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首页> 外文期刊>Contributions to Mineralogy and Petrology >The influence of melt composition on the partitioning of trace elements between anorthite and silicate melt
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The influence of melt composition on the partitioning of trace elements between anorthite and silicate melt

机译:熔体组合物对钙铜和硅酸盐熔体之间微量元素分配的影响

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摘要

The effect of melt composition on the partitioning of trace elements between anorthite and silicate melts has been studied experimentally in five compositions in the system CaO-Al2O3-SiO2 (CAS) at similar to 1400 degrees C and four compositions in the system CaO-MgO-Al2O3-SiO2 (CMAS) at 1332 degrees C. Melt composition has a significant impact on the substitution of trace elements into anorthite, particularly if the trace-element substitution is aliovalent and requires a charge balance for substitution. Melt composition strongly influences the partitioning of the trivalent rare earth element (REE) cations into the large-cation site (M) of anorthite. Due to charge balance requirements, the activity of alumina in the melt is the most important compositional variable for the REE partitioning in anorthite. Scandium, another trivalent cation, is much more compatible than is predicted for trivalent cations partitioning on the M-site. Therefore, scandium is likely partitioning onto the tetrahedral site in place of aluminium, which requires no charge balance and therefore is not affected strongly by melt composition. Similarly, the partitioning of the small divalent cations (Be and Mg) show a stronger relationship with changing melt composition than the large divalent cations (Ca, Sr, and Ba) and therefore are likely to partition on the tetrahedral site (T) of plagioclase rather than the large-cation site (M). Detailed thermodynamic modelling of the effects of melt composition is required for an adequate parameterization of trace-element mineral/melt partition coefficients, in addition to models of the effects of mineral composition.
机译:在系统CaO-Al 2 O 3-SiO 2(CAS)中的五种组合物中,在类似于1400℃和Syste CaO-MgO - Al 2 O 3-SiO 2(CMA)在1332℃下C.熔融组合物对钙质物的取代具有显着的影响,特别是如果痕量元素取代是铝化合物并且需要电荷平衡以取代。熔融组合物强烈影响三价稀土元素(REE)阳离子的分配到钙铜的大阳离子点(M)中。由于电荷平衡要求,熔体中氧化铝的活性是钙硫石中的REE分配最重要的成分变量。钪,另一个三价阳离子,比在M-Site上预测的三价阳离子分区更兼容。因此,钪可能在四面体场地上分配到铝的原位上,这不需要平衡,因此不受熔体组成强烈的影响。类似地,小二价阳离子(BE和Mg)的分区显示与改变熔体组合物的较强的关系,而不是大二价阳离子(Ca,Sr和Ba),因此可能会在Plagioclase的四面体位点(T)上分配而不是大阳离子网站(m)。除了矿物组合物的影响的模型之外,还需要熔融组合物的效果的详细的熔融组合物的效果。

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