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Additive effect of alkaline earth metals on ammonia decomposition reaction over Ni/Y2O3 catalysts

机译:碱土金属对Ni / Y 2 O 3催化剂氨分解反应的添加作用

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摘要

( Recently, ammonia has attracted much attention as a promising hydrogen carrier due to various advantages for on-site hydrogen generation. In this study, Ni/Y2O3 catalysts modified by alkaline earth metals were prepared and their catalytic activity for ammonia decomposition was examined. The addition of a small amount of Sr or Ba species remarkably improved the performance of Ni/Y2O3, while the Mg- and Ca- modification were not effective. The XRD analysis elucidated that the composite oxides consisting of alkaline earth metals and nickel were formed in the as-calcined Sr- and Ba-modified Ni/Y2O3 catalysts, and were decomposed by the reduction treatment. This suggested that the Sr and Ba components were located in the vicinity of Ni particles, resulting in the strong interaction with the Ni species. The NH3-temperature programmed surface reaction measurement revealed that the desorption of nitrogen atoms strongly-adsorbed on the Ni surface has terminated at lower temperatures over the Sr-and Ba-modified catalysts than over the others. This characteristic desorption behavior would be mainly attributed to the enhancement of the electron density in the Ni metal by the strong basic property of Sr and Ba components and the strong Ni-Sr and Ni-Ba interaction. Considering the nitrogen desorption step was kinetically significant, this change in the electronic state of the Ni surface should be responsible for the promotion effect of the Sr-and Ba-modification.
机译:(最近,由于现场氢气产生的各种优点,氨是由于现场氢气产生的各种优点而引起了许多关注。在该研究中,制备由碱土金属改性的Ni / Y 2 O 3催化剂,并检查它们的氨分解的催化活性。该添加少量Sr或BA物种显着提高了Ni / Y 2 O 3的性能,而Mg-和Ca-改性无效。XRD分析阐明了由碱土金属和镍组成的复合氧化物如煅烧的SR-和BA改性的Ni / Y 2 O 3催化剂,并通过还原处理分解。这表明Sr和Ba组分位于Ni颗粒附近,导致与Ni种类的强相互作用。该NH 3温度编程的表面反应测量显示,在Ni表面上强烈吸附的氮原子的解吸在较低温度下终止SR-and Ba改性催化剂比其他催化剂。这种特征解吸行为主要归因于通过Sr和Ba组分的强基本性能和强Ni-Sr和Ni-Ba相互作用来增强Ni金属中的电子密度。考虑到氮沉积步骤是重要的,Ni表面的电子状态变化应负责SR和BA改性的促进效果。

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  • 来源
    《RSC Advances》 |2016年第88期|共7页
  • 作者单位

    Kyoto Univ Dept Energy &

    Hydrocarbon Chem Grad Sch Engn Nishikyo Ku Kyoto 6158510 Japan;

    Kyoto Univ Dept Energy &

    Hydrocarbon Chem Grad Sch Engn Nishikyo Ku Kyoto 6158510 Japan;

    Kyoto Univ Dept Energy &

    Hydrocarbon Chem Grad Sch Engn Nishikyo Ku Kyoto 6158510 Japan;

    Kyoto Univ Dept Energy &

    Hydrocarbon Chem Grad Sch Engn Nishikyo Ku Kyoto 6158510 Japan;

    Kyoto Univ Dept Energy &

    Hydrocarbon Chem Grad Sch Engn Nishikyo Ku Kyoto 6158510 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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