Deep Earth carbon reactions through time and space

The authors acknowledge partial support from the Sloan Foundation grant G-2016-7157.Reactions involving carbon in the deep Earth have limited manifestation on Earth’s surface, yet they have played a critical role in the evolution of our planet. The metal-silicate partitioning reaction promoted carbon capture during Earth’s accretion and may have sequestered substantial carbon in Earth’s core. The freezing reaction involving iron-carbon liquid could have contributed to the growth of Earth’s inner core and the geodynamo. The redox melting/freezing reaction largely controls the movement of carbon in the modern mantle, and reactions between carbonates and silicates in the deep mantle also promote carbon mobility. The ten-year activity of the Deep Carbon Observatory has made important contributions to our knowledge of how these reactions are involved in the cycling of carbon throughout our planet, both past and present, and helped to identify gaps in our understanding that motivate and give direction to future studies.Publisher PDFPeer reviewe

Chapter 5 - X-Ray Diffraction Structure Measurements

This chapter describes how the structure of molten silicates under high pressures may be measured by synchrotron X-ray diffraction, using either large-volume presses or diamond-anvil cells, the latter combined with resistive-heating or laser-heating techniques. A brief summary of the data obtained so far is given, followed by a description of both energy-dispersive and angle-dispersive techniques, including challenges and how they may be overcome. Three areas of research are then highlighted: (1) structural measurements at extreme pressure conditions up to 100 GPa, (2) tracking the structural environment of minor/trace elements in magmas, and (3) the different ways to obtain the density of melts from X-ray diffraction data. Finally, some future prospects are discussed

Bonding of xenon to oxygen in magmas at depth

The field of noble gases chemistry has witnessed amazing advances in the last decade with over 100 compounds reported including Xe oxides and Xe–Fe alloys stable at the pressure-temperature conditions of planetary interiors. The chemistry of Xe with planetary materials is nonetheless still mostly ignored, while Xe isotopes are used to trace a variety of key planetary processes from atmosphere formation to underground nuclear tests. It is indeed difficult to incorporate the possibility of Xe reactivity at depth in isotopic geochemical models without a precise knowledge of its chemical environment. The structure of Xe doped hydrous silica-rich melts is investigated by in situ high energy synchrotron X-ray diffraction using resistive heating diamond anvil cells. Obtained pair distribution functions reveal the oxidation of Xe between 0.2 GPa and 4 GPa at high T up to 1000 K. In addition to the usual interatomic distances, a contribution at 2.05 ± 0.05 Å is observed. This contribution is not observed in the undoped melt, and is interpreted as the Xe–O bond, with a coordination number of about 12 consistent with Xe insertion in rings of the melt structure. Xe solubility measurements by electron microprobe and particle induced X-rays emission analysis confirm that Xe and Ar have similar solubility values in wt% in silicate melts. These values are nonetheless an order of magnitude higher than those theoretically calculated for Xe. The formation of Xe–O bonds explains the enhanced solubility of Xe in deep continental crust magmas, revealing a mechanism that could store Xe and fractionate its isotopes. Xenon is indeed atypical among noble gases, the atmosphere being notably depleted in elemental Xe, and very strongly depleted in Xe light isotopes. These observations are known as the ‘missing’ Xe paradox, and could be solved by the present findings

Development of chemical and topological structure in aluminosilicate liquids and glasses at high pressure

International audienceThe high pressure structure of liquid and glassy anorthite (CaAl(2)Si(2)O(8)) and calcium aluminate (CaAl(2)O(4)) glass was measured by using in situ synchrotron x-ray diffraction in a diamond anvil cell up to 32.4(2) GPa. The results, combined with ab initio molecular dynamics and classical molecular dynamics simulations using a polarizable ion model, reveal a continuous increase in Al coordination by oxygen, with 5-fold coordinated Al dominating at 15 GPa and a preponderance of 6-fold coordinated Al at higher pressures. The development of a peak in the measured total structure factors at 3.1 Å(-1) is interpreted as a signature of changes in topological order. During compression, cation-centred polyhedra develop edge- and face- sharing networks. Above 10 GPa, following the pressure-induced breakdown of the network structure, the anions adopt a structure similar to a random close packing of hard spheres

High P-T transformations of nitrogen to 170 GPa

International audienceX-ray diffraction and optical spectroscopy techniques are used to characterize stable and metastable transformations of nitrogen compressed up to 170GPa and heated above 2500K. X-ray diffraction data show that ɛ-N2 undergoes two successive structural changes to complex molecular phases ζ at 62GPa and a newly discovered κ at 110GPa. The latter becomes an amorphous narrow gap semiconductor on further compression and if subjected to very high temperatures (∼2000K ) crystallizes to the crystalline cubic-gauche-N structure (cg-N) above 150GPa. The diffraction data show that the transition to cg-N is accompanied by 15% volume reduction

Dissociative melting of ice VII at high pressure

International audienceWe have used x-ray diffraction to determine the structure factor of water along its melting line to a static pressure of 57 GPa (570 kbar) and a temperature of more than 1500 K, conditions which correspond to the lower mantle of the Earth, and the interiors of Neptune and Uranus up to a depth of 7000 km. We have also performed corresponding first principles and classical molecular dynamics simulations. Above a pressure of 4 GPa the O-O structure factor is found to be very close to that of a simple soft sphere liquid, thus permitting us to determine the density of liquid water near the melting line. By comparing these results with the density of ice, also determined in this study, we find that the enthalpy of fusion (ΔHf) increases enormously along the melting line, reaching approximately 120 kJ/mole at 40 GPa (compared to 6 kJ/mole at 0 GPa), thus revealing significant molecular dissociation of water upon melting. We speculate that an extended two-phase region could occur in planetary processes involving the adiabatic compression of water