Kinetics of Decomposition in MAX Phases at Elevated Temperature
dc.contributor.author | Low, It-Meng (Jim) | |
dc.contributor.author | Pang, W. | |
dc.date.accessioned | 2017-01-30T13:43:12Z | |
dc.date.available | 2017-01-30T13:43:12Z | |
dc.date.created | 2012-03-23T01:19:45Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Low, I.M. and Pang, W.K. 2011. Kinetics of Decomposition in MAX Phases at Elevated Temperature. Materials Australia. 45 (2): pp. 33-35. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/34403 | |
dc.description.abstract |
The susceptibility of MAX phases to thermal dissociation at 1300-1800 °C in high vacuum has been studied using in-situ neutron diffraction. Above 1400 °C, MAX phases decomposed to binary carbide (e.g. TiCx) or binary nitride (e.g. TiNx), primarily through the sublimation of A-elements such as Al or Si, which results in a porous surface layer of MXx being formed. Positive activation energies were determined for the decomposition of MAX phases except for Ti3AlC2 where negative activation energy of 71.9 kJ mol-1 was obtained due to formation of fine pores on TiCx. The kinetics of isothermal phase decomposition at 1550 °C was modelled using a modified Avrami equation. An Avrami exponent (n)of < 1.0 was determined, indicative of the highly restricted diffusion of Al or Si between the channels ofM6X octohedra. The characteristics of thermal stability and phase transition are discussed. | |
dc.publisher | Institute of Materials Engineering Australasia Ltd | |
dc.title | Kinetics of Decomposition in MAX Phases at Elevated Temperature | |
dc.type | Journal Article | |
dcterms.source.volume | 45 | |
dcterms.source.number | 2 | |
dcterms.source.startPage | 33 | |
dcterms.source.endPage | 35 | |
dcterms.source.title | Materials Australia | |
curtin.department | Department of Imaging and Applied Physics | |
curtin.accessStatus | Fulltext not available |