TY - JOUR
T1 - Theoretical analysis of the direct decomposition of methane gas in a laminar stagnation-point flow
T2 - CO2-free production of hydrogen
AU - Bautista, O.
AU - Méndez, F.
AU - Treviñoc, C.
N1 - Funding Information:
O. Bautista acknowledges DGAPA of UNAM for supporting this work.
PY - 2008/12
Y1 - 2008/12
N2 - In this work, a theoretical analysis is developed to predict the decomposition temperature of methane gas, CH4, in a planar stagnation-point flow over a catalytic carbon surface. Hydrogen is produced (without CO2 as a byproduct) by means of a heterogeneous reaction mechanism, which is modeled with five heterogeneous reactions, including adsorption and desorption reactions. The mass species, momentum, and energy conservation equations for the gas phase are solved, taking into account that the temperature of decomposition is characterized by the Damköhler number. Therefore, the critical temperature conditions for the catalytic thermal decomposition are found by using a high activation energy analysis for the desorption kinetics of the adsorbed hydrogen component, H(s). Specifically, the numerical estimations show that, for increasing values of the velocity gradient associated with the stagnation flow, the temperature of decomposition grows, depending on the surface coverages of the product species.
AB - In this work, a theoretical analysis is developed to predict the decomposition temperature of methane gas, CH4, in a planar stagnation-point flow over a catalytic carbon surface. Hydrogen is produced (without CO2 as a byproduct) by means of a heterogeneous reaction mechanism, which is modeled with five heterogeneous reactions, including adsorption and desorption reactions. The mass species, momentum, and energy conservation equations for the gas phase are solved, taking into account that the temperature of decomposition is characterized by the Damköhler number. Therefore, the critical temperature conditions for the catalytic thermal decomposition are found by using a high activation energy analysis for the desorption kinetics of the adsorbed hydrogen component, H(s). Specifically, the numerical estimations show that, for increasing values of the velocity gradient associated with the stagnation flow, the temperature of decomposition grows, depending on the surface coverages of the product species.
KW - Endothermic reaction
KW - Hydrogen production
KW - Methane
KW - Surface coverage
KW - Thermal decomposition
UR - http://www.scopus.com/inward/record.url?scp=57549084504&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2008.09.060
DO - 10.1016/j.ijhydene.2008.09.060
M3 - Artículo
SN - 0360-3199
VL - 33
SP - 7419
EP - 7426
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 24
ER -