW oxides. The catalytic activity of the MoVW mixed oxide show a good conversion of methanol and selectivity to formaldehyde. © 2005 Springer Science+Business Media, Inc.(Partial oxidation of methanol to formaldehyde on molybdenum based mixed oxide catalyst) Badekai Ramachandra, B.; Choi, J.-S.; Choo, K.-Y.; Sung, J.-S.; Song, S.-D.; Kim, T.-H.2005Item Synthesis and characterization of nanocrystalline Mo-V-W-Fe-O mixed oxide catalyst and its performance in selective methanol oxidation(2007) Badekai Ramachandra, B.; Choi, J.-S.; Kim, T.-H.A mixed oxide catalyst containing Mo, V, W and Fe with the composition of 63, 23, 09 and 06 wt% respectively for the selective oxidation of the methanol to formaldehyde is in reported in this paper for the first time. The characterization of the catalyst was done using BET surface analysis, X-ray diffraction (XRD), Infrared spectroscopy (FTIR), Scanning electron microscopy (SEM) and Energy dispersive X-ray (EDX). The mixed oxide after calcination at 673 K in N2 which was subjected for the thermal activation in N 2flow at 813 K was used for the methanol selective oxidation. The thermal treatment shows enhanced catalytic performance. Thermal activation of the nanocrystalline Mo0.63V23W0.09Fe 0.06O x precursor oxide in nitrogen atmospheres induces partial crystallization of a Mo5O14-type oxide only in a narrow temperature range up to 813 K. XRD showed that the thermally activated mixed oxide consists of a mixture of a majority of crystalline Mo 5O14-type oxide and of small amounts of crystalline MoO3-type and MoO2-type oxides. The structural analysis suggests that the improvement of the catalytic performance of the MoVWFe oxide catalyst in the selective oxidation of methanol is related to the formation of the catalytic active site such as Mo5O14-type mixed oxide. © 2007 Springer Science+Business Media, LLC.Item Analytical properties of p-[N,N-bis(2-chloroethyl)amino]benzaldehyde thiosemicarbazone: Spectrophotometric determination of palladium(II) in alloys, catalysts, and complexes(2011) Karthikeyan, J.; Parameshwara, P.; Nityananda Shetty, A.N.p-[N,N-bis(2-chloroethyl)amino]benzaldehyde thiosemicarbazone (CEABT) is proposed as a new, sensitive, and selective analytical reagent for the spectrophotometric determination of palladium(II). The reagent reacts with palladium(II) in the pH range 1-2 to form a yellow-colored complex. Beer's law is obeyed in the concentration range up to 2.64 ?g cm-3. The optimum concentration range for minimum photometric error as determined by Ringbom's plot method is 0.48-2.40 ?g cm-3. The yellowish Pd(II)-reagent complex shows a maximum absorbance at 395 nm, with molar absorptivity of 4.05 × 104 dm3 mol-1 cm-1 and Sandell's sensitivity of the complex from Beer's data, for D= 0.001, is 0.0026 ?g cm-2. The composition of the Pd(II)-CEABT reagent complex is found to be 1:2 (M-L). The interference of various cations and anions in the method were studied. The proposed method was successfully used for the determination of Pd(II) in alloys, catalysts, complexes, water samples, and synthetic alloy mixtures with a fair degree of accuracy. © 2010 Springer Science+Business Media B.V.Item Kinetics of esterification of acetic acid with methanol in the presence of ion exchange resin catalysts(2011) JagadeeshBabu, P.E.; Sandesh, K.; Saidutta, M.B.Esterification kinetics of acetic acid with methanol was studied with solid acid catalyst in an isothermal batch reactor at 333-353 K. Different types of ion exchange catalyst (Indion 130, Indion 190, and Amberlyst 15 wet) were used for the esterification of acetic acid. It was found that Indion 130 was an effective catalyst for acetic acid esterification. The effects of stirrer speed, reaction temperature, initial reactant concentration, and catalyst loading on reaction rate were investigated and optimized. Temperature dependence of the reaction rates and activation energies was determined by an Arrhenius plot. A complete kinetic equation for describing the reaction catalyzed by Indion 130 was developed. This equation can be used in the simulation and design of the catalytic distillation column for the synthesis of methyl acetate. © 2011 American Chemical Society.Item Degradation of paracetamol in aqueous solution by Fenton Oxidation and photo-Fenton Oxidation processes using iron from Laterite soil as catalyst(2011) Manu, B.; MahamoodFor the treatment of paracetamol in water, the photo-Fenton Oxidation process and Classic Fenton oxidation process have been demonstrated and found effective. An iron catalyst extracted from lateritic soil is used to exhibit the degradation and mineralization of paracetamol. Paracetamol reduction and chemical oxygen demand (COD) removal are measured as the objective functions to be maximized. The experimental conditions of the degradation of paracetamol are optimized by Fenton process. the optimum conditions observed for 10 mg/L initial paracetamol concentration are influent pH 3, initial H 2O 2 dosage 30 mg/L, [paracetamol]/[H 2O 2] ratio 1:3 (w/w) and [H 2O 2] / [Laterite iron] ratio 30:0.75 (w/w). At the optimum conditions, for 10 mg/L of initial paracetamol concentration, 76% paracetamol reduction and 69% COD removal by Fenton oxidation and 79% paracetamol reduction and 77% COD removal by UV-C Fenton process are observed in 120 minutes reaction time. At the above optimum conditions, HPLC analysis has demonstrated 100% removal of paracetamol for Fenton oxidation process in 240 minutes and for UV-C photo- Fenton process in 120 minutes. The methods are effective and they may be used in the paracetamol industry. © 2011 CAFET-INNOVA TECHNICAL SOCIETY.Item Condensation of malononitrile with salicylaldehydes and o-aminobenzaldehydes revisited: Solvent and catalyst free synthesis of 4H-chromenes and quinolines(Royal Society of Chemistry, 2012) Bhat, S.I.; Choudhury, A.R.; Trivedi, D.R.The reaction of malononitrile with salicylaldehyde under solvent and catalyst free conditions was re-investigated using mechanochemical mixing, thermal heating and a direct crystallization process. The resulting condensation product by all three types of molecular activation, was found to be (2-amino-3-cyano-4H-chromene-4-yl)malononitrile, which is not the previously reported benzofuran-2-carbonitrile. The structure of the resulting chromene derivative was confirmed by FT-IR, MS, 1H, 13C NMR and single crystal and powder X-ray diffraction. The reaction pathway under neat conditions (mechanochemical mixing) at ambient temperature was monitored by IR spectral measurements. The versatility of the current green protocol was examined through the reaction of eleven derivatives of o-hydroxybenzaldehyde with malononitrile to obtain 2-amino-3-cyano-4H-chromene derivatives. In addition, malononitrile was further reacted with o-aminobenzaldehydes under neat conditions to yield quinoline derivatives. © 2012 The Royal Society of Chemistry.