Oxidation of nano-sized aluminum powders

[Display omitted] •Weight gain measured in TG oxidation experiments was split between particles of different sizes.•Reaction kinetics obtained by isoconversion explicitly accounting for the effect of size distribution.•Activation energy is obtained as a function of oxide thickness for growth of amor...

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Veröffentlicht in:Thermochimica acta 2016-07, Vol.636, p.48-56
Hauptverfasser: Vorozhtsov, A.B., Lerner, M., Rodkevich, N., Nie, H., Abraham, A., Schoenitz, M., Dreizin, E.L.
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Sprache:eng
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Zusammenfassung:[Display omitted] •Weight gain measured in TG oxidation experiments was split between particles of different sizes.•Reaction kinetics obtained by isoconversion explicitly accounting for the effect of size distribution.•Activation energy is obtained as a function of oxide thickness for growth of amorphous alumina.•Oxidation mechanism for nanopowders remains the same as for coarser aluminum powders. Oxidation of aluminum nanopowders obtained by electro-exploded wires is studied. Particle size distributions are obtained from transmission electron microscopy (TEM) images. Thermo-gravimetric (TG) experiments are complemented by TEM and XRD studies of partially oxidized particles. Qualitatively, oxidation follows the mechanism developed for coarser aluminum powder and resulting in formation of hollow oxide shells. Sintering of particles is also observed. The TG results are processed to account explicitly for the particle size distribution and spherical shapes, so that oxidation of particles of different sizes is characterized. The apparent activation energy is obtained as a function of the reaction progress using model-free isoconversion processing of experimental data. A complete phenomenological oxidation model is then proposed assuming a spherically symmetric geometry. The oxidation kinetics of aluminum powder is shown to be unaffected by particle sizes reduced down to tens of nm. The apparent activation energy describing growth of amorphous alumina is increasing at the very early stages of oxidation. The higher activation energy is likely associated with an increasing homogeneity in the growing amorphous oxide layer, initially containing multiple defects and imperfections. The trends describing changes in both activation energy and pre-exponent of the growing amorphous oxide are useful for predicting ignition delays of aluminum particles. The kinetic trends describing activation energies and pre-exponents in a broader range of the oxide thicknesses are useful for prediction of aging behavior of aluminum powders.
ISSN:0040-6031
1872-762X
DOI:10.1016/j.tca.2016.05.003