Effects of nano size mischmetal and its oxide on improving the hydrogen sorption behaviour of MgH2

This paper reports the catalytic effects of mischmetal (Mm) and mischmetal oxide (Mm-oxide) on improving the dehydrogenation and rehydrogenation behaviour of magnesium hydride (MgH₂). It has been found that 5 wt.% is the optimum catalyst (Mm/Mm-oxide) concentration for MgH₂. The Mm and Mm-oxide catalyzed MgH₂ exhibits hydrogen desorption at significantly lower temperature and also fast rehydrogenation kinetics compared to ball-milled MgH₂ under identical conditions of temperature and pressure. The onset desorption temperature for MgH₂ catalyzed with Mm and Mm-oxide are 323 °C and 305 °C, respectively. Whereas the onset desorption temperature for the ball-milled MgH₂ is 381 °C. Thus, there is a lowering of onset desorption temperature by 58 °C for Mm and by 76 °C for Mm-oxide. The dehydrogenation activation energy of Mm-oxide catalyzed MgH₂ is 66 kJ/mol. It is 35 kJ/mol lower than ball-milled MgH₂. Additionally, the Mm-oxide catalyzed dehydrogenated Mg exhibits faster rehydrogenation kinetics. It has been noticed that in the first 10 min, the Mm-oxide catalyzed Mg (dehydrogenated MgH₂) has absorbed up to 4.75 wt.% H₂ at 315 °C under 15 atmosphere hydrogen pressure. The activation energy determined for the rehydrogenation of Mm-oxide catalyzed Mg is ∼62 kJ/mol, whereas that for the ball-milled Mg alone is ∼91 kJ/mol. Thus, there is a decrease in absorption activation energy by ∼29 kJ/mol for the Mm-oxide catalyzed Mg. In addition, Mm-oxide is the native mixture of CeO₂ and La₂O₃ which makes the duo a better catalyst than CeO₂, which is known to be an effective catalyst for MgH₂. This takes place due to the synergistic effect of CeO₂ and La₂O₃. It can thus be said that Mm-oxide is an effective catalyst for improving the hydrogen sorption behaviour of MgH₂.