Isothermal nature of martensite formation in Pt-modified β-NiAl alloys

Numerous experimental and modeling efforts to describe the cyclic behavior of β-NiAl-based coatings have recognized and considered the propensity of Ni-rich β compositions to exhibit a reversible martensitic transformation upon cooling. However, until now it has not been clear whether this martensit...

Full description

Saved in:
Bibliographic Details
Published inActa materialia Vol. 55; no. 7; pp. 2433 - 2441
Main Authors Sordelet, D.J., Besser, M.F., Ott, R.T., Zimmerman, B.J., Porter, W.D., Gleeson, B.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.04.2007
Elsevier Science
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Numerous experimental and modeling efforts to describe the cyclic behavior of β-NiAl-based coatings have recognized and considered the propensity of Ni-rich β compositions to exhibit a reversible martensitic transformation upon cooling. However, until now it has not been clear whether this martensite forms by an athermal process or if the transformation is isothermal in nature, exhibiting time-dependent kinetics. In this study model Ni–37Al– xPt ( x = 5, 10 and 30) alloys (all at.%) were examined primarily using thermal analysis, which showed that the martensite transformation is isothermal in nature with a single activation energy. In addition, the temperature range where this reversible transformation occurs increases with higher Pt contents. The autocatalytic behavior of this transformation was further illustrated during slow cooling in the differential scanning calorimeter, whereupon a series of ‘bursts’ corresponding to a sequence of individual exothermic peaks were observed. The potential implications of the isothermal martensite transformation in the β-based coatings is discussed.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
IS-J 7204
DE-AC02-07CH11358
USDOE Office of Science (SC)
ISSN:1359-6454
1873-2453
DOI:10.1016/j.actamat.2006.11.038