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Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.

The application of highly active nano catalysts in advanced oxidation processes (AOPs) improves the production of non-selective hydroxyl radicals and co-oxidants for complete remediation of polluted water. This study focused on the synthesis and characterisation of a highly active visible light C–N-co-doped TiO2 nano catalyst that we prepared via the sol-gel method and pyrolysed at 350 °C for 105 min in an inert atmosphere to prevent combustion of carbon moieties. Then we prolonged the pyrolysis holding time to 120 and 135 min and studied the effect of these changes on the crystal structure, particle size and morphology, electronic properties and photocatalytic performance. The physico-chemical characterisation proved that alteration of pyrolysis holding time allows control of the amount of carbon in the TiO2 catalyst causing variations in the band gap, particle size and morphology and induced changes in electronic properties. The C–N–TiO2 nano composites were active under both visible and UV light. Their improved activity was ascribed to a low electron–hole pair recombination rate that enhanced the generation of OH· and related oxidants for total deactivation of O.II dye. This study shows that subtle differences in catalyst preparation conditions affect its physico-chemical properties and catalytic efficiency under solar and UV light.