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  4. Lead in zircon at the atomic scale
 
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Lead in zircon at the atomic scale

Journal
American Mineralogist
Journal Volume
97
Journal Issue
7
Start Page
1094
End Page
1102
ISSN
0003-004X
Date Issued
2012-06-25
Author(s)
Kogawa, M.
Watson, E. B.
Ewing, R. C.
SATOSHI UTSUNOMIYA  
DOI
10.2138/am.2012.3993
URI
https://www.scopus.com/pages/publications/84864839749
https://scholars.lib.ntu.edu.tw/handle/123456789/736888
Abstract
Lead-doped zircon crystals, which were synthesized under three different conditions (Watson et al. 1997): dry at 1430 °C at atmospheric pressure without P2O5; wet at 900 °C at 1.5 GPa in the presence of P2O5; and wet at 800 °C at 1.0 GPa without P 2O5, have been investigated to understand the mechanisms of Pb incorporation into zircon at the sub-micrometer scale, using various electron microscopy techniques including high-resolution transmission electron microscopy (HRTEM) and high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). Four different mechanisms in which Pb may be incorporated into zircon have been identified. In the P-free synthesis, Pb-oxide hydrate particles, 50-200 nm in size, are embedded in zircon. Each Pb-particle is associated with a single vesicle, ∼50 nm. Lead in the zircon structure is possibly incorporated under the detection limit value of energy-dispersive X-ray analysis (EDX) by means of: (1) Zr4+ = Pb2+ + 2H+ at less than -0.1 wt%. In the system with P, Pb-phases occur in three different forms: Pb-rich domains concentrated along cleavage planes or grain boundaries without any evident crystal form; numerous Pb-phosphate particles, as large as 100 nm, embedded heterogeneously in the zircon crystal; and homogeneous distribution of Pb in the zircon structure at less than -1 wt% as determined by EDX. These results suggest that charge balance is maintained by the xenotime-type coupled substitution: (2) Zr4+ + 2Si4+ = Pb2+ + 2P5+ with a possible minor contribution from mechanism 1. The apparent solubility limit of Pb, <1 wt%, is constrained mainly by the xenotime-type coupled substitution mechanism, which is probably due to increasing strain at higher Pb-concentrations. The presence of Pb 2+ in natural zircon is consistent with the low-level Pb allowed by substitution mechanism 2, with only a minor contribution from substitution mechanism 1, the latter of which causes distortion in the local structure.
Subjects
Lead
Nanoscale
TEM
Zircon
Publisher
Mineralogical Society of America
Type
journal article

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