首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >The dependence of metal-silicate partitioning of moderately volatile elements on oxygen fugacity and Si contents of Fe metal: Implications for their valence states in silicate liquids
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The dependence of metal-silicate partitioning of moderately volatile elements on oxygen fugacity and Si contents of Fe metal: Implications for their valence states in silicate liquids

机译:金属硅酸盐分配对中等挥发性元素对Fe金属的氧逃逸性和Si含量的依赖性:硅酸盐液体的价值

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摘要

The volatile siderophile elements are important tracers of the delivery of volatile elements to the Earth. Their concentrations in the bulk silicate Earth are a function of the relative timing of their accretion and their sequestration into the core: a comprehensive understanding of their metal-silicate partitioning behaviour is therefore required in order to infer the volatile element accretion history. We present new partitioning data between liquid metal and liquid silicate at 11 GPa for a suite of volatile siderophile elements: Ag, As, Au, Cu, Ge, P, Pb, Sb, Sn. We focus particularly on determining their valence states and the effects of Si on partitioning, which are required in order to extrapolate from experimental conditions to core-formation conditions. It was found that all elements have weak to strong positive interaction parameters with Si. At lowfO2, redox equilibria dictate that the siderophile elements should become more siderophile. However, at lowfO2, Si also partitions more strongly into the metal. Given the repulsive nature of the interaction between Si and the elements of interest, the increased Si concentration at lowfO2will counteract the expected increase in the partition coefficient, making these elements less siderophile than expected at very reducing conditions. This causes the linear relationship betweenfO2and log(D) to become non-linear at lowfO2, which we account for by fitting an interaction parameter between Si and the elements of interest. This has implications for the interpretation of experimental results, because the valence cannot be determined from the slope of log(D) vs. logfO2if lowfO2, high Si metal compositions are employed without applying an activity correction. This also has implications for the extrapolation of experimental partitioning data to core-formation conditions: reducing conditions in the early stages of core formation do not necessarily result in complete or even strong depletion of siderophile elements when Si i
机译:挥发性的长三角形元素是将挥发性元素输送到地球的重要示踪剂。它们在散装硅酸盐地球中的浓度是它们的增生的相对定时的函数和它们在核心中的封存:因此需要综合理解其金属 - 硅酸盐分配行为,以便推断挥发性元素积累历史。我们在11GPa下呈现出液态金属和液体硅酸盐之间的新分区数据,用于促挥发的挥发性元件:Ag,As,Au,Cu,Ge,p,pb,sb,sn。我们特别专注于确定其价态和Si对分区的影响,这是为了从实验条件从实验条件外推动到核心形成条件。发现所有元素都有弱与SI的强阳性相互作用参数弱。在Lowfo2,氧化还原均衡决定了Siderophile元素应该变得更加普及。然而,在Lowfo2,Si也更强烈地分配到金属中。鉴于Si与感兴趣的元素之间的相互作用的排斥性质,Lowfo2的浓度增加抵消了分区系数的预期增加,使得这些元素比在非常还原条件下的预期不太长。这导致效率之间的线性关系在LOGFO2处变得非线性,我们通过拟合SI与感兴趣的元素之间的交互参数来解释。这对实验结果的解释具有影响,因为可以从Log(D)的斜率与LogFO2IF LogFO2的斜率确定,但在不施加活性校正的情况下使用高Si金属组合物。这也对核心形成条件的实验分区数据的外推的影响:在SI i时,核心地层早期阶段的减少条件并不一定会导致Si I

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