Rheological properties and concentration cross-overs of anionic acrylamide copolymers in saline solutions (potassium chloride) were investigated by using capillary viscometer method. Area of non-overlapping coils between the crossover concentration and the concentration of fluctuation mesh formation was determined; it was shown that with increase of salt concentration this area practically disappears, i.e. mass transfer mechanism changes near the crossover concentration. It was shown that at low concentrations of potassium chloride increasing the content of ionic groups of macromolecules leads to reduction in the crossover concentration and increase in the effective volume. It is found that the kaolin adsorption capacity decreases when polymers are adsorbed from saline solution, and the adsorption constant is significantly higher in the presence of salt than in water.

Dissolution of acrylamide anionic (co)polymers in saline solutions (potassium and sodium chlorides) with concentration of 3.4 mol/l was studied by atomic absorption spectroscopy, optical microscopy, gel-test and capillary viscosimetry. It has been established that with increasing in the content of ionogenic groups and the transition from sodium chloride to potassium chloride solutions the dissolution rate of (co)polymer increases. The concentration of cations of low molecular weight electrolytes is higher in the swollen polymer phase than in the solution in the swelling stage of polymers, the difference in the counter ion content decreases with increasing dissolution time. Comparative analysis of the Huggins constant and the hydrodynamic radii of acrylamide (co)polymers has showed that increase in the interaction in polymer-solvent system is accompanied by the increase in size of macromolecular coils. The Kuhn segment of polymer macromolecules is higher in sodium chloride solutions than in potassium chloride solutions and increases with the decrease in ionogenic group content.

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