Faculty Publications
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Item Soot Oxidation Activity of Redox and Non-Redox Metal Oxides Synthesised by EDTA–Citrate Method(Springer New York LLC barbara.b.bertram@gsk.com, 2017) Anjana, A.P.; Prasad Dasari, H.P.; Lee, J.-H.; Harshini, H.; Babu, G.U.B.Abstract: In the present study, redox (CeO2, SnO2, Pr6O11 and Mn3O4) and non-redox (Gd2O3, La2O3 ZrO2 and HfO2) metal oxides were successfully synthesised using the EDTA–citrate complexing method and tested for soot oxidation activity. The characterization of the metal oxides is carried out using FTIR, XRD, BET surface area, pore volume analyser, SEM and TEM. The redox nature and metal–oxygen bond information of the metal oxides are obtained from XPS analysis. In redox metal oxides, three critical parameters [lattice oxygen binding energy, reduction temperature and ?r (ionic size difference of the corresponding metal oxide oxidation states)] govern the soot oxidation activity. Among the redox metal oxide samples, Mn3O4 and Pr6O11 samples showed lower binding energy for oxygen (O?—529.4, 528.9 eV respectively), lower reduction temperature (T?—317 and 512 °C respectively) and have smaller ?r value (9 pm and 17 pm respectively). Thus, displayed a better soot oxidation activity (T50 = 484 and 482 °C respectively) than compared to other redox metal oxides. Among the non-redox metal oxides, HfO2 sample displayed higher BET surface area (21.06 m2/g), lattice strain (0.0157), smaller ionic radius (58.2 pm) and higher relative surface oxygen ratio (58%) and thus resulted in a significantly better soot oxidation activity (T50 = 483 °C) than compared to other non-redox metal oxides. Graphical Abstract: [Figure not available: see fulltext.]. © 2017, Springer Science+Business Media, LLC.Item Praseodymium doped ceria as electrolyte material for IT-SOFC applications(Elsevier Ltd, 2018) Shajahan, I.; Ahn, J.; Nair, P.; Medisetti, S.; Patil, S.; Niveditha, V.; Uday Bhaskar Babu, G.; Prasad Dasari, H.P.; Lee, J.-H.Praseodymium-doped ceria (PDC, Ce0.9Pr0.1O2) electrolyte material for intermediate temperature solid oxide fuel cells (IT-SOFCs) has been successfully synthesised by EDTA-citrate method. From X-Ray diffraction (XRD), fluorite structure along with a crystallite size of 5.4 nm is obtained for PDC nanopowder calcined at 350 °C/24 h. Raman spectroscopy confirmed the structure, presence of oxygen vacancies with the manifestation of the main peak at 457 cm?1 and with a secondary peak at 550 cm?1. From Transmission Electron Microscopy (TEM) analysis, the average particle size is around 7–10 nm and selected area electron diffraction (SAED) patterns further confirmed the fluorite structure of PDC nanopowder. The PDC nanopowder displayed a BET surface area of 65 m2/g with a primary particle size of ?13 nm (calculated from BET surface area). Dilatometer studies revealed a multi-step shrinkage behaviour with the multiple peaks at 522, 1171 and 1461 °C which may be originated due to the presence of multiple size hard agglomerates. The PDC electrolyte pellet sintered at 1500 °C displayed an ionic conductivity of 1.213E-03 S cm?1 along with an activation energy of 1.28eV. Instead of a single fluorite structure, XRD of sintered PDC pellet showed multiple structures (Fluorite structure (CeO2) and cubic structure (PrO2). © 2018 Elsevier B.V.Item Photocatalytic degradation of ciprofloxacin & norfloxacin and disinfection studies under solar light using boron & cerium doped TiO2 catalysts synthesized by green EDTA-citrate method(Elsevier B.V., 2021) Manjunatha, M.; Chandewar, P.R.; Mahalingam, H.The presence of antibiotic residues in water bodies is an emerging global concern due to its potential development of antimicrobial resistance. Hence, it is essential to develop photocatalysts that not only degrade the antibiotics but can also simultaneously disinfect. Four different boron and cerium doped TiO2 photocatalysts, synthesized by the EDTA-citrate method, are studied for the degradation of two common fluoroquinolone-based antibiotics: ciprofloxacin (CIP) and norfloxacin (NOR) under sunlight. The catalysts are characterized by SEM, TEM, Raman spectroscopy, XPS, DRS, BET surface area and particle size analyzer. At optimized conditions, the synthesized catalysts showed 90–93% degradation for both CIP and NOR. The effects of catalyst loading and initial concentration are studied, and the reaction is found to be pseudo-first-order. The degradation is analyzed by COD reduction and LC–MS, and the by-products of degradation determined. The recycle studies showed that the catalysts are stable up to three consecutive runs. The scavenging experiments indicated e? and OH? as the dominant species responsible for the photocatalytic activity. The disinfection studies using these catalysts under solar light gave 95–99.99% efficiency for E.coli confirming that they are very efficient and can be further exploited for large scale treatment. © 2020 Elsevier B.V.Item Study of CO oxidation activity of NiO-PDC and NiO-YSZ catalysts coated on alumina wash-coated honeycomb cordierite monolith(Springer Science and Business Media Deutschland GmbH, 2025) Wagay, A.A.; Shourya, A.; Patil, S.S.; Shirasangi, R.; Prasad Dasari, H.P.In this study, the EDTA-Citrate method was employed to synthesize NiO-PDC (NPC) and NiO-YSZ (NYZ) powder catalysts in nanostructured form. Subsequently, the catalysts were slurry dip-coated onto monolith cordierite substrates with alumina, using a one-step coating approach, and their CO oxidation activity was tested. The coating was achieved by first mixing the catalyst with the alumina suspension to prepare a homogeneous slurry, which was then used for dip coating onto the monolith. The adherence test was performed on the coated monolith to evaluate the mechanical stability of the catalyst-alumina composite layer. The coating was visually confirmed through optical imaging. The remaining powders (after coating) were then subjected to BET surface area, XRD, Raman spectroscopy, H2 TPR and O2 TPD analysis for characterization. Raman spectra showed that NPC exhibited higher oxygen vacancies than NYZ. H2 TPR and O2 TPD provided better evidence of the reduction potential and O2 desorption of NPC respectively. NPC/cord demonstrated the highest catalytic activity (T50 = 165 °C) compared to NYZ/cord (T50 = 215 °C) and bare cordierite (T50 = 777 °C), which is attributed to its better redox properties and higher oxygen vacancies. The effect of flow rate and heating rate on CO oxidation was studied on NPC/cord and NYZ/cord. The long-term stability of the NPC/cord and NYZ/cord were tested through 5-h and 50-h isothermal studies. © The Author(s) under exclusive licence to Associação Brasileira de Engenharia Química 2025.