Characterisation of Mg-x wt.% FeTi (x=5-30) and Mg-40 wt.% FeTiMn hydrogen absorbing materials prepared by mechanical alloying

被引:51
|
作者
Vijay, R
Sundaresan, R
Maiya, MP
Murthy, SS
Fu, Y
Klein, HP
Groll, M
机构
[1] Univ Stuttgart, Inst Kernenerget & Energiesyst, D-70569 Stuttgart, Germany
[2] Int Adv Res Ctr Powder Met & New Mat, Hyderabad 500005, Andhra Pradesh, India
[3] Indian Inst Technol, Dept Mech Engn, Refrigerat & Airconditioning Lab, Madras 600036, Tamil Nadu, India
关键词
hydrogen storage materials; high-energy ball milling; scanning electron microscopy; X-ray diffraction;
D O I
10.1016/j.jallcom.2004.04.115
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Composites based on Mg with intermetallic FeTi (up to 30 wt.%) and FeTiMn (40 wt.%) were prepared by mechanical alloying for evaluation of their hydrogen storage characteristics. In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proportions. Powders milled under argon had to be activated by remilling under hydrogen. In the second case FeTiMn prepared by melting was milled together with MgH2 under hydrogen. Hydrogen storage characteristics, pressure-composition isotherms and kinetics were investigated under different parameters. Among the FeTi composites, Mg-5 wt.% FeTi had the maximum absorption capacity of 5.80 wt.% at 300degreesC and 5.12 wt.% at 200degreesC. At 300degreesC the initial desorption rate was the highest for Mg-10 wt.% FeTi, but its final desorption capacity was less than that of Mg-5 wt.% FeTi. None of the compositions showed any desorption at 200degreesC. In the case of composites with FeTiMn, absorption and desorption temperatures decreased by ball milling and higher storage capacities were achieved. In Mg-40 wt.% FeTiMn, the lowest absorption and desorption temperatures were 80 and 240degreesC, respectively, with the material absorbing 4 wt.% hydrogen even at 80degreesC. The kinetics improved with increasing milling time. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:283 / 295
页数:13
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