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Phase Transition and EOS of Marmatite (Zn0.76Fe0.23S) up to 623K and 17GPa |
JIANG Xi1,3;ZHOU Wen-Ge1;XIE Hong-Sen1;LIU Yong-Gang1;FAN Da-Wei1,3;LIU Jing1,2;LI Yan-Chun2;LUO Chong-Ju2;MA Mai-Ning3 |
1Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550002
2Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049
3Graduate School of Chinese Academy of Sciences, Beijing 100049 |
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Cite this article: |
JIANG Xi, ZHOU Wen-Ge, XIE Hong-Sen et al 2007 Chin. Phys. Lett. 24 287-290 |
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Abstract In situ energy dispersive x-ray diffraction for natural marmatite (Zn0.76Fe0.23S) is performed up to 17.7GPa and 623K. It is fitted by the Birch--Murnaghan equation of state (EOS) that K0 and α0 for marmatite are 85(3)GPa and 0.79(16)×10-4K-1, respectively. Fe2+ isomorphic replacing to Zn2+ in natural crystal is responsible for high bulk modulus and thermal expansivity of marmatite. Temperature derivative of bulk modulus (∂K/∂T)P for marmatite is fitted to be -0.044(23)GPaK-1. The unambiguous B3--B1 phase boundaries for marmatite are determined to be Pupper(GPa)=15.50-0.016 T(°C) and Plower (GPa)=9.94--0.012T(°C) at 300--623K.
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Keywords:
91.60.Fe
91.60.Hg
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Published: 01 January 2007
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