均相化学沉积含镁储氢材料的制备及其氢化性能

Hayao Imamura, Yoshihiro Usui, Masaharu Takashima
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引用次数: 12

摘要

使用金属镁在液氨中的溶解使得能够制备新型的含镁储氢材料。使用金属蒸气技术在77K下将镁原子分散在氨基质中,产生溶解的镁金属在液氨中的均匀溶液。使用氨的溶剂能力制备的储氢材料有两种类型。(i) 镁从溶解的镁在液氨中的溶液中结晶出来;结晶是在存在或不存在催化活性镍粉末(分别为Mg-Ni或Mg)的情况下进行的;(ii)通过用溶液(称为MgAC)浸渍活性碳(AC)载体,使镁高度分散在活性碳(DC)载体上。使用先前负载有催化活性镍的AC,样品的制备进一步扩展到包括二元体系(Mg-NiAC)。结合制备方法对这些样品进行了研究。镁样品对氢吸收极为活跃。对于Mg-Ni和Mg-NiAC样品,镍的增加显著加速了母体镁金属的初始氢化速率。
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Preparation and hydriding properties of magnesium-containing hydrogen storage materials chemically deposited from a homogeneous phase

Use of the dissolution of magnesium metal in liquid ammonia enabled novel magnesium-containing hydrogen storage materials to be prepared. The dispersion of magnesium atoms in ammonia matrices at 77 K using a metal vapour technique gave rise to a homogeneous solution of dissolved magnesium metal in liquid ammonia. Hydrogen storage materials prepared using the solvent power of ammonia are of two types. (i) Magnesium was crystallized out of the solution of dissolved magnesium in liquid ammonia; the crystallization was carried out in the presence or absence of catalytically active nickel powders (respectively Mg-Ni or Mg); (ii) Magnesium was highly dispersed on an active carbon (AC) support by impregnating the AC with the solution (referred to as MgAC). Using AC on which catalytically active nickel had been previously supported, the preparation of samples was further extended to include binary systems (Mg-NiAC). These samples were investigated in connection with the preparation methods. The magnesium samples were extremely active toward hydrogen absorption. For the Mg-Ni and Mg-NiAC samples an increase in nickel markedly accelerated the initial hydriding rates of the parent magnesium metal.

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