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Modeling mass transfer of CO2 in brine at high pressures by chemical potential gradient
KTH, School of Architecture and the Built Environment (ABE), Civil and Architectural Engineering, Structural Engineering and Bridges. Southeast University, China.
2013 (English)In: Science China Chemistry, ISSN 1674-7291, Vol. 56, no 6, 821-830 p.Article in journal (Refereed) Published
Abstract [en]

To investigate long-term CO2 behavior in geological formations and quantification of possible CO2 leaks, it is crucial to investigate the potential mobility of CO2 dissolved in brines over a wide range of spatial and temporal scales and density distributions in geological media. In this work, the mass transfer of aqueous CO2 in brines has been investigated by means of a chemical potential gradient model based on non-equilibrium thermodynamics in which the statistical associating fluid theory equation of state was used to calculate the fugacity coefficient of CO2 in brine. The investigation shows that the interfacial concentration of aqueous CO2 and the corresponding density both increase with increasing pressure and decreasing temperature; the effective diffusion coefficients decrease initially and then increase with increasing pressure; and the density of the CO2-disolved brines increases with decreasing CO2 pressure in the CO2 dissolution process. The aqueous CO2 concentration profiles obtained by the chemical potential gradient model are considerably different from those obtained by the concentration gradient model, which shows the importance of considering non-ideality, especially when the pressure is high.

Place, publisher, year, edition, pages
2013. Vol. 56, no 6, 821-830 p.
Keyword [en]
CO2 geological sequestration, density, diffusion, dissolution, mass transport, non-equilibrium thermodynamics, SAFT EoS
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Other Chemistry Topics
URN: urn:nbn:se:kth:diva-134268DOI: 10.1007/s11426-013-4834-8ISI: 000319775900016ScopusID: 2-s2.0-84878770696OAI: diva2:666261

QC 20131122

Available from: 2013-11-22 Created: 2013-11-20 Last updated: 2013-11-22Bibliographically approved

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