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Keywords = planetary mantles and cores

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15 pages, 9640 KB  
Article
Electrical Resistivity and Phase Evolution of Fe–N Binary System at High Pressure and High Temperature
by Yunzhe Wang, Fan Yang, Chunhua Shen, Jing Yang, Xiaojun Hu and Yingwei Fei
Minerals 2024, 14(5), 467; https://doi.org/10.3390/min14050467 - 28 Apr 2024
Cited by 2 | Viewed by 2781
Abstract
Partitioning experiments and the chemistry of iron meteorites indicate that the light element nitrogen could be sequestered into the metallic core of rocky planets during core–mantle differentiation. The thermal conductivity and the mineralogy of the Fe–N system under core conditions could therefore influence [...] Read more.
Partitioning experiments and the chemistry of iron meteorites indicate that the light element nitrogen could be sequestered into the metallic core of rocky planets during core–mantle differentiation. The thermal conductivity and the mineralogy of the Fe–N system under core conditions could therefore influence the planetary cooling, core crystallization, and evolution of the intrinsic magnetic field of rocky planets. Limited experiments have been conducted to study the thermal properties and phase relations of Fe–N components under planetary core conditions, such as those found in the Moon, Mercury, and Ganymede. In this study, we report results from high-pressure experiments involving electrical resistivity measurements of Fe–N phases at a pressure of 5 GPa and temperatures up to 1400 K. Four Fe–N compositions, including Fe–10%N, Fe–6.4%N, Fe–2%N, and Fe–1%N (by weight percent), were prepared and subjected to recovery experiments at 5 GPa and 1273 K. These experiments show that Fe–10%N and Fe–6.4%N form a single hexagonal close-packed phase (ɛ-nitrides), while Fe–2%N and Fe–1%N exhibit a face-centered cubic structure (γ-Fe). In separate experiments, the resistivity data were collected during the cooling after compressing the starting materials to 5 GPa and heating to ~1400 K. The resistivity of all compositions, similar to the pure γ-Fe, exhibits weak temperature dependence. We found that N has a strong effect on the resistivity of metallic Fe under rocky planetary core conditions compared to other potential light elements such as Si. The temperature-dependence of the resistivity also revealed high-pressure phase transition points in the Fe–N system. A congruent reaction, ε ⇌ γ’, occurs at ~673 K in Fe–6.4%N, which is ~280 K lower than that at ambient pressure. Furthermore, the resistivity data provided constraints on the high-pressure phase boundary of the polymorphic transition, γ ⇌ α, and an eutectoid equilibrium of γ’ ⇌ α + ε. The data, along with the recently reported phase equilibrium experiments at high pressures, enable construction of a phase diagram of the Fe–N binary system at 5 GPa. Full article
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49 pages, 2930 KB  
Review
Natural Iron Silicides: A Systematic Review
by Michael A. Rappenglück
Minerals 2022, 12(2), 188; https://doi.org/10.3390/min12020188 - 31 Jan 2022
Cited by 14 | Viewed by 12790
Abstract
This review systematically presents all finds of geogenic, impact-induced, and extraterrestrial iron silicide minerals known at the end of 2021. The respective morphological characteristics, composition, proven or reasonably suspected genesis, and possible correlations of different geneses are listed and supported by the available [...] Read more.
This review systematically presents all finds of geogenic, impact-induced, and extraterrestrial iron silicide minerals known at the end of 2021. The respective morphological characteristics, composition, proven or reasonably suspected genesis, and possible correlations of different geneses are listed and supported by the available literature (2021). Artificially produced iron silicides are only dealt with insofar as the question of differentiation from natural minerals is concerned, especially regarding dating to pre-industrial and pretechnogenic times. Full article
(This article belongs to the Special Issue Iron Silicide Minerals)
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20 pages, 1651 KB  
Review
Sample Digestion and Combined Preconcentration Methods for the Determination of Ultra-Low Gold Levels in Rocks
by Yan-hong Liu, Bo Wan and Ding-shuai Xue
Molecules 2019, 24(9), 1778; https://doi.org/10.3390/molecules24091778 - 8 May 2019
Cited by 24 | Viewed by 8211
Abstract
The gold abundance in basic rocks, which normally varies between 0.5 and 5 ppb, has served as a very important indicator in many geoscience studies, including those focused on the planetary differentiation, redistribution of elements during the crustal process, and ore genesis. However, [...] Read more.
