Dresselhaus-Cooper Leora E, Martynowych Dmitro J, Zhang Fan, Tsay Charlene, Ilavsky Jan, Wang SuYin Grass, Chen Yu-Sheng, Nelson Keith A
Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Institute for Soldier Nanotechnology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
J Phys Chem A. 2020 Apr 30;124(17):3301-3313. doi: 10.1021/acs.jpca.9b07637. Epub 2020 Apr 15.
We demonstrate a strongly thresholded response in cyclotrimethylene trinitramine (RDX) when it is cylindrically shocked using a novel waveguide geometry. Using ultrafast single-shot multi-frame imaging, we demonstrate that <100 μm diameter single crystals of RDX embedded in a polymer host deform along preferential planes for >100 ns after the shock first arrives in the crystal. We use in situ imaging and time-resolved photoemission to demonstrate that short-lived chemistry occurs with complex deformation pathways. Using scanning electron microscopy and ultra-small-angle X-ray scattering, we demonstrate that the shock-induced dynamics leave behind porous crystals, with pore shapes and sizes that change significantly with shock pressure. A threshold pressure of ∼12 GPa at the center of convergence separated the single-mode planar crystal deformations from the chemistry-coupled multi-plane dynamics at higher pressures. Our observations indicate preferential directions for deformation in our cylindrically shocked system, despite the applied stress along many different crystallographic planes.
当使用新型波导几何结构对环三亚甲基三硝胺(RDX)进行柱面冲击时,我们展示了其强烈的阈值响应。通过超快单次多帧成像,我们证明嵌入聚合物主体中的直径小于100μm的RDX单晶在冲击首次到达晶体后,会沿着优先平面变形超过100 ns。我们使用原位成像和时间分辨光发射来证明,在复杂的变形路径中会发生短寿命化学反应。通过扫描电子显微镜和超小角X射线散射,我们证明冲击诱导的动力学过程会留下多孔晶体,其孔隙形状和大小会随冲击压力而显著变化。在汇聚中心处约12 GPa的阈值压力将单模平面晶体变形与更高压力下化学耦合的多平面动力学区分开来。我们的观察结果表明,尽管沿许多不同晶面施加了应力,但在我们的柱面冲击系统中仍存在优先的变形方向。