Catalytic activity, selectivity and stability of a Pt/CeO2 (5wt% Pt) catalyst were investigated in the low temperature ethanol steam reforming reaction for hydrogen production. Experimental results showed that the catalyst is very active and selective, with negligible CO production and complete ethanol conversion already at 300 ◦C. The main promoted reactions are ethanol decomposition, ethanol steam reforming and CO water gas shift, and a preliminary kinetic investigation showed that the apparent reaction orders are 0.5 and 0 for ethanol and steam respectively, with an apparent activation energy of 18 kJ mol−1 evaluated in the range 300–450 ◦C. Kinetic evaluations and temperature programmed desorption experiments suggest a surface reaction mechanism involving the following step: (i) ethanol dissociative adsorption on catalyst surface to form acetaldehyde intermediate, (ii) decarbonylation to produce mainlyH2, CH4 and CO, and (iii)WGSreaction of CO adsorbed on Pt sites to produce H2 and CO2.
Low temperature catalytic steam reforming of ethanol. 2. Preliminary kinetic investigation of Pt/CeO2 catalysts
CIAMBELLI, Paolo;PALMA, Vincenzo;
2010-01-01
Abstract
Catalytic activity, selectivity and stability of a Pt/CeO2 (5wt% Pt) catalyst were investigated in the low temperature ethanol steam reforming reaction for hydrogen production. Experimental results showed that the catalyst is very active and selective, with negligible CO production and complete ethanol conversion already at 300 ◦C. The main promoted reactions are ethanol decomposition, ethanol steam reforming and CO water gas shift, and a preliminary kinetic investigation showed that the apparent reaction orders are 0.5 and 0 for ethanol and steam respectively, with an apparent activation energy of 18 kJ mol−1 evaluated in the range 300–450 ◦C. Kinetic evaluations and temperature programmed desorption experiments suggest a surface reaction mechanism involving the following step: (i) ethanol dissociative adsorption on catalyst surface to form acetaldehyde intermediate, (ii) decarbonylation to produce mainlyH2, CH4 and CO, and (iii)WGSreaction of CO adsorbed on Pt sites to produce H2 and CO2.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
