Abstract

AbstractBACKGROUND: Hydrophobically modified polyelectrolytes are widely used polymers due to their good water solubility, stretched configuration in water and strong hydrophobic association. The study reported here aimed at researching the double action of hydrophobic association and electrostatic effect of novel hydrophobically modified polyelectrolytes in solution.RESULTS: A series of novel hydrophobically modified polyelectrolytes were synthesized by micellar copolymerization with various feed ratios of sodium 2‐acrylamido‐2‐methylpropanesulfonate, N‐n‐dodecylamine and sodium dodecylsulfonate. Their structure was characterized using Fourier transform infrared spectroscopy, nuclear magnetic resonance and gel permeation chromatography, and the viscosities of their aqueous and salt solutions were studied.CONCLUSION: The results show that the addition of the hydrophobic comonomer results in a decrease in molecular weight (Mw). The smaller the initial number of hydrophobes in one micelle, the higher is Mw of the resulting copolymer. The viscosity of PAD‐1.73 polyelectrolyte is less sensitive to salt than those of the others. According to the zero shear viscosity and corresponding concentration, the critical cluster‐forming concentration, critical overlap concentration and critical entanglement concentration of these polymer solutions were determined. Moreover, in the dilute regime the viscosity decreases with increasing salinity, while in the semi‐dilute regime the viscosity decreases first and then increases. It is suggested that in dilute and semi‐dilute regimes, hydrophobic intramolecular association and intermolecular association dominate, respectively. Copyright © 2009 Society of Chemical Industry

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