K. Eskilsson et al., Effects of adsorption of low-molecular-weight triblock copolymers on interactions between hydrophobic surfaces in water, LANGMUIR, 15(9), 1999, pp. 3242-3249
in this work, we report on the interaction forces between hydrophobed silic
a surfaces immersed in polymer solutions. The polymers studied were a serie
s of poly(ethylene oxide)-polytetrahydrofuranpoly(ethylene oxide) (PEO-PTHF
-PEO) triblock copolymers and a poly(ethylene oxide) homopolymer. The inter
action forces were measured by the interfacial gauge technique. We show how
the interactions are changed by the adsorbed state of the copolymers. This
depends on both the copolymer concentration and the adsorption time. Above
a critical surface coverage, the interaction between approaching surfaces
at first shows a steric repulsion due to overlap of the adsorbed polymer la
yers. This repulsion increases as the distance between the surfaces decreas
es. In this regime the energy-distance curve could be accounted for by the
theory of grafted polymer brushes of de Gennes. However, for small surface-
to-surface distances the interaction curves do not follow this prediction.
Instead, the repulsion stabilized at a more or less constant level with dec
reasing intersurface separation. Finally, however, hard wall contact was es
tablished between the two surfaces. We infer that adsorbed copolymers to a
large extent are expelled from the gap between the surfaces in this small s
urface-to-surface distance range. The force needed to expel copolymers from
the intersurface gap was shown to be equal to the surface pressure at the
solid-liquid interface. We also studied the influence of the rate of approa
ch and the separation of the surfaces on the energy-distance curves The pro
cess of expelling polymers from the surface-to-surface gap was shown to dep
end on the velocity of the approaching surfaces and the surface coverage. F
or high approach rates and/or large surface coverages, the lateral mobility
of the polymers was such that it inhibited the expulsion process of polyme
rs from the gap. However, rapidly repeated force curves, measured at a cons
tant rate, and successively, were found to be perfectly reproducible.