Development of Ti-Cr-Mn-Fe based alloys with high hydrogen desorption pressures for hybrid hydrogen storage vessel application

被引:64
作者
Chen, Zhiwen [1 ]
Xiao, Xuezhang [1 ]
Chen, Lixin [1 ]
Fan, Xiulin [1 ]
Liu, Langxia [1 ]
Li, Shouquan [1 ]
Ge, Hongwei [1 ]
Wang, Qidong [1 ]
机构
[1] Zhejiang Univ, Key Lab Adv Mat & Applicat Batteries Zhejiang Pro, Dept Mat Sci & Engn, Hangzhou 310027, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Metal hydrides; Ti-Cr-Mn-Fe based alloys; Laves phase; Hydrogen storage properties; High hydrogen desorption pressure; METAL HYDRIDE; INTERMETALLIC COMPOUNDS; MICROSTRUCTURE; COMPRESSORS; SYSTEM;
D O I
10.1016/j.ijhydene.2013.07.073
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
Three series of Ti-Cr-Mn-Fe based alloys with high hydrogen desorption plateau pressures for hybrid hydrogen storage vessel application were prepared by induction levitation melting, as well as their crystallographic characteristics and hydrogen storage properties were investigated. The results show that all of the alloys were determined as a single phase of C14-type Laves structure. As the Fe content in the TiCr1.9-xMn0.1Fex (x = 0.4-0.6) alloys increases, the hydrogen absorption and desorption plateau pressures increase, and the hydrogen storage capacity and plateau slope factor decrease respectively. The same trends are observed when increasing the Mn content in the TiCr1.4-yMnyFe0.6 ( y = 0.1-0.3) alloys, except for the plateau slope factor. Compared with the stoichiometric TiCr1.1Mn0.3Fe0.6 alloy, the titanium super-stoichiometric Ti1+zCr1.1Mn0.3Fe0.6 (z = 0.02, 0.04) alloys have larger hydrogen storage capacities and lower hydrogen desorption plateau pressures. Among the studied alloys, Ti1.02Cr1.1Mn0.3Fe0.6 has the best overall properties for hybrid hydrogen storage application. Its hydrogen desorption pressure at 318 K is 41.28 MPa, its hydrogen storage capacity is 1.78 wt.% and its dissociation enthalpy (Delta H-d) is 16.24 kJ/mol H-2. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12803 / 12810
页数:8
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