Site preference and local geometry of Sc in garnets: I. Multifarious mechanisms in the pyrope-grossular join.
Articolo
Data di Pubblicazione:
2006
Abstract:
We applied different independent techniques (electron microprobe analysis, structure reÞ nement,
and X-ray absorption spectroscopy) to unravel the possible mechanisms of Sc incorporation in the
pyrope-grossular join. Samples were synthesized at elevated pressure and temperature by adding 5
wt% of Sc2O3 to selected nominal compositions (pyrope, pyrope60grossular40, pyrope20grossular80,
and grossular). In this way, the site of incorporation was not pre-determined, and only depends on the
availability of a mechanism for local charge-balance. The EXAFS spectra of the two end-members
could be analyzed by a multi-shell Þ t procedure, whereas the chemical heterogeneity of the Sc-doped
solid-solution terms prevented this approach. However, the available information allows detection of
different mechanisms of incorporation, which are active as a function of the bulk composition. In pyrope,
Sc mainly enters the dodecahedral X site, and the local charge balance is achieved by incorporation of
Mg at the adjacent tetrahedral Z site. Local charge-balance requirements suggest that a Z site occupied
by Mg bridges two X sites occupied by Sc. When the entrance of Ca provides relaxation of the averaged
structure, Sc may enter all the three available cation sites via the coupled heterovalent exchange
XSc1
ZSc1
XMg.1
ZSi.1 and the homovalent exchange YSc1
YAl.1. In the samples of this work, there is an
apparent limit in the Sc incorporation at the Y site, which is in contrast to the favored mechanism of
incorporation in Sc-doped andradites. This limit can be explained in terms of relative dimensions of
the structural sites when Al is the dominant Y cation. These results must be taken into account when
evaluating trace-element behavior in garnets for geochemical purposes. In particular, they explain why
DSc can be treated together with DREE in models based on the elastic strain theory in garnets close to
the pyrope composition, but deviate from the parabolic Þ t in grossular-rich garnets.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Crystal structure; garnet; trace elements and REE; scandium; XAS
Elenco autori:
Oberti, ROBERTA MARIA
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