The effects of nanonickel additive on the decomposition of complex metal hydride LiAlH4 (lithium alanate)

被引:45
|
作者
Varin, Robert A. [1 ]
Zbroniec, Leszek [1 ]
Czujko, Tomasz [2 ]
Wronski, Zbigniew S. [1 ,2 ]
机构
[1] Univ Waterloo, Dept Mech & Mechatron Engn, Waterloo, ON N2L 3G1, Canada
[2] Nat Resources Canada, CanmetENERGY, Hydrogen Fuel Cells & Transportat Energy, Ottawa, ON K1A 1M1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Solid state hydrogen storage; Desorption temperature and kinetics; Nanonickel additives; Hydrogen storage materials; Lithium alanate (LiAlH4); Ball milling; HYDROGEN DESORPTION PROPERTIES; RELEASE; NICKEL;
D O I
10.1016/j.ijhydene.2010.06.090
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
High energy ball milling up to at least 1h does not lead to the transformation of undoped LiAlH4 as well as LiAlH4 doped with n-Ni into Li3AlH6. In a DSC test the melting of LiAlH4 is completely eliminated by the addition of 5 wt% n-Ni incorporated by high energy ball milling. The LiAlH4 + 5 wt% n-Ni system processed by ball milling desorbs similar to 4.8 wt% H-2 at 120 degrees C within 2000 s. At 120 degrees C within a 5000 s time interval the desorption reaction occurs fully in a solid state in one step according to the following reaction: LiAlH4 -> 1/3Li(3)AlH(6) + 2/3Al + H-2. This reaction is completely non-volatile. At 140 degrees C and higher temperatures the desorption reaction of ball milled LiAlH4 + 5 wt% n-Ni occurs fully in a solid state most likely in two steps according to the following reactions: (1) LiAlH4 -> 1/3Li(3)AlH(6) + 2/3Al + H-2 and (2) 1/3Li(3)AlH(6) -> LiH + 1/3Al + 0.5H(2). However, XRD patterns after reaction (2) do not show the presence of LiH but instead, they show the presence of LiOH. It is possible that LiH is transformed rapidly into LiOH by a mechanism which is now under investigation. When stored for a long time at room temperature the heavily ball milled LiAlH4 + 5 wt% n-Ni system gradually degrades losing H-2 capacity. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1167 / 1176
页数:10
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