Journal
POLYMERS
Volume 9, Issue 10, Pages -Publisher
MDPI
DOI: 10.3390/polym9100548
Keywords
polyetherimides; crystallization; molecular dynamics; nanocomposite; pi-pi interactions
Categories
Funding
- Ministry of Education and Science of the Russian Federation (Government of the Russian Federation) [14.Z50.31.0002, 220]
- Army Research Office (ARO) [W911NF-16-R-0356]
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Crystallization of all-aromatic heterocyclic polymers typically results in an improvement of their thermo-mechanical properties. Nucleation agents may be used to promote crystallization, and it is well known that the incorporation of nanoparticles, and in particular carbon-based nanofillers, may induce or accelerate crystallization through nucleation. The present study addresses the structural properties of polyetherimide-based nanocomposites and the initial stages of polyetherimide crystallization as a result of single-walled carbon nanotube (SWCNT) incorporation. We selected two amorphous thermoplastic polyetherimides ODPA-P3 and aBPDA-P3 based on 3,3,4,4-oxydiphthalic dianhydride (ODPA), 2,3,3,4-biphenyltetracarboxylic dianhydride (aBPDA) and diamine 1,4-bis[4-(4-aminophenoxy)phenoxy]benzene (P3) and simulated the onset of crystallization in the presence of SWCNTs using atomistic molecular dynamics. For ODPA-P3, we found that the planar phthalimide and phenylene moieties show pronounced ordering near the CNT (carbon nanotube) surface, which can be regarded as the initial stage of crystallization. We will discuss two possible mechanisms for ODPA-P3 crystallization in the presence of SWCNTs: the spatial confinement caused by the CNTs and - interactions at the CNT-polymer matrix interface. Based on our simulation results, we propose that ODPA-P3 crystallization is most likely initiated by favorable - interactions between the carbon nanofiller surface and the planar ODPA-P3 phthalimide and phenylene moieties.
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