%0 Journal Article %T Catalytic Hydrogenation Reactions on Molybdenum Oxide %A H. Al-Kandari %A S. Al-Kandari %A A. M. Mohamed %A F. Al-Kharafi %A A. Katrib %J Modern Research in Catalysis %P 36-42 %@ 2168-4499 %D 2015 %I Scientific Research Publishing %R 10.4236/mrc.2015.41005 %X Partially reduced molybdenum trioxide deposited on titania under hydrogen at 673 K for 12 h ena- bled to convert several surface atomic layers to the catalytically active bifunctional (metal-acid) MoO2-x(OH)y/TiO2 (MoTi) structure. The formed metallic function is the result of ¦Ð bonding between adjacent Mo-Mo atoms placed along the C-axis of the rutile structure of MoO2. Delocalization of these ¦Ð electrons produces a wire like atomic metal. This resembles in a way, the small Pt particles deposited on a support. Moreover, dissociated hydrogen atoms are bonded to sample surface oxygen to produce Br&oslash;nsted acid Mo-OH function(s). These metal-acidic properties have been tested for several catalytic reactions requiring one or bothcatalytic functions. In this order, 2-propanol species could be considered as a model test of the acidic function via dehydration of the molecule to propene, while hydrogenation of the produced propene to propane is performed by the metallic function. Moreover, hydrogenation of 2-propanol to acetone, requires relatively strong metallic function. In this order, addition of small amount of alkali metal like rubidium will suppress the acidic function in MoO2-x(OH)y/TiO2 and enhance the metallic function strength. The performance of the metallic function alone in this case will be evaluated. Titanium dioxide is employed in this catalytic system as a support. It does not have any catalytic effect. Association of XPS-UPS, ISS sur-face techniques with catalytic performances of this catalytic MoTi system will be presented. %K MoO< %K sub> %K 2-x< %K /sub> %K (OH)< %K sub> %K y< %K /sub> %K Catalyst %K XPS %K Acid-Metal Functions %K Hydrogenation %K 2-Propanol %U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=53050