The Fe-Si-C system at extreme P-T conditions: a possible core crystallization pathway for reduced planets

1,2F.Miozzi,1,3G.Morard,1D.Antonangeli,1M.A.Baron,5A.Pakhomova,1,4A.N.Clark,6M.Mezoua,1G.Fiquet
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2022.01.013]
1Sorbonne Université, Muséum National d’Histoire Naturelle, UMR CNRS 7590, Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie, IMPMC, 75005 Paris, France
2Earth and Planets Laboratory, Carnegie Institution for Science, Washington, DC, USA1
3Univ. Grenoble Alpes, Univ. Savoie Mont Blanc, CNRS, IRD, UGE, ISTerre, Grenoble 38000, France1
4University of Colorado, Boulder, CO 80309-0399, USA
5Deutsches Elektronen-Synchrotron (DESY), Hamburg, Germany
6European Synchrotron Radiation Facility (ESRF), Grenoble, France
Copyright Elsevier

Several characteristics of a planet, including its internal dynamics, hinge on the composition and crystallization regime of the core, which, in turn, depends on the phase relations, melting behaviour and thermodynamic properties of constituent materials. The Fe-Si-C ternary system can serve as a proxy for core composition and formation processes under reducing conditions. We conducted laser-heated diamond anvil cell experiments coupled with in situ X-ray diffraction and electron microscopy analysis of the recovered samples, on four different starting compositions in the Fe-Si-C ternary system. Phase relations up to 200 GPa and up to 4000 K were determined. An FeSi phase with a B2 structure and iron carbides with different stoichiometries (i.e. Fe3C and Fe7C3) are the main observed phases, along with pure C (diamond) that has an extended stability field in the subsolidus regime. Carbon is largely soluble in B2-structured FeSi, whereas Si does not partition into the carbides. The melting curve determined for the starting material containing the least amount of light elements is consistent with the one for the Fe-C system. The other starting materials display higher melting temperatures than that of Fe-C, suggesting the existence of at least two different invariant points in the Fe-Si-C system. Applied to planetary interiors, our observations highlight how a small variation in light elements content would deeply affect the solidification style of a core. Bottom-up (Fe-enriched systems) and top-down regimes (C-rich systems), as well as solidification of a crystal mush (Si-enriched systems). These three crystallization regimes influence significantly the possibility of starting and sustaining a dynamo. Our results provide new insights into the differentiation of terrestrial planets in the Solar System and beyond, contributing to the study of planetary diversity.

Metal compositions of carbonaceous chondrites

1,2Elishevah M.M.E. van Kooten,1Edith Kubik,1Julien Siebert,3Benjamin D.Heredia,3Tonny B.Thomsen,1Frédéric Moynier
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2022.01.008]
1Université de Paris, Institut de Physique du Globe de Paris, CNRS UMR 7154, 1 rue Jussieu, 75238 Paris, France
2Center for Star and Planet Formation, Globe Institute, University of Copenhagen, Øster Voldgade 5-7, 1350 Copenhagen, Denmark
3Geological Survey of Denmark, GEUS, Øster Voldgade 10, 1350 Copenhagen, Denmark
Copyright Elsevier

FeNi metals represent an important fraction of chondritic components that remains relatively unexplored within most carbonaceous chondrite groups. The compositions of these metals can place constraints on the nature of their precursor materials as well as the physicochemical conditions of chondrule formation. In this study, we have analyzed the major, minor and trace element compositions of metal grains from relatively unaltered carbonaceous chondrites NWA 801 (CR), Leoville (CV3.1), Paris (CM2.9), Maribo (CM2.8) and Bells (CM-an). We observe a predominant and constant sub-solar Co/Ni ratio of CR, CM and CM-an metal grains. In Ni versus Co space, the metal grains fall below modelled curves for equilibrium condensation of metals from a solar gas. From Ni versus Cr plots, we infer that Paris (and possibly Leoville) metal grains could have maintained a primary condensation signature, although for most grains, condensation must have occurred under disequilibrium conditions. CR and isolated CM-an metals mostly fall outside of the predicted condensation fields. Based on metal-silicate partition coefficients of Ni and Co that vary with pressure, we interpret their Co/Ni signatures as having a planetary origin, with presumable extraction by impact jetting. Considering that almost all CM and CR metal grains have the same Co/Ni ratio, we cannot rule out a planetary origin for CM metal grains. We relate the highly siderophile element (HSE) patterns of carbonaceous chondrite metal to mixing and subsequent equilibration of refractory metal nuggets (RMN), FeNi alloys and silicate chondrule precursors. As with the Co/Ni ratios, the HSE patterns of CM, CM-an, CR and CV metal grains are nearly identical, suggesting that the abundance and nature of the metal precursor materials were similar for carbonaceous chondrites. The overall volatility patterns of CV, CM and CR chondrites, suggest that the latter form under more oxidizing conditions than CV chondrites. The volatility patterns of Paris metal grains overlap with CV and CR chondrule metals, implying variable P-T-fO2 conditions during CM chondrule formation. Finally, we comment on the origin of metal grains in various petrological settings. Chondrule rim and isolated metal grains are likely derived and expelled from the equilibrated core metal and were subsequently altered to include and re-equilibrate with materials from the disk. Trace element analyses of the anomalous CM chondrite Bells metal grains show potential relationships with CM chondrite and CH chondrite metal for the chondrule cores and isolated grains, respectively. Small metal grains from CM chondrite Maribo, which are located in the chondrite matrix, potentially have distinct volatility patterns from CR and Paris isolated grains, hinting at a distinct origin for small metal grains and large chondrule-derived metal. Future work on carbonaceous chondrite metal should include an extensive dataset of metal-silicate equilibration calculations on individual chondrules and an investigation of small (micron scale) versus large isolated metal grains.