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A method for estimating the activity of titania in magmatic liquids from the compositions of coexisting rhombohedral and cubic iron-titanium oxides

机译:一种从菱面体和立方铁钛氧化物共存的成分估算岩浆液中二氧化钛活性的方法

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摘要

A method is described for estimating the activity of titania (TiO_2 in a magmatic liquid from the compositions of coexisting cubic oxide (spinel) and rhombohedral oxide (ihnenite). These estimates are derived from the thermody-namic models of Ghiorso and Evans (Am J Sci 308: 957-1039, 2008; see also Sack and Ghiorso in Contrib Mineral Petrol 106:474-505, 1991a; Am Mineral 76:827-847, 1991b) and may be computed self consistently along with temperature and oxygen fugacity for an assumed pressure. The method is applied to a collection of 729 naturally occurring oxide pairs from rhyolites and dacites. For this suite of oxides, values of titania activity relative to rutile saturation range from 0.3 to 0.9. Genetically related groups of oxide pairs display activity-temperature trends with negative slopes at higher activities (0.6-0.9) or positive slopes at lower activities (0.3-0.7). Thermodynamic analysis supports the assumption of two-oxide, liquid equilibrium for the former group, but suggests that such an interpretation for oxide sequences with positive activity-temperature trends may be problematic. Application of the estimation method to oxide pairs from the Shiveluch Volcano and the Bishop Tuff reveals that the former are consistent with having equilibrated with known matrix glass compositions, whereas the latter pairs are inconsistent with equilibration with preemptive liquids trapped in quartz inclusions.
机译:描述了一种根据共存的立方氧化物(尖晶石)和菱面体氧化物(亚铁矿)的成分估算岩浆液中二氧化钛(TiO_2)活性的方法,这些估算值是根据Ghiorso和Evans(Am J Sci 308:957-1039,2008;另请参见Sack和Ghiorso,在Contrib Mineral Petrol 106:474-505,1991a; Am Mineral 76:827-847,1991b)中,并且对于温度和氧气逸度,该方法适用于从流纹岩和dacits收集的729对天然存在的氧化物对的集合。对于这组氧化物,相对于金红石饱和度的二氧化钛活性值介于0.3到0.9之间。较高活动度为负斜率(0.6-0.9)或较低活动度为正斜率(0.3-0.7)的温度趋势。热力学分析支持前者的两氧化物,液体平衡假设,但建议这说明对具有正活性-温度趋势的氧化物序列的这种解释可能是有问题的。将估算方法应用于Shiveluch火山和Bishop Tuff的氧化物对后发现,前者与已知基质玻璃成分的平衡相符,而后者与捕获在石英夹杂物中的先发液体的平衡相矛盾。

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