热液条件下k -长石晶体结构各向异性对溶蚀动力学影响的实验研究

M. Pollet-Villard , D. Daval , P. Ackerer , G.D. Saldi , K.G. Knauss , B. Wild , B. Fritz
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引用次数: 7

摘要

我们提出了在Soultz-sous-Forêts增强型地热系统中,各向异性对热液条件下k -长石溶解动力学影响的实验研究结果。我们试图量化钾长石各向异性对溶解速率的影响,以建立一个更全面的硅酸盐矿物反应表面演化模型,并提出可用于水岩相互作用模型和反应输运代码的替代动力学速率定律。我们的研究结果表明,钾晶石溶解速率与吉布斯反应自由能(ΔGr)之间的关系明显不同于地球化学代码中通常采用的过渡态理论:它取决于钾晶石矿物的晶体取向,不同晶面之间存在显著差异。至于远离平衡的溶解速率,这一结果突出表明,使用一个独特的理论速率定律来描述溶解速率作为ΔGr的函数仍然是非常值得怀疑的。这些结果对我们理解和模拟溶解机制的挑战非常重要,它们证明了溶解各向异性在这些机制中起着根本作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental Study of Dissolution Kinetics of K-feldspar as a Function of Crystal Structure Anisotropy under Hydrothermal Conditions

We present the results of an experimental study of the effect of anisotropy on the kinetics of K-Feldspar dissolution under hydrothermal conditions as encountered in the Soultz-sous-Forêts enhanced geothermal system. We try to quantify the impact of K-feldspar anisotropy on dissolution rates in order to develop a more comprehensive model of the evolution of the reactive surface of silicate minerals in order to propose alternate kinetic rate laws to be implemented into water-rock interaction models and reactive transport codes. Our results evidence a relation between K-spar dissolution rate and the Gibbs free energy of reaction (ΔGr) which clearly differs from the transition state theory usually implemented into geochemical codes: it depends on the crystallographic orientation of K-spar mineral with significant differences between the different crystal faces. As for the far-from-equilibrium dissolution rate, this result highlights that using a unique theoretical rate law to describe dissolution rate as a function of ΔGr remains highly questionable. These results are very important for our challenge of understanding and modelling the dissolution mechanisms and they evidence that the dissolution anisotropy plays a fundamental role in these mechanisms.

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