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An experimental study of element partitioning between magnetite, clinopyroxene and iron-bearing silicate liquids with particular emphasis on vanadium

机译:磁铁矿,亚铁辉石和含铁硅酸盐液体中元素分配的实验研究,特别是钒

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摘要

Mineral-melt partition coefficients of vanadium and a series of divalent trace elements (Ni, Co, Mn, Sr) have been determined for ferrobasaltic bulk compositions at one atmosphere. Experiments were performed at constant temperature (1,068 °C) and oxygen fugacity from 0.7 log units below to 2.6 log units above the NNO buffer (NNO–0.7 to NNO+2.6). All experiments were saturated in clinopyroxene and titanomagnetite. Partition coefficients for divalent cations between the liquid and these two minerals are found to be controlled by the ionic radius of the cation and the composition of the coexisting liquid, coefficients being significantly higher in more polymerised melts. Vanadium partitioning is strongly dependent on oxygen fugacity, decreasing by approximately one order of magnitude with increasing $ f_{O_2 } $ from NNO–0.7 to NNO+2.6 for both clinopyroxene and magnetite. Based upon thermodynamic modelling of the relative proportions of V3+, V4+ and V5+ in our liquids, this behaviour is inferred to be dominated by partitioning of V3+, despite the fact that this valence state is predicted to occur in low relative abundance. Derived values of $ {rm D}_{{rm V}^{{rm 3 + }} } $ show no systematic dependence on melt polymerisation, but do show a systematic dependence on mineral composition. In particular, our data and those of the literature are combined to show that $ {rm D}_{{rm V}^{{rm 3 + }} }^{{rm Cpx/Liq}} $ increases significantly as clinopyroxenes become more iron-rich. The partition coefficients for vanadium determined in this study have been used to model the V concentration of liquid and magnetite as a function of differentiation in a ferrobasaltic system at different oxygen fugacities. These results show that extreme enrichments of V2O5 in magnetite will only occur for a relatively small range of $ f_{O_2 } $ , between NNO and NNO–1.5. The results of our modelling are shown to be consistent with observations made on the V-rich magnetite layers of the Bushveld intrusion.
机译:钒和一系列二价微量元素(Ni,Co,Mn,Sr)的矿物熔体分配系数已在一个大气压下确定了铁基玄武岩大块成分。实验是在恒定温度(1,068°C)和氧逸度从NNO缓冲液以下0.7 log单位到NNO缓冲液上方2.6 log单位(NNO–0.7至NNO + 2.6)下进行的。所有实验均在斜发ino和钛磁铁矿中饱和。发现液体和这两种矿物质之间的二价阳离子分配系数受阳离子的离子半径和共存液体的组成控制,在聚合程度更高的熔体中,该系数明显更高。钒的分配强烈依赖于氧逸度,对于clinopyroxene和磁铁矿,钒的含量从NNO-0.7增加到NNO + 2.6,降低了大约一个数量级。根据我们液体中V3 + ,V4 + 和V5 + 的相对比例的热力学模型,尽管存在以下事实,但这种行为被认为是由V3 + 的分配决定的该价态预计会以较低的相对丰度发生。 $ {rm D} _ {{rm V} ^ {{rm 3 +}}} $的推导值没有显示出对熔融聚合的系统依赖性,但显示出了对矿物成分的系统性依赖性。尤其是,我们的数据和文献数据相结合后,发现随着{{Cld / Liq}}}的增加,随着{{Cl}} {$ {rm D} _ {{{rm V}}} {铁含量更高。在这项研究中确定的钒分配系数已被用来模拟液体和磁铁矿的V浓度,作为在不同氧逸散度下铁碱体系中微分的函数。这些结果表明,磁铁矿中V2 O5 的极度富集只会在$ f_ {O_2} $的相对较小范围内发生,介于NNO和NNO–1.5之间。结果表明,我们的建模结果与对Bushveld侵入体的富V磁铁矿层所做的观察一致。

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    《Contributions to Mineralogy and Petrology》 |2002年第1期|22-37|共16页
  • 作者单位

    Centre de Recherches Pétrographiques et Géochimiques BP 20 54501 Vandoeuvre-lès-Nancy cedex France;

    Centre de Recherches Pétrographiques et Géochimiques BP 20 54501 Vandoeuvre-lès-Nancy cedex France;

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