Study of the dry reforming of methane and ethanol using Rh catalysts supported on doped alumina

Asmaa Drif (1, 2, 3) , Nicolas Bion (2) , Rachid Brahmia (3) , Satu Ojala (1) , Laurence Pirault-Roy (2) , Esa Turpeinen (1) , Kuma Prem Seelam (1) , Riitta L. Keiski (1) , Florence Epron (2)

1 University of Oulu
2 IC2MP [Poitiers] - Institut de chimie des milieux et matériaux de Poitiers [UMR 7285]
3 UCD - Université Chouaib Doukkali

Abstract Various MxOy-Al2O3 oxides (M =Zr, Mg, Ni, Ce, La), prepared by a sol-gel method, were used as supports for rhodium catalysts in methane and ethanol dry reforming. After calcination, the Rh/MxOy-Al2O3 catalysts present BET surface areas between 85 and 208 m(2) g(-1). For the CH4 dry reforming, the highest yields in hydrogen are obtained in the following ranking: Rh/NiO-Al2O3 > Rh/Al2O3 > Rh/MgO-Al2O3 approximate to Rh/CeO2-Al2O3 > Rh/ZrO2-Al2O3 > Rh/La2O3-Al2O3, not very different from the one for ethanol dry reforming at 800 degrees C which is: Rh/NiO-Al2O3 >> Rh/Al2O3 Rh/MgO-Al2O3 approximate to Rh/CeO2-Al2O3 > Rh/ZrO2-Al2O3 approximate to Rh/La2O3-Al2O3, although the reaction temperature is different. For the two reactions, the best catalyst is Rh/NiO-Al2O3 even if it deactivates during the reaction due to carbon deposition. This high activity may be explained by both the presence of the NiAl2O4 spinel phase, avoiding the deactivation of rhodium by migration in alumina, and the high dispersion of Rh favored by the presence of nickel particles at the support surface. Moreover, Ni particles on the support surface also contribute to the activity as demonstrated by the high hydrogen yield obtained in the presence of NiO-Al2O3, which is similar to the one obtained with Rh/Al2O3

Mots clés: Rh catalysts; Alumina-based mixed oxides; Ethanol dry reforming; Methane dry reforming

Domaines: Chimie; Catalyse

Asmaa Drif, Nicolas Bion, Rachid Brahmia, Satu Ojala, Laurence Pirault-Roy, et al.. Study of the dry reforming of methane and ethanol using Rh catalysts supported on doped alumina . Applied Catalysis A : General, 2015, 504 pp. 576-584 ⟨10.1016/j.apcata.2015.02.019⟩. ⟨hal-01266339⟩