氢化镁
氢气储存
氢化物
球磨机
解吸
吸附
结构精修
差示扫描量热法
动力学
镁
氢
化学
材料科学
焓
分析化学(期刊)
无机化学
结晶学
冶金
晶体结构
物理化学
热力学
吸附
色谱法
有机化学
物理
量子力学
作者
Jacques Huot,Guoxian Liang,S. Boily,A. Van Neste,Robert Schulz
标识
DOI:10.1016/s0925-8388(99)00474-0
摘要
It has recently been discovered that energetic ball milling of hydrides can improve their hydrogen sorption properties significantly. In this work, we present a systematic study of structural modifications and hydrogen absorption–desorption kinetics of ball-milled magnesium hydride. Structural investigations showed that after only 2 h of milling, a metastable orthorhombic (γ) magnesium hydride phase is formed. A Rietveld analysis of the X-ray diffraction spectrum of the 20 h milled sample gave a proportion of 74 wt.% MgH2, 18 wt.% γ MgH2 and 8 wt.% MgO. The hydrogen capacity and sorption kinetics were measured before and after milling. We found that the sorption kinetics are much faster for the milled sample compared to the unmilled one. This explains the fact that the hydrogen desorption temperature of the ball-milled sample as measured by pressured differential scanning calorimetry (PDSC), is reduced by 64 K compared to the unmilled sample. There is no significant change of the storage capacity upon milling and the absorption plateau pressure does not change. From the desorption curves, the activation energy was deduced. The milling also increased the specific surface area. This was confirmed by SEM micrographs and BET measurements. Possible mechanisms explaining the improved kinetics are presented.
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