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Bulk and interfacial behavior of nanoparticle/polymer blends.

Conference ·
OSTI ID:949006

We have investigated a model athermal system consisting of polystyrene (PS) nanoparticles (NPs) in PS melts. Neutron scattering shows that the chain dimensions expand in the presence of the NPs. We investigate this result theoretically using self-consistent PRISM theory, and also find an expansion in chain dimensions as a function of NP volume fraction. Recently it has been shown that nanoparticles can suppress dewetting in thin polymer films, a counterintuitive result since particles usually induce dewetting. Neutron reflectivity measurements have shown that the NPs phase separate to the surface, so one proposed mechanism for the inhibition of dewetting is that this segregation changes the surface energies. We calculate the density profiles for dilute NPs in polymer melts near a substrate using classical density functional theory, which shows that the NPs do indeed segregate to the surface.

Research Organization:
Sandia National Laboratories
Sponsoring Organization:
USDOE
DOE Contract Number:
AC04-94AL85000
OSTI ID:
949006
Report Number(s):
SAND2005-1883C
Country of Publication:
United States
Language:
English

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