The monomers containing phenylsulfonamide N-allyl-4-methylbenzenesulfonamide (TCAP) and N,N-diallyl-4-methyl benzenesulfonamide (TCDAP) were copolymerized with acrylamide (AM), acrylic acid (AA), and 3-(3-methacrylamidopropyl-dimethylammonio)-propane-1-sulfonate (MDPS), respectively, through free-radical micellar copolymerization in deionized water for enhanced oil recovery (EOR). Then, the effect of the synthesis conditions was investigated simultaneously; the copolymers were characterized by Fourier transform infraredFTIR, nuclear magnetic resonance, scanning electron microscopy, and thermogravimetric analysis. It was found that the thickening function, high-temperature resistance (120 C), and anti-shear ability were improved significantly. It was also found that the copolymers had excellent viscoelasticity at the lower shear frequencies. When the copolymers were dissolved in 10,000 mg L −1 NaCl, 2000 mg L −1 CaCl 2 , and 2000 mg L −1 MgCl 2 solutions, the viscosity retention rates of AM/AA/TCAP/MDPS and AM/AA/TCDAP/MDPS were 13.3, 11.1, 10.6% and 18.6, 15.2, 11.7%, respectively. In addition, the copolymers for EOR at 60 C were 11.4 and 13.8%, respectively, which demonstrated that the copolymers possessed excellent performance for potential application in EOR.
Herein, novel hyperbranched polyamidoamine guanidinium salts (GS-h-PAMAM) and two cationic acrylamide copolymers P(AM-DAC-ABSM) and P(AM-DAC-AMTU) were successfully prepared. Then, self-assembly supramolecular systems were synthesized by directly mixing GS-h-PAMAM with copolymers in aqueous solution, and the mechanism of the self-assembly process was speculated. FT-IR, NMR, and SEM were used for structural confirmation. Furthermore, the excellent solution properties revealed that the supramolecular systems had potential application in clay hydration inhibitors. More importantly, utilizing functionalized hyperbranched polyamidoamine in the synthesis self-assembly supramolecular systems was an effective strategy for expanding their application fields and developing new functional materials, providing a powerful reference for the next study.
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