Quantification of the rate of mass transfer in diagenetic and hydrothe
rmal systems requires a knowledge of the kinetics of mineral-fluid rea
ctions at elevated temperature and pressure and at chemical conditions
close to equilibrium. This communication describes an experimental st
udy of the reaction kinetics of laumontite, a Ca-zeolite, at 80, 120 a
nd 150-degrees-C, 50 MPa using batch (close to equilibrium) and flow (
far from equilibrium) experimental techniques in the-pH range 7-10. Fl
uid and mineral buffers were employed to constrain chemical conditions
during the experiments. The dissolution of laumontite is non-stoichio
metric, with Ca being preferentially removed from the laumontite struc
ture. SEM observations of reacted laumontite grains are consistent wit
h a surface controlled reaction mechanism. Dissolution rates obtained
by the batch and flow techniques showed good agreement. The dissolutio
n rate of laumontite is independent of hydrogen ion activity in the fl
uid phase at 80-degrees-C, but increases slightly with increasing hydr
ogen ion activity at 120 and 150-degrees-C. Measured dissolution rates
range from 3x10(-11) (80-degrees-C) to 1x10(-9) (150-degrees-C) molm-
2s-1 and are 10-50 times greater than that of heulandite at 25-degrees
-C. The activation energy of dissolution is almost-equal-to 58 kJmol-1
.