Journal of Mineralogical and Petrological Sciences
Online ISSN : 1349-3825
Print ISSN : 1345-6296
ISSN-L : 1345-6296
ORIGINAL ARTICLES
Laihunite in planetary materials: An FTIR and TEM study of oxidized synthetic and meteoritic Fe-rich olivine
Naotaka TOMIOKAAndreas MORLOKChiyoe KOIKEMelanie KÖHLERMonica GRADY
Author information
JOURNALS FREE ACCESS

2012 Volume 107 Issue 4 Pages 157-166

Details
Abstract

In situ mid-infrared transmission measurements of matrices from carbonaceous chondrites heated up to 572 °C in air were conducted by FTIR spectroscopy. The FTIR spectra of the matrices mainly showed olivine bands. With increasing temperature, up to 477 °C, the spectra did not show significant changes. However, at 572 °C, the ~11-μm band split into a doublet, and the intensity of the ∼ 10-μm band relative to that of the ∼ 11-μm band increased significantly. In synthetic Fe-rich olivine (Fo47) samples heated at 600 °C in air, their mid-infrared spectra showed changes similar to those in meteoritic samples. A TEM observation of the recovered meteoritic samples showed that most olivine grains had a stacking disorder on (001). Selected area electron diffraction patterns of the grains also exhibited extra reflections, corresponding to a similar superstructure to three-fold periodicity along col known as laihunite-3M in Fe2SiO4. Although the synthetic Fe-rich olivine did not have any defect structures before heating, the olivine commonly had a stacking disorder on (001) after heating at 600 °C. Therefore, the changes in mid-infrared spectra of the matrices of carbonaceous chondrites were not caused by chemical reactions among their constituent minerals, but were mainly caused by oxidation of iron within the olivine structure. The mid-infrared spectra of olivine-dominating samples from this study are potential reference data for the oxidation state of olivine in in situ mid-infrared measurements on the Martian surface, in partially oxidized meteorites, on asteroidal surfaces, and in interplanetary dust particles.

Information related to the author
© 2012 Japan Association of Mineralogical Sciences
Next article
feedback
Top