Hydrogen incorporation in orthopyroxene: interaction of different trivalent cations |
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| Authors: | Email author" target="_blank">Roland?StalderEmail author Stephan?Klemme Thomas?Ludwig Henrik?Skogby |
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| Institution: | 1.Abteilung Angewandte und Experimentelle Mineralogie,Geowissenschaftliches Zentrum der Universit?t G?ttingen,G?ttingen,Germany;2.Mineralogisches Institut der Universit?t Heidelberg,Heidelberg,Germany;3.Naturhistoriska riksmuseet,Sektionen f?r mineralogi,Stockholm,Sweden |
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| Abstract: | The incorporation of hydrogen into ferrosilite, Fe-bearing enstatite and orthopyroxene containing different trivalent cations (Cr3+ and Al3+, Cr3+ and Fe3+) was investigated experimentally at 25 kbar. Hydrogen concentration was determined by FTIR-spectroscopy on oriented crystal sections and by secondary ion mass spectroscopy, whereas Mößbauer spectroscopy and optical spectroscopy were used to characterise the valence state of Fe in orthopyroxene. Results suggest that hydrogen incorporation in ferrosilite is achieved by a similar mechanism as in pure enstatite. In Cr-bearing samples, however, hydrogen incorporation is reduced by the presence of other trivalent cations by an increased tendency to form Tschermaks substitutions, e.g. Si T 4+ + Mg M1 2+ ? Al T 3+ + Cr M1 3+ . Thus, hydrogen solubility in natural orthopyroxenes from the Earth’s mantle, containing significant amounts of Cr3+, Al3+, and Fe3+, may be much more limited than expected from their trivalent cation content, as a large fraction of the trivalent cations does not participate in H-incorporating reactions as 2 Mg M1 2+ ? M M1 3+ + VM1 + H i + . |
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| Keywords: | Orthopyroxene Hydrogen incorporation Trivalent cation High pressure Spectroscopy |
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