Abstract:
Catalytic reduction of NO with CO at a lower temperature is an extremely challenging task, thus requiring conceivable surfaces to overcome such issues. Ru-substituted CeO sub(2) catalysts prepared via the solution combustion method were employed in CO oxidation and NO-CO conversion studies. The characterization for material formation and surface structure was carried out through XRD, SEM, TEM, and BET surface area. The catalytic study revealed the promising behavior of 5 percent Ru in CeO sub(2) for the 100 percent conversion of NO-CO at 150 degrees C, proving it to be an excellent exhaust material. These observed results are also supported by temperature-programmed studies, i.e. TPD of NO and CO in addition to NH sub(3)-TPD and H sub(2)-TPR for their convincible surface interaction that is inclined toward a significant change in the conversion path. Additionally, the proposed mechanism, based on the experimental evidence, sheds light on the NO-CO redox reaction, directing the reaction pathway toward the Langmuir-Hinshelwood and Mars-Van Krevelen-type route. Moreover, the exceptional performance can be attributed to the strategic incorporation of Ru in CeO sub(2), where the strong interaction of Ru-Ce is able to gain a high synergy for NO and CO conversion.
