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Improvement of hydrogen-storage properties of MgH_2 by Ni,LiBH_4, and Ti addition

机译:Ni,LiBH_4和Ti的添加改善MgH_2的储氢性能

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摘要

In this work, differently from our previous work, MgH_2 instead of Mg was used as a starting material. Ni, Ti, and LiBH_4 with a high hydrogen-storage capacity of 18.4 wt% were added. A sample with a composition of MgH_2-10Ni-2LiBH_4-2Ti was prepared by reactive mechanical grinding. MgH_2-10Ni-2LiBH_4-2Ti after reactive mechanical grinding contained MgH_2, Mg, Ni, TiH_(1.924), and MgO phases. The activation of MgH_2-10Ni-2LiBH_4-2Ti for hydriding and dehydriding reactions was not required. At the number of cycles, n = 2, MgH_2-10Ni-2LiBH_4-2Ti absorbed 4.09 wt% H for 5 min, 4.25 wt% H for 10 min, and 4.44 wt % H for 60 min at 573 K under 12 bar H_2. At n = 1, MgH_2-10Ni-2LiBH_4-2Ti desorbed 0.13 wt % H for 10 min, 0.54 wt% H for 20 min, 1.07 wt% H for 30 min, and 1.97 wt% H for 60 min at 573 K under 1.0 bar H_2. The PCT (Pressure-Composition-Temperature) curve at 593 K for MgH_2-10Ni-2LiBH_4-2Ti showed that its hydrogen-storage capacity was 5.10 wt%. The inverse dependence of the hydriding rate on temperature is partly due to a decrease in the pressure differential between the applied hydrogen pressure and the equilibrium plateau pressure with the increase in temperature. The rate-controlling step for the dehydriding reaction of the MgH_2-10Ni-2LiBH_4-2Ti at n = 1 was analyzed.
机译:在这项工作中,与我们以前的工作不同,MgH_2代替了Mg作为起始原料。添加具有18.4重量%的高储氢容量的Ni,Ti和LiBH_4。通过反应机械研磨制备具有MgH_2-10Ni-2LiBH_4-2Ti组成的样品。反应性机械研磨后的MgH_2-10Ni-2LiBH_4-2Ti包含MgH_2,Mg,Ni,TiH_(1.924)和MgO相。不需要为了氢化和脱水反应而活化MgH_2-10Ni-2LiBH_4-2Ti。在周期数n = 2时,MgH_2-10Ni-2LiBH_4-2Ti在12 bar H_2下在573 K下吸收4.09 wt%H持续5 min,4.25 wt%H持续10 min,以及4.44 wt%H持续60 min。在n = 1时,MgH_2-10Ni-2LiBH_4-2Ti在1.0的573 K下脱附了0.13 wt%的H 10分钟,0.54 wt%的H 20分钟,1.07 wt%的H 30分钟和1.97 wt%的H 60分钟。 H_2条。 MgH_2-10Ni-2LiBH_4-2Ti在593 K下的PCT(压力-温度-温度)曲线表明,其储氢能力为5.10 wt%。氢化率与温度成反比,部分原因是随着温度的升高,施加的氢气压力和平衡平台压力之间的压力差减小。分析了在n = 1时MgH_2-10Ni-2LiBH_4-2Ti脱水反应的速率控制步骤。

著录项

  • 来源
    《International journal of hydrogen energy》 |2013年第4期|1910-1917|共8页
  • 作者单位

    Diuision of Advanced Materials Engineering, Research Center of Advanced Materials Development, Engineering Research Institute,Chonbuk National Uniuersity, 567 Baefeje-daero, Deofejin-gu, Jeonju 561-756, South Korea;

    Department of Materials Engineering, Graduate School, Chonbuk National Uniuersity, 567 Baefeje-daero, Deofejin-gu, Jeonju 561-756,South Korea;

    Thin film Technology laboratory, School of Chemical Engineering, Chonbufe National Uniuersity, 567 Baefeje-daero, Deofejin-gu,Jeonju 561-756, South Korea;

    Diuision of Advanced Materials Engineering, Research Center of Advanced Materials Development, Engineering Research Institute,Chonbuk National Uniuersity, 567 Baefeje-daero, Deofejin-gu, Jeonju 561-756, South Korea;

    Korea Energy Materials Ltd., 409 Daegu Technoparfe, 1-11 Hosan-Dong, Dalseo-Gu, Daegu 704-230, South Korea;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    starting material MgH_2; Ni,LiBH_4,and Ti addition; reactive mechanical grinding; activation; Mg_2Ni formation;

    机译:起始原料MgH_2;Ni;LiBH_4和Ti的添加;反应机械研磨;活化;Mg_2Ni的形成;
  • 入库时间 2022-08-18 00:27:38

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