Magnesium hydride is a very attractive material for solid state hydrogen storage due to their high mass and volume capacity, but its slow absortion/desortion kinetics does not favours its practical use in mobile applications. Recently it has been observed that the addition of small quantities of tra
Kinetics of dehydrogenation of the Mg–Ti–H hydrogen storage system
✍ Scribed by H.Y. Sohn; S. Emami
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 525 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0360-3199
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✦ Synopsis
Among the proposed hydrogen storage systems, magnesium alloys have proved to be promising since they are rechargeable with high hydrogen capacities (theoretically up to 7.6 wt.%), reversibility and low costs. Small particle size, which can be achieved by milling, and small amounts of transition-metal compounds as catalysts result in increased hydrogen release/uptake kinetics. In this work, we developed the rate expression for the dehydrogenation of milled 7MgH 2 /TiH 2 , 10MgH 2 /TiH 2 , and MgH 2 samples. The complete rate expressions, together with the values of activation energy and other rate parameters, were determined for the three milled samples by analyzing data obtained from nonisothermal thermogravimetric analysis (TGA). The MgH 2 doped with TiH 2 by high-energy milling displayed substantially reduced apparent activation energy of 107e118 kJ/mol and significantly faster kinetics, compared with 226 kJ/mol for similarly milled MgH 2 without TiH 2 doping.
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