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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Trace element partitioning between vapor, brine and halite under extreme phase separation conditions
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Trace element partitioning between vapor, brine and halite under extreme phase separation conditions

机译:在极端相分离条件下,微量元素在蒸气,盐水和盐岩之间分配

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摘要

Experiments were conducted to investigate the partitioning of Li, Br, Rb, Cs and B between vapor, brine and halite during subcritical and supercritical phase separation in the NaCl-H2O system (388-550 degrees C, 250-350 bars). Results indicate that Li and Br partition preferentially into the low-salinity vapor fluids, while Rb and Cs become more enriched in the coexisting brines. Under more extreme conditions of pressure and temperature in the two-phase region, especially near the vapor-brine-halite boundary, strong salting-out effects imposed on neutral aqueous species enhance significantly partitioning of all trace elements into the low-salinity fluid. Dissolved boron is strongly affected by this and a particularly strong enrichment into vapors is observed, a trend that can be effectively correlated with changes in reduced density. Exclusion of Li, Br, Rb, Cs and B from halite, when precipitated, further increases the solubility of these species in the coexisting Cl-poor fluid. In general, the lack of distortion in the partitioning behavior of trace elements between vapor, brine and/or halite with the transition from subcritical to supercritical conditions in the NaCl-H2O system precludes the need for special reference to the critical point of seawater when interpreting phase relations in submarine hydrothermal systems. The combination of experimentally determined trace element partitioning data with constraints imposed by mineral solubility provides a means to better understand the origin and evolution of hot spring vent fluids. For example, in Brandon hydrothermal system (21 degrees S EPR) supercritical phase separation and subseafloor mixing appear to be the main heat and mass transport mechanisms fueled by a shallow magmatic intrusion, with boron systematics ruling out major contributions from magmatic degassing processes accompanying the near-seafloor volcanism. (c) 2007 Elsevier Ltd. All rights reserved.
机译:进行了实验,以研究在NaCl-H2O系统(388-550摄氏度,250-350巴)中的亚临界和超临界相分离过程中,Li,Br,Rb,Cs和B在蒸气,盐水和盐岩之间的分配。结果表明,Li和Br优先分配到低盐度蒸汽流体中,而Rb和Cs在共存盐水中更富集。在两相区域更极端的压力和温度条件下,尤其是在蒸气-卤化物-卤化物边界附近,强加于中性水族的盐析作用会显着增强所有微量元素向低盐度流体的分配。溶解的硼受到此的强烈影响,并且观察到蒸汽中的富集特别强,这种趋势可以与密度降低的变化有效相关。当析出锂,锂,溴,R,铯和硼时,它们从盐石中排除会进一步增加这些物质在贫氯液体中的溶解度。通常,NaCl-H2O系统中的微量元素在亚临界条件下转变为超临界条件时,蒸气,盐水和/或盐岩中微量元素的分配行为没有畸变,因此在解释时无需特别参考海水的临界点海底热液系统的相位关系。实验确定的微量元素分配数据与矿物溶解度所施加的限制相结合,为更好地了解温泉排放液的起源和演化提供了一种手段。例如,在布兰登热液系统(南太平洋21度)中,超临界相分离和海底混合似乎是浅岩浆侵入推动的主要传热和传质机制,硼系统排除了伴随岩浆脱气过程的主要贡献海底火山活动。 (c)2007 Elsevier Ltd.保留所有权利。

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