Faculty Publications
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Item Effect of fuel and solvent on soot oxidation activity of ceria nanoparticles synthesized by solution combustion method(KeAi Communications Co., 2019) Patil, S.S.; Prasad Dasari, H.P.Effect of fuel (glycine and urea) and solvent (water, acetone and ethanol) on the soot oxidation activity of ceria nanoparticles synthesized by solution combustion method is carried out in the present study. X-ray diffraction (XRD) patterns displayed a fluorite structure and the Tauc's plot obtained from UV-Diffusive Reflectance spectroscopy (UV-DRS) showed that the band gap value was around 2.9–3.1 eV for the synthesized ceria nanoparticles irrespective of the fuel and solvent used. Ceria nanoparticles synthesized using glycine and acetone resulted in lower crystallite size, higher facet ratios ([1 0 0]/[1 1 1] and [1 1 0]/[1 1 1]) and higher lattice strain than compared to other solvents and fuels and thus resulted in better soot oxidation activity (T50 = 416 °C). The present synthesis method has played a significant role in improving the reactive facet ratios, providing lower crystallite size and high lattice strain. © 2019Item Effect of morphology and oxidation state of nickel on diesel soot oxidation activity(Elsevier Ltd, 2022) Vijay, M.P.A.; Patil, S.S.; Madhura, D.R.; Anjana, A.P.; Gouramma, P.; Prasad Dasari, H.P.; Arya, S.B.; Harshini, H.NiO sample is synthesized using the EDTA citrate complex method and calcined at 600 °C/5 h. Ni sample was acquired by reducing NiO to Ni at 600 °C in 4% H2/N2 atmosphere. Its physicochemical properties were obtained by XRD and Raman spectroscopy analysis, where it confirmed the complete reduction of NiO to Ni. SEM and TEM micrographs revealed a drastic particle growth for the Ni, indicating NiO sintering during the reduction process and a considerable surface morphology change. Ozawa and KAS methods were used to calculate the mean activation energy (Ea) value. NiO displayed lower Ea than Ni. Hence, NiO showed better catalytic activity than Ni. © 2022Item A Negative Effect of Niobium-Doped Ceria on Soot Oxidation Activity‡(John Wiley and Sons Inc, 2022) Patil, S.S.; Naik, S.; Ramesh, M.D.; Harshini, H.; Prasad Dasari, H.P.Niobium-doped ceria catalysts were synthesized to study soot oxidation activity. X-Ray diffraction (XRD) and Raman analysis of the samples revealed the presence of a fluorite structure of CeO2 for all the doped samples. The T50 temperature of the pure CeO2 sample was more significant than that of bare soot. The high catalytic activity of the CeO2 catalyst can be attributed to the low crystallite size, high facet ratio, and the large Brunauer-Emmett-Teller (BET) surface area as compared to Nb-doped samples. The activation energy calculated by both Ozawa and KAS methods were found to be low for CeO2 when compared to Nb-doped samples. CeO2 resulted in better soot oxidation activity with low activation energy. © 2022 Wiley-VCH GmbHItem An investigation on copper-loaded ceria-praseodymium catalysts for soot oxidation activity and its kinetics(Springer Science and Business Media Deutschland GmbH, 2024) Patil, S.S.; Prasad Dasari, H.P.The Cu-loaded Ce-Pr catalyst series was successfully developed to study their performance on soot oxidation activity and its kinetic behavior. The doped samples showed a similar trend for cubic fluorite structure except for CuO, which possessed a monoclinic structure from the XRD analysis. Facet ratios [{100}/{111} and {110}/{111}] for the reactive planes were calculated from XRD spectra; the ratio was high for the 5 Cu-CP catalysts. The oxygen vacancy peaks were noticed from Raman spectra for the doped samples. 5 Cu-CP displayed the better catalytic activity of T50 = 402 °C, which may be attributed to high reactive planes and better reducibility. The addition of Cu showed a slight enhancement in catalytic activity compared to CP and pure Ce. The kinetic triplets were evaluated: the activation energy (Ea), pre-exponential factor (A), and the reaction model. Pure Ce displayed the lowest Ea and A values, whereas pure Cu showed high Ea and A values by all the methods. Graphical abstract: (Figure presented.) © The Author(s) under exclusive licence to Associação Brasileira de Engenharia Química 2023.Item Ceria-Terbium-based electrospun nanofiber catalysts for soot oxidation activity and its kinetics(Taiwan Institute of Chemical Engineers, 2024) Patil, S.S.; Kumar, R.; Prasad Dasari, H.P.Background: Ceria-based materials have an excellent potential to be catalysts for catalytic three-way converters in the automobile industry. Developing Ceria-based nanofiber catalysts can be a significant approach for further exploring the application of these materials in automobile industries. Methods: In this study, Ag, Cu, or Co doped Ceria–Terbium nanofibers were synthesized using the electrospinning technique. The obtained nanofiber catalysts were characterized using FE-SEM, XRD, FT-Raman Spectroscopy, and BET-BJH analysis and tested for soot oxidation activity and its kinetics. Significant findings: FE-SEM examination reveals that the obtained nanofibers have a diameter ranging from around 100 to 600 nm. CeTbCo nanofibers exhibited a reduced particle size and enhanced pore formation. The XRD investigation revealed that all the nanofibers displayed a face-centered fluorite structure of CeO2. In Raman spectroscopy analysis, CeTbCo nanofibes showed the emergence of a secondary Co3O4 phase. The CeTbCo nanofiber catalyst showed better SBET (specific surface area) (66 m2/g) and average pore size (12.08 