The gold abundance in basic rocks, which normally varies between 0.5 and 5 ppb, has served as a very important indicator in many geoscience studies, including those focused on the planetary differentiation, redistribution of elements during the crustal process, and ore genesis. However, because gold is a monoisotopic element that exhibits a nugget effect, it is very difficult to quantify its ultra-low levels in rocks, which significantly limits our understanding of the origin of gold and its circulation between the Earth crust, mantle, and core. In this work, we summarize various sample digestion and combined preconcentration methods for the determination of gold amounts in rocks. They include fire assay, fire assay combined with Te coprecipitation and instrumental neutron activation analysis (INAA) or laser ablation inductively coupled plasma mass spectrometry, fusion combined with Te coprecipitation and anion exchange resins, dry chlorination, wet acid digestion combined with precipitation, ion exchange resins, solvent extraction, polyurethane foam, extraction chromatography, novel solid adsorbents, and direct determination by INAA. In addition, the faced challenges and future perspectives in this field are discussed. Full article
(This article belongs to the Special Issue Modern Sample Preparation Approaches for Separation Science)
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31 pages, 5765 KB  
Review
Silicon Isotope Geochemistry: Fractionation Linked to Silicon Complexations and Its Geological Applications
by Wei Wang, Hai-Zhen Wei, Shao-Yong Jiang, Xi Liu, Fang Lei, Yi-Bo Lin and Yao Zhao
Molecules 2019, 24(7), 1415; https://doi.org/10.3390/molecules24071415 - 10 Apr 2019
Cited by 18 | Viewed by 8585
Abstract
The fundamental advances in silicon isotope geochemistry have been systematically demonstrated in this work. Firstly, the continuous modifications in analytical approaches and the silicon isotope variations in major reservoirs and geological processes have been briefly introduced. Secondly, the silicon isotope fractionation linked to [...] Read more.
The fundamental advances in silicon isotope geochemistry have been systematically demonstrated in this work. Firstly, the continuous modifications in analytical approaches and the silicon isotope variations in major reservoirs and geological processes have been briefly introduced. Secondly, the silicon isotope fractionation linked to silicon complexation/coordination and thermodynamic conditions have been extensively stressed, including silicate minerals with variable structures and chemical compositions, silica precipitation and diagenesis, chemical weathering of crustal surface silicate rocks, biological uptake, global oceanic Si cycle, etc. Finally, the relevant geological implications for meteorites and planetary core formation, ore deposits formation, hydrothermal fluids activities, and silicon cycling in hydrosphere have been summarized. Compared to the thermodynamic isotope fractionation of silicon associated with high-temperature processes, that in low-temperature geological processes is much more significant (e.g., chemical weathering, biogenic/non-biogenic precipitation, biological uptake, adsorption, etc.). The equilibrium silicon isotope fractionation during the mantle-core differentiation resulted in the observed heavy isotope composition of the bulk silicate Earth (BSE). The equilibrium fractionation of silicon isotopes among silicate minerals are sensitive to the Si–O bond length, Si coordination numbers (CN), the polymerization degrees of silicate unites, and the electronegativity of cations in minerals. The preferential enrichment of different speciation of dissoluble Si (DSi) (e.g., silicic acid H4SiO40 (H4) and H3SiO4 (H3)) in silica precipitation and diagenesis, and chemical weathering, lead to predominately positive Si isotope signatures in continental surface waters, in which the dynamic fractionation of silicon isotope could be well described by the Rayleigh fractionation model. The role of complexation in biological fractionations of silicon isotopes is more complicated, likely involving several enzymatic processes and active transport proteins. The integrated understanding greatly strengthens the potential of δ30Si proxy for reconstructing the paleo terrestrial and oceanic environments, and exploring the meteorites and planetary core formation, as well as constraining ore deposits and hydrothermal fluid activity. Full article
(This article belongs to the Special Issue Advances in Silicon Chemistry 2018)
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