Abstract
We report results of small angle neutron scattering measurements made on sodium polystyrene sulfonate in aqueous salt solutions. The correlation length (ξ) and osmotic compressibility are measured as a function of polymer (c) and added salt (c(S)) concentrations, and the results are compared with scaling predictions and the random-phase approximation (RPA). In Dobrynin et al.'s scaling model the osmotic pressure consists of a counter-ion contribution and a polymer contribution. The polymer contribution is found to be two orders of magnitude smaller than expected from the scaling model, in agreement with earlier observations made on neutral polymers in good solvent condition. RPA allows the determination of single-chain dimensions in semidilute solutions at high polymer and added salt concentrations, but fails for c(S)≤ 2 M. The χ parameter can be modelled as the sum of an intrinsic contribution (χ(0)) and an electrostatic term: χ∼χ(0) + K'/√c(S), where χ(0) > 0.5 is consistent with the hydrophobic nature of the backbone of NaPSS. The dependence of χ(elec)∼ 1/√c(S) disagrees with the random-phase approximation (χ(elec)∼ 1/c(s)), but agrees with the light scattering results in dilute solution and Dobrynin et al.'s scaling treatment of electrostatic excluded volume.