Abstract
A dual framing camera system was coupled with custom-designed ultrafast imaging spectrometer optics to yield simultaneous imaging and imaging spectroscopy of extremely short detonation interaction events in reactive materials. For short exposures of 100 ns or less, spectral resolutions of 2.4 Å are achievable, allowing for time-resolved identification of key intermediate species evolving from prompt reaction. Under some circumstances, emission can be fit to a local emission temperature, assuming the optically thin limit. Applications to reactive metal systems involving aluminum, magnesium, titanium, boron, and silicon are demonstrated.
Original language | English (US) |
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Pages (from-to) | 78-86 |
Number of pages | 9 |
Journal | Applied Spectroscopy |
Volume | 71 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2017 |
Keywords
- Detonation chemistry
- energetic materials spectroscopy
- optical and spectroscopic imaging array
- reactive materials spectroscopy
- simultaneous imaging and spectroscopy
- spatially resolved spectroscopy
- temporally resolved spectroscopy
- ultrafast imaging spectrometer
ASJC Scopus subject areas
- Instrumentation
- Spectroscopy