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

被引:0
作者
Bui, Khang Quang [1 ]
Barbosa, Gabriel D. [1 ]
Le, Tran Thi-Bao [1 ]
Papavassiliou, Dimitrios V. [1 ]
Razavi, Sepideh [1 ]
Striolo, Alberto [1 ]
机构
[1] Univ Oklahoma, Sch Sustainable Chem Biol & Mat Engn, Norman, OK 73019 USA
基金
美国国家科学基金会;
关键词
SHAPED SILICA NANOPORES; MOLECULAR-DYNAMICS; DIFFUSION-COEFFICIENTS; WATER MIXTURES; MASS-TRANSPORT; ION SOLVATION; HYDROGEN; SIMULATION; ASSOCIATION; HYDRATION;
D O I
10.1063/5.0251946
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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-& Aring; 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.
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页数:13
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共 107 条
  • [1] Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
    Abraham, Mark James
    Murtola, Teemu
    Schulz, Roland
    Páll, Szilárd
    Smith, Jeremy C.
    Hess, Berk
    Lindah, Erik
    [J]. SoftwareX, 2015, 1-2 : 19 - 25
  • [2] Aksu I., 2015, GeoResJ, V7, P1, DOI 10.1016/j.grj.2015.02.003
  • [3] The effect of clay on initial and residual saturation of hydrogen in clay-rich sandstone formation: Implications for underground hydrogen storage
    Al-Yaseri, Ahmed
    Esteban, Lionel
    Yekeen, Nurudeen
    Giwelli, Ausama
    Sarout, Joel
    Sarmadivaleh, Mohammad
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2023, 48 (13) : 5175 - 5185
  • [4] Blue hydrogen: Current status and future technologies
    AlHumaidan, Faisal S.
    Halabi, Mamun Absi
    Rana, Mohan S.
    Vinoba, Mari
    [J]. ENERGY CONVERSION AND MANAGEMENT, 2023, 283
  • [5] Cushion gas effects on clay-hydrogen-brine wettability at conditions relevant to underground gas storage
    Ali, Azeezat
    Cole, David R.
    Striolo, Alberto
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2024, 58 : 668 - 677
  • [6] CO2 Solubility in Aqueous Electrolyte Solutions Confined in Calcite Nanopores
    Ali, Azeezat
    Striolo, Alberto
    Cole, David R.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2021, 125 (22) : 12333 - 12341
  • [7] Allen M. P., 1987, Computer Simulation of Liquids
  • [8] Fluids and Electrolytes under Confinement in Single-Digit Nanopores
    Aluru, Narayana R.
    Aydin, Fikret
    Bazant, Martin Z.
    Blankschtein, Daniel
    Brozena, Alexandra H.
    de Souza, J. Pedro
    Elimelech, Menachem
    Faucher, Samuel
    Fourkas, John T.
    Koman, Volodymyr B.
    Kuehne, Matthias
    Kulik, Heather J.
    Li, Hao-Kun
    Li, Yuhao
    Li, Zhongwu
    Majumdar, Arun
    Martis, Joel
    Misra, Rahul Prasanna
    Noy, Aleksandr
    Tuan Anh Pham
    Qu, Haoran
    Rayabharam, Archith
    Reed, Mark A.
    Ritt, Cody L.
    Schwegler, Eric
    Siwy, Zuzanna
    Strano, Michael S.
    Wang, YuHuang
    Yao, Yun-Chiao
    Zhan, Cheng
    Zhang, Ze
    [J]. CHEMICAL REVIEWS, 2023, 123 (06) : 2737 - 2831
  • [9] Preferential Adsorption from Liquid Water-Ethanol Mixtures in Alumina Pores
    Anh Phan
    Cole, David R.
    Striolo, Alberto
    [J]. LANGMUIR, 2014, 30 (27) : 8066 - 8077
  • [10] Aqueous Methane in Slit-Shaped Silica Nanopores: High Solubility and Traces of Hydrates
    Anh Phan
    Cole, David R.
    Striolo, Alberto
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (09) : 4860 - 4868