Equilibrium melting relations at shallow lower mantle P-T conditions probed by the laser-heated diamond anvil cell

IF 1.2 4区 地球科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY
L. Pison Pacynski, E. Gardés, D. Andrault
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引用次数: 0

Abstract

Laser-heated diamond anvil cell (LH-DAC) is needed to investigate melting properties of deep planetary interiors. Interpretation of the melting behavior is however challenging because extreme temperature gradients are inevitable. In this work, we investigate how the peak temperature at the center of the laser spot, from sample solidus to 1000 K above (ΔT), affects the chemical relations between melt and solid residue. We investigate the melting behavior of two possible mantle compositions, pyrolite and chondritic type material, at pressures corresponding to depths of ~ 1000 km and higher (40–73 GPa). Recovered samples are characterized at nanoscale spatial resolution using electron microscopy. Samples tend to show that chemical composition of melts and bridgmanite-melt relations vary largely with peak temperature. With increasing ΔT, the (Mg,Fe) exchange coefficient (KFe-MgBg/melt) decreases from 0.29 to 0.11, and SiO2 contents in melt ([SiO2]melt) from 43 to 18 wt%. In addition, we observe that the higher ΔT, the more the liquid is depleted in bridgmanitic-type composition. These experimental features are contrary with those expected from the known melting diagram of typical mantle material. Instead, they are well explained by considering fast solidification of bridgmanite (Bg) at the edge of the molten zone, in disequilibrium conditions. The sample prepared at solidus temperature and for short duration presents a central melt pool of Ca-bearing melt in close contact with Bg and ferropericlase. The degree of partial melting is coherently estimated to 18(2) wt% by two independent observations. This corresponds to pseudo-eutectic conditions where only the third mineral, davemaoite, is exhausted. For a pressure of 40.5 GPa, KFe-MgBg/melt and [SiO2]melt are found to be 0.29 and 43 wt%, respectively, in good agreement with multi-anvil press experiments. Altogether, this work shows that erroneous solid–liquid chemical relations can arise from samples synthesized at temperatures well above solidus in the LH-DAC.

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来源期刊
Physics and Chemistry of Minerals
Physics and Chemistry of Minerals 地学-材料科学:综合
CiteScore
2.90
自引率
14.30%
发文量
43
审稿时长
3 months
期刊介绍: Physics and Chemistry of Minerals is an international journal devoted to publishing articles and short communications of physical or chemical studies on minerals or solids related to minerals. The aim of the journal is to support competent interdisciplinary work in mineralogy and physics or chemistry. Particular emphasis is placed on applications of modern techniques or new theories and models to interpret atomic structures and physical or chemical properties of minerals. Some subjects of interest are: -Relationships between atomic structure and crystalline state (structures of various states, crystal energies, crystal growth, thermodynamic studies, phase transformations, solid solution, exsolution phenomena, etc.) -General solid state spectroscopy (ultraviolet, visible, infrared, Raman, ESCA, luminescence, X-ray, electron paramagnetic resonance, nuclear magnetic resonance, gamma ray resonance, etc.) -Experimental and theoretical analysis of chemical bonding in minerals (application of crystal field, molecular orbital, band theories, etc.) -Physical properties (magnetic, mechanical, electric, optical, thermodynamic, etc.) -Relations between thermal expansion, compressibility, elastic constants, and fundamental properties of atomic structure, particularly as applied to geophysical problems -Electron microscopy in support of physical and chemical studies -Computational methods in the study of the structure and properties of minerals -Mineral surfaces (experimental methods, structure and properties)
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