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首页> 外文期刊>Shock Waves >SHOCK WAVES IN MOLECULAR SOLIDS - ULTRAFAST VIBRATIONAL SPECTROSCOPY OF THE FIRST NANOSECOND
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SHOCK WAVES IN MOLECULAR SOLIDS - ULTRAFAST VIBRATIONAL SPECTROSCOPY OF THE FIRST NANOSECOND

机译:分子固体中的电击波-第一个纳米的超快振动光谱

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摘要

A novel technique which uses a microfabricated shock target array assembly is described, where the passage of a shock front through a thin (0.5 mu m) polycrystalline layer and the subsequent unloading process is monitored in real time with ultrafast coherent Raman spectroscopy. Using a high repetition rate laser shock generation technique, high resolution, coherent Raman spectra are obtained in shocked anthracene and in a high explosive material, NTO, with time resolution of similar to 50 ps, Spectroscopic measurements are presented which yield the shock pressure (up to 5 GPa), the shock velocity (similar to 4 km/s), the shock front rise-time (t(r) < 25 ps), and the temperature (similar to 400 degrees C). A brief discussion is presented, how this new technique can be used to determine the Hugoniot, the equation of state, the entropy increase across the shock front, and monitor shock induced chemical reactions in real time. [References: 34]
机译:描述了一种使用微加工的冲击靶阵列组件的新颖技术,其中,通过超快相干拉曼光谱实时监测冲击前沿穿过薄的(0.5微米)多晶层的过程以及随后的卸载过程。使用高重复频率激光冲击发生技术,可以在震惊的蒽和高爆炸性材料NTO中获得高分辨率,相干的拉曼光谱,其时间分辨率接近50 ps,并提出了能产生冲击压力的光谱测量值(最高至5 GPa),冲击速度(类似于4 km / s),冲击前沿上升时间(t(r)<25 ps)和温度(类似于400摄氏度)。进行了简短的讨论,该新技术如何用于确定Hugoniot,状态方程,整个激波前沿的熵增加以及实时监视激波诱发的化学反应。 [参考:34]

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