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

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL Journal of Chemical Physics Pub Date : 2025-03-28 DOI:10.1063/5.0251946
Khang Quang Bui, Gabriel D Barbosa, Tran Thi-Bao Le, Dimitrios V Papavassiliou, Sepideh Razavi, Alberto Striolo
{"title":"Structural and dynamical properties of aqueous NaCl brines confined in kaolinite nanopores.","authors":"Khang Quang Bui, Gabriel D Barbosa, Tran Thi-Bao Le, Dimitrios V Papavassiliou, Sepideh Razavi, Alberto Striolo","doi":"10.1063/5.0251946","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":15313,"journal":{"name":"Journal of Chemical Physics","volume":"162 12","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1063/5.0251946","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
高岭石纳米孔中NaCl盐水的结构和动力学性质。
量化粘土孔隙中盐水的热力学、结构和动力学性质对于各种地能应用至关重要,包括地下储氢(UHS)和碳捕集与封存(CCS)。本文应用原子分子动力学模拟研究了10个-Å高岭石狭缝孔内的NaCl盐水。NaCl浓度分别为5%、10%、12.5和15wt . %,均低于溶解度极限,但足以提供统计学上相关的信息。离子在纳米孔中的分布是不均匀的。显然,Na+阳离子优先被硅氧烷表面吸引,聚集在水密度低的区域,而Cl-阴离子被高岭石的三水石表面吸引,聚集在水化层内。约束影响离子的性质,在相同的温度、压力和成分下,孔内的离子配对比散装水溶液中更明显。相反,离子会影响承压水的性质。例如,水-水氢键在封闭条件下的寿命在水化壳内被缩短;当盐度从5%增加到12.5 wt. %时,可降低高岭石表面附近水密度波动的可能性,但当NaCl浓度从12.5 wt. %增加到15 wt. %时,Cl-阴离子可增强三水石表面附近水化层密度波动的可能性。进一步研究模拟的分子轨迹,提取扩散系数。虽然限制在高岭石纳米孔中降低了所有物种的迁移率,但观察到盐浓度的非单调趋势。这种趋势似乎与离子配对的可能性有关。此外,预测阳离子的扩散系数高于阴离子的扩散系数,这与在散装盐水中通常观察到的相反。由于密度波动与气体在密闭水中的溶解度等性质相关,因此我们的观察结果可能对UHS和CCS等地能应用具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Chemical Physics
Journal of Chemical Physics 物理-物理:原子、分子和化学物理
CiteScore
7.40
自引率
15.90%
发文量
1615
审稿时长
2 months
期刊介绍: The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance. Topical coverage includes: Theoretical Methods and Algorithms Advanced Experimental Techniques Atoms, Molecules, and Clusters Liquids, Glasses, and Crystals Surfaces, Interfaces, and Materials Polymers and Soft Matter Biological Molecules and Networks.
期刊最新文献
Crystallization and structural rearrangement in nearly hard-sphere model colloidal suspensions: A long-time study across concentration regimes. Excitonic-coupling enhancement in double π-helical dimers for highly efficient and robust circularly polarized luminescence. Formal O(N3) scaling GW calculations by block tensor decomposition for large molecule systems. Neutral barium in solid neon: Optical spectroscopy and first excited state lifetime. A universal metric for classifying gas transport regimes in nanoconfined media.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1