Eur. Phys. J. B 7, 573-583 (1999)
https://doi.org/10.1007/s100510050650

Free energy of semiflexible polymers and structure of interfaces

Department of Physics, Kyoto University, Kyoto 606-8502, Japan

Received: 28 May 1998
Revised: 12 August 1998
Accepted: 8 September 1998
Published online: 15 February 1999

Abstract

The free energy of semiflexible polymers is calculated as a functional of the compositional scalar order parameter ϕ and the orientational order parameter of second-rank tensor S_ij on the basis of a microscopic model of wormlike chains with variable segment lengths. We use a density functional theory and a gradient expansion to evaluate the entropic part of the free energy, which is given in a power series of . The interaction term of the free energy is derived with a random phase approximation. For the rigid rod limit, the nematic-isotropic transition point is given by , N and w being the degree of polymerization and the anisotropic interaction parameter, respectively, and the degree of ordering at the transition point is 0.33448. We also find that the contour length of polymer chains becomes larger in a nematic phase than in an isotropic phase. Interface profiles are obtained numerically for some typical cases. In the neighborhood of isotropic-isotropic interfaces, polymer chains tend to align parallel to the interface on the polymer-rich side and perpendicular on the poor side. When an isotropic region and a nematic region coexist, orientational order parallel to the interface is preferred in the nematic region.