首页> 外文期刊>The American mineralogist >The effect of f_(O2) on the partitioning and valence of v and Cr in garnet/melt pairs and the relation to terrestrial mantle v and Cr content
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The effect of f_(O2) on the partitioning and valence of v and Cr in garnet/melt pairs and the relation to terrestrial mantle v and Cr content

机译:f_(O2)对石榴石/熔体对中v和Cr的分配和价态的影响以及与地幔中v和Cr含量的关系

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Chromium and vanadium are stable in multiple valence states in natural systems, and their distribution between garnet and silicate melt is not well understood. Here, the partitioning and valence state of V and Cr in experimental garnet/melt pairs have been studied at 1.8-3.0 GPa, with variable oxygen fugacity between IW-1.66 and the Ru-RuO_2 (IW+9.36) buffer. In addition, the valence state of V and Cr has been measured in several high-pressure (majoritic garnet up to 20 GPa) experimental garnets, some natural megacrystic garnets from the western United States, and a suite of mantle garnets from South Africa. The results show that Cr remains in trivalent in garnet across a wide range of oxygen fugacities. Vanadium, on the other hand, exhibits variable valence state from 2.5 to 3.7 in the garnets and from 3.0 to 4.0 in the glasses. The valence state of V is always greater in the glass than in the garnet. Moreover, the garnet/melt partition coefficient, D(V), is highest when V is trivalent, at the most reduced conditions investigated (IW-1.66 to FMQ). The V~(2.5+) measured in high P-T experimental garnets is consistent with the reduced nature of those metal-bearing systems. The low V valence state measured in natural megacrystic garnets is consistent with f _(O2) close to the IW buffer, overlapping the range of f_(O2) measured independently by Fe~(2+)/Fe~(3+) techniques on similar samples. However, the valence state of V measured in a suite of mantle garnets from South Africa is constant across a 3 log f_(O2) unit range (FMQ-1.8 to FMQ-4.5), suggesting that the valence state of V is controlled by the crystal chemistry of the garnets rather than f_(O2) variations. The compatibility of V and Cr in garnets and other deep mantle silicates indicates that the depletion of these elements in the Earth's primitive upper mantle could be due to partitioning into lower mantle phases as well as into metal.
机译:铬和钒在自然系统中以多种价态稳定,人们对它们在石榴石和硅酸盐熔体之间的分布了解甚少。在这里,研究了石榴石/熔体对中V和Cr的分配和化合价状态,为1.8-3.0 GPa,氧逸度在IW-1.66和Ru-RuO_2(IW + 9.36)缓冲液之间变化。此外,已在几种高压(最高20 GPa的硬质石榴石),美国西部的天然大晶石榴石和南非的一组地幔石榴石中测量了V和Cr的价态。结果表明,在各种氧气逸度中,Cr仍以三价形式存在于石榴石中。另一方面,钒在石榴石中的价态变化为2.5到3.7,在玻璃杯中的价态为3.0到4.0。玻璃中V的价态始终比石榴石中的V大。此外,在研究的还原度最高的条件下(IW-1.66至FMQ),当V为三价时,石榴石/熔体分配系数D(V)最高。在高P-T实验石榴石中测得的V〜(2.5+)与那些含金属系统的还原性质一致。在天然超大石榴石中测得的低V价态与接近IW缓冲液的f _(O2)一致,重叠了Fe〜(2 +)/ Fe〜(3+)技术独立测量的f_(O2)范围。类似的样本。但是,在南非的一套地幔石榴石中测得的V的价态在3 log f_(O2)单位范围内(FMQ-1.8至FMQ-4.5)是恒定的,这表明V的价态受电子价的控制。石榴石的晶体化学,而不是f_(O2)的变化。石榴石和其他深地幔硅酸盐中V和Cr的相容性表明,地球原始上地幔中这些元素的消耗可能是由于划分为下地幔相以及金属。

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