Abstract
Fe-Ni materials with varying Ni loading are developed for separate H2
and CO production by CH4-CO2 chemical looping. The product streams are
obtained by first feeding CH4, which decomposes to H2 and carbon. The
latter acts as reductant for the subsequent CO2 feed, which together
with Fe re-oxidation yields CO. After 25 CH4-CO2 cycles, 10Fe5Ni@Zr has
a higher H2 space-time-yield than 10Fe0Ni@Zr
(〖20mmol∙s〗^(-1)∙kg_(Fe+Ni)^(-1) vs.
〖15mmol∙s〗^(-1)∙kg_(Fe+Ni)^(-1)), a 2.6 times higher CO
(〖57mmol∙s〗^(-1)∙kg_(Fe+Ni)^(-1)) and lower deactivation. This
improvement has two reasons: (i) CH4 activation over Ni leading to
cracking, (ii) product hydrogen causing deeper FeO reduction.
Deactivation follows from accumulated carbon, non-reactive for CO2. On
Ni and Fe sites, carbon can be removed by lattice oxygen or CO2,
yielding more CO compared to the theoretical value for Fe oxidation.
However, carbon that migrates away from the metals requires oxygen for
removal, which restores the activity of the Ni-containing samples.