Microstructure evolution during phase separation in Ti-Zr-CShow others and affiliations
2016 (English)In: International journal of refractory metals & hard materials, ISSN 0263-4368, Vol. 61, p. 238-248Article in journal (Refereed) Published
Abstract [en]
(Ti,Zr)C powder was synthesized by carbothermal reduction and subsequently aged at 1150–2000 °C. The phase composition and microstructure was investigated using X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, and electron backscatter diffraction. It was found that the as-synthesized (Ti,Zr)C particles have a concentration gradient with a higher concentration of Ti at the surface of the particles. Furthermore, during aging the (Ti,Zr)C decomposes into Ti-rich and Zr-rich lamellae. During aging at 1400 and 1800 °C for 10 h, most Zr-rich and Ti-rich domains precipitate at grain boundaries, inheriting the crystal orientation of the parent grain behind the growth front. When the precipitate grows into another (Ti,Zr)C grain, that grain adopts the same crystal orientation as the parent grain. The crystallographic misorientation between adjacent lamellae is 0–5°. Based on these microstructural observations it is hypothesized that the mechanism of decomposition is discontinuous precipitation.
Place, publisher, year, edition, pages
Elsevier, 2016. Vol. 61, p. 238-248
Keywords [en]
Carbides, Discontinuous precipitation, Electron backscatter diffraction, Energy-dispersive X-ray spectroscopy, Phase separation, Backscattering, Carbothermal reduction, Electron diffraction, Energy dispersive spectroscopy, Grain boundaries, Grain growth, Microstructure, Precipitation (chemical), Scanning electron microscopy, X ray diffraction, X ray spectroscopy, Concentration gradients, Electron back scatter diffraction, Energy dispersive X ray spectroscopy, Mechanism of decomposition, Micro-structural observations, Micro-structure evolutions, Mis-orientation, Crystal orientation
National Category
Materials Engineering
Identifiers
URN: urn:nbn:se:kth:diva-195185DOI: 10.1016/j.ijrmhm.2016.09.019ISI: 000388048300032Scopus ID: 2-s2.0-84989814061OAI: oai:DiVA.org:kth-195185DiVA, id: diva2:1053104
Funder
VINNOVA, 2014-03392
Note
QC 20161208
2016-12-082016-11-022022-09-15Bibliographically approved
In thesis