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Chemical and isotopic fractionation during the evaporation of the FeO-MgO-SiO2-CaO-Al2O3-TiO2 rare earth element melt system

A synthetic material with solar elemental proportions of iron, magnesium, silicon, titanium, calcium, and aluminum oxides and doped with rare earth elements was evaporated in a vacuum furnace at 1800 and 2000 C for different durations to study its chemical and isotopic evolution during the evaporati...

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Bibliographic Details
Published in:Geochimica et cosmochimica acta 2001-02, Vol.65 (3), p.479-494
Main Authors: Wang, Jianhua, Davis, Andrew M, Clayton, Robert N, Mayeda, Toshiko K, Hashimoto, Akihiko
Format: Article
Language:English
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Summary:A synthetic material with solar elemental proportions of iron, magnesium, silicon, titanium, calcium, and aluminum oxides and doped with rare earth elements was evaporated in a vacuum furnace at 1800 and 2000 C for different durations to study its chemical and isotopic evolution during the evaporation process. It is demonstrated that kinetic evaporation of solar composition material can produce residues of calcium-, aluminum-rich inclusion bulk chemistry. The evaporation sequence of the main constituents in this solar composition material is iron > silicon about magnesium > titanium. Calcium and aluminum remain unevaporated after evaporation of 95 percent of the solar composition material. The chemical fractionation between the gas and condensed phase is a function not only of temperature and pressure, but also of the bulk chemical composition of the condensed phase. During the evaporation process, cerium is almost as volatile as iron. The 2000-fold cerium depletion found in some refractory inclusions in carbonaceous chondrites was reproduced in the evaporation experiment and can be readily explained as a result of evaporation of preexisting meteoritic material. Kinetic isotopic fractionation of magnesium, oxygen, and silicon follows the Rayleigh distillation law during the laboratory evaporation of synthetic solar composition material. This implies that the residue is well mixed during the evaporation process and that the evaporation kinetic processes are surface reaction-controlled. (Author)
ISSN:0016-7037
DOI:10.1016/S0016-7037(00)00529-9