Startseite Behavior of hydrogen defect and framework of Fe-bearing wadsleyite and ringwoodite at high temperature and high pressure
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Behavior of hydrogen defect and framework of Fe-bearing wadsleyite and ringwoodite at high temperature and high pressure

  • Yang Jin , Weihua Huang , ZhongPing Wang , Wei Sun , Yan Liu , Qunke Xia ORCID logo und Yan Yang
Veröffentlicht/Copyright: 10. Juli 2023
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Abstract

The transition zone is dominated by polymorphs of olivine, wadsleyite, and ringwoodite, which are to date considered the main water carriers in the Earth’s mantle. Despite considerable studies on water solubility and its impact on physical properties of the two minerals, knowledge of their hydrogen defects and framework behavior at high temperature and high pressure is still lacking. Here, we systematically assess this issue, by in situ high-temperature (20–800 °C) infrared spectroscopic studies, in situ high-temperature (20–800 °C) and high temperature-pressure (14.27 and 18.84 GPa, 20–400 °C) Raman spectroscopic studies on the iron-bearing wadsleyite and ringwoodite. The results show that dehydrogenation in wadsleyite happens at a higher temperature than in ringwoodite. The infrared absorption patterns of hydrogen defects in wadsleyite and ringwoodite are temperature sensitive, resulting from hydrogen defects transfer and site-specific stabilities. As for the framework, it is more sensitive to temperature and pressure for ringwoodite than wadsleyite. These results provide new knowledge about hydrogen defects and framework of wadsleyite and ringwoodite at high temperature and high pressure, which is indispensable for understanding water solubility and its impacts on physical properties of these two minerals.

Acknowledgments and Funding

Sylvie Demouchy is warmly thanked for manuscript discussion. Suwen Qiu is thanked for the EPMA experiment. This work was supported by the National Natural Science Foundation of China (42172041, 41972038) and Fundamental Research Funds for the Central Universities (Grant K20210168).

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Received: 2022-04-02
Accepted: 2022-08-25
Published Online: 2023-07-10
Published in Print: 2023-07-26

© 2023 by Mineralogical Society of America

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