MOLECULAR-WEIGHT DEPENDENCE OF DIBLOCK COPOLYMER SEGREGATION AT A POLYMER-POLYMER INTERFACE

Utilizing forward recoil spectrometry (FRES), we have determined the segregation isotherm which describes the interfacial excess z(i)* of diblock copolymers of poly(d8-styrene-b-2-vinylpyridine) (dPS-PVP) at the interface between the homopolymers PS and PVP as a function of phi(infinity) the volume fraction of diblock copolymer remaining in the host homopolymer. All the samples were analyzed after annealing at temperatures and times sufficient to achieve equilibrium segregation. The effect of the degree of polymerization of both the diblock copolymers and the host homopolymers on the segregation isotherm is investigated. When the degree of polymerization of the homopolymer is much larger than that of the diblock copolymer, the normalized interfacial excess (z(i)*/R(g)), where R(g) is the radius of gyration of an isolated block copolymer chain, is a universal function of that portion of the block copolymer chemical potential due to chain stretching. The existence of such a universal function is predicted by theory and its form is in good agreement with self-consistent mean field calculations. Using these results, one can predict important aspects of the block copolymer segregation (e.g., the saturation interfacial excess) without recourse to the time-consuming numerical calculations. (C) 1994 John Wiley & Sons, Inc.