Aromaticity of five- and six-membered heterocycles present in crude oils – An electronic description for hydrotreatment process
[Display omitted] ► DFT study of five- and six-membered compounds present in hydrotreatment process was performed. ► Proton affinities of aromatic compounds were calculated. ► Geometrical modifications were observed for five-membered heterocyclic compounds. ► Hückel’s rule was satisfied in pyridine...
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Veröffentlicht in: | Fuel (Guildford) 2012-10, Vol.100, p.177-185 |
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Format: | Artikel |
Sprache: | eng |
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► DFT study of five- and six-membered compounds present in hydrotreatment process was performed. ► Proton affinities of aromatic compounds were calculated. ► Geometrical modifications were observed for five-membered heterocyclic compounds. ► Hückel’s rule was satisfied in pyridine protonated compounds, not for five-membered ones. ► Aromatic stabilization energy explains the refractory character and catalyst poisoning by pyridine derivatives.
The present work is focused on attempt to understand the importance of aromaticity in the elimination of N, O and S atoms from five-membered heterocycles and catalyst poisoning by basic nitrogen six-membered heterocyclic compounds in the hydrotreatment (HDT) process. Pyrrole, furan, thiophene and pyridine, and their fused benzene ring derivatives have been studied by means of density functional theory (DFT). Proton affinities (PAs) were calculated for all these compounds, geometrical modifications were observed during protonation. Five-membered aromatic compounds break planarity due to proton interaction of the heteroatom, while pyridine-type compounds do not. Aromatic stabilization energy (ASE) was calculated by homodesmotic chemical reactions for all heterocyclic compounds. The energetic trends for protonated and unprotonated compounds confirm the less reactivity of dibenzo-compounds in the HDT process and catalyst’s poisoning by pyridine derivatives present in crude oils. |
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ISSN: | 0016-2361 1873-7153 |
DOI: | 10.1016/j.fuel.2012.05.011 |