纳米孔隙度对含碳流体行为的影响

D. Cole, A. Striolo
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引用次数: 6

摘要

孔隙度和渗透率是连接含碳流体的起源、形态、运动和数量的关键变量,共同决定了流体-气-岩系统的物理和化学演化。孔隙的分布、孔隙体积及其连通性因地球物质、地质环境和历史的不同而有很大差异。总的趋势是孔隙度和渗透率随着深度的增加,以及孔隙尺寸和/或裂缝孔径宽度的增加而减小。例外情况包括变形带(如断层或剪切带)、岩浆侵位区和俯冲带。孔隙或裂缝显示三维层次结构,表现出可变的连通性,定义了孔隙和/或裂缝网络。这种网络结构和拓扑控制:(1)内部孔隙体积,矿物相,以及流体,水溶液,挥发物,包裹体等可接近的潜在反应表面;(2)扩散路径长度、弯曲度以及平流或扩散输运的优势。对于由更细的网络控制的固体,传输主要是缓慢的平流和/或扩散。尽管流体-矿物相互作用在地质系统中可以发生广泛的空间和时间尺度,但包括矿物表面或埋藏界面(如孔隙、孔喉、晶界、微裂缝和位错)中的流体在内的界面现象(图12.1)会影响地质系统中多相流和反应性输运的性质。流体-矿物系统的复杂性表现为多种形式,包括水中溶解成分的相互作用、矿物表面的润湿膜、溶解和挥发物质的吸附、反应的启动以及流动物质的运输。当考虑到典型的最小长度尺度的孔隙和裂缝特征及其扩展的三维网络结构时,物理(输运)和化学性质(反应性)以及相关相互作用的直接观察和建模是具有挑战性的。各种孔隙类型及其在与流体反应过程中的演化是控制流体可达孔隙体积分布、流动动力学、流体滞留、化学反应性和污染物运移的重要因素。而在浅地壳环境中,裂缝主导流在体积上可能占主导地位
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The Influence of Nanoporosity on the Behavior of Carbon-Bearing Fluids
Porosity and permeability are key variables linking the origin, form, movement, and quantity of carbon-bearing fluids that collectively dictate the physical and chemical evolution of fluid–gas–rock systems. The distribution of pores, pore volume, and their connectedness vary widely, depending on the Earth material, its geologic context, and its history. The general tendency is for porosity and permeability to decrease with increasing depth, along with pore size and/or fracture aperture width. Exceptions involve zones of deformation (e.g. fault or shear zones), regions bounding magma emplacement and subduction zones. Pores or fractures display three-dimensional hierarchical structures, exhibiting variable connectivity defining the pore and/or fracture network. This network structure and topology control: (1) internal pore volumes, mineral phases, and potentially reactive surfaces accessible to fluids, aqueous solutions, volatiles, inclusions, etc.; and (2) diffusive path lengths, tortuosity, and the predominance of advective or diffusive transport. For solids dominated by finer networks, transport is dominated by slow advection and/or diffusion. Despite the extensive spatial and temporal scales over which fluid–mineral interactions can occur in geologic systems, interfacial phenomena including fluids at mineral surfaces or contained within buried interfaces such as pores, pore throats, grain boundaries, microfractures, and dislocations (Figure 12.1) impact the nature of multiphase flow and reactive transport in geologic systems. Complexity in fluid–mineral systems takes many forms, including the interaction of dissolved constituents in water, wetting films on mineral surfaces, adsorption of dissolved and volatile species, the initiation of reactions, and transport of mobile species. Direct observations and modeling of physical (transport) and chemical properties (reactivity) and associated interactions are challenging when considering the smallest length scales typical of pore and fracture features and their extended three-dimensional network structures. The various void types and their evolution during reaction with fluids are critically important factors controlling the distribution of the fluid-accessible pore volume, flow dynamics, fluid retention, chemical reactivity, and contaminant species transport. While fracture-dominated flow can be volumetrically dominant in shallow crustal settings
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