Impact ignition and combustion of micron-scale aluminum particles pre-stressed with different quenching rates

Pre-stressing aluminum (Al) particles by annealing and quenching alters dilatational strain and is linked to increased particle reactivity. The quenching rate associated with pre-stressing is a key parameter affecting the final stress state within the Al particle, with faster quenching rates theoretically favoring a higher, more desirable stress state. Micron scale Al particles are annealed to 573 K, then quenched at different rates (i.e., 200 and 900 K/min), mixed with bismuth oxide (Bi2O3), and the Al + Bi2O3 mixtures are examined under low-velocity, drop-weight impact conditions. Both quenching rates showed increased impact ignition sensitivity (i.e., between 83% and 89% decrease in ignition energy). However, the slower quenching rate showed a 100% increase in pressurization rate compared to untreated particles, while the faster quenching rate showed a 97% increase in peak pressure, indicating that these two quenching rates affect Al particles differently. Surprisingly, synchrotron X-ray diffraction data show that the 200 K/min quenched particles have a higher dilatational strain than the untreated particles or the 900 K/min quenched particles. Results are rationalized with the help of a simple mechanical model that takes into account elastic stresses, creep in the alumina shell, and delamination of shell from the core. The model predicts that Al powder quenched at 200 K/min did not experience delamination. In contrast, Al quenched at 900 K/min did not have creep but does have delamination, and under impact, delamination led to major fracture, greater oxygen access to the core, and significant promotion of reaction. Thus, the increase in quenching rate and shell-core delamination are more important for the increase in Al reactivity than pre-stressing alone

Internal stresses in pre-stressed micron-scale aluminum core-shell particles and their improved reactivity

Dilatation of aluminum (Al) core for micron-scale particles covered by alumina (Al2O3) shell was measured utilizing x-ray diffraction with synchrotron radiation for untreated particles and particles after annealing at 573 K and fast quenching at 0.46 K/s. Such a treatment led to the increase in flame rate for Al + CuO composite by 32% and is consistent with theoretical predictions based on the melt-dispersion mechanism of reaction for Al particles. Experimental results confirmed theoretical estimates and proved that the improvement of Al reactivity is due to internal stresses. This opens new ways of controlling particle reactivity through creating and monitoring internal stresses

Influence of Aluminum Passivation on the Reaction Mechanism: Flame Propagation Studies

Currently, two main known mechanisms of aluminum (Al) nanoparticle reaction are discussed in the literature, namely those based on diffusion through an oxide shell and melt-dispersion. The two mechanisms lead to opposite predictions in nanoparticle design. The diffusion mechanism suggests that the reduction or complete elimination of the oxide shell will increase Al reactivity, whereas the meltdispersion mechanism suggests an increase in initial oxide thickness up to an optimal value. The goal of this study is to perform critical experiments in a confined flame tube apparatus to compare these two predictions. Specifically, the flame propagation rates of perfluoroalkyl carboxylic acid (C 13F27COOH)-treated Al nanoparticles with and without an alumina shell were measured. Results show that when there is no alumina passivation shell encasing the Al core, the flame rate decreases by a factor of 22-95 and peak pressure deceases by 3 orders of magnitude, in comparison with the Al particles with an oxide shell. These results imply that the melt-dispersion reaction mechanism is responsible for high flame propagation rates observed in these confined tube experiments

High-density amorphous phase of silicon carbide obtained under large plastic shear and high pressure

In situ x-ray diffraction study of the hexagonal 6H SiC under pressure and shear in rotational diamond anvil cell is performed that reveals phase transformation to the new high-density amorphous (hda) phase SiC. In contrast to known low-density amorphous SiC, hda-SiC is promoted by pressure and unstable under pressure release. The critical combination of pressure ∼30 GPa and rotation of an anvil of 2160° that causes disordering is determined