Thermal interaction of inert additives in energetic materials

The inclusion of insulating inert particles in energetic materials has shown burning rate enhancement in certain cases, contradictory to the traditional laminar flame theory. Flame front corrugation that increases the reaction front area observed at micron to sub-millimeter scales was proposed previously to explain the phenomenon. However, a recent simulation study observed a significant temperature gradient within the inert particle, implying that the residence time of the inert particle in the flame front could play a role in the thermal interaction between additives and surrounding energetic materials. In this work, we tested these hypotheses by employing a high-speed microscopic imaging system to quantify the burning rate and flame morphology of Al/CuO nanothermites with various SiO2 2 particle sizes and mass loading. Additionally, we performed flame propagation simulations to quantify the thermal interactions between the energetic materials and the embedded single inert particle. The experimental results show that the burning rate depends on the particle size as well as mass loading. Specifically, as the SiO2 2 particle size increases from 100 nm to 100 mu m, the burning rate is enhanced by 26% at a mass loading of 7.5%. Further computational studies reveal that flame corrugation may not be the sole factor to alter the burning rate. Non-dimensional analyses show that energy absorption and temperature non-uniformity in inert particles have strong correlations with particle diameter. When the characteristic time of heating the inert particle is shorter than the flame residence time, the inert particle acts as a heat sink, leading to a negative impact on burning rates due to the heat removal from the surrounding energetic materials. This reveals that both flame front morphology and heat transfer, altered by inert additives with different particle sizes, play a key role in burning rates.