Nanostructures in Water-in-CO₂ Microemulsions Stabilized by Double-Chain Fluorocarbon Solubilizers

High-pressure small-angle neutron scattering (HP-SANS) studies were conducted to investigate nanostructures and interfacial properties of water-in-supercritical CO₂ (W/CO₂) microemulsions with double-fluorocarbon-tail anionic surfactants, having different fluorocarbon chain lengths and linking groups (glutarate or succinate). At constant pressure and temperature, the microemulsion aqueous cores were found to swell with an increase in water-to-surfactant ratio, <i>W</i>₀, until their solubilizing capacities were reached. Surfactants with fluorocarbon chain lengths of <i>n</i> = 4, 6, and 8 formed spherical reversed micelles in supercritical CO₂ even at <i>W</i>₀ over the solubilizing powers as determined by phase behavior studies, suggesting formation of Winsor-IV W/CO₂ microemulsions and then Winsor-II W/CO₂ microemulsions. On the other hand, a short C2 chain fluorocarbon surfactant analogue displayed a transition from Winsor-IV microemulsions to lamellar liquid crystals at <i>W</i>₀ = 25. Critical packing parameters and aggregation numbers were calculated by using area per headgroup, shell thickness, the core/shell radii determined from SANS data analysis: these parameters were used to help understand differences in aggregation behavior and solubilizing power in CO₂. Increasing the microemulsion water loading led the critical packing parameter to decrease to ∼1.3 and the aggregation number to increase to >90. Although these parameters were comparable between glutarate and succinate surfactants with the same fluorocarbon chain, decreasing the fluorocarbon chain length <i>n</i> reduced the critical packing parameter. At the same time, reducing chain length to 2 reduced negative interfacial curvature, favoring planar structures, as demonstrated by generation of lamellar liquid crystal phases