This work presents the adsorption process of nitrogen compounds, namely quinoline (Q), pyridine (Pyr), and indole (In), from liquid fuels such as gasoline and diesel containing dibenzothiophene (DBT) as sulfur-containing molecules. These compounds were adsorbed on mesoporous materials, namely SBA-15 and SBA-16, in calcined form in batch mode using dodecane as a solvent represent to a diesel mixture. The main conclusion of this research is that SBA-15 showed a higher nitrogen adsorption capacity than SBA-16 for all molecules containing nitrogen and sulfur. A comparative study of nitrogen and sulfur adsorption confirms that selective removal of nitrogen compounds from fuels using SBA-15 was better than that of sulfur compounds. Moreover, an increase in the adsorption of Q was found with SBA-15 material compared to SBA-16. To explain this behavior, the solids were characterized using X-ray diffraction (XRD), nitrogen physisorption, and High-Resolution Transmission Electron Microscopy (HRTEM). A pseudo-second-order kinetic model, rather than a first-order one, fitted the nitrogen adsorption data best. Moreover, the Langmuir model was suitable for describing the adsorption of nitrogen compounds from simulated diesel fuel, instead of the Freundlich model, which means that nitrogen compounds are adsorbed in a monolayer.
Reactions involved in photocatalytic hydrogen production through water splitting combined with a hole scavenger involve several stages that make kinetic analysis quite complicated. In the present work, a kinetic model for the photocatalytic production of hydrogen has been developed based on competitive adsorption, considering the photocatalytic decomposition of an organic molecule coupled to hydrolysis through photocatalytic water splitting. Parameter estimation is performed by using the Levenberg‐Marquardt method. Model validation results give an estimation of the strength of adsorption of acetol and the acetaldehyde.
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