高等学校化学学报 ›› 2016, Vol. 37 ›› Issue (4): 688.doi: 10.7503/cjcu20150848

• 物理化学 • 上一篇    下一篇

3LiBH4/CeF3体系的放氢性能及机制

顾润, 张明, 王春阳, 黄维军, 柳东明()   

  1. 安徽工业大学材料科学与工程学院, 马鞍山 243002
  • 收稿日期:2015-11-04 出版日期:2016-04-10 发布日期:2016-01-24
  • 基金资助:
    国家自然科学基金(批准号: 51371008)资助

Dehydrogenation Property and Mechanism of 3LiBH4/CeF3System

GU Run, ZHANG Ming, WANG Chunyang, HUANG Weijun, LIU Dongming*()   

  1. School of Materials Science and Engineering Anhui University of Technology,Maanshan 243002, China
  • Received:2015-11-04 Online:2016-04-10 Published:2016-01-24
  • Contact: LIU Dongming E-mail:ldm_ahut@163.com
  • Supported by:
    † Supported by the National Natural Science Foundation of China(No.51371008)

摘要:

采用球磨法制备了3LiBH4/CeF3反应体系, 通过压力-组成-温度(PCT)测试仪、 X射线衍射仪(XRD)和傅里叶变换红外光谱仪(FTIR)研究了体系的放氢性能、 反应机制及性能改善机理. 结果表明, 3LiBH4/CeF3体系在295 ℃左右快速放氢, 总放氢量为4.1%(质量分数). 放氢过程中CeF3与LiBH4直接发生反应: 3LiBH4+CeF31/2CeB6+1/2CeH2+3LiF+11/2H2. 与纯LiBH4相比, 放氢热力学稳定性和表观活化能的降低是3LiBH4/CeF3体系放氢温度下降的主要原因.

关键词: 硼氢化锂, 氟化铈, 放氢性能, 放氢机制

Abstract:

The 3LiBH4/CeF3 reactive system was prepared by ball-milling treatment. Its dehydrogenation property and reaction as well as the property improvement mechanism were investigated by pressure-composition-temperature(PCT) analyser, X-ray diffractometer(XRD) and Fourier transform infrared spectrometer(FTIR). It was found that the 3LiBH4/CeF3 system fast released hydrogen at about 295 ℃ with about 4.1%(mass fraction) of hydrogen totally desorbed. During the dehydrogenation process, CeF3 reacted directly with LiBH4 according to the reaction 3LiBH4+CeF3 1/2CeB6+1/2CeH2+3LiF+11/2H2. In comparison with pristine LiBH4, the decrease in dehydrogenation thermodynamic stability and apparent activation energy are the main reasons for the declined dehydrogenation temperature of the 3LiBH4/CeF3 system.

Key words: LiBH4, CeF3, Dehydrogenation property, Dehydrogenation mechanism

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