Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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University of Bristol

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2019Molybdenum isotope fractionation between Mo4+ and Mo6+ in silicate liquid and metallic Mo10citations
  • 2015The influence of melt infiltration on the Li and Mg isotopic composition of the Horoman Peridotite Massif80citations
  • 2015The influence of melt infiltration on the Li and Mg isotopic composition of the Horoman Peridotite Massif80citations

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Chart of shared publication
Walter, Michael J.
1 / 4 shared
Gianolio, Diego
1 / 10 shared
Hin, Remco C.
1 / 1 shared
Lai, Yi Jen
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Dohmen, Ralf
2 / 7 shared
Strandmann, Philip A. E. Pogge Von
1 / 1 shared
Takazawa, Eiichi
2 / 2 shared
Pogge Von Strandmann, Philip A. E.
1 / 1 shared
Chart of publication period
2019
2015

Co-Authors (by relevance)

  • Walter, Michael J.
  • Gianolio, Diego
  • Hin, Remco C.
  • Lai, Yi Jen
  • Dohmen, Ralf
  • Strandmann, Philip A. E. Pogge Von
  • Takazawa, Eiichi
  • Pogge Von Strandmann, Philip A. E.
OrganizationsLocationPeople

article

Molybdenum isotope fractionation between Mo4+ and Mo6+ in silicate liquid and metallic Mo

  • Elliott, Tim
  • Walter, Michael J.
  • Gianolio, Diego
  • Hin, Remco C.
Abstract

<p>Previous work has shown that Mo isotopes measurably fractionate between metal and silicate liquids, even at temperatures appropriate for core formation. However, the effect of variations in the structural environment of Mo in the silicate liquid, especially as a function of valence state, on Mo isotope fractionation remained poorly explored. We have investigated the role of valence state in metal-silicate experiments in a gas-controlled furnace at 1400 °C and at oxygen fugacities between 10<sup>−12.7</sup> and 10<sup>–9.9</sup>, i.e. between three and 0.2 log units below the iron-wüstite buffer. Two sets of experiments were performed, both with a silicate liquid in the CaO-Al<sub>2</sub>O<sub>3</sub>-SiO<sub>2</sub> system. One set used molybdenum metal wire loops as the metal source, the other liquid gold alloyed with 2.5 wt% Mo contained in silica glass tubes. X-ray absorption near-edge spectroscopy analysis indicates that Mo<sup>6+</sup>/ΣMo in the silicate glasses varies between 0.24 and 0.77 at oxygen fugacities of 10<sup>–12.0</sup> and 10<sup>–9.9</sup> in the wire loop experiments and between 0.15 and 0.48 at 10<sup>–11.4</sup> and 10<sup>–9.9</sup> in the experiments with Au-Mo alloys. Double-spiked analysis of Mo isotope compositions furthermore shows that Mo isotope fractionation between metal and silicate is a linear function of Mo<sup>6+</sup>/ΣMo in the silicate glasses, with a difference of 0.51‰ in <sup>98</sup>Mo/<sup>95</sup>Mo between purely Mo<sup>4+</sup>-bearing and purely Mo<sup>6+</sup>-bearing silicate liquid. The former is octahedrally and the latter tetrahedrally coordinated. Our study implies that previous experimental work contained a mixture of Mo<sup>4+</sup> and Mo<sup>6+</sup> species in the silicate liquid. Our refined parameterisation for Mo isotope fractionation between metal and silicate can be described as Δ<sup>98/95</sup>Mo<sub>metal–silicate</sub>=[Formula presented] Molybdenum isotope ratios therefore have potential as a proxy to constrain the oxygen fugacity during core formation on planetary bodies if the parameterisation of Mo<sup>6+</sup>/ΣMo variation with oxygen fugacity is expanded, for instance to include iron-bearing systems. On Earth literature data indicate that the upper mantle is depleted in heavy Mo isotopes relative to the bulk Earth, as represented by chondrites. As previously highlighted, this difference is most likely not caused by core formation, which either enriches the mantle in heavy Mo isotopes or causes no significant fractionation, depending on temperature and, as we determined here, Mo<sup>6+</sup> content. We reaffirm that core formation does not account for the Mo isotope composition of the modern upper mantle, which may instead reflect the effect of fractionation during subduction as part of global plate recycling.</p>

Topics
  • impedance spectroscopy
  • molybdenum
  • experiment
  • Oxygen
  • glass
  • glass
  • gold
  • iron
  • wire
  • fractionation