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Updated: Sep 23, 2026

Simulation of the Planetary Interior Differentiation Processes in the Laboratory
Published on: November 15, 2013
Carbon solubility and liquid-liquid immiscibility in Fe-C-S ternary system up to 6 GPa: implications for the core of
Bin Zhao1,2, Guillaume Morard1, Geeth Manthilake3
1UMR CNRS 7590, Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie, IMPMC, Muséum National d'Histoire Naturelle, Sorbonne Université, 75005 Paris, France.
Abstract:
High-pressure, high-temperature experiments were conducted in a multi-anvil press using seven different starting compositions to investigate the phase relations of Fe-C-S liquids at pressures up to 6 GPa and temperatures up to 2000 K. Quenched samples revealed immiscible C-rich and S-rich metallic liquids at 2 and 4 GPa, manifesting as either large immiscible zones or emulsified smaller droplets. On the contrary, no immiscibility was observed at 5 or 6 GPa. At these higher pressures, the carbon solubility limit, significantly reduced by increasing sulfur content in the ternary liquid, prevents the formation of a liquid phase rich in both C and S. Our findings thus indicate that super-liquidus immiscibility in Fe-rich compositions does not occur at pressures above 5 GPa, due to the differential pressure dependence of C solubility and miscibility. The limited C solubility in S-rich liquids at higher pressures effectively suppresses immiscibility. Based on these results, terrestrial planetary bodies with fluid cores at pressures exceeding 5 GPa are unlikely to experience liquid-liquid immiscibility, even when both carbon and sulfur are abundant, as sulfur limits carbon solubility and promotes its exsolution. For the Moon, immiscibility-induced core stratification is not expected, though local emulsification could occur near the core-mantle boundary (CMB). In smaller bodies, a two-liquid Fe-C-S core may form at high temperatures, but progressive cooling may lead to graphite crystallization and the potential development of a graphitic crust.
Supplementary Information:
The online version contains supplementary material available at https://doi.org/10.1186/s40645-026-00846-3.
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