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The in situ saponification of crude oil lowers the interfacial tensions of oil–water systems in chemical-enhanced oil recovery (cEOR). When the interfacial tension is sufficiently low, emulsion phases occur, and the fluid phase distribution in the pore space changes, affecting oil displacement efficiency. This change in capillarity allows the injection water to penetrate different classes of pores, which must be reflected in the distribution of fluids in the pore space. This issue still needs to be adequately researched and is not reflected in the classic analyses of oil cluster size. We have performed μCT-based coreflood experiments to study the displacement efficiency of crude oil by alkaline solutions acting as cEOR agents for in situ saponification. The measured fluid distributions were analyzed using oil-cluster size statistics. In addition, the pore classes from which the oil was preferentially displaced and the degree of displacement as a function of alkali concentration were determined. Despite ultralow interfacial tension and emulsion formation, a clear separation of the oil and aqueous phases was observed over a wide range of alkali concentrations, allowing a two-phase analysis of the microscopic fluid distribution. It was found that (a) a Lorentz analysis of the cluster volume distribution is useful to characterize the cEOR displacement efficiency. It shows the tendency of oil clusters toward a more uniform size distribution toward optimal alkali concentration. (b) the additional oil recovery toward optimal displacement conditions comes from the fraction of smaller pores; at optimal conditions, all pore classes are flooded almost equally and to a high degree, equivalent to miscible displacement, i.e., extremely low interfacial tension.
The in situ saponification of crude oil lowers the interfacial tensions of oil–water systems in chemical-enhanced oil recovery (cEOR). When the interfacial tension is sufficiently low, emulsion phases occur, and the fluid phase distribution in the pore space changes, affecting oil displacement efficiency. This change in capillarity allows the injection water to penetrate different classes of pores, which must be reflected in the distribution of fluids in the pore space. This issue still needs to be adequately researched and is not reflected in the classic analyses of oil cluster size. We have performed μCT-based coreflood experiments to study the displacement efficiency of crude oil by alkaline solutions acting as cEOR agents for in situ saponification. The measured fluid distributions were analyzed using oil-cluster size statistics. In addition, the pore classes from which the oil was preferentially displaced and the degree of displacement as a function of alkali concentration were determined. Despite ultralow interfacial tension and emulsion formation, a clear separation of the oil and aqueous phases was observed over a wide range of alkali concentrations, allowing a two-phase analysis of the microscopic fluid distribution. It was found that (a) a Lorentz analysis of the cluster volume distribution is useful to characterize the cEOR displacement efficiency. It shows the tendency of oil clusters toward a more uniform size distribution toward optimal alkali concentration. (b) the additional oil recovery toward optimal displacement conditions comes from the fraction of smaller pores; at optimal conditions, all pore classes are flooded almost equally and to a high degree, equivalent to miscible displacement, i.e., extremely low interfacial tension.
This research investigates the interactions between a novel environmentally friendly chemical fluid consisting of Xanthan gum and bio-based surfactants, and crude oil. The surfactants, derived from various leaves using the spray drying technique, were characterized using Fourier-transform infrared (FTIR) spectroscopy, zeta potential analysis, Dynamic light scattering, and evaluation of critical micelle concentration. Static emulsion tests were conducted to explore the emulsification between crude oil and the polymer-surfactant solution. Analysis of the bulk oil FTIR spectra revealed that saturated hydrocarbons and light aromatic hydrocarbons exhibited a higher tendency to adsorb onto the emulsion phase. Furthermore, the increased presence of polar hydrocarbons in emulsion phases generated by polar surfactants confirmed the activation of electrostatic forces in fluid–fluid interactions. Nuclear magnetic resonance spectroscopy showed that the xanthan solution without surfactants had a greater potential to adsorb asphaltenes with highly fused aromatic rings, while the presence of bio-based surfactants reduced the solution's ability to adsorb asphaltenes with larger cores. Microfluidic tests demonstrated that incorporating surfactants derived from Morus nigra and Aloevera leaves into the xanthan solution enhanced oil recovery. While injection of the xanthan solution resulted in a 49.8% recovery rate, the addition of Morus nigra and Aloevera leaf-derived surfactants to the xanthan solution increased oil recovery to 58.1% and 55.8%, respectively.
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