Creep attenuation in glassy polymer nanocomposites with variable polymer-nanoparticle interactions.


Journal

Soft matter
ISSN: 1744-6848
Titre abrégé: Soft Matter
Pays: England
ID NLM: 101295070

Informations de publication

Date de publication:
07 Oct 2020
Historique:
pubmed: 9 9 2020
medline: 9 9 2020
entrez: 8 9 2020
Statut: ppublish

Résumé

The use of nanoparticle reinforced polymer matrices in continuous fiber composites for infrastructure applications requires a comprehensive understanding of viscoelastic creep. Critical parameters affecting the mechanical reinforcement offered by nanoparticles include nanoparticle size and concentration, as well as the interaction between the nanoparticle surface and polymer matrix. Here, we study the viscoelastic creep of nanocomposite systems comprised of glassy thermoplastic polymers and spherical silica nanoparticles of varying sizes and surface functionalization using a dynamic mechanical analysis (DMA) accelerated testing methodology. Significant differences in the nanoparticle dispersions in these nanocomposites were observed via transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) and are attributed to differences in the polymer-polymer and polymer-particle interaction strengths. The DMA measurements indicate a decrease in compliance at short times with increased nanoparticle loading that is largely independent of nanoparticle dispersion morphology and polymer-particle interaction strength. Conversely, long term creep behavior shows a much stronger dependence on these parameters with the creep onset time increasing by up to three orders of magnitude. For similar nanoparticle loadings, the time to critical deformation in systems with well-distributed, networked nanoparticle morphologies was larger by an order of magnitude compared to systems exhibiting strong nanoparticle aggregation. The networked systems delayed the time to critical deformation by three orders of magnitude over that of neat polymer. The increase in time to critical deformation is also greater in composites with smaller nanoparticles at similar loadings, which we attribute to the development of percolated nanoparticle networks. These results demonstrate the significant effects polymer-particle interactions and dispersion morphologies can have on the long-term creep compliance of thermoplastic nanocomposites.

Identifiants

pubmed: 32895688
doi: 10.1039/d0sm01247e
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8912-8924

Auteurs

C Francisco Buitrago (CF)

Department of Materials Science & Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA. winey@seas.upenn.edu.

James F Pressly (JF)

Department of Materials Science & Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA. winey@seas.upenn.edu.

Anita S Yang (AS)

Department of Chemical & Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.

Peter A Gordon (PA)

ExxonMobil Research and Engineering Company, Annandale, NJ 08801, USA. bharath.natarajan@exxonmobil.com.

Robert A Riggleman (RA)

Department of Chemical & Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.

Bharath Natarajan (B)

ExxonMobil Research and Engineering Company, Annandale, NJ 08801, USA. bharath.natarajan@exxonmobil.com.

Karen I Winey (KI)

Department of Materials Science & Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA. winey@seas.upenn.edu and Department of Chemical & Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.

Classifications MeSH