Publication | Open Access
Evaluation of hydrophobically associated polyacrylamide‐containing aqueous fluids and their potential use in petroleum recovery
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Citations
15
References
2004
Year
Industrial PolyacrylamideEngineeringAbstract AcrylamidePotential UsePolymersChemical EngineeringPolymer TechnologyMacromolecular EngineeringPetroleum ChemistryPolymer ProcessingRheologyCommercial PolyacrylamidePolymer ChemistryPolymer EngineeringPetroleum RecoveryBiopolymersPolymer AnalysisChemical Enhanced Oil RecoveryPolymer SolutionPolymer SciencePolymer CharacterizationAqueous FluidsPetroleum Engineering
Abstract Acrylamide and tridecyl acrylate copolymers were synthesized by micellar copolymerization to obtain water‐soluble, hydrophobically modified polymers. Rheological properties of the obtained polymer solutions were evaluated and compared to those of solutions of a commercial polyacrylamide currently used in the petroleum industry. The behavior of the copolymer solutions was studied as a function of the variation of hydrophobic monomer content incorporated in the copolymer as well as the salt content of the aqueous medium, for diluted and semi‐diluted regimens. Comparative studies of such effects on the intrinsic viscosity and the critical concentration of those polymers were conducted. The increase in hydrophobic monomer content produced a sudden increase in the bulk and absolute viscosity of the polymeric solutions, a trend that was more intense from a certain concentration typical for each polymer. Salt addition led to lower bulk viscosity caused by a stronger interaction among hydrophobic groups, resulting from minimized exposure of such groups and water. The same effect was observed for the critical concentration. A comparison of the synthesized polymers with industrial polyacrylamide showed that the synthesized polymers were characterized by advantageously high shear strength and high salt resistance. However, in the absence of salts, higher copolymer amounts were needed to prepare solutions whose viscosity was the same as that of commercial polyacrylamide. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3686–3692, 2004
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