高温高压下水镁石与水之间H同位素分馏的路径积分分子动力学预测

IF 4.5 1区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Caihong Gao , Yun Liu
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引用次数: 0

摘要

含氢矿物脱水过程中的氢(H)同位素分馏对追踪俯冲过程至关重要。前人的研究表明,水镁石与水之间的H同位素分馏对压力的变化非常敏感。然而,氢同位素在高温高压下的详细行为仍然知之甚少。在这项研究中,我们利用路径积分分子动力学(PIMD)模拟研究了水镁石和水在高温(300-1273 K)和压力(0-8 GPa)下的D/H同位素分馏,以解释核量子效应(NQEs)。采用基于第一性原理分子动力学(FPMD)数据训练的深电位模型来加速模拟。在实验温度下,水的减配函数比随压力的增加而减小,而水石膏的减配函数比随压力的增加而增大。由于压力对水镁石和水的rfrs有相反的影响,水镁石和水之间的D/H同位素分馏对压力变化非常敏感,并且在高压下(例如在2 GPa和200℃)分馏是相反的。水镁石和水中氢键环境对压力变化的响应不同,导致了D/H同位素分异的逆转。利用水镁石作为俯冲带含h矿物的代表,我们模拟了三个不同俯冲带中陆块中保留水和释放到地幔中的水的δD值。结果表明,板坯水和释放水的δD值与板坯压力和温度密切相关。模拟的释放水δD值主要在−40‰~−70‰之间,与衰竭地幔δD平均值(−60±5‰)重叠。由于同位素分异的逆转,输往地球深部(>200 km)的水表现出较高的δD值(>−50±10‰),表明极低的δD特征(例如<;—200‰)可能不是过去深俯冲作用的结果。模拟结果还表明,输送到地球深部的循环水的δD值可能与原始地幔储层的δD值不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Path-integral molecular dynamics predictions of H isotope fractionation between brucite and water at elevated temperatures and pressures
Hydrogen (H) isotope fractionation during the dehydration of H-bearing minerals is crucial for tracing the subduction processes. Previous studies have shown that H isotope fractionation between brucite and water is highly sensitive to the change of pressure. However, the detailed behaviors of H isotopes at high temperatures and high pressures remain poorly understood. In this study, we investigate the D/H isotope fractionation between brucite and water at elevated temperatures (300–1273 K) and pressures (0–8 GPa) using path-integral molecular dynamics (PIMD) simulations to account for the nuclear quantum effects (NQEs). The deep potential models trained on the first-principles molecular dynamics (FPMD) data were used to accelerate the simulations. The calculated reduced partition function ratios (RPFRs) of water decrease with increasing pressure at all the temperatures studied in this work, while the RPFRs of brucite increase with pressure. Due to the opposing pressure effects on RPFRs of these two phases, the D/H isotope fractionation between brucite and water is highly sensitive to the pressure change, and the fractionations are inversed at high pressures (e.g., at 2 GPa and 200 °C). The reversal of D/H isotope fractionation is attributed to the distinct responses of H bonding environments in brucite and water to the pressure changes.
Using brucite as a proxy for H-bearing minerals in subduction zones, we modeled the δD values of both the water retained in the slab and the water released into the mantle in three different subduction zones. The results demonstrate that the δD values of both the slab water and the released water are closely related to the pressures and temperatures of the slabs. The modeled δD values of the released water mainly range from − 40 ‰ to − 70 ‰, overlapping with the average δD value of the depleted mantle (−60 ± 5 ‰). Due to the reversal of isotope fractionation, the water transported into the deep Earth (>200 km) exhibit relatively high δD values (>−50 ± 10 ‰), suggesting that the extremely low δD signatures (e.g., < −200 ‰) reported in previous works may not be the results of the past deep subductions. The modeled results also indicate that recycled water transported into the deep Earth may have δD values distinct from those of primitive mantle reservoirs.
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来源期刊
Geochimica et Cosmochimica Acta
Geochimica et Cosmochimica Acta 地学-地球化学与地球物理
CiteScore
9.60
自引率
14.00%
发文量
437
审稿时长
6 months
期刊介绍: Geochimica et Cosmochimica Acta publishes research papers in a wide range of subjects in terrestrial geochemistry, meteoritics, and planetary geochemistry. The scope of the journal includes: 1). Physical chemistry of gases, aqueous solutions, glasses, and crystalline solids 2). Igneous and metamorphic petrology 3). Chemical processes in the atmosphere, hydrosphere, biosphere, and lithosphere of the Earth 4). Organic geochemistry 5). Isotope geochemistry 6). Meteoritics and meteorite impacts 7). Lunar science; and 8). Planetary geochemistry.
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