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Chain Entanglement in Thin Freestanding Polymer...
Journal article

Chain Entanglement in Thin Freestanding Polymer Films

Abstract

When a thin glassy film is strained uniaxially, a shear deformation zone (SDZ) can be observed. The ratio of the thickness of the SDZ to that of the undeformed film is related to the maximum extension ratio, lambda, which depends on the entanglement molecular weight, M(e). We have measured lambda as a function of film thickness in strained freestanding films of polystyrene as a probe of M(e) in confinement. It is found that thin films stretch further than thick films before failure, consistent with the interpretation that polymers in thin films are less entangled than bulk polymers, thus the effective value of M(e) in thin films is significantly larger than that of the bulk. Our results are well described by a conceptually simple model based on the probability of finding intermolecular entanglements near an interface.

Authors

Si L; Massa MV; Dalnoki-Veress K; Brown HR; Jones RAL

Journal

Physical Review Letters, Vol. 94, No. 12,

Publisher

American Physical Society (APS)

Publication Date

April 1, 2005

DOI

10.1103/physrevlett.94.127801

ISSN

0031-9007

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