Actinide crystal-liquid partitioning for clinopyroxene and Ca3(PO4)2 |
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Authors: | T. Benjamin W.R. Heuser D.S. Burnett M.G. Seitz |
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Affiliation: | Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, U.S.A.;Argonne National Laboratory, Argonne, IL 64039, U.S.A. |
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Abstract: | ![]() Using fission and alpha track radiography techniques, we have measured partition coefficients (D) for the actinide elements Th, U and Pu between diopsidic clinopyroxene, whitlockite [β-Ca3 (PO4)2] and silicate liquid at 20kbar. Equilibrium partitioning at the crystal-liquid interface is assumed, and corrections for actinide zoning have been applied to the measured D values. Reproducibility for both actinide and minor element D values is carefully examined as a criterion for crystal-liquid interface equilibrium. The data are mostly compatible with interface equilibrium except for experiments at high cooling rates ( ? 30 deg/hr). Partition coefficients for Th/U/Pu of about 0.002/0.002/0.06 are measured for clinopyroxene and 1.2/0.5/3.4 for whitlockite. At an oxygen fugacity of 10?8.5, Pu is much more readily incorporated into the crystalline phases than is U or Th because of the importance of trivalent Pu. The DPu(cpx) is similar to D(cpx) of the light rare earths supporting the concept of Pu/(rare earth) dating. |
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