Microstructure of experimentally oxidized olivine from a mantle nodule: I.Modes of Fe3+ and OH- occurrence

Citation
Nr. Khisina et al., Microstructure of experimentally oxidized olivine from a mantle nodule: I.Modes of Fe3+ and OH- occurrence, GEOCHEM INT, 39(4), 2001, pp. 327-335
Citations number
29
Categorie Soggetti
Earth Sciences
Journal title
GEOCHEMISTRY INTERNATIONAL
ISSN journal
00167029 → ACNP
Volume
39
Issue
4
Year of publication
2001
Pages
327 - 335
Database
ISI
SICI code
0016-7029(200104)39:4<327:MOEOOF>2.0.ZU;2-2
Abstract
Olivine (Fa 8.2%) from a mantle nodule in kimberlite (Udachnaya pipe, Yakut ia) was heated in air at 700 degreesC for 9 h and then examined by optical spectroscopy (IR and UV spectroscopy), electron microprobe analysis (EMPA), and transmission electron microscopy (TEM) using the method of electron en ergy-loss spectroscopy (EELS). Ultraviolet spectra recorded along the [001] plane showed the inward decrease of Fe3+. Three zones can be distinguished : (1) an oxidized rim containing Fe3+ as Fe3+-bearing phases and point defe cts within the olivine matrix; (2) a zone containing on by point Fe3+-beari ng defects; and (3) an unoxidized core. Hydroxyl OH-absorption bands in the IR spectrum are typical of mantle olivine and are normally assigned to poi nt OH-defects. However, the TEM-EELS study of the oxidized rim (with an ele ctron beam diameter of 4 nm) established that OH- does not occur as point d efects, but interacts with Fe3+ to form iron hydroxides (feroxyhyte, FeOOH, and bernalite, Fe(OH)(3)), which compose polyphase inclusions several hund red nanometers in size. Our investigations showed that IR spectroscopy comb ined with a TEM study is required to determine the modes of OH- occurrence in olivines and to correct the interpretation of OH- absorption bands in th e IR spectra. Our data also indicate that hydroxyl-bearing olivine is princ ipally oxidized differently to anhydrous olivine. In this case, instead of the typical oxidation products (laihunite, magnetite, hematite), Fe3+ and O H- defects interact to form iron hydroxides.