Isothermal compression of low-cordierite to 30 kbar (25° C)

The compression of cordierite (Mg, Fe)₂Al₄Si₅O₁₈·n (H₂O, CO₂; Na⁺, K⁺) has been studied up to 30 kbar (25° C) by volumetric measurements with a piston cylinder apparatus and by X-ray measurements with a diamond-anvil cell. Natural cordierite of intermediate Mg-Fe composition and synthetic Mg-cordierite served as samples. Two discontinuities at 2.2±0.3 and 9.0±0.6 kbar which are correlated with very small volume changes (0.3?0.05%) have been found. The X-ray data indicate, however, no symmetry change of the crystal structure. The two discontinuities are interpreted as phase transitions. The two discontinuities establish three pressure dependent phases referred to as low-pressure (LP)-, first high-pressure (HP1)- and second high-pressure (HP2)-phase. The gross compressibility of cordierite decreases from 1.1 Mbar^?1 at low pressure to 0.7 Mbar^?1 at 30 kbar for the intermediate Mg-Fe cordierite, and to 0.4 Mbar^?1 for Mg-cordierite. Depending on the pressure transmitting medium used in the two different compression techniques, two kinds of compression behavior are observed for cordierite. The measurements with the piston cylinder apparatus where lead is used as quasihydrostatic pressure medium indicate normal compression properties. The X-ray data, however, obtained with the diamond anvil cell where a methanol-ethanol mixture provides hydrostatic pressure conditions yield, e.g. for the HP1-phase a dramatic decrease in compressibility to almost zero. IR-spectra from samples of augmenting experiments with methanol, deuteromethanol and D₂O as pressure media indicate that pressure media of which the molecule size is comparable with the dimensions of the cordierite channels may be incorporated in the structure. This suggests that under such hydrostatic conditions the compression of cordierite is modified by a structure internal component which is acting via the channel system.