skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Cation ordering in synthetic and natural Ni-Mg olivine

Journal Article · · Am. Mineral.; (United States)
OSTI ID:5203665

The crystal structures of natural liebenbergite-(Ni/sub 1.52/Co/sub 0.05/Fe/sub 0.09/Mg/sub 0.34/)SiO/sub 4/-from Barberton, South Africa, and of synthetic liebenbergite-(Ni/sub 1.16/Mg/sub 0.84/)SiO/sub 4/-synthesized at 500/sup 0/C, have been studied in order to determine the intracrystalline Ni-Mg distribution. The natural liebenbergite is fully ordered, with Ml occupied only by Ni, whereas the synthetic sample is only partially ordered with K/sub D/ = (Mg(M2) . Ni(Ml))/(Ni(M2) . Mg(Ml)) = 9.9(4), ..delta..G/sup o//sub ex/ = -3.5 kcal/mole. Comparison with the results of Rajamani et al. (1975), who found K/sub D/ = 9.2(2) and ..delta..G/sup o//sub ex/ = -6.9 kcal/mole for a sample synthesized at 1280/sup 0/C, implies that the 500/sup 0/C synthetic sample in the present study crystallized metastably in a disordered or partially ordered state and ordering proceeded slowly. Although site size effects are small in Fe-Mg, Ni-Mg, and Co-Mg olivines, the crystal field stabilization energy is important in determining the observed cation distribution in Ni-Mg and Co-Mg olivines. Electronegativity or covalency effects are known only qualitatively, but there is a preference of less electronegative ions (Mg, Ca) for M2. Ordering of Ni into the Ml site of olivine should appreciably affect Ni partitioning between olivine and melt, and activity-composition relations have been examined assuming ideal solution behavior. Deviations from Raoult's law increase with increasng order, but variations in activity coefficients are less than 10 percent below 10 mole% Ni.

Research Organization:
Harvard Univ., Cambridge, MA
OSTI ID:
5203665
Journal Information:
Am. Mineral.; (United States), Vol. 66
Country of Publication:
United States
Language:
English