Faculty Publications

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    Ceria-samarium binary metal oxides: A comparative approach towards structural properties and soot oxidation activity
    (Elsevier B.V., 2018) Anjana, A.P.; Geethu, J.; P, M.R.; Prasad Dasari, H.P.; Lee, J.-H.; Harshini, H.; Bhaskar Babu, G.U.
    Binary metal oxides of CeO2-Sm2O3 (CSx, x varies from 10 to 90 mol%) along with pure CeO2 and Sm2O3 were synthesised successfully by the EDTA-Citrate method. From XRD, Raman spectroscopy and UV–vis DRS results, the whole composition of metal oxides exist in three phases: (fluorite phase (F) (CS10-CS30), bi-phase (fluorite (F) + cubic (C)) (CS30-CS90) and cubic phase (C) (Sm2O3)). For CSx samples, the calculated band gap energy values obtained from the UV–vis DRS results were in between 3.0–5.1 eV and fluorite phase samples (CS10–CS30) displayed lower band gap energy values (3.04–3.07 eV) than compared to the samples in other phases. Similarly, from XPS analysis, fluorite phase samples (CS10–CS30) showed higher surface oxygen vacancy concentration than compared to samples in other phases. Catalytic activity for soot oxidation is carried out on CSx samples, and the T50 temperature is in between 480–540 °C. Fluorite phase samples (CS10 CS30) showed higher surface area, lower degree of agglomeration, lower band gap energy, higher oxygen vacancy concentration and better catalytic activity for soot oxidation. Among all the CSx samples, CS10 sample displayed highest surface area (38 m2/g), lowest degree of agglomeration (0.36), lowest band gap energy (3.04 eV), highest oxygen vacancy concentration (64%) and highest soot oxidation activity (T50 = 480 °C). The order of the soot oxidation activity of CSx samples followed the same trend of band gap energy values. © 2018 Elsevier B.V.
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    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.
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    Effect of ionic radius on soot oxidation activity for ceria-based binary metal oxides
    (John Wiley and Sons Ltd vgorayska@wiley.com Southern Gate Chichester, West Sussex PO19 8SQ, 2019) Anjana, A.P.; Prasad Dasari, H.P.; Harshini, H.; Babu, G.U.B.
    CeO2 (C) along with binary metal oxides of Ce0.9M0.1O2-? (M = Sn, Hf, Zr, Gd, Sm, and La; CT, CH, CZ CG, CS, and CL) are synthesized using the EDTA–citrate method. Samples having an ionic radius smaller (CT, CH, and CZ) and larger (CG, CS, and CL) than Ce4+ are classified separately, and their soot oxidation activity is analyzed. The incorporation of dopant is confirmed from lattice constant variation in X-ray diffraction result. The critical descriptors for the activity are dopant nature (ionic radius and oxidation-state), single-phase solid solution, lattice strain, reactive (200) and (220) planes, Raman intensity ration (Iov/IF2g), optical bandgap, reducibility ratio, and surface oxygen vacancy. Smaller ionic radius, isovalent dopants (CH and CZ) create a defect site by lowering the optical bandgap along with improved surface oxygen vacancy concentration and thus enhanced soot oxidation activity. Aliovalent dopant with larger ionic radius shows the involvement of lattice oxygen in oxidation reaction by charge compensation mechanism. CL showed the highest activity amongst larger ionic radius samples. © 2019 Curtin University and John Wiley & Sons, Ltd.
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    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.