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高能量富氮碳氮化物三聚氰酸三叠氮化物的高压研究

High pressure study of a highly energetic nitrogen-rich carbon nitride, cyanuric triazide.

作者信息

Laniel Dominique, Downie Laura E, Smith Jesse S, Savard Didier, Murugesu Muralee, Desgreniers Serge

机构信息

Laboratoire de physique des solides denses, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.

Department of Physics and Atmospheric Science, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada.

出版信息

J Chem Phys. 2014 Dec 21;141(23):234506. doi: 10.1063/1.4902984.

Abstract

Cyanuric triazide (CTA), a nitrogen-rich energetic material, was compressed in a diamond anvil cell up to 63.2 GPa. Samples were characterized by x-ray diffraction, Raman, and infrared spectroscopy. A phase transition occurring between 29.8 and 30.7 GPa was found by all three techniques. The bulk modulus and its pressure derivative of the low pressure phase were determined by fitting the 300 K isothermal compression data to the Birch-Murnaghan equation of state. Due to the strong photosensitivity of CTA, synchrotron generated x-rays and visible laser radiation both lead to the progressive conversion of CTA into a two dimensional amorphous C=N network, starting from 9.2 GPa. As a result of the conversion, increasingly weak and broad x-ray diffraction lines were recorded from crystalline CTA as a function of pressure. Hence, a definite structure could not be obtained for the high pressure phase of CTA. Results from infrared spectroscopy carried out to 40.5 GPa suggest the high pressure formation of a lattice built of tri-tetrazole molecular units. The decompression study showed stability of the high pressure phase down to 13.9 GPa. Finally, two CTA samples, one loaded with neon and the other with nitrogen, used as pressure transmitting media, were laser-heated to approximately 1100 K and 1500 K while compressed at 37.7 GPa and 42.0 GPa, respectively. In both cases CTA decomposed resulting in amorphous compounds, as recovered at ambient conditions.

摘要

氰尿酸三叠氮化物(CTA)是一种富氮含能材料,在金刚石对顶砧中被压缩至63.2吉帕。通过X射线衍射、拉曼光谱和红外光谱对样品进行了表征。所有这三种技术都发现了在29.8吉帕至30.7吉帕之间发生的相变。通过将300K等温压缩数据拟合到Birch-Murnaghan状态方程,确定了低压相的体积模量及其压力导数。由于CTA具有很强的光敏性,从9.2吉帕开始,同步加速器产生的X射线和可见激光辐射都会导致CTA逐渐转化为二维非晶态C=N网络。由于这种转化,随着压力的增加,从结晶CTA记录到的X射线衍射线越来越弱且越来越宽。因此,无法获得CTA高压相的明确结构。在高达40.5吉帕的压力下进行的红外光谱研究结果表明,高压下形成了由三唑分子单元构成的晶格。减压研究表明,高压相在减压至13.9吉帕时仍保持稳定。最后,将两个分别以氖气和氮气作为压力传递介质的CTA样品,在分别为37.7吉帕和42.0吉帕的压力下进行激光加热,加热温度分别约为1100K和1500K。在这两种情况下,CTA均发生分解,在环境条件下恢复时生成非晶态化合物。

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