Perylene tetracarboxylic anhydride (PTCDA) was reacted with 6-aminocaproic acid to form the corresponding perylene bisimide (PBI). PBI was used as foundation an oligomerisation of glycidol in a ring-opening reaction of glycidol leading to a hyper branched, water soluble glycidol derivative of perylene (PBI-HPG). PBI-HPG was bound to the reduced graphene oxide via π-π stacking resulting in a compound termed PBI-HPG/RGO. The structure and morphology of PBI-HPG/RGO were investigated by infrared spectroscopy (FT-IR), wide angle X-ray diffractometry (WAXD), transmission electron microscopy (TEM), atomic force microscope (AFM) and X-ray photoelectron spectroscopy (XPS). PBI-HPG/RGO was blended into at different loadings in order to improve the thermal and mechanical properties of epoxy composites. The maximum Tg of the epoxy composites was about 20 o C and the decomposition temperature (Td) was 26 o C higher than that of neat epoxy. The incorporation of PBI-HPG/RGO yields a material with an impact strength of 39.6 KJ/m 2 and a tensile strength at 0.7 wt%. It increased by 50.8% and 62.3%, respectively, compared to the neat epoxy.
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RSC Adv.2 | RSC Adv., 2015, 00, 1-3This journal is