Vibrational Energy Transfer in High Explosives: Nitromethane

1995 ◽  
Vol 418 ◽  
Author(s):  
Xiaoyu Hong ◽  
Jeffrey R. Hill ◽  
Dana D. Dlott

AbstractTime resolved vibrational spectroscopy with picosecond tunable mid-infrared pulses is used to measure the rates and investigate the detailed mechanisms of multiphonon up-pumping and vibrational cooling in a condensed high explosive, nitromethane. Both processes occur on the ˜100 ps time scale under ambient conditions. The mechanisms involve sequential climbing or descending the ladder of molecular vibrations. Efficient intermolecular vibrational energy transfer from various molecules to the symmetric stretching excitation of NO2 is observed. The implications of these measurements for understanding shock initiation to detonation and the sensitivities of energetic materials to shock initiation are discussed briefly.

2010 ◽  
Vol 9 (2) ◽  
pp. 102-108 ◽  
Author(s):  
Tian-Xiang Xiang ◽  
Sheng Sun ◽  
Shun-Sheng Gong ◽  
Jia-Min Wang

2021 ◽  
Author(s):  
Neil Cole-Filipiak ◽  
Robert Knepper ◽  
Mitchell A. Wood ◽  
Krupa Ramasesha

Herein, we report on the sub-picosecond to sub-nanosecond vibrational energy transfer (VET) dynamics of the solid energetic material 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) using broadband, ultrafast infrared transient absorption spectroscopy. Experiments reveal VET occurring on three distinct timescales: sub-picosecond, 5 ps, and 200 ps. The ultrafast appearance of signal at all probed modes in the mid-infrared suggests strong anharmonic coupling of all vibrations in the solid whereas the long-lived evolution demonstrates that VET is incomplete, and thus thermal equilibrium is not attained, even on the hundred picosecond timescale. Mode-selectivity of the longest dynamics suggests coupling of the N–N and axial NO<sub>2</sub> stretching modes with the long-lived, excited phonon bath.


2021 ◽  
Author(s):  
Neil Cole-Filipiak ◽  
Robert Knepper ◽  
Mitchell A. Wood ◽  
Krupa Ramasesha

Herein, we report on the sub-picosecond to sub-nanosecond vibrational energy transfer (VET) dynamics of the solid energetic material 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) using broadband, ultrafast infrared transient absorption spectroscopy. Experiments reveal VET occurring on three distinct timescales: sub-picosecond, 5 ps, and 200 ps. The ultrafast appearance of signal at all probed modes in the mid-infrared suggests strong anharmonic coupling of all vibrations in the solid whereas the long-lived evolution demonstrates that VET is incomplete, and thus thermal equilibrium is not attained, even on the hundred picosecond timescale. Mode-selectivity of the longest dynamics suggests coupling of the N–N and axial NO<sub>2</sub> stretching modes with the long-lived, excited phonon bath.


2000 ◽  
Vol 112 (14) ◽  
pp. 6349-6354 ◽  
Author(s):  
G. Seifert ◽  
R. Zürl ◽  
T. Patzlaff ◽  
H. Graener

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