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Trace element partitioning between wollastonite and silicate-carbonate melt

Published online by Cambridge University Press:  05 July 2018

K. M. Law ,
J. D. Blundy ,
B. J. Wood  and
K. V. Ragnarsdottir
K. M. Law
Affiliation:
CETSEI, Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, UK
J. D. Blundy*
Affiliation:
CETSEI, Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, UK
B. J. Wood
Affiliation:
CETSEI, Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, UK
K. V. Ragnarsdottir
Affiliation:
CETSEI, Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, UK
*
*E-mail: jon.blundy@bris.ac.uk
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Abstract

We have performed an experimental study of the influence of varying size and charge on cation partitioning between wollastonite and silicate-carbonate melt in the system CaCO3-SiO2. The experimental conditions (3 GPa, 1420°C) lie close to the wollastonite II tc/I tc phase boundary. Results for 1+, 2+, 3+ and 4+ partitioning show parabolic dependence of partition coefficients on ionic radius, which can be fitted to the elastic strain model of Blundy and Wood (1994), wherein partitioning is described using three parameters: site radius (r0), site elasticity (apparent Young's Modulus) and the ‘strain-free’ partition coefficient (D0) for an element with radius r0. The apparent Young's Modulus of the Ca site in wollastonite, obtained from modelling the 2+ partitioning data, is 99±3 GPa, similar to the bulk-crystal value for the polymorph wollastonite I tc. r0 decreases with increasing charge on the substituent cation, while D0 also shows an approximately parabolic dependence on charge, with a maximum for 2+ cations. Partition coefficients for divalent cations Zn, Co, Fe, Cd, Mn and Pb are lower than would be predicted from their ionic radii alone, indicating a preference for the melt. This may be a consequence either of cation-carbonate complexation in the melt, or of the more distorted nature of cation co-ordination environments in melts.

Keywords

trace element partitioningwollastonitemetasomatismcarbonate melt
Type
Research Article
Information
Mineralogical Magazine , Volume 64 , Issue 4 , August 2000 , pp. 651 - 661
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2000

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