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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >HIGH PRESSURE AND HIGH TEMPERATURE METAL-SILICATE PARTITIONING OF SIDEROPHILE ELEMENTS - THE IMPORTANCE OF SILICATE LIQUID COMPOSITION
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HIGH PRESSURE AND HIGH TEMPERATURE METAL-SILICATE PARTITIONING OF SIDEROPHILE ELEMENTS - THE IMPORTANCE OF SILICATE LIQUID COMPOSITION

机译:硅单晶元素的高压高温金属硅酸盐分配-硅酸盐液体组成的重要性

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We have determined liquid metal-liquid silicate partition coefficients for Ni, Co, Mo, W, P, Ga, and Ge at 10 GPa and 2000 degrees C in a multi-anvil apparatus. Our sample containers were either MgO or Al2O3. The two different capsule materials imposed different redox states on our samples as well as producing very different silicate liquid compositions. The samples run in Al2O3 containers were at an fO(2) 1.1-1.4 log units below the iron-wustite (IW) buffer, and samples run in the MgO containers were 2.3 log units below the TW buffer. Although the partition coefficients we determine for Ni, Co, Mo, and W agree well with our previous work, we have obtained some rather surprising results. In the experiments reported here the partition coefficients for W, P, and Ge decrease with decreasing oxygen fugacity which is opposite to what is expected. We also find that partition coefficients for Mo and Ga do not increase as much as expected with decreasing oxygen fugacity, and although Ni and Co behave in a more normal manner, their partition coefficients also do not increase as much as expected with decreasing oxygen fugacity as a +2 valence for the two elements would predict. Simple analysis of the structures of the two different silicate melts shows that the MgO-rich melt is considerably more depolymerized than the Al2O3-rich melt. The partitioning behavior of all the elements indicates that all the cations are stabilized ill the more depolymerized MgO-rich melt. This is in accord with previous work on compositional effects on forsterite-liquid partitioning and the partitioning of metal cations between immiscible silicate liquids. Our results emphasize the need for thorough investigation of all variables that could potentially effect partitioning including the composition of the silicate melt. In addition, they suggest that mantle composition may play an important role during core formation. [References: 27]
机译:我们已经确定了在多砧装置中在10 GPa和2000摄氏度下Ni,Co,Mo,W,P,Ga和Ge的液态金属-液态硅酸盐分配系数。我们的样品容器是MgO或Al2O3。两种不同的胶囊材料在我们的样品上施加了不同的氧化还原状态,并产生了完全不同的硅酸盐液体成分。在Al2O3容器中运行的样品位于铁-铁水母(IW)缓冲区下方的fO(2)1.1-1.4 log单位下,而在MgO容器中运行的样品位于TW缓冲区以下2.3 log单位处。尽管我们确定的Ni,Co,Mo和W的分配系数与我们以前的工作非常吻合,但我们已经获得了一些相当令人惊讶的结果。在这里报道的实验中,W,P和Ge的分配系数随着氧逸度的降低而降低,这与预期的相反。我们还发现,随着氧逸度的降低,Mo和Ga的分配系数不会像预期的那样增加,尽管Ni和Co表现出更正常的行为,但随着氧逸度的降低,它们的分配系数也不会像预期的那样增加。两个元素的+2价将预测。对两种不同硅酸盐熔体的结构的简单分析表明,富MgO的熔体比富Al2O3的熔体解聚的多得多。所有元素的分配行为表明,随着富含MgO的聚合物解聚,所有阳离子都变得稳定。这与先前关于镁橄榄石-液体分配和金属阳离子在不混溶的硅酸盐液体之间分配的组成作用的先前研究一致。我们的结果强调需要彻底研究所有可能影响分配的变量,包括硅酸盐熔体的组成。此外,他们认为地幔成分可能在岩心形成过程中起重要作用。 [参考:27]

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