高等学校化学学报 ›› 2011, Vol. 32 ›› Issue (6): 1330.

• 研究论文 • 上一篇    下一篇

LiAlH4与LiNH2的相互作用机理及储氢特性

任晓, 王新华, 李寿权, 葛红卫   

  1. 浙江大学材料系, 杭州 310027
  • 收稿日期:2011-01-24 修回日期:2011-03-10 出版日期:2011-06-10 发布日期:2011-05-10
  • 通讯作者: 王新华 E-mail:xinhwang@zju.edu.cn
  • 基金资助:

    国家自然科学基金(批准号: 50671094)资助.

Reaction Mechanism and Hydrogen Storage Properties of LiAlH4 and LiNH2

REN Xiao, WANG Xin-Hua*, LI Shou-Quan,  GE Hong-Wei   

  • Received:2011-01-24 Revised:2011-03-10 Online:2011-06-10 Published:2011-05-10
  • Contact: WANG Xin-Hua E-mail:xinhwang@zju.edu.cn
  • Supported by:

    国家自然科学基金(批准号: 50671094)资助.

摘要: 将LiAlH4和LiNH2按摩尔比1:2进行球磨复合,随后将复合物进行加热放氢特性研究,然后对其完全放氢后的产物进行再吸氢特性研究。通过X射线衍射分析(XRD)、热分析(DSC)和红外 (FTIR)分析等测试手段对其反应过程进行了系统分析研究。研究结果表明,LiAlH4/2LiNH2加热放氢分为3个反应阶段,放氢后生成Li3AlN2,总放氢量达到8.65wt%。放氢生成的Li3AlN2在10MPaH2压力和400℃条件下,可以可逆吸氢5.0wt%,吸氢后的产物为 LiNH2 、AlN和LiH,而不能再生成LiAlH4。本文对LiAlH4/2LiNH2复合物放氢/再氢化过程机理进行了分析。

关键词: 储氢材料, 储氢性能, 配位氢化物, 化学氢化物, 金属氮氢化物

Abstract: LiAlH4 and LiNH2 was ball milled at molar ratio of 1:2, thus prepared composite was heated for dehydrogenation, the fully dehydrogenated samples were re-hydrogenated. The dehydrogenation/re-hydrogenation processes were studied by means of XRD, DSC and FTIR analysis. The experimental results showed that the dehydrogenation process of LiAlH4/2LiNH2 composite is a three-stage reaction, and Li3AlN2 was formed after releasing 8.65wt% of hydrogen。The derived Li3AlN2 can be re-hydrogenated under conditions of 10MPaH2 and 400℃, and LiNH2 、AlN and LiH were formed. The reversible hydrogen storage capacity reached 5.0wt%. The dehydrogenation/re-hydrogenation mechanism of LiAlH4/2LiNH2 composite was discussed.

Key words: Hydrogen storage materials, Hydrogen storage properties, Complex hydride, Chemical hydride, Metal-nitrogen-hydride

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