Synchrotron high-resolution XRD and thermal expansion of synthetic Mg calcites

Abstract

The structural parameters and the thermal behavior of a complete series of Ca–Mg carbonates synthesized at high pressure and temperature (1–1.5 GPa, 1273–1373 K) in the range 0–50 mol% MgCO₃ have been investigated by in situ powder synchrotron high-resolution X-ray diffraction at ambient and up to 1073 K under self-controlled CO₂ partial pressure. The crystal structures are disordered Mg calcite in the range 1–41 mol% MgCO₃, and Ca dolomite at 49 mol% MgCO₃. New calibration curves of the cell parameters for the Mg content and thermal expansion from ambient to 1073 K are given. Short-range structural effects of cation substitution and ordering and their thermal behavior as a function of Mg content were identified from three sets of data: the peak broadening, the cell parameter strains and the Raman band enlargements. Both intra- and inter-crystalline levels of compositional heterogeneity are identified and allow splitting the Mg calcites into two groups: low- and high-Mg calcites. The low-Mg calcites (up to 22 mol% MgCO₃) are homogeneous in Mg content with short-range ordering. High-Mg calcite (up to 41 mol% MgCO₃) displays domains with different local ordering configurations and similar or slightly different Mg contents, and to which is added a compositional variation between crystals, as determined by EMP, of the order of  ± 0.8 mol% MgCO₃. The cation ordering in Ca-rich dolomites similarly occurs in high-Mg synthetic calcites. The role of (CO₃)²⁻ group ordering is shown to be an important factor in the formation of Ca–Mg carbonates.