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A novel amphiphilic polymer, APAM, for enhanced oil recovery (EOR), was synthesized by radical copolymerization of acrylamide, dodecyl polyoxyethylene acrylate (DPEA), and N-(1,1,3,3-tetramethyl butyl) acrylamide (TBA), using potassium persulfate-sodium bisulfite as initiator-activator. The aggregation morphological observation of APAM in aqueous and NaCl solutions was performed using scanning electron microscope. The ability of APAM to solubilize and emulsify n-heptane and crude oil was investigated by visual methods, microscopy, and particle size analyses. The results show that APAM forms supramolecular aggregates in aqueous and NaCl solutions and has strong emulsification ability. As a result, the emulsion consisting of APAM aqueous solution and n-heptane (or crude oil) is much more stable than that of HPAM (partially hydrolyzed polyacrylamide, widely used in EOR), indicating a important function of APAM to emulsify oil component. [ABSTRACT FROM AUTHOR]

With the vacuum sublimation freezing-drying and rheological techniques, the salt/alkali/surfactant effects on the solution properties and the aggregate conformations of the polymers, synthesized hydrophobically modified poly (acrylamide) (HMPAM), were investigated. The experimental methods included viscosity measurements, the photomicroscopy, scan electron microscopy, and the freeze fracture transmission electron microscopy. The variety of conformations of the ultramolecular aggregates, the hydrophobical region, and the spatial network structures resulted from the hydrophobical interaction were studied. Combined results confirmed that HMPAM could form several of interesting three-dimensional network structures either in distilled water or NaCl solution. The results have revealed the mechanism of the salt/alkali/surfactant effects on the peculiar rheological properties of the solution. [ABSTRACT FROM AUTHOR]

The viscous properties, scanning electronic microscopy (SEM), and water/oil interfacial tension (IFT) of partially hydrolyzed polyacryamide (HPAM) and hydrophobically associating hydrolyzed polyacryamides modified with N-dodecylacrylamide were studied with the objective of investigating the influence on destabilization of emulsions. As expected, the copolymers exhibit significant viscosity enhancing capacity and three-dimensional network structures due to intermolecular hydrophobic associations, and also present high interfacial activities as the IFT decrease with increasing polymer concentration. As a result, the existences of copolymers increased both the viscosity of emulsions and the intensity of interfacial film, in which case slow down the diffusion of demulsifier molecules and enhance the stability of emulsions, finally, the separation of water from oil becomes more difficult. [ABSTRACT FROM AUTHOR]