Magnesium hydride has a high theoretically storage capacity, which amounts to 7.6 wt%. It is therefore a promising candidate for hydrogen storage applications. However, its major drawback is its high desorption temperature of well over 300 °C, which is related to the high stability of the Mg-H bonds and expressed in the high enthalpy of hydride formation (77 kJ/mol). The preparation of Mg composites with other hydrogen storage compounds is an effective method to improve the hydrogen storage properties of Mg. Thus we prepared Mg-50 wt% ZrCrFe alloy composite by high energy ball milling under argon atmosphere. X-ray diffraction (XRD) studies on the composite before and after hydriding cycles suggest no intermetalic phase is formed between Mg and the elements of the alloy. The morphological studies carried on by Scanning Electron Microscope (SEM) technique suggest that the alloy particles are homogeneously distributed throughout the Mg surface. A particle reduction after hydrogenation is also visible. Hydriding/dehydriding properties of the composites are investigated by PCT measurements using a dynamic system. The maximum hydrogen capacity for this composite is found to be 4.5 wt%. The reaction kinetics have also been recorded in a temperature range from RT to 300 °C and the thermodynamic parameters calculated from Van't Hoff plot. From the results it is found that the alloy reacts with hydrogen also when cooled to room temperature while at higher temperature it works as catalyst. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
All Science Journal Classification (ASJC) codes
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Condensed Matter Physics
- Energy Engineering and Power Technology
Jain, A., Agarwal, S., Jain, P., Gislon, P., Prosini, P. P., & Jain, I. P. (2012). Hydriding behavior of Mg-50 wt% ZrCrFe composite Prepared by high energy ball milling. International Journal of Hydrogen Energy, 37(4), 3665 - 3670. https://doi.org/10.1016/j.ijhydene.2011.04.042