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    Nanoscale gold clusters in arsenopyrite controlled by growth rate not concentration: Evidence from atom probe microscopy

    242323_242323.pdf (1.217Mb)
    Access Status
    Open access
    Authors
    Fougerouse, Denis
    Reddy, Steven
    Saxey, David
    Rickard, William
    Van Riessen, Arie
    Micklethwaite, S.
    Date
    2016
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Fougerouse, D. and Reddy, S. and Saxey, D. and Rickard, W. and Van Riessen, A. and Micklethwaite, S. 2016. Nanoscale gold clusters in arsenopyrite controlled by growth rate not concentration: Evidence from atom probe microscopy. American Mineralogist. 101 (8): pp. 1916-1919.
    Source Title
    American Mineralogist
    DOI
    10.2138/am-2016-5781CCBYNCND
    ISSN
    0003-004X
    School
    John de Laeter CoE in Mass Spectrometry
    Remarks

    This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by-nc-nd/4.0/

    URI
    http://hdl.handle.net/20.500.11937/24300
    Collection
    • Curtin Research Publications
    Abstract

    Auriferous sulfides, most notably pyrite (FeS2) and arsenopyrite (FeAsS), are among the most important economic minerals on Earth because they can host large quantities of gold in many of the world's major gold deposits. Here we present the first atom probe study of gold distribution in arsenopyrite to characterize the three-dimensional (3D) distribution of gold at the nanoscale and provide data to discriminate among competing models for gold incorporation in refractory ores. In contrast to models that link gold distribution to gold concentration, gold incorporation in arsenopyrite is shown to be controlled by the rate of crystal growth, with slow growth rate promoting the formation of gold clusters and rapid growth rate leading to homogeneous gold distribution. This study yields new information on the controls of gold distribution and incorporation in sulfides that has important implications for ore deposit formation. More broadly this study reveals new information about crystal-fluid interface dynamics that determine trace element incorporation into growing mineral phases.

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