Pt-Fe合金的矿物学及Pt-Fe二元体系中的相关系

L. Cabri, T. Oberthür, D. Schumann
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引用次数: 5

摘要

提出了一个修订的Pt-Fe相图来取代材料科学文献中使用的相图(例如,Okamoto 2004),并通过添加矿物学文献中发表的高温相平衡数据来改进Cabri和Feather(1975)的相图。在纯Pt - Fe体系中,室温下预测的固溶场大致如下:γ(Pt,Fe)从Pt到Pt0.78Fe0.22, Pt3Fe从Pt3.04Fe0.96到Pt2.64Fe1.36, PtFe从Pt1.16Fe0.84到Pt0.67Fe0.33, PtFe3从Pt1.26Fe2.94到Pt0.68Fe3.32。本文讨论并评价了原始侵入岩和矿石以及由原始侵入岩和矿石经长期物理和化学风化作用形成的淋积物和砂矿床中Pt-Fe合金的相关系和相界。尽管微量元素和微量元素的浓度不同,但天然Pt-Fe合金矿物与纯Pt-Fe二元体系中的相关系良好。
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The Mineralogy of Pt-Fe Alloys and Phase Relations in the Pt–Fe Binary System
A revised Pt–Fe phase diagram is proposed to replace those used in the materials science literature (e.g., Okamoto 2004), and to improve the one of Cabri & Feather (1975) by adding high-temperature phase equilibria data published in the mineralogical literature. The projected solid-solution fields at room temperature in the pure Pt–Fe system lie at the following approximate compositions: for γ(Pt,Fe) from Pt to Pt0.78Fe0.22, for Pt3Fe from Pt3.04Fe0.96 to Pt2.64Fe1.36, for PtFe from Pt1.16Fe0.84 to Pt0.67Fe0.33, and for PtFe3 from Pt1.26Fe2.94 to Pt0.68Fe3.32. The phase relations and phase boundaries are discussed and evaluated for Pt-Fe alloys occurring in pristine intrusive rocks and ores as well as in eluvial and placer deposits derived from the former by physical and chemical weathering over long periods of geologic time. In spite of the variable concentrations of minor and trace elements, the natural Pt-Fe alloy minerals correlate well with phase relations in the pure Pt–Fe binary system.
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