Hydrogen desorption properties of the Ca-N-H system

被引:50
|
作者
Hino, S
Ichikawa, T
Leng, HY
Fujii, H
机构
[1] Hiroshima Univ, Grad Sch Adv Sci Matter, Hiroshima 7398530, Japan
[2] Hiroshima Univ, Ctr Mat Res, Hiroshima 7398526, Japan
关键词
hydrogen storage materials; gas-solid reactions; high-energy ball millings; mechanochemical synthesis; thermal analysis;
D O I
10.1016/j.jallcom.2005.01.052
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
After synthesizing calcium amide (Ca(NH2)(2)) through the reaction of calcium hydride (CaH2) with ammonia (NH3), the thermal decomposition properties have been examined. The results indicated that Ca(NH2)(2) decomposed to calcium imide (CaNH) and NH3 gas with increasing temperature, where the desorption of NH3 started from about 60 degrees C and peaked around 300 degrees C in the thermal desorption mass spectra (TDMS). From the X-ray diffraction profiles, the product after heat treatment up to 350 degrees C was CaNH, but an unknown phase appeared in further heating up to 500 degrees C. Hydrogen (H-2) desorption properties of a mixture of Ca(NH2)(2) and CaH2 with 1:3 molar ratio were also examined. The H-2 gas of 3.5 wt.% in total was desorbed with two-peak structure in TDMS. The first peak corresponds to the reaction: Ca(NH2)(2) + CaH2 -> 2CaNH + 2H(2), and the second one originates from the reaction: CaNH + CaH2 -> Ca2NH + H-2. Simultaneously performed differential thermal analysis indicated that the former and the latter reactions were, respectively, exothermic and endothermic, so that the H, desorption corresponding to the first peak in TDMS disappeared after long-time-milling at room temperature. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 66
页数:5
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