Hydrogen production from hydrolysis of ammonia borane with limited water supply

被引:30
作者
Chou, Chang-Chen [1 ]
Lee, Duu-Jong [2 ]
Chen, Bing-Hung [1 ,3 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
[2] Natl Taiwan Univ, Dept Chem Engn, Tainan 10617, Taiwan
[3] Natl Cheng Kung Univ, Res Ctr Energy Technol & Strategy, Tainan 70101, Taiwan
关键词
Ammonia borane; Hydrogen generation; Hydrolysis reaction; Limited water supply; GENERATION SYSTEM; ROOM-TEMPERATURE; THERMAL-DECOMPOSITION; ORTHOBORIC ACID; CATALYST; STORAGE; DEHYDROGENATION; FUEL; NANOCLUSTERS; DISSOCIATION;
D O I
10.1016/j.ijhydene.2012.05.108
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
Effect of limited water supply to hydrolysis of ammonia borane for hydrogen evolution is studied over the cases in which the initial molar ratio of water to ammonia borane (H2O/AB) is set at 1.28, 2.57 and 4.50. The conversion efficiency of ammonia borane to hydrogen is estimated from the accumulated volume of produced hydrogen gas and the quantitative analysis of hydrolysate by solid-state B-11 NMR. Characteristics of hydrogen evolution are significantly influenced by both water dosage and injection rate of water. In the case that water is a limiting agent, namely, H2O/AB = 1.28, less hydrogen is produced than that predicted stoichiometrically. In contrast, conversion efficiency of ammonia borane reaches nearly 100% for the case with H2O/AB = 4.50. Injection rate of water to ammonia borane also affect profoundly the produced volume and production rate of hydrogen, if water is used as a limiting agent in the hydrolysis of ammonia borane. Nonetheless, boric acid and metaboric acid are found to be the dominant products in the hydrolysate from XRD, FT-IR and solid-state B-11 NMR analysis. The hydrogen storage capacity using limited water supply in this work could reach as high as about 5.33 wt%, based on combined mass of reactants and catalyst. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:15681 / 15690
页数:10
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