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Poisoning effect of oxygen on hydrogenation performance of a Zr-V-Ni Laves phase alloy

机译:氧中毒对Zr-V-Ni Laves相合金氢化性能的影响

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摘要

Zr-based Laves phase alloys have been considered as suitable getter materials for hydrogen isotopes recovery, storage and delivery and received considerable attention during past decades. This work focuses on hydrogenation performance of a pseudo-binary Zr-V-Ni Laves phase alloy with the composition of Zr(V0.95Ni0.05)(2) after pre-exposure in different contents of O-2. It is found that introduced pure oxygen can be rapidly absorbed by the fully activated Zr(V(0.95)Ni(0.052)n alloy within 40 s. All of the experimental samples pre-exposed in oxygen consist dominant C15 type ZrV2 Laves phase and minor Zr3V3O oxides. With the further increase the oxygen pressure to 4.0 kPa in specimen chamber, Bragg peaks of Zr2V, V-rich BCC solid solution phase and ZrO2 phase, including baddeleyite (alpha-ZrO2) with monoclinic structure and a small amount of tazheranite (gamma-ZrO2) with cubic structure are observed in addition to the dominant ZrV2 and minor Zr3V3O phases. Meanwhile, it can be seen that the lattice parameter of cubic C15 type ZrV2 calculated from Rietveld refinement increases from 7.402 to 7.432 angstrom with the increase of O-2 content and the corresponding unit cell volume increases 0.86 vol.% as the O-2 pressure from 1.0 to 4.0 kPa, which indicates more oxygen atoms have been dissolved into the lattice of ZrV2. All of the oxygen poisoned Zr(V0.95Ni0.05)(2) alloys can absorb hydrogen and the capacity decreases from 3.39 to 2.22 H A(-1) with the increase of oxygen pressure from 1.0 to 4.0 kPa, comparing with the maximum hydrogen storage capacity (4.34 H A(-1)) of the fully activated fresh alloy. The existence of oxygen is found to decrease both capacity and kinetics of Zr(V0.95Ni0.05)(2) by forming passivation layer oxides which block the dissociation of H-2 molecule on the surface. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:Zr基Laves相合金被认为是用于氢同位素回收,储存和输送的合适的吸气材料,在过去的几十年中受到了广泛的关注。这项工作的重点是在不同含量的O-2下预暴露Zr(V0.95Ni0.05)(2)组成的准二元Zr-V-Ni Laves相合金的氢化性能。发现引入的纯氧可以在40 s内被完全活化的Zr(V(0.95)Ni(0.052)n合金迅速吸收,所有预先暴露在氧气中的实验样品均由占主导地位的C15型ZrV2 Laves相和次要的Zr3V3O氧化物。随着样品室中的氧气压力进一步升高至4.0 kPa,Zr2V,富V的BCC固溶体相和ZrO2相的布拉格峰,包括具有单斜晶结构的斜方晶石(α-ZrO2)和少量的Tazheranite(除了主要的ZrV2相和次要的Zr3V3O相以外,还观察到立方结构的γ-ZrO2),同时可以看出,随着O的增加,由Rietveld精炼计算出的立方C15型ZrV2的晶格参数从7.402增大到7.432埃O-2压力从1.0到4.0 kPa时-2含量和相应的晶胞体积增加0.86 vol。%,这表明更多的氧原子已溶解到ZrV2的晶格中。所有氧中毒的Zr(V0.95Ni0 。 05)(2)合金可以吸收氢,并且随着氧气压力从1.0 kPa增加到4.0 kPa,容量从3.39降低到2.22 HA(-1),而最大氢存储容量(4.34 HA(-1))完全活化的新鲜合金。发现氧的存在通过形成钝化层氧化物来阻止Zr(V0.95Ni0.05)(2)的容量和动力学,钝化层氧化物会阻止H-2分子在表面解离。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2016年第42期|19114-19122|共9页
  • 作者单位

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

    Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China;

  • 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

    Laves phase alloy; Hydrogen storage; Gaseous impurities; Poisoning effect; Kinetics;

    机译:Laves相合金储氢气态杂质中毒作用动力学;

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