Ammonia borane decomposition in the presence of cobalt halides

被引:35
作者
Chiriac, R. [1 ]
Toche, F. [1 ]
Demirci, U. B. [1 ,2 ]
Krol, O. [1 ]
Miele, P. [2 ]
机构
[1] Univ Lyon 1, CNRS, UMR 5615, Lab Multimat & Interfaces, F-69622 Villeurbanne, France
[2] Univ Montpellier 2, Inst Europeen Membranes, UMR 5253, CNRS,Lab Agregats Interfaces & Mat Energie, F-34095 Montpellier 5, France
关键词
Ammonia borane; Chemical hydrogen storage; Cobalt halides; Hydrogen release; Thermolysis; THERMAL-DECOMPOSITION; HYDROGEN STORAGE; HYDROLYSIS;
D O I
10.1016/j.ijhydene.2011.07.040
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
In the present work we studied the effect of cobalt halides (CoF2, CoCl2, CoBr2 and CoI2; also denoted CoX2) on the thermal decomposition of ammonia borane NH3BH3 (AB) over the range 25-220 degrees C. The reaction was followed by thermogravimetric analysis and differential scanning calorimetry. The gaseous products analyzed by gas chromatography and mass spectrometry, and the solid by-products identified by elemental analysis: powder X-ray diffraction, infrared and X-ray photoelectron spectroscopies. Compared to pristine AB, the presence of CoCl2 and CoBr2 reduces both the induction period of the AB decomposition and the content of unwanted borazine in the H-2 stream, whereas the presence of CoI2 or CoF2 has little or no effect, respectively. We propose that the positive effect of CoX2 comes from their electronic and steric effects, and that CoCl2 is the compound which shows the best properties relative to these effects. Herein, the roles of Co and X are discussed and a revised mechanism of the AB dehydrocoupling initiation is proposed. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12955 / 12964
页数:10
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