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1 Bayerisches Geoinstitut, Universitaet Bayreuth, 95440 Bayreuth, Germany
2 Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EQ, U.K.
Correspondence: * E-mail: tiziana.boffa-ballaran{at}uni-bayreuth.de
The local mixing and ordering behavior of the otavite-magnesite solid solution has been characterized using infrared powder absorption spectroscopy in the spectral region 502000 cm1 at room temperature. Lattice modes due to Cd translations (75200 cm1) and Mg translations (200350 cm1) were both observed in the IR spectra for samples of intermediate composition. Peak positions of Cd translations remain constant as a function of composition, whereas those of Mg translations decrease in wavenumber with increasing otavite content. This suggests that the otavite-magnesite solid solution displays a combination of one-mode and two-mode behavior, most likely due to the large difference in atomic weight between magnesium and cadmium. Vibrational bands relating to the CO32 groups in the spectral region 600900 cm1 vary linearly as a function of composition and are not sensitive to the degree of order. The vibrational band at ~14001450 cm1 also varies linearly with composition, but R
ordered samples show a marked increase in frequency compared to their R
c counterparts. Positive deviations from linearity are observed for the effective line width determined using the autocorrelation method (expressed in terms of
corr values) for both lattice modes and bending vibrations of the CO32 molecular groups, whereas a linear variation as a function of composition of the
corr values of the CO32 stretching mode is observed for the 800 °C solid solution. Only in the region 600900 cm1 is an effect of order observed as a reduction in
corr values with respect to the sample with R
c symmetry. The difference in
corr values between the ordered and disordered samples was used to determine the local order parameter, q, which is consistent with a tricritical order-disorder transition.
Key Words: IR spectroscopy otavite-magnesite solid solution autocorrelation phase transition carbonates
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