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Kinetics of iron redox reaction in silicate melts: A high temperature Xanes study on an alkali basalt

B Cochain et al 2009 J. Phys.: Conf. Ser. 190 012182 (5pp)   doi: 10.1088/1742-6596/190/1/012182  Help

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B Cochain1, D R Neuville1, D de Ligny2, J Roux1, F Baudelet3, E Strukelj1 and P Richet1
1 Physique des Minéraux et Magmas, Géochimie-Cosmochimie, CNRS-IPGP, 4 place Jussieu, 75005 Paris, France
2 Université Claude Bernard Lyon 1, LPCML, F-69622 Villeurbanne, France
3 Synchrotron SOLEIL, L'Orme des Merisiers, Saint Aubin, France
E-mail: cochain@ipgp.jussieu.fr

Abstract. In Earth and Materials sciences, iron is the most important transition element. Glass and melt properties are strongly affected by iron content and redox state with the consequence that some properties (i.e. viscosity, heat capacity, crystallization...) depend not only on the amounts of Fe2+ and Fe3+, but also on the coordination state of these ions. In this work we investigate iron redox reactions through XANES experiments at the K-edge of iron. Using a high-temperature heating device, pre-edge of XANES spectra exhibits definite advantages to make in-situ measurements and to determine the evolution of redox state with time, temperature and composition of synthetic silicate melts. In this study, new kinetics measurements are presented for a basalt melt from the 31,000-BC eruption of the Puy de Lemptegy Volcano in France. These measurements have been made between 773 K and at superliquidus temperatures up to 1923 K.

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