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Goverapet Srinivasan S, Shivaramaiah R, Kent PR, et al. A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry. Phys Chem Chem Phys. 2017;19(11):7820-7832doi: 10.1039/c7cp00811b.
Goverapet Srinivasan, S., Shivaramaiah, R., Kent, P. R., Stack, A. G., Riman, R., Anderko, A., Navrotsky, A., & Bryantsev, V. S. (2017). A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry. Physical chemistry chemical physics : PCCP, 19(11), 7820-7832. https://doi.org/10.1039/c7cp00811b
Goverapet Srinivasan, Sriram, et al. "A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry." Physical chemistry chemical physics : PCCP vol. 19,11 (2017): 7820-7832. doi: https://doi.org/10.1039/c7cp00811b
Goverapet Srinivasan S, Shivaramaiah R, Kent PR, Stack AG, Riman R, Anderko A, Navrotsky A, Bryantsev VS. A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry. Phys Chem Chem Phys. 2017 Mar 15;19(11):7820-7832. doi: 10.1039/c7cp00811b. PMID: 28262886.
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Phys Chem Chem Phys. 2017 Mar 15;19(11):7820-7832. doi: 10.1039/c7cp00811b.

A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry.

Physical chemistry chemical physics : PCCP

Sriram Goverapet Srinivasan, Radha Shivaramaiah, Paul R C Kent, Andrew G Stack, Richard Riman, Andre Anderko, Alexandra Navrotsky, Vyacheslav S Bryantsev

Affiliations

  1. Chemical Sciences Division, Oak Ridge National Laboratory, 1 Bethel Valley Road, Oak Ridge, TN 37831, USA. [email protected].
  2. Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California Davis, 1 Shields Avenue, Davis, CA 95616, USA. [email protected].
  3. Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, 1 Bethel Valley Road, Oak Ridge, TN 37831, USA and Computer Science and Mathematics Division, Oak Ridge National Laboratory, 1 Bethel Valley Road, Oak Ridge, TN 37831, USA.
  4. Department of Materials Science and Engineering, Rutgers, The State University of New Jersey, 607 Taylor Road, Piscataway, New Jersey 08855, USA.
  5. OLI Systems, Inc., 240 Cedar Knolls Road, Suite 301, Cedar Knolls, New Jersey 07927, USA.

PMID: 28262886 DOI: 10.1039/c7cp00811b

Abstract

Bastnäsite, a fluoro-carbonate mineral, is the single largest mineral source of light rare earth elements (REE), La, Ce and Nd. Enhancing the efficiency of separation of the mineral from gangue through froth flotation is the first step towards meeting an ever increasing demand for REE. To design and evaluate collector molecules that selectively bind to bastnäsite, a fundamental understanding of the structure and surface properties of bastnäsite is essential. In our earlier work (J. Phys. Chem. C, 2016, 120, 16767), we carried out an extensive study of the structure, surface stability and water adsorption energies of La-bastnäsite. In this work, we make a comparative study of the surface properties of Ce-bastnäsite, La-bastnäsite, and calcite using a combination of density functional theory (DFT) and water adsorption calorimetry. Spin polarized DFT+U calculations show that the exchange interaction between the electrons in Ce 4f orbitals is negligible and that these orbitals do not participate in bonding with the oxygen atom of the adsorbed water molecule. In agreement with calorimetry, DFT calculations predict larger surface energies and stronger water adsorption energies on Ce-bastnäsite than on La-bastnäsite. The order of stabilities for stoichiometric surfaces is as follows: [101[combining macron]0] > [101[combining macron]1] > [101[combining macron]2] > [0001] > [112[combining macron]2] > [101[combining macron]4] and the most favorable adsorption sites for water molecules are the same as for La-bastnäsite. In agreement with water adsorption calorimetry, at low coverage water molecules are strongly stabilized via coordination to the surface Ce

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