Ionized poly(acrylic acid) gels were studied both at concentrations close to the concentration of preparation and at swelling equilibrium. In the first experimental condition, the introduction of electrostatic interactions decreases the shear modulus. The addition of salt screens these interactions and allows one to recover the shear modulus of unneutralized gels. The correlation of these effects with light scattering results suggests that they are related to a change of the gel microstructure with electrostatic interactions. The swelling equilibrium of these gels if found to scale like the ratio of the ionization degree to the Debye-Huckel screening parameter with an exponent 6/5. The shear modulus at swelling equilibrium is given by the simple affine deformation law for not too high smelling degrees (<200). For larger swelling ratios, the shear modulus increases with swelling ratio due to deviations from Gaussian elasticity. These results can be partly explained by a recently proposed model. Finally, the cooperative diffusion coefficient can be measured by kinetics of swelling experiments and its behavior does not follow the predictions of the same model, possibly due to the coupling of cooperative diffusion with the establishment of a Donnan equilibrium.