Effect of imidazolium-based ionic liquid on CO2 sequestration: a study on solubility, interfacial properties, and X-ray imaging in water-wet formations
Amany A. Aboulrous , Nihal Mounir Darraj , Vincenzo Cunsolo , David Uko , J.P. Martin Trusler , Martin J. Blunt
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引用次数: 0
Abstract
The efficiency of geological CO₂ sequestration is often limited by low CO₂ solubility, which poses challenges for long-term storage stability. This study addresses these limitations by exploring the potential of 1-butyl-3-methylimidazolium bromide (BMIM-Br) to enhance CO₂ storage in water-wet subsurface formations. BMIM-Br was synthesized via a microwave-assisted method and the structure was confirmed using different spectroscopic methods including Fourier Transform Infrared Spectroscopy (FTIR), and Proton Nuclear Magnetic Resonance (1H NMR) analysis.
Under conditions of 3 MPa and 323.15 K, the solubility of CO₂ in a 5 wt% BMIM-Br solution was more than double the solubility in pure water. At 0.3 MPa, the interfacial tension (IFT) between CO₂ and the BMIM-Br solution decreased from 36.3 mN/m to 32.9 mN/m at 293.15 and 323.15 K, respectively compared to the pure water values 69.9 mN/m and 63.8 mN/m respectively at the same conditions. When CO2 was injected into a Bentheimer sandstone rock sample fully saturated with the aqueous phase. There was a significant increase in CO₂ saturation (SCO2), rising from 0.58 with pure water to 0.72 with BMIM-Br. The lowered interfacial tension allows more of the pore space to be accessed at the same imposed capillary pressure. When the aqueous phase was injected to displace CO2, the residual saturation was 0.21 with pure water, but only 0.16 for the BMIM-Br solution. This is likely a consequence of increased dissolution of CO2 in BMIM-Br. These results suggest that BMIM-Br significantly improves CO₂ solubility and injectivity by reducing interfacial tension. Its overall impact points to a promising strategy for optimizing CO₂ sequestration in subsurface formations.
期刊介绍:
The journal includes papers in the following areas:
– Simple organic liquids and mixtures
– Ionic liquids
– Surfactant solutions (including micelles and vesicles) and liquid interfaces
– Colloidal solutions and nanoparticles
– Thermotropic and lyotropic liquid crystals
– Ferrofluids
– Water, aqueous solutions and other hydrogen-bonded liquids
– Lubricants, polymer solutions and melts
– Molten metals and salts
– Phase transitions and critical phenomena in liquids and confined fluids
– Self assembly in complex liquids.– Biomolecules in solution
The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include:
– Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.)
– Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.)
– Light scattering (Rayleigh, Brillouin, PCS, etc.)
– Dielectric relaxation
– X-ray and neutron scattering and diffraction.
Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.