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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Boron isotope geochemistry during diagenesis. Part I. Experimental determination of fractionation during illitization of smectite
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Boron isotope geochemistry during diagenesis. Part I. Experimental determination of fractionation during illitization of smectite

机译:成岩过程中的硼同位素地球化学。第一部分。蒙脱石非法化过程中分馏的实验测定

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Experiments were performed to measure the isotopic fractionation of boron between illite/smectite (I/S) clay minerals and water as a function of temperature (300 degrees and 350 degreesC) and degree of illitization. Corresponding changes in the oxygen isotopes were monitored as an indication of the approach to equilibrium. The kinetics of the B-isotope exchange follows the mineralogical restructuring of smectite as it recrystallizes to illite. An initial decline in delta B-11(I/S) occurs when the I/S is randomly ordered (RO). The delta B-11(I/S) values reach a plateau during R1 ordering of the I/S, representing a metastable condition. The greatest change in delta B-11(I/S) is observed during long-range (R3) ordering of the I/S when neoformation occurs. Values of delta B-11(I/S) measured on the equilibrium reaction products were used to construct a B-isotope fractionation curve. There is a linear correlation among data from these experiments and 1100 degreesC basaltic melt-fluid fractionation experiments (Hervig and Moore, 2000) that can be extrapolated to include adsorption experiments at 25 degreesC (Palmer et al,, 1987), Unlike other stable isotopic systems (e.g., oxygen) there is no mineral-specific fractionation of B-isotopes, bur rather a coordination dependence of the fractionation. Under diagenetic conditions B is predominantly in trigonal coordination in fluids but substitutes in tetrahedral sites of silicates. The preference of B-10 for tetrahedral bonds is the major fractionating factor of B in silicates. Copyright (C) 2001 Elsevier Science Ltd. [References: 52]
机译:进行实验以测量伊利石/蒙脱石(I / S)黏土矿物和水之间的硼同位素分馏随温度(300度和350摄氏度)和硅化程度的变化。氧同位素的相应变化被监测以指示达到平衡的方法。 B-同位素交换的动力学遵循蒙脱石重结晶为伊利石时的矿物学结构调整。当I / S被随机排序(RO)时,会出现增量B-11(I / S)的初始下降。在I / S的R1排序过程中,增量B-11(I / S)值达到平稳状态,表示亚稳态。当发生新形成时,在I / S的远程(R3)排序期间,可以观察到B-11(I / S)的最大变化。在平衡反应产物上测得的δB-11(I / S)值用于构建B-同位素分馏曲线。这些实验数据与1100摄氏度的玄武岩熔体流体分馏实验(Hervig and Moore,2000)的数据之间存在线性相关性,可以推断为包括25摄氏度的吸附实验(Palmer等,1987),这与其他稳定同位素不同在系统(例如氧气)中,不存在B同位素的矿物特异性分馏,bur而是分馏的配位依赖性。在成岩条件下,B主要在流体中处于三角配位状态,但在硅酸盐的四面体位点被替代。 B-10对于四面体键的优先选择是B在硅酸盐中的主要分馏因子。版权所有(C)2001 Elsevier Science Ltd. [引用:52]

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