Hydrodesulfurization of dibenzothiophene and its hydrogenated intermediates over sulfided Mo/γ-Al2O3

Two intermediates of dibenzothiophene (DBT)—tetrahydro-DBT (THDBT) and hexahydro-DBT (HHDBT)—were synthesized, and their hydrodesulfurization (HDS) mechanism was investigated over Mo/γ-Al2O3 at 300–340 °C and 5 MPa in the absence and presence of H2S and 2-methylpiperidine. The rate constants of all steps in the kinetic network of the HDS of DBT were measured. THDBT underwent desulfurization by hydrogenolysis to 1-phenylcyclohexene, followed by hydrogenation to phenylcyclohexane. The desulfurization of HHDBT occurred by hydrogenolysis of the aryl Csingle bondS bond and then cleavage of the cycloalkyl Csingle bondS bond of the resulting thiol by elimination to 1-phenylcyclohexene and by hydrogenolysis to phenylcyclohexane. H2S strongly inhibited the desulfurization of all three molecules but did not inhibit (de)hydrogenation. 2-Methylpiperidine also had a strong inhibitory effect, especially on (de)hydrogenation and, to a lesser extent, on desulfurization. The order of the inhibition of DBT, THDBT, and HHDBT was explained by the adsorption constants of these three molecules.