Abstract

Nanoenergetic materials have some advantages against micrometric and bulk materials. This is due to enhanced surface area and intimacy between reactive components that leads to increase in the reaction rate and decrease in the ignition delay. However, till now there is very limited understanding of fundamental physical processes that control reaction and combustion wave propagation. The heat transfer in the case of nanoparticles is characterized some specifi c features which determine the sometime unusual ignition and combustion behavior. The paper is focused on discussing the ignition and combustion of nano Al particles in conditions of a shock tube and in a plastic tube. It is shown that tiny metal particles at high temperatures and pressures become “thermally isolated” from ambient gas environment and experimentally observed ignition delays may be two order magnitudes longer of those calculated without accounting real energy accommodation and sticking coeffi cients. When going to conditions of reaction propagation in a plastic tube, some different ways for heat transfer have to be carefully analyzed. Actually, there are no evidences for unique dominant process which may provide propagation of combustion wave with observed speed through the loose Al/CuO particles mixture. It can be stated that the process comprises 2 stages with very fast ignition, releasing large amount of heat and propelling hot gas and condensed material in direction of unreacted mixture followed by more slow reaction of remaining metal with evolved in oxide decomposition oxygen. Common conclusion is that further detailed studying the fundamental properties of nanoenergetics materials and their reaction behavior may open ways for purposed control of the combustion behavior and for effective use of nanoenergetics in practical applications.

Highlights

  • The works in nanochemistry opened a bottom-up approach in the architecture of matter, from the atom to millimeter scale

  • In the case of low density samples of loosely-packed nanoenergetic material the high “burning rate” reaching 1000 m/s was experimentally recorded while for densely-packed samples a moderate rate was recorded comprising ≈ 1 m/sec which was typical of the systems with micron-sized powders

  • These results indicate that observed very high velocities of luminescent front propagation during combustion of nanoenergetic systems in thin channels are probably caused by the hot gas exhaustion but not by the kinetics of heterogeneous chemical reactions in nanosystems

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Summary

Introduction

The works in nanochemistry opened a bottom-up approach in the architecture of matter, from the atom to millimeter scale. Another example of possible effects of gas phase chemistry and difficulties of interpretation of experimental data can be demonstrated while analyzing the displacement of the luminescent front in the plastic tubes filled with energetic material It was shown in experiments [4] with loosely-packed aluminum/copper oxide (Al/CuO) nano thermites in acrylic burn tube, composed of fully and partially filled sections, that the velocity of the luminous front in partially filled region approached 1000 m/s and was about 600 m/s in the filled region. In the case of low density samples of loosely-packed nanoenergetic material the high “burning rate” reaching 1000 m/s was experimentally recorded while for densely-packed samples a moderate rate was recorded comprising ≈ 1 m/sec which was typical of the systems with micron-sized powders These results indicate that observed very high velocities of luminescent front propagation during combustion of nanoenergetic systems in thin channels are probably caused by the hot gas exhaustion but not by the kinetics of heterogeneous chemical reactions in nanosystems. The present paper illustrates this issue on the examples of fast reaction of individual Al particles in a shock tube and Al/CuO mixtures in a plastic burn tube

Ignition and combustion of nanoAl in a shock tube
Ignition and combustion of nanoAl in a plastic burn tube
Findings
Conclusions
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