Hydrogen pressures, ranging from 80 to 1 atm, were utilized to study t
he hydriding kinetics of small, well-shaped LaAl0.25Ni4.75 samples at
temperatures between 246 K and 281 K. The hydrogen absorption was moni
tored as a function of time at constant temperature and approximately
constant pressure. Either a shrinking core (sc) or a low-dimensional n
ucleation and growth (ng) models fit the experimental data. in one cas
e an interesting feature of thin cracked layer, consisting of bent fla
kes was revealed in a SEM micrograph of a partly hydrogenated sample.
This observation is examined in view of the above models. The pressure
dependence of the rate constants indicates an interface-controlled ph
ase transition as the hydride formation rate-determining step. The act
ivation energy for the hydriding process is estimated from Arrhenius p
lots of the reaction rates to be 0.25 eV/H atom. The results are compa
red with kinetic data of hydride formation in massive LaNi5 and powder
ed LaAl0.25Ni4.75 samples.