A four component clay-polymer-salt-water system, consisting of n-butyl
ammonium vermiculite, poly(ethylene oxide), n-butylammonium chloride,
and heavy water, was studied by neutron scattering. The volume fractio
n of clay in the system and the salt concentration were held constant,
at r = 0.01 and c = 0.1 M, respectively, and the volume fraction of p
olymer v was varied between 0 and 0.04. The addition of polymer, up to
v 0.04, had no effect on the phase transition temperature between the
tactoid and gel phases of the clay system. However, even for v values
as low as 0.001, the clay plates in the gel phase were more parallel
and more regularly spaced than in the system without added polymer. In
the gel phase, the lattice constant d along the swelling axis of the
clay colloid decreased as a function of the polymer volume fraction, f
rom 12 nm at v = 0 to 6 nm at v = 0.04. This behavior is qualitatively
similar to that observed in the vermiculite system with added poly(vi
nyl methyl ether). Possible mechanisms for the observed contraction ar
e discussed, including the possibility of bridging flocculation of the
clay plates. In one experiment, the d value in the gel phase was obse
rved to increase with temperature prior to collapse into the tactoid p
hase, which is a new effect that seems to depend on cycling of the sys
tem between the gel and tactoid phases.