Mechanical activation of TiFe for hydrogen storage by cold rolling under inert atmosphere

被引:77
作者
Vega, L. E. R. [1 ]
Leiva, D. R. [2 ]
Leal Neto, R. M. [3 ]
Silva, W. B. [1 ]
Silva, R. A. [2 ]
Ishikawa, T. T. [2 ]
Kiminami, C. S. [2 ]
Botta, W. J. [2 ]
机构
[1] Univ Fed Sao Carlos UFSCar, Programa Posgrad Ciencia & Engn Mat, Rod Washington Luis,Km 235, BR-13565905 Sao Carlos, SP, Brazil
[2] Univ Fed Sao Carlos UFSCar, Dept Engn Mat, Rod Washington Luis,Km 235, BR-13565905 Sao Carlos, SP, Brazil
[3] IPEN, Ctr Ciencia & Tecnol Mat, Av Lineu Prestes,2242 Cidade Univ, BR-05508000 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Cold rolling under inert atmosphere; Hydrogen storage; TiFe; HIGH-PRESSURE TORSION; NANOCRYSTALLINE TIFE; ALLOYS; PERFORMANCE; ABSORPTION; FETI;
D O I
10.1016/j.ijhydene.2017.12.054
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
TiFe is a very interesting material for hydrogen storage in the solid state, due to its hydrogen capacity of 1.9 wt % and to the fact it can be absorb/desorb hydrogen at room temperature. However, the TiFe produced by casting does not absorb hydrogen, unless a procedure called activation is applied, which is based on a repetition of several thermal cycles. This study evaluates the effects of a mechanical activation route for the TiFe intermetallic compound, namely, cold rolling (CR) under inert atmosphere. Stoichiometric TiFe was prepared from elementary powders by arc melting. Ingot was grinded and then cold rolled for 20 and 40 passes under argon inside a glove box, with moisture and oxygen contents below 0.1 ppm. Cold rolled samples consisted of two parts: powder particles and thin cracked flakes. The results showed that mechanically activated samples by CR exhibited rapid absorption of hydrogen at room temperature, without using a thermal activation process. In general, the average storage capacity of hydrogen was 1.4 wt% H-2 for the first absorption, regardless of the number of passes for both flake and powder samples. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2913 / 2918
页数:6
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