Abstract
The performance of hydrophobic associating polymers could be significantly affected by addition of a small amount of surfactant, especially around the critical association concentration. In this work, a CO2 stimuli responsive surfactant, N, N-dimethyl oleoaminde-propylamine (PKO), was introduced into the hydrophobic associating polymer solution (PMA), which endowed the conventional hydrophobic associating polymer solution with CO2 stimuli responsive performance. The conductivity measurements indicated the molecular structure and properties of PKO could be regulated with bubbling and removal of CO2 and the protonated surfactant exhibited superior surface activity. In the presence of CO2, PKO interacted with hydrophobic monomer to be mixed micelles, which prompted the transition of PMA aggregation from intramolecular association to intermolecular association, exhibiting a gel-like fluid. With removal of CO2, the mixed micelles were dissociated and the viscosity of the solution decreased significantly, leading a water-like fluid. The reversible transition of aggregation and performance could be regulated reversibly through the presence and removal of CO2. The PMA-PKO systems with CO2 switchable performance would have wide applications in hydraulic fracturing and oil production.