4.8 Article

Wetting-Dewetting and Dispersion Aggregation Transitions Are Distinct for Polymer Grafted Nanoparticles in Chemically Dissimilar Polymer Matrix

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 33, Pages 10624-10631

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b05291

Keywords

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Funding

  1. U.S. Department of Energy [DE-SC0003912]
  2. NSF graduate fellowship [DGE 1144083]
  3. ExxonMobil Chemical Company
  4. National Science Foundation [NSF DMR 1040446, DMR-0944772]
  5. U.S. Department of Energy (DOE) [DE-SC0003912] Funding Source: U.S. Department of Energy (DOE)

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Simulations and experiments are conducted on mixtures containing polymer grafted nanoparticles in a chemically distinct polymer matrix, where the graft and matrix polymers exhibit attractive enthalpic interactions at low temperatures that become progressively repulsive as temperature is increased. Both coarse-grained molecular dynamics simulations, and X-ray scattering and neutron scattering experiments with deuterated polystyrene (dPS) grafted silica and poly(vinyl methyl ether) PVME matrix show that the sharp phase transition from (mixed) dispersed to (demixed) aggregated morphologies due to the increasingly repulsive effective interactions between the blend components is distinct from the continuous wetting-dewetting transition. Strikingly, this is unlike the extensively studied chemically identical graft-matrix composites, where the two transitions have been considered to be synonymous, and is also unlike the free (ungrafted) blends of the same graft and matrix homopolymers, where the wetting-dewetting is a sharp transition coinciding with the macrophase separation.

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