4.7 Article

Chlorine isotope fractionation during serpentinization and hydrothermal mineralization: A density functional theory study

期刊

CHEMICAL GEOLOGY
卷 581, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.chemgeo.2021.120406

关键词

Equilibrium chlorine isotope fractionation; Chlorine-bearing minerals; Serpentinization; Hydrothermal mineralization

资金

  1. National Natural Science Foundation of China [41973002, 41830428]
  2. China National Space Administration (CNSA) [D020205]

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This study investigates the chlorine isotope fractionation during serpentinization and hydrothermal mineralization, using density functional theory and ab initio molecular dynamics simulations. The results suggest a potential alternative for using apatite-group minerals to constrain the origin and evolution of hydrothermal fluids, alongside tracking sources of chloride in subduction zones and mineralizing fluids in ore deposits using chlorine isotopes.
Because of the large-scale recycling of volatile chlorine from the interior to the surface of the Earth, it is possible to use the isotopic composition of this element (delta Cl-32) in serpentinite to study mantle-crust interactions in subduction zones. It is also possible to use chlorine isotopes to track the evolution of fluids (through fluid inclusions/minerals) in hydrothermal ore-forming systems. Here, we report the results of a study of equilibrium chlorine isotope fractionation during serpentinization and hydrothermal mineralization based on density functional theory (DFT) and ab initio molecular dynamics simulations (AIMD). The chlorine isotope fractionation between lizardite and brine under variable thermodynamic conditions is described by the relationship 10001n alpha(lizardite-fluid) = 0.4170 x (1000/T)(2)-0.0281 x (1000/T) + 0.0582, which yielded Delta Cl-37(lizardite-fluid) values of +0.49 to +4.46 parts per thousand, +0.41 to +0.59 parts per thousand and + 0.49 to +3.57 parts per thousand for conditions at the seafloor, in the mantle wedge and in subduction zones. As a proxy for the diversity of metal-chloride complexes in hydrothermal fluids, the stable configurations of ferrous chloride complexes were acquired from long trajectories of AIMD simulation. Using this information, the chlorine isotope fractionation between minerals (i.e., apatite-group minerals, muscovite, phlogopite, tremolite, lizardite, marialite and metal halides) and ore-forming fluid was estimated. The relatively large chlorine isotope fractionation (Delta Cl-37(minerals-hydrothermal fluid) values from -1.99 to +2.18 parts per thousand) might partly explain the large variation of delta Cl-32 in individual fluid inclusions observed in hydrothermal ore deposits. Because of the limited chlorine isotope fractionation between apatite and hydrothermal fluid (i.e., delta Cl-32 (apatite-ore-forming fluid) of 0.06 parts per thousand-0.69 parts per thousand), apatite-group minerals might be an alternative to fluid inclusions for constraining the origin and evolution of hydrothermal fluids using delta Cl-32 values. The theoretical constraints provided in this paper will facilitate the use of chlorine isotopes in tracking the sources of chloride in subduction zones and the origin of mineralizing fluids in ore deposits.

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