TY - JOUR
T1 - Formation of hydrous stishovite from coesite in high-pressure hydrothermal environments
AU - Spektor, Kristina
AU - Nylen, Johanna
AU - Mathew, Renny
AU - Edén, Mattias
AU - Stoyanov, Emil
AU - Navrotsky, Alexandra
AU - Leinenweber, Kurt
AU - Häussermann, Ulrich
N1 - Funding Information:
National Science Foundation (NSF) through Grants 2013-4690 and DMR-1007557
Publisher Copyright:
© 2016 2016 by Walter de Gruyter Berlin/Boston.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - In low-Temperature, high-pressure hydrothermal environments coesite transforms into hydrous forms of stishovite. We studied hydrous stishovite produced from hydrothermal treatment of silica glass as initial SiO2 source at temperatures of 350-550 °C and pressures around 10 GPa. The P-T quenched samples were analyzed by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermal analysis, and IR and magic-Angle spinning (MAS) NMR spectroscopy. The presence of significant amounts of H2O (ranging from 0.5 to 3 wt%) is shown from thermogravimetric measurements. PXRD reveals that at temperatures below 400 °C, hydrous stishovite is obtained as two distinct phases that may relate to the solid ice-VII environment present at prevailing P-T conditions. Initially formed hydrous stishovite is metastable and dehydrates over time in the low-Temperature, high-pressure hydrothermal environment. The primary mechanism of H incorporation in stishovite is a direct substitution of 4H+ for Si4+ yielding unique octahedral hydrogarnet defects. In IR spectra this defect manifests itself by two broad but distinct bands at 2650 and 2900 cm-1, indicating strong hydrogen bonding. These bands are shifted in the deuteride to 2029 and 2163 cm-1, respectively. Protons of the octahedral hydrogarnet defect produce
AB - In low-Temperature, high-pressure hydrothermal environments coesite transforms into hydrous forms of stishovite. We studied hydrous stishovite produced from hydrothermal treatment of silica glass as initial SiO2 source at temperatures of 350-550 °C and pressures around 10 GPa. The P-T quenched samples were analyzed by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermal analysis, and IR and magic-Angle spinning (MAS) NMR spectroscopy. The presence of significant amounts of H2O (ranging from 0.5 to 3 wt%) is shown from thermogravimetric measurements. PXRD reveals that at temperatures below 400 °C, hydrous stishovite is obtained as two distinct phases that may relate to the solid ice-VII environment present at prevailing P-T conditions. Initially formed hydrous stishovite is metastable and dehydrates over time in the low-Temperature, high-pressure hydrothermal environment. The primary mechanism of H incorporation in stishovite is a direct substitution of 4H+ for Si4+ yielding unique octahedral hydrogarnet defects. In IR spectra this defect manifests itself by two broad but distinct bands at 2650 and 2900 cm-1, indicating strong hydrogen bonding. These bands are shifted in the deuteride to 2029 and 2163 cm-1, respectively. Protons of the octahedral hydrogarnet defect produce
KW - Coesite-stishovite transition
KW - high-pressure hydro-Thermal environments
KW - hydrous minerals
KW - octahedral defects
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U2 - 10.2138/am-2016-5609
DO - 10.2138/am-2016-5609
M3 - Article
AN - SCOPUS:84994593653
SN - 0003-004X
VL - 101
SP - 2514
EP - 2524
JO - American Mineralogist
JF - American Mineralogist
IS - 11
ER -