Published March 20, 2009 | Version v1
Journal article

Hydrogen storage in TiCr1.2(FeV)x BCC solid solutions

  • 1. Institut de Recherche sur l'hydrogene, Universite du Quebec a Trois-Rivieres 3351, Boul. des Forges, Trois-Rivieres, Quebec G9A 5H7 (Canada)

Description

The Ti-V-based BCC solid solutions have been considered attractive candidates for hydrogen storage due to their relatively large hydrogen absorbing capacities near room temperature. In spite of this, improvements of some issues should be achieved to allow the technological applications of these alloys. Higher reversible hydrogen storage capacity, decreasing the hysteresis of PCI curves, and decrease in the cost of the raw materials are needed. In the case of vanadium-rich BCC solid solutions, which usually have large hydrogen storage capacities, the search for raw materials with lower cost is mandatory since pure vanadium is quite expensive. Recently, the substitutions of vanadium in these alloys have been tried and some interesting results were achieved by replacing vanadium by commercial ferrovanadium (FeV) alloy. In the present work, this approach was also adopted and TiCr1.2(FeV)x alloy series was investigated. The XRD patterns showed the co-existence of a BCC solid solution and a C14 Laves phase in these alloys. SEM analysis showed the alloys consisted of dendritic microstructure and C14 colonies. The amount of C14 phase increases when the amount of (FeV) decreases in these alloys. Concerning the hydrogen storage, the best results were obtained for the TiCr1.2(FeV)0.4 alloy, which achieved 2.79 mass% of hydrogen storage capacity and 1.36 mass% of reversible hydrogen storage capacity

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2008.04.062

Additional details

Identifiers

DOI
10.1016/j.jallcom.2008.04.062;
PII
S0925-8388(08)00661-0;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
472
Journal Issue
1-2
Journal Page Range
p. 247-251
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.