Though the transition from cylindrical micelles to spherical micelles of the anionic surfactant potassium oleate in the presence of oils has been studied, these changes have not been studied for long-tail zwitterionic surfactants. The effects of n-decane, crude oil (CO), extra virgin olive oil (EVOO) and polyglycolic acid (PGA) on the zero-shear viscosity of an aqueous solution of a sulfobetaine surfactant system were investigated at 30 C and 60 C. The main surfactant in the system was erucamidopropyl hydroxypropyl sulfobetaine. The methods employed were rheology and cryo-TEM. The solution with 3.96 wt% surfactant system and 6.2 wt% CaCl 2 was viscoelastic at both test temperatures due to the formation of entangled cylindrical micelle networks. n-Decane induced the following regimes of zeroshear viscosity change at both temperatures: (i) the high viscosity regime (HVR), (ii) the transition regime (TR), and (iii) the low viscosity regime (LVR). The HVR was characterized by high zero-shear viscosities.The TR was characterized by a sharp drop in zero-shear viscosity due to the formation of untangled micelles. The LVR was due to the formation of microemulsions. The formation of these regimes depended on the balance between micellization and oil solubilization. We reveal for the first time that the number of regimes depends on the type of oil: both CO and EVOO induced only one and two regimes at 30 C and 60 C, respectively. PGA did not significantly affect the solution at either temperature with increasing concentration, meaning the solution was resistant to decreasing pH even at higher temperatures.
High-temperature/high-salinity (HTHS) reservoirs contain a significant fraction of the world's remaining oil in place and are potential candidates for enhanced oil recovery (EOR). Selection of suitable surfactants for such reservoirs is a challenging task. In this work, two synthesized zwitterionic surfactants bearing a saturated and an unsaturated tail, namely 3-(N-stearamidopropyl-N,N-dimethyl ammonium) propanesulfonate and 3-(N-oleamidopropyl-N,N-dimethyl ammonium) propanesulfonate, respectively, were evaluated. The surfactant with the unsaturated tail showed excellent solubility in synthetic seawater (57,643 ppm) and in formation brine (213,734 ppm). However, the unsaturated surfactant with a saturated tail showed poor solubility, and therefore it was not evaluated further. The thermal stability of the synthesized unsaturated surfactant solution in seawater was evaluated by heating the solution at 90 C in a sealed aging tube for 2 weeks. The thermal stability of the unsaturated surfactant was confirmed by FTIR and NMR analysis of the aged samples at such harsh conditions. The critical micelle concentration (CMC) of the synthesized unsaturated surfactant in seawater was 1.02 × 10 −4 mol L −1 , while the surface tension at CMC was 30 mN m −1 . The synthesized unsaturated surfactant was able to reduce the oil-water interfacial tension tõ 10 −1 mN m −1 at different conditions. A commercial copolymer of acrylamide and 2-acrylamido-2-methylpropane sulfonic acid (AM-AMPS) was tested for EOR applications in HTHS conditions. The addition of the synthesized unsaturated surfactant to the AM-AMPS copolymer increased the viscosity of the system. The increase in oil recovery by injecting the unsaturated surfactant solution and the surfactant-polymer mixture in solution was 8 and 21%, respectively. The excellent properties of the synthesized unsaturated surfactant show that surfactants with an unsaturated tail can be an excellent choice for HTHS reservoirs.
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