Polymer ''brushes'' are formed when long-chain molecules are somehow a
ttached by one end at an interface with a relatively small area per ch
ain. Such adsorbed brushes in the presence of solvent may be used to m
odify surface properties, stabilize colloidal particles, etc. Strongly
segregated block copolymer phases, or interfacial layers of such ''po
lymeric surfactants'' may also be modeled in terms of ''melt brushes,'
' (i.e., brushes without solvent). In both cases, when chain attachmen
ts are crowded on the interface, the chains stretch out to avoid neigh
boring chains. The resulting physical state has properties markedly di
fferent from polymer solutions, gels, or weakly adsorbed polymer layer
s. When the chains are strongly stretched, their statistical mechanics
become simpler, as fluctuations around the set of most probable confo
rmations are suppressed. This makes possible many pencil-and-paper cal
culations of brush properties, including bending and compressional mod
uli, and detailed knowledge of the chain conformations. As a recent ex
ample, I will describe calculations of phase diagrams of strongly segr
egated block copolymers including bicontinuous double-diamond phases.
(C) 1994 John Wiley and Sons, Inc.