Long-Term Aging in Miscible Polymer Nanocomposites

We find that the initial, solvent-cast state of nanoparticles (NPs) in a polymer matrix temporally evolves during thermal annealing such that, at steady state, NPs maximize their distance from each other subject to mass balance constraints. The observed timescales for this unexpected structural reor...

Full description

Saved in:
Bibliographic Details
Published inMacromolecules Vol. 55; no. 11; pp. 4502 - 4515
Main Authors Jhalaria, Mayank, Jimenez, Andrew M., Mathur, Reha, Tekell, Marshall C., Huang, Yucheng, Narayanan, Suresh, Benicewicz, Brian C., Kumar, Sanat K.
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 14.06.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:We find that the initial, solvent-cast state of nanoparticles (NPs) in a polymer matrix temporally evolves during thermal annealing such that, at steady state, NPs maximize their distance from each other subject to mass balance constraints. The observed timescales for this unexpected structural reorganization, as probed by small-angle X-ray scattering, are temperature-dependent and can be prohibitively large, especially at temperatures around and below 1.2T g. X-ray photon correlation spectroscopy measurements during reorganization reveal that the collective NP dynamics slow down with annealing at constant temperature; this is accompanied by changes in the low-frequency regime in macroscopic viscoelastic measurements in equilibrated materials. By ruling out other potential sources for these effects (i.e., electrostatic interactions, adsorbed layers), we attribute these results to a long-ranged repulsive force between the NPs caused by fluctuations in the polymer phase, i.e., the “anti-Casimir” effect proposed by Obhukhov and Semenov [ Long-range interactions in polymer melts: The anti-Casimir effect. Phys Rev Lett 2005, 95 (3), 038305]. Thus, our results highlight the important role of long-term, slow NP reorganization on the structure and, subsequently, the properties of polymer nanocomposites (PNCs), even in the case of nominally miscible polymer nanoparticle hybrids.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
AC02-06CH11357; DGE-2036197
USDOE Office of Science (SC), Basic Energy Sciences (BES)
National Science Foundation (NSF)
ISSN:0024-9297
1520-5835
1520-5835
DOI:10.1021/acs.macromol.2c00332