TY - JOUR
T1 - Aqueous phase reforming in a microchannel reactor
T2 - The effect of mass transfer on hydrogen selectivity
AU - Neira d'Angelo, M.F.
AU - Ordomskiy, V.
AU - Schaaf, van der, J.
AU - Schouten, J.C.
AU - Nijhuis, T.A.
PY - 2013/10/1
Y1 - 2013/10/1
N2 - Aqueous phase reforming of sorbitol was carried out in a 1.7 m long, 320 μm ID microchannel reactor with a 5 μm Pt-based washcoated catalyst layer, combined with nitrogen stripping. The performance of this microchannel reactor is correlated to the mass transfer properties, reaction kinetics, hydrogen selectivity and product distribution. Mass transfer does not affect the rate of sorbitol consumption, which is limited by the kinetics of the reforming reaction. Mass transfer significantly affects the hydrogen selectivity and the product distribution. The rapid consumption of hydrogen in side reactions at the catalyst surface is prevented by a fast mass transfer of hydrogen from the catalyst site to the gas phase in the microchannel reactor. This results in a decrease of the concentration of hydrogen at the catalyst surface, which was found to enhance the desired reforming reaction rate at the expense of the undesired hydrogen consuming reactions. Compared to a fixed bed reactor, the selectivity to hydrogen in the microchannel reactor was increased by a factor of 2. The yield of side products (mainly C3 and heavier hydrodeoxygenated species) was suppressed while the yield of hydrogen was increased from 1.4 to 4 moles per mole of sorbitol fed.
AB - Aqueous phase reforming of sorbitol was carried out in a 1.7 m long, 320 μm ID microchannel reactor with a 5 μm Pt-based washcoated catalyst layer, combined with nitrogen stripping. The performance of this microchannel reactor is correlated to the mass transfer properties, reaction kinetics, hydrogen selectivity and product distribution. Mass transfer does not affect the rate of sorbitol consumption, which is limited by the kinetics of the reforming reaction. Mass transfer significantly affects the hydrogen selectivity and the product distribution. The rapid consumption of hydrogen in side reactions at the catalyst surface is prevented by a fast mass transfer of hydrogen from the catalyst site to the gas phase in the microchannel reactor. This results in a decrease of the concentration of hydrogen at the catalyst surface, which was found to enhance the desired reforming reaction rate at the expense of the undesired hydrogen consuming reactions. Compared to a fixed bed reactor, the selectivity to hydrogen in the microchannel reactor was increased by a factor of 2. The yield of side products (mainly C3 and heavier hydrodeoxygenated species) was suppressed while the yield of hydrogen was increased from 1.4 to 4 moles per mole of sorbitol fed.
UR - http://www.scopus.com/inward/record.url?scp=84884162554&partnerID=8YFLogxK
U2 - 10.1039/c3cy00577a
DO - 10.1039/c3cy00577a
M3 - Article
SN - 2044-4753
VL - 3
SP - 2834
EP - 2842
JO - Catalysis Science & Technology
JF - Catalysis Science & Technology
IS - 10
ER -