Internal stress plasticity occurs when a small external stress biases inter
nal mismatch strains produced by, e.g., phase transformation or thermal exp
ansion mismatch. At small applied stresses, this deformation mechanism is c
haracterized by a deformation rate which is proportional to the applied str
ess and is higher than for conventional creep mechanisms. In this work. we
demonstrate the operation of internal stress plasticity due to internal che
mical stresses produced by chemical composition gradients. We subject speci
mens of beta -phase Ti-6Al-4V to cyclic charging/discharging with hydrogen
(by cyclic exposure of specimens to gaseous H-2), under a small external te
nsile stress. As expected for internal stress plasticity, the average strai
n rate during chemical cycles at 1030 degreesC is larger than for creep at
constant composition hydrogen-free or -saturated), and a linear stress depe
ndence is observed at small applied stresses. Additionally, we present an a
nalytical model which couples elastic and creep deformation with a transien
t diffusion problem, wherein the diffusant species induces swelling of the
host lattice. Without the use of any adjustable parameters, the model accur
ately predicts both the observed strain evolution during hydrogen cycling o
f Ti-6Al-4V and the measured stress dependence of the deformation. (C) 2001
Acta Materialia Inc. Published by Elsevier Science Ltd. All rights reserve
d.