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Improving thermal and mechanical properties of epoxy composites by using functionalized graphene
Perylene tetracarboxylic anhydride (PTCDA) was reacted with 6-aminocaproic acid to form the corresponding perylene bisimide (PBI). PBI was used as the foundation for oligomerisation of glycidol in a ring-opening reaction of glycidol leading to a hyper branched, water-soluble glycidol derivative of p...
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Published in: | RSC advances 2015-01, Vol.5 (74), p.60596-60607 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Perylene tetracarboxylic anhydride (PTCDA) was reacted with 6-aminocaproic acid to form the corresponding perylene bisimide (PBI). PBI was used as the foundation for 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 microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). PBI-HPG/RGO was blended at different loadings in order to improve the thermal and mechanical properties of epoxy composites. The maximum
T
g
of the epoxy composites was about 20 °C and the decomposition temperature (
T
d
) was 26 °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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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C5RA09410K |