Literature DB >> 16721503

Dramatic stiffening of ultrathin polymer films in the rubbery regime.

P A O'Connell1, G B McKenna.   

Abstract

Recently, we (P.A. O'Connell, G.B. McKenna, Science 307, 1760 (2005)) introduced a novel nano-bubble inflation method to measure the absolute creep compliance of nanometer thick polymer films. In that work it was shown that even at film thicknesses as small as 27.5nm the glass temperature was unchanged for poly(vinyl acetate) (PVAc). Perhaps more importantly, and the subject of the present work, was the observation that these ultrathin films show a dramatic stiffening in the rubbery plateau regime, i.e., the compliance was reduced by over two orders of magnitude compared to the bulk material. In the present work we substantiate the previous results in a study of the thickness dependence of the rubbery compliance of PVAc and polystyrene (PS) films for thicknesses from 13nm to 276nm. We show the substantial stiffening of the plateau region for both materials. Furthermore, the rubbery compliance (inverse of stiffness) scales with approximately the second power ( 1.8+/-0.2) in the film thickness for both materials.

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Year:  2006        PMID: 16721503     DOI: 10.1140/epje/i2005-10125-4

Source DB:  PubMed          Journal:  Eur Phys J E Soft Matter        ISSN: 1292-8941            Impact factor:   1.890


  14 in total

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9.  Confinement and processing effects on glass transition temperature and physical aging in ultrathin polymer films: novel fluorescence measurements.

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10.  Glass transition temperature of freely-standing films of atactic poly(methyl methacrylate).

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Journal:  Eur Phys J E Soft Matter       Date:  2003-11-05       Impact factor: 1.890

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  2 in total

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2.  Thin Film Elastic Modulus of Degradable Tyrosine-Derived Polycarbonate Biomaterials and Their Blends.

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