Structural and dynamical properties of aqueous NaCl brines confined in kaolinite nanopores

K Khang Quang Bui (School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,) G Gabriel D. Barbosa (School of Sustainable Chemical, Biological and Materials Engineering, The University of Oklahoma 1 , Norman, Oklahoma 73019,) T Tran Thi-Bao Le (School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,) D Dimitrios V. Papavassiliou (School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,) S Sepideh Razavi (School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,) A Alberto Striolo (Department of Chemical Engineering)

Abstract

Quantifying thermodynamics, structural, and dynamical properties of brine confined in clay pores is critical for a variety of geo-energy applications, including underground hydrogen storage (UHS) and carbon capture and sequestration (CCS). Atomistic molecular dynamics simulations are applied here to study aqueous NaCl brines within 10-Å kaolinite slit pores. NaCl concentrations are chosen at 5, 10, 12.5, and 15 wt. %, all below the solubility limit and high enough to provide statistically relevant information. The distribution of the ions within the nanopores is found not to be homogeneous. Explicitly, Na+ cations, preferentially attracted to the siloxane surface, accumulate in regions with low water density, whereas Cl− anions, attracted to the gibbsite surface of kaolinite, are found within the hydration layers. Confinement affects the properties of ions, with ion pairing being more pronounced within the pore than in bulk aqueous solutions at similar temperatures, pressures, and compositions. Conversely, the ions affect the properties of confined water. For example, the lifetime of water–water hydrogen bonds in confinement is shortened within the hydration shells; increasing salinity from 5 to 12.5 wt. % reduces the likelihood of water density fluctuations near the kaolinite surfaces, although when the NaCl concentration rises from 12.5 to 15 wt. %, Cl− anions enhance the likelihood of density fluctuations for the hydration layer near the gibbsite surface. The simulated molecular trajectories are studied further to extract diffusion coefficients. While confinement in the kaolinite nanopore reduces the mobility of all species, non-monotonic trends are observed as a function of salt concentration. The trends seem associated with the likelihood of ion pairing. Furthermore, the diffusion coefficients for the cations are predicted to be higher than those for the anions, which is contrary to what is typically observed in bulk brines. Because density fluctuations are correlated with properties such as the solubility of gases in confined water, our observations may have important implications for geo-energy applications such as UHS and CCS.

Article Details

Volume / Issue Vol. 162, Issue 12
Published March 28, 2025
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (6)

K

Khang Quang Bui

School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,

G

Gabriel D. Barbosa

School of Sustainable Chemical, Biological and Materials Engineering, The University of Oklahoma 1 , Norman, Oklahoma 73019,

T

Tran Thi-Bao Le

School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,

D

Dimitrios V. Papavassiliou

School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,

S

Sepideh Razavi

School of Sustainable Chemical, Biological, and Materials Engineering, The University of Oklahoma , Norman, Oklahoma 73019,

A

Alberto Striolo

Department of Chemical Engineering