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Fe-Mg partitioning between ringwoodite and magnesiowustite and the effect of pressure, temperature and oxygen fugacity

机译:铁镁镁铁矿和镁硅铁矿之间的分配以及压力,温度和氧逸度的影响

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The partitioning of Mg and Fe between magnesiowustite and ringwoodite solid solutions has been measured between 15 and 23 GPa and 1200-1600 ℃ using both Fe and Re capsule materials to vary the oxidation conditions. The partitioning results show a clear dependence on the capsule material used due to the variation in Fe~(3+) concentrations as a consequence of the different oxidation environments. Using results from experiments performed in Fe capsules, where metallic Fe was also added to the starting materials, the difference in the interaction parameters for the two solid solutions (W_(FeMg)~(mw) - W_(FeMg)~(ring)) is calculated to be 8.5 ± 1 kJ mol~(-1). Similar experiments performed in Re metal capsules result in a value for W_(FeMg)~(mw) - W_(FeMg)~(ring) that is apparently 4 kJ higher, if all Fe is assumed to be FeO. Electron energy-loss near-edge structure (ELNES) spectroscopic analyses, however, show Fe~(3+) concentrations to be approximately three times higher in magnesiowustite produced in Re capsules than in Fe capsules and that Fe~(3+) partitions preferentially into magnesiowustite, with K_(D_(Fe~(3+)))~(ring/mw) estimated between 0.1 and 0.6. Using an existing activity composition model for magnesiowustite, a least-squares fit to the partitioning data collected in Fe capsules results in a value for the ringwoodite interaction parameter (W_(FeMg)~(ring)) of 3.5 ± 1 kJ mol~(-1). The equivalent regular interaction parameter for magnesiowustite (W_(FeMg)~(mw)) is 12.1 ± 1.8 kJ mol. These determinations take into account the Fe~(3+) concentrations that occur in both phases in the presence of metallic Fe. The free energy change in J mol~(-1) for the Fe exchange reaction can be described, over the range of experimental conditions, by 912 + 4.15 (T - 298) + 18.9P with T in K, Pin kbar. The estimated volume change for this reaction is smaller than that predicted using current compilations of equation of state data and is much closer to the volume change at ambient conditions. These results are therefore a useful test of high pressure and temperature equation of state data. Using thermodynamic data consistent with this study the reaction of ringwoodite to form magnesiowustite and stishovite is calculated from the data collected using Fe capsules. Comparison of these results with previous studies shows that the presence of Fe~(3+) in phases produced in multianvil experiments using Re capsules can have a marked effect on apparent phase relations and determined thermodynamic properties.
机译:使用Fe和Re胶囊材料来改变氧化条件,已在15至23 GPa和1200-1600℃之间测量了镁和铁石固溶体中镁和铁的分配。由于不同的氧化环境,Fe〜(3+)浓度的变化,分配结果显示出对所用胶囊材料的明显依赖性。利用在Fe胶囊中进行的实验结果(其中还向原料中添加了金属Fe),两种固溶体(W_(FeMg)〜(mw)-W_(FeMg)〜(ring))相互作用参数的差异计算为8.5±1 kJ mol〜(-1)。如果假设所有的Fe都是FeO,则在Re金属胶囊中进行的类似实验得出的W_(FeMg)〜(mw)-W_(FeMg)〜(ring)的值显然要高4 kJ。然而,电子能损近缘结构(ELNES)光谱分析表明,Re胶囊中生成的菱镁矿中的Fe〜(3+)浓度大约是Fe胶囊中的Fe〜(3+)浓度的三倍,并且Fe〜(3+)优先分配进入菱镁矿,K_(D_(Fe〜(3 +)))〜(ring / mw)估计在0.1至0.6之间。使用现有的菱镁矿活动组成模型,对Fe胶囊中收集的分区数据进行最小二乘拟合,得出的林铁矿相互作用参数值(W_(FeMg)〜(ring))为3.5±1 kJ mol〜(- 1)。镁硅钙石的等效正则相互作用参数(W_(FeMg)〜(mw))为12.1±1.8 kJ mol。这些确定考虑了在金属铁的存在下在两个相中出现的Fe〜(3+)浓度。在实验条件范围内,Fe交换反应的J mol〜(-1)的自由能变化可以用912 + 4.15(T-298)+ 18.9P表示,其中T在K,Pin kbar。该反应的估计体积变化小于使用状态数据方程的当前汇编预测的体积变化,并且更接近环境条件下的体积变化。因此,这些结果是对高压和高温状态数据方程式的有用测试。使用与本研究一致的热力学数据,从铁胶囊收集的数据中计算出林伍德石形成菱镁矿和菱镁矿的反应。这些结果与先前研究的比较表明,在使用Re胶囊的多砧实验中产生的相中Fe〜(3+)的存在可能对表观相关系和确定的热力学性质产生显着影响。

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