A comparative study of Pt/γ-Al2O3, Au/α-Fe2O3 and CuO–CeO2 catalysts for the selective oxidation of carbon monoxide in excess hydrogen

@article{Avgouropoulos2002ACS,
  title={A comparative study of Pt/$\gamma$-Al2O3, Au/$\alpha$-Fe2O3 and CuO–CeO2 catalysts for the selective oxidation of carbon monoxide in excess hydrogen},
  author={George Avgouropoulos and Theophilos Ioannides and Ch. Papadopoulou and Jurka Batista and Stanko Hocevar and Haralambos K. Matralis},
  journal={Catalysis Today},
  year={2002},
  volume={75},
  pages={157-167}
}

Bimetallic Au-Cu/CeO2 catalyst: Synthesis, structure, and catalytic properties in the CO preferential oxidation

The preparation of bimetallic Au-Cu catalysts via the decomposition of the double complex salt [Au(en)2]2[Cu(C2O4)2]3 · 8H2O is considered. It is found that this method of preparation allows us to

Selective oxidation of CO in the presence of H2, H2O and CO2 utilising Au/α-Fe2O3 catalysts for use in fuel cells

Au/Fe2O3 catalysts prepared using co-precipitation are described and discussed for the preferential oxidation of CO in the presence of H2, H2O and CO2. A catalyst prepared using a two-stage
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Abstract The selective oxidation of CO on Au/Al 2 O 3 and Au/MO x /Al 2 O 3 (M=Mg, Mn) in the presence of H 2 was studied. The addition of MgO and MnO x improves the CO oxidation activity and

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The selective CO oxidation (also referred to as PROX) on a Au/α-Fe2O3catalyst in simulated reformer gas (low concentrations of CO and O2, 75 kPa H2, balance N2) at atmospheric pressure was

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Abstract The selective CO oxidation reaction on Pt/γ-Al2O3insimulated reformer gas (75% H2; the rest is N2) was investigated over a wide range of CO concentrations (0.02–1.5%)at low stoichiometric

Carbon Monoxide Removal from Hydrogen-Rich Fuel Cell Feedstreams by Selective Catalytic Oxidation

Indirect methanol fuel cells currently being investigated at General Motors for transportation applications require removal of carbon monoxide from the hydrogen-rich gas stream produced by the fuel

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The oxidation of carbon monoxide catalyzed by Pt(111) was studied in ultrahigh vacuum using reactive molecular beam–surface scattering. Under all conditions studied, the reaction follows a