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American Mineralogist

Journal of Earth and Planetary Materials

Ed. by Baker, Don / Xu, Hongwu / Swainson, Ian


IMPACT FACTOR 2017: 2.645

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1945-3027
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Volume 101, Issue 5

Issues

Thermodynamics of bastnaesite: A major rare earth ore mineral

Radha Shivaramaiah
  • Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California Davis, Davis, California 95616, U.S.A
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/ Andre Anderko / Richard E. Riman
  • Department of Materials Science and Engineering, The State University of New Jersey, Piscataway, New Jersey 08854-8066, U.S.A
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/ Alexandra Navrotsky
  • Corresponding author
  • Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California Davis, Davis, California 95616, U.S.A
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Published Online: 2016-04-30 | DOI: https://doi.org/10.2138/am-2016-5565

Abstract

Bastnaesite, [RE-CO3-OH/F] (RE = rare earth) is one of the major sources of rare earth elements found in commercial deposits at Mountain Pass, California, Bayan Obo, China, and elsewhere. Synthetic forms of bastnaesite have been explored for applications including optical devices and phosphors. Determination of thermodynamic properties of these phases is critical for understanding their origin, mining, and processing. We report the first experimental determination of formation enthalpies of several OH and F bastnaesites based on high-temperature oxide melt solution calorimetry of well-characterized synthetic samples. The formation enthalpies from binary oxides and fluorides for all the bastnaesite samples are highly exothermic, consistent with their stability in the garnet zone of the Earth’s crust. Fluoride bastnaesite, which is more abundant in nature than its hydroxide counterpart, is thermodynamically more stable. For both OH and F bastnaesite, the enthalpy of formation becomes more negative with increasing ionic radius of the RE3+ cation. This periodic trend is also observed among rare earth phosphates and several other rare earth ternary oxides. For a given RE, the formation enthalpies from binary oxides are more negative for orthophosphates than for bastnaesites, supporting the argument that monazite could have formed by reaction of bastnaesite and apatite at high temperature. The difference in formation enthalpy of monazite and bastnaesite provides insight into energetics of such reactions along the rare earth series.

Keywords: Rare earths; bastnaesite; stability; monazite

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About the article

Received: 2015-09-20

Accepted: 2015-11-30

Published Online: 2016-04-30

Published in Print: 2016-05-01


Citation Information: American Mineralogist, Volume 101, Issue 5, Pages 1129–1134, ISSN (Online) 1945-3027, ISSN (Print) 0003-004X, DOI: https://doi.org/10.2138/am-2016-5565.

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© 2016 by Walter de Gruyter Berlin/Boston.

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