Conferences

TRANSFORMATIONS BETWEEN MN-LIKE PHASES IN THE FE–MO–CR–C SYSTEM

  
A.M.Zaslavskii 2,
  
S.D. Kharchenko 3
 

1 I. M. Frantsevich Institute for Problems of Materials Science of the NAS of Ukraine, Omeliana Pritsaka str.,3, Kyiv, 03142, Ukraine
2 Institute of Food Resources (IFR) of the National Academy of Agrarian Sciences (NAAS) of Ukraine, str. Yevgena Sverstyuk, 4A, Kyiv, 02000, Ukraine
3 General Energy Institute of National Academy of Sciences of Ukraine , 172, Antonovycha St., Kyiv, 03150, Ukraine
tavbenya@ukr.net

Powder Metallurgy - Kiev: Frantsevich Institute for Problems of Materials Science NASU, 2025, #01/02
http://www.materials.kiev.ua/article/3848

Abstract

Transmission electron microscopy was employed to establish the nature of transformations between Mn-like phases in the Fe–Mo–Cr–C system illustrated by the example of structural and phase states of the rapidly quenched Fe51.9Mo11.1Cr26.3C10.7 (at.%) alloy. The alloy was produced as ribbons by melt spinning at a cooling rate of 5 × 106 K/sec using the planar flow casting technique. The phase constituents of the alloy were πFe,Mo,Cr,C and  χFe,Mo,Cr,C phases, corresponding to the β- and α-polymorphs of Mn, respectively. The direct πFe,Mo,Cr,C → χFe,Mo,Cr,C transformation was established to occur in the alloy. This transition proceeded completely, without changes in the composition or in the specific volume of the unit cell, which is ~0.012 nm3/atom for both phases. In electron microscopy images, the πFe,Mo,Cr,C → χFe,Mo,Cr,C transformation appears as a two-level nanoscale deformation contrast within the grains of the polygonal πFe,Mo,Cr,C phase. Specifically, it is manifested as a conglomerate of lamellar packets that are perpendicular to the spinning ribbon surface (with lamellae 10–20 nm wide), containing a substructure of transverse fragments (~ 10 nm in width). It was concluded that the πFe,Mo,Cr,C → χFe,Mo,Cr,C phase transition displayed the features of a diffusionless martensitic-type transformation between coherent phases. The transformation occurs within 700–727 °C, the same temperature range as in the decomposition of the π phase in rapidly quenched Fe–Mo–C alloys and as in the β-Mn α-Mn polymorphic transformation in elemental manganese. The quaternary πFe,Mo,Cr,C phase is manifested morphologically in two microstructural types. One corresponds to the metastable state of the πFe,Mo,Cr,C phase: elongated crystallites without signs of solid-state transformation, ranging in size from 200 nm to several microns. This type of microstructure is preserved from the crystallization temperature of the πFe,Mo,Cr,C phase to the observation temperature in regions adjacent to the spinning ribbon surface. The other microstructural type consists of polyhedral crystallites shaped as regular pentagons and convex deltoids with an average linear size of 50–200 nm. This polyhedral microstructure of the πFe,Mo,Cr,C phase, characteristic of the annealed state, forms in the ‘thermal bath’ within the ribbon under near-equilibrium conditions. It persists from the πFe,Mo,Cr,C phase crystallization temperature to the πFe,Mo,Cr,C → χFe,Mo,Cr,C transformation temperature. The χFe,Mo,Cr,C solid solutions appear morphologically as nanoscale deformation substructures within the grains of the initial polygonal πFe,Mo,Cr,C phase and are observed from the πFe,Mo,Cr,C → χFe,Mo,Cr,C transformation temperature to room temperature. Similar to the metastable πFe,Mo,Cr,C phase, the metastable χFe,Mo,Cr,C solid solutions exhibit high kinetic stability at room temperature.


DIFFUSIONLESS TRANSFORMATIONS, FE–MO–CR–C SYSTEM, MN-LIKE PHASES, RAPIDLY QUENCHED ALLOYS