Ar. Pawley et al., VOLUME MEASUREMENTS OF ZOISITE AT SIMULTANEOUSLY ELEVATED PRESSURE AND TEMPERATURE, The American mineralogist, 83(9-10), 1998, pp. 1030-1036
Unit-cell parameters of zoisite, Ca2Al3Si3O12(OH), have been measured
at simultaneously high pressures and temperatures (up to 6.1 GPa and 8
00 degrees C) in a Walker-style multi-anvil apparatus at the synchrotr
on radiation source at Daresbury Laboratory, U.K. Measurements were ma
de in a series of heating cycles at increasing loads. Sample pressure,
measured using an internal NaCl standard, increased during heating. C
ell parameters vary smoothly with pressure and temperature; individual
expansivities and compressibilities vary in the order c > b > a. Isot
hermal bulk moduli were calculated from the volumes measured at 30, 20
0, 400, 600, and 800 degrees C by fitting the Murnaghan equation of st
ate to each isothermal data set. This assumes K' = 4. Ambient-pressure
volumes calculated from previous measurements of thermal expansivity
of zoisite were included in the Murnaghan fits. A linear fit of the bu
lk moduli with temperature gave values for the bulk modulus at 298 K,
K-298 = 125(3) Gpa, and its variation with temperature, partial deriva
tive K-T/partial derivative T = -0.029(6) GPa K-1. K-298 is slightly h
igher than the recent value for a single crystal in a diamond-anvil ce
ll, indicating a lower maximum pressure stability of zoisite than woul
d be calculated using that value. Our data allow zoisite volumes to be
calculated at P-T conditions relevant to the Earth and show that, in
a typical subduction zone, zoisite becomes more dense as subduction pr
oceeds, helping to stabilize it to high pressures.