FCC HCP MARTENSITIC-TRANSFORMATION IN THE FE-MN SYSTEM - EXPERIMENTAL-STUDY AND THERMODYNAMIC ANALYSIS OF PHASE-STABILITY/

Citation
S. Cotes et al., FCC HCP MARTENSITIC-TRANSFORMATION IN THE FE-MN SYSTEM - EXPERIMENTAL-STUDY AND THERMODYNAMIC ANALYSIS OF PHASE-STABILITY/, Metallurgical and materials transactions. A, Physical metallurgy andmaterials science, 26(8), 1995, pp. 1957-1969
Citations number
103
Categorie Soggetti
Metallurgy & Metallurigical Engineering","Material Science
ISSN journal
10735623
Volume
26
Issue
8
Year of publication
1995
Pages
1957 - 1969
Database
ISI
SICI code
1073-5623(1995)26:8<1957:FHMITF>2.0.ZU;2-Y
Abstract
A new experimental study of A(s) and M(s) in the Fe-Mn system has been performed by using two complementary experimental techniques, viz., d ilatometry and electrical resistivity measurements, which are applied to the whole composition range where the transformation can be detecte d, i.e., between 10 and 30 pet Mn. We used the A(s) and M(s) temperatu res as input information in an analysis based on thermodynamic models for the Gibbs energy of the face-centered cubic (fcc) and hexagonal cl ose-packed (hcp) phases. In these models, the magnetic contribution to Gibbs energy is accounted for, which allows us to study, by calculati on, the influence of the entropy of magnetic ordering upon the relativ e stability of the phases. The picture of magnetic effects upon the fc c/hcp transformation that emerges from our work is as follows. At low Mn contents, the martensitic transformation temperatures are larger th an the Neel temperature of the fcc phase, and both A(s) and M(s) decre ase linearly with increasing Mn. This encourages an extrapolation to z ero Mn content, and we use that to critically discuss the available in formation on the fcc/hcp equilibrium temperature for Fe at atmospheric pressure. At sufficiently large Mn contents, we have M(s) < T-N(gamma ) which implies that the fcc phase orders antiferromagnetically before transforming to the hcp phase. Since hcp remains paramagnetic down to lower temperatures, the ordering reaction in fee leads to a relative stabilization of this phase, which is reflected in a drastic, nonlinea r decrease of M(s).