首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >In Situ Small-Angle Neutron Scattering Analysis of the Initial Deuteride Formation of Deuterium-Cerium Reactions under a Controlled Gas Flow
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In Situ Small-Angle Neutron Scattering Analysis of the Initial Deuteride Formation of Deuterium-Cerium Reactions under a Controlled Gas Flow

机译:原位小角中子散射分析在受控气流下氘 - 铈反应的初始氘形成

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摘要

"Real-life" metals inevitably form the oxide layer, thus leading to complex initial hydriding processes, which are still unclear because of the experimental challenges in monitoring elemental steps including surface sorption, permeation, and concentration of hydrogen. In this study, the deuteride precipitation caused by the concentration of deuterium was successfully measured by the in situ small-angle neutron scattering (SANS) method, which used a self-designed reaction chamber to give rise to the scattering signals of the surface structure. In addition, in the measurements of activated cerium samples, surface sorption of deuterium could be modified to form a constant flow in order to further explore the initial hydriding processes. The formation of deuterides was found to occur as soon as deuterium was absorbed in the samples with a thin oxide layer and the subsequent growth of deuterides depended on the amount of consumed D-2. However, the sample with a thick oxide layer showed the delayed precipitation of deuterides and the decelerated subsequent growth of deuterides without inhibiting the surface absorption of deuterium. The in situ SANS method showed the high sensitivity to the deuteride phase on the surface at a deuterium amount of 0.2 mu mol cm(-2) D-2 for cerium and a great potential in exploring the mechanism of early incipient stages of hydrogen reactions.
机译:“现实生活”金属不可避免地形成氧化物层,从而导致复杂的初始水合过程,这仍然不清楚,因为在包括表面吸附,渗透和氢浓度的情况下监测元素步骤的实验挑战。在该研究中,通过使用自行设计的反应室的原位小角中子散射(SAN)方法成功地测量由氘的浓度引起的氘沉淀,其使用自行设计的反应室产生表面结构的散射信号。另外,在活性铈样品的测量中,可以改变氘的表面吸附以形成恒定流动,以进一步探索初始水合过程。发现氘甲醚的形成在用薄氧化物层吸收氘中,并且随后氘化氘的随后生长依赖于消耗的D-2的量。然而,具有厚氧化物层的样品显示了氘氘的延迟沉淀和氘的后续生长而不抑制氘的表面吸收。原位SANS方法在铈的氘量为0.2μmmolcm(-2)d-2的表面上对表面的氘化相的高敏感性和探索氢反应的早期初期阶段的机制的巨大潜力。

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  • 作者单位

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Inst Nucl Phys &

    Chem Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Inst Nucl Phys &

    Chem Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Key Lab Neutron Phys Mianyang 621999 Sichuan Peoples R China;

    China Acad Engn Phys Inst Nucl Phys &

    Chem Mianyang 621999 Sichuan Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
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