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Incomplete reactions in nanothermite composites

机译:纳米热复合材料的不完全反应

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摘要

Exothermic reactions between oxophilic metals and transition/post transition metal-oxides have been well documented owing to their fast reaction time scales (≈10 μs). This article examines the extent of the reaction in nano-aluminum based thermite systems through a forensic inspection of the products formed during reaction. Three nanothermite systems (Al/CuO, Al/Bi_2O_3, and Al/ WO_3) were selected owing to their diverse combustion characteristics, thereby providing sufficient generality and breadth to the analysis. Microgram quantities of the sample were coated onto a fine platinum wire, which was resistively heated at high heating rates (≈10~5K/s) to ignite the sample. The subsequent products were captured/quenched very rapidly («500 [μs] in order to preserve the chemistry/morphology during initiation and subsequent reaction and were quantitatively analyzed using electron microscopy and focused ion beam cross-sectioning followed by energy dispersive X-ray spectroscopy. Elemental examination of the cross-section of the quenched particles shows that oxygen is predominantly localized in the regions containing aluminum, implying the occurrence of the redox reaction. The Al/CuO system, which has simultaneous gaseous oxygen release and ignition (T_(Ignition ≈ T_(oxygen Release)), shows a substantially lower oxygen content within the product particles as opposed to Al/Bi_2O_3 and Al/WO_3 thermites, which are postulated to undergo a condensed phase reaction (T_(Ignition) 《 T_(Oxygen Release)). An effective A1:0 composition for the interior section was obtained for all the mixtures, with the smaller particles generally showing a higher oxygen content than the larger ones. The observed results were further corroborated with the reaction temperature, obtained using a high-speed spectro-pyrometer, and bomb calorimetry conducted on larger samples (≈l5 mg). The results suggest that thermites that produce sufficient amounts of gaseous products generate smaller product particles and achieve higher extents of completion.
机译:亲氧性金属与过渡/过渡金属氧化物之间的放热反应由于其快速的反应时间范围(≈10μs)而得到了充分的证明。本文通过对反应过程中形成的产物进行法医检查,检查了纳米铝基铝热体系中的反应程度。由于其不同的燃烧特性,选择了三种纳米热液体系(Al / CuO,Al / Bi_2O_3和Al / WO_3),从而为分析提供了足够的通用性和广度。将微克量的样品涂在细铂丝上,将其以高加热速率(≈10〜5K / s)电阻加热以点燃样品。后续产物被快速捕获/猝灭(«500 [μs],以便保留引发和后续反应过程中的化学/形态),并使用电子显微镜和聚焦离子束横截面,然后进行能量色散X射线光谱法进行定量分析对淬火颗粒的横截面进行元素检查表明,氧主要分布在含铝区域,这意味着发生了氧化还原反应.Al / CuO系统具有同时释放和点燃气态氧气的功能(T_(点火≈T_(氧气释放)),与Al / Bi_2O_3和Al / WO_3铝热剂相比,产品颗粒中的氧含量低得多,后者假定会发生冷凝相反应(T_(点火)《 T_(氧气释放) )。对于所有混合物,均获得了有效的内部A1:0组成,较小的颗粒通常显示出较高的氧含量。更大的。观察到的结果进一步得到了反应温度的证实,反应温度是使用高速分光热度计获得的,并且对较大的样品(约15 mg)进行了炸弹量热。结果表明,产生足够量气态产物的铝热剂产生较小的产物颗粒,并达到较高的完井程度。

著录项

  • 来源
    《Journal of Applied Physics》 |2017年第5期|054307.1-054307.10|共10页
  • 作者单位

    Department of Chemical and Biomolecular Engineering and Department of Chemistry and Biochemistry, University of Maiyland, College Park, Maryland 20706, USA;

    Materials Measurement Science Division, National Institute of Standards and Technology, Gaithershurg, Maryland 20899, USA;

    Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA;

    Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA;

    Department of Chemical and Biomolecular Engineering and Department of Chemistry and Biochemistry, University of Maiyland, College Park, Maryland 20706, USA;

  • 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
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