Phase relations in the carbon-saturated C–Mg–Fe–Si–O system and C and Si solubility in liquid Fe at high pressure and temperature: implications for planetary interiors

2013 ◽  
Vol 40 (8) ◽  
pp. 647-657 ◽  
Author(s):  
Suguru Takahashi ◽  
Eiji Ohtani ◽  
Hidenori Terasaki ◽  
Yoshinori Ito ◽  
Yuki Shibazaki ◽  
...  
2015 ◽  
Vol 1 (5) ◽  
pp. e1400260 ◽  
Author(s):  
Barbara Lavina ◽  
Yue Meng

The iron-oxygen system is the most important reference of rocks’ redox state. Even as minor components, iron oxides can play a critical role in redox equilibria, which affect the speciation of the fluid phases chemical differentiation, melting, and physical properties. Until our recent finding of Fe4O5, iron oxides were assumed to comprise only the polymorphs of FeO, Fe3O4, and Fe2O3. Combining synthesis at high pressure and temperature with microdiffraction mapping, we have identified yet another distinct iron oxide, Fe5O6. The new compound, which has an orthorhombic structure, was obtained in the pressure range from 10 to 20 GPa upon laser heating mixtures of iron and hematite at ~2000 K, and is recoverable to ambient conditions. The high-pressure orthorhombic iron oxides Fe5O6, Fe4O5, and h-Fe3O4 display similar iron coordination geometries and structural arrangements, and indeed exhibit coherent systematic behavior of crystallographic parameters and compressibility. Fe5O6, along with FeO and Fe4O5, is a candidate key minor phase of planetary interiors; as such, it is of major petrological and geochemical importance. We are revealing an unforeseen complexity in the Fe-O system with four different compounds—FeO, Fe5O6, Fe4O5, and h-Fe3O4—in a narrow compositional range (0.75 < Fe/O < 1.0). New, finely spaced oxygen buffers at conditions of the Earth’s mantle can be defined.


2006 ◽  
Vol 155 (1-2) ◽  
pp. 146-151 ◽  
Author(s):  
Wendy L. Mao ◽  
Andrew J. Campbell ◽  
Dion L. Heinz ◽  
Guoyin Shen

2020 ◽  
Vol 105 (3) ◽  
pp. 333-343
Author(s):  
Katherine Armstrong ◽  
Nicki C. Siersch ◽  
Tiziana Boffa-Ballaran ◽  
Daniel J. Frost ◽  
Tony Yu ◽  
...  

Abstract Experimental studies and measurements of inclusions in diamonds show that ferric iron components are increasingly stabilized with depth in the mantle. To determine the thermodynamic stability of such components, their concentration needs to be measured at known oxygen fugacities. The metal-oxide pair Ru and RuO2 are ideal as an internal oxygen fugacity buffer in high-pressure experiments. Both phases remain solid to high temperatures and react minimally with silicates, only exchanging oxygen. To calculate oxygen fugacities at high pressure and temperature, however, requires information on the phase relations and equation of state properties of the solid phases. We have made in situ synchrotron X-ray diffraction measurements in a multi-anvil press on mixtures of Ru and RuO2 to 19.4 GPa and 1473 K with which we have determined phase relations of the RuO2 phases and derived thermal equations of state (EoS) parameters for both Ru and RuO2. Rutile-structured RuO2 was found to undergo two phase transformations, first at ~7 GPa to an orthorhombic structure and then above 12 GPa to a cubic structure. The phase boundary of the cubic phase was constrained for the first time at high pressure and temperature. We have derived a continuous Gibbs free energy expression for the tetragonal and orthorhombic phases of RuO2 by fitting the second-order phase transition boundary and P-V-T data for both phases, using a model based on Landau theory. The transition between the orthorhombic and cubic phases was then used along with EoS terms derived for both phases to determine a Gibbs free energy expression for the cubic phase. We have used these data to calculate the oxygen fugacity of the Ru + O2 = RuO2 equilibrium, which we have parameterized as a single polynomial across the stability fields of all three phases of RuO2. The expression is log10fO2(Ru – RuO2) = (7.782 – 0.00996P + 0.001932P2 – 3.76 × 10–5P3) + (–13 763 + 592P – 3.955P2)/T + (–1.05 × 106 – 4622P)/T2, which should be valid from room pressure up to 25 GPa and 773–2500 K, with an estimated uncertainty of 0.2 log units. Our calculated fO2 is shown to be up to 1 log unit lower than estimates that use previous expressions or ignore EoS terms.


2021 ◽  
Vol 154 (14) ◽  
pp. 144701
Author(s):  
Nico Alexander Gaida ◽  
Ken Niwa ◽  
Takuya Sasaki ◽  
Masashi Hasegawa

Author(s):  
Egor Koemets ◽  
Timofey Fedotenko ◽  
Saiana Khandarkhaeva ◽  
Maxim Bykov ◽  
Elena Bykova ◽  
...  

Author(s):  
Egor Koemets ◽  
Timofey Fedotenko ◽  
Saiana Khandarkhaeva ◽  
Maxim Bykov ◽  
Elena Bykova ◽  
...  

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