In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum

The susceptibility of Ti2AlN to thermal dissociation at 1500–1800 °C in high-vacuum has been studied using in situ neutron diffraction. Above 1500 °C, Ti2AlN decomposed to TiNx primarily through the sublimation of aluminium (Al). The kinetics of isothermal phase decomposition at 1550 °C was modelled...

Full description

Bibliographic Details
Main Authors: Pang, Wei Kong, Low, It-Meng (Jim), Kennedy, S., Smith, R.
Format: Journal Article
Published: Elsevier 2010
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/35541
_version_ 1848754524790980608
author Pang, Wei Kong
Low, It-Meng (Jim)
Kennedy, S.
Smith, R.
author_facet Pang, Wei Kong
Low, It-Meng (Jim)
Kennedy, S.
Smith, R.
author_sort Pang, Wei Kong
building Curtin Institutional Repository
collection Online Access
description The susceptibility of Ti2AlN to thermal dissociation at 1500–1800 °C in high-vacuum has been studied using in situ neutron diffraction. Above 1500 °C, Ti2AlN decomposed to TiNx primarily through the sublimation of aluminium (Al). The kinetics of isothermal phase decomposition at 1550 °C was modelled using a modified Avrami equation. An Avrami exponent (n) of 0.338 was determined, indicative of the highly restricted out-diffusion of Al between the channels of Ti6N octahedra. The characteristics of thermal stability and phase transition in Ti2AlN are discussed. Characterisation of surface compositions and examination of cross-sectional microstructures of decomposed Ti2AlN, using synchrotron radiation diffraction and SEM, respectively, verify the findings of the neutron diffraction; that Ti2AlN decomposes to TiNx at the surface primarily via the sublimation of Al from grain boundaries.
first_indexed 2025-11-14T08:41:47Z
format Journal Article
id curtin-20.500.11937-35541
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T08:41:47Z
publishDate 2010
publisher Elsevier
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-355412019-02-19T04:28:06Z In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum Pang, Wei Kong Low, It-Meng (Jim) Kennedy, S. Smith, R. Neutron diffraction MAX phase TiN Decomposition Ti2AlN The susceptibility of Ti2AlN to thermal dissociation at 1500–1800 °C in high-vacuum has been studied using in situ neutron diffraction. Above 1500 °C, Ti2AlN decomposed to TiNx primarily through the sublimation of aluminium (Al). The kinetics of isothermal phase decomposition at 1550 °C was modelled using a modified Avrami equation. An Avrami exponent (n) of 0.338 was determined, indicative of the highly restricted out-diffusion of Al between the channels of Ti6N octahedra. The characteristics of thermal stability and phase transition in Ti2AlN are discussed. Characterisation of surface compositions and examination of cross-sectional microstructures of decomposed Ti2AlN, using synchrotron radiation diffraction and SEM, respectively, verify the findings of the neutron diffraction; that Ti2AlN decomposes to TiNx at the surface primarily via the sublimation of Al from grain boundaries. 2010 Journal Article http://hdl.handle.net/20.500.11937/35541 10.1016/j.msea.2010.08.012 Elsevier fulltext
spellingShingle Neutron diffraction
MAX phase
TiN
Decomposition
Ti2AlN
Pang, Wei Kong
Low, It-Meng (Jim)
Kennedy, S.
Smith, R.
In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title_full In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title_fullStr In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title_full_unstemmed In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title_short In situ diffraction study on decomposition of Ti2AlN at 1500–1800 °C in vacuum
title_sort in situ diffraction study on decomposition of ti2aln at 1500–1800 °c in vacuum
topic Neutron diffraction
MAX phase
TiN
Decomposition
Ti2AlN
url http://hdl.handle.net/20.500.11937/35541