Fate of Carbon During the Formation of Earth’s Core

Author(s):  
Ingrid Blanchard ◽  
Eleanor Jennings ◽  
Ian Franchi ◽  
Zuchao Zhao ◽  
Sylvain Petitgirard ◽  
...  

<p>Carbon is an element of great importance in the Earth, because it is intimately linked to the presence of life at the surface, and, as a light element, it may contribute to the density deficit of the Earth’s iron-rich core. Carbon is strongly siderophile at low pressures and temperatures (1), hence it should be stored mainly in the Earth’s core. Nevertheless, we still observe the existence of carbon at the surface, stored in crustal rocks, and in the mantle, as shown by the exhumation of diamonds. The presence of carbon in the crust and mantle could be the result of the arrival of carbon during late accretion, after the process of core formation ceased, or because of a change in its metal–silicate partitioning behavior at the conditions of core formation (P >40 GPa – T >3500 K). Previous studies reported metal–silicate partitioning of carbon based on experiments using large volume presses up to 8 GPa and 2200°C (2). Here, we performed laser-heated diamond anvil cell experiments in order to determine carbon partitioning between liquid metal and silicate at the extreme conditions of Earth’s core–mantle differentiation. We recovered our samples using the Focused Ion Beam technique and welded a 3 μm thick slice of each sample onto a TEM grid. Major elements were analyzed by electron microprobe, whereas the concentrations of carbon in the silicate were analyzed by nanoSIMS. We thus have obtained metal–silicate partitioning results for carbon at PT conditions relevant to planetary core formation, where C remains siderophile in all experiments, but partition coefficients are up to two orders of magnitude lower than in low PTexperiments. We derive a new parameterization of the pressure–temperature dependence of the metal–silicate partitioning of carbon and apply this in a state-of-the-art model of planet formation and differentiation (3,4) that is based on astrophysical N-body accretion simulations. Results show that BSE carbon concentrations increase strongly starting at a very early stage of Earth’s accretion and, depending on the concentration of carbon in accreting bodies, can easily reach or exceed estimated BSE values.</p><p> </p><p>(1) Dasgupta et al., 2013. Geochimica et Cosmochimica Acta 102, 191-212</p><p>(2) Li et al., 2016. Nature Geoscience 9, 781–785</p><p>(3) Rubie et al., 2015. Icarus 248, 89–108</p><p>(4) Rubie et al., 2016. Science 353, 1141–1144</p><p> </p>

2012 ◽  
Vol 1433 ◽  
Author(s):  
Andrew A. Woodworth ◽  
Ali Sayir ◽  
Philip G. Neudeck ◽  
Balaji Raghothamachar ◽  
Michael Dudley

ABSTRACTCommercially available bulk silicon carbide (SiC) has a high number (>2000/cm2) of screw dislocations (SD) that have been linked to degradation of high-field power device electrical performance properties. Researchers at the NASA Glenn Research Center have proposed a method to mass-produce significantly higher quality bulk SiC. In order for this bulk growth method to become reality, growth of long single crystal SiC fibers must first be achieved. Therefore, a new growth method, Solvent-Laser Heated Floating Zone (Solvent-LHFZ), has been implemented. While some of the initial Solvent-LHFZ results have recently been reported, this paper focuses on further characterization of grown crystals and their growth fronts. To this end, secondary ion mass spectroscopy (SIMS) depth profiles, cross section analysis by focused ion beam (FIB) milling and mechanical polishing, and orientation and structural characterization by X-ray transmission Laue diffraction patterns and X-ray topography were used. Results paint a picture of a chaotic growth front, with Fe incorporation dependant on C concentration.


2020 ◽  
Vol 117 (45) ◽  
pp. 27893-27898
Author(s):  
Dongyang Huang ◽  
James Badro ◽  
Julien Siebert

The bulk silicate Earth (BSE), and all its sampleable reservoirs, have a subchondritic niobium-to-tantalum ratio (Nb/Ta). Because both elements are refractory, and Nb/Ta is fairly constant across chondrite groups, this can only be explained by a preferential sequestration of Nb relative to Ta in a hidden (unsampled) reservoir. Experiments have shown that Nb becomes more siderophile than Ta under very reducing conditions, leading the way for the accepted hypothesis that Earth’s core could have stripped sufficient amounts of Nb during its formation to account for the subchondritic signature of the BSE. Consequently, this suggestion has been used as an argument that Earth accreted and differentiated, for most of its history, under very reducing conditions. Here, we present a series of metal–silicate partitioning experiments of Nb and Ta in a laser-heated diamond anvil cell, at pressure and temperature conditions directly comparable to those of core formation; we find that Nb is more siderophile than Ta under any conditions relevant to a deep magma ocean, confirming that BSE’s missing Nb is in the core. However, multistage core formation modeling only allows for moderately reducing or oxidizing accretionary conditions, ruling out the need for very reducing conditions, which lead to an overdepletion of Nb from the mantle (and a low Nb/Ta ratio) that is incompatible with geochemical observations. Earth’s primordial magma ocean cannot have contained less than 2% or more than 18% FeO since the onset of core formation.


