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Catalytic effect of Mg2Ni and Mg12RE on MgH2 formation and decomposition

机译:Mg2Ni和Mg12RE对MgH2形成和分解的催化作用

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In this study, several binary and ternary as-cast Mg-Ni-RE alloys were subjected to an electrochemical hydriding process to determine the catalytic effect of intermetallic phases on MgH2 formation and decomposition. The alloys were electrochemically hydrided in a 6 mol/1KOH solution at 80 degrees C. To assess the catalytic effect of the Mg2Ni and Mg12RE phases on electrochemical hydriding performance, an optical emission spectrometer with glow discharge was employed. The temperature of dehydriding was observed by the temperature-programmed desorption technique. It was found that the only hydride formed after the electrochemical hydriding of all investigated alloys was MgH2. Both the Mg2Ni and Mg12RE phases support hydrogen absorption but in different manners. The Mg2Ni phase maximizes the hydrogen concentration beneath the surface of the binary alloys. In contrast, the Mg12RE phase decreases the maximum hydrogen surface concentration but supports inward hydrogen diffusion. The influence of the Mg12RE phase on hydrogen diffusion is most likely responsible for the reduction of the MgH2 decomposition temperature by more than 190 K compared to commercial MgH2. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在这项研究中,对几种二元和三元铸态Mg-Ni-RE合金进行了电化学氢化处理,以确定金属间相对MgH2形成和分解的催化作用。合金在80摄氏度下于6 mol / 1KOH溶液中进行电化学氢化。为了评估Mg2Ni和Mg12RE相对电化学氢化性能的催化作用,使用了具有辉光放电的光发射光谱仪。通过程序升温脱附技术观察脱水温度。已发现所有研究的合金进行电化学氢化后形成的唯一氢化物是MgH2。 Mg2Ni和Mg12RE相均支持氢吸收,但方式不同。 Mg2Ni相使二元合金表面下的氢浓度最大化。相反,Mg12RE相降低了最大氢表面浓度,但支持了向内的氢扩散。与商用MgH2相比,Mg12RE相对氢扩散的影响最有可能导致MgH2分解温度降低190 K以上。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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