Time-Dependent Multi-Particle Model Describing the Hydrogen Absorption of Nanocrystalline Magnesium Powders: A Case Study
Ádám Révész () and
Áron Pintér
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Ádám Révész: Department of Materials Physics, Eötvös University (ELTE), P.O.B. 32, H-1518 Budapest, Hungary
Áron Pintér: Department of Materials Physics, Eötvös University (ELTE), P.O.B. 32, H-1518 Budapest, Hungary
Energies, 2024, vol. 17, issue 10, 1-14
Abstract:
Classical kinetic models describing the hydrogen absorption of nanocrystalline metallic hydrides generally do not involve any parameter related to the change in the crystallite size during the hydrogenation at constant temperature. In the present investigation, ball-milled nanocrystalline Mg powders exhibiting lognormal crystallite size distribution have been subjected to hydrogen absorption in a Sievert-type apparatus. Partially absorbed states were achieved by interrupting the hydrogenation cycle at different hydrogen content, i.e., when 15%, 50%, and 90% of Mg powder transformed to MgH 2 . The evolution of the characteristic size of the nucleating MgH 2 phase was determined from X-ray diffraction analysis. Considering the crystallite size distribution of the as-milled powder agglomerate as well as the growth during the isothermal hydrogenation process, a time-dependent multi-particle reaction function ∝ C V ¯ t ; R ( t ) was developed. It was shown unambiguously for this case study that the measured hydrogen absorption curve of the ball-milled Mg powder shows the best correlation with this model when it is compared to classical kinetic functions or the previously developed multi-particle reaction function excluding the change in the average crystallite size during hydrogenation.
Keywords: hydrogen storage; kinetics; magnesium; growth; time-dependent multi-particle reaction model (search for similar items in EconPapers)
JEL-codes: Q Q0 Q4 Q40 Q41 Q42 Q43 Q47 Q48 Q49 (search for similar items in EconPapers)
Date: 2024
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