Abstract

Abstract— The partitioning of the rare earth elements (REE) between hibonite and silicate melt has been investigated at 1470 °C in the system calcium tschermak's molecule‐diopside. Oxygen fugacity was varied between air and the iron‐wustite buffer using conventional gas mixing, and to “infinitely reducing” using Sr2+ as a surrogate for Eu2+. The partition coefficient (D) pattern is light REE enriched with D(La) = 7.15 and D(Yb) = 0.1. D(Eu) varied from about 2 in air to about 0.55 in an “infinitely reducing” atmosphere. Experiments were reversed for Eu and, by implication, a close approach to equilibrium was achieved for other elements. Absolute activity coefficients for REE in hibonite were estimated, yielding γLa = 330, γEu3+ = 1200, and γYb = 24 000. These results suggest that unless the principal phase(s) into which a trace element is dissolving and the activity—composition relationships for that trace element in that phase(s) are known, condensation temperatures based on assumed ideal solution behavior will generally be in error.

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