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High‐Pressure Investigation in the System SiO 2 –GeO 2 : Mutual Solubility of Si and Ge in Quartz, Coesite and Rutile Phases
Author(s) -
Gullikson Amber L.,
Leinenweber Kurt,
Stoyanov Emil,
Zhang Hui,
Malik AbdsSami
Publication year - 2015
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/jace.13352
Subject(s) - coesite , stishovite , solubility , rutile , quartz , mineralogy , analytical chemistry (journal) , phase (matter) , geology , materials science , chemistry , metallurgy , chromatography , organic chemistry , paleontology , eclogite , subduction , tectonics
Mutual solubilities in crystalline phases in the system SiO 2 –GeO 2 have been investigated up to 10 GPa pressure and 1500°C temperature, using a bulk composition of 50 mol% GeO 2 . Solid solution of up to 40 mol% GeO 2 into the mineral quartz has been confirmed as well as solubility of Si into GeO 2 rutile (argutite) and Ge into SiO 2 rutile (stishovite) phases and limited Ge into coesite. Solubility of Ge in quartz is very high, and decreases with pressure, with the univariant quartz‐out reaction occurring near 3.4 GPa at 1200°C. The solubility of GeO 2 in coesite is highest at 3.4 GPa (about 8 mol%) and decreases with increasing pressure. Significantly more extensive solubility than previously reported for the rutile phases has been found and measured in detail as a function of pressure and temperature. Extensive solubility of SiO 2 in GeO 2 is found in argutite at 1200°C, increasing strongly with pressure and reaching a maximum of 25.2 mol% SiO 2 in GeO 2 at 9 GPa. At this point coesite (ss) plus argutite (ss) react to form a stishovite phase with 18 mol% GeO 2 , and the mutual solubility in both phases decreases above this pressure. At 1500°C, similar solubilities are observed but the maximum SiO 2 solubility in argutite of just over 25 mol% occurs near 10 GPa. All these solid solutions can be recovered to ambient temperature and pressure. Phase diagrams and unit cell information of the phases are presented here. Based on these results, a useful and industrially relevant, application for accurately measuring high pressure is suggested.

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