TY - JOUR
T1 - High temperature hydrogenation of Ti-V alloys
T2 - The effect of cycling and carbon monoxide on the bulk and surface properties
AU - Suwarno, S.
AU - Solberg, J. K.
AU - Krogh, B.
AU - Raaen, S.
AU - Yartys, V. A.
N1 - Publisher Copyright:
© 2015 Hydrogen Energy Publications, LLC.
PY - 2016/1/21
Y1 - 2016/1/21
N2 - In the present work, the high temperature (425-575 °C) hydrogen storage properties of Ti-V alloys have been studied, both at static conditions and in a flow of hydrogen gas. The selected isothermal temperature range is considered as an optimal condition for hydrogen sorption enhanced steam reforming. When hydrogenation and dehydrogenation were performed in pure hydrogen gas and in vacuum, a large reversible hydrogen capacity of 3.95 wt. % H was obtained, demonstrating completeness of the formation and decomposition of (Ti,V)-dihydrides. However, when cycling was performed in a flow of hydrogen gas, the reversible hydrogen capacity decreased to ∼2 wt. % H caused by the formation of stable lower (Ti,V)-hydrides. A further decrease in the reversible hydrogen storage capacity took place when pure hydrogen gas was replaced by a mixture of hydrogen and carbon monoxide CO. This decrease was caused by the formation of an oxygen rich layer on the surface of the alloy, which was partially blocking the hydrogen exchange between the surface and the bulk of the sample.
AB - In the present work, the high temperature (425-575 °C) hydrogen storage properties of Ti-V alloys have been studied, both at static conditions and in a flow of hydrogen gas. The selected isothermal temperature range is considered as an optimal condition for hydrogen sorption enhanced steam reforming. When hydrogenation and dehydrogenation were performed in pure hydrogen gas and in vacuum, a large reversible hydrogen capacity of 3.95 wt. % H was obtained, demonstrating completeness of the formation and decomposition of (Ti,V)-dihydrides. However, when cycling was performed in a flow of hydrogen gas, the reversible hydrogen capacity decreased to ∼2 wt. % H caused by the formation of stable lower (Ti,V)-hydrides. A further decrease in the reversible hydrogen storage capacity took place when pure hydrogen gas was replaced by a mixture of hydrogen and carbon monoxide CO. This decrease was caused by the formation of an oxygen rich layer on the surface of the alloy, which was partially blocking the hydrogen exchange between the surface and the bulk of the sample.
KW - Carbon monoxide
KW - High-temperature hydrogen storage
KW - Hydrogen production
KW - Metal hydrides
KW - Titanium-vanadium alloys
UR - http://www.scopus.com/inward/record.url?scp=84954497364&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2015.11.077
DO - 10.1016/j.ijhydene.2015.11.077
M3 - Article
AN - SCOPUS:84954497364
SN - 0360-3199
VL - 41
SP - 1699
EP - 1710
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 3
ER -