Abstract
Temperature programmed desorption - mass spectrometry was utilized to study the non-isothermal hydrogen desorption from as-received and pre-oxidized TiH 2 powder samples. Above the temperature of 750 °C, hydrogen desorption from the thermally decomposed as-received powder is kinetically delayed compared to that from the pre-oxidized samples. The scanning electron microscopy observations suggest that the delay stems from simultaneous surface coarsening and particles sintering that occur predominantly in the as-received powder at lower temperatures. It is also suggested that the difference in morphology evolution of the as-received and pre-oxidized powders originates from the dependence of Ti diffusion on the concentration of oxygen dissolved in Ti, since the oxide layer itself was found to dissociate at lower temperatures (∼500 °C).
Original language | English |
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Pages (from-to) | 6045-6054 |
Number of pages | 10 |
Journal | International Journal of Hydrogen Energy |
Volume | 44 |
Issue number | 12 |
DOIs | |
State | Published - 1 Mar 2019 |
Keywords
- Dehydrogenation
- SEM
- Sintering
- Surface coarsening
- Temperature programmed desorption – mass spectrometry (TPD-MS)
- Titanium hydride
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Condensed Matter Physics
- Energy Engineering and Power Technology