Shear induced changes in the demixing conditions are discussed for the copo
lymer blends of the present type in terms of a distortion of quasichemical
equilibria established in the stagnant systems between the two different ki
nds of polymer segments. Calculations were performed in an attempt to ratio
nalize experimental results obtained with blends exhibiting upper critical
solution temperatures. The proposed model accounts for the experience that
the first observable effect of shear consists of an enlargement of the two-
phase regime (a behavior which differs fundamentally from that of homopolym
er blends or homopolymer solutions) and yields the correct order of magnitu
de for the effects. The influences of copolymer composition, number of segm
ents of the components, and temperature dependence of the Flory-Huggins int
eraction parameter are discussed in detail. Furthermore, it is demonstrated
how the present considerations relate to an earlier approach based on the
energy a system can store while it flows. (C) 1999 American Institute of Ph
ysics. [S0021-9606(99)50115-3].