Title of article :
TiO2–SiO2 supported hydrotreating catalysts: physico-chemical characterization and activities Original Research Article
Author/Authors :
M.S. Rana، نويسنده , , S.K Maity، نويسنده , , J. Ancheyta، نويسنده , , G.Murali Dhar، نويسنده , , T.S.R. Prasada Rao، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Abstract :
Hydrotreating of model molecules over high specific surface area (SSA) Co(Ni)Mo/TiO2–SiO2 mixed oxide supported catalysts has been investigated in a micro-catalytic reactor at 400 °C and atmospheric pressure. Activity studies are carried out for thiophene hydrodesulfurization (HDS) and 1-cyclohexene hydrogenation (HYD). The effect of support composition, molybdenum content (2–14 wt.% Mo) and promoters contents (1–5 wt.% Co or Ni) is examined. Supported catalysts are characterized by BET specific surface area, X-ray diffraction (XRD), pore volume, zero point charge (ZPC) and low temperature oxygen chemisorptions (LTOC). Sulfided catalysts showed wide range of activity variation with support composition which relishes that molybdenum sulfided active phases strongly depend on the nature and composition of support. LTOC and catalytic activity results showed similar trend with the effect of molybdenum variation indicating that the number of anion vacancies varies with variation of MoS2 phases. The highest activities were observed at 8 wt.% Mo loading and after that activity decreases with decreasing the anionic vacancies. The characterization results of XRD, ZPC and LTOC are well agreed about the Mo monolayer formation. Incorporation of TiO2 with SiO2 alters the nature of weak interaction of active phases with SiO2 support, and overcome it through poor dispersion on the support surface. Therefore, TiO2 counterpart plays a role to provide high intrinsic activity and generate favorable morphology of MoS2 phases and metal support interaction.
Keywords :
XRD and O2 chemisorptions , CoMo , HDS , TiO2–SiO2 , HYD
Journal title :
Applied Catalysis A:General
Journal title :
Applied Catalysis A:General