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MgCO3 + SiO2 Reaction at Pressures up to 32 GPa Studied Using in-Situ X-Ray Diffraction and Synchrotron Radiation. / Litasov, K. D.; Shatskiy, A. F.
In: Geochemistry International, Vol. 57, No. 9, 01.09.2019, p. 1024-1033.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - MgCO3 + SiO2 Reaction at Pressures up to 32 GPa Studied Using in-Situ X-Ray Diffraction and Synchrotron Radiation
AU - Litasov, K. D.
AU - Shatskiy, A. F.
N1 - Publisher Copyright: © 2019, Pleiades Publishing, Ltd.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Abstract: The paper reports results of an experimental study of decarbonation and melting reactions in the MgCO3–SiO2 system at pressures up to 32 GPa, using multianvil technique and in-situ X-ray diffraction with synchrotron radiation. At 3–7 GPa and 1400–1700 K, the reaction proceeds with the release of carbon dioxide and the formation of enstatite. At 9–13 GPa and 1850–1930 K, clinoenstatite, carbonate–silicate melt, and CO2 were found among the reaction products. At 16 GPa and 1825 K, the reaction is associated with the formation of wadsleyite and, at a higher temperature, by the generation of carbonated melt (with Mg/Si ratio close to wadsleyite) stishovite, and CO2 fluid. At this pressure, which coincides with the stability field of the wadsleyite–stishovite assemblage in the MgSiO3 phase diagram, the reaction temperature decreases by about 100 K. At higher pressures, the reaction proceeds with the formation of the MgSiO3 (akimotoite or bridgmanite) + melt assemblage. The reaction temperature at 25–35 GPa does not change and is about 2000 K. With a further increase in temperature to 2100 K, bridgmanite melts incongruently, reacting with the carbonate–silicate melt to form stishovite. The composition of the eutectic mixture shifts towards MgCO3 with increasing pressure. The reaction marks the upper temperature limit for the stability of magnesite and a free SiO2 phase in the Earth’s mantle and generally coincides with the mantle adiabat at depths of 300–900 km.
AB - Abstract: The paper reports results of an experimental study of decarbonation and melting reactions in the MgCO3–SiO2 system at pressures up to 32 GPa, using multianvil technique and in-situ X-ray diffraction with synchrotron radiation. At 3–7 GPa and 1400–1700 K, the reaction proceeds with the release of carbon dioxide and the formation of enstatite. At 9–13 GPa and 1850–1930 K, clinoenstatite, carbonate–silicate melt, and CO2 were found among the reaction products. At 16 GPa and 1825 K, the reaction is associated with the formation of wadsleyite and, at a higher temperature, by the generation of carbonated melt (with Mg/Si ratio close to wadsleyite) stishovite, and CO2 fluid. At this pressure, which coincides with the stability field of the wadsleyite–stishovite assemblage in the MgSiO3 phase diagram, the reaction temperature decreases by about 100 K. At higher pressures, the reaction proceeds with the formation of the MgSiO3 (akimotoite or bridgmanite) + melt assemblage. The reaction temperature at 25–35 GPa does not change and is about 2000 K. With a further increase in temperature to 2100 K, bridgmanite melts incongruently, reacting with the carbonate–silicate melt to form stishovite. The composition of the eutectic mixture shifts towards MgCO3 with increasing pressure. The reaction marks the upper temperature limit for the stability of magnesite and a free SiO2 phase in the Earth’s mantle and generally coincides with the mantle adiabat at depths of 300–900 km.
KW - bridgmanite
KW - carbonate
KW - coesite
KW - enstatite
KW - magnesite
KW - mantle
KW - melting
KW - stishovite
KW - transition zone
KW - 32 GPA
KW - SYSTEM
KW - HIGH-PRESSURE
KW - CARBONATED ECLOGITE
KW - HIGH-TEMPERATURE
KW - PERIDOTITE
KW - LOWER MANTLE
KW - DIAMOND FORMATION
KW - MAGNESITE
KW - PHASE-RELATIONS
UR - http://www.scopus.com/inward/record.url?scp=85071365746&partnerID=8YFLogxK
U2 - 10.1134/S0016702919090064
DO - 10.1134/S0016702919090064
M3 - Article
AN - SCOPUS:85071365746
VL - 57
SP - 1024
EP - 1033
JO - Geochemistry International
JF - Geochemistry International
SN - 0016-7029
IS - 9
ER -
ID: 21344191