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Solubility of FeO in (Mg,Fe)SiO3 perovskite and the post-perovskite phase transition
被引:56
|作者:
Tateno, Shigehiko
Hirose, Kei
Sata, Nagayoshi
Ohishi, Yasuo
机构:
[1] Tokyo Inst Technol, Dept Earth & Planetary Sci, Tokyo Inst Technol, Tokyo 1528551, Japan
[2] Japan Agcy Marine Earth Sci & Technol, Inst Res Earth Evolut, Kanagawa 2370061, Japan
[3] Japan Synchrotron Radiat Res Inst, Sayo, Hyogo 679519, Japan
基金:
日本学术振兴会;
关键词:
post-perovskite;
perovskite;
iron;
D '' layer;
phase transition;
in situ X-ray observation;
D O I:
10.1016/j.pepi.2006.11.010
中图分类号:
P3 [地球物理学];
P59 [地球化学];
学科分类号:
0708 ;
070902 ;
摘要:
Phase relations in Mg0.5Fe0.5SiO3 and Mg0.25Fe0.75SiO3 were investigated in a pressure range from 72 to 123 GPa on the basis of synchrotron X-ray diffraction measurements in situ at high-pressure and -temperature in a laser-heated diamond-anvil cell (LHDAC). Results demonstrate that Mg0.5Fe0.5SiO3 perovskite is formed as a single phase at 85-108 GPa and 1800-2330 K, indicating a high solubility of FeO in (Mg,Fe)SiO3 perovskite at high pressures. Post-perovskite appears coexisting with perovskite in Mg0.5Fe0.5SiO3 above 106 GPa at 1410 K, the condition very close to the post-perovskite phase transition boundary in pure MgSiO3. The coexistence of perovskite and post-perovskite was observed to 123 GPa. In addition, post-perovskite was formed coexisting with perovskite also in Mg0.25Fe0.75SiO3 bulk composition at 106-123 GPa. In contrast to earlier experimental and theoretical studies, these results show that incorporation of FeO stabilizes perovskite at higher pressures. This could be due to a larger ionic radius of Fe2+ ion, which is incompatible with a small Mg2+ site in the post-perovskite phase. (c) 2006 Elsevier B.V. All rights reserved.
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页码:319 / 325
页数:7
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