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    Comparison of thermal stability in MAX211 and 312 phases

    154870_154870.pdf (151.1Kb)
    Access Status
    Open access
    Authors
    Pang, Wei Kong
    Low, It-Meng
    O'Connor, Brian
    Studer, A.
    Peterson, V.
    Sun, Z.
    Palmquist, J-P.
    Date
    2010
    Type
    Conference Paper
    
    Metadata
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    Citation
    Pang, W.K. and Low, I.M. and O'Connor, B.H. and Studer, A.J. and Peterson, V.K. and Sun, Z.M. and Palmquist, J-P. 2010. Comparison of thermal stability in MAX211 and 312 phases, International Conference on Neutron Scattering 2009, May 3 2009. Knoxville, Tennessee, USA: Institute of Physics (IOP).
    Source Title
    Journal of Physics: Conference Series Volume 251
    Source Conference
    International Conference on Neutron Scattering 2009
    DOI
    10.1088/1742-6596/251/1/012025
    ISSN
    1742-6596
    School
    Department of Imaging and Applied Physics
    Remarks

    © 2010 IOP Institute of Physics

    URI
    http://hdl.handle.net/20.500.11937/15298
    Collection
    • Curtin Research Publications
    Abstract

    The susceptibility of four MAX phases (Ti2AlC, Cr2AlC, Ti3AlC2, and Ti3SiC2) to high-temperature thermal dissociation in vacuum has been investigated using in-situ neutron diffraction. In high vacuum, these phases decomposed above 1400°C through the sublimation of M and A elements, forming a surface coating of MC. The apparent activation energies for the decomposition of sintered Ti3SiC2, Ti3AlC2, and Ti2AlC were determined to be 179.3, -71.9, and 85.7 kJ mol−1, respectively. The spontaneous release of Ti2AlC and TiC from de-intercalation during decomposition of Ti3AlC2 resulted in a negative activation energy.

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