nm) and total pore volume (0.223 cc/g)), better soot oxidation activity (T50 = 347 ℃) than other nanofiber catalysts. The CeTbCo nanofiber catalyst exhibited an activation energy of 132 kJ mol−1 and a pre-exponential factor (ln (A)) of 25.63 min−1. © 2024 Taiwan Institute of Chemical EngineersItem Soot oxidation activity and kinetics of Ce0.9M0.1O2-δ (M = Cs, Mg, Ca) catalysts: Impact of Cs doping in ceria and impact of nanorods on catalytic activity(Institution of Chemical Engineers, 2024) Nayak, A.S.; Patil, S.S.; Prasad Dasari, H.P.; Telaginatot, D.; Rynjah, M.; Cheruku, S.Solution combustion method is used to synthesize Ce0.9M0.1O2-δ (M = Cs, Mg, Ca) catalysts and calcined at 600 °C/5 h. XRD and Raman Spectroscopy Analyses the chemical structure, the phases observed, and the oxygen defects in the synthesized catalysts. A cubic fluorite structure of CeO2 has been noticed for all the catalysts from XRD and Raman Spectroscopy analyses. FE-SEM micrographs are used to analyze the morphology of the Ce0.9M0.1O2-δ (M = Cs, Mg, Ca) catalysts. Ce0.9Cs0.1O2-δ catalyst shows the presence of nanorods (diameter: 63 nm), which are not seen in the other catalysts. The redox and surface properties of the synthesized catalysts are tested by H2-Temperature Programmed Reduction (H2-TPR) and O2-Temperature Programmed Desorption (O2-TPD), respectively. The Ce0.9Cs0.1O2-δ catalyst shows the greatest degree of reducibility from TPR studies and for the Ce0.9Cs0.1O2-δ catalyst, the oxygen species evolved from the O2-TPD studies are also the highest. Thermogravimetric Analysis (TGA) has been used to carry the soot oxidation activity of the developed catalysts. Soot oxidation kinetic studies have been conducted at different heating rates (5, 10, and 15 °C/min) for the catalysts. The kinetic triplets for the developed catalysts have been obtained, and rate plots ([Formula presented] vs. temperature) and Arrhenius plots (ln(k) vs. [Formula presented]) have been developed for the catalysts. From the soot oxidation and kinetic studies for the developed catalysts, Ce0.9Cs0.1O2-δ shows better soot oxidation activity (T50 = 372 °C) than the other two catalysts, while Ce0.9Mg0.1O2-δ (T50 = 556 °C) shows the lowest soot oxidation activity. All the catalysts follow a non-integral exponential model for soot oxidation, and the Ce0.9Cs0.1O2-δ catalyst has the lowest activation energy. © 2024 Institution of Chemical EngineersItem Soot Oxidation Kinetics on Nickel Oxide: Effects of Various Synthesis Techniques(Pleiades Publishing, 2024) Patil, S.S.; Prasad Dasari, H.P.; Gouramma, P.; Harshini, H.Abstract: Nickel oxide (NiO) nanoparticles were synthesized using four different methods: microwave co-precipitation (MCP), solution combustion synthesis (SCS), direct nitrate calcination (DNC), and the sol-gel process (SGP), incorporating organic additives such as glucose and fructose. X-ray diffraction and Raman spectroscopy analyses revealed that the NiO nanoparticles formed a face-centered cubic phase characterized by Ni–O bond stretching. The SCS method produced NiO nanoparticles with higher lattice strain, smaller crystallite size, and an increased facet ratio ({110}) compared to the other methods. Transmission electron microscopy indicated that the order of nano-agglomeration size for the NiO nanoparticles was DNC > MCP > SGP > SCS. The NiO nanoparticles synthesized via SCS, SGP and MCP exhibited irregular hexagonal shapes. Among the synthesized nanoparticles, those produced by the SCS method demonstrated the highest catalytic activity (T50 = 478°C), followed by DNC (T50 = 492°C), MCP (T50 = 495°C), and SGP (T50 = 538°C). A kinetic study was conducted to evaluate key parameters, including activation energy, preexponential factor, and reaction model. The experimental curves of soot conversion were compared with theoretical curves derived from the evaluated kinetic parameters. The NiO nanoparticles synthesized via SCS exhibited the highest kinetic activity with the enhanced reaction rate at lower temperatures. © Pleiades Publishing, Ltd. 2024.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.Item Diesel soot oxidation over Mn–Pr–Ce oxide catalysts: structural changes and the impact of Mn doping(Royal Society of Chemistry, 2025) Patil, S.S.; Prasad Dasari, H.P.; Shirasangi, R.; Harshini, H.The soot oxidation activity of manganese-doped ceria-praseodymium catalysts, synthesized via solution combustion synthesis, was evaluated. The analyses performed with XRD and Raman spectroscopy indicated that the Mn-doped CP catalysts displayed the typical fluorite structure of CeO2. The addition of Mn to CP led to a reduction in crystallite size from 14 nm to below 10 nm. The F2g Raman active mode of fluorite-structured Ce and the oxygen vacancies resulting from the addition of Mn and Pr (bands B 560 cm–1 to 580 cm–1) were consistently observed across all Mn-doped CP catalysts. 15 and 20 Mn-CP exhibited an additional secondary phase identified as Mn2O3. The analysis of BET surface area and BJH pore size revealed that the Mn-doped CP catalysts exhibited both micro and mesoporous characteristics. The H2-TPR and O2-TPD profiles indicated enhanced reducibility resulting from the incorporation of Mn and Pr into CeO2-doped catalysts. The improved T50 (365 ± 1 1C) for the 5 Mn-CP catalytic system is primarily due to its increased specific surface area of 45 m2 g–1 and the presence of active surface adsorbed oxygen species identified in the XPS and O2-TPD studies. 5 Mn-CP exhibited the lowest activation energy value compared to all other Mn-doped catalysts. © 2025 The Author(s)