Abstract

Recent progress in the understanding of the binding of surfactants to hydrophobically modified polymers (HMP), and the consequences of such binding, is reviewed. HMP are water-soluble polymers onto which low proportions of hydrophobic sidechains (hydrophobes) have been grafted. In an aqueous environment, the HMP hydrophobes associate among themselves and with added surfactant molecules into micelle-like aggregates. An HMP may therefore be considered as a ‘modified surfactant’, and the binding of surfactants to HMP is analogous to the mixed micellisation in mixed surfactant solutions. The binding isotherm gives the concentration of free (monomeric) surfactant and the stoichiometry of the HMP/surfactant complex at different total compositions. In mixtures involving ionic surfactants, it is found that the free surfactant often dominates, and gives important contributions to the ionic strength. Characteristic properties of HMP/surfactant mixtures may be related to stoichiometries of the mixed complexes. Thus, the maximum in solution viscosity, which is commonly found in HMP/surfactant mixtures, occurs at a similar hydrophobe stoichiometry (ratio of bound surfactant to HMP hydrophobe) for many different systems, although the total concentrations of surfactant at the maximum may vary by orders of magnitude, depending on the surfactant cmc. The solubility of a complex of oppositely charged HMP and surfactant is related to the charge stoichiometry of the complex. The phase separation/redissolution phenomena occurring in the bulk solution influence the HMP adsorption to surfaces and the forces between surfaces with adsorbed HMP.

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