SHOCK-INDUCED CHEMICAL-REACTIONS IN TITANIUM-SILICON POWDER MIXTURES OF DIFFERENT MORPHOLOGIES - TIME-RESOLVED PRESSURE MEASUREMENTS AND MATERIALS ANALYSIS
Nn. Thadhani et al., SHOCK-INDUCED CHEMICAL-REACTIONS IN TITANIUM-SILICON POWDER MIXTURES OF DIFFERENT MORPHOLOGIES - TIME-RESOLVED PRESSURE MEASUREMENTS AND MATERIALS ANALYSIS, Journal of applied physics, 82(3), 1997, pp. 1113-1128
The response of porous titanium (Ti) and silicon (Si) powder mixtures
with small, medium, and coarse particle morphologies is studied under
high-pressure shock loading, employing postshock materials analysis as
well as nanosecond, time-resolved pressure measurements. The objectiv
e of the work was to provide an experimental basis for development of
models describing shock-induced solid-state chemistry. The time-resolv
ed measurements of stress pulses obtained with piezoelectric polymer (
poly-vinyl-di-flouride) pressure gauges provided extraordinary sensiti
vity for determination of rate-dependent shock processes. Both techniq
ues showed clear evidence for shock-induced chemical reactions in medi
um-morphology powders, while fine and coarse powders showed no evidenc
e for reaction. It was observed that the medium-morphology mixtures ex
perience simultaneous plastic deformation of both Ti and Si particles.
Fine morphology powders show particle agglomeration, while coarse Si
powders undergo extensive fracture and entrapment within the plastical
ly deformed Ti; such processes decrease the propensity for initiation
of shock-induced reactions. The change of deformation mode between fra
cture and plastic deformation in Si powders of different morphologies
is a particularly critical observation. Such a behavior reveals the ov
erriding influence of the shock-induced, viscoplastic deformation and
fracture response, which controls the mechanochemical nature of shock-
induced solid-state chemistry. The present work in conjunction with ou
r prior studies, demonstrates that the initiation of chemical reaction
s in shock compression of powders is controlled by solid-state mechano
chemical processes, and cannot be qualitatively or quantitatively desc
ribed by thermochemical models. (C) 1997 American Institute of Physics
.