Comparison Of Post-Detonation Combustion In Explosives Incorporating Aluminum Nanoparticles: Influence Of The Passivation Layer
JOURNAL OF APPLIED PHYSICS(2013)
Abstract
Aluminum nanoparticles and explosive formulations that incorporate them have been a subject of ongoing interest due to the potential of aluminum particles to dramatically increase energy content relative to conventional organic explosives. We have used time-resolved atomic and molecular emission spectroscopy to monitor the combustion of aluminum nanoparticles within the overall chemical dynamics of post-detonation fireballs. We have studied the energy release dynamics of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) charges incorporating three types of aluminum nanoparticles: commercial oxide-passivated nanoparticles, oleic acid-capped aluminum nanoparticles (AlOA), and nanoparticles in which the oxide shell of the particle has been functionalized with an acrylic monomer and copolymerized into a fluorinated acrylic matrix (AlFA). The results indicate that the commercial nanoparticles and the AlFA nanoparticles are oxidized at a similar rate, while the AlOA nanoparticles combust more quickly. This is most likely due to the fact that the commercial nano-Al and the AlFA particles are both oxide-passivated, while the AlOA particles are protected by an organic shell that is more easily compromised than an oxide layer. The peak fireball temperatures for RDX charges containing 20 wt. % of commercial nano-Al, AlFA, or AlOA were similar to 3900 K, similar to 3400 K, and similar to 4500 K, respectively. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4790159]
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Key words
aluminum,chemical reactions,copolymers,formulations,combustion,monomers,emission spectra,explosives,energy transfer,oxidation,acrylic resins,copolymerization,nanoparticles
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