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    Incorporation of impurity anions into DSP: insights into structure and stability from computer modelling

    Access Status
    Fulltext not available
    Authors
    Lowe, Jennifer
    Rohl, Andrew
    Gale, Julian
    Parkinson, Gordon
    Smith, P.
    Date
    2006
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Lowe, Jennifer Louise and Rohl, Andrew and Gale, Julian and Parkinson, Gordon and Smith, P.G.. 2006. Incorporation of impurity anions into DSP: insights into structure and stability from computer modelling. Molecular Simulation 32 (1): 35-44.
    Source Title
    Molecular Simulation
    DOI
    10.1080/08927020500529301
    Additional URLs
    http://www.informaworld.com
    Faculty
    Department of Applied Chemistry
    Division of Engineering, Science and Computing
    Faculty of Science
    Remarks

    This is an electronic version of the article:

    Incorporation of impurity anions into DSP: insights into structure and stability from computer modelling

    J. L. Lowe; A. L. Rohl; J. D. Gale; P. G. Smith; G. M. Parkinson. Molecular Simulation; January 2006; Volume 32(1):35-44.

    Molecular Simulation is available online at:

    http://www.informaworld.com/openurl?doi:10.1080/08927020500529301

    URI
    http://hdl.handle.net/20.500.11937/44690
    Collection
    • Curtin Research Publications
    Abstract

    DSP is an important by-product of alumina production via the Bayer process. Under Western Australian processing conditions, the DSP has a sodalite-type structure that can incorporate anions within its framework. This is particularly useful for removal of impurity anions from liquor recycled in the circuit. As a first step to gaining a fundamental understanding of the incorporation process, we have undertaken molecular mechanics calculations to examine the interaction energy between a series of anions and the sodalite framework, as a measure of the affinity of the anions for the sodalite cage. Our calculations predict that the ions have an increased affinity for the cage along the series aluminate, chloride, carbonate, sulfate and hydroxide. These calculations have successfully predicted the trends that we observe from competitive-uptake experiments in our laboratory.

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