首页> 外文期刊>Doklady Earth Sciences >Phase Relations and Melting in the Systems of Peridotite-H_2O-CO_2 and Eclogite-H_2O-CO_2 at Pressures up to 27 GPa
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Phase Relations and Melting in the Systems of Peridotite-H_2O-CO_2 and Eclogite-H_2O-CO_2 at Pressures up to 27 GPa

机译:橄榄岩-H_2O-CO_2和榴辉岩-H_2O-CO_2在高达27 GPa的压力下的相关系和熔融

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摘要

Experimental study of phase equilibria with volatile components is the most important task for solution of the problems related to the processes of melting and distribution of matter in the Earth's mantle [1]. The main volatile components in the mantle may be described in the C—O—H system. Oxidized compounds, namely H_2O and CO_2 dominate in the upper mantle at depths up to 100—200 km. CH_4, as well as possibly other hydrocarbons, and H_2 become more important on deeper levels at a gradual decrease of f_(O_2) values [2, 3]. However oxidized species may be preserved at a depth up to at least 600—700 km [4], as well as participate in "redox-melting" [5]. Because of this, it is important to study their influence on phase relations in mantle rocks at high pressures. Solidus and phase equilibria of H_2O-bearing peridotite and eclog-ite systems have been studied in detail up to a pressure of 25 GPa [6, 7]. The same systems with CO_2 are studied up to pressures of 20—32 GPa [8—11]. However, the systems containing both H_2O and CO_2 are studied only at low pressures up to 6 GPa [5, 12—14]. In this paper we report the main results of the experimental study of the systems peridotite—H_2O—CO_2 and eclog-ite—H_2O—CO_2 up to a pressure of 27 GPa.
机译:解决具有挥发性成分的相平衡的实验是解决与地球地幔中物质融化和分布过程有关的问题的最重要任务[1]。地幔中的主要挥发性成分可以在CH系统中描述。氧化的化合物,即H_2O和CO_2在上地幔中占主导地位,深度达100-200 km。随着f_(O_2)值的逐渐降低,CH_4以及可能的其他碳氢化合物和H_2在更深的水平上变得更加重要[2,3]。但是,被氧化的物种可以保留至少600-700 km的深度[4],并参与“氧化还原融化” [5]。因此,重要的是研究它们在高压下对地幔岩石中相关系的影响。含H_2O的橄榄岩和榴辉岩系统的固相和相平衡已被详细研究,压力高达25 GPa [6,7]。研究了具有CO_2的相同系统,压力最高为20-32 GPa [8-11]。但是,仅在高达6 GPa的低压下研究同时包含H_2O和CO_2的系统[5,12-14]。在本文中,我们报告了橄榄石-H_2O-CO_2和榴辉岩-H_2O-CO_2压力高达27 GPa的实验研究的主要结果。

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  • 来源
    《Doklady Earth Sciences》 |2011年第2期|p.498-502|共5页
  • 作者单位

    V.S. Sobolev Institute of Geology and Mineralogy, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia;

    V.S. Sobolev Institute of Geology and Mineralogy, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia;

    V.S. Sobolev Institute of Geology and Mineralogy, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia;

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