A novel hyperbranched polymer was synthesized using acrylamide (AM), acrylic acid (AA),N-vinyl-2-pyrrolidone (NVP), and dendrite functional monomer as raw materials by redox initiation system in an aqueous medium. The hyperbranched polymer was characterized by infrared (IR) spectroscopy,1H NMR spectroscopy,13C NMR spectroscopy, elemental analysis, and scanning electron microscope (SEM). The viscosity retention rate of the hyperbranched polymer was 22.89% higher than that of the AM/AA copolymer (HPAM) at 95°C, and the viscosity retention rate was 8.17%, 12.49%, and 13.68% higher than that of HPAM in 18000 mg/L NaCl, 1800 mg/L CaCl2, and 1800 mg/L MgCl2·6H2O brine, respectively. The hyperbranched polymer exhibited higher apparent viscosity (25.2 mPa·s versus 8.1 mPa·s) under 500 s−1shear rate at 80°C. Furthermore, the enhanced oil recovery (EOR) of 1500 mg/L hyperbranched polymer solutions was up to 23.51% by the core flooding test at 80°C.
A novel copolymer containing nano-SiO2was synthesized by free radical polymerization using acrylamide (AM), acrylic acid (AA), and nano-SiO2functional monomer (NSFM) as raw materials under mild conditions. The AM/AA/NSFM copolymer was characterized by infrared (IR) spectroscopy,1H NMR spectroscopy, elemental analysis, and scanning electron microscope (SEM). It was found that the AM/AA/NSFM copolymer exhibited higher viscosity than the AM/AA copolymer at 500 s−1shear rate (18.6 mPa·s versus 8.7 mPa·s). It was also found that AM/AA/NSFM could achieve up to 43.7% viscosity retention rate at 95°C. Mobility control results indicated that AM/AA/NSFM could establish much higher resistance factor (RF) and residual resistance factor (RRF) than AM/AA under the same conditions (RF: 16.52 versus 12.17, RRF: 3.63 versus 2.59). At last, the enhanced oil recovery (EOR) of AM/AA/NSFM was up to 20.10% by core flooding experiments at 65°C.
Amphoteric hyperbranched polymers (AMHPMs) that respond to shear rate, temperature, salt, and pH were synthesized using a water free radical polymerization technique.
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