Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 39, Issue 15, Pages 7834-7841Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2014.02.118
Keywords
Hydrogen storage; Magnesium hydride; Alanate; Destabilized system; Catalyst
Categories
Funding
- Malaysian Government through the Research Acculturation Grant Scheme (RAGS) [57087]
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In this paper, the hydrogen storage properties and reaction mechanism of the 4MgH(2) + LiAlH4 composite system with the addition of Fe2O3 nanopowder were investigated. Temperature-programmed-desorption results show that the addition of 5 wt.% Fe2O3 to the 4MgH(2) + LiAlH4 composite system improves the onset desorption temperature to 95 degrees C and 270 degrees C for the first two dehydrogenation stage, which is lower 40 degrees C and 10 degrees C than the undoped composite. The dehydrogenation and rehydrogenation kinetics of 5 wt.% Fe2O3-doped 4MgH(2) + LiAlH4 composite were also improved significantly as compared to the undoped composite. Differential scanning calorimetry measurements indicate that the enthalpy change in the 4MgH(2)-LiAlH4 composite system was unaffected by the addition of Fe2O3 nanopowder. The Kissinger analysis demonstrated that the apparent activation energy of the 4MgH(2) + LiAlH4 composite (125.6 kJ/mol) was reduced to 117.1 kJ/mol after doping with S wt.% Fe2O3. Meanwhile, the X-ray diffraction analysis shows the formation of a new phase of Li2Fe3O4 in the doped composite after the dehydrogenation and rehydrogenation process. It is believed that Li2Fe3O4 acts as an actual catalyst in the 4MgH(2) + LiAH(4) + 5 wt.% Fe2O3 composite which may promote the interaction of MgH2 and LilH(4) and thus accelerate the hydrogen sorption performance of the MgH2 + LiAlH4 composite system. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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