4.7 Article

Segmental dynamics and rheology of miscible poly(vinylidene fluoride)/poly(methyl methacrylate) (70/30 by weight) blend filled with titania or poly(methyl methacrylate)-grafted titania

Journal

COMPOSITES SCIENCE AND TECHNOLOGY
Volume 123, Issue -, Pages 39-48

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.compscitech.2015.11.031

Keywords

Nanoparticles; Polymer-matrix composites (PMCs); Surface treatments; Rheology; Dielectric relaxation

Funding

  1. National Natural Science Foundation of China [51003093, 51273173]
  2. Program for Zhejiang Provincial Innovative Research Team [2009R50004]
  3. Research Foundation of Education Bureau of Zhejiang Province [Y200908238]

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Titania (TiO2) or poly (methyl methacrylate) (PMMA)-grafted titania (TiO2-g-PMMA) were incorporated into miscible poly (vinylidene fluoride) (PVDF)/PMMA (70/30 by weight) blend by melt mixing. TiO2 particles exhibited aggregation in the composites as displayed by scanning electron microscopy observations and the storage modulus (G') plateau in the low frequency (omega) region. This is accompanied with the restriction of molecular mobility and the elevation of glass transition temperature (T-g). Conversely, TiO2-g-PMMA nanoparticles with well-defined cross-linked PMMA shells of 5 nm in thickness are well distributed in the matrix, without the influence on T-g and the appearance of low-omega plateau. The dispersion of TiO2 is not stable during the thermal annealing of the composite in the melt while the TiO2-g-PMMA nanoparticles demonstrate excellent dispersion stability. Broadband dielectric spectroscopies indicate that TiO2 influenced the molecular relaxations of alpha(a) and alpha(c), while the effect of TiO2-g-PMMA was negligible. Furthermore, the core shell structured TiO2-g-PMMA nanoparticles produced considerable smaller interfacial polarization than TiO2 in the composites. (C) 2015 Elsevier Ltd. All rights reserved.

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