Pore-scale simulation of H2-brine system relevant for underground hydrogen storage: A lattice Boltzmann investigation

被引:3
|
作者
Wang, Yuhang [1 ]
Chakrapani, Thejas Hulikal [2 ]
Wen, Zhang [1 ]
Hajibeygi, Hadi [2 ]
机构
[1] China Univ Geosci, Sch Environm Studies, Wuhan 430078, Peoples R China
[2] Delft Univ Technol, Fac Civil Engn & Geosci, Dept Geosci & Engn, NL-2628 CV Delft, Netherlands
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Underground hydrogen storage; Flow in porous media; Pore-scale modeling; Relative permeability; RELATIVE PERMEABILITY; 2-PHASE FLOW; POROUS-MEDIA; CAPILLARY-PRESSURE; MODEL; FLUID; DISPLACEMENT; STATE; HYSTERESIS; DYNAMICS;
D O I
10.1016/j.advwatres.2024.104756
中图分类号
TV21 [水资源调查与水利规划];
学科分类号
081501 ;
摘要
Underground hydrogen (H-2) storage in saline aquifers is a viable solution for large-scale H-2 storage. Due to its remarkably low viscosity and density, the flow of H-2 within saline aquifers exhibits strong instability, which needs to be thoroughly investigated to ensure safe operations at the storage site. For the first time, we develop a lattice Boltzmann model tailored for pore-scale simulations of the H-2-brine system under typical subsurface storage conditions. The model captures the significant contrast of fluid properties between H-2 and brine, and it offers the flexibility to adjust the contact angle to suit varying wetting conditions. We show that the snap-off is enhanced in a system with a high capillary number and a small contact angle. These conditions lead to a low recovery factor, which is unfavorable for H-2 production from the aquifer. Moreover, the relative permeability curves, computed from the simulation results, exhibit distinct behaviors for H-2 and brine. In the case of the wetting phase, the relative permeability can be quantified using the quadratic expression, whereas for the non-wetting phase, the relative permeability exhibits a nearly linear behavior, and saturation alone appears insufficient to characterize the relative permeability at large saturations of non-wetting phase. This implies that different formula for liquid and gas phases may be employed for continuum-scale simulations.
引用
收藏
页数:11
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