In situ pair distribution function analysis of crystallizing Fe-silicate melts

Abstract

The structures of a series of Na2O–FeO–Fe2O3–SiO2 melts with Si/Fe = 1, 2, or 3 have been characterized via synchrotron X-ray total scattering using aerodynamic levitation, a containerless technique, paired with laser heating. The melt structure has been simulated using empirical potential structure refinement (EPSR) based on X-ray scattering data and molecular dynamics (MD) simulations with effective partial charge potentials. Pair distribution functions and coordination numbers of cations in the melt were obtained from the data refinement and from the MD simulations. Iron redox and accompanying density were modeled for each composition assuming either (1) oxidized (all Fe3+) or (2) reduced (some Fe2+) to the level predicted for the Ar levitator environment from a literature model. The actual redox of the melts appears to be intermediate, with some Fe2+ but not as much as assumed from the literature model of redox. Comparison of EPSR and MD models at the same redox conditions indicates generally good agreement, and precise values of coordination numbers depend sensitively on the assumptions for cutoff lengths. Stepwise cooling of each melt in the series resulted in formation of magnetite on the free surface of the sample, but no silica-containing crystalline phases were observed. This study provides a comprehensive assessment of coupled factors (composition, redox, density) needed to assess high-temperature in situ structural measurements of simplified iron silicates.