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Thermodynamic and Kinetic Destabilization of Magnesium Hydride Using Mg-In Solid Solution Alloys

机译:含镁固溶合金的氢化镁热力学和动力学失稳

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摘要

Efforts to thermodynamically destabilize magnesium hydride (MgH_2), so that it can be used for practical hydrogen storage applications, have been a difficult challenge that has eluded scientists for decades. This letter reports that MgH_2 can indeed be destabilized by forming solid solution alloys of magnesium with group Ⅲ and ⅣB elements, such as indium. Results of this research showed that the equilibrium hydrogen pressure of a Mg-0.1In alloy is 70% higher than that of pure MgH_2. The temperature at 1 bar hydrogen pressure (T_(1bar)) of Mg-0.1In alloy was reduced to 262.9 ℃ from 278.9 ℃, which is the T_(1bar) of pure MgH_2. Furthermore, the kinetic rates of dehydrogenation of Mg-0.1In alloy hydride doped with a titanium intermetallic (TiMn_2) catalyst were also significantly improved compared with those of MgH_2.
机译:努力使氢化镁(MgH_2)热力学不稳定,使其可用于实际的储氢应用,这是数十年来科学家们一直难以克服的挑战。这封信报道说,MgH_2的确可以通过与第Ⅲ和ⅣB族元素(如铟)形成镁的固溶合金而失稳。研究结果表明,Mg-0.1In合金的平衡氢压比纯MgH_2高70%。 Mg-0.1In合金在1 bar氢气压力下的温度(T_(1bar))从278.9℃降至262.9℃,这是纯MgH_2的T_(1bar)。此外,与MgH_2相比,掺杂金属间化合物(TiMn_2)的Mg-0.1In合金氢化物的脱氢动力学速率也得到了显着提高。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第30期|10982-10985|共4页
  • 作者单位

    Department of Metallurgical Engineering, The University of Utah, 135 South 1460 East, Room 412, Salt Lake City, Utah 84112-0114, United States;

    Department of Metallurgical Engineering, The University of Utah, 135 South 1460 East, Room 412, Salt Lake City, Utah 84112-0114, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South, Cass Avenue, Argonne, Illinois 60439,United States;

    X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, 9700 South, Cass Avenue, Argonne, Illinois 60439,United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:12:45

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