Magnesium isotope fractionation in silicate melts by chemical and thermal diffusion
Magnesium isotope fractionation in silicate melts by chemical and thermal diffusion
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DOI:
10.1016/j.gca.2007.10.016
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发表时间:
2008
影响因子:
5
通讯作者:
F. Richter;E. Watson;R. Mendybaev;F. Teng;P. Janney
中科院分区:
文献类型:
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作者:
F. Richter;E. Watson;R. Mendybaev;F. Teng;P. Janney
Two types of laboratory experiments were used to quantify magnesium isotopic fractionations associated with chemical and thermal (Soret) diffusion in silicate liquids. Chemical diffusion couples juxtaposing a molten natural basalt (SUNY MORB) and a molten natural rhyolite (Lake County Obsidian) were run in a piston cylinder apparatus and used to determine the isotopic fractionation of magnesium as it diffused from molten basalt to molten rhyolite. The thermal diffusion experiments were also run in a piston cylinder apparatus but with a sample made entirely of molten SUNY MORB displaced from the hotspot of the assembly furnace so that the sample would have a temperature difference of about 100–200°C from one end to the other. The chemical diffusion experiments showed fractionations of26Mg/24Mg by as much as 7‰, which resulted in an estimate for the mass dependence of the self-diffusion coefficients of the magnesium isotopes corresponding to [Formula: see text] with β=0.05. The thermal diffusion experiments showed that a temperature difference of about 100°C resulted in the MgO, CaO, and FeO components of the basalt becoming slightly enriched by about 1wt% in the colder end while SiO2was enriched by several wt% in the hotter end. The temperature gradient also fractionated the magnesium isotopes. A temperature difference of about 150°C produced an 8‰ enrichment of26Mg/24Mg at the colder end relative to the hotter end. The magnesium isotopic fractionation as a function of temperature in molten basalt corresponds to 3.6×10−2‰/°C/amu.