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离子效应对超临界 CO2-盐水界面张力的影响:分子动力学模拟及与离子强度、温度和压力的通用相关性。

Ionic Effects on Supercritical CO2-Brine Interfacial Tensions: Molecular Dynamics Simulations and a Universal Correlation with Ionic Strength, Temperature, and Pressure.

机构信息

Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy & Environment, Southeast University , Nanjing, Jiangsu 210096, China.

Department of Mechanical Engineering, Materials Science & Engineering Program, FAMU-FSU College of Engineering, Florida State University , Tallahassee, Florida 32310, United States.

出版信息

Langmuir. 2016 Sep 13;32(36):9188-96. doi: 10.1021/acs.langmuir.6b02485. Epub 2016 Sep 2.

Abstract

For geological CO2 storage in deep saline aquifers, the interfacial tension (IFT) between supercritical CO2 and brine is critical for the storage security and design of the storage capacitance. However, currently, no predictive model exists to determine the IFT of supercritical CO2 against complex electrolyte solutions involving various mixed salt species at different concentrations and compositions. In this paper, we use molecular dynamics (MD) simulations to investigate the effect of salt ions on the incremental IFT at the supercritical CO2-brine interface with respect to that at the reference supercritical CO2-water interface. Supercritical CO2-NaCl solution, CO2-CaCl2 solution and CO2-(NaCl+CaCl2) mixed solution systems are simulated at 343 K and 20 MPa under different salinities and salt compositions. We find that the valence of the cations is the primary contributor to the variation in IFT, while the Lennard-Jones potentials for the cations pose a smaller impact on the IFT. Interestingly, the incremental IFT exhibits a general linear correlation with the ionic strength in the above three electrolyte systems, and the slopes are almost identical and independent of the solution types. Based on this finding, a universal predictive formula for IFTs of CO2-complex electrolyte solution systems is established, as a function of ionic strength, temperature, and pressure. The predicted IFTs using the established formula agree perfectly (with a high statistical confidence level of ∼96%) with a wide range of experimental data for CO2 interfacing with different electrolyte solutions, such as those involving MgCl2 and Na2SO4. This work provides an efficient and accurate route to directly predict IFTs in supercritical CO2-complex electrolyte solution systems for practical engineering applications, such as geological CO2 sequestration in deep saline aquifers and other interfacial systems involving complex electrolyte solutions.

摘要

对于深部盐水层中的地质 CO2 储存,超临界 CO2 与盐水之间的界面张力(IFT)对于储存安全性和储存电容的设计至关重要。然而,目前尚无预测模型能够确定涉及不同混合盐种类、不同浓度和组成的复杂电解质溶液中超临界 CO2 的 IFT。在本文中,我们使用分子动力学(MD)模拟来研究盐离子对超临界 CO2-盐水界面相对于参考超临界 CO2-水界面的增量 IFT 的影响。在 343 K 和 20 MPa 下,模拟了超临界 CO2-NaCl 溶液、CO2-CaCl2 溶液和 CO2-(NaCl+CaCl2)混合溶液系统在不同盐度和盐组成下的情况。我们发现,阳离子的价态是导致 IFT 变化的主要因素,而阳离子的 Lennard-Jones 势能对 IFT 的影响较小。有趣的是,在上述三种电解质体系中,增量 IFT 与离子强度呈普遍线性关系,斜率几乎相同且与溶液类型无关。基于这一发现,建立了一个用于 CO2-复杂电解质溶液体系 IFT 的通用预测公式,作为离子强度、温度和压力的函数。所建立的公式预测的 IFT 与广泛的实验数据完全吻合(置信水平约为 96%),这些实验数据涉及 CO2 与不同电解质溶液的界面,例如涉及 MgCl2 和 Na2SO4 的电解质溶液。这项工作为直接预测深部盐水层中地质 CO2 封存和其他涉及复杂电解质溶液的界面系统中的超临界 CO2-复杂电解质溶液体系的 IFT 提供了一种高效准确的途径,为实际工程应用提供了便利。

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