| Abstract: | The thermodynamic properties of polymer solutions are frequently described in terms of the Flory-Huggins equation. This equation includes a parameter χ, which depends upon the intermolecular forces acting between the molecules in a solution. The experimental determination of χ was performed by an improved microtechnique and extended to a wide range of polar and nonpolar diluents of polyethylene. Careful correlations are prescribed for calculating χ from pure-component properties; they are based on an extension of the Hildebrand-Scatchard theory of solutions and on the theory of intermolecular forces. Polar (τ) and nonpolar (δ) solubility parameters are presented for a variety of solvents. For polyethylene—nonpolar solvent systems we have emphasized the factor deciding the sign of heat of mixing, while for polyethylene-polar solvent systems we have determined the contribution of dipole-induced dipole interactions ψ (δτ) in interchange-energy density B and, hence, χ. |
