Equilibrium properties of three anion exchange membranes were studied in aqueous solutions of HCl under symmetrical conditions. Measurements of exchange capacities, sorption, water content, electrical conductivity and self-diffusion flux of chloride ions showed that the classical gel-phase model does not account for the experimental data. So, we had to consider two simultaneous mechanisms of transport of Cl− ions: on the one hand, a hopping mechanism in the active region including the exchange fixed sites and the counter-ions, and, on the other hand, a dragging mechanism in the interstitial region. The mobility of the counter-ions balancing the exchanging sites increased with the HCl concentration in the external solution while that of the Cl− ions in the interstitial phase of the membrane remained practically constant.