A Correlative Four-Dimensional Study of Phase-Separation at the Subnanoscale To Nanoscale of a Ni-Al Alloy

Abstract

The temporal evolution of ordered gamma'(L1(2))-precipitates precipitating in a disordered gamma(f.c.c.) matrix is studied in extensive detail for a Ni-12.5 Al at.% alloy aged at 823 K (550 degrees C), for times ranging from 0.08 to 4096 h. Three-dimensional atom-probe tomography (3-D APT) results are compared to monovacancy-mediated lattice-kinetic Monte Carlo (LKMC1) simulations on a rigid lattice, which include monovacancy-solute binding energies through 4th nearest-neighbor distances, for the same mean composition and aging temperature. The temporal evolution of the measured values of the mean radius, (R(t)>, number density, aluminum supersaturations, and volume fraction of the gamma'(L1(2))-precipitates are compared to the predictions of a modified version of the Lifshitz-Slyozov diffusion-limited coarsening model due to Calderon, Voorhees et al. The resulting experimental rate constants are used to calculate the Gibbs interfacial free-energy between the gamma(f.c.c.)- and gamma'(L1(2))-phases, which enter the model, using data from two thermodynamic databases, and its value is compared to all exiting values. The diffusion coefficient for coarsening is calculated utilizing the same rate-constants and compared to all archival diffusivities, not determined from coarsening experiments, and it is demonstrated to be the inter-diffusivity, (D) over tilde, of Ni and Al. The monovacancy-mediated LKMC1 simulation results are in good agreement with our 3-D APT data. The compositional interfacial width, for the (100)-interface, between the gamma(f.c.c.)- and gamma'(L1(2))-phases, decreases continuously with increasing aging time and < R(t)>, both for the 3-D APT results and the monovacancy-mediated LKMC1 simulations, in disagreement with an ansatz intrinsic to the trans-interface diffusion-controlled coarsening model, which assumes the exact opposite trend for binary alloys. (C) 2019 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.