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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >The trace-component trapping effect: Experimental evidence, theoretical interpretation, and geochemical applications
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The trace-component trapping effect: Experimental evidence, theoretical interpretation, and geochemical applications

机译:痕量组分的捕获效应:实验证据,理论解释和地球化学应用

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摘要

Experimental data indicating increase of crystal-melt (fluid) partition coefficients in the range of microconcentrations of trace elements are reviewed and analyzed in detail. This concentration dependence of partition coefficients has been referred to as either deviations from Henry's law or the trace-component trapping effect. A critical review of a variety of models proposed to explain this phenomenon is also given. It is shown that the most reasonable and developed of these models relate changes in trace element partition coefficient at low concentrations to interactions between the trace element ions and metastable lattice defects (i.e., linear and planar defects) at low temperatures or intrinsic point defects of thermal origin at higher temperatures. The mechanism of interaction between trace element substituent atoms and intrinsic defects is considered in detail, with particular consideration given to the creation of pair associates, coupled substitutions, and the influence of other impurities on the trace element dissolution. The models developed are fit to the available experimental data to provide descriptions of the dependence of partition coefficients on composition and to estimate the concentrations and free energies of formation of the intrinsic defects (i.e., vacancies and interstitial atoms) in a matrix crystal. Some probable geochemical applications and manifestations of the trapping effect are discussed. This leads to the conclusion that there is an urgent need for further consideration of the problem.
机译:回顾并详细分析了表明微量元素微量浓度范围内的熔体(流体)分配系数增加的实验数据。分配系数的这种浓度依赖性已被称为与亨利定律的偏离或痕量组分的捕获效应。还对提出用来解释这种现象的各种模型进行了严格审查。结果表明,这些模型中最合理,最完善的模型是,低浓度时痕量元素分配系数的变化与低温时痕量元素离子与亚稳晶格缺陷(即线性和平面缺陷)或热的固有点缺陷之间的相互作用有关。起源于更高的温度。详细考虑了微量元素取代原子与固有缺陷之间的相互作用机理,特别考虑了缔合缔合体,偶联取代以及其他杂质对微量元素溶解的影响。所开发的模型适合于可用的实验数据,以描述分配系数对成分的依赖性,并估计基质晶体中固有缺陷(即空位和间隙原子)形成的浓度和自由能。讨论了一些可能的地球化学应用和圈闭作用的表现形式。由此得出结论,迫切需要进一步考虑该问题。

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