压力为4 GPa,温度为1400 ~ 1500℃时,铁对CaCO3±橄榄石±蛇纹石基体的渗透特性(实验数据)

V. Sonin, E. Zhimulev, A. Chepurov, A. Turkin, A. Chepurov
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引用次数: 0

摘要

研究课题。我们提出了在高P-T参数下,与CaCO3-Fe体系相比,在橄榄石和蛇纹石存在下CaCO3与金属铁相互作用的建模的第一个结果。这项研究的相关性与在全球碳循环的背景下研究地壳物质向地球还原地幔俯冲过程中的脱碳反应的需要有关。方法。实验在bar高压仪器上进行,压力为4.0 GPa,温度为1400-1500°С,随后在配备化学微量分析系统的扫描电子显微镜上对所得样品进行研究。结果。CaCO3在实现的条件下是不稳定的。反应产物为碳化铁和有硅酸盐相存在的钙镁乌斯特或钙镁乌斯特。结论。在高压下,即使组分处于固态,CaCO3也会与金属铁发生相互作用。在相互作用过程中,由于Fe-C体系中共晶的熔融温度相对较低,液态金属的出现提供了较高的反应速率。确定了重力对铁渗入碳酸盐基体的影响,主要表现为碳酸盐晶粒间液态金属的渗透。H2O的存在显著降低了碳酸盐的熔点,导致组分扩散加快,脱碳反应速率加快,同时在高流化环境下,由于液态Fe的密度与其他组分存在差异,也会产生重力的影响。
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Peculiarities of Fe penetration into the matrix of CaCO3 ± olivine ± serpentine at a pressure of 4 GPa and temperature of 1400-1500°C (experimental data)
Research subject. We present the first results on modeling of the interaction of CaCO3 with metallic Fe in the presence of olivine and serpentine at high P-T parameters in comparison with the CaCO3-Fe system. The relevance of the study is related to the need to study decarbonatization reactions during subduction of crustal matter into the Earth's reduced mantle within the context of the global carbon cycle. Methods. The experiment was carried out using a BARS high-pressure apparatus at a pressure of 4.0 GPa and temperatures of 1400-1500°С with a subsequent study of the obtained samples on a scanning electron microscope equipped with a chemical microanalysis system. Results. CaCO3 was found to be unstable under the implemented conditions. The reaction products were iron carbide and Ca-wustite or Ca-magnesiowustite in the presence of silicate phases. Conclusions. The interaction of CaCO3 with metallic Fe at high pressure occurs even if the components are in the solid state. High reaction rates during interaction are provided by the appearance of liquid metal due to the relatively low melting temperature of the eutectic in Fe-C systems. The influence of gravity on the penetration of Fe into the carbonate matrix, which consists in the predominant infiltration of liquid metal between carbonate grains, was established. The presence of H2O significantly reduces the melting point of carbonate, which leads to an increase in the diffusion of components and decarbonization reaction rate, while the effect of gravity also takes place due to the difference in the density of liquid Fe in comparison with other components in a highly fluidized environment.
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