Pressure-composition-isotherm behaviors of MgHx-BCY composites by reactive mechanical alloying

The aim of the present paper is to report results on hydrogenation behavior of a new composite material, MgH x -BCY10. Rare earth element-doped ABO 3 perovskite oxides have been studied for their possibility use in hydrogen storage. Especially, materials based on BaCeO 3 are known not only for their...

Full description

Saved in:
Bibliographic Details
Published inMetals and materials international Vol. 19; no. 6; pp. 1351 - 1353
Main Authors Lee, Soo-Sun, Lee, Na-Ri, Kim, Kyeong-Il, Hong, Tae-Whan
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.11.2013
대한금속·재료학회
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The aim of the present paper is to report results on hydrogenation behavior of a new composite material, MgH x -BCY10. Rare earth element-doped ABO 3 perovskite oxides have been studied for their possibility use in hydrogen storage. Especially, materials based on BaCeO 3 are known not only for their proton conductivity in hydrogen but also for the fact that they have higher hydrogen solubility than that of other metal oxides. So, the admixing of perovskite-type oxide in storage materials has to consider the possibility of MgH x leading to sorption kinetics. And, these materials can be new materials for hydrogen storage. This research considers Pressure-Composition-Isothermal behavior according to perovskite-type oxide powder ratio and hydrogen pressure. The effects of added amount of BCY show a temperature of dehydrogenation that has decreased.From the results shown in the P-C-T curves, the MgHx-5wt% BCY composite was evaluated as having a 2.81 wt% maximum hydrogen storage capacity at 623 K. The absorption curves show that the MgH x -10wt% BCY was composite evaluated at a maximum 0.43wt%/s hydrogen absorption rate at 623 K. From the results of the hydrogenation behavior observed, the role of BCY as a catalyst in hydrogen absorption is confirmed.
Bibliography:G704-000797.2013.19.6.012
ISSN:1598-9623
2005-4149
DOI:10.1007/s12540-013-0639-8