作者: David P. Serrano , Juan Ángel Botas , Patricia Pizarro , Gema Gómez
DOI: 10.1016/J.IJHYDENE.2013.02.112
关键词: Hydrogen production 、 Autocatalysis 、 Chemical kinetics 、 Hydrogen 、 Inorganic chemistry 、 Catalysis 、 Carbon 、 Reaction rate 、 Chemistry 、 Methane
摘要: Abstract The reaction kinetics of methane decomposition to yield hydrogen and carbon has been investigated comparing different types carbonaceous catalysts: two ordered mesoporous carbons (CMK-3 CMK-5) commercial blacks (CB-bp CB-v). evolution the rate along time analyzed concluding that it is governed by opposite events: reduction active sites deposition, autocatalytic effects deposits pore blockage diffusional constraints. A relatively simple kinetic model developed fits quite well experimental curves in spite complexity involved phenomena. Both CMK carbons, particularly CMK-5, present highest initial rates longest stability at long times. In these materials, a part remains accessible, since formed from are capable growing through catalyst mesopores toward outer particles. activation energies calculated follow sequence CMK-3