2020 ◽  
Vol 117 (16) ◽  
pp. 8743-8749 ◽  
Author(s):  
Rebecca A. Fischer ◽  
Elizabeth Cottrell ◽  
Erik Hauri ◽  
Kanani K. M. Lee ◽  
Marion Le Voyer

Earth’s core is likely the largest reservoir of carbon (C) in the planet, but its C abundance has been poorly constrained because measurements of carbon’s preference for core versus mantle materials at the pressures and temperatures of core formation are lacking. Using metal–silicate partitioning experiments in a laser-heated diamond anvil cell, we show that carbon becomes significantly less siderophile as pressures and temperatures increase to those expected in a deep magma ocean during formation of Earth’s core. Based on a multistage model of core formation, the core likely contains a maximum of 0.09(4) to 0.20(10) wt% C, making carbon a negligible contributor to the core’s composition and density. However, this accounts for ∼80 to 90% of Earth’s overall carbon inventory, which totals 370(150) to 740(370) ppm. The bulk Earth’s carbon/sulfur ratio is best explained by the delivery of most of Earth’s volatiles from carbonaceous chondrite-like precursors.


Author(s):  
Andrew P Jephcoat ◽  
M. Ali Bouhifd ◽  
Don Porcelli

The present state of the Earth evolved from energetic events that were determined early in the history of the Solar System. A key process in reconciling this state and the observable mantle composition with models of the original formation relies on understanding the planetary processing that has taken place over the past 4.5 Ga. Planetary size plays a key role and ultimately determines the pressure and temperature conditions at which the materials of the early solar nebular segregated. We summarize recent developments with the laser-heated diamond anvil cell that have made possible extension of the conventional pressure limit for partitioning experiments as well as the study of volatile trace elements. In particular, we discuss liquid–liquid, metal–silicate (M–Sil) partitioning results for several elements in a synthetic chondritic mixture, spanning a wide range of atomic number—helium to iodine. We examine the role of the core as a possible host of both siderophile and trace elements and the implications that early segregation processes at deep magma ocean conditions have for current mantle signatures, both compositional and isotopic. The results provide some of the first experimental evidence that the core is the obvious replacement for the long-sought, deep mantle reservoir. If so, they also indicate the need to understand the detailed nature and scale of core–mantle exchange processes, from atomic to macroscopic, throughout the age of the Earth to the present day.


2021 ◽  
Vol 27 (S1) ◽  
pp. 1012-1015
Author(s):  
Gudrun Wilhelm ◽  
Ute Golla-Schindler ◽  
Katharina Wöhrl ◽  
Christian Geisbauer ◽  
Graham Cooke ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Terry-Ann Suer ◽  
Julien Siebert ◽  
Laurent Remusat ◽  
James M. D. Day ◽  
Stephan Borensztajn ◽  
...  

AbstractHighly siderophile elements (HSE), including platinum, provide powerful geochemical tools for studying planet formation. Late accretion of chondritic components to Earth after core formation has been invoked as the main source of mantle HSE. However, core formation could also have contributed to the mantle’s HSE content. Here we present measurements of platinum metal-silicate partitioning coefficients, obtained from laser-heated diamond anvil cell experiments, which demonstrate that platinum partitioning into metal is lower at high pressures and temperatures. Consequently, the mantle was likely enriched in platinum immediately following core-mantle differentiation. Core formation models that incorporate these results and simultaneously account for collateral geochemical constraints, lead to excess platinum in the mantle. A subsequent process such as iron exsolution or sulfide segregation is therefore required to remove excess platinum and to explain the mantle’s modern HSE signature. A vestige of this platinum-enriched mantle can potentially account for 186Os-enriched ocean island basalt lavas.


2013 ◽  
Vol 592-593 ◽  
pp. 781-784 ◽  
Author(s):  
Jaroslav Polák ◽  
Jiří Man ◽  
Ivo Kuběna

Persistent slip markings (PSMs) were experimentally studied in 316L steel fatigued to early stages of the fatigue life. High resolution SEM, combined with focused ion beam (FIB) technique and atomic force microscopy (AFM) were used to assess the true shape of PSMs in their early stage of development. General features of PSMs in fatigued metals are extrusions and intrusions. Their characteristic features were determined. They were discussed in relation with the theories of surface relief formation and fatigue crack initiation based on the formation, migration and annihilation of point defects in the bands of intensive cyclic slip - persistent slip bands (PSBs)


2012 ◽  
Vol 706-709 ◽  
pp. 2496-2501
Author(s):  
Junji Yamanaka ◽  
Chiaya Yamamoto ◽  
Yasuhiro Kuno ◽  
Minoru Doi

We have been studying the microstructure change of B2 cubic precipitates into an A2+B2 complex structure in Fe-Al-Ni alloy. In this study, we carried out detailed observation using focused ion beam (FIB) and scanning transmission electron microscopy (STEM). First, Fe-14.3at%Al-10.3at%Ni solid solution was prepared. Secondly, the specimens were heated at 1173 K, at which they formed B2 cubic precipitates (ordered bcc) dispersed in an A2 matrix (disordered bcc). After that, the B2/A2 two-phase specimen was annealed at 973 K. Then we fabricated STEM specimens using FIB, followed by high-resolution secondary electron imaging. We repeated this slice-and-observation procedure to determine the detailed microstructure of this heat-treated alloy. At the early stage of the 973 K annealing, the A2 phase appeared in the original B2 precipitates and showed a spongelike structure, whereas small nanometer-order B2 particles appeared in the A2 matrix. The A2/B2 interface at this stage showed no anisotropic morphology. Therefore, the main driving force of this process may not be strain energy, but chemical and interface energies. Further annealing at 973 K decreased the number of small B2 particles in the A2 matrix, and these particles dissolved into the matrix eventually. The annealing also changed the A2/B2 spongelike structure, which was observed in the original B2 precipitates, into simple structures such as the A2 core and B2 crust. Then the B2 phase showed ordinal coarsening behavior. When B2 precipitates, which had hollow cubic morphology, were observed to be very close to each other, the face-centered area of the B2 crust tended to dissolve and only large B2 precipitates remained.


Sign in / Sign up

Export Citation Format

Share Document