HDS of benzothiophene and dihydrobenzothiophene over sulfided Mo/γ-Al2O3

The hydrodesulfurization (HDS) of benzothiophene (BT) and dihydrobenzothiophene (DHBT) was studied over a sulfided Mo/γ-Al2O3 catalyst at 5 MPa and 280 and 300 °C. In the absence of H2S, benzothiophene reacted by hydrogenation to dihydrobenzothiophene and by hydrogenolysis to ethylbenzene (EB), and dihydrobenzothiophene reacted by hydrogenolysis to ethylbenzene. H2S inhibited both hydrogenation and hydrogenolysis, but the latter much more strongly. The reverse inhibition was observed for 2-methylpiperidine (MPi). In the presence of H2S and/or 2-methylpiperidine, dihydrobenzothiophene reacted to ethylbenzene as well as by total hydrogenation to octahydrobenzothiophene, and on to ethylcyclohexenes and ethylcyclohexane. Dihydrobenzothiophene did not react back to benzothiophene at and below 300 °C, while the equivalent tetrahydrodibenzothiophene reacted fast to an equilibrium with tetrahydrodibenzothiophene, due to stabilization of the vinylic bond by the alkyl groups. The observed products and kinetic results were explained by a model in which the CS bonds were mainly broken by hydrogenolysis.

Graphical abstractThe hydrodesulfurization of benzothiophene and dihydrobenzothiophene was studied over a sulfided Mo/γ-Al2O3 catalyst at 5 MPa and 280 and 300 °C. Bnzothiophene reacted by hydrogenation to dihydrobenzothiophene and by hydrogenolysis to ethylbenzene, and dihydrobenzothiophene reacted by hydrogenolysis to ethylbenzene. H2S inhibited both hydrogenation and hydrogenolysis, but the latter much more strongly. The reverse inhibition was observed for 2-methylpiperidine.Figure optionsDownload full-size imageDownload as PowerPoint slide