H. Tanaka, M. Kuriyama, Y. Ishida, S.-I. Ito and K. Tomishige, “Preferential CO Oxidation in Hydrogen-rich Stream over Pt Catalysts Modified with Alkali Metals: Part II. Catalyst Characterization and Role of Alkali Metals,” Applied Catalysis A: Generl, Vol. 343, No. 1-2, 2008, pp. 125-133 doi:10.1016/j.apcata.2008.03.029

has been cited by the following article:

• TITLE: Removal of Carbon Monoxide from Hydrogen-rich Fuels over CeO2-promoted Pt/Al2O3

  AUTHORS: Akkarat Wongkaew, Pichet Limsuwan

  KEYWORDS: CO Oxidation; CeO2-Pt/alumina; CO Adsorption; Selective CO Oxidation; Fuel Processing

  JOURNAL NAME: Advances in Chemical Engineering and Science, Vol.3 No.4B, October 25, 2013

  ABSTRACT: A comparative study of catalytic CO oxidation and selective CO oxidation over Pt/Al2O3 and CeO2-promoted Pt/Al2O3 catalysts has been investigated for the removal of a trace amount of CO from the reformed gas. The catalysts were prepared by sol gel and incipient wetness impregnation. CO oxidation and selective CO oxidation were carried out with a 5%Pt/Al2O3 and a 5%Pt/15%CeO2/Al2O3. The presence of 15%CeO2 inthe 5%Pt/Al2O3 dramatically improves the activities to CO oxidation and selective CO oxidation at low temperature (0℃). FTIR results indicate that CO could react with lattice oxygen from ceria and release CO2 as a product. Low space velocity would obtain high CO conversion at low temperatures while high space velocity would obtain high CO conversion at high temperatures. The results also show that a 5%Pt/15%CeO2/Al2O3 can completely oxidize 1% CO at180℃with selectivity of 52% and space velocity of70,000 cm3·g-1·h-1. Under the realistic gas feed with 1%O2, this catalyst is very stable and retains its activity and selectivity at180℃during 72 h.