Ultrahydrous stishovite from high-pressure hydrothermal treatment of SiO2
Author(s) -
Kristina Spektor,
Johanylén,
Emil Stoyanov,
Alexandra Navrotsky,
R. L. Hervig,
Kurt Leinenweber,
Gregory P. Holland,
Ulrich Häußermann
Publication year - 2011
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1117152108
Subject(s) - stishovite , coesite , hydrothermal circulation , anhydrous , rutile , mineral , silicon , chemistry , crystallography , infrared spectroscopy , mineralogy , analytical chemistry (journal) , calorimetry , materials science , geology , quartz , organic chemistry , thermodynamics , subduction , seismology , eclogite , composite material , paleontology , tectonics , physics
Stishovite (SiO2 with the rutile structure and octahedrally coordinated silicon) is an important high-pressure mineral. It has previously been considered to be essentially anhydrous. In this study, hydrothermal treatment of silica glass and coesite at 350–550 °C near 10 GPa produces stishovite with significant amounts of H2 O in its structure. A combination of methodologies (X-ray diffraction, thermal analysis, oxide melt solution calorimetry, secondary ion mass spectrometry, infrared and nuclear magnetic resonance spectroscopy) indicate the presence of 1.3 ± 0.2 wt % H2 O and NMR suggests that the primary mechanism for the H2 O uptake is a direct hydrogarnet-like substitution of 4H+ for Si4+ , with the protons clustered as hydroxyls around a silicon vacancy. This substitution is accompanied by a substantial volume decrease for the system (SiO2 + H2 O), although the stishovite expands slightly, and it is only slightly unfavorable in energy. Stishovite could thus be a host for H2 O at convergent plate boundaries, and in other relatively cool high-pressure environments.
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