Compatibilized polypropylene nanocomposites containing expanded graphite and graphene nanoplatelets

We present a non-covalent compatibilization approach to prepare polypropylene (PP) composites containing expanded graphite (EG) and graphene nanoplatelets (GNPs) by melt compounding. This method involves PP matrix functionalization with pyridine (Py) moieties, which are capable of engaging in pi-pi interactions with the surface of the EG and GNPs. The addition of 10 wt% of PP grafted with amino-pyridine (PP-g-Py) to neat PP facilitated the break-up of EG particles, by intercalating between their layers and facilitating their separation into smaller tactoids. GNPs were prepared starting from EG through a thermomechanical exfoliation method. Addition of GNPs to PP resulted in well-dispersed platelets having aspect ratios as high as 40, whereas in the presence of the PP-g-Py compatibilizer the matrix contained sub-micron scale platelets. The electrical percolation thresholds were in the vicinity of 6 and 10 vol% in the compatibilized PP-EG and PP-GNP composites, respectively, and the maximum value of the electrical conductivity achieved was 10(-1) S/m for the compatibilized GNP composites. Addition of GNPs resulted in increases in the flexural moduli by as much as 95% compared to the unfilled PP, whereas the impact strength remained unaffected up to 10 wt% GNP content.

Automated summary

A non-covalent compatibilization approach was utilized to prepare polypropylene composites containing expanded graphite and graphene nanoplatelets. Functionalizing the PP matrix with Py moieties facilitated the dispersion of EG and GNPs, with improved aspect ratios of the platelets. Electrical percolation thresholds were around 6% and 10%, with a maximum electrical conductivity achieved of 10(-1) S/m.