(De)hydration Front Propagation Into Zero-Permeability Rock

IF 2.9 2区 地球科学 Q2 GEOCHEMISTRY & GEOPHYSICS
Stefan M. Schmalholz, Lyudmila Khakimova, Yury Podladchikov, Erwan Bras, Philippe Yamato, Timm John
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Abstract

Hydration and dehydration reactions play pivotal roles in plate tectonics and the deep water cycle, yet many facets of (de)hydration reactions remain unclear. Here, we study (de)hydration reactions where associated solid density changes are predominantly balanced by porosity changes, with solid rock deformation playing a minor role. We propose a hypothesis for three scenarios of (de)hydration front propagation and test it using one-dimensional hydro-mechanical-chemical models. Our models couple porous fluid flow, solid rock volumetric deformation, and (de)hydration reactions described by equilibrium thermodynamics. We couple our transport model with reactions through fluid pressure: the fluid pressure gradient governs porous flow and the fluid pressure magnitude controls the reaction boundary. Our model validates the hypothesized scenarios and shows that the change in solid density across the reaction boundary, from lower to higher pressure, dictates whether hydration or dehydration fronts propagate: decreasing solid density causes dehydration front propagation in the direction opposite to fluid flow while increasing solid density enables both hydration and dehydration front propagation in the same direction as fluid flow. Our models demonstrate that reactions can drive the propagation of (de)hydration fronts, characterized by sharp porosity fronts, into a viscous medium with zero porosity and permeability; such propagation is impossible without reactions, as porosity fronts become trapped. We apply our model to serpentinite dehydration reactions with positive and negative Clapeyron slopes and granulite hydration (eclogitization). We use the results of systematic numerical simulations to derive a new equation that allows estimating the transient, reaction-induced permeability of natural (de)hydration zones.

Abstract Image

(零渗透性岩石中的(脱)水化前沿传播
水化和脱水反应在板块构造和深层水循环中起着举足轻重的作用,但(脱)水化反应的许多方面仍不清楚。在这里,我们研究了(脱)水合反应,在这种反应中,相关的固体密度变化主要由孔隙度变化来平衡,而固体岩石变形只起次要作用。我们提出了(脱)水化前沿传播的三种情况,并使用一维水文机械化学模型进行了测试。我们的模型将多孔流体流动、固体岩石体积变形和平衡热力学描述的(脱)水化反应结合起来。我们通过流体压力将传输模型与反应结合起来:流体压力梯度控制多孔流,流体压力大小控制反应边界。我们的模型验证了假设的情况,并表明反应边界上固体密度从低压到高压的变化决定了水合或脱水前沿的传播:降低固体密度会导致脱水前沿向与流体流动相反的方向传播,而增加固体密度则会使水合和脱水前沿向与流体流动相同的方向传播。我们的模型证明,反应可以推动(脱)水合前沿向孔隙度和渗透率为零的粘性介质传播,而孔隙度和渗透率为零的粘性介质则以尖锐的孔隙度前沿为特征;如果没有反应,这种传播是不可能的,因为孔隙度前沿会被困住。我们将模型应用于克拉皮隆斜率为正和负的蛇纹岩脱水反应以及花岗岩水化(蚀变)。我们利用系统数值模拟的结果推导出一个新方程,该方程可以估算天然(脱)水化带的瞬态反应诱导渗透率。
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来源期刊
Geochemistry Geophysics Geosystems
Geochemistry Geophysics Geosystems 地学-地球化学与地球物理
CiteScore
5.90
自引率
11.40%
发文量
252
审稿时长
1 months
期刊介绍: Geochemistry, Geophysics, Geosystems (G3) publishes research papers on Earth and planetary processes with a focus on understanding the Earth as a system. Observational, experimental, and theoretical investigations of the solid Earth, hydrosphere, atmosphere, biosphere, and solar system at all spatial and temporal scales are welcome. Articles should be of broad interest, and interdisciplinary approaches are encouraged. Areas of interest for this peer-reviewed journal include, but are not limited to: The physics and chemistry of the Earth, including its structure, composition, physical properties, dynamics, and evolution Principles and applications of geochemical proxies to studies of Earth history The physical properties, composition, and temporal evolution of the Earth''s major reservoirs and the coupling between them The dynamics of geochemical and biogeochemical cycles at all spatial and temporal scales Physical and cosmochemical constraints on the composition, origin, and evolution of the Earth and other terrestrial planets The chemistry and physics of solar system materials that are relevant to the formation, evolution, and current state of the Earth and the planets Advances in modeling, observation, and experimentation that are of widespread interest in the geosciences.
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