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Effect of Magneto-Mechanical Synergism in the Process-Structure Correlation in Fe-C Alloys: A Phase-Field Modeling Approach

Soumya Bandyopadhyay, Sourav Chatterjee, Dallas R. Trinkle, Richard G. Hennig, Victoria Miller, Michael S. Kesler, Michael R. Tonks

Abstract

Applied magnetic fields can alter phase equilibria and kinetics in steels; however, quantitatively resolving how magnetic, chemical, and elastic driving forces jointly influence the microstructure remains challenging. We develop a quantitative magneto-mechanically coupled phase-field model for the Fe-C system that couples a CALPHAD-based chemical free energy with demagnetization-field magnetostatics and microelasticity. The model reproduces single- and multi-particle evolution during the alpha to gamma inverse transformation at 1023 K under external fields up to 20 T, including ellipsoidal morphologies observed experimentally at 8 T. Chemically driven growth is isotropic; a magnetic interaction introduces an anisotropic driving force that elongates gamma precipitates along the field into ellipsoids, while elastic coherency promotes faceting, yielding elongated cuboidal or ``brick-like" particles under combined magneto-elastic coupling. Growth kinetics increase with C content, and decrease with field strength and misfit strain. Multi-particle simulations reveal dipolar interaction-mediated coalescence for field-parallel neighbors and ripening for field-perpendicular neighbors. Incorporating field-dependent diffusivity from experiment slows kinetics as expected; a first-principles-motivated anisotropic diffusivity correction is estimated to be small (<2%). These results establish a process-structure link for magnetically assisted heat treatments of Fe-C alloys and provide guidance for microstructure control via chemo-magneto-mechanical synergism.

Effect of Magneto-Mechanical Synergism in the Process-Structure Correlation in Fe-C Alloys: A Phase-Field Modeling Approach

Abstract

Applied magnetic fields can alter phase equilibria and kinetics in steels; however, quantitatively resolving how magnetic, chemical, and elastic driving forces jointly influence the microstructure remains challenging. We develop a quantitative magneto-mechanically coupled phase-field model for the Fe-C system that couples a CALPHAD-based chemical free energy with demagnetization-field magnetostatics and microelasticity. The model reproduces single- and multi-particle evolution during the alpha to gamma inverse transformation at 1023 K under external fields up to 20 T, including ellipsoidal morphologies observed experimentally at 8 T. Chemically driven growth is isotropic; a magnetic interaction introduces an anisotropic driving force that elongates gamma precipitates along the field into ellipsoids, while elastic coherency promotes faceting, yielding elongated cuboidal or ``brick-like" particles under combined magneto-elastic coupling. Growth kinetics increase with C content, and decrease with field strength and misfit strain. Multi-particle simulations reveal dipolar interaction-mediated coalescence for field-parallel neighbors and ripening for field-perpendicular neighbors. Incorporating field-dependent diffusivity from experiment slows kinetics as expected; a first-principles-motivated anisotropic diffusivity correction is estimated to be small (<2%). These results establish a process-structure link for magnetically assisted heat treatments of Fe-C alloys and provide guidance for microstructure control via chemo-magneto-mechanical synergism.

Paper Structure

This paper contains 18 sections, 33 equations, 12 figures, 2 tables.

Figures (12)

  • Figure 1: Optical micrographs of Fe–0.4 mass% C aged at 1023 K, showing microstructure formation: (a) without applied magnetic field; (b) with a vertically applied magnetic field. Black and white regions correspond to the martensite (transformed from $\gamma$) and $\alpha$ phases, respectively. The $\gamma$ phase transforms into martensite during quenching. Taken from Ohtsuka et al.ohtsuka2000alignment. Ellipsoidal grains nucleated in samples with an applied field: (c) microstructures of Fe–0.1%C alloy subjected to the inverse transformation under magnetic field of 8T. Dark spots are $\gamma$ particles and the gray matrix is $\alpha$ phase maruta2002magnetic; (d) scanning electron micrographs of steel specimen showing the nucleation of $\alpha$ particles inside a $\gamma$ grain. shimotomai2003formation. Ellipsoidal particles are outlined in red.
  • Figure 2: Fitted Gibbs free energies of the $\gamma$ and $\alpha$ phases obtained from CALPHAD databases naraghi2014thermodynamicsgustafson1985thermodynamic.
  • Figure 3: (a)-(b) Representative sections of the microstructures (shown in Fig. \ref{['fig:experiment']}(c)) obtained from the experimental report by Maruta et al.maruta2002magnetic for Fe-0.1 %C under 8T magnetic field. (c) Simulated morphology for the same system with similar experimental conditions and misfit strain of $0.3\%$. The simulated morphology displays an elliptical shape under these condition, which agrees well with the experimental observation.
  • Figure 4: Microstructural evolution of an austenite precipitate within a ferrite matrix in a Fe-0.4 wt%C system: (a) initial configuration; (b) shape resulting from chemical effects alone, showing an isotropic profile; (c–e) evolution under 1 T, 10 T, and 20 T magnetic fields, transitioning from a lens shape at 1 T to a perfectly elliptical morphology at higher fields; (f) profile arising from combined chemical and elastic interactions, yielding a cuboidal precipitate; (g–i) combined magneto-elastic effects at 20 T, evolving from a faceted ellipse at low misfit strain to a brick-like morphology at higher misfit strain.
  • Figure 5: Power spectrum analysis (b,e,h,k) and angular power distribution (c,f,i,l) for austenite precipitates (a,d,g,j) in a Fe-0.4 wt%C system for (a-c) chemical effects along, (d-e) elastic‐only interactions with $\epsilon_{ls} = -0.03$, (g-i) magnetic interaction with $B^{ext} = 20$ T, and (j-i) under combined magnetic and elastic interactions with $\epsilon_{ls} = -0.03$ and $B^{ext} = 20$ T.
  • ...and 7 more figures