Elucidation of promotion effect of nickel on Mo/Al 2O 3 and Co-Mo/Al 2O 3 catalysts in hydrodesulfurization using a [formula omitted] radioisotope tracer method

Abstract

Hydrodesulfurization (HDS) reactions of radioactive 35 S -labeled dibenzothiophene (DBT) were carried out over a series of Ni-promoted Mo/Al 2O 3 and Co-Mo/Al 2O 3 catalysts at temperatures between 220 and 280 °C and under 5.00 MPa pressure. HDS and hydrogenation (HYD) activity of Mo/Al 2O 3 catalyst were remarkably enhanced with the addition of nickel, the maximum promotional effect of Ni occurred with a Ni/Mo ratio of ca. 0.5. The amount of labile sulfur ( S 0) and the release rate constant of [ 35 S ]H 2S ( k RE) increased significantly with the addition of nickel, indicating that nickel makes the sulfur on the catalysts more mobile. The promoting effect of nickel on the activity of Mo/Al 2O 3 catalyst was attributed to the formation of more active sites. Further, the HDS activity of Co-Mo/Al 2O 3 catalyst was also enhanced with the addition of nickel; its maximum promotional effect occurred with a Ni/Mo ratio of ca. 0.2 for Ni-Co-Mo catalysts. Ni-promoted Co-Mo/Al 2O 3 catalysts with lower Ni/Mo ratio had greater S 0 and k RE values than Co-Mo/Al 2O 3 catalyst and resulted in higher HDS activity. This indicates that more active sites were formed with adding Ni to Co-Mo/Al 2O 3 catalyst, although their numbers were limited. On the other hand, the promoting effect of nickel to Mo/Al 2O 3 almost disappeared with adding cobalt into Ni-Mo/Al 2O 3 catalysts, suggesting that cobalt hindered the formation of more active Ni-Mo-S phase or covered the phase.